A valve situated at the entrance to the pulmonary trunk from the right ventricle.
The pathologic narrowing of the orifice of the PULMONARY VALVE. This lesion restricts blood outflow from the RIGHT VENTRICLE to the PULMONARY ARTERY. When the trileaflet valve is fused into an imperforate membrane, the blockage is complete.
Backflow of blood from the PULMONARY ARTERY into the RIGHT VENTRICLE due to imperfect closure of the PULMONARY VALVE.
The valve between the left ventricle and the ascending aorta which prevents backflow into the left ventricle.
A combination of congenital heart defects consisting of four key features including VENTRICULAR SEPTAL DEFECTS; PULMONARY STENOSIS; RIGHT VENTRICULAR HYPERTROPHY; and a dextro-positioned AORTA. In this condition, blood from both ventricles (oxygen-rich and oxygen-poor) is pumped into the body often causing CYANOSIS.
Pathological conditions involving any of the various HEART VALVES and the associated structures (PAPILLARY MUSCLES and CHORDAE TENDINEAE).
The valve between the left atrium and left ventricle of the heart.
The valve consisting of three cusps situated between the right atrium and right ventricle of the heart.
A congenital heart defect characterized by the narrowing or complete absence of the opening between the RIGHT VENTRICLE and the PULMONARY ARTERY. Lacking a normal PULMONARY VALVE, unoxygenated blood in the right ventricle can not be effectively pumped into the lung for oxygenation. Clinical features include rapid breathing, CYANOSIS, right ventricle atrophy, and abnormal heart sounds (HEART MURMURS).
Animals produced by the mating of progeny over multiple generations. The resultant strain of animals is virtually identical genotypically. Highly inbred animal lines allow the study of certain traits in a relatively pure form. (Segen, Dictionary of Modern Medicine, 1992)
A pathological constriction that can occur above (supravalvular stenosis), below (subvalvular stenosis), or at the AORTIC VALVE. It is characterized by restricted outflow from the LEFT VENTRICLE into the AORTA.
Occlusion of the outflow tract in either the LEFT VENTRICLE or the RIGHT VENTRICLE of the heart. This may result from CONGENITAL HEART DEFECTS, predisposing heart diseases, complications of surgery, or HEART NEOPLASMS.
Prosthesis, usually heart valve, composed of biological material and whose durability depends upon the stability of the material after pretreatment, rather than regeneration by host cell ingrowth. Durability is achieved 1, mechanically by the interposition of a cloth, usually polytetrafluoroethylene, between the host and the graft, and 2, chemically by stabilization of the tissue by intermolecular linking, usually with glutaraldehyde, after removal of antigenic components, or the use of reconstituted and restructured biopolymers.
Surgical insertion of synthetic material to repair injured or diseased heart valves.
Pathological condition characterized by the backflow of blood from the ASCENDING AORTA back into the LEFT VENTRICLE, leading to regurgitation. It is caused by diseases of the AORTIC VALVE or its surrounding tissue (aortic root).
Use or insertion of a tubular device into a duct, blood vessel, hollow organ, or body cavity for injecting or withdrawing fluids for diagnostic or therapeutic purposes. It differs from INTUBATION in that the tube here is used to restore or maintain patency in obstructions.
A device that substitutes for a heart valve. It may be composed of biological material (BIOPROSTHESIS) and/or synthetic material.
Cardiac manifestation of gastrointestinal CARCINOID TUMOR that metastasizes to the liver. Substances secreted by the tumor cells, including SEROTONIN, promote fibrous plaque formation in ENDOCARDIUM and its underlying layers. These deposits cause distortion of the TRICUSPID VALVE and the PULMONARY VALVE eventually leading to STENOSIS and valve regurgitation.
Procedures in which placement of CARDIAC CATHETERS is performed for therapeutic or diagnostic procedures.
Developmental abnormalities in any portion of the VENTRICULAR SEPTUM resulting in abnormal communications between the two lower chambers of the heart. Classification of ventricular septal defects is based on location of the communication, such as perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular defect.
A type of heart valve surgery that involves the repair, replacement, or reconstruction of the annuli of HEART VALVES. It includes shortening the circumference of the annulus to improve valve closing capacity and reinforcing the annulus as a step in more complex valve repairs.
Widening of a stenosed HEART VALVE by the insertion of a balloon CATHETER into the valve and inflation of the balloon.
Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life.
Ultrasonic recording of the size, motion, and composition of the heart and surrounding tissues. The standard approach is transthoracic.
Narrowing below the PULMONARY VALVE or well below it in the infundibuluar chamber where the pulmonary artery originates, usually caused by a defective VENTRICULAR SEPTUM or presence of fibrous tissues. It is characterized by restricted blood outflow from the RIGHT VENTRICLE into the PULMONARY ARTERY, exertional fatigue, DYSPNEA, and chest discomfort.
Backflow of blood from the RIGHT VENTRICLE into the RIGHT ATRIUM due to imperfect closure of the TRICUSPID VALVE.
The short wide vessel arising from the conus arteriosus of the right ventricle and conveying unaerated blood to the lungs.
Backflow of blood from the LEFT VENTRICLE into the LEFT ATRIUM due to imperfect closure of the MITRAL VALVE. This can lead to mitral valve regurgitation.
The hemodynamic and electrophysiological action of the right HEART VENTRICLE.
Surgery performed on the heart.
Inflammation of the inner lining of the heart (ENDOCARDIUM), the continuous membrane lining the four chambers and HEART VALVES. It is often caused by microorganisms including bacteria, viruses, fungi, and rickettsiae. Left untreated, endocarditis can damage heart valves and become life-threatening.
Flaps of tissue that prevent regurgitation of BLOOD from the HEART VENTRICLES to the HEART ATRIA or from the PULMONARY ARTERIES or AORTA to the ventricles.
Abnormal protrusion or billowing of one or both of the leaflets of MITRAL VALVE into the LEFT ATRIUM during SYSTOLE. This allows the backflow of blood into left atrium leading to MITRAL VALVE INSUFFICIENCY; SYSTOLIC MURMURS; or CARDIAC ARRHYTHMIA.
Inflammation of the ENDOCARDIUM caused by BACTERIA that entered the bloodstream. The strains of bacteria vary with predisposing factors, such as CONGENITAL HEART DEFECTS; HEART VALVE DISEASES; HEART VALVE PROSTHESIS IMPLANTATION; or intravenous drug use.
Flaps within the VEINS that allow the blood to flow only in one direction. They are usually in the medium size veins that carry blood to the heart against gravity.
Narrowing of the passage through the MITRAL VALVE due to FIBROSIS, and CALCINOSIS in the leaflets and chordal areas. This elevates the left atrial pressure which, in turn, raises pulmonary venous and capillary pressure leading to bouts of DYSPNEA and TACHYCARDIA during physical exertion. RHEUMATIC FEVER is its primary cause.
The plan and delineation of prostheses in general or a specific prosthesis.
Measurement of intracardiac blood flow using an M-mode and/or two-dimensional (2-D) echocardiogram while simultaneously recording the spectrum of the audible Doppler signal (e.g., velocity, direction, amplitude, intensity, timing) reflected from the moving column of red blood cells.
A genetically heterogeneous, multifaceted disorder characterized by short stature, webbed neck, ptosis, skeletal malformations, hypertelorism, hormonal imbalance, CRYPTORCHIDISM, multiple cardiac abnormalities (most commonly including PULMONARY VALVE STENOSIS), and some degree of INTELLECTUAL DISABILITY. The phenotype bears similarities to that of TURNER SYNDROME that occurs only in females and has its basis in a 45, X karyotype abnormality. Noonan syndrome occurs in both males and females with a normal karyotype (46,XX and 46,XY). Mutations in a several genes (PTPN11, KRAS, SOS1, NF1 and RAF1) have been associated the the NS phenotype. Mutations in PTPN11 are the most common. LEOPARD SYNDROME, a disorder that has clinical features overlapping those of Noonan Syndrome, is also due to mutations in PTPN11. In addition, there is overlap with the syndrome called neurofibromatosis-Noonan syndrome due to mutations in NF1.
The pathologic narrowing of the orifice of the TRICUSPID VALVE. This hinders the emptying of RIGHT ATRIUM leading to elevated right atrial pressure and systemic venous congestion. Tricuspid valve stenosis is almost always due to RHEUMATIC FEVER.
The heart of the fetus of any viviparous animal. It refers to the heart in the postembryonic period and is differentiated from the embryonic heart (HEART/embryology) only on the basis of time.
Evaluation undertaken to assess the results or consequences of management and procedures used in combating disease in order to determine the efficacy, effectiveness, safety, and practicability of these interventions in individual cases or series.
A condition in which the RIGHT VENTRICLE of the heart was functionally impaired. This condition usually leads to HEART FAILURE or MYOCARDIAL INFARCTION, and other cardiovascular complications. Diagnosis is made by measuring the diminished ejection fraction and a depressed level of motility of the right ventricular wall.
Absence of the orifice between the RIGHT ATRIUM and RIGHT VENTRICLE, with the presence of an atrial defect through which all the systemic venous return reaches the left heart. As a result, there is left ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR) because the right ventricle is absent or not functional.
A condition of abnormally low AMNIOTIC FLUID volume. Principal causes include malformations of fetal URINARY TRACT; FETAL GROWTH RETARDATION; GESTATIONAL HYPERTENSION; nicotine poisoning; and PROLONGED PREGNANCY.
The lower right and left chambers of the heart. The right ventricle pumps venous BLOOD into the LUNGS and the left ventricle pumps oxygenated blood into the systemic arterial circulation.
The protrusion of an organ or part of an organ into a natural or artificial orifice.
A repeat operation for the same condition in the same patient due to disease progression or recurrence, or as followup to failed previous surgery.
Studies in which individuals or populations are followed to assess the outcome of exposures, procedures, or effects of a characteristic, e.g., occurrence of disease.
The visualization of tissues during pregnancy through recording of the echoes of ultrasonic waves directed into the body. The procedure may be applied with reference to the mother or the fetus and with reference to organs or the detection of maternal or fetal disease.
An infant during the first month after birth.
Echocardiography applying the Doppler effect, with the superposition of flow information as colors on a gray scale in a real-time image.
A benign tumor of fibrous or fully developed connective tissue.
Ultrasonic recording of the size, motion, and composition of the heart and surrounding tissues using a transducer placed in the esophagus.
Abnormalities in any part of the HEART SEPTUM resulting in abnormal communication between the left and the right chambers of the heart. The abnormal blood flow inside the heart may be caused by defects in the ATRIAL SEPTUM, the VENTRICULAR SEPTUM, or both.
The movement and the forces involved in the movement of the blood through the CARDIOVASCULAR SYSTEM.
The muscular structure separating the right and the left lower chambers (HEART VENTRICLES) of the heart. The ventricular septum consists of a very small membranous portion just beneath the AORTIC VALVE, and a large thick muscular portion consisting of three sections including the inlet septum, the trabecular septum, and the outlet septum.
ENDOCARDIUM infection that is usually caused by STREPTOCOCCUS. Subacute infective endocarditis evolves over weeks and months with modest toxicity and rare metastatic infection.
This structure includes the thin muscular atrial septum between the two HEART ATRIA, and the thick muscular ventricular septum between the two HEART VENTRICLES.
'Abnormalities, Multiple' is a broad term referring to the presence of two or more structural or functional anomalies in an individual, which may be genetic or environmental in origin, and can affect various systems and organs of the body.
A fetal blood vessel connecting the pulmonary artery with the descending aorta.
Enlargement of the RIGHT VENTRICLE of the heart. This increase in ventricular mass is often attributed to PULMONARY HYPERTENSION and is a contributor to cardiovascular morbidity and mortality.
Pathophysiological conditions of the FETUS in the UTERUS. Some fetal diseases may be treated with FETAL THERAPIES.
Tumors in any part of the heart. They include primary cardiac tumors and metastatic tumors to the heart. Their interference with normal cardiac functions can cause a wide variety of symptoms including HEART FAILURE; CARDIAC ARRHYTHMIAS; or EMBOLISM.
A type of heart valve surgery that involves the repair, replacement, or reconstruction of the annulus of the MITRAL VALVE. It includes shortening the circumference of the annulus to improve valve closing capacity and reinforcing the annulus as a step in more complex valve repairs.
Studies used to test etiologic hypotheses in which inferences about an exposure to putative causal factors are derived from data relating to characteristics of persons under study or to events or experiences in their past. The essential feature is that some of the persons under study have the disease or outcome of interest and their characteristics are compared with those of unaffected persons.
Developmental abnormalities in any portion of the ATRIAL SEPTUM resulting in abnormal communications between the two upper chambers of the heart. Classification of atrial septal defects is based on location of the communication and types of incomplete fusion of atrial septa with the ENDOCARDIAL CUSHIONS in the fetal heart. They include ostium primum, ostium secundum, sinus venosus, and coronary sinus defects.
Echocardiography amplified by the addition of depth to the conventional two-dimensional ECHOCARDIOGRAPHY visualizing only the length and width of the heart. Three-dimensional ultrasound imaging was first described in 1961 but its application to echocardiography did not take place until 1974. (Mayo Clin Proc 1993;68:221-40)
Pathologic processes that affect patients after a surgical procedure. They may or may not be related to the disease for which the surgery was done, and they may or may not be direct results of the surgery.
A congenital cardiovascular malformation in which the AORTA arises entirely from the RIGHT VENTRICLE, and the PULMONARY ARTERY arises from the LEFT VENTRICLE. Consequently, the pulmonary and the systemic circulations are parallel and not sequential, so that the venous return from the peripheral circulation is re-circulated by the right ventricle via aorta to the systemic circulation without being oxygenated in the lungs. This is a potentially lethal form of heart disease in newborns and infants.
Elements of limited time intervals, contributing to particular results or situations.
Endoscopic examination, therapy or surgery of the fetus and amniotic cavity through abdominal or uterine entry.
A conical fibro-serous sac surrounding the HEART and the roots of the great vessels (AORTA; VENAE CAVAE; PULMONARY ARTERY). Pericardium consists of two sacs: the outer fibrous pericardium and the inner serous pericardium. The latter consists of an outer parietal layer facing the fibrous pericardium, and an inner visceral layer (epicardium) resting next to the heart, and a pericardial cavity between these two layers.
The dilatation of the aortic wall behind each of the cusps of the aortic valve.
The act of dilating.
A birth defect characterized by the narrowing of the AORTA that can be of varying degree and at any point from the transverse arch to the iliac bifurcation. Aortic coarctation causes arterial HYPERTENSION before the point of narrowing and arterial HYPOTENSION beyond the narrowed portion.
Studies to determine the advantages or disadvantages, practicability, or capability of accomplishing a projected plan, study, or project.
A value equal to the total volume flow divided by the cross-sectional area of the vascular bed.
Radiography of blood vessels after injection of a contrast medium.

Investigation of the theory and mechanism of the origin of the second heart sound. (1/356)

To investigate further the origin of the second heart sound we studied human subjects, dogs, and a model in vitro of the cardiovascular system. Intra-arterial sound, pressure, and, where possible, flow and high speed cine (2,000 frames/sec) were utilized. The closure sound of the semilunar valves was of higher amplitude in be ventricles than in their respective arterial cavities. The direction of inscription of the main components of intra-arterial sound were opposite in direction to the components of intraventricular sound. Notches, representative of pressure increments, were noted on the ventricular pressure tracings and were coincident with the components of sound. The amplitude of the closure sound varied with diastolic pressure, but remained unchanged with augmentation of forward and retrograde aortic flow. Cines showed second sound to begin after complete valvular closure, and average leaflet closure rate was constant regardless of pressure. Hence, the semilunar valves, when closed, act as an elastic membrane and, when set into motion, generate compression and expansion of the blood, producing transient pressure changes indicative of sound. The magnitude of the initial stretch is related to the differential pressure between the arterial and ventricular chambers. Sound transients which follow the major components of the second sound appear to be caused by the continuing stretch and recoil of the leaflets. Clinically unexplained findings such as the reduced or absent second sound in calcific aortic stenosis and its paradoxical presence in congenital aortic stenosis may be explained by those observations.  (+info)

Noninvasive evaluation of pulmonary capillary wedge pressure in patients with acute myocardial infarction by deceleration time of pulmonary venous flow velocity in diastole. (2/356)

OBJECTIVES: This study investigates the correlation between deceleration time of diastolic pulmonary venous flow (PV-DT) and of early filling mitral flow (LV-DT), and pulmonary capillary wedge pressure (PCWP) in patients with acute myocardial infarction (AMI). BACKGROUND: An earlier study suggests that Doppler-derived LV-DT provides an accurate means of estimating PCWP in postinfarction patients with left ventricular systolic dysfunction. Furthermore, recent studies have suggested that PCWP correlates better with PV-DT than with LV-DT. However, the value of PV-DT and LV-DT for assessment of PCWP in patients with AMI has not been evaluated. METHODS: In 141 consecutive patients with AMI, we measured PV-DT and LV-DT by Doppler echocardiography, and compared these variables with PCWP measured using a Swan-Ganz catheter. RESULTS: There was a weak negative correlation between the LV-DT and PCWP (r = -0.54). Although the sensitivity of < or =130 ms in LV-DT in predicting > or =18 mm Hg in PCWP was high (86%), its specificity was low (59%). On the other hand, a very close negative correlation was found between PV-DT and PCWP (r = -0.89). The sensitivity and specificity of < or =160 ms in PV-DT in predicting > or =18 mm Hg in PCWP were 97% and 96%, respectively. CONCLUSIONS: In patients with AMI, Doppler-derived PV-DT showed a stronger correlation with PCWP than LV-DT.  (+info)

Pulmonary ventricular outflow reconstruction with a size-reduced cryopreserved pulmonary valve allograft: mid-term follow-up. (3/356)

Surgical reduction of pulmonary allografts is being performed because of the shortage of allografts of suitable size for pediatric use. However, the outcome of size-reduced pulmonary allografts for pulmonary conduits is unknown. In the present study, cryopreserved pulmonary allografts harvested from adults at the time of kidney donation were size-reduced and used in 4 children, 2 with pulmonary atresia and ventricular septal defect and 2 with atrioventricular discordance, pulmonary atresia and ventricular septal defect. They all had undergone right and/or left modified Blalock-Taussig shunt operations with a 5-mm synthetic graft prior to the reparative operations. They underwent definitive repair with a size-reduced cryopreserved pulmonary allograft valved conduit and were followed up for 2-5 years. Postoperative echocardiographic and cineangiographic assessments revealed excellent function of the pulmonary bicuspidalized valves with a minimal pressure gradient and no, or only trivial, regurgitation. Although the long-term result of a cryopreserved bicuspid pulmonary valved conduit remains unknown, the remodeled bicuspid pulmonary allograft conduits showed excellent hemodynamic characteristics in mid-term follow-up and appear to be a reasonable alternative to other types of conduits when an appropriate-sized allograft is not available.  (+info)

