BMJ  2005;330:1059-1063 (7 May), doi:10.1136/bmj.330.7499.1059

Primary care

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

Julia Hippisley-Cox, professor of clinical epidemiology and general practice1, Carol Coupland, senior lecturer in medical statistics1

1 Division of Primary Care, School of Community Health Sciences, University Park, Nottingham NG2 7RD

Correspondence to: J Hippisley-Cox julia.hippisley-cox{at}nottingham.ac.uk

Objective To determine the effect of combinations of statins, aspirin, {beta} 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, {beta} 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 {beta} blockers (83% reduction, 95% confidence interval 77% to 88%); statins, aspirin, {beta} 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 {beta} 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 {beta} 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.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to StumbleUpon StumbleUpon   Add to Technorati Technorati    What's this?

Relevant Articles

Derivation and validation of QRISK, a new cardiovascular disease risk score for the United Kingdom: prospective open cohort study
Julia Hippisley-Cox, Carol Coupland, Yana Vinogradova, John Robson, Margaret May, and Peter Brindle
BMJ 2007 335: 136. [Abstract] [Full Text] [PDF]

Drug combinations and all cause mortality in heart disease: No new insights were gained
Staffan Bjorck
BMJ 2005 331: 159. [Extract] [Full Text] [PDF]

Drug combinations and all cause mortality in heart disease: Use of statins is not supported by study
Eddie Vos
BMJ 2005 331: 159. [Extract] [Full Text]

Drug combinations and all cause mortality in heart disease: Dosages and types of ACE inhibitors need to be known
Frank A Snyder
BMJ 2005 331: 159. [Extract] [Full Text]

Hit parade
BMJ 2005 331: 115. [Extract] [Full Text]

For newly diagnosed ischaemic heart disease give a statin, aspirin, and {beta} blocker
BMJ 2005 330: 0. [Full Text]

The polypill and cardiovascular disease
Tom Fahey, Peter Brindle, and Shah Ebrahim
BMJ 2005 330: 1035-1036. [Extract] [Full Text] [PDF]

A strategy to reduce cardiovascular disease by more than 80%
N J Wald and M R Law
BMJ 2003 326: 1419. [Abstract] [Full Text] [PDF]

The electronic patient record in primary care—regression or progression? A cross sectional study
Julia Hippisley-Cox, Mike Pringle, Ruth Cater, Alison Wynn, Vicky Hammersley, Carol Coupland, Rhydian Hapgood, Peter Horsfield, Sheila Teasdale, and Christine Johnson
BMJ 2003 326: 1439-1443. [Abstract] [Full Text] [PDF]

Risk of venous thromboembolism among users of third generation oral contraceptives compared with users of oral contraceptives with levonorgestrel before and after 1995: cohort and case-control analysis
Hershel Jick, James A Kaye, Catherine Vasilakis-Scaramozza, and Susan S Jick
BMJ 2000 321: 1190-1195. [Abstract] [Full Text] [PDF]

Implementing findings of research
A Haines and R Jones
BMJ 1994 308: 1488-1492. [Extract] [Full Text]

This article has been cited by other articles:

  • Corp, E.V., Antoniou, S., Wright, P.G., Khachi, H., Vercaeren, S., Wald, D.S. (2009). Use and cost of branded and generic drugs in patients with coronary heart disease--results from a prospective survey of 1008 patients in two London hospitals. QJM 0: hcp127v1-hcp127 [Abstract] [Full text]  
  • Kasanuki, H., Hagiwara, N., Hosoda, S., Sumiyoshi, T., Honda, T., Haze, K., Nagashima, M., Yamaguchi, J.-i., Origasa, H., Urashima, M., Ogawa, H., for the HIJ-CREATE Investigators, (2009). Angiotensin II receptor blocker-based vs. non-angiotensin II receptor blocker-based therapy in patients with angiographically documented coronary artery disease and hypertension: the Heart Institute of Japan Candesartan Randomized Trial for Evaluation in Coronary Artery Disease (HIJ-CREATE). Eur Heart J 30: 1203-1212 [Abstract] [Full text]  
  • Coleman, L. A., Kottke, T. E., Rank, B., Reding, D. J., Selna, M., Isham, G. J., Nelson, A. F., Greenlee, R. T. (2008). Partnering Care Delivery and Research to Optimize Health. Clin Med Res 6: 113-118 [Abstract] [Full text]  
  • Suissa, S. (2008). Immeasurable Time Bias in Observational Studies of Drug Effects on Mortality. Am J Epidemiol 168: 329-335 [Abstract] [Full text]  
  • Choudhry, N. K., Patrick, A. R., Antman, E. M., Avorn, J., Shrank, W. H. (2008). Cost-Effectiveness of Providing Full Drug Coverage to Increase Medication Adherence in Post-Myocardial Infarction Medicare Beneficiaries. Circulation 117: 1261-1268 [Abstract] [Full text]  
  • Badger, S. A., Soong, C. V., Lee, B., Swain, G. R., McGuigan, K. E. (2008). Prescribing Practice of General Practitioners in Northern Ireland for Peripheral Arterial Disease. ANGIOLOGY 59: 57-63 [Abstract]  
  • DeWilde, S, Carey, I M, Richards, N, Whincup, P H, Cook, D G (2008). Trends in secondary prevention of ischaemic heart disease in the UK 1994 2005: use of individual and combination treatment. Heart 94: 83-88 [Abstract] [Full text]  
  • Hippisley-Cox, J., Vinogradova, Y., Coupland, C., Parker, C. (2007). Risk of Malignancy in Patients With Schizophrenia or Bipolar Disorder: Nested Case-Control Study. Arch Gen Psychiatry 64: 1368-1376 [Abstract] [Full text]  
  • Thomas, R. J. (2007). Cardiac Rehabilitation/Secondary Prevention Programs: A Raft for the Rapids: Why Have We Missed the Boat?. Circulation 116: 1644-1646 [Full text]  
  • van der Elst, M. E, Bouvy, M. L, de Blaey, C. J, de Boer, A. (2007). Effect of drug combinations on admission for recurrent myocardial infarction. Heart 93: 1226-1230 [Abstract] [Full text]  
  • Wald, D. S, Morton, G., Walker, K., Iosson, N., Curzen, N. P (2007). Long-Term Continuation on Cardiovascular Drug Treatment in Patients with Coronary Heart Disease. The Annals of Pharmacotherapy 41: 1644-1647 [Abstract] [Full text]  
  • Hippisley-Cox, J., Coupland, C., Vinogradova, Y., Robson, J., May, M., Brindle, P. (2007). Derivation and validation of QRISK, a new cardiovascular disease risk score for the United Kingdom: prospective open cohort study. BMJ 335: 136-136 [Abstract] [Full text]  
  • Ford, E. S., Ajani, U. A., Croft, J. B., Critchley, J. A., Labarthe, D. R., Kottke, T. E., Giles, W. H., Capewell, S. (2007). Explaining the Decrease in U.S. Deaths from Coronary Disease, 1980-2000. NEJM 356: 2388-2398 [Abstract] [Full text]  
  • Sekhri, N, Feder, G S, Junghans, C, Hemingway, H, Timmis, A D (2007). How effective are rapid access chest pain clinics? Prognosis of incident angina and non-cardiac chest pain in 8762 consecutive patients. Heart 93: 458-463 [Abstract] [Full text]  
  • Goyal, A., Alexander, J. H., Hafley, G. E., Graham, S. H., Mehta, R. H., Mack, M. J., Wolf, R. K., Cohn, L. H., Kouchoukos, N. T., Harrington, R. A., Gennevois, D., Gibson, C. M., Califf, R. M., Ferguson, T. B. Jr, Peterson, E. D., PREVENT IV Investigators, (2007). Outcomes Associated With the Use of Secondary Prevention Medications After Coronary Artery Bypass Graft Surgery. Ann. Thorac. Surg. 83: 993-1001 [Abstract] [Full text]  
  • Choudhry, N. K., Avorn, J., Antman, E. M., Schneeweiss, S., Shrank, W. H. (2007). Should Patients Receive Secondary Prevention Medications For Free After A Myocardial Infarction? An Economic Analysis. Health Aff (Millwood) 26: 186-194 [Abstract] [Full text]  
  • Kaplan, N. M. (2005). An Updated Meta-Analysis With a Few Surprises. Hypertension 46: 257-258 [Full text]  
  • Bjorck, S. (2005). Drug combinations and all cause mortality in heart disease: No new insights were gained. BMJ 331: 159-159 [Full text]  
  • Vos, E. (2005). Drug combinations and all cause mortality in heart disease: Use of statins is not supported by study. BMJ 331: 159-159 [Full text]  
  • Snyder, F. A (2005). Drug combinations and all cause mortality in heart disease: Dosages and types of ACE inhibitors need to be known. BMJ 331: 159-159 [Full text]  
  • (2005). Hit parade. BMJ 331: 115-115 [Full text]  
  • (2005). Drug Combinations That Reduce Mortality in CHD Patients. JWatch General 2005: 6-6 [Full text]  
  • Fahey, T., Brindle, P., Ebrahim, S. (2005). The polypill and cardiovascular disease. BMJ 330: 1035-1036 [Full text]  

Rapid Responses:

Read all Rapid Responses

We must consider also Single Patient Based Medicine in therapy decisions.
Sergio Stagnaro
bmj.com, 7 May 2005 [Full text]
Use of statins not supported by study
Eddie Vos
bmj.com, 6 May 2005 [Full text]
For newly diagnosed ischaemic heart disease: less drugs, low costs and ... don’t forget lifestyle changes!
Emanuele Cereda, et al.
bmj.com, 8 May 2005 [Full text]
Are all angiotensin converting enzyme inhibitors equally ineffective?
Robert J. Richards
bmj.com, 10 May 2005 [Full text]
What were dosages of ACE-1, and as prev asked, which ones.
Frank A. Snyder, et al.
bmj.com, 11 May 2005 [Full text]
angiotensin converting enzyme inhibition in ischaemic heart disease
Staffan Bjorck
bmj.com, 11 May 2005 [Full text]
ACE Inhibitors and Ischaemic heart disease
Ramachandran Sivakumar
bmj.com, 19 May 2005 [Full text]



Access jobs at BMJ Careers
Whats new online at Student 

BMJ