Cargando…
A comprehensive study of congenital unilateral absence of branch pulmonary artery associated with other congenital heart defects and ipsilateral non-unifocalizable major aorto-pulmonary collateral arteries: A single-center retrospective study
INTRODUCTION: Congenital unilateral absence of pulmonary artery (UAPA) is a rare congenital anomaly with the complete absence of intrapericardial segment of one of the branch pulmonary arteries. Sixty percent are associated with other congenital heart defects (CHD) that often need correction. AIM: T...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174626/ https://www.ncbi.nlm.nih.gov/pubmed/34103851 http://dx.doi.org/10.4103/apc.APC_99_20 |
_version_ | 1783702942064312320 |
---|---|
author | Ramamurthy, Harpanahalli Ravi Walavalkar, Varsha Siddaiah, Satheesh Maheshwari, Sunita |
author_facet | Ramamurthy, Harpanahalli Ravi Walavalkar, Varsha Siddaiah, Satheesh Maheshwari, Sunita |
author_sort | Ramamurthy, Harpanahalli Ravi |
collection | PubMed |
description | INTRODUCTION: Congenital unilateral absence of pulmonary artery (UAPA) is a rare congenital anomaly with the complete absence of intrapericardial segment of one of the branch pulmonary arteries. Sixty percent are associated with other congenital heart defects (CHD) that often need correction. AIM: To analyze the data of patients with UAPA and ipsilateral non-unifocalizable major aortopulmonary collateral arteries (MAPCAs) associated with other CHD to identify the commonly associated CHD, their management strategies and outcomes. MATERIALS AND METHODS: Retrospective data of patients admitted for congenital UAPA with other CHD was compiled from hospital records from 2002 to 2015. The associated CHD were categorized as group I with the decreased pulmonary flow and group II with increased pulmonary flow to the unaffected contralateral pulmonary artery. The determinants of their management were analyzed. RESULTS: Sixty-five patients of UAPA and ipsilateral non-unifocalizable MAPCAs associated with other CHD were identified. Group I had 41 patients and Group II had 24. The most common CHD associated with UAPA was tetralogy of Fallot (TOF) in 31 patients (47.7%). Fifty-three patients underwent surgery, 48 (73.8%) underwent single lung corrective surgery, 5 (7.6%) palliative surgery and 12 (18.4) received no surgery. Four operated patients died in the immediate postoperative period. The lowest Mc Goon ratio and Nakata index to undergo corrective surgery were 1.0 and 87.4 mm2/m2. A follow-up of 21 patients was done, among which 11 patients who underwent single-stage corrective surgery, all are in NYHA class II and saturating above 95%. CONCLUSIONS: Congenital UAPA is a rare anomaly and associated with a variety of CHDs, TOF being the most common. Single lung corrective surgery in patients with ipsilateral non-unifocalizable MAPCAs has good immediate and long term survival. |
format | Online Article Text |
id | pubmed-8174626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-81746262021-06-07 A comprehensive study of congenital unilateral absence of branch pulmonary artery associated with other congenital heart defects and ipsilateral non-unifocalizable major aorto-pulmonary collateral arteries: A single-center retrospective study Ramamurthy, Harpanahalli Ravi Walavalkar, Varsha Siddaiah, Satheesh Maheshwari, Sunita Ann Pediatr Cardiol Original Article INTRODUCTION: Congenital unilateral absence of pulmonary artery (UAPA) is a rare congenital anomaly with the complete absence of intrapericardial segment of one of the branch pulmonary arteries. Sixty percent are associated with other congenital heart defects (CHD) that often need correction. AIM: To analyze the data of patients with UAPA and ipsilateral non-unifocalizable major aortopulmonary collateral arteries (MAPCAs) associated with other CHD to identify the commonly associated CHD, their management strategies and outcomes. MATERIALS AND METHODS: Retrospective data of patients admitted for congenital UAPA with other CHD was compiled from hospital records from 2002 to 2015. The associated CHD were categorized as group I with the decreased pulmonary flow and group II with increased pulmonary flow to the unaffected contralateral pulmonary artery. The determinants of their management were analyzed. RESULTS: Sixty-five patients of UAPA and ipsilateral non-unifocalizable MAPCAs associated with other CHD were identified. Group I had 41 patients and Group II had 24. The most common CHD associated with UAPA was tetralogy of Fallot (TOF) in 31 patients (47.7%). Fifty-three patients underwent surgery, 48 (73.8%) underwent single lung corrective surgery, 5 (7.6%) palliative surgery and 12 (18.4) received