Accumulation of oxidized LDL in human semilunar valves correlates with coronary atherosclerosis. (4/356)

OBJECTIVE: Recent data indicate that oxidized low-density lipoprotein (ox-LDL) has several proatherogenic effects, e.g. induction of macrophage chemoattractants, adhesion molecules, cytokines, type-1 plasminogen activator inhibitor and platelet-derived growth factor A-chain by smooth muscle cells. Therefore, ox-LDL has been utilized as a marker of oxidative modification of proteins in atherosclerosis. Because heart valves consist of smooth muscle cells, fibroblasts and endothelial cells, and because valvular disease and coronary atherosclerosis could result from similar biological processes, we investigated ox-LDL accumulation in isolated aortic and pulmonary valves and coronary arteries from patients with angiographically proven coronary heart disease (CHD, n = 19), patients with idiopathic congestive heart failure (IDCM = idiopathic dilated cardiomyopathy, n = 20), and transplant donors. METHODS: Masson-Goldner staining and immunohistochemistry utilizing anti ox-LDL and CD68 were performed on paraffin sections of freshly isolated semilunar valves. Data were analyzed by digital image planimetry and by visual scoring of staining intensity. RESULTS: Ox-LDL immunoreactivity was identified in the vascular aspect of the attachment line, in the deep valve stroma, and in the ventricular and vascular endothelium of the semilunar valves, colocalizing with macrophages. Valvular ox-LDL area was significantly increased in CHD-patients (P < 0.03) and IDCM-patients (P < 0.04) compared with controls. More ox-LDL was accumulating in the pulmonary valves than in the aortic valves (P = 0.04) as assessed by area and staining intensity. Valvular ox-LDL area in pulmonary valve and aortic valve was significantly correlated with ox-LDL accumulation in the intimal layer (P < 0.001) and medial layer (P < 0.001) of coronary arteries from the same patients. CONCLUSION: The data suggest that the biological process leading to ox-LDL accumulation in coronary atherosclerosis also involves heart valves. Therefore, accumulation of the oxidative stress marker ox-LDL in heart valves illustrates atherosclerosis as an additional mechanisms accelerating valvular degeneration in these patients.  (+info)

The Ross operation: initial Israeli experience. (5/356)

BACKGROUND: The need for aortic valve replacement in children and young adults poses a special problem to cardiologists and surgeons. Replacing the sick aortic valve with the patient's pulmonary valve as described by Ross has proven to be a good option in this special age group. OBJECTIVE: To review our initial experience in order to assess the short-term results. METHODS: From January 1996 to June 1999, 40 patients (age 8 months to 41 years) underwent aortic valve replacement with pulmonary autograft. Indications for surgery were congenital aortic valve disease in 30 patients, bacterial endocarditis in 5, rheumatic fever in 3, and complex left ventricular outflow tract obstruction in 3. Trans-esophageal echocardiography was performed preoperatively and post-bypass in all patients, and transthoracic echocardiography was done prior to discharge and on follow-up. RESULTS: There was no preoperative or late mortality. All patients remain in functional class I (New York Heart Association) and are free of complications and medication. None showed progression of autograft insufficiency or LVOT obstruction. Homograft insufficiency in the pulmonary position has progressed from mild to moderate in one patient, and three developed mild homograft stenosis. CONCLUSIONS: The Ross procedure can be performed with good results in the young population and is considered an elegant surgical alternative to prosthetic values and homografts.  (+info)

Transcatheter implantation of a bovine valve in pulmonary position: a lamb study. (6/356)

BACKGROUND: Pulmonary regurgitation can lead to severe right ventricular dysfunction, which is a delicate postoperative problem in the long-term follow-up of patients who had surgery for congenital heart diseases. Clinical conditions of patients suffering from pulmonary valve incompetence are improved by valve replacement with a prosthetic valve. To date, the surgical approach is the only option to replace a pulmonary valve. We report the first experience of percutaneous pulmonary valve implantation. METHODS AND RESULTS: A fresh bovine jugular vein containing a native valve was sutured into a vascular stent and then cross-linked with a 0.6% glutaraldehyde solution for 36 hours. After being hand-crimped onto a balloon catheter, the device was inserted percutaneously according to standard stent-placing techniques. The valved stent was finally deployed in the position of the native pulmonary valve of the lamb. Hemodynamic evaluation was carried out before and 2 months after implantation. Anatomic evaluation was finally performed. Percutaneous pulmonary valve replacement was successful in 5 lambs. No complications were noted. Early and late angiographic and hemodynamic studies confirmed a good position of the stents with a competent valve at the end of the protocol. One stent was slightly stenotic, with macroscopically visible calcifications. CONCLUSIONS: Nonsurgical implantation of pulmonary valves is possible in the lamb. This new technique is similar to standard stent implantation. Thus, it should be feasible in humans, in whom it will lead to a significant reduction of reoperations in patients in need of pulmonary valve replacement.  (+info)

Tissue Doppler imaging consistently detects myocardial contraction and relaxation abnormalities, irrespective of cardiac hypertrophy, in a transgenic rabbit model of human hypertrophic cardiomyopathy. (7/356)

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is diagnosed clinically by the presence of left ventricular hypertrophy (LVH). However, LVH is absent in a significant number of genotype-positive patients. Because myocyte dysfunction and disarray are the primary abnormalities in HCM, we reasoned that tissue Doppler imaging could identify contraction and relaxation abnormalities, irrespective of hypertrophy, in a transgenic rabbit model of human HCM. METHODS AND RESULTS: M-mode, 2D, Doppler echocardiography and tissue Doppler imaging were performed in nontransgenic (n=24), wild-type beta-myosin heavy chain-arginine(403) (n=14), and mutant beta-myosin heavy chain-glutamic acid(403) (n=24) transgenic rabbits. Mean septal thicknesses were 2.0+/-0.3, 2.0+/-0.25, and 2.75+/-0.3 mm in the 3 groups, respectively (P:=0.001). LVH was absent in 9 of the 24 mutant rabbits. Left ventricular dimensions, systolic function, heart rate, mitral inflow velocities, and time intervals were similar in the groups. However, the difference between atrial reversal and transmitral A wave duration was increased in the mutant rabbits (P:<0.001). More importantly, systolic and early diastolic tissue Doppler velocities were significantly lower in all mutant rabbits (7.45+/-2.2 versus 10.8+/-2.3 cm/s in nontransgenic and 9. 0+/-0.76 cm/s in wild-type; P:<0.001), including the 9 without LVH. A systolic velocity <8.5 cm/s had an 86% sensitivity and 100% specificity in identifying the mutant transgenic rabbits. CONCLUSIONS: Myocardial contraction and relaxation were reduced in the mutant beta-myosin heavy chain-glutamic acid(403) transgenic rabbit model of human HCM, irrespective of the presence or absence of LVH. In addition, tissue Doppler imaging is more sensitive than conventional echocardiography for HCM screening.  (+info)

Pulmonary valve replacement in adults late after repair of tetralogy of fallot: are we operating too late? (8/356)

OBJECTIVES: The purpose of this study is to evaluate right ventricular (RV) volume and function after pulmonary valve replacement (PVR) and to address the issue of optimal surgical timing in these patients. BACKGROUND: Chronic pulmonary regurgitation (PR) following repair of tetralogy of Fallot (TOF) leads to RV dilation and an increased incidence of sudden cardiac death in adult patients. METHODS: We studied 25 consecutive adult patients who underwent PVR for significant PR late after repair of TOF. Radionuclide angiography was performed in all at a mean of 8.2 months (+/- 8 months) before PVR and repeated at a mean of 28.0 months (+/- 22.8 months) after the operation. Right ventricular (RV) end-systolic volume (RVESV), RV end-diastolic volume (RVEDV) and RV ejection fraction (RVEF) were measured. RESULTS: Mean RVEDV, RVESV and RVEF remained unchanged after PVR (227.1 ml versus 214.9 ml, p = 0.74; 157.4 ml versus 155.4 ml, p = 0.94; 35.6% versus 34.7%, p = 0.78, respectively). Of the 10 patients with RVEF > or = 0.40 before PVR, 5 patients (50%) maintained a RVEF > or = 0.40 following PVR, whereas only 2 out of 15 patients (13%) with pre-operative values <0.40 reached an RVEF > or = 0.40 postoperatively (p < 0.001). CONCLUSIONS: Right ventricular recovery following PVR for chronic significant pulmonary regurgitation after repair of TOF may be compromised in the adult population. In order to maintain adequate RV contractility, pulmonary valve implant in these patients should be considered before RV function deteriorates.  (+info)

The pulmonary valve, also known as the pulmonic valve, is a semilunar valve located at the exit of the right ventricle of the heart and the beginning of the pulmonary artery. It has three cusps or leaflets that prevent the backflow of blood from the pulmonary artery into the right ventricle during ventricular diastole, ensuring unidirectional flow of blood towards the lungs for oxygenation.

Pulmonary Valve Stenosis is a cardiac condition where the pulmonary valve, located between the right ventricle and the pulmonary artery, has a narrowed opening. This stenosis (narrowing) can cause obstruction of blood flow from the right ventricle to the lungs. The narrowing can be caused by a fusion of the valve leaflets, thickened or calcified valve leaflets, or rarely, a dysplastic valve.

The severity of Pulmonary Valve Stenosis is classified based on the gradient pressure across the valve, which is measured during an echocardiogram. A mild stenosis has a gradient of less than 30 mmHg, moderate stenosis has a gradient between 30-59 mmHg, and severe stenosis has a gradient of 60 mmHg or higher.

Mild Pulmonary Valve Stenosis may not require treatment, while more severe cases may need to be treated with balloon valvuloplasty or surgical valve replacement. If left untreated, Pulmonary Valve Stenosis can lead to right ventricular hypertrophy, heart failure, and other complications.

Pulmonary Valve Insufficiency, also known as Pulmonary Regurgitation, is a cardiac condition in which the pulmonary valve located between the right ventricle and the pulmonary artery does not close properly. This leads to the backward leakage or regurgitation of blood from the pulmonary artery into the right ventricle during diastole, causing an increased volume load on the right ventricle.

The severity of Pulmonary Valve Insufficiency can vary from mild to severe and may be caused by congenital heart defects, infective endocarditis, Marfan syndrome, rheumatic heart disease, or as a result of aging, or following certain cardiac procedures such as pulmonary valvotomy or ventriculostomy.

Mild Pulmonary Valve Insufficiency may not cause any symptoms and may only require periodic monitoring. However, severe Pulmonary Valve Insufficiency can lead to right-sided heart failure, arrhythmias, and other complications if left untreated. Treatment options for Pulmonary Valve Insufficiency include medication, surgical repair or replacement of the pulmonary valve, or a combination of these approaches.

The aortic valve is the valve located between the left ventricle (the lower left chamber of the heart) and the aorta (the largest artery in the body, which carries oxygenated blood from the heart to the rest of the body). It is made up of three thin flaps or leaflets that open and close to regulate blood flow. During a heartbeat, the aortic valve opens to allow blood to be pumped out of the left ventricle into the aorta, and then closes to prevent blood from flowing back into the ventricle when it relaxes. Any abnormality or damage to this valve can lead to various cardiovascular conditions such as aortic stenosis, aortic regurgitation, or infective endocarditis.

Tetralogy of Fallot is a congenital heart defect that consists of four components: ventricular septal defect (a hole between the lower chambers of the heart), pulmonary stenosis (narrowing of the pulmonary valve and outflow tract), overriding aorta (the aorta lies directly over the ventricular septal defect), and right ventricular hypertrophy (thickening of the right ventricular muscle). This condition results in insufficient oxygenation of the blood, leading to cyanosis (bluish discoloration of the skin and mucous membranes) and other symptoms such as shortness of breath, fatigue, and poor growth. Treatment typically involves surgical repair, which is usually performed during infancy or early childhood.

Heart valve diseases are a group of conditions that affect the function of one or more of the heart's four valves (tricuspid, pulmonic, mitral, and aortic). These valves are responsible for controlling the direction and flow of blood through the heart. Heart valve diseases can cause the valves to become narrowed (stenosis), leaky (regurgitation or insufficiency), or improperly closed (prolapse), leading to disrupted blood flow within the heart and potentially causing symptoms such as shortness of breath, fatigue, chest pain, and irregular heart rhythms. The causes of heart valve diseases can include congenital defects, age-related degenerative changes, infections, rheumatic heart disease, and high blood pressure. Treatment options may include medications, surgical repair or replacement of the affected valve(s), or transcatheter procedures.

The mitral valve, also known as the bicuspid valve, is a two-leaflet valve located between the left atrium and left ventricle in the heart. Its function is to ensure unidirectional flow of blood from the left atrium into the left ventricle during the cardiac cycle. The mitral valve consists of two leaflets (anterior and posterior), the chordae tendineae, papillary muscles, and the left atrial and ventricular myocardium. Dysfunction of the mitral valve can lead to various heart conditions such as mitral regurgitation or mitral stenosis.

The tricuspid valve is the heart valve that separates the right atrium and the right ventricle in the human heart. It is called "tricuspid" because it has three leaflets or cusps, which are also referred to as flaps or segments. These cusps are named anterior, posterior, and septal. The tricuspid valve's function is to prevent the backflow of blood from the ventricle into the atrium during systole, ensuring unidirectional flow of blood through the heart.

Pulmonary atresia is a congenital heart defect where the pulmonary valve, which controls blood flow from the right ventricle to the lungs, doesn't form properly and instead of being open, there is a membranous obstruction or atresia. This results in an absence of communication between the right ventricle and the pulmonary artery.

The right ventricle is often small and underdeveloped due to this condition, and blood flow to the lungs can be severely limited. In some cases, there may be additional heart defects present, such as a ventricular septal defect (a hole between the two lower chambers of the heart) or patent ductus arteriosus (an abnormal connection between the pulmonary artery and the aorta).

Pulmonary atresia can range from mild to severe, and treatment options depend on the specific anatomy and physiology of each individual case. Treatment may include medications, catheter-based procedures, or open-heart surgery, and in some cases, a heart transplant may be necessary.

Inbreeding in animals refers to the mating of closely related individuals, such as siblings or offspring of siblings, over multiple generations. An inbred strain is a population of animals produced by this repeated mating of close relatives, which results in a high degree of genetic similarity among members of the strain.

Inbreeding can lead to an increase in homozygosity, where identical alleles are present at corresponding loci on both chromosomes. This can result in the expression of recessive traits, some of which may be deleterious or even lethal. However, inbred strains also have advantages, such as reduced genetic variability, which makes them useful for scientific research.

Inbred strains are commonly used in biomedical research, including genetics, immunology, and behavioral studies. They provide a consistent and controlled genetic background, allowing researchers to study the effects of specific genes or environmental factors with greater precision. Additionally, inbred strains can be crossed with other strains to create hybrid populations, which can be used to map quantitative trait loci (QTL) and identify genes associated with complex traits.

Aortic valve stenosis is a cardiac condition characterized by the narrowing or stiffening of the aortic valve, which separates the left ventricle (the heart's main pumping chamber) from the aorta (the large artery that carries oxygen-rich blood to the rest of the body). This narrowing or stiffening prevents the aortic valve from opening fully, resulting in reduced blood flow from the left ventricle to the aorta and the rest of the body.

The narrowing can be caused by several factors, including congenital heart defects, calcification (hardening) of the aortic valve due to aging, or scarring of the valve due to rheumatic fever or other inflammatory conditions. As a result, the left ventricle must work harder to pump blood through the narrowed valve, which can lead to thickening and enlargement of the left ventricular muscle (left ventricular hypertrophy).

Symptoms of aortic valve stenosis may include chest pain or tightness, shortness of breath, fatigue, dizziness or fainting, and heart palpitations. Severe aortic valve stenosis can lead to serious complications such as heart failure, arrhythmias, or even sudden cardiac death. Treatment options may include medications to manage symptoms, lifestyle changes, or surgical intervention such as aortic valve replacement.

Ventricular outflow obstruction is a term used in cardiology to describe a condition where there is an obstruction or narrowing in the flow of blood as it exits the heart's ventricles (the lower chambers of the heart). This obstruction can occur due to various reasons such as congenital heart defects, hypertrophic cardiomyopathy, or calcification of the aortic valve.

In a normal heart, the left ventricle pumps oxygenated blood into the aorta through the aortic valve, and the right ventricle pumps deoxygenated blood into the pulmonary artery through the pulmonic valve. Any obstruction in these outflow tracts can lead to increased pressure within the ventricles, which can result in various symptoms such as shortness of breath, chest pain, dizziness, or fatigue.

The severity of the obstruction and the resulting symptoms can vary depending on the location and extent of the narrowing. Treatment options may include medications, surgical procedures, or catheter-based interventions to alleviate the obstruction and improve blood flow.

A bioprosthesis is a type of medical implant that is made from biological materials, such as heart valves or tendons taken from animals (xenografts) or humans (allografts). These materials are processed and sterilized to be used in surgical procedures to replace damaged or diseased tissues in the body.

Bioprosthetic implants are often used in cardiac surgery, such as heart valve replacement, because they are less likely to cause an immune response than synthetic materials. However, they may have a limited lifespan due to calcification and degeneration of the biological tissue over time. Therefore, bioprosthetic implants may need to be replaced after several years.

Bioprostheses can also be used in other types of surgical procedures, such as ligament or tendon repair, where natural tissue is needed to restore function and mobility. These prostheses are designed to mimic the properties of native tissues and provide a more physiological solution than synthetic materials.

Heart valve prosthesis implantation is a surgical procedure where an artificial heart valve is inserted to replace a damaged or malfunctioning native heart valve. This can be necessary for patients with valvular heart disease, including stenosis (narrowing) or regurgitation (leaking), who do not respond to medical management and are at risk of heart failure or other complications.

There are two main types of artificial heart valves used in prosthesis implantation: mechanical valves and biological valves. Mechanical valves are made of synthetic materials, such as carbon and metal, and can last a long time but require lifelong anticoagulation therapy to prevent blood clots from forming. Biological valves, on the other hand, are made from animal or human tissue and typically do not require anticoagulation therapy but may have a limited lifespan and may need to be replaced in the future.

The decision to undergo heart valve prosthesis implantation is based on several factors, including the patient's age, overall health, type and severity of valvular disease, and personal preferences. The procedure can be performed through traditional open-heart surgery or minimally invasive techniques, such as robotic-assisted surgery or transcatheter aortic valve replacement (TAVR). Recovery time varies depending on the approach used and individual patient factors.

Aortic valve insufficiency, also known as aortic regurgitation or aortic incompetence, is a cardiac condition in which the aortic valve does not close properly during the contraction phase of the heart cycle. This allows blood to flow back into the left ventricle from the aorta, instead of being pumped out to the rest of the body. As a result, the left ventricle must work harder to maintain adequate cardiac output, which can lead to left ventricular enlargement and heart failure over time if left untreated.

