Does statin increase the risk of intracerebral hemorrhage in stroke survivors? A meta-analysis and trial sequential analysis

Author:

Teoh Ru Jian Jonathan1,Huang Chi-Jung2,Chan Chi Peng3,Chien Li-Yin14,Chung Chih-Ping56,Sung Shih-Hsien789,Chen Chen-Huan81011,Chiang Chern-En712,Cheng Hao-Min13ORCID

Affiliation:

1. International Health Program, National Yang-Ming University, Taipei

2. Center for Evidence-based Medicine, Taipei Veterans General Hospital, Taipei

3. Royal Infirmary of Edinburgh, NHS Lothian, Edinburgh, UK

4. Institute of Community Health Care, National Yang-Ming University, Taipei

5. Department of Neurology, National Yang-Ming University, Taipei

6. Department of Neurology, Taipei Veterans General Hospital, Taipei

7. Department of Medicine, National Yang-Ming University, Taipei

8. Department of Internal Medicine, Taipei Veterans General Hospital, Taipei

9. Institute of Public Health and Community Medicine Research Center, National Yang-Ming University, Taipai

10. Institute of Public Health and Community Medicine Research Center, National Yang-Ming University, Taipei

11. Department of Medical Education, Taipei Veterans General Hospital, Taipei

12. General Clinical Research Center, Taipei Veterans General Hospital, Taipei

13. Center for Evidence-based Medicine, Taipei Veterans General Hospital, No. 201, Sec. 2, Shih-Pai Road, Beitou District, Taipei 11217

Abstract

Background: It remains debatable whether statin increases the risk of intracerebral hemorrhage (ICH) in poststroke patients. Methods: We systematically searched PubMed, EMBASE, and CENTRAL for randomized controlled trials. Trial sequential analysis (TSA) was conducted to assess the reliability and conclusiveness of the available evidence in the meta-analysis. To evaluate the overall effectiveness, the net composite endpoints were derived by totaling ischemic stroke, hemorrhagic stroke, transient ischemic attack (TIA), myocardial infarction, and cardiovascular mortality. Results: A total of 17 trials with 11,576 subjects with previous ischemic stroke, TIA, or ICH were included, in which statin therapy increased the risk of hemorrhagic stroke (risk ratio [RR], 1.42; 95% confidence interval [CI], 1.07–1.87), but reduced the risk of ischemic stroke (RR, 0.85; 95% CI, 0.75–0.95). For the net composite endpoints, statin therapy was associated with a 17% risk reduction (95% CI, 12–21%; number needed to treat = 6). With a control event rate 2% and RR increase 40%, the TSA suggested a conclusive signal of an increased risk of hemorrhagic stroke in stroke survivors taking statin. However, with the sensitivity analysis by changing assumptions, the conclusions about hemorrhagic stroke risk were less robust. Conclusions: Statin therapy in poststroke patients increased the risk of hemorrhagic stroke but effectively reduced ischemic stroke risk. Weighing the benefits and potential harms, statin has an overall beneficial effect in patients with previous stroke or TIA. However, more studies are required to investigate the conclusiveness of the increased hemorrhagic stroke risk revealed in our study.

Funder

Taiwan International Cooperation and Development Fund International Higher Education Scholarship program

Ministry of Health and Welfare

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology,Pharmacology

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