A Randomized Clinical Trial of Dexmedetomidine on Delirium, Cognitive Dysfunction, and Sleep After Non-Ambulatory Orthopedic Surgery With Regional Anesthesia.
{"title":"A Randomized Clinical Trial of Dexmedetomidine on Delirium, Cognitive Dysfunction, and Sleep After Non-Ambulatory Orthopedic Surgery With Regional Anesthesia.","authors":"Vlasios Karageorgos,Panagiota Darivianaki,Anastasia Spartinou,Maria Christofaki,Aikaterini Chatzimichali,Vasileia Nyktari,Panagiotis Simos,Alexandra Papaioannou","doi":"10.1213/ane.0000000000007548","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nPostoperative delirium (POD), emergence delirium (ED), and postoperative cognitive dysfunction (POCD) are disorders of the neuropsychiatric spectrum affecting the elderly during the postoperative period, potentially sharing a common pathophysiological pathway. Disrupted sleep postoperatively correlates with both POD and POCD, revealing overlapping risk factors. This study investigates the potential of dexmedetomidine anesthesia to reduce the incidence of POD (primary outcome), ED, POCD, impairment of sleep quality, and emergent chronic pain (secondary outcomes) in older adults undergoing major orthopedic surgery under regional anesthesia.\r\n\r\nMETHODS\r\nIn this double-blind randomized control trial, patients scheduled for major lower limb orthopedic surgery under regional anesthesia were randomized to receive either dexmedetomidine or propofol for sedation at a 1:1 ratio. POD, ED, and POCD were assessed with the Confusion Assessment Method tool, the Riker Sedation-Agitation scale, and the European Battery of psychometric tests, respectively. Sleep quality was assessed using the Pittsburg Sleep Quality Index and chronic pain with the painDETECT tool. Assessments of all outcome variables were performed before surgery, and at 48 hours and 3 months postoperatively.\r\n\r\nRESULTS\r\nA total of 80 patients (dexmedetomidine group n = 41) were enrolled in the study and completed the follow-up. POD, ED, and early POCD incidence were significantly lower in dexmedetomidine compared to propofol group (4.8% vs 38.4%, P = .001; 2.4% vs 38.4%, P < .001; 2.4% vs 56.4%, P < .001, respectively). Patients in the dexmedetomidine group reported improved sleep quality in the immediate postoperative period (lower PSQI score) and lower painDETECT scores at 3 months (4.4 ± 0.7 vs 13.4 ± 0.8, P < .001; 2.4 ± 0.9 vs 5.3 ± 0.9, P = .023, respectively). Intraoperative bradycardia and hemodynamic instability episodes were more common in the dexmedetomidine group while a single patient presented airway obstruction (2.4% vs 30.8%, P = .002) in the dexmedetomidine group.\r\n\r\nCONCLUSIONS\r\nSedation with dexmedetomidine resulted in a statistically and clinically important reduction in the incidence of POD, ED, and early POCD, while it improved self-reported postoperative sleep quality and reduced chronic pain scores in patients undergoing major elective lower limb surgery under regional anesthesia.","PeriodicalId":7799,"journal":{"name":"Anesthesia & Analgesia","volume":"130 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Anesthesia & Analgesia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1213/ane.0000000000007548","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
BACKGROUND
Postoperative delirium (POD), emergence delirium (ED), and postoperative cognitive dysfunction (POCD) are disorders of the neuropsychiatric spectrum affecting the elderly during the postoperative period, potentially sharing a common pathophysiological pathway. Disrupted sleep postoperatively correlates with both POD and POCD, revealing overlapping risk factors. This study investigates the potential of dexmedetomidine anesthesia to reduce the incidence of POD (primary outcome), ED, POCD, impairment of sleep quality, and emergent chronic pain (secondary outcomes) in older adults undergoing major orthopedic surgery under regional anesthesia.
METHODS
In this double-blind randomized control trial, patients scheduled for major lower limb orthopedic surgery under regional anesthesia were randomized to receive either dexmedetomidine or propofol for sedation at a 1:1 ratio. POD, ED, and POCD were assessed with the Confusion Assessment Method tool, the Riker Sedation-Agitation scale, and the European Battery of psychometric tests, respectively. Sleep quality was assessed using the Pittsburg Sleep Quality Index and chronic pain with the painDETECT tool. Assessments of all outcome variables were performed before surgery, and at 48 hours and 3 months postoperatively.
RESULTS
A total of 80 patients (dexmedetomidine group n = 41) were enrolled in the study and completed the follow-up. POD, ED, and early POCD incidence were significantly lower in dexmedetomidine compared to propofol group (4.8% vs 38.4%, P = .001; 2.4% vs 38.4%, P < .001; 2.4% vs 56.4%, P < .001, respectively). Patients in the dexmedetomidine group reported improved sleep quality in the immediate postoperative period (lower PSQI score) and lower painDETECT scores at 3 months (4.4 ± 0.7 vs 13.4 ± 0.8, P < .001; 2.4 ± 0.9 vs 5.3 ± 0.9, P = .023, respectively). Intraoperative bradycardia and hemodynamic instability episodes were more common in the dexmedetomidine group while a single patient presented airway obstruction (2.4% vs 30.8%, P = .002) in the dexmedetomidine group.
CONCLUSIONS
Sedation with dexmedetomidine resulted in a statistically and clinically important reduction in the incidence of POD, ED, and early POCD, while it improved self-reported postoperative sleep quality and reduced chronic pain scores in patients undergoing major elective lower limb surgery under regional anesthesia.
背景术后谵妄(POD)、出现性谵妄(ED)和术后认知功能障碍(POCD)是影响术后老年人的神经精神谱系障碍,可能具有共同的病理生理途径。术后睡眠中断与POD和POCD均相关,揭示了重叠的危险因素。本研究探讨了右美托咪定麻醉对在区域麻醉下接受骨科大手术的老年人降低POD(主要结局)、ED、POCD、睡眠质量损害和突发慢性疼痛(次要结局)发生率的潜力。方法在本双盲随机对照试验中,在区域麻醉下进行下肢骨科大手术的患者,按1:1的比例随机接受右美托咪定或异丙酚镇静。POD、ED和POCD分别用混淆评估方法工具、Riker镇静-躁动量表和欧洲系列心理测试进行评估。使用匹兹堡睡眠质量指数评估睡眠质量,使用painDETECT工具评估慢性疼痛。术前、术后48小时和术后3个月对所有结果变量进行评估。结果共80例患者(右美托咪定组n = 41)入组并完成随访。与异丙酚组相比,右美托咪定组POD、ED和早期POCD发生率显著降低(4.8% vs 38.4%, P = 0.001;2.4% vs 38.4%, P < 0.001;2.4% vs 56.4%, P < 0.001)。右美托咪定组患者术后即刻睡眠质量改善(PSQI评分较低),3个月时painDETECT评分较低(4.4±0.7 vs 13.4±0.8,P < 0.001);2.4±0.9 vs 5.3±0.9,P = 0.023)。右美托咪定组术中心动过缓和血流动力学不稳定事件更为常见,而右美托咪定组有1例患者出现气道阻塞(2.4% vs 30.8%, P = 0.002)。结论右美托咪定镇静可显著降低区域麻醉下重大选择性下肢手术患者POD、ED和早期POCD的发生率,同时改善患者术后自我报告的睡眠质量,降低慢性疼痛评分。