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Abstract

OBJECTIVES

We evaluated 4384 procedures performed between 1957 and 2018, collected in the National Register for Congenital Heart Defects, conducted on 997 patients with 1823 pulmonary valve replacements (PVRs), including 226 implanted via catheter [transcatheter valve (TCV)]. Main study targets are as follows: TCV benefit, valve type durability, decade-wise treatment changes and procedure frequencies over the lifetime of a PVR patient.

METHODS

We studied TCV impact on surgical valve replacement (via Kaplan–Meier); pulmonary valve type-specific performance (Kaplan–Meier and Cox regressions with age group as stratification or ordinary variable); procedure interval changes over the decades (Kaplan–Meier); procedure load, i.e. frequency of any procedure/surgical PVR/interventional or surgical PVR by patient age (multistate analyses).

RESULTS

TCV performance was equivalent to surgical PVRs and extended durability significantly. Homografts were most durable; Contegras lasted comparably less in older; and Hancock devices lasted less in younger patients. Matrix P-valves showed poorer performance. Age group stratification improves the precision of valve-specific explantation hazard estimations. The current median interval between procedures is 2.6 years; it became significantly shorter in most age groups below 40 years. At 30 years, 80% of patients had undergone ≥3 procedures, 20% ≥3 surgical PVRs and 42% ≥3 surgical or interventional PVRs.

CONCLUSIONS

TCVs doubled freedom from explantation of conventional valves. Homografts’ age group-specific explantation hazard ratio was lowest; Matrix P’s hazard ratio was highest. Age-stratified Cox regressions improve the precision of prosthesis durability evaluations. The median time between procedures for PVR patients shortened significantly to 2.6 years. At 30 years, 42% had ≥3 PVRs.

Details

Title
Pulmonary valve prostheses: patient’s lifetime procedure load and durability. Evaluation of the German National Register for Congenital Heart Defects
Author
Boethig, Dietmar 1 ; Avsar, Murat 1 ; Bauer, Ulrike M M 2 ; Sarikouch, Samir 1 ; Beerbaum, Philipp 3 ; Berger, Felix 4 ; Cesnjevar, Robert 5 ; Dähnert, Ingo 6 ; Dittrich, Sven 7 ; Ewert, Peter 8 ; Haverich, Axel 1 ; Hörer, Jürgen 8 ; Kostelka, Martin 6 ; Photiadis, Joachim 9 ; Sandica, Eugen 10 ; Schubert, Stephan 10 ; Urban, Aleksandra 2 ; Bobylev, Dmitry 1 ; Horke, Alexander 1 

 Department of Cardiac, Thoracic, Transplantation and Vascular Surgery, Hanover Medical School , Hanover, Germany 
 National Register for Congenital Heart Defects, German Centre for Cardiovascular Research (DZHK) , Berlin, Germany 
 Department of Pediatric Cardiology and Intensive Care Medicine, Hanover Medical School , Hanover, Germany 
 Department of Congenital HeartDisease/Pediatric Cardiology, German Heart Institute Berlin, Berlin, Germany 
 Department of Pediatric Cardiac Surgery, University of Erlangen , Erlangen, Germany 
 Department of Cardiac Surgery, Heart Centre, University of Leipzig, Clinic for Pediatric Cardiology , Leipzig, Germany 
 Divisions of Pediatric Cardiology, University of Erlangen , Erlangen, Germany 
 Department of Paediatric Cardiology and Congenital Heart Defects and Congenital Heart Surgery, German Heart Centre of the Technical University of Munich , Munich, Germany 
 Department of Congenital Heart Disease, German Heart Institute, German Centre for Cardiovascular Research (DZHK) partner site Berlin , Berlin, Germany 
10  Department of Congenital Heart Disease, Heart and Diabetes Centre , Bad Oeynhausen, Germany 
Pages
297-306
Publication year
2022
Publication date
Feb 2022
Publisher
Oxford Publishing Limited (England)
ISSN
15699293
e-ISSN
15699285
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3191818336
Copyright
© The Author(s) 2021. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.