Foertsch Madeline J, Winter Jessica B, Rhoades Abigail G, Martin Lukas T, Droege Christopher A, Ernst Neil E
Department of Pharmacy Services, UC Health-University of Cincinnati Medical Center, Ohio (Drs Foertsch, Winter, Droege, and Ernst); University of Cincinnati James L. Winkle College of Pharmacy, Ohio (Drs Foertsch, Winter, Rhoades, Martin, Droege, and Ernst); Department of Pharmacy Services, The Christ Hospital Health Network, Cincinnati, Ohio (Dr Rhoades); and Department of Pharmacy Services, St Elizabeth Healthcare, Edgewood, Kentucky (Dr Martin).
Crit Care Nurs Q. 2019 Jan/Mar;42(1):12-29. doi: 10.1097/CNQ.0000000000000233.
Alcohol withdrawal syndrome (AWS) is a complex neurologic disorder that develops after an acute reduction in or cessation of chronic alcohol consumption that alters neurotransmitter conduction. The incidence of AWS in the intensive care unit varies, but has been associated with poor outcomes. This is primarily driven by downregulation of gamma-aminobutyric acid (GABA) leading to autonomic excitability and psychomotor agitation. No clinical assessment tools have been validated to assess for AWS in the intensive care unit, particularly for patients requiring mechanical ventilation. The Clinical Institute Withdrawal Assessment for Alcohol Scale, Revised, may be considered to gauge the extent of withdrawal, but is not particular with acute presentations in this population. Symptom-triggered use of GABA agonist such as benzodiazepines remains the mainstay of pharmacotherapeutic intervention. Nonbenzodiazepine GABA agonists such as barbiturates and propofol as well as non-GABA adjunctive agents such as dexmedetomidine, ketamine, and antipsychotic agents may help reduce the need for symptom-triggered benzodiazepine dosing, but lack robust data. Agent selection should be based on patient-specific factors such as renal and hepatic metabolism, duration of action, and clearance. Institution-specific protocols directing GABA-acting medications and adjunctive medications for excitatory, adrenergic, and delirium assessments could be considered to improve patient outcomes and caregiver satisfaction.
酒精戒断综合征(AWS)是一种复杂的神经系统疾病,在长期饮酒后急性减少或停止饮酒导致神经递质传导改变时发生。重症监护病房中AWS的发生率各不相同,但与不良预后相关。这主要是由γ-氨基丁酸(GABA)下调导致自主神经兴奋性和精神运动性激越引起的。目前尚无经过验证的临床评估工具可用于评估重症监护病房中的AWS,特别是对于需要机械通气的患者。修订后的酒精临床研究所戒断评估量表可用于评估戒断程度,但对于该人群的急性表现并不特别适用。症状触发使用GABA激动剂如苯二氮䓬类药物仍然是药物治疗干预的主要手段。非苯二氮䓬类GABA激动剂如巴比妥类药物和丙泊酚以及非GABA辅助药物如右美托咪定、氯胺酮和抗精神病药物可能有助于减少症状触发的苯二氮䓬类药物给药需求,但缺乏有力的数据支持。药物选择应基于患者的特定因素,如肾和肝代谢、作用持续时间和清除率。可以考虑制定针对GABA作用药物和辅助药物用于兴奋性、肾上腺素能和谵妄评估的机构特定方案,以改善患者预后和护理人员满意度。