Pulmonary Atresia
"Pulmonary Atresia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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).
Descriptor ID |
D018633
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MeSH Number(s) |
C14.240.850.937 C14.280.484.640 C16.131.240.850.906
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Concept/Terms |
Pulmonary Atresia- Pulmonary Atresia
- Atresia, Pulmonary Valve
- Valve Atresia, Pulmonary
- Valve Atresias, Pulmonary
- Atresias, Pulmonary
- Pulmonary Atresias
- Pulmonary Valve Atresia
- Pulmonary Valve Atresias
- Atresia, Pulmonary
- Atresias, Pulmonary Valve
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Below are MeSH descriptors whose meaning is more general than "Pulmonary Atresia".
Below are MeSH descriptors whose meaning is more specific than "Pulmonary Atresia".
This graph shows the total number of publications written about "Pulmonary Atresia" by people in this website by year, and whether "Pulmonary Atresia" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2001 | 0 | 1 | 1 | 2003 | 1 | 1 | 2 | 2004 | 1 | 1 | 2 | 2006 | 0 | 1 | 1 | 2008 | 1 | 0 | 1 | 2010 | 0 | 1 | 1 | 2012 | 0 | 1 | 1 | 2020 | 1 | 1 | 2 |
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Below are the most recent publications written about "Pulmonary Atresia" by people in Profiles.
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Agasthi P, Graziano JN, Pophal SG. Percutaneous Closure of a "Doughnut Leak" Around an Atrial Septal Occluder Device in a Patient With Recurrent Migraines. J Invasive Cardiol. 2020 Sep; 32(9):E242-E243.
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Ganigara M, Sagiv E, Buddhe S, Bhat A, Chikkabyrappa SM. Tetralogy of Fallot With Pulmonary Atresia: Anatomy, Physiology, Imaging, and Perioperative Management. Semin Cardiothorac Vasc Anesth. 2021 Sep; 25(3):208-217.
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Eltayeb O, Mongé MC, Popescu AR, Sarwark AE, Harris T, Backer CL. Discontinuous Pulmonary Artery. World J Pediatr Congenit Heart Surg. 2017 01; 8(1):106-110.
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Mongeon FP, Gurvitz MZ, Broberg CS, Aboulhosn J, Opotowsky AR, Kay JD, Valente AM, Earing MG, Lui GK, Fernandes SM, Gersony DR, Cook SC, Ting JG, Nickolaus MJ, Landzberg MJ, Khairy P. Aortic root dilatation in adults with surgically repaired tetralogy of fallot: a multicenter cross-sectional study. Circulation. 2013 Jan 15; 127(2):172-9.
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Mavroudis C, Dodge-Khatami A, Stewart RD, Jacobs ML, Backer CL, Lorber RE. An overview of surgery options for congenital coronary artery anomalies. Future Cardiol. 2010 Sep; 6(5):627-45.
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Khairy P, Aboulhosn J, Gurvitz MZ, Opotowsky AR, Mongeon FP, Kay J, Valente AM, Earing MG, Lui G, Gersony DR, Cook S, Ting JG, Nickolaus MJ, Webb G, Landzberg MJ, Broberg CS. Arrhythmia burden in adults with surgically repaired tetralogy of Fallot: a multi-institutional study. Circulation. 2010 Aug 31; 122(9):868-75.
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Nagashima M, Hibino N, Yamamoto E, Higaki T. Total cavopulmonary connection for functionally single ventricle with pulmonary atresia and abnormal arborization of pulmonary arteries--exclusion of overwhelmed area by collateral arteries from Fontan circulation. Interact Cardiovasc Thorac Surg. 2008 Dec; 7(6):1180-2.
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Trivedi KR, Karamlou T, Yoo SJ, Williams WG, Freedom RM, McCrindle BW. Outcomes in 45 children with ductal origin of the distal pulmonary artery. Ann Thorac Surg. 2006 Mar; 81(3):950-7.
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Vricella LA, Kanani M, Cook AC, Cameron DE, Tsang VT. Problems with the right ventricular outflow tract: a review of morphologic features and current therapeutic options. Cardiol Young. 2004 Oct; 14(5):533-49.
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Dyamenahalli U, McCrindle BW, McDonald C, Trivedi KR, Smallhorn JF, Benson LN, Coles J, Williams WG, Freedom RM. Pulmonary atresia with intact ventricular septum: management of, and outcomes for, a cohort of 210 consecutive patients. Cardiol Young. 2004 Jun; 14(3):299-308.
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