Clinical Events After Deferral of LAD Revascularization Following Physiological Coronary Assessment.


Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
05 02 2019
Historique:
received: 24 07 2018
revised: 04 10 2018
accepted: 22 10 2018
entrez: 2 2 2019
pubmed: 2 2 2019
medline: 22 11 2019
Statut: ppublish

Résumé

Physicians are not always comfortable deferring treatment of a stenosis in the left anterior descending (LAD) artery because of the perception that there is a high risk of major adverse cardiac events (MACE). The authors describe, using the DEFINE-FLAIR (Functional Lesion Assessment of Intermediate Stenosis to Guide Revascularisation) trial, MACE rates when LAD lesions are deferred, guided by physiological assessment using fractional flow reserve (FFR) or the instantaneous wave-free ratio (iFR). The purpose of this study was to establish the safety of deferring treatment in the LAD using FFR or iFR within the DEFINE-FLAIR trial. MACE rates at 1 year were compared between groups (iFR and FFR) in patients whose physiological assessment led to LAD lesions being deferred. MACE was defined as a composite of cardiovascular death, myocardial infarction (MI), and unplanned revascularization at 1 year. Patients, and staff performing follow-up, were blinded to whether the decision was made with FFR or iFR. Outcomes were adjusted for age and sex. A total of 872 patients had lesions deferred in the LAD (421 guided by FFR, 451 guided by iFR). The event rate with iFR was significantly lower than with FFR (2.44% vs. 5.26%; adjusted HR: 0.46; 95% confidence interval [CI]: 0.22 to 0.95; p = 0.04). This was driven by significantly lower unplanned revascularization with iFR and numerically lower MI (unplanned revascularization: 2.22% iFR vs. 4.99% FFR; adjusted HR: 0.44; 95% CI: 0.21 to 0.93; p = 0.03; MI: 0.44% iFR vs. 2.14% FFR; adjusted HR: 0.23; 95% CI: 0.05 to 1.07; p = 0.06). iFR-guided deferral appears to be safe for patients with LAD lesions. Patients in whom iFR-guided deferral was performed had statistically significantly lower event rates than those with FFR-guided deferral.

Sections du résumé

BACKGROUND
Physicians are not always comfortable deferring treatment of a stenosis in the left anterior descending (LAD) artery because of the perception that there is a high risk of major adverse cardiac events (MACE). The authors describe, using the DEFINE-FLAIR (Functional Lesion Assessment of Intermediate Stenosis to Guide Revascularisation) trial, MACE rates when LAD lesions are deferred, guided by physiological assessment using fractional flow reserve (FFR) or the instantaneous wave-free ratio (iFR).
OBJECTIVES
The purpose of this study was to establish the safety of deferring treatment in the LAD using FFR or iFR within the DEFINE-FLAIR trial.
METHODS
MACE rates at 1 year were compared between groups (iFR and FFR) in patients whose physiological assessment led to LAD lesions being deferred. MACE was defined as a composite of cardiovascular death, myocardial infarction (MI), and unplanned revascularization at 1 year. Patients, and staff performing follow-up, were blinded to whether the decision was made with FFR or iFR. Outcomes were adjusted for age and sex.
RESULTS
A total of 872 patients had lesions deferred in the LAD (421 guided by FFR, 451 guided by iFR). The event rate with iFR was significantly lower than with FFR (2.44% vs. 5.26%; adjusted HR: 0.46; 95% confidence interval [CI]: 0.22 to 0.95; p = 0.04). This was driven by significantly lower unplanned revascularization with iFR and numerically lower MI (unplanned revascularization: 2.22% iFR vs. 4.99% FFR; adjusted HR: 0.44; 95% CI: 0.21 to 0.93; p = 0.03; MI: 0.44% iFR vs. 2.14% FFR; adjusted HR: 0.23; 95% CI: 0.05 to 1.07; p = 0.06).
CONCLUSIONS
iFR-guided deferral appears to be safe for patients with LAD lesions. Patients in whom iFR-guided deferral was performed had statistically significantly lower event rates than those with FFR-guided deferral.

