A randomized controlled trial of a physiology-guided percutaneous coronary intervention optimization strategy: Rationale and design of the TARGET FFR study.


Journal

Clinical cardiology
ISSN: 1932-8737
Titre abrégé: Clin Cardiol
Pays: United States
ID NLM: 7903272

Informations de publication

Date de publication:
May 2020
Historique:
received: 18 11 2019
revised: 23 01 2020
accepted: 27 01 2020
pubmed: 11 2 2020
medline: 24 4 2021
entrez: 11 2 2020
Statut: ppublish

Résumé

Post-percutaneous coronary intervention (PCI) fractional flow reserve (FFR) ≥0.90 confers an improved cardiac prognosis. There are currently limited data available to determine how often it is possible to improve an angiographically acceptable but physiologically suboptimal result. A physiology-guided optimization strategy can achieve a clinically meaningful increase in the proportion of patients achieving a final post-PCI FFR ≥0.90 compared to standard care. Following angiographically successful PCI procedures, 260 patients will be randomized (1:1) to receive either a physiology-guided incremental optimization strategy (intervention group) or blinded post-PCI coronary physiology measurements (control group). Patients undergoing successful, standard-of-care PCI for either stable angina or non-ST-segment-elevation myocardial infarction who meet the study's inclusion and exclusion criteria will be eligible for randomization. The primary endpoint is defined as the proportion of patients with a final post-PCI FFR result ≥0.90. Secondary endpoints include change from baseline in Seattle Angina Questionnaire and EQ-5D-5L scores at 3 months and the rate of target vessel failure and its components (cardiac death, myocardial infarction, stent thrombosis, unplanned rehospitalization with target vessel revascularization) at 3 months and 1 year. 260 individual patients were successfully randomized between March 2018 and November 2019. Key baseline demographics of the study population are reported within. TARGET FFR is an investigator-initiated, prospective, single-center, randomized controlled trial of an FFR-guided PCI optimization strategy. The study has completed recruitment and is now in clinical follow-up. It is anticipated that primary results will be presented in Autumn 2020. ClinicalTrials.gov Identifier: NCT03259815. [Correction added on Apr 3 2020, after first online publication: Clinical Trials identifier added.].

Identifiants

pubmed: 32037592
doi: 10.1002/clc.23342
pmc: PMC7244297
doi:

Banques de données

ClinicalTrials.gov
['NCT03259815']

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

414-422

Subventions

Organisme : NHS National Waiting Times Centre Board endowment funds
Organisme : British Heart Foundation
ID : PG/17/25/32884
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RE/18/6134217
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/14/15/30661
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG-17-25-32884
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS172632744
Pays : United Kingdom

Informations de copyright

© 2020 The Authors. Clinical Cardiology published by Wiley Periodicals, Inc.

Références

Catheter Cardiovasc Interv. 2018 Nov 15;92(6):1063-1074
pubmed: 29446567
JACC Cardiovasc Interv. 2019 Oct 28;12(20):1991-2001
pubmed: 31648761
Heart. 2005 Feb;91(2):203-6
pubmed: 15657233
N Engl J Med. 1996 Jun 27;334(26):1703-8
pubmed: 8637515
J Invasive Cardiol. 2015 Aug;27(8):346-51
pubmed: 26232010
Glob J Health Sci. 2015 Dec 18;8(7):240-44
pubmed: 26925913
Heart. 2016 Dec 15;102(24):1988-1994
pubmed: 27492942
Z Kardiol. 2002;91 Suppl 3:132-6
pubmed: 12641028
JACC Cardiovasc Interv. 2012 Oct;5(10):1013-8
pubmed: 23078728
Am Heart J. 2016 Dec;182:119-124
pubmed: 27914491
J Am Heart Assoc. 2016 Nov 29;5(12):
pubmed: 27899365
Am Heart J. 2017 Jan;183:1-9
pubmed: 27979031
Circ Cardiovasc Interv. 2019 May;12(5):e007428
pubmed: 31018666
Circulation. 2016 Sep 27;134(13):906-17
pubmed: 27573032
Circulation. 2002 Jun 25;105(25):2950-4
pubmed: 12081986
Am Heart J. 2017 Feb;184:10-16
pubmed: 27892882
EuroIntervention. 2019 Aug 29;15(5):457-464
pubmed: 30561367
Catheter Cardiovasc Interv. 2001 Mar;52(3):322-6; discussion 327
pubmed: 11246245
Catheter Cardiovasc Interv. 2017 Feb 1;89(2):233-242
pubmed: 27219714
Am J Cardiol. 2011 Jun 15;107(12):1763-7
pubmed: 21481828
J Invasive Cardiol. 2015 May;27(5):222-8
pubmed: 25929298
JACC Cardiovasc Interv. 2017 May 22;10(10):986-995
pubmed: 28456699
J Am Coll Cardiol. 2014 Oct 21;64(16):1641-54
pubmed: 25323250
Cardiovasc Interv Ther. 2013 Apr;28(2):170-7
pubmed: 23161151
Clin Cardiol. 2020 May;43(5):414-422
pubmed: 32037592
J Cardiol. 2017 Apr;69(4):613-618
pubmed: 27876181
Catheter Cardiovasc Interv. 2015 Mar;85(4):585-92
pubmed: 24678006
Eur Heart J. 2006 Aug;27(15):1811-7
pubmed: 16822812
Catheter Cardiovasc Interv. 2002 Dec;57(4):452-9
pubmed: 12455078
Circulation. 1999 Mar 2;99(8):1015-21
pubmed: 10051294
EuroIntervention. 2016 Dec 20;12(12):1473-1480
pubmed: 27998839
N Engl J Med. 2009 Jan 15;360(3):213-24
pubmed: 19144937
Lancet. 2018 Oct 27;392(10157):1530-1540
pubmed: 30266412
JACC Cardiovasc Interv. 2016 May 23;9(10):1022-31
pubmed: 27198682
JACC Cardiovasc Interv. 2009 Apr;2(4):357-63
pubmed: 19463450
BMC Cardiovasc Disord. 2016 Sep 08;16(1):177
pubmed: 27608682
Heart Vessels. 2011 Nov;26(6):572-81
pubmed: 21221600
J Am Coll Cardiol. 2017 Dec 26;70(25):3088-3096
pubmed: 29268922
Heart. 2013 Dec;99(23):1740-8
pubmed: 24047640
Circ Cardiovasc Interv. 2017 Aug;10(8):
pubmed: 28790165
EuroIntervention. 2018 Dec 20;14(12):e1324-e1331
pubmed: 29784630
Circ J. 2006 Oct;70(10):1327-31
pubmed: 16998268
Am J Physiol Heart Circ Physiol. 2016 Sep 1;311(3):H520-31
pubmed: 27342881
Circulation. 2001 Oct 16;104(16):1917-22
pubmed: 11602494
EuroIntervention. 2018 Sep 20;14(7):806-814
pubmed: 29790478
Int J Cardiol. 2014 Sep 20;176(2):399-404
pubmed: 25125008

Auteurs

Damien Collison (D)

West of Scotland Regional Heart and Lung Centre, Golden Jubilee National Hospital, Clydebank, UK.
Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.

John D McClure (JD)

Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.

Colin Berry (C)

West of Scotland Regional Heart and Lung Centre, Golden Jubilee National Hospital, Clydebank, UK.
Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.

Keith G Oldroyd (KG)

West of Scotland Regional Heart and Lung Centre, Golden Jubilee National Hospital, Clydebank, UK.
Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH