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Time-Related Risk of Pulmonary Conduit Re-replacement: A Congenital Heart Surgeons’ Society Study

  • Congenital Heart Surgeons’ Society Pulmonary Conduit Working Group
    ,
  • Connor P. Callahan
    ,
  • Anusha Jegatheeswaran
    ,
  • Eugene H. Blackstone
    ,
  • Tara Karamlou
    ,
  • Christopher W. Baird
*Corresponding author for this work
  • University of Toronto
    ,
  • Cleveland Clinic Foundation
    ,
  • Harvard University
    ,
  • Children's National Medical Center
    ,
  • Indiana University Bloomington
    ,
  • Nemours Children's Clinic
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Background: Patients receiving a right ventricle to pulmonary artery conduit (PC) in infancy will require successive procedures or replacements, each with variable longevity. We sought to identify factors associated with time-related risk of a subsequent surgical replacement (PC3) or transcatheter pulmonary valve insertion (TPVI) after a second surgically placed PC (PC2). Methods: From 2002 to 2016, 630 patients from 29 Congenital Heart Surgeons’ Society member institutions survived to discharge after initial valved PC insertion (PC1) at age ≤ 2 years. Of those, 355 underwent surgical replacement (PC2) of that initial conduit. Competing risk methodology and multiphase parametric hazard analyses were used to identify factors associated with time-related risk of PC3 or TPVI. Results: Of 355 PC2 patients (median follow-up, 5.3 years), 65 underwent PC3 and 41 TPVI. Factors at PC2 associated with increased time-related risk of PC3 were smaller PC2 Z score (hazard ratio [HR] 1.6, P <.001), concomitant aortic valve intervention (HR 7.6, P =.009), aortic allograft (HR 2.2, P =.008), younger age (HR 1.4, P <.001), and larger Z score of PC1 (HR 1.2, P =.04). Factors at PC2 associated with increased time-related risk of TPVI were aortic allograft (HR: 3.3, P =.006), porcine unstented conduit (HR 4.7, P <.001), and older age (HR 2.3, P =.01). Conclusions: Aortic allograft as PC2 was associated with increased time-related risk of both PC3 and TPVI. Surgeons may reduce risk of these subsequent procedures by not selecting an aortic homograft at PC2, and by oversizing the conduit when anatomically feasible.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 623-629 (7 pages)

Journal (Volume, Issue Number)

Annals of Thoracic Surgery (Volume 113, Issue 2)

Publication milestones

  • Accepted/In press - 2021
  • Published - 02/2022

Publication status

Published - 02/2022

ISSN

0003-4975

Publication IDs

  • Scopus: 85109441959
  • PubMed: 34097895

Publication metrics

Metrics

Scopus
citations
Fractional count
2
Fractional count
0.12
Fractional count
15
Fractional count
0.88
Fractional count
2
Fractional count
1

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Captures
14
Citation count
21

Funding Details

Funding for Dr Callahan was provided by the Congenital Heart Surgeons’ Society ( CHSS ) John W. Kirklin / David Ashburn Fellowship, and the Hospital for Sick Children Division of Cardiovascular Surgery. A Children’s Heart Foundation grant provided funding early in this cohort’s enrollment. The authors are grateful for the assistance of CHSS data center staff (Nabi Aghaei, Sally Cai, Anna Wasiak, Tharini Paramananthan, Uroosa Khan, Maha Rahmen, Lauren Graham, and Sunita O’Shea) in coordinating patient enrollment, data abstraction, and management of data. We also thank all CHSS member surgeons and institutions for their ongoing contributions to this and all CHSS data center studies.
FundersFunding numbers
Congenital Heart Surgeons' Society
-
Hospital for Sick Children Division of Cardiovascular Surgery
-
CHF
-
CHSS
-