Department of Anesthesia, Stanford University School of Medicine, 300 Pasteur Drive, Grant Building Room S268C, Stanford, CA, 94305, United States.
Department of Anesthesia, Stanford University School of Medicine, 300 Pasteur Drive, Grant Building Room S268C, Stanford, CA, 94305, United States.
Drug Alcohol Depend. 2018 Feb 1;183:176-183. doi: 10.1016/j.drugalcdep.2017.06.043. Epub 2017 Aug 14.
In this study, we investigated the co-administration of ondansetron with morphine, and whether it could prevent the development of physical dependence in patients taking opioids for the treatment of chronic pain.
A total of 48 chronic back pain patients (N = 48) participated in this double-blinded, placebo-controlled, randomized study. Patients were titrated onto sustained-release oral morphine and randomized to take 8 mg ondansetron or placebo three times daily concurrently with morphine during the 30-day titration. Following titration, patients underwent Naloxone induced opioid withdrawal. Opioid withdrawal signs and symptoms were then assessed by a blinded research assistant (objective opioid withdrawal score: OOWS) and by the research participant (subjective opioid withdrawal score: SOWS).
We observed clinically significant signs of naloxone-precipitated opioid withdrawal in all participants (ΔOOWS = 4.3 ± 2.4, p < 0.0001; ΔSOWS = 14.1 ± 11.7, p < 0.0001), however no significant differences in withdrawal scores were detected between treatment groups.
We hypothesized that ondansetron would prevent the development of physical dependence in human subjects when co-administered with opioids, but found no difference in naloxone-precipitated opioid withdrawal scores between ondansetron and placebo treatment groups. These results suggest that further studies are needed to determine if 5HT receptor antagonists are useful in preventing opioid physical dependence.
本研究旨在探讨昂丹司琼与吗啡联合应用能否预防接受阿片类药物治疗慢性疼痛的患者产生躯体依赖性。
共有 48 例慢性背痛患者(N=48)参与了这项双盲、安慰剂对照、随机研究。患者接受缓释口服吗啡滴定,并随机分为三组,在 30 天滴定期间同时每日服用 8mg 昂丹司琼或安慰剂 3 次。滴定后,患者接受纳洛酮诱导的阿片类药物戒断。然后由盲法研究助理(客观阿片类戒断评分:OOWS)和研究参与者(主观阿片类戒断评分:SOWS)评估阿片类药物戒断症状和体征。
我们观察到所有参与者均出现明显的纳洛酮诱发的阿片类药物戒断迹象(ΔOOWS=4.3±2.4,p<0.0001;ΔSOWS=14.1±11.7,p<0.0001),但治疗组之间戒断评分无显著差异。
我们假设昂丹司琼与阿片类药物联合应用时可预防人体产生躯体依赖性,但在昂丹司琼和安慰剂治疗组之间,纳洛酮诱发的阿片类药物戒断评分无差异。这些结果表明,需要进一步研究以确定 5-HT 受体拮抗剂是否有助于预防阿片类药物的躯体依赖性。