The aortic valve is a trileaflet valve that lies between the left ventricle and the aorta. During systole (the contraction phase of the heart cycle), the aortic valve opens to allow blood to be pumped out of the left ventricle into the aorta and then distributed to the rest of the body. During diastole (the relaxation phase of the heart cycle), the aortic valve closes to prevent blood from flowing back into the left ventricle.

Aortic valve insufficiency can be caused by various conditions, including congenital heart defects, infective endocarditis, rheumatic heart disease, Marfan syndrome, and trauma. Symptoms of aortic valve insufficiency may include shortness of breath, fatigue, chest pain, palpitations, and edema (swelling). Diagnosis is typically made through physical examination, echocardiography, and other imaging studies. Treatment options depend on the severity of the condition and may include medication, surgery to repair or replace the aortic valve, or a combination of both.

Catheterization is a medical procedure in which a catheter (a flexible tube) is inserted into the body to treat various medical conditions or for diagnostic purposes. The specific definition can vary depending on the area of medicine and the particular procedure being discussed. Here are some common types of catheterization:

1. Urinary catheterization: This involves inserting a catheter through the urethra into the bladder to drain urine. It is often performed to manage urinary retention, monitor urine output in critically ill patients, or assist with surgical procedures.
2. Cardiac catheterization: A procedure where a catheter is inserted into a blood vessel, usually in the groin or arm, and guided to the heart. This allows for various diagnostic tests and treatments, such as measuring pressures within the heart chambers, assessing blood flow, or performing angioplasty and stenting of narrowed coronary arteries.
3. Central venous catheterization: A catheter is inserted into a large vein, typically in the neck, chest, or groin, to administer medications, fluids, or nutrition, or to monitor central venous pressure.
4. Peritoneal dialysis catheterization: A catheter is placed into the abdominal cavity for individuals undergoing peritoneal dialysis, a type of kidney replacement therapy.
5. Neurological catheterization: In some cases, a catheter may be inserted into the cerebrospinal fluid space (lumbar puncture) or the brain's ventricular system (ventriculostomy) to diagnose or treat various neurological conditions.

These are just a few examples of catheterization procedures in medicine. The specific definition and purpose will depend on the medical context and the particular organ or body system involved.

A heart valve prosthesis is a medical device that is implanted in the heart to replace a damaged or malfunctioning heart valve. The prosthetic valve can be made of biological tissue (such as from a pig or cow) or artificial materials (such as carbon or polyester). Its function is to allow for the proper directional flow of blood through the heart, opening and closing with each heartbeat to prevent backflow of blood.

There are several types of heart valve prostheses, including:

1. Mechanical valves: These are made entirely of artificial materials and have a longer lifespan than biological valves. However, they require the patient to take blood-thinning medication for the rest of their life to prevent blood clots from forming on the valve.
2. Bioprosthetic valves: These are made of biological tissue and typically last 10-15 years before needing replacement. They do not require the patient to take blood-thinning medication, but there is a higher risk of reoperation due to degeneration of the tissue over time.
3. Homografts or allografts: These are human heart valves that have been donated and preserved for transplantation. They have similar longevity to bioprosthetic valves and do not require blood-thinning medication.
4. Autografts: In this case, the patient's own pulmonary valve is removed and used to replace the damaged aortic valve. This procedure is called the Ross procedure and has excellent long-term results, but it requires advanced surgical skills and is not widely available.

The choice of heart valve prosthesis depends on various factors, including the patient's age, overall health, lifestyle, and personal preferences.

Carcinoid heart disease is a rare complication that occurs in some people with carcinoid tumors, which are slow-growing tumors that typically originate in the digestive tract. These tumors can release hormones and other substances into the bloodstream, which can cause various symptoms. In carcinoid heart disease, these substances cause fibrous plaques to form on the heart valves, leading to thickening and stiffening of the valve leaflets. This can result in leakage or obstruction of the heart valves, causing symptoms such as shortness of breath, fatigue, and fluid retention. Carcinoid heart disease is most commonly affects the tricuspid and pulmonary valves, which are located on the right side of the heart. If left untreated, carcinoid heart disease can lead to serious complications, including heart failure. Treatment typically involves a combination of medications to manage symptoms and control the growth of the tumor, as well as surgery to repair or replace damaged heart valves.

Cardiac catheterization is a medical procedure used to diagnose and treat cardiovascular conditions. In this procedure, a thin, flexible tube called a catheter is inserted into a blood vessel in the arm or leg and threaded up to the heart. The catheter can be used to perform various diagnostic tests, such as measuring the pressure inside the heart chambers and assessing the function of the heart valves.

Cardiac catheterization can also be used to treat certain cardiovascular conditions, such as narrowed or blocked arteries. In these cases, a balloon or stent may be inserted through the catheter to open up the blood vessel and improve blood flow. This procedure is known as angioplasty or percutaneous coronary intervention (PCI).

Cardiac catheterization is typically performed in a hospital cardiac catheterization laboratory by a team of healthcare professionals, including cardiologists, radiologists, and nurses. The procedure may be done under local anesthesia with sedation or general anesthesia, depending on the individual patient's needs and preferences.

Overall, cardiac catheterization is a valuable tool in the diagnosis and treatment of various heart conditions, and it can help improve symptoms, reduce complications, and prolong life for many patients.

A ventricular septal defect (VSD) is a type of congenital heart defect that involves a hole in the wall separating the two lower chambers of the heart, the ventricles. This defect allows oxygenated blood from the left ventricle to mix with deoxygenated blood in the right ventricle, leading to inefficient oxygenation of the body's tissues. The size and location of the hole can vary, and symptoms may range from none to severe, depending on the size of the defect and the amount of blood that is able to shunt between the ventricles. Small VSDs may close on their own over time, while larger defects usually require medical intervention, such as medication or surgery, to prevent complications like pulmonary hypertension and heart failure.

Cardiac valve annuloplasty is a surgical procedure that involves repairing and reinforcing the ring-like structure (annulus) surrounding the heart valves, primarily the mitral or tricuspid valves. This procedure is often performed to correct valve leaks or regurgitation caused by various conditions such as valve disease or dilated cardiomyopathy.

During the annuloplasty procedure, the surgeon typically uses an artificial ring-like device (annuloplasty ring) made of fabric, metal, or a combination of both to reshape and stabilize the damaged annulus. The ring is sewn in place, reducing the size of the valve opening and helping the valve leaflets to coapt properly, thereby preventing valve leaks and improving heart function.

Annuloplasty can be performed as a standalone procedure or in combination with other cardiac surgeries such as valve replacement or repair. The specific technique and approach may vary depending on the individual patient's needs and the surgeon's preference.

Balloon valvuloplasty is a medical procedure used to treat heart valve stenosis or narrowing. It involves the use of a thin, flexible tube (catheter) with a balloon at its tip, which is guided through a blood vessel to the narrowed heart valve. Once in position, the balloon is inflated to stretch and widen the valve opening, improving blood flow. After the valve is widened, the balloon is deflated and the catheter is removed. This procedure can be performed on various heart valves, including the aortic, mitral, and pulmonary valves.

Congenital heart defects (CHDs) are structural abnormalities in the heart that are present at birth. They can affect any part of the heart's structure, including the walls of the heart, the valves inside the heart, and the major blood vessels that lead to and from the heart.

Congenital heart defects can range from mild to severe and can cause various symptoms depending on the type and severity of the defect. Some common symptoms of CHDs include cyanosis (a bluish tint to the skin, lips, and fingernails), shortness of breath, fatigue, poor feeding, and slow growth in infants and children.

There are many different types of congenital heart defects, including:

1. Septal defects: These are holes in the walls that separate the four chambers of the heart. The two most common septal defects are atrial septal defect (ASD) and ventricular septal defect (VSD).
2. Valve abnormalities: These include narrowed or leaky valves, which can affect blood flow through the heart.
3. Obstruction defects: These occur when blood flow is blocked or restricted due to narrowing or absence of a part of the heart's structure. Examples include pulmonary stenosis and coarctation of the aorta.
4. Cyanotic heart defects: These cause a lack of oxygen in the blood, leading to cyanosis. Examples include tetralogy of Fallot and transposition of the great arteries.

The causes of congenital heart defects are not fully understood, but genetic factors and environmental influences during pregnancy may play a role. Some CHDs can be detected before birth through prenatal testing, while others may not be diagnosed until after birth or later in childhood. Treatment for CHDs may include medication, surgery, or other interventions to improve blood flow and oxygenation of the body's tissues.

Echocardiography is a medical procedure that uses sound waves to produce detailed images of the heart's structure, function, and motion. It is a non-invasive test that can help diagnose various heart conditions, such as valve problems, heart muscle damage, blood clots, and congenital heart defects.

During an echocardiogram, a transducer (a device that sends and receives sound waves) is placed on the chest or passed through the esophagus to obtain images of the heart. The sound waves produced by the transducer bounce off the heart structures and return to the transducer, which then converts them into electrical signals that are processed to create images of the heart.

There are several types of echocardiograms, including:

* Transthoracic echocardiography (TTE): This is the most common type of echocardiogram and involves placing the transducer on the chest.
* Transesophageal echocardiography (TEE): This type of echocardiogram involves passing a specialized transducer through the esophagus to obtain images of the heart from a closer proximity.
* Stress echocardiography: This type of echocardiogram is performed during exercise or medication-induced stress to assess how the heart functions under stress.
* Doppler echocardiography: This type of echocardiogram uses sound waves to measure blood flow and velocity in the heart and blood vessels.

Echocardiography is a valuable tool for diagnosing and managing various heart conditions, as it provides detailed information about the structure and function of the heart. It is generally safe, non-invasive, and painless, making it a popular choice for doctors and patients alike.

Pulmonary subvalvular stenosis is a rare cardiac condition that refers to the narrowing or obstruction of the pulmonary valve or the outflow tract below it, within the right ventricle of the heart. This results in restricted blood flow from the right ventricle to the pulmonary artery and subsequently to the lungs.

The narrowing can be caused by various factors such as a membranous shelf-like structure (dysplasia), a fibrous ring, or a tunnel-like narrowing of the outflow tract (tunneling). The severity of the stenosis may vary from mild to severe, and symptoms can range from shortness of breath, fatigue, and chest pain to more serious complications like heart failure or arrhythmias.

Diagnosis typically involves imaging tests such as echocardiography, cardiac MRI, or cardiac catheterization. Treatment options depend on the severity of the stenosis and may include monitoring, medications, or invasive procedures such as balloon dilation or surgical repair.

Tricuspid valve insufficiency, also known as tricuspid regurgitation, is a cardiac condition in which the tricuspid valve located between the right atrium and right ventricle of the heart does not close properly, allowing blood to flow back into the right atrium during contraction of the right ventricle. This results in a portion of the blood being pumped inefficiently, which can lead to volume overload of the right side of the heart and potentially result in symptoms such as fatigue, weakness, shortness of breath, and fluid retention. The condition can be congenital or acquired, with common causes including dilated cardiomyopathy, infective endocarditis, rheumatic heart disease, and trauma.

The pulmonary artery is a large blood vessel that carries deoxygenated blood from the right ventricle of the heart to the lungs for oxygenation. It divides into two main branches, the right and left pulmonary arteries, which further divide into smaller vessels called arterioles, and then into a vast network of capillaries in the lungs where gas exchange occurs. The thin walls of these capillaries allow oxygen to diffuse into the blood and carbon dioxide to diffuse out, making the blood oxygen-rich before it is pumped back to the left side of the heart through the pulmonary veins. This process is crucial for maintaining proper oxygenation of the body's tissues and organs.

Mitral valve insufficiency, also known as mitral regurgitation, is a cardiac condition in which the mitral valve located between the left atrium and left ventricle of the heart does not close properly, causing blood to flow backward into the atrium during contraction of the ventricle. This leads to an increased volume load on the left heart chamber and can result in symptoms such as shortness of breath, fatigue, and fluid retention. The condition can be caused by various factors including valve damage due to degenerative changes, infective endocarditis, rheumatic heart disease, or trauma. Treatment options include medication, mitral valve repair, or replacement surgery depending on the severity and underlying cause of the insufficiency.

Right Ventricular Function refers to the ability of the right ventricle (RV) of the heart to receive and eject blood during the cardiac cycle. The right ventricle is one of the four chambers of the heart and is responsible for pumping deoxygenated blood from the body to the lungs for re-oxygenation.

Right ventricular function can be assessed by measuring various parameters such as:

1. Right Ventricular Ejection Fraction (RVEF): It is the percentage of blood that is ejected from the right ventricle during each heartbeat. A normal RVEF ranges from 45-75%.
2. Right Ventricular Systolic Function: It refers to the ability of the right ventricle to contract and eject blood during systole (contraction phase). This can be assessed by measuring the tricuspid annular plane systolic excursion (TAPSE) or tissue Doppler imaging.
3. Right Ventricular Diastolic Function: It refers to the ability of the right ventricle to relax and fill with blood during diastole (relaxation phase). This can be assessed by measuring the right ventricular inflow pattern, tricuspid valve E/A ratio, or deceleration time.
4. Right Ventricular Afterload: It refers to the pressure that the right ventricle must overcome to eject blood into the pulmonary artery. Increased afterload can impair right ventricular function.

Abnormalities in right ventricular function can lead to various cardiovascular conditions such as pulmonary hypertension, heart failure, and arrhythmias.

Cardiac surgical procedures are operations that are performed on the heart or great vessels (the aorta and vena cava) by cardiothoracic surgeons. These surgeries are often complex and require a high level of skill and expertise. Some common reasons for cardiac surgical procedures include:

1. Coronary artery bypass grafting (CABG): This is a surgery to improve blood flow to the heart in patients with coronary artery disease. During the procedure, a healthy blood vessel from another part of the body is used to create a detour around the blocked or narrowed portion of the coronary artery.
2. Valve repair or replacement: The heart has four valves that control blood flow through and out of the heart. If one or more of these valves become damaged or diseased, they may need to be repaired or replaced. This can be done using artificial valves or valves from animal or human donors.
3. Aneurysm repair: An aneurysm is a weakened area in the wall of an artery that can bulge out and potentially rupture. If an aneurysm occurs in the aorta, it may require surgical repair to prevent rupture.
4. Heart transplantation: In some cases, heart failure may be so severe that a heart transplant is necessary. This involves removing the diseased heart and replacing it with a healthy donor heart.
5. Arrhythmia surgery: Certain types of abnormal heart rhythms (arrhythmias) may require surgical treatment. One such procedure is called the Maze procedure, which involves creating a pattern of scar tissue in the heart to disrupt the abnormal electrical signals that cause the arrhythmia.
6. Congenital heart defect repair: Some people are born with structural problems in their hearts that require surgical correction. These may include holes between the chambers of the heart or abnormal blood vessels.

Cardiac surgical procedures carry risks, including bleeding, infection, stroke, and death. However, for many patients, these surgeries can significantly improve their quality of life and longevity.

Endocarditis is an inflammation of the inner layer of the heart chambers and heart valves, called the endocardium. This inflammation typically results from a bacterial or, less commonly, fungal infection that travels through the bloodstream and attaches to damaged areas of the heart.

There are two main types of endocarditis:

1. Acute Endocarditis: Develops quickly and can be severe, causing fever, chills, shortness of breath, fatigue, and heart murmurs. It may lead to serious complications like heart failure, embolism (blood clots that travel to other parts of the body), and damage to heart valves.

2. Subacute Endocarditis: Develops more slowly, often causing milder symptoms that can be mistaken for a cold or flu. Symptoms may include fatigue, weakness, fever, night sweats, weight loss, joint pain, and heart murmurs. Subacute endocarditis is more likely to affect people with previously damaged heart valves or congenital heart conditions.

Treatment usually involves several weeks of intravenous antibiotics or antifungal medications, depending on the cause of the infection. In some cases, surgery may be required to repair or replace damaged heart valves. Preventive measures include good oral hygiene and prompt treatment of infections, especially in individuals at a higher risk for endocarditis, such as those with congenital heart defects, artificial heart valves, or previous history of endocarditis.

Heart valves are specialized structures in the heart that ensure unidirectional flow of blood through its chambers during the cardiac cycle. There are four heart valves: the tricuspid valve and the mitral (bicuspid) valve, located between the atria and ventricles, and the pulmonic (pulmonary) valve and aortic valve, located between the ventricles and the major blood vessels leaving the heart.

The heart valves are composed of thin flaps of tissue called leaflets or cusps, which are supported by a fibrous ring. The aortic and pulmonic valves have three cusps each, while the tricuspid and mitral valves have three and two cusps, respectively.

The heart valves open and close in response to pressure differences across them, allowing blood to flow forward into the ventricles during diastole (filling phase) and preventing backflow of blood into the atria during systole (contraction phase). A properly functioning heart valve ensures efficient pumping of blood by the heart and maintains normal blood circulation throughout the body.

Mitral valve prolapse (MVP) is a heart condition where the mitral valve, which separates the left atrium and left ventricle in the heart, doesn't function properly. In MVP, one or both of the mitral valve flaps (known as leaflets) bulge or billow into the left atrium during the contraction of the left ventricle. This prolapse can cause a leakage of blood back into the atrium, known as mitral regurgitation. In many cases, MVP is asymptomatic and doesn't require treatment, but in some instances, it may lead to complications such as infective endocarditis or arrhythmias. The exact causes of MVP are not fully understood, but it can be associated with certain genetic factors, connective tissue disorders, and mitral valve abnormalities present at birth.

Bacterial endocarditis is a medical condition characterized by the inflammation and infection of the inner layer of the heart, known as the endocardium. This infection typically occurs when bacteria enter the bloodstream and attach themselves to damaged or abnormal heart valves or other parts of the endocardium. The bacteria can then multiply and cause the formation of vegetations, which are clusters of infected tissue that can further damage the heart valves and lead to serious complications such as heart failure, stroke, or even death if left untreated.

Bacterial endocarditis is a relatively uncommon but potentially life-threatening condition that requires prompt medical attention. Risk factors for developing bacterial endocarditis include pre-existing heart conditions such as congenital heart defects, artificial heart valves, previous history of endocarditis, or other conditions that damage the heart valves. Intravenous drug use is also a significant risk factor for this condition.

Symptoms of bacterial endocarditis may include fever, chills, fatigue, muscle and joint pain, shortness of breath, chest pain, and a new or changing heart murmur. Diagnosis typically involves a combination of medical history, physical examination, blood cultures, and imaging tests such as echocardiography. Treatment usually involves several weeks of intravenous antibiotics to eradicate the infection, and in some cases, surgical intervention may be necessary to repair or replace damaged heart valves.

Venous valves are one-way flaps made of thin, flexible tissue that lie inside your veins. They allow blood to flow towards the heart but prevent it from flowing backward. These valves are especially important in the veins of the legs, where they help to counteract the force of gravity and ensure that blood flows back up to the heart. When venous valves become damaged or weakened, blood can pool in the veins, leading to conditions such as varicose veins or chronic venous insufficiency.

