Systematic review: Pharmacological interventions for the treatment of post-stroke fatigue

Author:

Chu Shuk Han1ORCID,Zhao Xu2,Komber Ahmad1,Cheyne Joshua3,Wu Simiao4ORCID,Cowey Eileen5,Kutlubaev Mansur6,Mead Gillian1ORCID

Affiliation:

1. Usher Institute, The University of Edinburgh, Edinburgh, UK

2. Department of Chemistry, Oxford University, Oxford, UK

3. Library Services, University of the West of Scotland, Paisley, UK

4. Department of Neurology, West China Hospital, Sichuan University, Chengdu, China

5. Nursing & Health Care School, University of Glasgow, Glasgow, UK

6. Department of Neurology, Bashkir State Medical University, Ufa, Russia

Abstract

Background: Post-stroke fatigue (PSF) affects around 50% of stroke survivors. Previous systematic reviews of randomized controlled trials found insufficient evidence to guide practice, but most excluded Chinese studies. Furthermore, their searches are now out-of-date. Aims: To systematically review and perform a meta-analysis of randomized placebo-controlled trials of pharmacological interventions for treating PSF. Methods: We screened Airitri, CNKI, VIP, CINAHL, ClinicalTrials.gov, CENTRAL, Cochrane Stroke Group Trial Register, EMBASE, EU Clinical Trial Register, ISRCTN, MEDLINE, PsycINFO, Wanfang, and WHO ICTRP up to 11 November 2022. Our primary outcome was fatigue severity. We conducted subgroup analysis by drug type and sensitivity analysis after excluding the trials at high risk of bias. Secondary outcomes included mood and quality of life. Results: We screened 33,297 citations and identified 10 published completed trials, 6 unpublished completed trials, and 6 ongoing trials. Pharmacological treatments were associated with lower fatigue severity at the end of treatment (10 published completed trials, 600 participants, pooled standardized mean difference (SMD) = −0.80, 95% confidence interval (CI): −1.29 to −0.31; I2 = 86%, p < 0.00001), but not at follow-up (265 participants, pooled SMD = −0.14, 95% CI: −0.38 to 0.10; I2 = 0, p = 0.51). However, these trials were small and had considerable risk of bias. Beneficial effects were seen in trials with low risk of bias on randomization, missing outcome data, and reporting bias. There were insufficient data on secondary outcomes for meta-analysis, but six trials reported improved quality of life. Conclusion: There is insufficient evidence to support a particular pharmacological treatment for PSF, thus current clinical guidelines do not require amendment.

Publisher

SAGE Publications

Subject

Neurology,Neurology (clinical)

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