Park Ju Nyeong, Serafinski Rachel, Ujeneza Merci, McKenzie Michelle, Tardif Jessica, Krotulski Alex J, Badea Adina, Grossman Elyse R, Green Traci C
Rhode Island Hospital, Providence, RI, United States.
Warren Alpert Medical School, Brown University, Providence, RI, United States.
Drug Alcohol Depend Rep. 2024 Jun 5;11:100247. doi: 10.1016/j.dadr.2024.100247. eCollection 2024 Jun.
Xylazine is an ⍺2 adrenergic receptor agonist and a veterinary sedative that can cause severe health complications yet interventions to detect and treat human exposure remain underdeveloped. Community-based drug checking services (DCS) involve the testing of small amounts of drugs to increase community knowledge of unregulated supplies and decrease harms. This study characterized xylazine awareness, desire, use and exposure among people who use drugs (PWUD) in Rhode Island, US.
We analyzed data from an ongoing PWUD cohort study. In 2023, 125 PWUD were enrolled and surveyed. Using point-of-care Fourier Transform infrared spectroscopy (FTIR-S), we tested a drug sample from each participant onsite and confirmed the results offsite at a laboratory. Results were conveyed in real-time, along with harm reduction education, referrals to resources and care.
Virtually all participants (99.2 %) wanted to avoid xylazine exposure. Half (51.2 %) knew what xylazine was, and a quarter (26.1 %) suspected previous exposure. Xylazine exposure was primarily surmised through sedating (45.2 %) and ulcerative (29.0 %) effects. Only 8.8 % of participants submitted a sample that they expected to contain xylazine. Xylazine was detected in 14.5 % of samples using FTIR-S and in 21.4 % of samples using a dual laboratory approach of gas chromatography mass spectrometry (GC-MS) and liquid chromatography quadrupole-time-of-flight mass spectrometry (LC-QTOF-MS). Participants thought that these xylazine-positive samples were fentanyl (78.3 %), heroin (13.0 %), or Percocet® (8.7 %).
Implementing point-of-care DCS at harm reduction organizations could be useful in rapidly increasing xylazine awareness and engaging at-risk individuals in prevention, harm reduction, treatment, and rapid care for xylazine-related wounds.
赛拉嗪是一种α2肾上腺素能受体激动剂和兽用镇静剂,可导致严重的健康并发症,但用于检测和治疗人类接触赛拉嗪的干预措施仍不完善。基于社区的药物检测服务(DCS)涉及对少量药物进行检测,以增加社区对不受监管药物供应的了解并减少危害。本研究描述了美国罗德岛州吸毒者(PWUD)对赛拉嗪的知晓情况、使用意愿、使用情况及接触情况。
我们分析了一项正在进行的PWUD队列研究的数据。2023年,招募了125名PWUD并进行了调查。使用即时护理傅里叶变换红外光谱法(FTIR-S),我们在现场对每位参与者的一份药物样本进行了检测,并在实验室进行了非现场结果确认。结果与减少危害教育、资源和护理转介一起实时传达。
几乎所有参与者(99.2%)都希望避免接触赛拉嗪。一半(51.2%)的人知道赛拉嗪是什么,四分之一(26.1%)的人怀疑之前接触过赛拉嗪。赛拉嗪接触主要是通过镇静作用(45.2%)和溃疡性作用(29.0%)推测出来的。只有8.8%的参与者提交了他们预期含有赛拉嗪的样本。使用FTIR-S在14.5%的样本中检测到了赛拉嗪,使用气相色谱-质谱联用(GC-MS)和液相色谱-四极杆飞行时间质谱联用(LC-QTOF-MS)的双重实验室方法在21.4%的样本中检测到了赛拉嗪。参与者认为这些赛拉嗪阳性样本是芬太尼(78.3%)、海洛因(13.0%)或羟考酮(8.7%)。
在减少危害组织中实施即时护理DCS可能有助于迅速提高对赛拉嗪的认识,并使高危个体参与到赛拉嗪相关伤口的预防、减少危害、治疗和快速护理中。