Mitral valve stenosis is a cardiac condition characterized by the narrowing or stiffening of the mitral valve, one of the four heart valves that regulate blood flow through the heart. This narrowing prevents the mitral valve from fully opening during diastole (relaxation phase of the heart cycle), leading to restricted flow of oxygenated blood from the left atrium into the left ventricle.

The narrowing or stiffening of the mitral valve can be caused by various factors, such as rheumatic heart disease, congenital heart defects, aging, or calcium deposits on the valve leaflets. As a result, the left atrium has to work harder to pump blood into the left ventricle, causing increased pressure in the left atrium and pulmonary veins. This can lead to symptoms such as shortness of breath, fatigue, coughing, and heart palpitations.

Mitral valve stenosis is typically diagnosed through a combination of medical history, physical examination, and imaging techniques like echocardiography or cardiac catheterization. Treatment options may include medications to manage symptoms and prevent complications, as well as surgical interventions such as mitral valve repair or replacement to alleviate the stenosis and improve heart function.

Prosthesis design is a specialized field in medical device technology that involves creating and developing artificial substitutes to replace a missing body part, such as a limb, tooth, eye, or internal organ. The design process typically includes several stages: assessment of the patient's needs, selection of appropriate materials, creation of a prototype, testing and refinement, and final fabrication and fitting of the prosthesis.

The goal of prosthesis design is to create a device that functions as closely as possible to the natural body part it replaces, while also being comfortable, durable, and aesthetically pleasing for the patient. The design process may involve collaboration between medical professionals, engineers, and designers, and may take into account factors such as the patient's age, lifestyle, occupation, and overall health.

Prosthesis design can be highly complex, particularly for advanced devices such as robotic limbs or implantable organs. These devices often require sophisticated sensors, actuators, and control systems to mimic the natural functions of the body part they replace. As a result, prosthesis design is an active area of research and development in the medical field, with ongoing efforts to improve the functionality, comfort, and affordability of these devices for patients.

Doppler echocardiography is a type of ultrasound test that uses high-frequency sound waves to produce detailed images of the heart and its blood vessels. It measures the direction and speed of blood flow in the heart and major blood vessels leading to and from the heart. This helps to evaluate various conditions such as valve problems, congenital heart defects, and heart muscle diseases.

In Doppler echocardiography, a small handheld device called a transducer is placed on the chest, which emits sound waves that bounce off the heart and blood vessels. The transducer then picks up the returning echoes, which are processed by a computer to create moving images of the heart.

The Doppler effect is used to measure the speed and direction of blood flow. This occurs when the frequency of the sound waves changes as they bounce off moving objects, such as red blood cells. By analyzing these changes, the ultrasound machine can calculate the velocity and direction of blood flow in different parts of the heart.

Doppler echocardiography is a non-invasive test that does not require any needles or dyes. It is generally safe and painless, although patients may experience some discomfort from the pressure applied by the transducer on the chest. The test usually takes about 30 to 60 minutes to complete.

Noonan Syndrome is a genetic disorder that affects various parts of the body and is characterized by distinctive facial features, short stature, heart defects, and developmental delays. It is caused by mutations in genes responsible for regulating cell growth and division. The syndrome is often identified at birth or in early childhood due to its physical manifestations, which may include widely spaced eyes, low-set ears, a short neck, a broad or webbed neck, chest deformities, and pulmonary valve stenosis. Noonan Syndrome affects both sexes and all races equally, with an estimated prevalence of 1 in 1,000 to 1 in 2,500 live births.

Tricuspid valve stenosis is a cardiac condition characterized by the narrowing or stiffening of the tricuspid valve, which is located between the right atrium and right ventricle in the heart. This narrowing or stiffening restricts the normal flow of blood from the right atrium into the right ventricle, causing increased pressure in the right atrium and reduced blood flow to the lungs.

The tricuspid valve typically has three leaflets or cusps that open and close to regulate the flow of blood between the right atrium and right ventricle. In tricuspid valve stenosis, these leaflets become thickened, calcified, or fused together, leading to a reduced opening size and impaired function.

The most common causes of tricuspid valve stenosis include rheumatic heart disease, congenital heart defects, carcinoid syndrome, and infective endocarditis. Symptoms may include fatigue, shortness of breath, swelling in the legs and abdomen, and irregular heartbeats. Treatment options depend on the severity of the condition and underlying causes but may involve medications, surgical repair or replacement of the valve, or catheter-based procedures.

The fetal heart is the cardiovascular organ that develops in the growing fetus during pregnancy. It starts to form around 22 days after conception and continues to develop throughout the first trimester. By the end of the eighth week of gestation, the fetal heart has developed enough to pump blood throughout the body.

The fetal heart is similar in structure to the adult heart but has some differences. It is smaller and more compact, with a four-chambered structure that includes two atria and two ventricles. The fetal heart also has unique features such as the foramen ovale, which is a hole between the right and left atria that allows blood to bypass the lungs, and the ductus arteriosus, a blood vessel that connects the pulmonary artery to the aorta and diverts blood away from the lungs.

The fetal heart is responsible for pumping oxygenated blood from the placenta to the rest of the body and returning deoxygenated blood back to the placenta for re-oxygenation. The rate of the fetal heartbeat is faster than that of an adult, typically ranging from 120 to 160 beats per minute. Fetal heart rate monitoring is a common method used during pregnancy and childbirth to assess the health and well-being of the developing fetus.

Treatment outcome is a term used to describe the result or effect of medical treatment on a patient's health status. It can be measured in various ways, such as through symptoms improvement, disease remission, reduced disability, improved quality of life, or survival rates. The treatment outcome helps healthcare providers evaluate the effectiveness of a particular treatment plan and make informed decisions about future care. It is also used in clinical research to compare the efficacy of different treatments and improve patient care.

Right ventricular dysfunction is a condition characterized by the impaired ability of the right ventricle (one of the two pumping chambers in the heart) to fill with blood during the diastolic phase or eject blood during the systolic phase. This results in reduced cardiac output from the right ventricle, which can lead to various complications such as fluid accumulation in the body, particularly in the abdomen and lower extremities, and ultimately congestive heart failure if left untreated.

Right ventricular dysfunction can be caused by various factors, including damage to the heart muscle due to a heart attack, high blood pressure in the lungs (pulmonary hypertension), chronic lung diseases, congenital heart defects, viral infections, and certain medications. Symptoms of right ventricular dysfunction may include shortness of breath, fatigue, swelling in the legs, ankles, or abdomen, and a decreased tolerance for physical activity.

Diagnosis of right ventricular dysfunction typically involves a combination of medical history, physical examination, imaging tests such as echocardiography, cardiac MRI, or CT scan, and other diagnostic procedures such as electrocardiogram (ECG) or cardiac catheterization. Treatment options depend on the underlying cause but may include medications to reduce fluid buildup, improve heart function, and manage symptoms, as well as lifestyle modifications such as reducing salt intake and increasing physical activity levels. In severe cases, more invasive treatments such as surgery or implantable devices like pacemakers or ventricular assist devices may be necessary.

Tricuspid atresia is a congenital heart defect where the tricuspid valve, which regulates blood flow between the right atrium and right ventricle, fails to develop properly. As a result, there is no direct pathway for blood to move from the right atrium to the right ventricle and then to the lungs for oxygenation.

In this condition, blood from the body returning to the heart enters the right atrium but cannot flow through the tricuspid valve into the right ventricle. Instead, it flows through an opening in the interatrial septum (atrial septal defect) into the left atrium and then into the left ventricle. The left ventricle pumps this blood to the body and a portion of it goes to the lungs via a patent ductus arteriosus or other collateral vessels.

Tricuspid atresia is often associated with other heart defects, such as transposition of the great arteries, pulmonary stenosis, or total anomalous pulmonary venous return. Symptoms can vary depending on the severity and associated defects but may include cyanosis (bluish discoloration of the skin), shortness of breath, fatigue, and poor growth. Treatment typically involves surgical interventions to create a path for blood to flow to the lungs and establish proper oxygenation.

Oligohydramnios is a medical condition that refers to an abnormally low amount of amniotic fluid surrounding the fetus in the uterus during pregnancy. The amniotic fluid is essential for the protection and development of the fetus, including lung maturation and joint mobility. Oligohydramnios is often diagnosed through ultrasound measurements of the pocket depth of the amniotic fluid and is defined as an amniotic fluid index (AFI) of less than 5 cm or a single deepest pocket (SDP) of less than 2 cm after 24 weeks of gestation.

The condition can be caused by various factors, such as fetal growth restriction, maternal high blood pressure, placental insufficiency, rupture of membranes, and genetic disorders. Oligohydramnios may increase the risk of complications during pregnancy and childbirth, including preterm labor, fetal distress, and stillbirth. The management of oligohydramnios depends on the underlying cause and gestational age, and may include close monitoring, delivery, or treatment of the underlying condition.

The heart ventricles are the two lower chambers of the heart that receive blood from the atria and pump it to the lungs or the rest of the body. The right ventricle pumps deoxygenated blood to the lungs, while the left ventricle pumps oxygenated blood to the rest of the body. Both ventricles have thick, muscular walls to generate the pressure necessary to pump blood through the circulatory system.

A prolapse is a medical condition where an organ or tissue in the body slips from its normal position and drops down into a lower part of the body. This usually occurs when the muscles and ligaments that support the organ become weak or stretched. The most common types of prolapses include:

* Uterine prolapse: When the uterus slips down into or protrudes out of the vagina.
* Rectal prolapse: When the rectum (the lower end of the colon) slips outside the anus.
* Bladder prolapse (cystocele): When the bladder drops into the vagina.
* Small bowel prolapse (enterocele): When the small intestine bulges into the vagina.

Prolapses can cause various symptoms, such as discomfort, pain, pressure, and difficulty with urination or bowel movements. Treatment options depend on the severity of the prolapse and may include lifestyle changes, physical therapy, medication, or surgery.

A reoperation is a surgical procedure that is performed again on a patient who has already undergone a previous operation for the same or related condition. Reoperations may be required due to various reasons, such as inadequate initial treatment, disease recurrence, infection, or complications from the first surgery. The nature and complexity of a reoperation can vary widely depending on the specific circumstances, but it often carries higher risks and potential complications compared to the original operation.

Follow-up studies are a type of longitudinal research that involve repeated observations or measurements of the same variables over a period of time, in order to understand their long-term effects or outcomes. In medical context, follow-up studies are often used to evaluate the safety and efficacy of medical treatments, interventions, or procedures.

In a typical follow-up study, a group of individuals (called a cohort) who have received a particular treatment or intervention are identified and then followed over time through periodic assessments or data collection. The data collected may include information on clinical outcomes, adverse events, changes in symptoms or functional status, and other relevant measures.

The results of follow-up studies can provide important insights into the long-term benefits and risks of medical interventions, as well as help to identify factors that may influence treatment effectiveness or patient outcomes. However, it is important to note that follow-up studies can be subject to various biases and limitations, such as loss to follow-up, recall bias, and changes in clinical practice over time, which must be carefully considered when interpreting the results.

Prenatal ultrasonography, also known as obstetric ultrasound, is a medical diagnostic procedure that uses high-frequency sound waves to create images of the developing fetus, placenta, and amniotic fluid inside the uterus. It is a non-invasive and painless test that is widely used during pregnancy to monitor the growth and development of the fetus, detect any potential abnormalities or complications, and determine the due date.

During the procedure, a transducer (a small handheld device) is placed on the mother's abdomen and moved around to capture images from different angles. The sound waves travel through the mother's body and bounce back off the fetus, producing echoes that are then converted into electrical signals and displayed as images on a screen.

Prenatal ultrasonography can be performed at various stages of pregnancy, including early pregnancy to confirm the pregnancy and detect the number of fetuses, mid-pregnancy to assess the growth and development of the fetus, and late pregnancy to evaluate the position of the fetus and determine if it is head down or breech. It can also be used to guide invasive procedures such as amniocentesis or chorionic villus sampling.

Overall, prenatal ultrasonography is a valuable tool in modern obstetrics that helps ensure the health and well-being of both the mother and the developing fetus.

A newborn infant is a baby who is within the first 28 days of life. This period is also referred to as the neonatal period. Newborns require specialized care and attention due to their immature bodily systems and increased vulnerability to various health issues. They are closely monitored for signs of well-being, growth, and development during this critical time.

Echocardiography, Doppler, color is a type of ultrasound test that uses sound waves to create detailed moving images of the heart and its blood vessels. In this technique, color Doppler is used to visualize the direction and speed of blood flow through the heart and great vessels. The movement of the red blood cells causes a change in frequency of the reflected sound waves (Doppler shift), which can be used to calculate the velocity and direction of the blood flow. By adding color to the Doppler image, it becomes easier for the interpreting physician to understand the complex three-dimensional motion of blood through the heart. This test is often used to diagnose and monitor various heart conditions, including valve disorders, congenital heart defects, and cardiac muscle diseases.

A fibroma is a benign (non-cancerous) tumor that consists primarily of fibrous or connective tissue. It can occur in various parts of the body, including the skin, mouth, and internal organs. The term "fibroma" is often used to describe any benign fibrous growth, but there are specific types of fibromas such as dermatofibroma (found in the skin), oral fibroma (found in the mouth), and benign fibrous histiocytoma (found in soft tissues).

It's important to note that while fibromas are generally harmless, they can cause discomfort or problems depending on their size and location. If a fibroma is causing issues or there's concern about its growth or malignancy, it should be evaluated by a healthcare professional for potential removal or further assessment.

Transesophageal echocardiography (TEE) is a type of echocardiogram, which is a medical test that uses sound waves to create detailed images of the heart. In TEE, a special probe containing a transducer is passed down the esophagus (the tube that connects the mouth to the stomach) to obtain views of the heart from behind. This allows for more detailed images of the heart structures and function compared to a standard echocardiogram, which uses a probe placed on the chest. TEE is often used in patients with poor image quality from a standard echocardiogram or when more detailed images are needed to diagnose or monitor certain heart conditions. It is typically performed by a trained cardiologist or sonographer under the direction of a cardiologist.

A heart septal defect is a type of congenital heart defect, which means it is present at birth. It involves an abnormal opening in the septum, the wall that separates the two sides of the heart. This opening allows oxygen-rich blood to leak into the oxygen-poor blood chambers in the heart.

There are several types of heart septal defects, including:

1. Atrial Septal Defect (ASD): A hole in the atrial septum, the wall between the two upper chambers of the heart (the right and left atria).
2. Ventricular Septal Defect (VSD): A hole in the ventricular septum, the wall between the two lower chambers of the heart (the right and left ventricles).
3. Atrioventricular Septal Defect (AVSD): A combination of an ASD and a VSD, often accompanied by malformation of the mitral and/or tricuspid valves.

The severity of a heart septal defect depends on the size of the opening and its location in the septum. Small defects may cause no symptoms and may close on their own over time. Larger defects can lead to complications, such as heart failure, pulmonary hypertension, or infective endocarditis, and may require medical or surgical intervention.

Hemodynamics is the study of how blood flows through the cardiovascular system, including the heart and the vascular network. It examines various factors that affect blood flow, such as blood volume, viscosity, vessel length and diameter, and pressure differences between different parts of the circulatory system. Hemodynamics also considers the impact of various physiological and pathological conditions on these variables, and how they in turn influence the function of vital organs and systems in the body. It is a critical area of study in fields such as cardiology, anesthesiology, and critical care medicine.

The ventricular septum is the thick, muscular wall that separates the left and right ventricles, which are the lower chambers of the heart. Its main function is to prevent the oxygen-rich blood in the left ventricle from mixing with the oxygen-poor blood in the right ventricle.

A congenital heart defect called a ventricular septal defect (VSD) can occur when there is an abnormal opening or hole in the ventricular septum, allowing blood to flow between the two ventricles. This can result in various symptoms and complications, depending on the size of the defect and the amount of blood that passes through it. VSDs are typically diagnosed and treated by pediatric cardiologists or cardiac surgeons.

Subacute bacterial endocarditis (SBE) is a type of infective endocarditis that typically has a more indolent course compared to acute bacterial endocarditis. It is caused by organisms that are less virulent and have a higher affinity for damaged heart valves or endocardium.

The most common causative organisms of SBE include Streptococcus viridans, Streptococcus bovis, and enterococci. The infection often develops over a period of weeks to months, with nonspecific symptoms such as fatigue, weakness, fever, weight loss, and night sweats.

SBE can lead to serious complications, including heart failure, valvular damage, embolic events, and even death if left untreated. Treatment typically involves prolonged courses of intravenous antibiotics, with surgical intervention reserved for cases with severe valvular damage or uncontrolled infection.

Preventive measures include appropriate management of underlying heart conditions, prophylactic antibiotic therapy in high-risk individuals undergoing dental or invasive procedures, and good oral hygiene.

The heart septum is the thick, muscular wall that divides the right and left sides of the heart. It consists of two main parts: the atrial septum, which separates the right and left atria (the upper chambers of the heart), and the ventricular septum, which separates the right and left ventricles (the lower chambers of the heart). A normal heart septum ensures that oxygen-rich blood from the lungs does not mix with oxygen-poor blood from the body. Any defect or abnormality in the heart septum is called a septal defect, which can lead to various congenital heart diseases.

'Abnormalities, Multiple' is a broad term that refers to the presence of two or more structural or functional anomalies in an individual. These abnormalities can be present at birth (congenital) or can develop later in life (acquired). They can affect various organs and systems of the body and can vary greatly in severity and impact on a person's health and well-being.

Multiple abnormalities can occur due to genetic factors, environmental influences, or a combination of both. Chromosomal abnormalities, gene mutations, exposure to teratogens (substances that cause birth defects), and maternal infections during pregnancy are some of the common causes of multiple congenital abnormalities.

Examples of multiple congenital abnormalities include Down syndrome, Turner syndrome, and VATER/VACTERL association. Acquired multiple abnormalities can result from conditions such as trauma, infection, degenerative diseases, or cancer.

The medical evaluation and management of individuals with multiple abnormalities depend on the specific abnormalities present and their impact on the individual's health and functioning. A multidisciplinary team of healthcare professionals is often involved in the care of these individuals to address their complex needs.

The Ductus Arteriosus is a fetal blood vessel that connects the pulmonary trunk (the artery that carries blood from the heart to the lungs) and the aorta (the largest artery in the body, which carries oxygenated blood from the heart to the rest of the body). This vessel allows most of the blood from the right ventricle of the fetal heart to bypass the lungs, as the fetus receives oxygen through the placenta rather than breathing air.

After birth, with the first breaths, the blood oxygen level increases and the pressure in the lungs rises. As a result, the circulation in the newborn's body changes, and the Ductus Arteriosus is no longer needed. Within the first few days or weeks of life, this vessel usually closes spontaneously, turning into a fibrous cord called the Ligamentum Arteriosum.

Persistent Patency of the Ductus Arteriosus (PDA) occurs when the Ductus Arteriosus does not close after birth, which can lead to various complications such as heart failure and pulmonary hypertension. This condition is often seen in premature infants and may require medical intervention or surgical closure of the vessel.

