Literature DB >> 28645241

Long-term outcome after right ventricle to pulmonary artery conduit surgery and reintervention.

Kristofer Skoglund1, Gunnar Svensson1, Ulf Thilén2, Mikael Dellborg1, Peter Eriksson1.   

Abstract

BACKGROUND: Reconstruction of the right ventricular outflow tract with a conduit is an established surgical procedure in congenital heart disease and reinterventions are common.
OBJECTIVE: An increasing number of patients have a conduit, but there are few population-based studies of long-term outcomes after conduit surgery, reoperations, and transcatheter pulmonary valve replacement.
METHODS: In April 2015, all adult patients with a conduit were identified in the Swedish National Registry for Congenital Heart Disease (SWEDCON). Data on patients who died before age of 16 years are not included in the registry and thus not included in the study.
RESULTS: We found 574 patients with a mean age 36.1 years. The largest proportion had tetralogy of Fallot (45%). In total there were 762 operations and 50 transcatheter pulmonary valve replacements. Mean age at first conduit operation was 20.2 years. Long-term survival up to 48 years including perioperative mortality (<1%) was 93% at 20 years. The most common cause of death was cardiac-related. Higher age at first conduit operation was associated with increased mortality risk. Reintervention-free survival was 77% and 54% at 10 and 20 years, respectively. Conduit reinterventions were common. Ten-year reintervention-free survival after first conduit reintervention (n = 176) was significantly lower than after first conduit operation (70% vs 77% p = .04). Higher age at first conduit operation was associated with a reduced risk of reintervention, whereas male sex and complex malformations were associated with increased risk of reintervention.
CONCLUSIONS: The mortality of repeated conduit reinterventions is low. The need for reintervention of conduits is considerable, and reintervention-free survival after the first conduit reintervention is poorer than after first conduit implantation. The findings in this study only applies for patients reaching 16 years of age.

Entities:  

Keywords:  Congenital heart disease; conduit; mortality; reintervention; transcatheter pulmonary valve replacement

Mesh:

Year:  2017        PMID: 28645241     DOI: 10.1080/14017431.2017.1343492

Source DB:  PubMed          Journal:  Scand Cardiovasc J        ISSN: 1401-7431            Impact factor:   1.589


  3 in total

1.  Multidisciplinary approach and treatment options in right ventricular outflow tract malformations.

Authors:  Kristofer Skoglund; Ludvig Clase; Mikael Dellborg
Journal:  J Multidiscip Healthc       Date:  2018-07-16

2.  Health-Related Quality of Life in Children With Earlier Surgical Repair for Right Ventricular Outflow Tract Anomalies and the Agreement Between Children and Their Parents.

Authors:  Birgitta Svensson; Ewa Idvall; Fredrik Nilsson; Petru Liuba
Journal:  Front Cardiovasc Med       Date:  2020-04-28

3.  Impact of valve fenestrations and structural changes in homografts on the long-term outcome in the recipient.

Authors:  Ida Axelsson; Torsten Malm; Johan Nilsson
Journal:  Cell Tissue Bank       Date:  2021-02-12       Impact factor: 1.522

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.