School of Social Dimensions of Health, University of Victoria, 3800 Finnerty Road, Victoria, BC, V8P 5C2, Canada.
Canadian Institute for Substance Use Research, 2300 McKenzie Ave, Victoria, BC, V8P 5C2, Canada.
Syst Rev. 2019 Jun 11;8(1):138. doi: 10.1186/s13643-019-1048-y.
North America is in the midst of an unabated opioid overdose epidemic due to the increasing non-medical use of fentanyl and ultra-potent opioids. Naloxone is an effective antidote to opioid toxicity, yet its optimal dosing in the context of fentanyl and ultra-potent opioid overdoses remains unknown. This review aims to determine the relationship between the first empiric dose of naloxone and reversal of toxicity, adverse events, and the total cumulative dose required among patients with undifferentiated opioid overdoses and those with suspected toxicity from ultra-potent opioids. Secondary objectives include evaluating the relationship between the cumulative naloxone dose and toxicity reversal and adverse events, among patients with undifferentiated opioid overdoses and those with suspected toxicity from ultra-potent opioids.
To identify studies, we will search MEDLINE, Embase, CENTRAL, DARE, CDAG, CINAHL, Science Citation Index, multiple trial registries, and the gray literature. Included studies will evaluate patients with suspected or confirmed opioid toxicity from undifferentiated opioids and ultra-potent opioids, who received an empiric and possibly additional doses of naloxone. The main outcomes of interest are the relationship between naloxone dose and toxicity reversal and adverse events. We will include controlled and non-controlled interventional studies, observational studies, case reports/series, and reports from poison control centers. We will extract data and assess study quality in duplicate with discrepancies resolved by consensus or a third party. We will use the Downs and Black and Cochrane risk of bias tools for observational and randomized controlled studies. If we find sufficient variation in dose, we will fit a random effects one-stage model to estimate a dose-response relationship. We will conduct multiple subgroup analyses, including by type of opioid used and by suspected high and low prevalence of ultra-potent opioid use based on geographic location and time of the original studies.
Our review will include the most up-to-date available data including ultra-potent opioids to inform the current response to the opioid epidemic, addressing the limitations of recent reviews. We anticipate limitations relating to study heterogeneity. We will disseminate study results widely to update overdose treatment guidelines and naloxone dosing in Take Home Naloxone programs.
由于芬太尼和超强效阿片类药物的非医疗使用不断增加,北美的阿片类药物过量流行仍在加剧。纳洛酮是阿片类药物毒性的有效解毒剂,但在芬太尼和超强效阿片类药物过量的情况下,其最佳剂量仍不清楚。本综述旨在确定未分化阿片类药物过量患者和疑似超强效阿片类药物毒性患者中,纳洛酮首次经验剂量与毒性逆转、不良事件和所需总累积剂量之间的关系。次要目标包括评估未分化阿片类药物过量患者和疑似超强效阿片类药物毒性患者中,纳洛酮累积剂量与毒性逆转和不良事件之间的关系。
为了确定研究,我们将搜索 MEDLINE、Embase、CENTRAL、DARE、CDAG、CINAHL、科学引文索引、多个试验登记处和灰色文献。纳入的研究将评估疑似或确诊的未分化阿片类药物和超强效阿片类药物毒性的患者,他们接受了经验性和可能的额外纳洛酮剂量。主要观察指标是纳洛酮剂量与毒性逆转和不良事件之间的关系。我们将纳入对照和非对照干预性研究、观察性研究、病例报告/系列和毒物控制中心的报告。我们将重复提取数据并评估研究质量,如果存在分歧,将通过共识或第三方解决。我们将使用唐斯和布莱克和 Cochrane 偏倚风险工具对观察性和随机对照研究进行评估。如果我们发现剂量存在足够的差异,我们将使用随机效应一阶段模型来估计剂量反应关系。我们将进行多个亚组分析,包括根据所使用的阿片类药物类型以及根据地理位置和原始研究的时间,疑似超强效阿片类药物使用的高和低流行率进行分析。
我们的综述将包括最新的可用数据,包括超强效阿片类药物,以告知当前对阿片类药物流行的反应,解决最近综述的局限性。我们预计会存在研究异质性的局限性。我们将广泛传播研究结果,以更新过量治疗指南和家庭携带纳洛酮计划中的纳洛酮剂量。