Right ventricular hypertrophy (RVH) is a medical condition characterized by an enlargement and thickening (hypertrophy) of the right ventricle of the heart. The right ventricle is one of the four chambers of the heart that is responsible for pumping deoxygenated blood to the lungs through the pulmonary artery.

In response to increased workload or pressure overload, such as in chronic lung diseases, pulmonary hypertension, or congenital heart defects, the right ventricle may undergo hypertrophy. This results in an increase in the size and thickness of the right ventricular muscle, which can impair its ability to fill with blood and pump it efficiently to the lungs.

RVH can be diagnosed through various tests, including electrocardiogram (ECG), echocardiography, cardiac magnetic resonance imaging (MRI), or cardiac catheterization. Treatment of RVH depends on the underlying cause and may include medications, oxygen therapy, surgery, or other interventions to reduce the workload on the right ventricle and improve its function.

Fetal diseases are medical conditions or abnormalities that affect a fetus during pregnancy. These diseases can be caused by genetic factors, environmental influences, or a combination of both. They can range from mild to severe and may impact various organ systems in the developing fetus. Examples of fetal diseases include congenital heart defects, neural tube defects, chromosomal abnormalities such as Down syndrome, and infectious diseases such as toxoplasmosis or rubella. Fetal diseases can be diagnosed through prenatal testing, including ultrasound, amniocentesis, and chorionic villus sampling. Treatment options may include medication, surgery, or delivery of the fetus, depending on the nature and severity of the disease.

Heart neoplasms are abnormal growths or tumors that develop within the heart tissue. They can be benign (noncancerous) or malignant (cancerous). Benign tumors, such as myxomas and rhabdomyomas, are typically slower growing and less likely to spread, but they can still cause serious complications if they obstruct blood flow or damage heart valves. Malignant tumors, such as angiosarcomas and rhabdomyosarcomas, are fast-growing and have a higher risk of spreading to other parts of the body. Symptoms of heart neoplasms can include shortness of breath, chest pain, fatigue, and irregular heart rhythms. Treatment options depend on the type, size, and location of the tumor, and may include surgery, radiation therapy, or chemotherapy.

Mitral valve annuloplasty is a surgical procedure that involves repairing and reinforcing the mitral valve in the heart, which helps control blood flow between the left atrium and left ventricle. The procedure typically aims to reduce the size of the mitral valve's dilated or stretched opening (annulus) by implanting a prosthetic ring or band around it. This reinforcement helps restore normal valve function, preventing regurgitation or backflow of blood into the atrium during heart contractions.

The procedure is often performed to treat mitral valve regurgitation, which can be caused by various factors such as age-related degenerative changes, infective endocarditis, rheumatic heart disease, or congenital abnormalities. Mitral valve annuloplasty may be done alone or in combination with other cardiac surgeries like mitral valve replacement or repair of the valve leaflets.

Retrospective studies, also known as retrospective research or looking back studies, are a type of observational study that examines data from the past to draw conclusions about possible causal relationships between risk factors and outcomes. In these studies, researchers analyze existing records, medical charts, or previously collected data to test a hypothesis or answer a specific research question.

Retrospective studies can be useful for generating hypotheses and identifying trends, but they have limitations compared to prospective studies, which follow participants forward in time from exposure to outcome. Retrospective studies are subject to biases such as recall bias, selection bias, and information bias, which can affect the validity of the results. Therefore, retrospective studies should be interpreted with caution and used primarily to generate hypotheses for further testing in prospective studies.

Atrial septal defect (ASD) is a type of congenital heart defect that involves the septum, which is the wall that separates the two upper chambers of the heart (atria). An ASD is a hole or abnormal opening in the atrial septum, allowing oxygen-rich blood to leak into the oxygen-poor blood chambers in the heart. This leads to an overload of blood in the right side of the heart, which can cause enlargement of the heart and increased work for the right ventricle.

ASDs can vary in size, and small defects may not cause any symptoms or require treatment. Larger defects, however, can result in symptoms such as shortness of breath, fatigue, and heart rhythm abnormalities. Over time, if left untreated, ASDs can lead to complications like pulmonary hypertension, atrial fibrillation, and stroke.

Treatment for ASD typically involves surgical closure of the defect or catheter-based procedures using devices to close the hole. The choice of treatment depends on factors such as the size and location of the defect, the patient's age and overall health, and the presence of any coexisting conditions.

Three-dimensional echocardiography (3DE) is a type of cardiac ultrasound that uses advanced technologies to create a real-time, detailed 3D image of the heart. This imaging technique provides a more comprehensive view of the heart's structure and function compared to traditional 2D echocardiography. By visualizing the heart from multiple angles, 3DE can help physicians better assess complex cardiac conditions, plan treatments, and monitor their effectiveness.

In a 3DE examination, a transducer (a handheld device that emits and receives sound waves) is placed on the chest to capture ultrasound data. This data is then processed by specialized software to create a 3D model of the heart. The procedure is non-invasive and typically takes less than an hour to complete.

Three-dimensional echocardiography has several clinical applications, including:

1. Evaluation of cardiac morphology and function in congenital heart disease
2. Assessment of valvular structure and function, such as mitral or aortic valve regurgitation or stenosis
3. Guidance during interventional procedures like transcatheter aortic valve replacement (TAVR)
4. Quantification of left ventricular volumes, ejection fraction, and mass
5. Assessment of right ventricular size and function
6. Detection and monitoring of cardiac tumors or other masses
7. Pre-surgical planning for complex heart surgeries

Overall, 3DE offers a more accurate and detailed view of the heart, allowing healthcare providers to make informed decisions about patient care and improve outcomes.

Postoperative complications refer to any unfavorable condition or event that occurs during the recovery period after a surgical procedure. These complications can vary in severity and may include, but are not limited to:

1. Infection: This can occur at the site of the incision or inside the body, such as pneumonia or urinary tract infection.
2. Bleeding: Excessive bleeding (hemorrhage) can lead to a drop in blood pressure and may require further surgical intervention.
3. Blood clots: These can form in the deep veins of the legs (deep vein thrombosis) and can potentially travel to the lungs (pulmonary embolism).
4. Wound dehiscence: This is when the surgical wound opens up, which can lead to infection and further complications.
5. Pulmonary issues: These include atelectasis (collapsed lung), pneumonia, or respiratory failure.
6. Cardiovascular problems: These include abnormal heart rhythms (arrhythmias), heart attack, or stroke.
7. Renal failure: This can occur due to various reasons such as dehydration, blood loss, or the use of certain medications.
8. Pain management issues: Inadequate pain control can lead to increased stress, anxiety, and decreased mobility.
9. Nausea and vomiting: These can be caused by anesthesia, opioid pain medication, or other factors.
10. Delirium: This is a state of confusion and disorientation that can occur in the elderly or those with certain medical conditions.

Prompt identification and management of these complications are crucial to ensure the best possible outcome for the patient.

Transposition of the Great Vessels is a congenital heart defect in which the two main vessels that carry blood from the heart to the rest of the body are switched in position. Normally, the aorta arises from the left ventricle and carries oxygenated blood to the body, while the pulmonary artery arises from the right ventricle and carries deoxygenated blood to the lungs. In transposition of the great vessels, the aorta arises from the right ventricle and the pulmonary artery arises from the left ventricle. This results in oxygen-poor blood being pumped to the body and oxygen-rich blood being recirculated back to the lungs, which can lead to serious health problems and is often fatal if not corrected through surgery soon after birth.

In the field of medicine, "time factors" refer to the duration of symptoms or time elapsed since the onset of a medical condition, which can have significant implications for diagnosis and treatment. Understanding time factors is crucial in determining the progression of a disease, evaluating the effectiveness of treatments, and making critical decisions regarding patient care.

For example, in stroke management, "time is brain," meaning that rapid intervention within a specific time frame (usually within 4.5 hours) is essential to administering tissue plasminogen activator (tPA), a clot-busting drug that can minimize brain damage and improve patient outcomes. Similarly, in trauma care, the "golden hour" concept emphasizes the importance of providing definitive care within the first 60 minutes after injury to increase survival rates and reduce morbidity.

Time factors also play a role in monitoring the progression of chronic conditions like diabetes or heart disease, where regular follow-ups and assessments help determine appropriate treatment adjustments and prevent complications. In infectious diseases, time factors are crucial for initiating antibiotic therapy and identifying potential outbreaks to control their spread.

Overall, "time factors" encompass the significance of recognizing and acting promptly in various medical scenarios to optimize patient outcomes and provide effective care.

Fetoscopy is a minimally invasive surgical procedure that allows direct visualization of the fetus and the intrauterine environment through the use of a fiber-optic scope. It is typically performed during the second trimester of pregnancy to diagnose or treat various fetal conditions, such as twin-to-twin transfusion syndrome, congenital diaphragmatic hernia, or spina bifida. The procedure involves inserting a thin tube called a fetoscope through the mother's abdomen and uterus to access the fetus. Fetoscopy can also be used for taking fetal tissue samples for genetic testing.

It is important to note that while fetoscopy can provide valuable information and treatment options, it does carry some risks, including preterm labor, premature rupture of membranes, infection, and bleeding. Therefore, the decision to undergo fetoscopy should be made carefully, in consultation with a medical professional, and based on a thorough evaluation of the potential benefits and risks.

The pericardium is the double-walled sac that surrounds the heart. It has an outer fibrous layer and an inner serous layer, which further divides into two parts: the parietal layer lining the fibrous pericardium and the visceral layer (epicardium) closely adhering to the heart surface.

The space between these two layers is filled with a small amount of lubricating serous fluid, allowing for smooth movement of the heart within the pericardial cavity. The pericardium provides protection, support, and helps maintain the heart's normal position within the chest while reducing friction during heart contractions.

The Sinus of Valsalva are three pouch-like dilations or outpouchings located at the upper part (root) of the aorta, just above the aortic valve. They are named after Antonio Maria Valsalva, an Italian anatomist and physician. These sinuses are divided into three parts:

1. Right Sinus of Valsalva: It is located to the right of the ascending aorta and usually gives rise to the right coronary artery.
2. Left Sinus of Valsalva: It is situated to the left of the ascending aorta and typically gives rise to the left coronary artery.
3. Non-coronary Sinus of Valsalva: This sinus is located in between the right and left coronary sinuses, and it does not give rise to any coronary arteries.

These sinuses play a crucial role during the cardiac cycle, particularly during ventricular contraction (systole). The pressure difference between the aorta and the ventricles causes the aortic valve cusps to be pushed into these sinuses, preventing the backflow of blood from the aorta into the ventricles.

Anatomical variations in the size and shape of the Sinuses of Valsalva can occur, and certain conditions like congenital heart diseases (e.g., aortic valve stenosis or bicuspid aortic valve) may affect their structure and function. Additionally, aneurysms or ruptures of the sinuses can lead to severe complications, such as cardiac tamponade, endocarditis, or stroke.

Dilation, also known as dilatation, refers to the process of expanding or enlarging a body passage or cavity. In medical terms, it typically refers to the widening of a bodily opening or hollow organ, allowing for increased flow or access. This can occur naturally, such as during childbirth when the cervix dilates to allow for the passage of a baby, or it can be induced through medical procedures or interventions.

For example, dilation of the pupils is a natural response to darkness or certain medications, while dilation of blood vessels is a common side effect of some drugs and can also occur in response to changes in temperature or emotional state. Dilation of the stomach or intestines may be necessary for medical procedures such as endoscopies or surgeries.

It's important to note that dilation can also refer to the abnormal enlargement of a body part, such as dilated cardiomyopathy, which refers to an enlarged and weakened heart muscle.

Aortic coarctation is a narrowing of the aorta, the largest blood vessel in the body that carries oxygen-rich blood from the heart to the rest of the body. This condition usually occurs in the part of the aorta that is just beyond where it arises from the left ventricle and before it divides into the iliac arteries.

In aortic coarctation, the narrowing can vary from mild to severe, and it can cause a variety of symptoms depending on the severity of the narrowing and the age of the individual. In newborns and infants with severe coarctation, symptoms may include difficulty breathing, poor feeding, and weak or absent femoral pulses (located in the groin area). Older children and adults with mild to moderate coarctation may not experience any symptoms until later in life, when high blood pressure, headaches, nosebleeds, leg cramps, or heart failure develop.

Aortic coarctation is typically diagnosed through physical examination, imaging tests such as echocardiography, CT angiography, or MRI, and sometimes cardiac catheterization. Treatment options include surgical repair or balloon dilation (also known as balloon angioplasty) to open the narrowed section of the aorta. If left untreated, aortic coarctation can lead to serious complications such as high blood pressure, heart failure, stroke, and rupture or dissection of the aorta.

A feasibility study is a preliminary investigation or analysis conducted to determine the viability of a proposed project, program, or product. In the medical field, feasibility studies are often conducted before implementing new treatments, procedures, equipment, or facilities. These studies help to assess the practicality and effectiveness of the proposed intervention, as well as its potential benefits and risks.

Feasibility studies in healthcare typically involve several steps:

1. Problem identification: Clearly define the problem that the proposed project, program, or product aims to address.
2. Objectives setting: Establish specific, measurable, achievable, relevant, and time-bound (SMART) objectives for the study.
3. Literature review: Conduct a thorough review of existing research and best practices related to the proposed intervention.
4. Methodology development: Design a methodology for data collection and analysis that will help answer the research questions and achieve the study's objectives.
5. Resource assessment: Evaluate the availability and adequacy of resources, including personnel, time, and finances, required to carry out the proposed intervention.
6. Risk assessment: Identify potential risks and challenges associated with the implementation of the proposed intervention and develop strategies to mitigate them.
7. Cost-benefit analysis: Estimate the costs and benefits of the proposed intervention, including direct and indirect costs, as well as short-term and long-term benefits.
8. Stakeholder engagement: Engage relevant stakeholders, such as patients, healthcare providers, administrators, and policymakers, to gather their input and support for the proposed intervention.
9. Decision-making: Based on the findings of the feasibility study, make an informed decision about whether or not to proceed with the proposed project, program, or product.

Feasibility studies are essential in healthcare as they help ensure that resources are allocated efficiently and effectively, and that interventions are evidence-based, safe, and beneficial for patients.

Blood flow velocity is the speed at which blood travels through a specific part of the vascular system. It is typically measured in units of distance per time, such as centimeters per second (cm/s) or meters per second (m/s). Blood flow velocity can be affected by various factors, including cardiac output, vessel diameter, and viscosity of the blood. Measuring blood flow velocity is important in diagnosing and monitoring various medical conditions, such as heart disease, stroke, and peripheral vascular disease.

Angiography is a medical procedure in which an x-ray image is taken to visualize the internal structure of blood vessels, arteries, or veins. This is done by injecting a radiopaque contrast agent (dye) into the blood vessel using a thin, flexible catheter. The dye makes the blood vessels visible on an x-ray image, allowing doctors to diagnose and treat various medical conditions such as blockages, narrowing, or malformations of the blood vessels.

There are several types of angiography, including:

* Cardiac angiography (also called coronary angiography) - used to examine the blood vessels of the heart
* Cerebral angiography - used to examine the blood vessels of the brain
* Peripheral angiography - used to examine the blood vessels in the limbs or other parts of the body.

Angiography is typically performed by a radiologist, cardiologist, or vascular surgeon in a hospital setting. It can help diagnose conditions such as coronary artery disease, aneurysms, and peripheral arterial disease, among others.

