Initiating buprenorphine to treat opioid use disorder without prerequisite withdrawal: an updated systematic review.

IF 3.7 2区 医学 Q1 SUBSTANCE ABUSE
Kathleen K Adams, Kristin Waters, Diana M Sobieraj
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引用次数: 0

Abstract

Background: Withdrawal prior to buprenorphine initiation may be intolerable or create barriers to therapy. We aim to update our previous systematic review on the efficacy and safety of buprenorphine initiation strategies that aim to omit prerequisite opioid withdrawal (POW).

Methods: We used the same search strategy for this update as in the original review with the modification of an additional term "low dose." We searched Embase and Scopus from April 11, 2020 to August 1, 2024 with searches in Google Scholar and www.

Clinicaltrials: gov . A study was included if it described patients with opioid use disorder or chronic pain that transitioned from a full mu-opioid agonist to buprenorphine without preceding withdrawal and reported withdrawal during initiation as an outcome. Two investigators independently screened citations and articles for inclusion, collected data using a standardized data collection tool, and assessed study risk of bias.

Results: Forty-four articles met our inclusion criteria; 31 were case reports/series reporting 84 cases and 13 were single-arm observational studies reporting a total of 576 cases. These studies were added to the literature from our original systematic review, totaling 59 studies and 682 patients. Sublingual buprenorphine was the most common initial formulation, comprising 55% (376/682) of cases. In case reports/series, use of a validated scale to measure withdrawal was uncommon; validated scales were only used in 36% of patients. All other patients had withdrawal assessed in a manner not utilizing a validated scale. Approximately half of these patients experienced any level of withdrawal (57/106 = 54%). The specific outcome of "any level of withdrawal" was not consistently reported in single-arm observational studies. Eight studies reported on any level of withdrawal, which occurred in 41% (177/428) of initiation attempts; some patients experienced more than one initiation attempt. Thirteen patients in case reports/series and 37 patients in the single-arm observational studies reported clinically significant withdrawal (50/682 = 7%). 81% (451/555) of patients transitioned to buprenorphine.

Conclusion: The prevalence of buprenorphine dosing strategies that aim to omit POW has vastly increased over the past 4 years. While quality of evidence remains low, the increased quantity of publications and integration into health-system guidelines and protocols demonstrates the need for prospective, controlled studies. It is unknown how selection bias impacts current findings, further highlighting the need for prospective, randomized, controlled trials evaluating these dosing strategies.

背景:丁丙诺啡起始治疗前的戒断可能令人难以忍受,或对治疗造成障碍。我们旨在更新之前关于丁丙诺啡起始策略疗效和安全性的系统综述,这些策略旨在省略阿片类药物戒断(POW)的前提条件:我们采用了与原始综述相同的检索策略,但增加了一个新词 "低剂量"。我们在 2020 年 4 月 11 日至 2024 年 8 月 1 日期间检索了 Embase 和 Scopus,并在 Google Scholar 和 www.Clinicaltrials: gov 中进行了检索。如果一项研究描述了阿片类药物使用障碍或慢性疼痛患者从全μ-阿片类激动剂过渡到丁丙诺啡而未出现戒断,并将起始治疗期间的戒断作为一项结果进行了报告,则该研究被纳入其中。两名研究人员独立筛选了引用文献和纳入文章,使用标准化数据收集工具收集数据,并评估了研究的偏倚风险:44篇文章符合我们的纳入标准;其中31篇为病例报告/系列研究,报告了84个病例,13篇为单臂观察研究,报告了共计576个病例。这些研究与我们最初的系统综述文献相加,共有 59 项研究和 682 名患者。舌下丁丙诺啡是最常见的初始制剂,占病例总数的 55%(376/682)。在病例报告/系列研究中,使用有效量表测量戒断情况的情况并不常见;仅有 36% 的患者使用了有效量表。所有其他患者的戒断评估方式均未使用验证量表。这些患者中约有一半出现过任何程度的戒断(57/106 = 54%)。在单臂观察研究中,"任何程度的戒断 "这一具体结果的报告并不一致。八项研究报告了任何程度的戒断,这发生在41%(177/428)的起始尝试中;一些患者经历了不止一次起始尝试。病例报告/系列研究中的 13 名患者和单臂观察研究中的 37 名患者报告了具有临床意义的戒断(50/682 = 7%)。81%(451/555)的患者过渡到使用丁丙诺啡:结论:在过去 4 年中,旨在避免 POW 的丁丙诺啡给药策略的普及率大幅提高。虽然证据的质量仍然较低,但出版物数量的增加以及纳入医疗系统指南和方案的情况表明,有必要开展前瞻性对照研究。目前尚不清楚选择偏倚如何影响目前的研究结果,这进一步凸显了对这些剂量策略进行前瞻性、随机对照试验评估的必要性。
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来源期刊
Addiction Science & Clinical Practice
Addiction Science & Clinical Practice Psychology-Clinical Psychology
CiteScore
3.90
自引率
10.80%
发文量
64
审稿时长
28 weeks
期刊介绍: Addiction Science & Clinical Practice provides a forum for clinically relevant research and perspectives that contribute to improving the quality of care for people with unhealthy alcohol, tobacco, or other drug use and addictive behaviours across a spectrum of clinical settings. Addiction Science & Clinical Practice accepts articles of clinical relevance related to the prevention and treatment of unhealthy alcohol, tobacco, and other drug use across the spectrum of clinical settings. Topics of interest address issues related to the following: the spectrum of unhealthy use of alcohol, tobacco, and other drugs among the range of affected persons (e.g., not limited by age, race/ethnicity, gender, or sexual orientation); the array of clinical prevention and treatment practices (from health messages, to identification and early intervention, to more extensive interventions including counseling and pharmacotherapy and other management strategies); and identification and management of medical, psychiatric, social, and other health consequences of substance use. Addiction Science & Clinical Practice is particularly interested in articles that address how to improve the quality of care for people with unhealthy substance use and related conditions as described in the (US) Institute of Medicine report, Improving the Quality of Healthcare for Mental Health and Substance Use Conditions (Washington, DC: National Academies Press, 2006). Such articles address the quality of care and of health services. Although the journal also welcomes submissions that address these conditions in addiction speciality-treatment settings, the journal is particularly interested in including articles that address unhealthy use outside these settings, including experience with novel models of care and outcomes, and outcomes of research-practice collaborations. Although Addiction Science & Clinical Practice is generally not an outlet for basic science research, we will accept basic science research manuscripts that have clearly described potential clinical relevance and are accessible to audiences outside a narrow laboratory research field.
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