O'Donnell Julie K, Halpin John, Mattson Christine L, Goldberger Bruce A, Gladden R Matthew
MMWR Morb Mortal Wkly Rep. 2017 Nov 3;66(43):1197-1202. doi: 10.15585/mmwr.mm6643e1.
Preliminary estimates of U.S. drug overdose deaths exceeded 60,000 in 2016 and were partially driven by a fivefold increase in overdose deaths involving synthetic opioids (excluding methadone), from 3,105 in 2013 to approximately 20,000 in 2016 (1,2). Illicitly manufactured fentanyl, a synthetic opioid 50-100 times more potent than morphine, is primarily responsible for this rapid increase (3,4). In addition, fentanyl analogs such as acetylfentanyl, furanylfentanyl, and carfentanil are being detected increasingly in overdose deaths (5,6) and the illicit opioid drug supply (7). Carfentanil is estimated to be 10,000 times more potent than morphine (8). Estimates of the potency of acetylfentanyl and furanylfentanyl vary but suggest that they are less potent than fentanyl (9). Estimates of relative potency have some uncertainty because illicit fentanyl analog potency has not been evaluated in humans. This report describes opioid overdose deaths during July-December 2016 that tested positive for fentanyl, fentanyl analogs, or U-47700, an illicit synthetic opioid, in 10 states participating in CDC's Enhanced State Opioid Overdose Surveillance (ESOOS) program.* Fentanyl analogs are similar in chemical structure to fentanyl but not routinely detected because specialized toxicology testing is required. Fentanyl was detected in at least half of opioid overdose deaths in seven of 10 states, and 57% of fentanyl-involved deaths also tested positive for other illicit drugs, such as heroin. Fentanyl analogs were present in >10% of opioid overdose deaths in four states, with carfentanil, furanylfentanyl, and acetylfentanyl identified most frequently. Expanded surveillance for opioid overdoses, including testing for fentanyl and fentanyl analogs, assists in tracking the rapidly changing illicit opioid market and informing innovative interventions designed to reduce opioid overdose deaths.
2016年美国药物过量致死的初步估计数超过6万例,部分原因是涉及合成阿片类药物(不包括美沙酮)的过量致死人数增长了五倍,从2013年的3105例增至2016年的约2万例(1,2)。非法制造的芬太尼是一种比吗啡效力强50至100倍的合成阿片类药物,主要导致了这一快速增长(3,4)。此外,在过量致死案例(5,6)以及非法阿片类药物供应(7)中,越来越多地检测到乙酰芬太尼、呋喃芬太尼和卡芬太尼等芬太尼类似物。据估计,卡芬太尼的效力比吗啡强1万倍(8)。乙酰芬太尼和呋喃芬太尼效力的估计值有所不同,但表明它们的效力比芬太尼弱(9)。由于尚未在人体中评估非法芬太尼类似物的效力,相对效力的估计存在一定不确定性。本报告描述了2016年7月至12月期间,参与美国疾病控制与预防中心强化州阿片类药物过量监测(ESOOS)项目的10个州中,对芬太尼、芬太尼类似物或U-47700(一种非法合成阿片类药物)检测呈阳性的阿片类药物过量致死案例。*芬太尼类似物的化学结构与芬太尼相似,但由于需要专门的毒理学检测,通常不会被检测到。在10个州中的7个州,至少一半的阿片类药物过量致死案例中检测到了芬太尼,在涉及芬太尼的死亡案例中,57%同时对其他非法药物(如海洛因)检测呈阳性。在4个州,超过10%的阿片类药物过量致死案例中存在芬太尼类似物,其中卡芬太尼、呋喃芬太尼和乙酰芬太尼最为常见。扩大对阿片类药物过量的监测,包括检测芬太尼和芬太尼类似物,有助于追踪迅速变化的非法阿片类药物市场,并为旨在减少阿片类药物过量致死的创新干预措施提供信息。