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"Pulmonary valve stenosis - Diagnosis and treatment - Mayo Clinic". www.mayoclinic.org. Retrieved 2021-08-07. synd/2283 at Who ... Balloon valvuloplasty is the most common treatment for pulmonary stenosis, a balloon is placed where the artery or valve is ... "Pulmonary valve stenosis - Symptoms and causes". Mayo Clinic. Retrieved 2020-04-14. Bhattacharya, Priyanka T.; Sharma, Sandeep ... It may cause valve regurgitation. If balloon valvuplasty is not an option open heart surgery must be performed where the valve ...
... valves= tricuspid valve; mitral valve † Semilunar valves= pulmonary valve; aortic valve The closure of the aortic valve causes ... Contractions in the right ventricle provide pulmonary circulation by pulsing oxygen-depleted blood through the pulmonary valve ... The mitral and tricuspid valves, also known as the atrioventricular, or AV valves, open during ventricular diastole to permit ... the aortic and pulmonary valves) to open-which results in separated blood volumes being ejected from the two ventricles. This ...
The pulmonary valve is surgically closed. From the right ventricle to the pulmonary bifurcation, a synthetic conduit and a ... using a pulmonary or aortic homograft conduit to relieve pulmonary obstruction in double outlet right ventricle with pulmonary ... pulmonary atresia; or pulmonary stenosis; or subpulmonary stenosis. The Rastelli procedure is typically performed between one ... Univariable analysis revealed that a straddling tricuspid valve (P =.04) and longer aortic crossclamping periods (P =.04) were ...
Heart problems may include pulmonary valve stenosis. The breast bone may either protrude or be sunken, while the spine may be ... pulmonary valve stenosis, variable intellectual development, and skin pigment changes. Cardiofaciocutaneous (CFC) syndrome - ... This includes pulmonary valvular stenosis (50-60%), atrial septal defects (10-25%), ventricular septal defects (5-20%) and ... valvular pulmonary stenosis, often had a characteristic physical appearance, with short stature, webbed neck, wide spaced eyes ...
... the aortic valve at the aorta, and the pulmonary valve at the pulmonary artery. The heart also has a coronary sinus valve and ... as in mitral valve stenosis, tricuspid valve stenosis, pulmonary valve stenosis and aortic valve stenosis. Stenosis of the ... the pressure in the pulmonary artery will close the pulmonary valve. The closure of the pulmonary valve contributes the P2 ... The pulmonary valve (sometimes referred to as the pulmonic valve) lies between the right ventricle and the pulmonary artery, ...
Ross, D (1966). "Correction of Pulmonary Atresia with a Homograft Aortic Valve". The Lancet. 288 (7479): 1446-1447. doi:10.1016 ... the first report of the use of a homograft aortic valve to repair pulmonary atresia. In 1975, Somerville, "always feisty and ... Somerville, J (1970). "Management of pulmonary atresia". Br Heart J. 32 (5): 641-51. doi:10.1136/hrt.32.5.641. PMC 487386. PMID ...
... is a congenital malformation of the pulmonary valve in which the valve orifice fails to develop. The valve is ... Heart valves Percutaneous pulmonary valve implantation "Pulmonary atresia: MedlinePlus Medical Encyclopedia". www.nlm.nih.gov. ... such as the pulmonary valve and the tricuspid valve, are abnormally small. Pulmonary atresia with ventricular septal defect (PA ... The pulmonary valve is located on the right side of the heart between the right ventricle and pulmonary artery. In a normal ...
"Tissue engineering of pulmonary heart valves on allogenic acellular matrix conduits: in vivo restoration of valve tissue". ... Tissue engineered heart valves offer certain advantages over traditional biological and mechanical valves: Living valve - The ... "Porcine small intestine submucosa as a pulmonary valve leaflet substitute". The Journal of Heart Valve Disease. 9 (6): 769-74, ... In 2000, Matheny conducted a study in which he used a pig's small intestinal submucosa to replace one pulmonary valve leaflet. ...
Part 1: aortic and pulmonary regurgitation (native valve disease)" (PDF). European Journal of Echocardiography. 11 (3): 223-244 ... Aortic valve regurgitation vs aortic valve stenosis Phonocardiograms from normal and abnormal heart sounds The physical ... Physiologically, in individuals with a normally functioning aortic valve, the valve is only open when the pressure in the left ... "Aortic valve replacement - Why it's done - NHS Choices". www.nhs.uk. Retrieved 4 June 2016. "Aortic insufficiency: MedlinePlus ...
333 pulmonary valve insufficiency secondary to distortion of the ribcage;: 335-341 and basilar invagination.: 106-107 The ... to the heart valves, to the vasculature,: 329 it is an integral part of the connective tissue of the lungs.: 336 As such, ... 335 The most obvious source of respiratory problems in OI is pulmonary insufficiency caused by problems in the architecture of ...
... or pulmonary autograft for aortic valve disease. He has said that his interest had lain "particularly with the valves- ... it involves replacing a patient's damaged aortic valve with his or her own pulmonary valve. Ross believed that, "with care, the ... He developed the pulmonary autograft, known as the Ross procedure, for treatment of aortic valve disease. Donald Ross was born ... Archived 15 April 2012 at the Wayback Machine Ross D.N. (1967). "Replacement of aortic and mitral valves with a pulmonary ...
In pulmonary valve stenosis, there is a reduction in blood flow to the lungs due to an obstruction of the heart at the pulmonic ... Pulmonary valve stenosis results in issues of blood flow to the lungs. Abdominal organs, including the liver, stomach, ... valve. This contributes to cyanosis and pulmonary hypertension. For proper diagnosis of situs ambiguus, cardiac and non-cardiac ... In right atrial isomerism, the pulmonary blood oxygen tract is damaged due to right-left shunting of blood. In addition, the ...
Right sided variables are represented by pulmonary valve open to close time. Inverted as diastolic chronotropy, the variables ... Left sided systolic chronotropy can be appreciated as Aortic Valve open to close time. ... are aortic valve close to open and pulmonic close to open time. Pharmaceutical manipulation of chronotropic properties was ...
... posterior to the pulmonary valve. The pulmonary trunk bifurcates into right and left pulmonary arteries below the arch of aorta ... Pulmonary circuit Transverse section of thorax, showing relations of pulmonary artery. Pulmonary artery Pulmonary artery.Deep ... The largest pulmonary artery is the main pulmonary artery or pulmonary trunk from the heart, and the smallest ones are the ... The pulmonary trunk splits into the right and the left main pulmonary artery. The left main pulmonary artery is shorter than ...
Cardiac arrhythmia Aortic valve insufficiency Pulmonary artery hypertension: PAH has the following symptoms; dyspnea and ... Fowler, Robin (2012). "Exercise Intolerance in Pulmonary Arterial Hypertension". Pulmonary Medicine. June: 359204. doi:10.1155/ ... Dysfunctions involving the pulmonary, cardiovascular or neuromuscular systems have been frequently found to be associated with ... The exercise intolerance is associated with reduced pulmonary function that is the origin of CF. Bronchiectasis Post-exertional ...
The human heart contains four valves: tricuspid valve, pulmonary valve, mitral valve and aortic valve. Their main purpose is to ... A pulmonary homograft (a pulmonary valve taken from a cadaver) is then used to replace the patient's own pulmonary valve. This ... is where the aortic valve is removed and replaced with the patient's own pulmonary valve (the valve between the right ventricle ... the first clinically available tilting-disc valve was the Bjork-Shiley valve. Tilting‑disc valves, a type of swing check valve ...
The murmur is heard due to a high velocity flow back across the pulmonary valve; this is usually a consequence of pulmonary ... The Graham Steell murmur is often heard in patients with chronic cor pulmonale (pulmonary heart disease) as a result of chronic ... A Graham Steell murmur is a heart murmur typically associated with pulmonary regurgitation. It is a high pitched early ... In cases of mitral obstruction the murmur is occasionally heard over the pulmonary area and below this region, for the distance ...
It is also used in corrective surgeries for Tetralogy of Fallot where the pulmonary valve is anomalous, persistent truncus ... The maneuver entails cutting the main pulmonary artery and moving it anterior to the aorta before reattaching the pulmonary ... "The Lecompte Maneuver for Relief of Airway Compression in Absent Pulmonary Valve Syndrome". The Annals of Thoracic Surgery. 81 ... or in surgery to correct absent pulmonary valve syndrome. ... If both pulmonary arteries are not mobilized adequately, they ...
Pulmonary, or pulmonic stenosis is an often congenital narrowing of the pulmonary valve; it can be present in ... Ali Khan, M.; Al-Yousef, S.; Huhta, J.; Bricker, J.; Mullins, C.; Sawyer, W. (May 1989). "Critical pulmonary valve stenosis in ... Brachydactyly of the distal phalanges, sensorineural deafness and pulmonary stenosis are common with Keutel syndrome. In Muenke ... Other characteristics seen with the syndrome include developmental delay, growth retardation, pulmonary stenosis (an ...
Both stenosis of the pulmonary artery and pulmonary valve stenosis are causes of pulmonic stenosis.[citation needed]In some ... Stenosis of the pulmonary artery is a condition where the pulmonary artery is subject to an abnormal constriction (or stenosis ... It should not be confused with a pulmonary valve stenosis, which is in the heart, but can have similar hemodynamic effects. ... For peripheral pulmonary artery stenosis in Alagille syndrome". Tex Heart Inst J. 25 (1): 79-82. PMC 325508. PMID 9566070. v t ...
... pulmonary valve-open to valve-closed; left ventricle, aortic valve-open to valve-closed. The sinoatrial node (S-A Node) is the ... The pulmonary (or pulmonic) valve in the right ventricle opens into the pulmonary trunk, also known as the pulmonary artery, ... The atrioventricular valves remain open while the aortic and pulmonary valves remain closed because the pressure gradient ... systole pulses oxygen-depleted blood through the pulmonary valve through the pulmonary arteries to the lungs, providing ...
Pulmonary atresia in PAVSD takes place during the first 8 weeks of fetal life, when the pulmonary valve that is supposed to ... Pulmonary atresia with ventricular septal defect is a rare birth defect characterized by pulmonary valve atresia occurring ... since the phenotype of pulmonary atresia is not compatible with life due to the pulmonary valve atresia resulting in reduced ... The condition consists of atresia affecting the pulmonary valve and a hypoplastic right ventricular outflow tract. The ...
An imperforate pulmonary valve.. *A ventricular septum that is intact or can present a ventricular septal defect: This is a ... Prenatal. Pulmonary valve atresia can be suspected prenatally based on ultrasonography but must be confirmed postnatally. ... Pulmonary valve atresia is a structural heart anomaly characterized clinically by cyanosis and anatomically by an imperforate ... Specify intracardiac anatomy, including the presence of valve atresia, the involvement of the tricuspid valve, and whether the ...
... the pressure in the pulmonary artery closes the pulmonary valve. The closure of the pulmonary valve contributes to the P2 ... The pulmonary valve (sometimes referred to as the pulmonic valve) is a valve of the heart that lies between the right ventricle ... the other being the aortic valve. Similar to the aortic valve, the pulmonary valve opens in ventricular systole when the ... Pulmonary valves Pulmonary valves Stradins, P (September 2004). "Comparison of biomechanical and structural properties between ...
Oxygen-poor blood flows through this valve from the heart to the lungs, where it picks up fresh ... Absent pulmonary valve is a rare defect in which the pulmonary valve is either missing or poorly formed. ... Absent pulmonary valve syndrome; Congenital absence of the pulmonary valve; Pulmonary valve agenesis; Cyanotic heart disease - ... pulmonary valve; Congenital heart disease - pulmonary valve; Birth defect heart - pulmonary valve ...
Clinicians should not assume that sildenafil is beneficial in pulmonary hypertension following valve surgery, warn Spanish ... Cite this: Sildenafil Warning in Pulmonary Hypertension After Valve Surgery - Medscape - Aug 28, 2017. ... He nevertheless said that the evidence in support of the drug when used to treat pulmonary hypertension related to left heart ... The only established treatment for valvular heart disease is the repair or replacement of the valve, either surgically or ...
Congenital absence of the pulmonary valve with an intact ventricular septum occurs, but this is much less common. ... characterized by features of tetralogy of Fallot with either rudimentary ridges or the complete absence of pulmonic valve ... with absent pulmonary valve is a rare congenital anomaly ... Tetralogy of Fallot With Absent Pulmonary Valve * Sections ... encoded search term (Tetralogy of Fallot With Absent Pulmonary Valve) and Tetralogy of Fallot With Absent Pulmonary Valve What ...
pulmonary valve disease (DOID:5749) Alliance: disease page Synonyms: pulmonary valve disorder Alt IDs: ICD9CM_2006:424.3, ...
Valve replacement to remove the problem valve and put a mechanical or tissue valve in its place ... Valve replacement to remove the problem valve and put a mechanical or tissue valve in its place ... Surgery may be done to repair or replace the problem valve. Choices are: *Balloon valvuloplasty to pass a balloon to the valve ... Surgery may be done to repair or replace the problem valve. Choices are: *Balloon valvuloplasty to pass a balloon to the valve ...
Transcatheter Pulmonary Valves Market Study by Global Industry Analysts, Inc. ... Global Transcatheter Pulmonary Valves Market to Reach $115 Million by 2030. The global market for Transcatheter Pulmonary ... Transcatheter Pulmonary Valves. A Global Strategic Business Report. MCP22971. .accordion_2.mt-4 button.accordion{ border:none ! ... The Transcatheter Pulmonary Valves market in the U.S. is estimated at US$22.2 Million in the year 2022. China, the world`s ...
... pulmonary valve replacement with the Magna Ease #25 bioprosthetic tissue valve, and pulmonary arterioplasty with a bovine ... Pulmonary Artery Augmentation and Pulmonary Valve Replacement After Arterial Switch Operation Monday, October 9, 2023 ... However, due to the short length of the main pulmonary artery, difficulty in any future endovascular pulmonary valve procedures ... Man Fong S, Him Ling T. Pulmonary Artery Augmentation and Pulmonary Valve Replacement After Arterial Switch Operation. October ...
... the shunt flows from the ductus arteriosus towards the pulmonary valve. Although hemodynamic c ... Echocardiographic images of the pulmonary valve in a healthy dog (a, b) and a dog with PDA (c, d). Valves opened during systole ... The transducer was placed on the root of the pulmonary artery with the ultrasound beam aimed toward the pulmonary valves to ... Online Resource 1 Epicardial echocardiographic sectional image of the pulmonary artery at the pulmonary valve level in a dog ...
Percutaneous pulmonary valve implantation (PPVI) has revolutionized the management of right ventricular outflow tract ... Bartonella henselae endocarditis of percutaneously implanted pulmonary valve Iryna Atamanyuk et al. J Heart Valve Dis. 2012 Sep ... Bartonella henselae endocarditis of percutaneously implanted pulmonary valve Iryna Atamanyuk 1 , Shahzad G Raja, Martin ... Atamanyuk I, Raja SG, Kostolny M. Atamanyuk I, et al. J Heart Valve Dis. 2011 Jan;20(1):94-7. J Heart Valve Dis. 2011. PMID: ...
The two main types of pulmonary valve disease are pulmonary valve regurgitation (leaking of the valve) and pulmonary stenosis ( ... Causes of Pulmonary Valve Disease. In adults, pulmonary regurgitation usually is caused by high blood pressure in the pulmonary ... Pulmonary Valve Disease Symptoms. Pulmonary valve regurgitation is often detected by a physician while listening to the heart ... The pulmonary valve allows blood to flow one way from the right ventricle (lower-right chamber) of the heart into the pulmonary ...
Pulmonary Valve Stenosis in Children - Learn about the causes, symptoms, diagnosis & treatment from the MSD Manuals - Medical ... Symptoms of Pulmonary Valve Stenosis in Children Most children with pulmonary valve stenosis have no symptoms. Severe pulmonary ... Pulmonary valve stenosis is a narrowing of the pulmonary valve (sometimes called the pulmonic valve), which opens to allow ... In most children with pulmonary valve stenosis, the valve is mildly to moderately narrowed, making the right ventricle pump a ...
Critical aortic valve stenosis in newborns is the cause of a severe clinical condition with the onset of symptoms during first ... Critical aortic valve stenosis; hybrid correction; hybrid Norwood; bilateral banding; hybrid Norwood procedure; acute pulmonary ... Emergency Hybrid Correction in a Newborn with Critical Aortic Valve Stenosis with Acute Pulmonary Edema in the First Hour after ... Emergency Hybrid Correction in a Newborn with Critical Aortic Valve Stenosis with Acute Pulmonary Edema in the First Hour after ...
Pulmonary valve stenosis is a condition, usually present at birth, where either the pulmonary valve or the pulmonary artery ... Pulmonary Valve Stenosis Pulmonary valve stenosis is a condition, usually present at birth, where either the pulmonary valve or ... and other conditions that can cause damage or scarring of the pulmonary valve.. Symptoms of Pulmonary Valve Stenosis Symptoms ... Causes of Pulmonary Valve Stenosis Pulmonary stenosis is most commonly caused by a malformation during fetal development. The ...
... is often incomplete after successful left-sided valve replacement (LSVR). Proximal pulmonary arterial (PPA) wall disease can be ... Despite normal PVR and DPG, Ipc-PH had a significant decrease in pulmonary arterial capacitance and RV-PA coupling impairment. ... Patients were classified as isolated post-capillary PH (Ipc-PH; pulmonary vascular resistance [PVR] ≤ 3 WU and/or diastolic ... RV-PA coupling was estimated by the tricuspid annular plane systolic excursion to systolic pulmonary arterial pressure ratio. ...
Pulmonary Valve 3D. *​Description ** Lies behind the medial end of the left third costal cartilage and the adjacent portion of ... Opens during ventricular systole and shuts slightly after closure of the aortic valve. ... Opens during ventricular systole and shuts slightly after closure of the aortic valve. ...
"Pulmonary Valve Stenosis" by people in this website by year, and whether "Pulmonary Valve Stenosis" was a major or minor topic ... "Pulmonary Valve Stenosis" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical ... This lesion restricts blood outflow from the RIGHT VENTRICLE to the PULMONARY ARTERY. When the trileaflet valve is fused into ... Below are the most recent publications written about "Pulmonary Valve Stenosis" by people in Profiles. ...
Nonrheumatic pulmonary valve incompetence Nonrheumatic pulmonary valve regurgitation MS-DRG Mapping * DRG Group #306-307 - ... the aortic and mitral valves on the left and the pulmonary and tricuspid valves on the right). These conditions occur largely ... Nonrheumatic pulmonary valve insufficiency BILLABLE Billable Code Billable codes are sufficient justification for admission to ... I37.1 is a billable ICD code used to specify a diagnosis of nonrheumatic pulmonary valve insufficiency. A billable code is ...
... a pulmonary valve replacement can be adjusted as a child grows, eliminating the need for invasive procedures. ... have congenital pulmonary valve disease, which impedes the flow of blood between the heart and lungs. Pulmonary valves that are ... The Autus Valves leaflets are made of a polymer with a long track record of use as a pediatric pulmonary valve leaflet.. ... "There is a huge need for better solutions for children with valve disease," Hofferberth says. "A pulmonary valve that can be ...
Learn more about how heart valves work and the common types of problems that can occur. ... The type of heart valve disease you have depends on which valve is affected and in what way. ... Heart valve diseases can cause problems in any of the hearts four valves: the aortic, mitral, pulmonary, and tricuspid valves ... There are two main types of heart valve atresia:. *Pulmonary atresia affects the pulmonary valve. In this condition, blood ...
Get access to cutting edge treatment via Pulmonary Valve Replacement Surgery. View duration, location, compensation, and ... Your doctors have suggested that you should have surgery to replace your pulmonary valve.. ... Idiopathic Pulmonary Fibrosis Clinical Trials 2023. Top 10 Idiopathic Pulmonary Fibrosis Clinical Trials [2023 Studies] , Power ... Pulmonary Arterial Hypertension Clinical Trials 2023. Top 10 Pulmonary Arterial Hypertension Clinical Trials [2023 Studies] , ...
My son, 29, teacher with Tetralogy of Fallot, has a leaky pulmonary valve-is he likely to need further surgery as he gets older ... In some cases, after repair of tetralogy of Fallot, the pulmonary valve can become leaky, and this sometimes does need further ...
Images in cardiovascular medicine Three-dimensional reconstruction of pulmonary valve ...
