Postoperative Dexmedetomidine Infusion and Chronic Postsurgical Pain in Thoracoscopic Pulmonary Nodule Surgery: A Retrospective Study with Propensity-Score-Matched Analysis.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY Pain and Therapy Pub Date : 2024-08-01 Epub Date: 2024-05-28 DOI:10.1007/s40122-024-00611-8
Hang Sun, Yiwei Zhong, Min Wang, Shujie Niu, Rusong Yang, Yali Tian, Bingbing Li
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Abstract

Introduction: Patients frequently suffer from debilitating chronic postsurgical pain (CPSP) subsequent to thoracoscopic surgery. The impact of postoperative dexmedetomidine infusion on CPSP remains elusive. This study aimed to scrutinize the effect of dexmedetomidine on both 1-year incidence of CPSP and the quality of recovery after thoracoscopic pulmonary nodule surgery.

Methods: This retrospective analysis encompassed clinical and follow-up data from 1148 patients undergoing thoracoscopic pulmonary nodule surgery at our institution between September 2021 and August 2022. Depending on whether dexmedetomidine was infused intravenously or not on the first night after surgery, patients were stratified into the dexmedetomidine group or the control group, with propensity score matching applied to harmonize baseline characteristics. Comparative analysis sought to delineate distinctions of CPSP and recovery quality 1 year after surgery.

Results: Following propensity score matching, a cohort of 258 patients in each group underwent analysis. Comparisons after matching revealed no statistically significant disparities in 1-year CPSP incidence [76/258 (29.5%) versus 78/258 (30.2%), P = 0.847], moderate-to-severe pain occurrence [17/76 (22.4%) versus 22/78 (28.2%), P = 0.405], neuropathic pain occurrence [11/76 (14.5%) versus 11/78 (14.1%), P = 0.948], and postoperative recovery quality assessed by 12-Item Short Form Health Survey (SF-12) score (113.1 [107.2, 116.0] versus 113.0 [107.4, 116.0], P = 0.328). Multivariate logistic regression analysis encompassing the entire cohort identified being female [odds ratio (OR) 2.10, 95% confidence interval (CI) 1.59-2.79, P < 0.001) and postoperative rescue analgesia (OR 1.47, 95% CI 1.09-1.96, P = 0.010) as risk factors for CPSP, while intraoperative fentanyl dosage (OR 0.92, 95% CI 0.87-0.98, P = 0.006) emerged as a protective factor.

Conclusion: The prolonged administration of dexmedetomidine did not yield discernible amelioration in either 1-year CPSP or the recovery quality after thoracoscopic surgery. Noteworthy risk factors for CPSP encompassed female sex, postoperative rescue analgesia, and diminished fentanyl dosage intraoperatively.

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胸腔镜肺结节手术术后右美托咪定输注与术后慢性疼痛:倾向分数匹配分析的回顾性研究
导言:胸腔镜手术后,患者经常会出现令人衰弱的慢性术后疼痛(CPSP)。术后右美托咪定输注对 CPSP 的影响仍不明确。本研究旨在探讨右美托咪定对胸腔镜肺结节手术后1年CPSP发生率和恢复质量的影响:这项回顾性分析涵盖了2021年9月至2022年8月期间在我院接受胸腔镜肺结节手术的1148名患者的临床和随访数据。根据术后第一晚是否静脉输注右美托咪定,将患者分为右美托咪定组或对照组,并采用倾向评分匹配法统一基线特征。对比分析旨在明确术后一年 CPSP 和恢复质量的区别:经过倾向评分匹配后,对每组 258 名患者进行了分析。匹配后的比较显示,1 年 CPSP 发生率[76/258(29.5%)对 78/258(30.2%),P = 0.847]、中度至重度疼痛发生率[17/76(22.4%)对 22/78(28.2%),P = 0.405]、神经病理性疼痛发生率[11/76(14.5%)对 11/78(14.1%),P = 0.948],以及术后恢复质量评估(12 项简表健康调查 (SF-12) 评分)(113.1 [107.2, 116.0] 对 113.0 [107.4, 116.0],P = 0.328)。在对整个队列进行多变量逻辑回归分析后发现,女性患者的几率比(OR)为 2.10,95% 置信区间(CI)为 1.59-2.79,P 结论:女性患者的几率比男性患者低:长时间使用右美托咪定并未明显改善胸腔镜手术后1年的CPSP或恢复质量。值得注意的CPSP风险因素包括女性性别、术后抢救镇痛和术中减少芬太尼用量。
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来源期刊
Pain and Therapy
Pain and Therapy CLINICAL NEUROLOGY-
CiteScore
6.60
自引率
5.00%
发文量
110
审稿时长
6 weeks
期刊介绍: Pain and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of pain therapies and pain-related devices. Studies relating to diagnosis, pharmacoeconomics, public health, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, acute pain, cancer pain, chronic pain, headache and migraine, neuropathic pain, opioids, palliative care and pain ethics, peri- and post-operative pain as well as rheumatic pain and fibromyalgia. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports, trial protocols, short communications such as commentaries and editorials, and letters. The journal is read by a global audience and receives submissions from around the world. Pain and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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