Elyn Antoine, Roussin Anne, Lestrade Cécile, Franchitto Nicolas, Jullian Bénédicte, Cantagrel Nathalie
Chronic Pain Center, University Hospital of Toulouse, Toulouse, France
General and Family Medicine University Department, University of Toulouse III - Paul Sabatier, Toulouse, France.
Reg Anesth Pain Med. 2025 May 6;50(5):421-428. doi: 10.1136/rapm-2023-105035.
Long-term opioid use is associated with pharmacological tolerance, a risk of misuse and hyperalgesia in patients with chronic pain (CP). Tapering is challenging in this context, particularly with comorbid opioid-use disorder (OUD). The antihyperalgesic effect of ketamine, through N-methyl-D-aspartate (NMDA) antagonism, could be useful. We aimed to describe the changes in the dose of opioids consumed over 1 year after a 5-day hospitalisation with ketamine infusion for CP patients with OUD.
We performed a historical cohort study using a medical chart from 1 January 2014 to 31 December 2019. Patients were long-term opioid users with OUD and CP, followed by the Pain Center of the University Hospital of Toulouse, for which outpatient progressive tapering failed. Ketamine was administered at a low dose to initiate tapering during a 5-day hospitalisation.
59 patients were included, with 64% of them female and a mean age of 48±10 years old. The most frequent CP aetiologies were back pain (53%) and fibromyalgia (17%). The baseline opioid daily dose was 207 mg (±128) morphine milligram equivalent (MME). It was lowered to 92±72 mg MME at discharge (p<0.001), 99±77 mg at 3 months (p<0.001) and 103±106 mg at 12 months. More than 50% tapering was achieved immediately for 40 patients (68%), with immediate cessation for seven patients (12%). 17 patients were lost to follow-up.
A 5-day hospitalisation with a low-dose ketamine infusion appeared useful to facilitate opioid tapering in long-term opioid users with CP and OUD. Ketamine was well tolerated, and patients did not present significant withdrawal symptoms. Prospective and comparative studies are needed to confirm our findings.
长期使用阿片类药物与药物耐受性、慢性疼痛(CP)患者的滥用风险和痛觉过敏有关。在这种情况下,逐渐减少阿片类药物用量具有挑战性,尤其是对于合并阿片类药物使用障碍(OUD)的患者。氯胺酮通过拮抗N-甲基-D-天冬氨酸(NMDA)产生的抗痛觉过敏作用可能会有所帮助。我们旨在描述因OUD而患有CP的患者在接受为期5天的氯胺酮输注住院治疗后1年内阿片类药物消耗量的变化。
我们使用了2014年1月1日至2019年12月31日的病历进行了一项历史性队列研究。患者为长期使用阿片类药物且患有OUD和CP的患者,由图卢兹大学医院疼痛中心随访,其门诊逐渐减少阿片类药物用量失败。在为期5天的住院期间,给予低剂量氯胺酮以开始逐渐减少阿片类药物用量。
纳入59例患者,其中64%为女性,平均年龄为48±10岁。最常见的CP病因是背痛(53%)和纤维肌痛(17%)。基线阿片类药物每日剂量为207毫克(±128)吗啡毫克当量(MME)。出院时降至92±72毫克MME(p<0.001),3个月时为99±77毫克(p<0.001),12个月时为103±106毫克。40例患者(68%)立即实现了超过50%的减量,7例患者(12%)立即停药。17例患者失访。
为期5天的低剂量氯胺酮输注住院治疗似乎有助于长期使用阿片类药物且患有CP和OUD的患者逐渐减少阿片类药物用量。氯胺酮耐受性良好,患者未出现明显的戒断症状。需要进行前瞻性和比较性研究来证实我们的发现。