Reaching cardiovascular prevention guideline targets with a polypill-based approach: a meta-analysis of randomised clinical trials.


Journal

Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087

Informations de publication

Date de publication:
01 2019
Historique:
received: 03 02 2018
revised: 17 05 2018
accepted: 24 05 2018
pubmed: 30 6 2018
medline: 4 4 2019
entrez: 30 6 2018
Statut: ppublish

Résumé

The aim of this study was to determine the effect of polypill-based care on the achievement of 2016 European Society of Cardiology (ESC) guideline targets for blood pressure (BP), low-density lipoprotein (LDL) cholesterol and antiplatelet therapy. We conducted an individual participant data meta-analysis of three randomised clinical trials that compared a strategy using a polypill containing aspirin, statin and antihypertensive therapy with usual care in patients with a prior cardiovascular disease (CVD) event or who were at high risk of their first event. Overall, the trials included 3140 patients from Australia, England, India, Ireland, the Netherlands and New Zealand (75% male, mean age 62 years and 76% with a prior CVD event). The primary outcome for this study was the proportion of people achieving ESC guideline targets for BP, LDL and antiplatelet therapy. Those randomised to polypill-based care were more likely than those receiving usual care to achieve recommended targets for BP (62% vs 58%, risk ratio (RR) 1.08, 95% CI 1.02 to 1.15), LDL (39% vs 34%, RR 1.13, 95% CI 1.02 to 1.25) and all three targets for BP, LDL and adherence to antiplatelet therapy (the latter only applicable to those with a prior CVD event) simultaneously (24% vs 19%, RR 1.27, 95% CI 1.10 to 1.47) at 12 months. There was no difference between groups in antiplatelet adherence (96% vs 96%, RR 1.00, 95% CI 0.98 to 1.01). There was heterogeneity by baseline treatment intensity such that treatment effects increased with the fewer the number of treatments being taken at baseline: for patients taking 3, 2 and 0-1 treatment modalities the RRs for reaching all three guideline goals simultaneously were 1.10 (95% CI 0.94 to 1.30, 22% vs 20%), 1.62 (95% CI 1.09 to 2.42, 27% vs 17%) and 3.07 (95% CI 1.77 to 5.33, 35% vs 11%), respectively. Polypill-based therapy significantly improved the achievement of all three ESC targets for BP, LDL and antiplatelet therapy compared with usual care, particularly among those undertreated at baseline.

Identifiants

pubmed: 29954855
pii: heartjnl-2018-313108
doi: 10.1136/heartjnl-2018-313108
doi:

Substances chimiques

Antihypertensive Agents 0
Cholesterol, LDL 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Platelet Aggregation Inhibitors 0
Aspirin R16CO5Y76E

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

42-48

Commentaires et corrections

Type : CommentIn

Informations de copyright

© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2019. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Déclaration de conflit d'intérêts

Competing interests: Support for the submitted work: RW is funded by an NHMRC early career fellowship. The authors have received grants from several research charities and national funding agencies for research on cardiovascular polypills, and from Dr Reddy’s Laboratories for coordination of the SPACE programme (www.spacecollaboration.org). The polypills used in the SPACE trials were manufactured and supplied by Dr Reddy’s Laboratories free of charge. Some authors received funding from Dr Reddy’s Laboratories to attend investigator meetings related to the polypill (VS, RW, AP, ST, NR, AW and AR). George Health Enterprises, the social enterprise arm of The George Institute for Global Health (employer of some coauthors) has received investment for the development of fixed dose combination therapy containing statin, aspirin and blood pressure lowering medications.

Auteurs

Vanessa Selak (V)

Department of Epidemiology and Biostatistics, University of Auckland, Auckland, New Zealand.

Ruth Webster (R)

The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.

Sandrine Stepien (S)

The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.

Chris Bullen (C)

National Institute for Health Innovation, University of Auckland, Auckland, New Zealand.

Anushka Patel (A)

The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.

Simon Thom (S)

International Centre for Circulatory Health, National Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.

Bruce Arroll (B)

Department of General Practice and Primary Healthcare, University of Auckland, Auckland, New Zealand.

Michiel L Bots (ML)

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Alex Brown (A)

South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.

Sue Crengle (S)

Department of Preventive and Social Medicine, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.

Prabhakaran Dorairaj (P)

Centre for Chronic Disease Control, New Delhi, India.

C Raina Elley (CR)

Department of General Practice and Primary Healthcare, University of Auckland, Auckland, New Zealand.

Diederick E Grobbee (DE)

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Matire Harwood (M)

Te Kupenga Hauora Māori, University of Auckland, Auckland, New Zealand.

Graham S Hillis (GS)

Department of Cardiology, Royal Perth Hospital, Perth, Western Australia, Australia.

Tracey-Lea Laba (TL)

Menzies Centre for Health Policy, School of Public Health, Sydney Medical School, The University of Sydney, Sydney, New South Wales, Australia.

Bruce Neal (B)

The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.

David Peiris (D)

The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.

Natasha Rafter (N)

Department of Epidemiology and Public Health Medicine, Royal College of Surgeons in Ireland, Dublin, Ireland.

Christopher Reid (C)

School of Public Health, Curtin University, Perth, Western Australia, Australia.

Alice Stanton (A)

Molecular and Cellular Therapeutics, Royal College of Surgeons in Ireland, Dublin, Ireland.

Andrew Tonkin (A)

Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.

Tim Usherwood (T)

The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.
Department of General Practice, Sydney Medical School Westmead, The University of Sydney, Sydney, New South Wales, Australia.

Angela Wadham (A)

National Institute for Health Innovation, University of Auckland, Auckland, New Zealand.

Anthony Rodgers (A)

The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.

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Classifications MeSH