no surgery. Four operated patients died in the immediate postoperative period. The lowest Mc Goon ratio and Nakata index to undergo corrective surgery were 1.0 and 87.4 mm2/m2. A follow-up of 21 patients was done, among which 11 patients who underwent single-stage corrective surgery, all are in NYHA class II and saturating above 95%. CONCLUSIONS: Congenital UAPA is a rare anomaly and associated with a variety of CHDs, TOF being the most common. Single lung corrective surgery in patients with ipsilateral non-unifocalizable MAPCAs has good immediate and long term survival. Wolters Kluwer - Medknow 2021 2021-04-10 /pmc/articles/PMC8174626/ /pubmed/34103851 http://dx.doi.org/10.4103/apc.APC_99_20 Text en Copyright: © 2021 Annals of Pediatric Cardiology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Ramamurthy, Harpanahalli Ravi Walavalkar, Varsha Siddaiah, Satheesh Maheshwari, Sunita A comprehensive study of congenital unilateral absence of branch pulmonary artery associated with other congenital heart defects and ipsilateral non-unifocalizable major aorto-pulmonary collateral arteries: A single-center retrospective study |
title | A comprehensive study of congenital unilateral absence of branch pulmonary artery associated with other congenital heart defects and ipsilateral non-unifocalizable major aorto-pulmonary collateral arteries: A single-center retrospective study |
title_full | A comprehensive study of congenital unilateral absence of branch pulmonary artery associated with other congenital heart defects and ipsilateral non-unifocalizable major aorto-pulmonary collateral arteries: A single-center retrospective study |
title_fullStr | A comprehensive study of congenital unilateral absence of branch pulmonary artery associated with other congenital heart defects and ipsilateral non-unifocalizable major aorto-pulmonary collateral arteries: A single-center retrospective study |
title_full_unstemmed | A comprehensive study of congenital unilateral absence of branch pulmonary artery associated with other congenital heart defects and ipsilateral non-unifocalizable major aorto-pulmonary collateral arteries: A single-center retrospective study |
title_short | A comprehensive study of congenital unilateral absence of branch pulmonary artery associated with other congenital heart defects and ipsilateral non-unifocalizable major aorto-pulmonary collateral arteries: A single-center retrospective study |
title_sort | comprehensive study of congenital unilateral absence of branch pulmonary artery associated with other congenital heart defects and ipsilateral non-unifocalizable major aorto-pulmonary collateral arteries: a single-center retrospective study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174626/ https://www.ncbi.nlm.nih.gov/pubmed/34103851 http://dx.doi.org/10.4103/apc.APC_99_20 |
work_keys_str_mv | AT ramamurthyharpanahalliravi acomprehensivestudyofcongenitalunilateralabsenceofbranchpulmonaryarteryassociatedwithothercongenitalheartdefectsandipsilateralnonunifocalizablemajoraortopulmonarycollateralarteriesasinglecenterretrospectivestudy AT walavalkarvarsha acomprehensivestudyofcongenitalunilateralabsenceofbranchpulmonaryarteryassociatedwithothercongenitalheartdefectsandipsilateralnonunifocalizablemajoraortopulmonarycollateralarteriesasinglecenterretrospectivestudy AT siddaiahsatheesh acomprehensivestudyofcongenitalunilateralabsenceofbranchpulmonaryarteryassociatedwithothercongenitalheartdefectsandipsilateralnonunifocalizablemajoraortopulmonarycollateralarteriesasinglecenterretrospectivestudy AT maheshwarisunita acomprehensivestudyofcongenitalunilateralabsenceofbranchpulmonaryarteryassociatedwithothercongenitalheartdefectsandipsilateralnonunifocalizablemajoraortopulmonarycollateralarteriesasinglecenterretrospectivestudy AT ramamurthyharpanahalliravi comprehensivestudyofcongenitalunilateralabsenceofbranchpulmonaryarteryassociatedwithothercongenitalheartdefectsandipsilateralnonunifocalizablemajoraortopulmonarycollateralarteriesasinglecenterretrospectivestudy AT walavalkarvarsha comprehensivestudyofcongenitalunilateralabsenceofbranchpulmonaryarteryassociatedwithothercongenitalheartdefectsandipsilateralnonunifocalizablemajoraortopulmonarycollateralarteriesasinglecenterretrospectivestudy AT siddaiahsatheesh comprehensivestudyofcongenitalunilateralabsenceofbranchpulmonaryarteryassociatedwithothercongenitalheartdefectsandipsilateralnonunifocalizablemajoraortopulmonarycollateralarteriesasinglecenterretrospectivestudy AT maheshwarisunita comprehensivestudyofcongenitalunilateralabsenceofbranchpulmonaryarteryassociatedwithothercongenitalheartdefectsandipsilateralnonunifocalizablemajoraortopulmonarycollateralarteriesasinglecenterretrospectivestudy |