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      Opioid substitution and antagonist therapy trials exclude the common addiction patient: a systematic review and analysis of eligibility criteria

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          Abstract

          Background

          Eligibility criteria that result in the exclusion of a substantial number of patients from randomized trials jeopardize the generalizability of treatment effect to much of the clinical population. This is important when evaluating opioid substitution and antagonist therapies (OSATs), especially given the challenges associated with treating the opioid-dependent population. We aimed to identify OSAT trials' eligibility criteria, quantify the percentage of the clinical population excluded by these criteria, and determine how OSAT guidelines incorporate evidence from these trials.

          Methods

          We performed a systematic review to identify the eligibility criteria used across trials. We searched Medline, EMBASE, PsycINFO, Web of Science, Cochrane Library, Cochrane Clinical Trials Registry (CTR), World Health Organization International CTR Platform Search Portal, and the National Institutes of Health CTR databases from inception to January 1, 2014. To quantify the effect of trials' eligibility criteria on generalizability, we applied these criteria to data from an observational study of opioid-dependent patients (n = 394). We then accessed the Canadian, American, British, and World Health Organization (WHO) OSAT guidelines to evaluate how evidence is used in the recommendations.

          Results

          Among the 60 trials identified the majority (≥50 % of trials) exclude patients with psychiatric (60 %) and physical comorbidity (51.7 %). Additionally, we found 19 trials exclude patients with current alcohol/substance-use problems (31.7 %), and 29 (48.3 %) exclude patients taking psychotropic medications. These criteria were restrictive and in some cases rendered 70 % of the observational sample ineligible. North American OSAT guidelines made strong recommendations supported by evidence with poor generalizability. National Institute of Health and Care Excellence (NICE) and WHO guidelines for opioid misuse provide a critical assessment of the literature used to inform their recommendations.

          Conclusions

          Trials assessing OSATs often exclude patients with concurrent disorders. If the excluded patients respond differently to treatment, results from these trials are likely to overestimate the true effectiveness of OSATs. North American guidelines should consider these limitations when drafting clinical recommendations.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s13063-015-0942-4) contains supplementary material, which is available to authorized users.

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          Most cited references80

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          Buprenorphine maintenance versus placebo or methadone maintenance for opioid dependence

          Cochrane Database of Systematic Reviews
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            Rates of opioid misuse, abuse, and addiction in chronic pain: a systematic review and data synthesis.

            Opioid use in chronic pain treatment is complex, as patients may derive both benefit and harm. Identification of individuals currently using opioids in a problematic way is important given the substantial recent increases in prescription rates and consequent increases in morbidity and mortality. The present review provides updated and expanded information regarding rates of problematic opioid use in chronic pain. Because previous reviews have indicated substantial variability in this literature, several steps were taken to enhance precision and utility. First, problematic use was coded using explicitly defined terms, referring to different patterns of use (ie, misuse, abuse, and addiction). Second, average prevalence rates were calculated and weighted by sample size and study quality. Third, the influence of differences in study methodology was examined. In total, data from 38 studies were included. Rates of problematic use were quite broad, ranging from <1% to 81% across studies. Across most calculations, rates of misuse averaged between 21% and 29% (range, 95% confidence interval [CI]: 13%-38%). Rates of addiction averaged between 8% and 12% (range, 95% CI: 3%-17%). Abuse was reported in only a single study. Only 1 difference emerged when study methods were examined, where rates of addiction were lower in studies that identified prevalence assessment as a primary, rather than secondary, objective. Although significant variability remains in this literature, this review provides guidance regarding possible average rates of opioid misuse and addiction and also highlights areas in need of further clarification.
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              Eligibility criteria of randomized controlled trials published in high-impact general medical journals: a systematic sampling review.