Identifiants

pubmed: 30704577
pii: S0735-1097(18)39304-5
doi: 10.1016/j.jacc.2018.10.070
pmc: PMC6354033
pii:
doi:

Types de publication

Comparative Study Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

444-453

Subventions

Organisme : Medical Research Council
ID : G1100443
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/11/46/28861
Pays : United Kingdom
Organisme : Medical Research Council
ID : G1000357
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/05/006
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 212183/Z/18/Z
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.

Références

Am J Cardiol. 2000 Dec 15;86(12):1322-6
pubmed: 11113406
Circ Cardiovasc Interv. 2014 Jun;7(3):301-11
pubmed: 24782198
N Engl J Med. 2009 Jan 15;360(3):213-24
pubmed: 19144937
Eur Heart J. 2014 Oct 1;35(37):2541-619
pubmed: 25173339
JACC Cardiovasc Interv. 2017 Dec 26;10(24):2525-2527
pubmed: 29268882
Circulation. 2001 Jun 19;103(24):2928-34
pubmed: 11413082
JACC Cardiovasc Interv. 2016 Dec 12;9(23):2390-2399
pubmed: 27838269
Circulation. 1994 May;89(5):2150-60
pubmed: 8181140
Circ Cardiovasc Interv. 2014 Aug;7(4):492-502
pubmed: 24987048
JACC Cardiovasc Interv. 2017 Dec 26;10(24):2514-2524
pubmed: 29268881
N Engl J Med. 2017 May 11;376(19):1824-1834
pubmed: 28317458
J Am Coll Cardiol. 2012 Apr 10;59(15):1392-402
pubmed: 22154731
J Am Coll Cardiol. 2012 Feb 28;59(9):857-81
pubmed: 22296741
JACC Cardiovasc Interv. 2018 Aug 13;11(15):1423-1433
pubmed: 30093048
J Am Coll Cardiol. 2002 Mar 6;39(5):852-8
pubmed: 11869852
N Engl J Med. 2017 May 11;376(19):1813-1823
pubmed: 28317438

Auteurs

Sayan Sen (S)

Hammersmith Hospital, Imperial College London, Cancer Research UK, London, United Kingdom. Electronic address: sayan.sen@imperial.ac.uk.

Yousif Ahmad (Y)

Hammersmith Hospital, Imperial College London, Cancer Research UK, London, United Kingdom.

Hakim-Moulay Dehbi (HM)

University College London Cancer Trials Centre, London, United Kingdom.

James P Howard (JP)

Hammersmith Hospital, Imperial College London, Cancer Research UK, London, United Kingdom.

Juan F Iglesias (JF)

Lausanne University Hospital, Switzerland.

Rasha Al-Lamee (R)

Hammersmith Hospital, Imperial College London, Cancer Research UK, London, United Kingdom.

Ricardo Petraco (R)

Hammersmith Hospital, Imperial College London, Cancer Research UK, London, United Kingdom.

Sukhjinder Nijjer (S)

Hammersmith Hospital, Imperial College London, Cancer Research UK, London, United Kingdom.

Ravinay Bhindi (R)

Royal North Shore Hospital, Sydney, New South Wales, Australia.

Sam Lehman (S)

Flinders University, Adelaide, South Australia, Australia.

Darren Walters (D)

Prince Charles Hospital, Brisbane, Queensland, Australia.

James Sapontis (J)

MonashHeart and Monash University, Melbourne, Victoria, Australia.

Luc Janssens (L)

Imelda Hospital, Bonheiden, Belgium.

Christiaan J Vrints (CJ)

Antwerp University Hospital, Antwerp, Belgium.

Ahmed Khashaba (A)

Ain Shams University, Cairo, Egypt.

Mika Laine (M)

Helsinki University Hospital, Helsinki, Finland.

Eric Van Belle (E)

INSERM Unité 1011, Lille, France.

Florian Krackhardt (F)

Institut Coeur Poumon, Lille University Hospital, and Charite Campus Virchow Klinikum, Universitaetsmedizin, Berlin, Germany.

Waldemar Bojara (W)

Gemeinschaftsklinikum Mittelrhein, Kemperhof Koblenz, Koblenz, Germany.

Olaf Going (O)

Sana Klinikum Lichtenberg, Lichtenberg, Germany.

