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Anaesthetic management of a child with “cor–triatriatum” and multiple ventricular septal defects – A rare congenital anomaly

Cor-triatriatum is a rare congenital cardiac anomaly. It accounts for 0.1% of congenital heart diseases. Its association with multiple ventricular septal defects (VSD) is even rarer. A five-month-old baby was admitted with respiratory distress and failure to thrive. Clinical examination revealed dia...

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Autores principales: Sabade, Sriram, Vagrali, Anand, Patil, Sharan, Kalligudd, Praveen, Dhulked, Vithal, Dixit, M D, Gan, Mohan, Dayal, A
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2933485/
https://www.ncbi.nlm.nih.gov/pubmed/20885873
http://dx.doi.org/10.4103/0019-5049.65375
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author Sabade, Sriram
Vagrali, Anand
Patil, Sharan
Kalligudd, Praveen
Dhulked, Vithal
Dixit, M D
Gan, Mohan
Dayal, A
author_facet Sabade, Sriram
Vagrali, Anand
Patil, Sharan
Kalligudd, Praveen
Dhulked, Vithal
Dixit, M D
Gan, Mohan
Dayal, A
author_sort Sabade, Sriram
collection PubMed
description Cor-triatriatum is a rare congenital cardiac anomaly. It accounts for 0.1% of congenital heart diseases. Its association with multiple ventricular septal defects (VSD) is even rarer. A five-month-old baby was admitted with respiratory distress and failure to thrive. Clinical examination revealed diastolic murmur over mitral area. Chest X-ray showed cardiomegaly. Haematological and biochemical investigations were within normal limits. Electrocardiogram showed left atrial enlargement. 2D echo showed double-chambered left atrium (cor-triatriatum), atrial septal defect (ASD) and muscular VSD with moderate pulmonary arterial hypertension. The child was treated with 100% oxygen, diuretics and digoxin and was stabilized medically. We used balanced anaesthetic technique using oxygen, air, isoflurane, fentanyl, midazolam and vecuronium. Patient was operated under cardiopulmonary bypass (CPB) with moderate hypothermia. Through right atriotomy abnormal membrane in the left atrium was excised to make one chamber. VSD were closed with Dacron patches and ASD was closed with autologous pericardial patch. Patient tolerated the whole procedure well and was ventilated electively for 12h in the intensive care unit. He was discharged on the 10(th) postoperative day.
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spelling pubmed-29334852010-09-30 Anaesthetic management of a child with “cor–triatriatum” and multiple ventricular septal defects – A rare congenital anomaly Sabade, Sriram Vagrali, Anand Patil, Sharan Kalligudd, Praveen Dhulked, Vithal Dixit, M D Gan, Mohan Dayal, A Indian J Anaesth Case Report Cor-triatriatum is a rare congenital cardiac anomaly. It accounts for 0.1% of congenital heart diseases. Its association with multiple ventricular septal defects (VSD) is even rarer. A five-month-old baby was admitted with respiratory distress and failure to thrive. Clinical examination revealed diastolic murmur over mitral area. Chest X-ray showed cardiomegaly. Haematological and biochemical investigations were within normal limits. Electrocardiogram showed left atrial enlargement. 2D echo showed double-chambered left atrium (cor-triatriatum), atrial septal defect (ASD) and muscular VSD with moderate pulmonary arterial hypertension. The child was treated with 100% oxygen, diuretics and digoxin and was stabilized medically. We used balanced anaesthetic technique using oxygen, air, isoflurane, fentanyl, midazolam and vecuronium. Patient was operated under cardiopulmonary bypass (CPB) with moderate hypothermia. Through right atriotomy abnormal membrane in the left atrium was excised to make one chamber. VSD were closed with Dacron patches and ASD was closed with autologous pericardial patch. Patient tolerated the whole procedure well and was ventilated electively for 12h in the intensive care unit. He was discharged on the 10(th) postoperative day. Medknow Publications 2010 /pmc/articles/PMC2933485/ /pubmed/20885873 http://dx.doi.org/10.4103/0019-5049.65375 Text en © Indian Journal of Anaesthesia http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sabade, Sriram
Vagrali, Anand
Patil, Sharan
Kalligudd, Praveen
Dhulked, Vithal
Dixit, M D
Gan, Mohan
Dayal, A
Anaesthetic management of a child with “cor–triatriatum” and multiple ventricular septal defects – A rare congenital anomaly
title Anaesthetic management of a child with “cor–triatriatum” and multiple ventricular septal defects – A rare congenital anomaly
title_full Anaesthetic management of a child with “cor–triatriatum” and multiple ventricular septal defects – A rare congenital anomaly
title_fullStr Anaesthetic management of a child with “cor–triatriatum” and multiple ventricular septal defects – A rare congenital anomaly
title_full_unstemmed Anaesthetic management of a child with “cor–triatriatum” and multiple ventricular septal defects – A rare congenital anomaly
title_short Anaesthetic management of a child with “cor–triatriatum” and multiple ventricular septal defects – A rare congenital anomaly
title_sort anaesthetic management of a child with “cor–triatriatum” and multiple ventricular septal defects – a rare congenital anomaly
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2933485/
https://www.ncbi.nlm.nih.gov/pubmed/20885873
http://dx.doi.org/10.4103/0019-5049.65375
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