              Selective eligibility criteria of randomized controlled trials (RCTs) are vital to trial feasibility and internal validity. However, the exclusion of certain patient populations may lead to impaired generalizability of results. To determine the nature and extent of exclusion criteria among RCTs published in major medical journals and the contribution of exclusion criteria to the representation of certain patient populations. The MEDLINE database was searched for RCTs published between 1994 and 2006 in certain general medical journals with a high impact factor. Of 4827 articles, 283 were selected using a series technique. Trial characteristics and the details regarding exclusions were extracted independently. All exclusion criteria were graded independently and in duplicate as either strongly justified, potentially justified, or poorly justified according to previously developed and pilot-tested guidelines. Common medical conditions formed the basis for exclusion in 81.3% of trials. Patients were excluded due to age in 72.1% of all trials (60.1% in pediatric populations and 38.5% in older adults). Individuals receiving commonly prescribed medications were excluded in 54.1% of trials. Conditions related to female sex were grounds for exclusion in 39.2% of trials. Of all exclusion criteria, only 47.2% were graded as strongly justified in the context of the specific RCT. Exclusion criteria were not reported in 12.0% of trials. Multivariable analyses revealed independent associations between the total number of exclusion criteria and drug intervention trials (risk ratio, 1.35; 95% confidence interval, 1.11-1.65; P = .003) and between the total number of exclusion criteria and multicenter trials (risk ratio, 1.26; 95% confidence interval, 1.06-1.52; P = .009). Industry-sponsored trials were more likely to exclude individuals due to concomitant medication use, medical comorbidities, and age. Drug intervention trials were more likely to exclude individuals due to concomitant medication use, medical comorbidities, female sex, and socioeconomic status. Among such trials, justification for exclusions related to concomitant medication use and comorbidities were more likely to be poorly justified. The RCTs published in major medical journals do not always clearly report exclusion criteria. Women, children, the elderly, and those with common medical conditions are frequently excluded from RCTs. Trials with multiple centers and those involving drug interventions are most likely to have extensive exclusions. Such exclusions may impair the generalizability of RCT results. These findings highlight a need for careful consideration and transparent reporting and justification of exclusion criteria in clinical trials.
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                Author and article information

                Contributors
                dennisbb@mcmaster.ca
                proshano@uwo.ca
                leennaji2@gmail.com
                baworm@mcmaster.ca
                james_paul@sympatico.ca
                cplater@toxpro.ca
                pareg@mcmaster.ca
                worster@mcmaster.ca
                MVarenbut@canatc.ca
                jdaiter@toxpro.ca
                dmarsh@nosm.ca
                dipika.desai@phri.ca
                samaanz@mcmaster.ca
                905-522-1155 , thabanl@mcmaster.ca
                Journal
                Trials
                Trials
                Trials
                BioMed Central (London )
                1745-6215
                21 October 2015
                21 October 2015
                2015
                : 16
                : 475
                Affiliations
                [ ]Department of Clinical Epidemiology and Biostatistics, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4L8 Canada
                [ ]Schulich School of Medicine and Dentistry, University of Western Ontario, 4, 1465 Richmond Street, London, ON N6G 2M1 Canada
                [ ]Michael G. Degroote School of Medicine, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4L8 Canada
                [ ]McMaster Integrative Neuroscience Discovery and Study Program, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4L8 Canada
                [ ]Department of Anesthesia, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4L8 Canada
                [ ]Canadian Addiction Treatment Centres, 13291 Yonge Street, Richmond Hill, ON L4E 4L6 Canada
                [ ]Department of Medicine, Hamilton General Hospital, 237 Barton St East, Hamilton, ON L8L 2X2 Canada
                [ ]Northern Ontario School of Medicine, Ramsey Lake Road, Sudbury, ON P0M Canada
                [ ]Population Genomics Program, Chanchlani Research Centre, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4K1 Canada
                [ ]Peter Boris Centre for Addictions Research, St. Joseph’s Healthcare Hamilton, 100 West 5th Street, Hamilton, ON L9C 0E3 Canada
                [ ]Department of Psychiatry and Behavioural Neurosciences, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4K1 Canada
                [ ]Centre for Evaluation of Medicine, 25 Main Street West, Hamilton, ON L8P 1H1 Canada
                [ ]System Linked Research Unit, 175 Longwood Road, South Hamilton, L8P 0A1 Canada
                Article
                942
                10.1186/s13063-015-0942-4
                4618532
                26489415
                1d9fde94-3512-4cdb-b8de-4ec55de8d5b0
                © Dennis et al. 2015

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 12 March 2015
                : 3 September 2015
                Categories
                Research
                Custom metadata
                © The Author(s) 2015

                Medicine
                opioid addiction,opioid dependence,opioid use disorder,generalizability,comorbidity,psychiatric comorbidity,methodology,methadone maintenance treatment

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