Elmati Praveen Reddy, Waseem Hira, Kogilathota Jagirdhar Gowthami Sai, Stewart Christhopher M, Bautista Alexander
Anesthesiology, Saint Clare's Health, Denville, USA.
Psychiatry, University of Louisville School of Medicine, Louisville, USA.
Cureus. 2024 Aug 28;16(8):e68007. doi: 10.7759/cureus.68007. eCollection 2024 Aug.
Opioid use disorder (OUD) remains a significant public health challenge with patients often facing barriers to initiating medications for opioid use disorder (MOUD). Traditional initiation methods for buprenorphine-naloxone (buprenorphine/naloxone) can be challenging due to the longer duration of transition and the risk of precipitated withdrawal. This manuscript presents a case series of four patients who successfully transitioned to buprenorphine/naloxone maintenance using a novel approach: low-dose intravenous (IV) buprenorphine initiation. These cases presented in the manuscript involved patients with dual diagnoses of OUD and difficult-to-treat pain. Intravenous buprenorphine was administered at a dose of 0.3 mg every half-hour, with a maximum of four doses. Patients' withdrawal symptoms were monitored using the Clinical Opioid Withdrawal Scale (COWS). Comfort medications were provided as needed. All four patients were successfully transitioned to sublingual (SL) buprenorphine/naloxone without experiencing precipitated withdrawal. Patients were discharged with follow-up appointments at buprenorphine/naloxone clinics and bridge supplies of buprenorphine/naloxone. Low-dose IV buprenorphine initiation offers a rapid and effective method for transitioning patients from full-agonist opioids (FAOs) to buprenorphine/naloxone without precipitated withdrawal. This approach has the potential to increase treatment retention and patient satisfaction. This case series highlights the success of low-dose IV buprenorphine initiation in patients with OUD and chronic pain. Further research is needed to standardize this approach and assess long-term outcomes. Initiating MOUD with this method may improve patient care and reduce the burden on the healthcare system.
阿片类物质使用障碍(OUD)仍然是一项重大的公共卫生挑战,患者在启动阿片类物质使用障碍药物治疗(MOUD)时常常面临障碍。由于转换期较长以及发生戒断反应的风险,丁丙诺啡-纳洛酮(丁丙诺啡/纳洛酮)的传统启动方法可能具有挑战性。本文介绍了一个包含四名患者的病例系列,他们采用一种新方法成功过渡到丁丙诺啡/纳洛酮维持治疗:低剂量静脉注射(IV)丁丙诺啡启动。本文呈现的这些病例涉及同时患有OUD和难以治疗的疼痛的患者。静脉注射丁丙诺啡的剂量为每半小时0.3毫克,最大剂量为四剂。使用临床阿片类物质戒断量表(COWS)监测患者的戒断症状。根据需要提供舒适药物。所有四名患者均成功过渡到舌下(SL)丁丙诺啡/纳洛酮,未出现戒断反应。患者出院时安排了在丁丙诺啡/纳洛酮诊所的随访预约以及丁丙诺啡/纳洛酮的过渡供应。低剂量静脉注射丁丙诺啡启动为患者从完全激动剂阿片类药物(FAO)过渡到丁丙诺啡/纳洛酮提供了一种快速有效的方法,且不会引发戒断反应。这种方法有可能提高治疗依从性和患者满意度。这个病例系列突出了低剂量静脉注射丁丙诺啡启动在患有OUD和慢性疼痛患者中的成功。需要进一步研究来规范这种方法并评估长期结果。用这种方法启动MOUD可能会改善患者护理并减轻医疗系统的负担。