Barends Clemens R M, Absalom Anthony, van Minnen Baucke, Vissink Arjan, Visser Anita
Department of Anesthesiology, University of Groningen and University Medical Center Groningen, Groningen, The Netherlands.
Department of oral and maxillofacial surgery, University of Groningen and University Medical Center Groningen, Groningen, The Netherlands.
PLoS One. 2017 Jan 20;12(1):e0169525. doi: 10.1371/journal.pone.0169525. eCollection 2017.
To systematically review the literature comparing the efficacy and safety of dexmedetomidine and midazolam when used for procedural sedation.
We searched MEDLINE, EMBASE and COCHRANE for clinical trials comparing dexmedetomidine and midazolam for procedural sedation up to June 20, 2016. Inclusion criteria: clinical trial, human subjects, adult subjects (≥18 years), article written in English, German, French or Dutch, use of study medication for conscious sedation and at least one group receiving dexmedetomidine and one group receiving midazolam. Exclusion criteria: patients in intensive care, pediatric subjects and per protocol use of additional sedative medication other than rescue medication. Outcome measures for efficacy comparison were patient and clinician satisfaction scores and pain scores; outcome measures for safety comparison were hypotension, hypoxia, and circulatory and respiratory complications.
We identified 89 papers, of which 12 satisfied the inclusion and exclusion criteria; 883 patients were included in these studies. Dexmedetomidine was associated with higher patient and operator satisfaction than midazolam. Patients receiving dexmedetomidine experienced less pain and had lower analgesic requirements. Respiratory and hemodynamic safety were similar.
Dexmedetomidine is a promising alternative to midazolam for use in procedural sedation. Dexmedetomidine provides more comfort during the procedure for the patient and clinician. If carefully titrated, the safety profiles are similar.
系统回顾比较右美托咪定和咪达唑仑用于操作过程中镇静时的疗效和安全性的文献。
我们检索了MEDLINE、EMBASE和COCHRANE数据库,查找截至2016年6月20日比较右美托咪定和咪达唑仑用于操作过程中镇静的临床试验。纳入标准:临床试验、人类受试者、成年受试者(≥18岁)、用英文、德文、法文或荷兰文撰写的文章、使用研究药物进行清醒镇静且至少有一组接受右美托咪定,一组接受咪达唑仑。排除标准:重症监护患者、儿科受试者以及除抢救药物外按方案使用其他镇静药物的情况。疗效比较的结局指标为患者和临床医生满意度评分以及疼痛评分;安全性比较的结局指标为低血压、低氧血症以及循环和呼吸并发症。
我们识别出89篇论文,其中12篇符合纳入和排除标准;这些研究共纳入883例患者。与咪达唑仑相比,右美托咪定使患者和操作者满意度更高。接受右美托咪定的患者疼痛较轻且镇痛需求较低。呼吸和血流动力学安全性相似。
右美托咪定是用于操作过程中镇静的一种有前景的替代咪达唑仑的药物。右美托咪定在操作过程中为患者和临床医生提供更多舒适感。如果仔细滴定,安全性概况相似。