Outcomes of Participants With Diabetes in the ISCHEMIA Trials.

Bayes theorem coronary artery disease diabetes mellitus insulin progression-free survival renal insufficiency, chronic ventricular function, left

Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
26 10 2021
Historique:
pubmed: 16 9 2021
medline: 30 12 2021
entrez: 15 9 2021
Statut: ppublish

Résumé

Among patients with diabetes and chronic coronary disease, it is unclear if invasive management improves outcomes when added to medical therapy. The ISCHEMIA (International Study of Comparative Health Effectiveness with Medical and Invasive Approaches) trials (ie, ISCHEMIA and ISCHEMIA-Chronic Kidney Disease) randomized chronic coronary disease patients to an invasive (medical therapy + angiography and revascularization if feasible) or a conservative approach (medical therapy alone with revascularization if medical therapy failed). Cohorts were combined after no trial-specific effects were observed. Diabetes was defined by history, hemoglobin A1c ≥6.5%, or use of glucose-lowering medication. The primary outcome was all-cause death or myocardial infarction (MI). Heterogeneity of effect of invasive management on death or MI was evaluated using a Bayesian approach to protect against random high or low estimates of treatment effect for patients with versus without diabetes and for diabetes subgroups of clinical (female sex and insulin use) and anatomic features (coronary artery disease severity or left ventricular function). Of 5900 participants with complete baseline data, the median age was 64 years (interquartile range, 57-70), 24% were female, and the median estimated glomerular filtration was 80 mL·min Despite higher risk for death or MI, chronic coronary disease patients with diabetes did not derive incremental benefit from routine invasive management compared with initial medical therapy alone. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01471522.

Sections du résumé

BACKGROUND
Among patients with diabetes and chronic coronary disease, it is unclear if invasive management improves outcomes when added to medical therapy.
METHODS
The ISCHEMIA (International Study of Comparative Health Effectiveness with Medical and Invasive Approaches) trials (ie, ISCHEMIA and ISCHEMIA-Chronic Kidney Disease) randomized chronic coronary disease patients to an invasive (medical therapy + angiography and revascularization if feasible) or a conservative approach (medical therapy alone with revascularization if medical therapy failed). Cohorts were combined after no trial-specific effects were observed. Diabetes was defined by history, hemoglobin A1c ≥6.5%, or use of glucose-lowering medication. The primary outcome was all-cause death or myocardial infarction (MI). Heterogeneity of effect of invasive management on death or MI was evaluated using a Bayesian approach to protect against random high or low estimates of treatment effect for patients with versus without diabetes and for diabetes subgroups of clinical (female sex and insulin use) and anatomic features (coronary artery disease severity or left ventricular function).
RESULTS
Of 5900 participants with complete baseline data, the median age was 64 years (interquartile range, 57-70), 24% were female, and the median estimated glomerular filtration was 80 mL·min
CONCLUSIONS
Despite higher risk for death or MI, chronic coronary disease patients with diabetes did not derive incremental benefit from routine invasive management compared with initial medical therapy alone. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01471522.

Identifiants

pubmed: 34521217
doi: 10.1161/CIRCULATIONAHA.121.054439
pmc: PMC8545918
mid: NIHMS1739854
doi:

Banques de données

ClinicalTrials.gov
['NCT01471522']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1380-1395

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001445
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL105462
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL105561
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL105907
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002243
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL105565
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL125991
Pays : United States

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Auteurs

Jonathan D Newman (JD)

New York University Grossman School of Medicine (J.D.N., R.A., S.B., H.R.R., D.F.K., J.S.H.).

Rebecca Anthopolos (R)

New York University Grossman School of Medicine (J.D.N., R.A., S.B., H.R.R., D.F.K., J.S.H.).

G B John Mancini (GBJ)

Center for Cardiovascular Innovation, University of British Columbia, Vancouver, Canada (G.B.J.M.).

Sripal Bangalore (S)

New York University Grossman School of Medicine (J.D.N., R.A., S.B., H.R.R., D.F.K., J.S.H.).

Harmony R Reynolds (HR)

New York University Grossman School of Medicine (J.D.N., R.A., S.B., H.R.R., D.F.K., J.S.H.).

Dennis F Kunichoff (DF)

New York University Grossman School of Medicine (J.D.N., R.A., S.B., H.R.R., D.F.K., J.S.H.).

Roxy Senior (R)

Northwick Park Hospital-Royal Brompton Hospital, London, UK (R.S.).

Jesus Peteiro (J)

Complejo Hospitalario Universitario de A Coruña (CHUAC), Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), Universidad de A Coruña, A Coruña, Spain (J.P.).

Balram Bhargava (B)

All India Institute of Medical Sciences, Delhi (B.B., S.M.).

Pallav Garg (P)

London Health Sciences Center, Western University, Ontario, Canada (P.G.).

Jorge Escobedo (J)

Instituto Mexicano del Seguro Social, Mexico City (J.E.).

Rolf Doerr (R)

Praxisklinik Herz und Gefaesse, Dresden, Germany (R.D.).

Tomasz Mazurek (T)

Medical University of Warsaw, Poland (T.M.).

Jose Gonzalez-Juanatey (J)

Cardiology Department, Hospital Clínico Universitario, Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares Institution, Spain (J.G-J.).

Grzegorz Gajos (G)

Department of Coronary Disease and Heart Failure, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland (G.G.).

Carlo Briguori (C)

Laboratory of Interventional Cardiology and Department of Cardiology, Mediterranea Cardiocentro, Naples, Italy (C.B.).

Hong Cheng (H)

Beijing Anzhen Hospital, Capital Medical University, China (H.C.).

Andras Vertes (A)

Dél-pesti Centrumkóház Hospital, National Institute of Hematology and Infectious Disease, Cardiovascular Department, Budapest, Hungary (A.V.).

Sandeep Mahajan (S)

All India Institute of Medical Sciences, Delhi (B.B., S.M.).

Luis A Guzman (LA)

Instituto Médico Docencia Asistencia Médica e Investigación Clínica, Cordoba, Argentina (L.A.G.).

Matyas Keltai (M)

Semmelweis University, Budapest, Hungary (M.K.).

Aldo P Maggioni (AP)

Associazione Nazionale Medici Cardiologi Ospedalieri Research Center, Florence, Italy (A.P.M.).

Gregg W Stone (GW)

The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, Cardiovascular Research Foundation, New York (G.W.S.).

Jeffrey S Berger (JS)

New York University Grossman School of Medicine (J.D.N., R.A., S.B., H.R.R., D.F.K., J.S.H.).

Yves D Rosenberg (YD)

National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD (Y.D.R., J.L.F.).

William E Boden (WE)

Veterans Affairs New England Healthcare System, Boston University School of Medicine, MA (W.E.B.).

Bernard R Chaitman (BR)

St Louis University School of Medicine Center for Comprehensive Cardiovascular Care, MO (B.R.C.).

Jerome L Fleg (JL)

National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD (Y.D.R., J.L.F.).

David J Maron (DJ)

Department of Medicine, Stanford University, CA (D.J.M.).

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