Adverse event reporting in nonpharmacologic, noninterventional pain clinical trials: ACTTION systematic review

被引:22
|
作者
Hunsinger, Matthew [1 ]
Smith, Shannon M. [2 ]
Rothstein, Daniel [2 ]
McKeown, Andrew [2 ]
Parkhurst, Melissa [3 ]
Hertz, Sharon [4 ]
Katz, Nathaniel P. [5 ,6 ]
Lin, Allison H. [4 ]
McDermott, Michael P. [7 ]
Rappaport, Bob A. [4 ]
Turk, Dennis C. [8 ]
Dworkin, Robert H. [2 ]
机构
[1] Univ Pacific, Sch Profess Psychol, Hillsboro, OR 97123 USA
[2] Univ Rochester, Sch Med & Dent, Dept Anesthesiol, Rochester, NY USA
[3] Univ Rochester, Sch Med & Dent, Dept Psychiat, Rochester, NY 14642 USA
[4] US FDA, Silver Spring, MD USA
[5] Analges Solut, Natick, MA USA
[6] Tufts Univ, Boston, MA 02111 USA
[7] Univ Rochester, Sch Med & Dent, Dept Biostat & Computat Biol, Rochester, NY USA
[8] Univ Washington, Dept Anesthesiol & Pain Med, Seattle, WA 98195 USA
关键词
Harms reporting; Safety reporting; Adverse events; Complementary and alternative medical treatments; RANDOMIZED CONTROLLED-TRIALS; PSYCHOLOGICAL TREATMENTS; IMMPACT RECOMMENDATIONS; DRUG-SAFETY; HARMS; MANAGEMENT; STATEMENT; SYMPTOMS;
D O I
10.1016/j.pain.2014.08.004
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Assessment of treatment safety is 1 of the primary goals of clinical trials. Organizations and working groups have created reporting guidelines for adverse events (AEs). Previous research examining AE reporting for pharmacologic clinical trials of analgesics in major pain journals found many reporting inadequacies, suggesting that analgesic trials are not adhering to existing AE reporting guidelines. The present systematic review documented AE reporting in 3 main pain journals for nonpharmacologic, non-interventional (NP/NI) trials examining pain treatments. To broaden our pool of nonpharmacologic trials, we also included trials examining acupuncture, leech therapy, and noninvasive stimulation techniques (eg, transcutaneous electrical nerve stimulation). We documented AE reporting at 2 levels of specificity using coding manuals based on the Consolidated Standards of Reporting Trials (CONSORT) harms reporting standards and Analgesic, Anesthetic, and Addiction Clinical Trial Translations, Innovations, Opportunities, and Networks (ACTTION) AE reporting checklist. We identified a number of inadequacies in AE reporting across the 3 journals. For example, using the ACTTION coding manual, we found that less than one-half of the trials reported specific AE assessment methods; approximately one-third of the trials reported withdrawals due to AEs for each study arm; and about one-fourth of the trials reported all specific AEs. We also examined differences in AE reporting across several trial characteristics, finding that AE reporting was generally more detailed in trials with patients versus those using healthy volunteers undergoing experimentally evoked pain. These results suggest that investigators conducting and reporting NP/NI clinical trials are not adequately describing the assessment and occurrence of AEs. (C) 2014 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2253 / 2262
页数:10
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