Dexmedetomidine Prevents Chronic Incisional Pain After Brain Tumor Resection: A Secondary Analysis of the Randomized Control Trial

被引:2
|
作者
Zeng, Min [1 ]
Xu, Xin [2 ]
Li, Ruowen [3 ]
Zhang, Xingyue [1 ]
Ma, Tingting [1 ]
Cui, Qianyu [1 ]
Wang, Juan [1 ]
Li, Shu [1 ]
Peng, Yuming [1 ]
机构
[1] Capital Med Univ, Beijing Tiantan Hosp, Dept Anesthesiol, 119 Nansihuan Xilu, Beijing 100160, Peoples R China
[2] Dept Anesthesiol Natl Canc Ctr Natl Clin Res Ctr C, Canc Hosp, Dept Anesthesiol,Natl Canc Ctr,Natl Clin Res Ctr C, Beijing, Peoples R China
[3] China Japan Friendship Hosp, Dept Anesthesiol, Beijing, Peoples R China
来源
ANESTHESIA AND ANALGESIA | 2024年 / 138卷 / 04期
关键词
CHRONIC POSTSURGICAL PAIN; POSTOPERATIVE PAIN; CONSUMPTION; RECOVERY; SURGERY;
D O I
10.1213/ANE.0000000000006563
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BACKGROUND: Dexmedetomidine was reported to reduce postoperative acute pain after neurosurgery. However, the efficacy of dexmedetomidine for preventing chronic incisional pain is uncertain. METHODS: This article is a secondary analysis of a randomized, double-blind, placebo-controlled trial. Eligible patients were randomly allocated to either the dexmedetomidine group or the placebo group. Patients assigned to the dexmedetomidine group were given a 0.6 mu g kg(-1 )dexmedetomidine bolus followed by a 0.4 mu g kg(-1) h(-1) maintenance dose until dural closure; placebo patients were given comparable amounts of normal saline. The primary end point was the incidence of incisional pain at 3 months after craniotomy evaluated by numerical rating scale scores and defined as any score >0. The secondary end points were postoperative acute pain scores, sleep quality, and Short-Form McGill Pain Questionnaire (SF-MPQ-2) at 3 months after craniotomy. RESULTS: From January 2021 to December 2021, a total of 252 patients were included in the final analysis: the dexmedetomidine group (n = 128) and the placebo group (n = 124). The incidence of chronic incisional pain was 23.4% (30 of 128) in the dexmedetomidine group versus 42.7% (53 of 124) in the placebo group (risk ratio, 0.55; 95% confidence interval, 0.38-0.80; P = .001). The overall severity of chronic incisional pain was mild in both groups. Patients in the dexmedetomidine group had lower acute pain severity on movement than those in the placebo group for the first 3 days after surgery (all adjusted P < .01). Sleep quality did not differ between groups. However, the SF-MPQ-2 total sensory (P = .01) and neuropathic pain descriptor (P = .023) scores in the dexmedetomidine group were lower than those in the placebo group. CONCLUSIONS: Prophylactic intraoperative dexmedetomidine infusion reduces the incidence of chronic incisional pain as well as acute pain score after elective brain tumor resections.
引用
收藏
页码:839 / 847
页数:9
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