Repair of "simple" total anomalous pulmonary venous connection: A review from the pediatric cardiac care consortium

James D. St. Louis, Brian A. Harvey, Jeremiah S. Menk, Geetha Raghuveer, James E. O'Brien, Roosevelt Bryant, Lazaros Kochilas

Research output: Contribution to journalArticlepeer-review

63 Scopus citations

Abstract

Background: Outcomes for repair of total anomalous pulmonary venous connection (TAPVC) from individual institutions suggest a significant improvement in mortality over the past several decades. The purpose of this study is to review the outcomes after repair of TAPVC from a large multiinstitutional registry. Methods: A retrospective review of the multiinstitutional database, the Pediatric Cardiac Care Consortium (PCCC), was used to identify patients with the diagnosis of TAPVC who underwent complete correction between 1982 and 2007. Data reviewed included age, decade of primary operation, anatomic type, presentation, and in-hospital mortality. Results: Of the 118,084 surgical procedures submitted to the PCCC, 2,191 (1.9%) consisted of primary surgical correction of TAPVC. Sixty-one percent of the cohort was male, with 6.8% reported as premature. Overall in-hospital surgical mortality for simple TAPVC was 13%. Mortality was 20% from 1982 to 1989, 16% from 1990 to 1999, and 8% from 2000 to 2007. Obstruction to the anomalous pulmonary venous connection occurred in 29%, with a mortality of 26%. Conclusions: Surgical outcomes from repair of congenital cardiac anomalies have significantly improved over the past several decades. Multiinstitutional large databases are needed to confirm results published from single-institution experiences. Although improvements in surgical repair of TAPVC have occurred over the past three decades, specific subtypes still experience significant mortality.

Original languageEnglish (US)
Pages (from-to)133-138
Number of pages6
JournalAnnals of Thoracic Surgery
Volume94
Issue number1
DOIs
StatePublished - Jul 2012

Bibliographical note

Funding Information:
This publication was supported by NIH/NCRR CTSA Grant Number UL1 RR033183 . Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH.

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