Georgia Poison Center, 50 Hurt Plaza SE, Suite 600, Atlanta, GA, 30303, USA.
Department of Emergency Medicine, Emory University School of Medicine, Atlanta, GA, USA.
J Med Toxicol. 2020 Jan;16(1):41-48. doi: 10.1007/s13181-019-00735-w. Epub 2019 Aug 30.
Illicitly manufactured fentanyl (IMF) is responsible for a growing number of deaths. Some case series have suggested that IMF overdoses require significantly higher naloxone doses than heroin overdoses. Our objective was to determine if the naloxone dose required to treat an opioid overdose is associated with the finding of fentanyl, opiates, or both on urine drug screen (UDS).
A retrospective chart review was conducted at a single emergency department and its affiliated emergency medical services (EMS) agency. The charts of all patients who received naloxone through this EMS from 1/1/2017 to 6/15/2018 were reviewed. The study included patients diagnosed with a non-suicidal opioid overdose whose UDS was positive for opiates, fentanyl, or both. Data collected included demographics, vital signs, initial GCS, EMS and ED naloxone administrations, response to treatment, laboratory findings, and ED disposition. The fentanyl-only and fentanyl + opiate groups were compared to the opiate-only group using the stratified (by ED provider) variant of the Mann-Whitney U test.
Eight hundred and thirty-seven charts were reviewed, and 121 subjects were included in the final analysis. The median age of included subjects was 38 years and 75% were male. In the naloxone dose analysis, neither the fentanyl-only (median 0.8 mg, IQR 0.4-1.6; p = 0.68) nor the fentanyl + opiate (median 0.8 mg, IQR 0.4-1.2; p = 0.56) groups differed from the opiate-only group (median 0.58 mg, IQR 0.4-1.6).
Our findings refute the notion that high potency synthetic opioids like illicitly manufactured fentanyl require increased doses of naloxone to successfully treat an overdose. There were no significant differences in the dose of naloxone required to treat opioid overdose patients with UDS evidence of exposure to fentanyl, opiates, or both. Further evaluation of naloxone stocking and dosing protocols is needed.
非法制造的芬太尼(IMF)导致的死亡人数不断增加。一些病例系列表明,IMF 过量需要明显高于海洛因过量的纳洛酮剂量。我们的目的是确定治疗阿片类药物过量所需的纳洛酮剂量是否与尿液药物筛查(UDS)中芬太尼、阿片类药物或两者的检测结果相关。
在一个急诊部及其附属的紧急医疗服务(EMS)机构进行了回顾性图表审查。对 2017 年 1 月 1 日至 2018 年 6 月 15 日期间通过该 EMS 接受纳洛酮治疗的所有患者的图表进行了审查。研究纳入了诊断为非自杀性阿片类药物过量且 UDS 检测结果为阿片类药物、芬太尼或两者均阳性的患者。收集的数据包括人口统计学、生命体征、初始 GCS、EMS 和 ED 纳洛酮给药、治疗反应、实验室检查结果和 ED 处置。使用分层(按 ED 提供者)曼-惠特尼 U 检验对芬太尼仅组和芬太尼+阿片类药物组与阿片类药物仅组进行比较。
共审查了 837 份图表,最终有 121 名患者纳入最终分析。纳入患者的中位年龄为 38 岁,75%为男性。在纳洛酮剂量分析中,芬太尼仅组(中位数 0.8mg,IQR 0.4-1.6;p=0.68)和芬太尼+阿片类药物组(中位数 0.8mg,IQR 0.4-1.2;p=0.56)与阿片类药物仅组(中位数 0.58mg,IQR 0.4-1.6)均无差异。
我们的研究结果反驳了这样一种观点,即非法制造的芬太尼等高纯度合成阿片类药物需要增加纳洛酮剂量才能成功治疗过量。UDS 检测结果显示芬太尼、阿片类药物或两者均暴露的阿片类药物过量患者所需的纳洛酮剂量无显著差异。需要进一步评估纳洛酮储备和剂量方案。