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Review
. 2013 Oct 1:347:f5577.
doi: 10.1136/bmj.f5577.

Comparative effectiveness of exercise and drug interventions on mortality outcomes: metaepidemiological study

Huseyin Naci  1 , John P A Ioannidis
Affiliations
Review

Comparative effectiveness of exercise and drug interventions on mortality outcomes: metaepidemiological study

Huseyin Naci et al. BMJ. .

Abstract

Objective: To determine the comparative effectiveness of exercise versus drug interventions on mortality outcomes.

Design: Metaepidemiological study.

Eligibility criteria: Meta-analyses of randomised controlled trials with mortality outcomes comparing the effectiveness of exercise and drug interventions with each other or with control (placebo or usual care).

Data sources: Medline and Cochrane Database of Systematic Reviews, May 2013.

Main outcome measure: Mortality.

Data synthesis: We combined study level death outcomes from exercise and drug trials using random effects network meta-analysis.

Results: We included 16 (four exercise and 12 drug) meta-analyses. Incorporating an additional three recent exercise trials, our review collectively included 305 randomised controlled trials with 339,274 participants. Across all four conditions with evidence on the effectiveness of exercise on mortality outcomes (secondary prevention of coronary heart disease, rehabilitation of stroke, treatment of heart failure, prevention of diabetes), 14,716 participants were randomised to physical activity interventions in 57 trials. No statistically detectable differences were evident between exercise and drug interventions in the secondary prevention of coronary heart disease and prediabetes. Physical activity interventions were more effective than drug treatment among patients with stroke (odds ratios, exercise v anticoagulants 0.09, 95% credible intervals 0.01 to 0.70 and exercise v antiplatelets 0.10, 0.01 to 0.62). Diuretics were more effective than exercise in heart failure (exercise v diuretics 4.11, 1.17 to 24.76). Inconsistency between direct and indirect comparisons was not significant.

Conclusions: Although limited in quantity, existing randomised trial evidence on exercise interventions suggests that exercise and many drug interventions are often potentially similar in terms of their mortality benefits in the secondary prevention of coronary heart disease, rehabilitation after stroke, treatment of heart failure, and prevention of diabetes.

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Conflict of interest statement

Competing interests: All authors have completed the ICMJE uniform disclosure form at http://www.icmje.org/coi_disclosure.pdf and declare: no support from any organisation for the submitted work; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years, no other relationships or activities that could appear to have influenced the submitted work.

Figures

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Fig 1 Steps involved in study identification and selection
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Fig 2 Network of available comparisons between exercise and individual drug interventions in coronary heart disease, stroke, heart failure, and prediabetes. Size of node is proportional to number of trial participants, and thickness of line connecting nodes is proportional to number of participants randomised in trials directly comparing the two treatments. ACE=angiotensin converting enzyme
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Fig 3 Network of available comparisons between exercise and all drug interventions in coronary heart disease, stroke, heart failure, and prediabetes. Size of node is proportional to number of trial participants, and thickness of line connecting nodes is proportional to number of participants randomised in trials directly comparing the two treatments
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Fig 4 Findings of network meta-analysis: effects of exercise and drug interventions compared with control on mortality outcomes in coronary heart disease, stroke, heart failure, and prediabetes. Results shown are odds ratios and 95% credible intervals. Odds ratios lower than 1.00 favour intervention compared with control. ACE=angiotensin converting enzyme. *Number of data points for thiazolidinediones was insufficient to obtain an estimate of odds ratio compared with control
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