International variation in characteristics and clinical outcomes of patients with type 2 diabetes and heart failure: Insights from TECOS.


Journal

American heart journal
ISSN: 1097-6744
Titre abrégé: Am Heart J
Pays: United States
ID NLM: 0370465

Informations de publication

Date de publication:
12 2019
Historique:
received: 13 03 2019
accepted: 19 08 2019
pubmed: 11 11 2019
medline: 13 3 2020
entrez: 11 11 2019
Statut: ppublish

Résumé

International differences in management/outcomes among patients with type 2 diabetes and heart failure (HF) are not well characterized. We sought to evaluate geographic variation in treatment and outcomes among these patients. METHODS AND RESULTS: Among 14,671 participants in the Trial Evaluating Cardiovascular Outcomes with Sitagliptin (TECOS), those with HF at baseline and a documented ejection fraction (EF) (N = 1591; 10.8%) were categorized by enrollment region (North America, Latin America, Western Europe, Eastern Europe, and Asia Pacific). Cox models were used to examine the association between geographic region and the primary outcome of all-cause mortality (ACM) or hospitalization for HF (hHF) in addition to ACM alone. Analyses were stratified by those with EF <40% or EF ≥40%. The majority of participants with HF were enrolled in Eastern Europe (53%). Overall, 1,267 (79.6%) had EF ≥40%. β-Blocker (83%) and angiotensin-converting enzyme inhibitor/angiotensin receptor blocker (86%) use was high across all regions in patients with EF <40%. During a median follow-up of 2.9 years, Eastern European participants had lower rates of ACM/hHF compared with North Americans (adjusted hazard ratio: 0.45; 95% CI: 0.32-0.64). These differences were seen only in the EF ≥40% subgroup and not the EF <40% subgroup. ACM was similar among Eastern European and North American participants (adjusted hazard ratio: 0.79; 95% CI: 0.44-1.45). CONCLUSIONS: Significant variation exists in the clinical features and outcomes of HF patients across regions in TECOS. Patients from Eastern Europe had lower risk-adjusted ACM/hHF than those in North America, driven by those with EF ≥40%. These data may inform the design of future international trials.

Identifiants

pubmed: 31707329
pii: S0002-8703(19)30221-2
doi: 10.1016/j.ahj.2019.08.016
pii:
doi:

Substances chimiques

Adrenergic beta-Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0
Diuretics 0
Hypoglycemic Agents 0
Sitagliptin Phosphate TS63EW8X6F

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

57-65

Subventions

Organisme : NHLBI NIH HHS
ID : K12 HL138030
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Ankeet S Bhatt (AS)

Brigham and Women's Hospital, Harvard Medical School, Boston, MA.

Nancy Luo (N)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC.

Nicole Solomon (N)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC.

Neha J Pagidipati (NJ)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC.

Giuseppe Ambrosio (G)

Division of Cardiology, University of Perugia School of Medicine, Perugia, Italy.

Jennifer B Green (JB)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC.

Darren K McGuire (DK)

Division of Cardiology, Department of Medicine, University of Texas Southwestern Medical Center, Dallas, TX.

Eberhard Standl (E)

Diabetes Research Group, Munich Helmholtz Center, Munich, Germany.

Jan H Cornel (JH)

Noordwest Ziekenhuisgroep, Department of Cardiology, Alkmaar, the Netherlands.

Sigrun Halvorsen (S)

Department of Cardiology, Oslo University Hospital, and University of Oslo, Oslo, Norway.

Renato D Lopes (RD)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC.

Harvey D White (HD)

Green Lane Cardiovascular Service, Auckland City Hospital, Auckland, New Zealand.

Rury R Holman (RR)

Diabetes Trials Unit, Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, United Kingdom.

Eric D Peterson (ED)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC.

Robert J Mentz (RJ)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC. Electronic address: robert.mentz@duke.edu.

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Classifications MeSH