Tobias Härle (T)

Klinikum Oldenburg, European Medical School, Carl von Ossietzky University, Oldenburg, Germany.

Ciro Indolfi (C)

University Magna Graecia, Catanzaro, Italy.

Giampaolo Niccoli (G)

Catholic University of the Sacred Heart, Rome, Italy.

Flavio Ribichini (F)

University Hospital Verona, Verona, Italy.

Nobuhiro Tanaka (N)

Tokyo Medical University, Tokyo, Japan.

Hiroyoshi Yokoi (H)

Fukuoka Sannou Hospital, Fukuoka, Japan.

Hiroaki Takashima (H)

Aichi Medical University Hospital, Aichi, Japan.

Yuetsu Kikuta (Y)

Fukuyama Cardiovascular Hospital, Fukuyama, Japan.

Andrejs Erglis (A)

Pauls Stradins Clinical University Hospital, Riga, Latvia.

Hugo Vinhas (H)

Hospital Garcia de Horta, Lisbon, Portugal.

Pedro Canas Silva (PC)

Hospital Santa Maria, Lisbon, Portugal.

Sérgio B Baptista (SB)

Hospital Prof. Doutor Fernando Fonseca, Amadora, Portugal.

Ali Alghamdi (A)

King Abdulaziz Medical City Cardiac Center, Riyadh, Saudi Arabia.

Farrel Hellig (F)

Sunninghill Hospital, Johannesburg, Germany.

Bon-Kwon Koo (BK)

Seoul National University Hospital, Seoul, South Korea.

Chang-Wook Nam (CW)

Keimyung University Dongsan Medical Center, Daegu, South Korea.

Eun-Seok Shin (ES)

Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, South Korea.

Joon-Hyung Doh (JH)

Inje University Ilsan Paik Hospital, Daehwa-Dong, South Korea.

Salvatore Brugaletta (S)

Cardiovascular Institute, Hospital Clinic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

Eduardo Alegria-Barrero (E)

Hospital Universitario de Torrejón and Universidad Francisco de Vitoria, Madrid, Spain.

Martijin Meuwissen (M)

Amphia Hospital, Breda, Amsterdam, the Netherlands.

Jan J Piek (JJ)

AMC Heart Center, Academic Medical Center, Amsterdam, the Netherlands.

Niels van Royen (N)

VU University Medical Center, Amsterdam, the Netherlands.

Murat Sezer (M)

Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.

Carlo Di Mario (C)

Royal Brompton Hospital, and University of Florence, Florence, Italy.

Robert T Gerber (RT)

Conquest Hospital, St. Leonards-on-Sea, United Kingdom.

Iqbal S Malik (IS)

Hammersmith Hospital, Imperial College London, Cancer Research UK, London, United Kingdom.

Andrew S P Sharp (ASP)

Royal Devon and Exeter Hospital and University of Exeter, Exeter, United Kingdom.

Suneel Talwar (S)

Royal Bournemouth General Hospital, Bournemouth, United Kingdom.

Kare Tang (K)

Essex Cardiothoracic Centre, Basildon, and Anglia Ruskin University, Chelmsford, United Kingdom.

Habib Samady (H)

Emory University, Atlanta, Georgia.

John Altman (J)

Colorado Heart and Vascular, Lakewood, Colorado.

Arnold H Seto (AH)

Veterans Affairs Long Beach Healthcare System, Long Beach, California.

Jasvindar Singh (J)

Washington University School of Medicine, St. Louis, Missouri.

Allen Jeremias (A)

Stony Brook University Medical Center, New York, New York.

Hitoshi Matsuo (H)

Gifu Heart Center, Gifu, Japan.

Rajesh K Kharbanda (RK)

John Radcliffe Hospital, Oxford University Hospitals Foundation Trust, Oxford, United Kingdom.

Manesh R Patel (MR)

Duke University, Durham, North Carolina.

Patrick Serruys (P)

Hammersmith Hospital, Imperial College London, Cancer Research UK, London, United Kingdom.

Javier Escaned (J)

Hammersmith Hospital, Imperial College London, Cancer Research UK, London, United Kingdom.

Justin E Davies (JE)

Hospital Clinico San Carlos and Universidad Complutense de Madrid, Madrid, Spain.

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