Usefulness of Routine Fractional Flow Reserve for Clinical Management of Coronary Artery Disease in Patients With Diabetes.
Aged
Cardiovascular Agents
/ therapeutic use
Clinical Decision-Making
Coronary Angiography
Coronary Artery Bypass
Coronary Artery Disease
/ therapy
Coronary Stenosis
/ diagnostic imaging
Cross-Sectional Studies
Diabetes Mellitus
Female
Fractional Flow Reserve, Myocardial
Humans
Male
Myocardial Infarction
/ epidemiology
Percutaneous Coronary Intervention
Prospective Studies
Journal
JAMA cardiology
ISSN: 2380-6591
Titre abrégé: JAMA Cardiol
Pays: United States
ID NLM: 101676033
Informations de publication
Date de publication:
01 03 2020
01 03 2020
Historique:
pubmed:
9
1
2020
medline:
12
1
2021
entrez:
9
1
2020
Statut:
ppublish
Résumé
Approximately one-third of patients considered for coronary revascularization have diabetes, which is a major determinant of clinical outcomes, often influencing the choice of the revascularization strategy. The usefulness of fractional flow reserve (FFR) to guide treatment in this population is understudied and has been questioned. To evaluate the usefulness and rate of major adverse cardiovascular events (MACE) of integrating FFR in management decisions for patients with diabetes who undergo coronary angiography. This cross-sectional study used data from the PRIME-FFR study derived from the merger of the POST-IT study (Portuguese Study on the Evaluation of FFR-Guided Treatment of Coronary Disease [March 2012-November 2013]) and R3F study (French Study of FFR Integrated Multicenter Registries Implementation of FFR in Routine Practice [October 2008-June 2010]), 2 prospective multicenter registries that shared a common design. A population of all-comers for whom angiography disclosed ambiguous lesions was analyzed for rates, patterns, and outcomes associated with management reclassification, including revascularization deferral, in patients with vs without diabetes. Data analysis was performed from June to August 2018. Death from any cause, myocardial infarction, or unplanned revascularization (MACE) at 1 year. Among 1983 patients (1503 [77%] male; mean [SD] age, 65 [10] years), 701 had diabetes, and FFR was performed for 1.4 lesions per patient (58.2% of lesions in the left anterior descending artery; mean [SD] stenosis, 56% [11%]; mean [SD] FFR, 0.81 [0.01]). Reclassification by FFR was high and similar in patients with and without diabetes (41.2% vs 37.5%, P = .13), but reclassification from medical treatment to revascularization was more frequent in the former (142 of 342 [41.5%] vs 230 of 730 [31.5%], P = .001). There was no statistical difference between the 1-year rates of MACE in reclassified (9.7%) and nonreclassified patients (12.0%) (P = .37). Among patients with diabetes, FFR-based deferral identified patients with a lower risk of MACE at 12 months (25 of 296 [8.4%]) compared with those undergoing revascularization (47 of 257 [13.1%]) (P = .04), and the rate was of the same magnitude of the observed rate among deferred patients without diabetes (7.9%, P = .87). Status of insulin treatment had no association with outcomes. Patients (6.6% of the population) in whom FFR was disregarded had the highest MACE rates regardless of diabetes status. Routine integration of FFR for the management of coronary artery disease in patients with diabetes may be associated with a high rate of treatment reclassification. Management strategies guided by FFR, including revascularization deferral, may be useful for patients with diabetes.
Identifiants
pubmed: 31913433
pii: 2758311
doi: 10.1001/jamacardio.2019.5097
pmc: PMC6990935
doi:
Substances chimiques
Cardiovascular Agents
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
272-281Références
Cardiovasc Diabetol. 2016 Jul 19;15:100
pubmed: 27431395
Int J Cardiol. 2016 Sep 15;219:56-62
pubmed: 27281577
Circ J. 2004 Nov;68(11):993-8
pubmed: 15502378
Circulation. 2012 Oct 16;126(16):2020-35
pubmed: 22923432
Circ Cardiovasc Interv. 2016 Jul;9(7):
pubmed: 27412867
Eur Heart J. 2015 Dec 1;36(45):3182-8
pubmed: 26400825
Circ Cardiovasc Interv. 2014 Apr;7(2):248-55
pubmed: 24642999
Cardiovasc Diabetol. 2017 Jan 13;16(1):7
pubmed: 28086778
N Engl J Med. 2009 Jan 15;360(3):213-24
pubmed: 19144937
N Engl J Med. 2014 Sep 25;371(13):1208-17
pubmed: 25176289
Circ Cardiovasc Interv. 2017 Jun;10(6):
pubmed: 28615234
N Engl J Med. 2017 May 11;376(19):1824-1834
pubmed: 28317458
Rev Esp Cardiol. 2008 Apr;61(4):352-9
pubmed: 18405515
N Engl J Med. 2012 Sep 13;367(11):991-1001
pubmed: 22924638
N Engl J Med. 2012 Dec 20;367(25):2375-84
pubmed: 23121323
Am J Cardiol. 2007 Feb 15;99(4):504-8
pubmed: 17293194
Clin Res Cardiol. 2014 Mar;103(3):191-201
pubmed: 24264473
JACC Cardiovasc Interv. 2018 Feb 26;11(4):354-365
pubmed: 29471949
Catheter Cardiovasc Interv. 2017 Dec 1;90(7):1084-1085
pubmed: 29226576
Circ Cardiovasc Imaging. 2017 Jul;10(7):
pubmed: 28687539
Circulation. 2014 Jan 14;129(2):173-85
pubmed: 24255062
Coron Artery Dis. 2009 Aug;20(5):317-21
pubmed: 19444091
N Engl J Med. 2017 May 11;376(19):1813-1823
pubmed: 28317438
Am J Cardiol. 2016 Nov 1;118(9):1293-1299
pubmed: 27614852