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Meta-Analysis
. 2023 Jun 16;13(6):e060274.
doi: 10.1136/bmjopen-2021-060274.

Efficacy and safety of botulinum toxin for treating motor dysfunction in patients with Parkinson's disease: a systematic review and meta-analysis

Affiliations
Meta-Analysis

Efficacy and safety of botulinum toxin for treating motor dysfunction in patients with Parkinson's disease: a systematic review and meta-analysis

Yuqi Yang et al. BMJ Open. .

Abstract

Objective: To evaluate the efficacy and safety of botulinum toxin (BTX) for motor dysfunction in Parkinson's disease (PD).

Design: Systematic review and meta-analysis.

Data sources: Searches of PubMed, EMBASE and the Cochrane Library, from database inception to 20 October 2022.

Eligibility criteria: Studies reported in English with adult PD patients treated with BTX.

Data extraction and synthesis: Primary outcomes were United Parkinson's Disease Rate Scale Section (UPDRS) III (or its items) and Visual Analogue Scale (VAS). Secondary outcomes were UPDRS-II (or its items), Freezing of Gait Questionnaire (FOG-Q), Timed Up and Go test (TUG) and treatment-related adverse events (TRAEs). Mean difference (MD) or standardised MD (SMD) before and after treatment with 95% CIs were used for continuous variables and risk ratios (RRs) with 95% CIs was used for TRAEs.

Results: Six randomised controlled trials (RCTs) and six non-RCTs (case series) were included (ntotal=224 participants, nRCT=165). No significant difference was found in pooled results of UPDRS-III (available in four RCTs and two non-RCTs, SMD=-0.19, 95% CI -0.98 to 0.60), UPDRS-II (four RCTs and one non-RCT, SMD=-0.55, 95% CI -1.22 to 0.13), FOG-Q (one RCT and one non-RCT, SMD=0.53, 95% CI -1.93 to 2.98) or the risk of TRAEs (five RCTs, RR 0.87, 95% CI 0.37 to 2.01). Significant decreases were found in pooled VAS score (three RCTs and five non-RCTs, MD=-2.14, 95% CI -3.05 to -1.23) and TUG (MD=-2.06, 95% CI -2.91 to -1.20) after BTX treatment.

Conclusions: BTX may not be associated with motor symptoms alleviation, although it benefits pain alleviation and functional mobility improvement.

Keywords: NEUROPHYSIOLOGY; Neuropathology; Parkinson-s disease.

PubMed Disclaimer

Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Meta-analysis of United Parkinson’s Disease Rate Scale Section III, by study design. IV, inverse-variance; RCT, randomised controlled trial.
Figure 2
Figure 2
Meta-analysis of VAS, by study design. IV, inverse-variance; RCT, randomised controlled trial; VAS, Visual Analogue Scale.
Figure 3
Figure 3
Meta-analysis of United Parkinson’s Disease Rate Scale Section II, by study design. IV, inverse-variance; RCT, randomised controlled trial.
Figure 4
Figure 4
Meta-analysis of TUG after BTX treatment. BTX, botulinum toxin; IV, inverse-variance; TUG, Timed Up and Go test.
Figure 5
Figure 5
Meta-analysis of TRAEs after BTX treatment. BTX, botulinum toxin; IV, inverse-variance; TRAEs, treatment-related adverse events.

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