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Effect of combinations of drugs on all cause mortality in patients with ischaemic heart disease: nested case-control analysis

BMJ 2005; 330 doi: https://doi.org/10.1136/bmj.330.7499.1059 (Published 05 May 2005) Cite this as: BMJ 2005;330:1059

This article has a correction. Please see:

  1. Julia Hippisley-Cox, professor of clinical epidemiology and general practice (julia.hippisley-cox{at}nottingham.ac.uk)1,
  2. Carol Coupland, senior lecturer in medical statistics1
  1. 1Division of Primary Care, School of Community Health Sciences, University Park, Nottingham NG2 7RD
  1. Correspondence to: J Hippisley-Cox
  • Accepted 22 March 2005

Abstract

Objective To determine the effect of combinations of statins, aspirin, β blockers, and angiotensin converting enzyme inhibitors in the secondary prevention of all cause mortality in patients with ischaemic heart disease.

Design Open prospective cohort study with nested case-control analysis.

Setting 1.18 million patients registered with 89 general practices across 23 strategic health authority areas within the United Kingdom. Practices had longitudinal data for a minimum of eight years and were contributing to QRESEARCH, a new database.

Patients All patients with a first diagnosis of ischaemic heart disease between January 1996 and December 2003. Cases were patients with ischaemic heart disease who died. Controls were patients with ischaemic heart disease who were matched for age, sex, and year of diagnosis and were alive at the time their matched case died.

Main outcome measures Odds ratio with 95% confidence interval for risk of death in cases compared with controls. Exposure was current use of different combinations of statins, aspirin, β blockers, and angiotensin converting enzyme inhibitors before death in cases, or the equivalent date in controls.

Results 13 029 patients had a first diagnosis of ischaemic heart disease (incidence rate 338 per 100 000 person years). 2266 cases were matched to 9064 controls. Drug combinations associated with the greatest reduction in all cause mortality were statins, aspirin, and β blockers (83% reduction, 95% confidence interval 77% to 88%); statins, aspirin, β blockers, and angiotensin converting enzyme inhibitors (75% reduction, 65% to 82%); and statins, aspirin, and angiotensin converting enzyme inhibitors (71% reduction, 59% to 79%). Treatments associated with the smallest reduction in all cause mortality were β blockers alone (19% reduction, 37% reduction to 4% increase), angiotensin converting enzyme inhibitors alone (20% reduction, 1% to 35%), and combined statins and angiotensin converting enzyme inhibitors (31% reduction, 57% reduction to 12% increase).

Conclusions Combinations of statins, aspirins, and β blockers improve survival in high risk patients with cardiovascular disease, although the addition of an angiotensin converting enzyme inhibitor conferred no additional benefit despite the analysis being adjusted for congestive cardiac failure.

Footnotes

  • Contributors JHC initiated and designed the study, obtained ethical approval, undertook the data extraction and manipulation and some of the analyses, and drafted the paper. She will act as guarantor for the paper. CC contributed to the study design and core ideas, undertook some of the analyses, advised on interpretation, and contributed to drafting the paper.

  • Funding None.

  • Competing interests None declared.

  • Ethical approval Trent multicentre research ethics committee.

  • Accepted 22 March 2005
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