Minimally Invasive Pulmonary Valve Replacement Following Tetralogy of Fallot Repair ... Minimally Invasive Pulmonary Valve Replacement Following Tetralogy of Fallot Repair. Joseph Nellis1, Steven Thornton, Jr2, ... Patients often need multiple pulmonary valve replacements (PVR) throughout their life, and the temporary setbacks associated ... BACKGROUND: Pulmonary insufficiency is a well-documented complication following Tetralogy of Fallot (ToF) repair. Traditionally ...
Pulmonary hemodynamics and angiography are required for definitive diagnosis. BPA may offer these patients successful short- ... We describe a severe syndrome of isolated PPS in the adult that mimics chronic pulmonary thromboembolic disease. ... Pulmonary Artery / embryology * Pulmonary Artery / pathology * Pulmonary Valve Stenosis / complications * Pulmonary Valve ... Balloon pulmonary angioplasty (BPA) to decrease RV hypertension and improve pulmonary flow distribution was performed in 11 ...
The purpose of this study is to clarify the characteristic of idiopathic VT arising above pulmonary valve. We analyzed 15 ... The purpose of this study is to clarify the characteristic of idiopathic VT arising above pulmonary valve. We analyzed 15 ... The purpose of this study is to clarify the characteristic of idiopathic VT arising above pulmonary valve. We analyzed 15 ... The purpose of this study is to clarify the characteristic of idiopathic VT arising above pulmonary valve. We analyzed 15 ...
A simplified resistance valve for the pneumatic treatment of pulmonary affections. Collection:. Medicine in the Americas, 1610- ...
A simplified resistance valve for the pneumatic treatment of pulmonary affections. Collection:. Medicine in the Americas, 1610- ...
  • In pulmonary valve regurgitation, the valve does not close completely, allowing blood to flow backward into the heart. (emoryhealthcare.org)
  • Pulmonary valve stenosis can cause the heart to work harder, ultimately damaging the muscle and leading to heart failure, while pulmonary valve regurgitation can cause enlargement in the right ventricle, one of the four chambers of the heart. (emoryhealthcare.org)
  • Pulmonary valve regurgitation may occur as a result of a number of conditions, including endocarditis and pulmonary hypertension (high blood pressure). (emoryhealthcare.org)
  • The absence of mature pulmonary valve tissue leads to severe pulmonary regurgitation, which is often associated with massive dilatation of the proximal branch pulmonary arteries and which is characteristic of this syndrome. (medscape.com)
  • The absence of a functioning pulmonary valve gives rise to pulmonary regurgitation (insufficiency) that results in aneurysmal dilatation of the main and branch pulmonary arteries, which can compress the tracheobronchial tree (see the following image). (medscape.com)
  • Harmonyâ„¢ TPV is the first FDA-approved transcatheter valve system specifically designed to treat severe pulmonary regurgitation in patients with a native or surgically-repaired right ventricular outflow tract (RVOT) - offering your patients a minimally invasive treatment option. (medtronic.com)
  • The Harmony Transcatheter Pulmonary Valve (TPV) System is indicated for use in the management of pediatric and adult patients with severe pulmonary regurgitation (i.e., severe pulmonary regurgitation as determined by echocardiography and/or pulmonary regurgitant fraction ≥ 30% as determined by cardiac magnetic resonance imaging) who have a native or surgically-repaired right ventricular outflow tract and are clinically indicated for surgical pulmonary valve replacement. (medtronic.com)
  • At 6 months, 96.7% of the implanted cohort with evaluable data had acceptable hemodynamic function (primary endpoint), with 87 patients having a mean RVOT gradient ≤ 30 mm Hg and none having moderate or worse pulmonary regurgitation, needing catheter-based reintervention, or requiring surgical RVOT conduit replacement. (tctmd.com)
  • Additionally, 1-year rates of freedom from catheter- or surgery-based reintervention and TPV dysfunction were 98.0% and 96.9%, respectively, and no patients had moderate or severe pulmonary regurgitation. (tctmd.com)
  • In that case, the valve may begin to allow blood to "leak" back into the heart over time-this is known as pulmonary valve regurgitation. (secondscount.org)
  • Mild to moderate pulmonary valve leakage (or pulmonary valve regurgitation) may produce no symptoms. (secondscount.org)
  • Scholars@Duke publication: Branch Pulmonary Artery Valve Implantation Reduces Pulmonary Regurgitation and Improves Right Ventricular Size/Function in Patients With Large Right Ventricular Outflow Tracts. (duke.edu)
  • METHODS: Retrospective data were collected on patients with significant pulmonary regurgitation who had a percutaneous branch PA valve attempted. (duke.edu)
  • The approval enables the treatment of adult and pediatric patients who suffer from either a narrowed pulmonary valve or moderate or greater pulmonary regurgitation caused by congenital heart disease. (dicardiology.com)
  • Although pulmonary valve stenosis or regurgitation is often tolerated over the short and intermediate terms, the long-term consequences are numerous and include, but are not limited to, right-sided heart failure, arrhythmias, and sudden cardiac death. (structuralheartdisease.org)
  • Our specialists recommend mitral valve repair based on the severity of your heart's mitral valve regurgitation and your symptoms. (barnesjewish.org)
  • Mitral valve repair is now an option for nearly every patient who needs surgery to correct mitral valve regurgitation. (barnesjewish.org)
  • The device is designed for patients who have severe pulmonary valve regurgitation (blood leaking backward into the right lower chamber of the heart), a condition that often results from congenital heart disease. (fda.gov)
  • The device, called the Harmony Transcatheter Pulmonary Valve (TPV) System, is intended to improve blood flow to the lungs in patients with severe pulmonary valve regurgitation without open-heart surgery, which is the current standard of care. (fda.gov)
  • After having one of these procedures, the patient may or may not have a working pulmonary valve, which could lead to pulmonary regurgitation. (fda.gov)
  • Severe pulmonary valve regurgitation may be corrected through open-heart surgery to place a right ventricle-pulmonary artery conduit or an artificial valve. (fda.gov)
  • citation needed] Heart valve Pulmonary atresia Interior of right side of heart. (wikipedia.org)
  • See Tetralogy of Fallot , Tetralogy of Fallot With Pulmonary Stenosis , and Tetralogy of Fallot With Pulmonary Atresia for more information on these topics. (medscape.com)
  • As part of a comprehensive interventional cardiology program, Morgan Stanley Children's Hospital offers a complete range of treatments for congenital heart conditions including atrial septal defects (ASD), ventricular septal defects (VSD), aortic stenosis (AS), patent ductus arteriosus (PDA), pulmonary atresia (PA) and more. (medindia.net)
  • Pulmonary atresia and truncus arteriosus - Repair of these conditions may involve the placement of a valved tube (conduit) or human tissue tube (homograft) between the right ventricle and pulmonary artery. (secondscount.org)
  • Pulmonary atresia, intact ventricular septum, and Ebstein anomaly of the tricuspid valve. (unipd.it)
  • Pulmonary atresia with intact ventricular septum is a disorder that involves the whole right ventricle. (unipd.it)
  • Ebstein anomaly of the tricuspid valve further complicates surgical management and outcome of pulmonary atresia and intact ventricular septum. (unipd.it)
  • Pulmonary valve stenosis is a narrowing of the valve between the lower right heart chamber and the lung arteries. (mayoclinic.org)
  • In addition to compression of the larger bronchi, Rabinovitch et al described abnormal tufts of the smaller pulmonary arteries that compress the intrapulmonary bronchi. (medscape.com)
  • A right aortic arch, a ventricular septal defect with overriding aortic valve, and massively dilated main and branch pulmonary arteries are present. (medscape.com)
  • This and the airway obstruction due to the dilated pulmonary arteries are the hallmarks of the condition. (medscape.com)
  • The RVOT is the part of the heart that takes blood from the lower pumping chamber (right ventricle) to the blood vessels (pulmonary arteries) that carry blood from the right side of the heart to the lungs. (secondscount.org)
  • The RVOT includes the area underneath the pulmonary valve, the pulmonary valve itself, and a portion of the main pulmonary artery (before it divides into the right and the left lung arteries). (secondscount.org)
  • hence, a CT pulmonary angiogram was done which showed septic pulmonary embolism and multiple mycotic aneurysms of the pulmonary arteries. (bmj.com)
  • Refers to the specific combination of defects with a severely dysplastic pulmonary valve and massively dilated branch pulmonary arteries. (beds.ac.uk)
  • The heart is made up of a series of valves, chambers, arteries, and veins that rhythmically pump and move blood through it and into the body. (healthline.com)
  • The other two valves are at the entrance to the arteries leaving the heart these are the semilunar valves - the aortic valve at the aorta , and the pulmonary valve at the pulmonary artery . (wikipedia.org)
  • Depending on the results of your cardiac evaluation, your doctor may recommend medications to reduce fluid retention, although there's currently no medication for the leaky valve itself. (secondscount.org)
  • Infective endocarditis is a life-threatening infection rect evidence of M. genitalium pathogenicity is weak of the cardiac endothelium that can manifest as a and often difficult to ascertain because of concomitant new cardiac murmur, heart failure, valve vegetations, sexually transmitted pathogens. (cdc.gov)
  • Multiple types of congenital heart defects-7 (CHTD7) is an autosomal dominant disorder with incomplete penetrance characterized mainly by tetralogy of Fallot but also including right-sided aortic arch, absent pulmonary valve, and other cardiac abnormalities (Jin et al. (beds.ac.uk)
  • Collectively and anatomically, the valves are part of the dense connective tissue makeup of the heart known as the cardiac skeleton . (wn.com)
  • Objective Pulmonary hypertension (PHT) has been considered a risk factor for mortality in cardiac surgery. (nebraska.edu)
  • Heart valves are situated around the fibrous rings of the cardiac skeleton . (wikipedia.org)
  • The primary safety outcome included the composite of acute (less than 7 days post-procedure) and chronic (more than 7 days post-procedure) major adverse events, including atrioesophageal fistula, symptomatic pulmonary vein stenosis, cardiac tamponade/perforation requiring intervention or surgery, stroke or systemic thromboembolism , persistent phrenic nerve injury, vascular access complications requiring surgery, coronary artery spasm, and death. (medscape.com)
  • The atrial and ventricular masses, conduction system tissue, and support structure of the fibroelastic cardiac skeleton allow coordinated actions of the tricuspid valve. (medscape.com)
  • and Balloon Pulmonary Angioplasty for Chronic Thromboembolic Pulmonary Hypertension. (elsevier.ca)
  • Spontaneous Tricuspid Valve Chordal Rupture in Idiopathic Pulmonary Hypertension. (ox.ac.uk)
  • We report herein a case of a patient with severe pulmonary hypertension, on the lung transplantation waiting list, who presented with spontaneous chordal rupture, exacerbation of tricuspid insufficiency and worsening of clinical status. (ox.ac.uk)
  • A contemporary analysis of pulmonary hypertension in patients undergoing mitral valve surgery: Is this a risk factor? (nebraska.edu)
  • Dive into the research topics of 'A contemporary analysis of pulmonary hypertension in patients undergoing mitral valve surgery: Is this a risk factor? (nebraska.edu)
  • Despite advances in drug therapy, pulmonary hypertension-particularly arterial hypertension (PAH)-remains a fatal disease. (revespcardiol.org)
  • Percutaneous balloon pulmonary angioplasty, another interventional therapy, has re-emerged in the last few years as a clear alternative for the management of patients with distal, inoperable, chronic thromboembolic pulmonary hypertension. (revespcardiol.org)
  • The current review discusses the physiological background, experimental evidence, and potential clinical and hemodynamic benefits of all these interventional therapies regarding their use in the setting of RHF due to severe pulmonary hypertension. (revespcardiol.org)
  • What are the potential complications of pulmonary valve stenosis? (healthline.com)
  • The pulmonary valve (sometimes referred to as the pulmonic valve) is a valve of the heart that lies between the right ventricle and the pulmonary artery, and has three cusps. (wikipedia.org)
  • Tetralogy of Fallot (TOF) with absent pulmonary valve is a rare congenital anomaly characterized by features of tetralogy of Fallot with either rudimentary ridges or the complete absence of pulmonic valve tissue and usually with a hypoplastic pulmonary valve annulus. (medscape.com)
  • Edwards Lifesciences Corp. announced U.S. Food and Drug Administration (FDA) approval to expand use of the Edwards Sapien XT transcatheter heart valve for pulmonic valve replacement procedures. (dicardiology.com)
  • U.S. approval of the Sapien XT valve for pulmonic procedures provides an important, minimally invasive treatment option for a small group of patients who typically face the burden of multiple open-heart surgeries, oftentimes beginning at birth or during childhood. (dicardiology.com)
  • FDA approval of the Edwards Sapien XT valve for pulmonic procedures was supported by data from the multicenter COMPASSION clinical trial and additional clinical data from Europe. (dicardiology.com)
  • Pulmonic stenosis is a heart valve disorder that involves the pulmonary valve. (medlineplus.gov)
  • Narrowing that occurs in the valve itself is called valvular pulmonic stenosis. (medlineplus.gov)
  • Pulmonary valve stenosis is a narrowing of the pulmonary valve (sometimes called the pulmonic valve), which opens to allow blood to flow from the right ventricle to the lungs. (msdmanuals.com)
  • Pulmonic Stenosis Pulmonic (pulmonary) stenosis is a narrowing of the pulmonary valve opening that blocks (obstructs) blood flow from the right ventricle to the pulmonary artery. (msdmanuals.com)
  • The pulmonary valve is between the heart's right chamber and the main pulmonary artery (MPA). (chp.edu)
  • Before the aortic cross-clamp, the main pulmonary artery (PA) was also snared. (ctsnet.org)
  • Similar to the aortic valve, the pulmonary valve opens in ventricular systole when the pressure in the right ventricle rises above the pressure in the pulmonary artery. (wikipedia.org)
  • At the end of ventricular systole, when the pressure in the right ventricle falls rapidly, the pressure in the pulmonary artery closes the pulmonary valve. (wikipedia.org)
  • Congenital absence of the pulmonary valve with an intact ventricular septum occurs, but this is much less common. (medscape.com)
  • However, when the pulmonary valve is absent and the ventricular septum is intact, a normal ductus arteriosus is also generally present. (medscape.com)
  • Tetralogy of Fallot (TOF) consists of a malalignment ventricular septal defect (VSD), infundibular pulmonary stenosis, overriding aorta, and right ventricular hypertrophy (RVH). (medscape.com)
  • Characteristic muscular right ventricular hypertrophy and infundibular pulmonary stenosis are present. (medscape.com)
  • Expanding on data from the Investigational Device Exemption (IDE) trial, a postapproval study confirms the short-term hemodynamic effectiveness of the Melody transcatheter pulmonary valve (TPV) in patients with right ventricular outflow tract (RVOT) conduit dysfunction. (tctmd.com)
  • Many forms of congenital heart disease (CHD) repaired in infancy and childhood involve surgery on the pulmonary valve and right ventricular outflow tract (RVOT). (secondscount.org)
  • BACKGROUND: Most patients with large right ventricular outflow tracts (RVOTs) are excluded from available percutaneous pulmonary valve options. (duke.edu)
  • CONCLUSIONS: Percutaneous branch PA valve implantation results in a reduction in right ventricular volume with clinical benefit in the intermediate term. (duke.edu)
  • A correlation between the degree of tricuspid valve dysplasia and right ventricular cavity size was observed in all. (unipd.it)
  • A prospective, non-randomized, open label clinical study of a Restorative Pulmonary Heart Valve in Right Ventricular Outflow Tract (RVOT) reconstruction. (xplore2md.com)
  • La insuficiencia ventricular derecha (IVD) debida a HAP refractaria a tratamiento finalmente se produce y permanece como una causa importante de muerte en estos pacientes. (revespcardiol.org)
  • Today, the U.S. Food and Drug Administration approved the first in the world non-surgical heart valve to treat pediatric and adult patients with a native or surgically-repaired right ventricular outflow tract (RVOT), the part of the heart that carries blood out of the right ventricle to the lungs. (fda.gov)
  • After the atrioventricular (AV) endocardial cushions fuse, each atrioventricular orifice is surrounded by local proliferations of mesenchymal tissue, from which the AV valves form and are attached to the ventricular wall by muscular cords. (medscape.com)
  • The upper or atrial surface of the valve is thick and resembles atrial endocardium, and the lower or ventricular surface of the valve is thin and resembles ventricular endocardium. (medscape.com)
  • J&J COVID-19 Vaccine and Thrombosis + Medtronic's Harmony Transcatheter Pulmonary Valve Approval - Xtalks Life Science Podcast Ep. (xtalks.com)
  • The minimally invasive procedure, which involves the implantation of the first-ever catheter-based pulmonary valve replacement, is currently performed by interventional cardiologists at Morgan Stanley Children's Hospital of NewYork-Presbyterian and Columbia University Medical Center-the only New York City site and one of only three sites nationally that is offering the procedure as part of an ongoing clinical research trial. (medindia.net)
  • We have read the interesting article from Bokma and colleagues 1 documenting the outcomes of pulmonary valve replacement (PVR) in patients with repaired tetralogy of Fallot (rTOF). (bmj.com)
  • Methods: Blinded retrospective analyses of 177 TOF patients undergoing pulmonary valve replacement (PVR) between 1997 and 2015 were performed. (lu.se)
  • Sometimes, these CHD conditions may require a pulmonary valve replacement later in life. (secondscount.org)
  • She was treated with antibiotics and underwent tricuspid valve replacement and was discharged well with a return to her baseline functional capacity on subsequent follow-ups. (bmj.com)
  • and Transcatheter Tricuspid Valve Replacement. (elsevier.ca)
  • after valve replacement. (cdc.gov)
  • Transcatheter pulmonary valve replacement is safe, effective, and performed at an increasing number of centers around the world. (structuralheartdisease.org)
  • Most valve replacement surgeries are successful. (medicalnewstoday.com)
  • Heart valve replacement surgery carries some risks, such as infection and bleeding. (medicalnewstoday.com)
  • Keep reading to learn more about heart valve replacement surgery, including when it may be necessary, how much it may cost, what to expect, and what risks come with it. (medicalnewstoday.com)
  • A heart valve replacement may be necessary if a person's heart valves are not working properly and are too damaged for a repair to be successful. (medicalnewstoday.com)
  • Sometimes, people may need a replacement for more than one valve. (medicalnewstoday.com)
  • According to a 2020 study , the average cost of aortic valve replacement surgery is about $59,000. (medicalnewstoday.com)
  • Preparation for a valve replacement depends on the type of procedure a person is having. (medicalnewstoday.com)
  • This type of replacement procedure involves opening up the chest to replace a damaged valve. (medicalnewstoday.com)
  • When you have symptoms from valvular heart disease, heart valve replacement or repair can restore your heart's function. (barnesjewish.org)
  • Heart Valve Replacement and Repair: Why Choose Us? (barnesjewish.org)
  • We have excellent outcomes for transcatheter aortic valve replacement (TAVR) and aortic valve surgery, according to U.S.News & World Report rankings. (barnesjewish.org)
  • We were one of the first programs in the world to learn and teach others how to perform transcatheter aortic valve replacement (TAVR). (barnesjewish.org)
  • Treatment may be with medication but often (depending on the severity) involves valve repair or replacement (insertion of an artificial heart valve ). (wn.com)
  • In all, 84% of patients undergoing valve implantation had concomitant interventional procedures, 78% of which involved stenting. (tctmd.com)
  • Unlike the IDE trial, the postapproval study also had no age or weight limit, which is important, they say, because 1 of the 2 pediatric patients in whom implantation was unsuccessful due to pulmonary hemorrhage before implantation would have been considered too small for the IDE trial. (tctmd.com)
  • In some of these patients, percutaneous branch PA valve implantation may be feasible. (duke.edu)
  • RESULTS: Percutaneous branch PA valve implantation was attempted in 34 patients (18 bilateral and 16 unilateral). (duke.edu)
  • Until percutaneous valve technology for large RVOTs is refined and more widely available, branch PA valve implantation remains an option for select patients. (duke.edu)
