'Off pump' self-expanding injectable tissue valves (IPVR) versus 'on pump' conventional tissue valves (PVR) for replacement of the pulmonary valve: trial protocol for a randomised controlled trial (InVITe trial).
Adolescent
Adult
Aged
Aged, 80 and over
Cardiopulmonary Bypass
/ methods
Child
Clinical Protocols
Female
Heart Valve Diseases
/ surgery
Heart Valve Prosthesis
Heart Valve Prosthesis Implantation
/ methods
Humans
Male
Middle Aged
Prosthesis Design
Pulmonary Valve
/ surgery
Single-Blind Method
Treatment Outcome
Young Adult
cardiac surgery
congenital heart disease
valvular heart disease
Journal
BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874
Informations de publication
Date de publication:
02 04 2019
02 04 2019
Historique:
entrez:
5
4
2019
pubmed:
5
4
2019
medline:
21
4
2020
Statut:
epublish
Résumé
Patients with congenital heart disease often need repeated operations throughout life to replace the pulmonary valve. Valve replacement with 'injectable' self-expanding valves (which is performed 'off pump' without the use of cardiopulmonary bypass, CPB) may result in quicker recovery and lower risk of major complications than valve replacement with conventional valves (which is performed 'on pump' with the use of CPB). We are conducting a multicentre, single-blind randomised controlled trial in patients with congenital heart disease and aged between 12 and 80 years. We will randomise participants in a 1:1 ratio to receive either 'off pump' injectable pulmonary valve replacement or 'on pump' conventional pulmonary valve replacement. The primary outcome will be the difference between the groups with respect to post-surgery blood loss (as measured by chest drain volume) in the first 24 hours. Secondary outcomes will include in-hospital outcomes (intensive care unit stay, inotropic/vasodilator support, chest drain volume in the first 12 hours post-surgery, time of readiness for extubation, blood products used in the first 24 hours post-surgery, time of fitness for discharge, valve and heart function 6 months post-surgery (assessed using cardiovascular magnetic resonance and ECHOCARDIOGRAPHY) and health-related quality of life 6 weeks and 6 months post-surgery. This trial has been approved by the South West Exeter Research Ethics Committee. Findings will be shared with participating hospitals and disseminated to the academic community through peer reviewed publications and presentation at national and international meetings. Patients will be informed of the results through patient organisations and newsletters to participants. ISRCTN23538073.
Identifiants
pubmed: 30944136
pii: bmjopen-2018-026221
doi: 10.1136/bmjopen-2018-026221
pmc: PMC6500208
doi:
Banques de données
ISRCTN
['ISRCTN23538073']
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e026221Subventions
Organisme : Medical Research Council
ID : MR/J015350/1
Pays : United Kingdom
Organisme : Department of Health
ID : EME/15/180/55
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CH/17/1/32804
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/13/9/29990
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/15/33/31394
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/11/19/28827
Pays : United Kingdom
Informations de copyright
© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: Pierson Ltd have agreed to provide the injectable tissue valves (BioPulmonic™, Biointegral Surgical Inc.) used in the trial at a discounted rate. Pierson Ltd paid for the expenses associated with Stefano Marianeschi to visit the trial centres and provide IPVR training.
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