Literature DB >> 32710282

Echocardiographic Identification of Pulmonary Artery Flow Reversal: An Indicator of Adverse Outcomes in Single Ventricle Physiology.

Andrew D Spearman1,2, Salil Ginde3,4,5, Benjamin H Goot3,4, Amy M Schaal3, Mingen Feng6, Amy Y Pan6, Michele A Frommelt3,4, Peter C Frommelt3,4.   

Abstract

Individuals with single ventricle congenital heart disease (CHD) undergo multiple staged surgical palliations. Staged single ventricle palliation with a superior cavopulmonary connection (SCPC) in infancy followed by a Fontan in early childhood relies on passive, unobstructed pulmonary blood flow and normal pulmonary vasculature. We hypothesized that patients with echocardiographic identification of retrograde flow in a branch pulmonary artery (PA) after SCPC or Fontan are at increased risk for adverse outcomes. We conducted a retrospective chart review of patients seen at Children's Wisconsin from 1999 to 2019. Inclusion criteria included a history of single ventricle congenital heart disease and surgical palliation with a superior cavopulmonary connection (SCPC). We created two cohorts based on transthoracic echocardiographic identification of branch PA flow patterns: those with color Doppler-defined pulmonary artery flow reversal (PA reversal cohort) and those with normal anterograde flow (Non-reversal cohort). We identified 21 patients in the PA reversal cohort and 539 patients in the Non-reversal cohort. The PA reversal cohort had increased hospital length of stay after SCPC palliation (p < 0.001) and decreased transplant-free survival (p = 0.032), but there was no difference in overall survival (p = 0.099). There was no difference in hospital length of stay after Fontan (p = 0.17); however, the PA reversal cohort was significantly less likely to progress to Fontan palliation during early childhood (p = 0.005). Echocardiographic color Doppler identification of branch PA flow reversal in patients with single ventricle physiology is a high-risk indicator for adverse short- and long-term outcomes.

Entities:  

Keywords:  Bidirectional Glenn; Cavopulmonary connection; Congenital heart disease; Fontan; Pulmonary vasculature; Single ventricle

Year:  2020        PMID: 32710282     DOI: 10.1007/s00246-020-02421-z

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  1 in total

1.  Longitudinal Assessment of Outcome From Prenatal Diagnosis Through Fontan Operation for Over 500 Fetuses With Single Ventricle-Type Congenital Heart Disease: The Philadelphia Fetus-to-Fontan Cohort Study.

Authors:  Michael Y Liu; Benjamin Zielonka; Brian S Snarr; Xuemei Zhang; J William Gaynor; Jack Rychik
Journal:  J Am Heart Assoc       Date:  2018-10-02       Impact factor: 5.501

  1 in total
  1 in total

1.  Obstruction of the Anomalous Pulmonary Venous Connection in Scimitar Syndrome: Progression to Spontaneous Anomalous Pulmonary Vein Atresia during Infancy without Intervention.

Authors:  Rachel E Henning; David E Segar; Peter C Frommelt
Journal:  CASE (Phila)       Date:  2022-04-05
  1 in total

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