  • However, another option is transcatheter aortic valve implantation (TAVI), a less invasive procedure. (medicalnewstoday.com)
  • In patients with congenital heart defects, restoration of the right ventricle outflow tract (RVOT) continuity by surgical or percutaneous bovine valve implantation is a common procedure. (biomedcentral.com)
  • Flow characteristics in such valves are complex, therefore the aim of this study was demonstrating the potential application of 4D MRI flow for the comprehensive assessment of pulmonary flow patterns after surgical and percutaneous bovine valve implantation in the RVOT. (biomedcentral.com)
  • Fifteen patients after percutaneous bovine valve implantation (17.2 ± 2.0 years), 15 patients after surgical implantation (15.8 ± 1.7 years), and 15 healthy volunteers (as a control group) (16.5 ± 1.5 years) were included. (biomedcentral.com)
  • Patients with percutaneous implantation showed an eccentric pulmonary flow (deviation angle from the midline 31 ± 10 degree) with vortex formation (vortex size 73 ± 18%), and a significant asymmetric elevated WSR at focal regions of the conduit. (biomedcentral.com)
  • In contrast, those after surgical implantation showed a laminar pulmonary flow with no visible vortex and had symmetric, although elevated WSR in the conduit regions. (biomedcentral.com)
  • During the implantation procedure of a Harmony valve, a thin, hollow tube (catheter) with a collapsed Harmony valve on the end is inserted through a vein in the groin or in the neck and into the right side of the heart, and then into the RVOT where it is placed into position. (fda.gov)
  • Analysis of ECG Changes in Relation to Pulmonary Valve Implantation. (bvsalud.org)
  • It increases the risk of developing pulmonary valve stenosis later in life. (mayoclinic.org)
  • An echocardiography showed poor left ventricle contractility with 25 percent LVEF and a small apical aneurysm, severe MV insufficiency that was due to anomalous posterior leaflet and annular dilatation, and the left coronary artery arising from anterior sinus of the pulmonary artery. (ctsnet.org)
  • Part II will focus on Interventional Therapy for Pulmonary Embolism, with editorial direction from Dr. Jay Giri. (elsevier.ca)
  • The image below compares the pulmonary artery branching between healthy patients and those with absent pulmonary valve syndrome. (medscape.com)
  • Pulmonary artery branching in a healthy person and in a patient with absent pulmonary valve syndrome. (medscape.com)
  • However, tetralogy of Fallot with absent pulmonary valve is rare, with approximately 3% of patients with tetralogy of Fallot having the absent pulmonary valve syndrome. (medscape.com)
  • Emmanoulides et al were the first to highlight the association of absent pulmonary valve syndrome with the absence of the ductus arteriosus. (medscape.com)
  • Drawing showing absence of the pulmonary valve with features of tetralogy of Fallot. (medscape.com)
  • Etiologic factors for tetralogy of Fallot (TOF) with absent pulmonary valve are not known in most cases. (medscape.com)
  • 1. After surgical relief of RVOT obstruction with a conduit or prosthetic valve , patients should be followed up on a 1- to 2-year basis with echocardiography Doppler assessment of RV systolic pressure and function, as well as a measurement of the gradient across the RVOT . (wikidoc.org)
  • However, only ~15% of potential patients with RVOT dysfunction are suitable for currently approved implantable valves (i.e. (structuralheartdisease.org)
  • The Venus P-valve (Venus Medtech, Shanghai, China) is a recently developed self-expanding transcatheter heart valve designed to adapt to a dilated RVOT and in such it provide patients with a percutaneous interventional option after transannular patch repair. (structuralheartdisease.org)
  • Pulmonary flow patterns differ significantly between patients with a surgical and percutaneously implanted bovine valve in the RVOT. (biomedcentral.com)
  • In severe cases, surgery may be required to replace the pulmonary valve. (healthline.com)
  • Some people may need heart surgery to repair or replace the pulmonary valve. (medlineplus.gov)
  • The pulmonary valve controls blood flow between the heart and the lungs. (emoryhealthcare.org)
  • In pulmonary valve stenosis, the valve narrows, restricting blood flow to the lungs. (emoryhealthcare.org)
  • This causes the heart to work harder to push blood through the valve and into the lungs. (chp.edu)
  • A properly functioning pulmonary valve keeps blood flowing from the heart's lower right pumping chamber (right ventricle) into the pulmonary artery and onto the lungs. (secondscount.org)
  • The pulmonary artery carries oxygen-poor blood to the lungs. (medlineplus.gov)
  • The heart valve between the right ventricle and the artery to the lungs is narrowed. (msdmanuals.com)
  • The pulmonary artery carries oxygen-poor blood from the right ventricle into the lungs, where oxygen enters the bloodstream. (rochester.edu)
  • A surgical procedure known as a valvuloplasty can stretch the pulmonary valve's walls to improve blood flow. (healthline.com)
  • In the Heart Catheterization Lab at UPMC Children's Hospital , we use a balloon to widen the pulmonary valve (valvuloplasty). (chp.edu)
  • Percutaneous balloon pulmonary dilation (valvuloplasty) may be performed when no other heart defects are present. (medlineplus.gov)
  • Balloon valvuloplasty to open the valve or surgery to reconstruct it is sometimes needed. (msdmanuals.com)
  • A congenital heart defect characterized by the narrowing or complete absence of the opening between the RIGHT VENTRICLE and the PULMONARY ARTERY. (bvsalud.org)
  • What are the symptoms of pulmonary valve stenosis? (healthline.com)
  • Some people with mild pulmonary valve stenosis don't have symptoms. (mayoclinic.org)
  • Pulmonary valve stenosis symptoms depend on how much blood flow is blocked. (mayoclinic.org)
  • Those with more-severe pulmonary stenosis may first notice symptoms while exercising. (mayoclinic.org)
  • You have symptoms of pulmonary valve stenosis. (medlineplus.gov)
  • You have been treated or have untreated pulmonary valve stenosis and have developed swelling (of the ankles, legs, or abdomen), difficulty breathing, or other new symptoms. (medlineplus.gov)
  • Most children with pulmonary valve stenosis have no symptoms. (msdmanuals.com)
  • 1. Either surgical or percutaneous therapy can be useful in symptomatic patients with discrete RV pulmonary artery conduit obstructive lesions with greater than 50% diameter narrowing or when a bioprosthetic pulmonary valve has a peak gradient by Doppler greater than 50 mm Hg or a mean gradient greater than 30 mm Hg. (wikidoc.org)
  • 2. Either surgical or percutaneous therapy can be useful in asymptomatic patients when a pulmonary bioprosthetic valve has a peak Doppler gradient greater than 50 mm Hg. (wikidoc.org)
  • OBJECTIVES: The authors sought to assess the intermediate-term effects of percutaneous placed valves in the branch pulmonary artery (PA) position. (duke.edu)
  • Reasons for not receiving a valve included: risk of coronary artery compression (n = 6), conduit not suitable for implant (n = 4), criteria not met during catheterization (n = 4), relief of conduit stenosis by angioplasty (n = 3), need for surgical repair of another heart condition (n = 1), and risk of branch pulmonary artery stent compression (n = 1). (tctmd.com)
  • The surgical incision that cuts through the pulmonary valve opening may leave it somewhat leaky during this procedure. (secondscount.org)
  • As risks increase with each open-heart surgery, a non-surgical option can help them receive treatment, recover and return to normal activities sooner," said Larry L. Wood, Edwards' corporate vice president, transcatheter heart valves. (dicardiology.com)
  • In two of our surgical patients, a protruding anterior tricuspid valve leaflet was identified and excised and both patients survived. (unipd.it)
  • And the more blood the valve allows to back up into the heart, the more work the heart's right chamber must do. (secondscount.org)
  • Ideally, before your heart's function is affected, your doctor will recommend that your pulmonary valve be fixed or replaced. (secondscount.org)
  • Defects may involve abnormal formation of the heart's walls or valves or of the blood vessels that enter. (msdmanuals.com)
  • The heart's four valves open and close to move blood through the heart's chambers. (healthline.com)
  • This is the name for the condition that causes changes to the heart's valves. (healthline.com)
  • This is the valve separating the right ventricle (one of the chambers in the heart) and the pulmonary artery. (medlineplus.gov)
  • Prompt diagnosis and treatment of pulmonary valve stenosis can help reduce the risk of complications. (mayoclinic.org)
  • Prenatal Diagnosis, Associations and Outcome for Fetuses with Congenital Absence of the Pulmonary Valve Syndrome. (beds.ac.uk)
  • Currently, babies with absent or defective pulmonary valves may require open-heart surgery to implant a valved-conduit (a two-inch tube with a valve inside) to open the connection between their right ventricle and pulmonary artery. (medindia.net)
  • It is one of the four valves of the heart and one of the two semilunar valves, the other being the aortic valve. (wikipedia.org)
  • The closure of the pulmonary valve contributes to the P2 component of the second heart sound (S2). (wikipedia.org)
  • Heart valves are labeled with "B", "T", "A", and "P". Pulmonary valves Pulmonary valves Stradins, P (September 2004). (wikipedia.org)
  • Pulmonary valve stenosis most often occurs as a result of a congenital defect (present from birth), but can also be caused by rheumatic fever (often associated with untreated strep throat or scarlet fever) or endocarditis (inflammation of the lining inside the heart), among other conditions. (emoryhealthcare.org)
  • The valve acts as a doorway that lets blood into and out of the heart. (healthline.com)
  • If you're diagnosed with pulmonary valve stenosis, your doctor will often recommend that you undergo additional tests to ensure your heart is healthy. (healthline.com)
  • If pulmonary valve stenosis is left untreated, the extra effort your heart must exert can lead to heart failure and death. (healthline.com)
  • Pulmonary valve stenosis can cause a heart murmur . (healthline.com)
  • Maintaining a heart-healthy lifestyle also can be beneficial when you have pulmonary valve stenosis. (healthline.com)
  • In a narrowed heart valve, the valve flaps may become thick or stiff. (mayoclinic.org)
  • Usually, pulmonary valve disease is caused by a heart problem that develops before birth. (mayoclinic.org)
  • Pulmonary valve stenosis usually results from a heart problem present at birth. (mayoclinic.org)
  • This complication of strep throat can cause permanent damage to the heart and heart valves. (mayoclinic.org)
  • Some people with this syndrome develop carcinoid heart disease, which damages heart valves. (mayoclinic.org)
  • People with heart valve problems, such as pulmonary stenosis, have an increased risk of developing bacterial infections that affect the inner lining of the heart. (mayoclinic.org)
  • In severe pulmonary stenosis, the lower right heart chamber must pump harder to force blood into the pulmonary artery. (mayoclinic.org)
  • The new transcatheter pulmonary valve (TPV) is designed to extend the lifespan of the conduit by improving the natural function of the patient's heart. (medindia.net)
  • This unique and innovative procedure allows us to replace the patient's heart valve by threading the device through a vein in their leg and into their heart. (medindia.net)
  • Approximately 22 percent, or 4,800, of these babies born with congenital heart disease have defects disrupting the blood flow from the right ventricle to the pulmonary artery. (medindia.net)
  • Valves are structures in the heart that prevent blood from leaking backward. (chp.edu)
  • How Do You Treat Pulmonary Valve Stenosis in the Heart Cath Lab? (chp.edu)
  • Zareenah's heart condition, pulmonary stenosis, was diagnosed at her mum, Homaira's 20 week scan. (tinytickers.org)
  • Pulmonary artery anastomoses between the distal PA and proximal PA that was reconstructed with the autopericardium was done again with the beating heart and sinus rhythm was restored. (ctsnet.org)
  • Suppose you were born with a heart condition that required surgery to repair your pulmonary valve and its nearby structures when you were an infant or child. (secondscount.org)
  • If the pulmonary valve begins to allow significant amounts of blood to leak back into the heart, the right pumping chamber must work harder to pump more blood than usual. (secondscount.org)
  • In addition, many operations, such as the Rastelli, Ross, and Damus-Kaye-Stanzel procedures performed to make other congenital heart repairs, may also involve the placement of a valved tube (conduit) or human tissue tube (homograft) between the right ventricle and pulmonary artery. (secondscount.org)
  • Treatments to address the valve problem may include a minimally invasive, nonsurgical procedure or open-heart surgery. (secondscount.org)
  • M. genitalium in a prosthetic heart valve of a woman who sought care lacks a cell wall, making -lactam, fosfomycin, and in Switzerland for acute aortic valve dysfunction 3 years glycopeptide antimicrobials ineffective ( 5 ). (cdc.gov)
  • Doctors often suspect pulmonary stenosis if they hear a certain kind of heart murmur while listening with a stethoscope. (msdmanuals.com)
  • A heart murmur is a sound created by turbulent blood flow through narrowed or leaking heart valves or through abnormal heart structures. (msdmanuals.com)
  • To address these limitations, the medical device company Xeltis developed a new generation of restorative heart valves to enable the body to restore new, living heart valves with patient's own tissue. (xplore2md.com)
  • They may therefore enable a completely new treatment approach in heart valve therapy. (xplore2md.com)
  • Xeltis' bio-restorative heart valves are made of supramolecular polymers, based on Nobel prize awarded science. (xplore2md.com)
  • There is growing appreciation for the long-term adverse impact of right-sided dysfunction of the pulmonary valve in patients with congenital heart disease. (structuralheartdisease.org)
  • When parts of the heart, such as the valves, do not work properly, it is possible to repair or replace them. (medicalnewstoday.com)
  • When a person's heart valves are damaged, the heart will have trouble pumping blood. (medicalnewstoday.com)
  • According to the American Heart Association (AHA) , aortic and mitral valve replacements are the most common. (medicalnewstoday.com)
  • Learn more about common heart valve disorders. (medicalnewstoday.com)
  • Replacing a heart valve often involves open-heart surgery. (medicalnewstoday.com)
  • To replace a valve, the medical team will have to stop the heart for 1 hour and use a heart-lung machine to continue circulating blood in the person's body. (medicalnewstoday.com)
  • The Washington University and Barnes-Jewish Heart & Vascular Center offers leading expertise in the region to treat every type of valve problem. (barnesjewish.org)
  • Our team is experienced in both open-heart and minimally invasive surgery techniques to repair or replace heart valves damaged by valvular heart disease . (barnesjewish.org)
  • Minimally invasive procedures often use a transcatheter approach to repair or replace leaking heart valves. (barnesjewish.org)
  • Using this method, doctors make tiny incisions to repair or replace your heart valve. (barnesjewish.org)
  • We continue to pioneer new approaches and devices to repair and replace leaky heart valves. (barnesjewish.org)
  • Our heart surgeons can perform other procedures along with valve surgery, including high-risk or reoperative surgeries. (barnesjewish.org)
  • When your heart valve no longer functions as it should, surgery may be the best option. (barnesjewish.org)
  • Open-heart surgery, whether it's minimally invasive or traditional, offers the ability to get excellent results and treat multiple valves. (barnesjewish.org)
  • When a leaky mitral valve allows too much blood to flow backward, your heart must work harder to pump blood. (barnesjewish.org)
  • Valvular heart disease is any disease process involving one or more of the four valves of the heart (the aortic and mitral valves on the left and the pulmonary and tricuspid valves on the right). (wn.com)
  • Misshapen or damaged heart valves often need repair. (healthline.com)
  • An annuloplasty can reshape or reinforce the ring (annulus) that surrounds a valve in the heart. (healthline.com)
  • The heart valves are particularly vulnerable to this. (healthline.com)
  • The valves are flaps that open and close to allow blood to flow into the heart but keep any blood from flowing backward. (healthline.com)
  • Valves of the heart in motion, the front wall of the heart is removed in this image. (wikipedia.org)
  • Sound of the heart valves closing in a healthy 16 year old girl. (wikipedia.org)
  • A heart valve is a one-way valve that allows blood to flow in one direction through the chambers of the heart . (wikipedia.org)
  • Four valves are usually present in a mammalian heart and together they determine the pathway of blood flow through the heart. (wikipedia.org)
  • A heart valve opens or closes according to differential blood pressure on each side. (wikipedia.org)
  • The four valves in the mammalian heart are two atrioventricular valves separating the upper atria from the lower ventricles - the mitral valve in the left heart, and the tricuspid valve in the right heart. (wikipedia.org)
  • The heart also has a coronary sinus valve and an inferior vena cava valve , not discussed here. (wikipedia.org)
  • The heart valves and the chambers are lined with endocardium . (wikipedia.org)
  • Heart valves separate the atria from the ventricles , or the ventricles from a blood vessel . (wikipedia.org)
  • 3D - loop of a heart viewed from the apex, with the apical part of the ventricles removed and the mitral valve clearly visible. (wikipedia.org)
  • The use of the Harmony valve may delay the time before a patient needs additional open-heart surgery. (fda.gov)
  • The aortic valve is one of two valves in charge of controlling the flow of blood as it leaves the heart. (kidshealth.org)
  • Instead of two separate valves allowing flow into the heart, there is one large common valve that might be quite malformed. (kidshealth.org)
  • If bacteria travel through the blood and get stuck on a heart valve, this can cause this infection in the heart. (kidshealth.org)
  • People with congenital heart disease or heart valve problems are most at risk of getting bacterial endocarditis. (kidshealth.org)
  • Heart valves, superior view. (medscape.com)
  • The following image shows the AV valve leaflet and its attachment to the fibrous skeleton of the heart. (medscape.com)
  • The initial feasibility study is sponsored by Medtronic, Inc. CardioVascular Business Unit of Minneapolis, Minn., makers of the Melody Transcatheter Pulmonary Valve (TPV) and Ensemble Transcatheter Delivery System used in the procedure. (medindia.net)
  • Melody valve from Medtronic and Edwards Sapien valves from Edwards Lifesciences). (structuralheartdisease.org)
  • We may reconstruct the aorta on its own or along with surgery to replace the aortic valve. (barnesjewish.org)
  • Among mitral valve surgery (MVS) patients, we sought to determine if severe PHT increases mortality risk and if patients who undergo concomitant tricuspid valve surgery (TVS) incur additional risk. (nebraska.edu)
  • Babliak O, Babliak D, Volodymyr D, Marchenko A. Minimally Invasive Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) and Mitral Valve Repair. (ctsnet.org)
  • This video presents the case of a minimally invasive mitral valve (MV) and anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) repair in a twenty-one-month-old female patient. (ctsnet.org)
  • Note the small nubbins of tissue at the pulmonary valve annulus in the center of the drawing. (medscape.com)
  • The pulmonary valve annulus is usually hypoplastic, resulting in pulmonary stenosis. (medscape.com)
  • Mitral valve revision showed marked annulus dilation and A2 segment prolapse because of lateral papillary muscle fibrosis and an anomalous posterior leaflet. (ctsnet.org)
  • The right atrioventricular valve complex (the tricuspid valve) is made up of the 3 valve leaflets, the annulus, the supporting chordae tendineae, and the papillary muscles. (medscape.com)
  • PRJEB60931) with a rocking motion of the prosthetic valve sug- against a custom database ( 8 ) using Kraken 2 ( 9 ) and gesting disinsertion, without vegetations (Figure). (cdc.gov)
  • They provide products to diagnose and treat diseases of the pulmonary and gastrointestinal conditions and they offer interventional cardiology products. (researchandmarkets.com)
  • Our surgeons and interventional cardiologists have extensive experience in successful valve procedures using both natural and mechanical valves. (barnesjewish.org)
  • Atrial septostomy, Potts anastomosis, and pulmonary artery denervation are interventional procedures serving this purpose. (revespcardiol.org)
  • In the immediate neonatal period, cyanosis may be present, which is a result of increased pulmonary vascular resistance (PVR) causing a right-to-left shunt at the level of the VSD or the inability to effectively ventilate the patient. (medscape.com)
  • After the fall in pulmonary vascular resistance, respiratory difficulties are the most prominent symptom in severe cases. (medscape.com)