Dexmedetomidine as adjunctive therapy for the treatment of alcohol withdrawal syndrome: a systematic review protocol.

Marco Fiore, Giacomo Torretta, Maria Beatrice Passavanti, Pasquale Sansone, Maria Caterina Pace, Aniello Alfieri, Caterina Aurilio, Vittorio Simeon, Paolo Chiodini, Vincenzo Pota
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Abstract

Objective: The purpose of this review is to evaluate the effectiveness and safety of dexmedetomidine as adjunctive therapy to the standard of care (benzodiazepines) compared to either the standard of care or other adjunctive treatment approaches (e.g. benzodiazepines plus propofol) for the treatment of alcohol withdrawal syndrome (AWS).

Introduction: Benzodiazepines have been the cornerstone of AWS therapy, but in some patients, AWS is refractory to high doses. Moreover, benzodiazepine use is burdened by excessive sedation, confusion and respiratory depression. Options for management of refractory AWS include the addition of phenobarbital, propofol and, more recently, dexmedetomidine to benzodiazepines therapy. The possible advantage of dexmedetomidine compared to benzodiazepines is that it does not cause respiratory depression, thus reducing the risk of intubation and hospitalization in the intensive care unit.

Inclusion criteria: This review will consider studies including patients who are 18 years or older and are diagnosed with AWS. The exclusion criteria are a history of psychoactive substances or withdrawal states and/or severe neurologic disorder (e.g. traumatic brain injury, acute stroke, severe dementia, seizure disorder).

Methods: This review will include only studies published in English, with no restrictions on the year of publication. Both randomized controlled trials and observational studies (including cohort and case-control studies) assessing the drug effectiveness and safety will be included. The databases utilized will include: PubMed, Embase and Cochrane Central Register of Controlled Trials. In addition, the trial registers to be searched will include: World Health Organization International Clinical Trials Registry Platform (ICTRP), U.S. National Library of Medicine Drug Information Portal and ClinicalTrials.gov.

Systematic review registration number: PROSPERO CRD42018084370.

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右美托咪定作为酒精戒断综合征的辅助治疗:一项系统评价方案
目的:本综述的目的是评估右美托咪定作为护理标准(苯二氮卓类药物)的辅助治疗与治疗酒精戒断综合征(AWS)的护理标准或其他辅助治疗方法(如苯二氮卓类药物加丙泊酚)的有效性和安全性AWS治疗,但在一些患者中,AWS对高剂量是难治的。此外,苯二氮卓类药物的使用会带来过度镇静、精神错乱和呼吸抑制的负担。难治性AWS的治疗方案包括在苯二氮卓类药物治疗中加入苯巴比妥、丙泊酚和最近的右美托咪定。与苯二氮卓类药物相比,右美托咪定的可能优势在于它不会引起呼吸抑制,从而降低插管和在重症监护室住院的风险。纳入标准:本综述将考虑包括18岁或以上被诊断为AWS的患者在内的研究。排除标准是精神活性物质或戒断状态和/或严重神经系统疾病(如创伤性脑损伤、急性中风、严重痴呆、癫痫发作)的病史。方法:本综述仅包括以英语发表的研究,对发表年份没有限制。评估药物有效性和安全性的随机对照试验和观察性研究(包括队列和病例对照研究)都将包括在内。所使用的数据库将包括:PubMed、Embase和Cochrane对照试验中央登记册。此外,要搜索的试验注册将包括:世界卫生组织国际临床试验注册平台(ICTRP)、美国国家医学图书馆药物信息门户网站和ClinicalTrials.gov。系统审查注册号:PROSPERO CRD42018084370。
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