Pioneer Family Practice, 5130 Corporate Ctr Ct SE, Lacey, Washington, 98503, USA.
Department of Family Medicine, University of Washington School of Medicine, 1959 N.E. Pacific St., Box 356390, Seattle, WA, 98195-6390, USA.
Addict Sci Clin Pract. 2024 Aug 29;19(1):60. doi: 10.1186/s13722-024-00494-2.
Many people with opioid use disorder who stand to benefit from buprenorphine treatment are unwilling to initiate it due to experience with or fear of both spontaneous and buprenorphine-precipitated opioid withdrawal (BPOW). An effective means of minimizing withdrawal symptoms would reduce patient apprehensiveness, lowering the barrier to buprenorphine initiation. Ketamine, approved by the FDA as a dissociative anesthetic, completely resolved BPOW in case reports when infused at a sub-anesthetic dose range in which dissociative symptoms are common. However, most patients attempt buprenorphine initiation in the outpatient setting where altered mental status is undesirable. We explored the potential of short-term use of ketamine, self-administered sublingually at a lower, sub-dissociative dose to assist ambulatory patients undergoing transition to buprenorphine from fentanyl and methadone.
Patients prescribed ketamine were either (1) seeking transition to buprenorphine from illicit fentanyl and highly apprehensive of BPOW or (2) undergoing transition to buprenorphine from illicit fentanyl or methadone and experiencing BPOW. We prescribed 4-8 doses of sublingual ketamine 16 mg (each dose bioequivalent to 3-6% of an anesthetic dose), monitored patients daily or near-daily, and adjusted buprenorphine and ketamine dosing based on patient response and prescriber experience.
Over a period of 14 months, 37 patients were prescribed ketamine. Buprenorphine initiation was completed by 16 patients, representing 43% of the 37 patients prescribed ketamine, and 67% of the 24 who reported trying it. Of the last 12 patients who completed buprenorphine initiation, 11 (92%) achieved 30-day retention in treatment. Most of the patients who tried ketamine reported reduction or elimination of spontaneous opioid withdrawal symptoms. Some patients reported avoidance of severe BPOW when used prophylactically or as treatment of established BPOW. We developed a ketamine protocol that allowed four of the last patients to complete buprenorphine initiation over four days reporting only mild withdrawal symptoms. Two patients described cognitive changes from ketamine at a dose that exceeded the effective dose range for the other patients.
Ketamine at a sub-dissociative dose allowed completion of buprenorphine initiation in the outpatient setting in the majority of patients who reported trying it. Further research is warranted to confirm these results and develop reliable protocols for a range of treatment settings.
许多患有阿片类药物使用障碍的人,如果能从丁丙诺啡治疗中获益,他们不愿意开始治疗,因为他们经历过或担心自发和丁丙诺啡诱发的阿片类药物戒断(BPOW)。一种有效的减轻戒断症状的方法可以降低患者的担忧,降低开始丁丙诺啡治疗的障碍。氯胺酮已被 FDA 批准为一种分离麻醉剂,当以亚麻醉剂量范围输注时,可完全解决案例报告中的 BPOW,在此剂量范围内会出现分离症状。然而,大多数患者试图在门诊环境中开始使用丁丙诺啡,因为在这种环境下,精神状态改变是不理想的。我们探讨了短期使用氯胺酮的可能性,患者自行将其舌下含服至较低的亚分离剂量,以帮助从芬太尼和美沙酮过渡到丁丙诺啡的门诊患者。
接受氯胺酮治疗的患者要么(1)寻求从非法芬太尼过渡到丁丙诺啡,并且对 BPOW 非常担心,要么(2)从非法芬太尼或美沙酮过渡到丁丙诺啡,并经历 BPOW。我们为患者开了 4-8 剂舌下氯胺酮 16 毫克(每剂剂量与 3-6%的麻醉剂量相当),每天或几乎每天监测患者,并根据患者的反应和医生的经验调整丁丙诺啡和氯胺酮的剂量。
在 14 个月的时间里,有 37 名患者接受了氯胺酮治疗。16 名患者完成了丁丙诺啡的启动,占接受氯胺酮治疗的 37 名患者的 43%,占报告尝试该药物的 24 名患者的 67%。在最后 12 名完成丁丙诺啡启动的患者中,有 11 名(92%)在治疗中保持了 30 天的保留率。大多数尝试过氯胺酮的患者报告说,自发的阿片类药物戒断症状减轻或消除。一些患者报告说,预防性使用氯胺酮或治疗已确立的 BPOW 可以避免严重的 BPOW。我们制定了氯胺酮方案,允许最后 4 名患者在 4 天内完成丁丙诺啡的启动,仅报告轻度戒断症状。有 2 名患者在使用超过其他患者有效剂量范围的剂量时描述了认知变化。
亚分离剂量的氯胺酮允许大多数报告尝试过该药物的患者在门诊环境中完成丁丙诺啡的启动。需要进一步研究来证实这些结果,并为各种治疗环境制定可靠的方案。