Profile of Acyanotic Congenital Heart Defects

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dc.contributor.authorGupta, Akashen_US
dc.contributor.authorAbqari, Shaaden_US
dc.contributor.authorShahab, Tabassumen_US
dc.contributor.authorRabbani, M Uen_US
dc.contributor.authorAli, S Manaziren_US
dc.contributor.authorFirdaus, Uzmaen_US
dc.date.accessioned2019-11-16T07:26:53Z
dc.date.available2019-11-16T07:26:53Z
dc.date.issued2016-10
dc.description.abstractBackground: Acyanotic CHD constitute majority of heart defect with significant morbidity, Profile of various defects is essential for identifying children who need urgent intervention and who need to be medically followed. Methods: The study was carried out in Department of Pediatrics and Center of Cardiology, Jawaharlal Nehru Medical College, Aligarh. All patients referred with complaints or clinical examination suggestive of congenital heart defects were further evaluated with echocardiography. On echocardiography patients having congenital heart defects were included as cases which were further divided into cyanotic and acyanotic heart defects, preterms having PDA and PFO and those with acquired heart defects were excluded. The profile and mode of presentation of various acyanotic CHDs was further described in detail. Results: Acyanotic heart defects were 290(72.50%) of the total heart defects, while the contribution of cyanotic heart defects was 110 (27.50%). Out of all CHDs, VSD was the most common lesion with contribution of 152 (38.00%) cases, followed by ASD (20.34%) , PDA (13.10%), PS (6.90%), Subaortic Membrane (2.00%), AV Canal valve defect (1.00%), RSOV (1.00%), Bicuspid Aortic Valve (1.00%), PAPVC (0.66%), Cortriatriatum (0.33%), Coarctation of Aorta(0.33%), ALCAPA(0.33%) and Aortic stenosis (0.33%). Age of presentation for most of the children was between 1 to 5 years. Conclusions: The profile and mode of presentation of various acyanotic heart defects was similar to other studies but diagnosis was delayed in majority of cases. The prevelance of various obstructive lesions like AS, coarctation and bicuspid aortic valve was much lower.en_US
dc.identifier.affiliationsDepartment of Pediatrics, J. N. Medical College, AMU Aligarhen_US
dc.identifier.affiliationsDepartment of Pediatrics, J. N. Medical College, AMU Aligarhen_US
dc.identifier.affiliationsDepartment of Pediatrics, J. N. Medical College, AMU Aligarhen_US
dc.identifier.affiliationsCentre of Cardiology, J. N. Medical College, AMU Aligarhen_US
dc.identifier.affiliationsDepartment of Pediatrics, J. N. Medical College, AMU Aligarhen_US
dc.identifier.affiliationsDepartment of Pediatrics, J. N. Medical College, AMU Aligarhen_US
dc.identifier.citationGupta Akash, Abqari Shaad, Shahab Tabassum, Rabbani M U, Ali S Manazir, Firdaus Uzma. Profile of Acyanotic Congenital Heart Defects. International Archives of BioMedical and Clinical Research. 2016 Oct-Dec; 2(4): 11-16en_US
dc.identifier.issn2454-9894
dc.identifier.issn2454-9886
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/184460
dc.languageenen_US
dc.publisherIbn Sina Academy of Medieval Medicine & Sciencesen_US
dc.relation.issuenumber4en_US
dc.relation.volume2en_US
dc.source.urihttps://doi.org/10.21276/iabcr.2016.2.4.3en_US
dc.subjectAcyanotic Congenital Heart Diseaseen_US
dc.subjectProfileen_US
dc.subjectVsden_US
dc.subjectAsden_US
dc.subjectPs,asen_US
dc.titleProfile of Acyanotic Congenital Heart Defectsen_US
dc.typeJournal Articleen_US
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