Adverse events in a chiropractic spinal manipulative therapy single blinded, placebo, randomized controlled trial for migraineurs

被引:10
作者
Chaibi, Aleksander [1 ,2 ]
Benth, Jurate Saltyte [2 ,3 ]
Tuchin, Peter J. [4 ]
Russell, Michael Bjorn [1 ,2 ]
机构
[1] Akershus Univ Hosp, Head & Neck Res Grp, Res Ctr, N-1478 Oslo, Norway
[2] Univ Oslo, Inst Clin Med, Campus Akershus Univ Hosp, N-1474 Oslo, Norway
[3] Akershus Univ Hosp, Res Ctr, HOKH, N-1478 Oslo, Norway
[4] Macquarie Univ, Dept Chiropract, Sydney, NSW 2109, Australia
关键词
Adverse events; Side effects; Migraine; Chiropractic; Spinal manipulative therapy; Randomized controlled trial; RCT; PAIN; PREVENTION; GUIDELINES; OUTCOMES; SAFETY; CARE;
D O I
10.1016/j.msksp.2017.03.003
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Background: Unlike pharmacological randomized controlled trials (RCTs), manual-therapy RCTs do not always report adverse events (AEs). The few manual-therapy RCTs that provide information on AEs are frequently without details, such as the type and-, severity of the AE and reason for withdrawal. Objective: To prospectively report all AEs in a chiropractic spinal manipulative therapy (CSMT) RCT. Design: A prospective 3-armed, single-blinded, placebo, RCT. Methods: Seventy migraineurs were randomized to the CSMT or a placebo, with 12 intervention sessions over three months. The recommendations by CONSORT and the International Headache Society's Task Force on AEs in migraine RCTs were followed. A standardized reporting scheme designed for pharmacological RCTs was used, and the AEs were described as frequencies and percentages within each group. The 95% confidence intervals (CIs) for the percentages (absolute risk) of AEs in each group were calculated when possible. Attributable risk (%) and relative risk were calculated with the corresponding 95% CIs. Results: AEs were assessed in 703 sessions, with 355 in the CSMT group and 348 in the placebo group. Local tenderness was the most common AE, reported by 11.3% and 6.9% of the CSMT group and the placebo group, respectively, and tiredness on the intervention day was reported by 8.5% and 1.4% of CSMT group and the placebo group, respectively. The highest attributable risk was for tiredness on the treatment day, 7.0% (CI 3.9-10.2%) which presented a relative risk of 5.9 (CI 2.3-15.0). Conclusions: AEs were mild and transient, and severe or serious AEs were not observed. (C) 2017 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:66 / 71
页数:6
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