Predictive factors for reporting adverse events following spinal manipulation in randomized clinical trials - secondary analysis of a systematic review

被引:5
|
作者
Gorrell, Lindsay M. [1 ]
Brown, Benjamin [2 ]
Lystad, Reidar P. [3 ]
Engel, Roger M. [2 ]
机构
[1] Univ Calgary, Fac Kinesiol, Human Performance Lab, KNB 222, Calgary, AB T2N 1N4, Canada
[2] Macquarie Univ, Dept Chiropract, Bldg C5C West, Sydney, NSW 2109, Australia
[3] Macquarie Univ, Australian Inst Hlth Innovat, Fac Med & Hlth Sci, Level 6,75 Talavera Rd, N Ryde, NSW 2109, Australia
关键词
Adverse events; Harms; Spinal manipulative therapy; Manipulation; Spinal; LOW-BACK-PAIN; MECHANICAL NECK PAIN; THORACIC THRUST MANIPULATION; TENSION-TYPE HEADACHE; NAPRAPATHIC MANUAL THERAPY; CHIROPRACTIC CARE; CERVICAL-SPINE; PRESSURE PAIN; HOME EXERCISE; MEDICAL-CARE;
D O I
10.1016/j.msksp.2017.05.002
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
While spinal manipulative therapy (SMT) is recommended for the treatment of spinal disorders, concerns exist about adverse events associated with the intervention. Adequate reporting of adverse events in clinical trials would allow for more accurate estimations of incidence statistics through meta-analysis. However, it is not currently known if there are factors influencing adverse events reporting following SMT in randomized clinical trials (RCTs). Thus our objective was to investigate predictive factors for the reporting of adverse events in published RCTs involving SMT. The Physiotherapy Evidence Database (PEDro) and Cochrane Central Register of Controlled Trials (CENTRAL) were searched for RCTs involving SMT. Domains of interest included: sample size; publication date relative to the 2010 CONSORT statement; risk of bias; the region treated; and number of intervention sessions. 7398 records were identified, of which 368 articles were eligible for inclusion. A total of 140 (38.0%) articles reported on adverse events. Articles were more likely to report on adverse events if they possessed larger sample sizes, were published after the 2010 CONSORT statement, had a low risk of bias and involved multiple intervention sessions. The region treated was not a significant predictor for reporting on adverse events. Predictors for reporting on adverse events included larger sample size, publication after the 2010 CONSORT statement, low risk of bias and trials involving multiple intervention sessions. We recommend that researchers focus on developing robust methodologies and participant follow-up regimens for RCTs involving SMT. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:34 / 41
页数:8
相关论文
共 50 条
  • [21] Quality of adverse events reporting in clinical trials of COVID-19 drugs: A systematic review
    Madi, Karima
    Flumian, Clara
    Olivier, Pascale
    Sommet, Agnes
    Montastruc, Francois
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2023, 32 : 219 - 219
  • [22] Systematic Review of adverse events reporting in clinical trials leading to approval of targeted therapy and immunotherapy
    Bossi, Paolo
    Botta, Laura
    Bironzo, Paolo
    Sonetto, Cristina
    Musettini, Gianna
    Sbrana, Andrea
    Di Giannantonio, Valerio
    Locati, Laura D.
    Di Maio, Massimo
    Antonuzzo, Andrea
    FUTURE ONCOLOGY, 2019, 15 (21) : 2543 - 2553
  • [23] Quality of reporting of adverse events in clinical trials of covid-19 drugs: systematic review
    Madi, Karima
    Flumian, Clara
    Olivier, Pascale
    Sommet, Agnes
    Montastruc, Francois
    BMJ MEDICINE, 2023, 2 (01):
  • [25] Adverse events in psychotherapy randomized controlled trials: A systematic review
    Klatte, Rahel
    Strauss, Bernhard
    Fluckiger, Christoph
    Rosendahl, Jenny
    PSYCHOTHERAPY RESEARCH, 2025, 35 (01) : 84 - 99
  • [26] Analysis and reporting of adverse events in randomised controlled trials: a review
    Phillips, Rachel
    Hazell, Lorna
    Sauzet, Odile
    Cornelius, Victoria
    BMJ OPEN, 2019, 9 (02):
  • [27] Spinal manipulation for asthma: A systematic review of randomised clinical trials
    Ernst, E.
    RESPIRATORY MEDICINE, 2009, 103 (12) : 1791 - 1795
  • [28] CONCORDANCE BETWEEN PATIENTS AND CLINICIANS' REPORTING OF SYMPTOMATIC ADVERSE EVENTS IN CANCER CLINICAL TRIALS: A SYSTEMATIC REVIEW
    Sparano, F.
    Aaronson, N.
    Cottone, F.
    Piciocchi, A.
    La Sala, E.
    Anota, A.
    Deliu, N.
    Kieffer, J. M.
    Efficace, F.
    VALUE IN HEALTH, 2018, 21 : S76 - S77
  • [29] Challenges in Coding Adverse Events in Clinical Trials: A Systematic Review
    Schroll, Jeppe Bennekou
    Maund, Emma
    Gotzsche, Peter C.
    PLOS ONE, 2012, 7 (07):
  • [30] Clinical Effectiveness and Adverse Events of Bee Venom Therapy: A Systematic Review of Randomized Controlled Trials
    Jang, Soobin
    Kim, Kyeong Han
    TOXINS, 2020, 12 (09)