Morris Stephen, Lone Nazir I, McKenzie Cathrine A, Weir Christopher J, Walsh Timothy S
Primary Care Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
Usher Institute, The University of Edinburgh, Edinburgh, United Kingdom.
JAMA Netw Open. 2025 May 1;8(5):e2517533. doi: 10.1001/jamanetworkopen.2025.17533.
Propofol and the α2 agonists dexmedetomidine and clonidine are used for sedation in patients with critical illness receiving mechanical ventilation. Evidence about the cost-effectiveness of intravenous (IV) sedation with these medications is lacking.
To investigate the cost-effectiveness of dexmedetomidine-, clonidine-, and propofol-based IV sedation in patients with critical illness receiving mechanical ventilation.
DESIGN, SETTING, AND PARTICIPANTS: This economic evaluation used within-trial cost-utility analysis with a 6-month time horizon comparing dexmedetomidine-, clonidine-, and propofol-based IV sedation from a UK National Health Service and Personal Social Services perspective, with individual-level data collected from the Alpha 2 Agonists for Sedation to Produce Better Outcomes From Critical Illness (A2B) trial. Adults with critical illness receiving mechanical ventilation, with an anticipated total requirement for mechanical ventilation of at least 2 days, from 41 intensive care units in the UK were included. Recruitment ran from December 2018 through October 2023; the last date of follow-up was December 10, 2023.
Dexmedetomidine, clonidine, or propofol IV sedation. Patients receiving α2 agonists were permitted to receive supplemental propofol to achieve the target sedation score if required.
Incremental costs and quality-adjusted life years (QALYs) gained between dexmedetomidine-based vs propofol-based and clonidine-based vs propofol-based IV sedation were assessed. Mean net monetary benefits with each medication were assessed.
Among 1404 adults with critical illness receiving mechanical ventilation (mean [SD] age, 59.2 [14.9] years; 901 male [64.2%]), the mean (SD) Acute Physiology and Chronic Health Evaluation (APACHE) II score was 20.3 (8.2). The incremental cost for dexmedetomidine vs propofol was $1273 (95% CI, -$5000 to $7545), and for clonidine vs propofol, it was -$1328 (-$7114 to $4459). For dexmedetomidine vs propofol, there were 0.0008 QALYs (95% CI, -0.0198 to 0.0214 QALYs) gained, and for clonidine vs propofol, there were -0.0019 QALYs (95% CI, -0.0221 to 0.0181 QALYs) gained. Mean net monetary benefits for dexmedetomidine, clonidine, and propofol were -$53 278 (95% CI, -$58 063 to -$48 493), -$50 882 (95% CI, -$55 003 to -$46 762), and -$52 036 (95% CI, -$56 230 to -$47 834), respectively, at a maximum willingness to pay for a QALY of $16 250.
In this study, dexmedetomidine-, clonidine-, and propofol-based IV sedation in patients with critical illness receiving mechanical ventilation had similar costs and QALYs. These findings suggest that economic considerations should not affect which sedative these patients receive.
丙泊酚以及α2激动剂右美托咪定和可乐定用于接受机械通气的危重病患者的镇静。缺乏关于这些药物静脉镇静成本效益的证据。
研究右美托咪定、可乐定和丙泊酚为基础的静脉镇静在接受机械通气的危重病患者中的成本效益。
设计、设置和参与者:这项经济评估采用试验内成本效用分析,时间跨度为6个月,从英国国家医疗服务体系和个人社会服务的角度比较右美托咪定、可乐定和丙泊酚为基础的静脉镇静,数据来自“α2激动剂用于镇静以改善危重病患者预后”(A2B)试验的个体层面数据。纳入了英国41个重症监护病房中接受机械通气且预计机械通气总时长至少2天的成年危重病患者。招募时间为2018年12月至2023年10月;最后随访日期为2023年12月10日。
右美托咪定、可乐定或丙泊酚静脉镇静。接受α2激动剂的患者如果需要可接受补充丙泊酚以达到目标镇静评分。
评估右美托咪定与丙泊酚、可乐定与丙泊酚为基础的静脉镇静之间的增量成本和获得的质量调整生命年(QALY)。评估每种药物的平均净货币效益。
在1404例接受机械通气的成年危重病患者中(平均[标准差]年龄为59.2[14.9]岁;901例男性[64.2%]),平均(标准差)急性生理与慢性健康状况评估(APACHE)II评分为20.3(8.2)。右美托咪定与丙泊酚相比的增量成本为1273美元(95%CI,-5000美元至7545美元),可乐定与丙泊酚相比为-1328美元(-7114美元至4459美元)。右美托咪定与丙泊酚相比,获得了0.0008个QALY(95%CI,-0.0198至0.0214个QALY),可乐定与丙泊酚相比,获得了-0.0019个QALY(95%CI,-0.0221至0.0181个QALY)。在每个QALY最高支付意愿为16250美元时,右美托咪定、可乐定和丙泊酚的平均净货币效益分别为-53278美元(95%CI,-58063至-48493美元)、-50882美元(95%CI,-55003至-46762美元)和-52036美元(95%CI,-56230至-47834美元)。
在本研究中,右美托咪定、可乐定和丙泊酚为基础的静脉镇静在接受机械通气的危重病患者中成本和QALY相似。这些发现表明经济因素不应影响这些患者接受哪种镇静剂。