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Fixed-dose gabapentin augmentation in the treatment of alcohol withdrawal syndrome: a retrospective, open-label study.固定剂量加巴喷丁辅助治疗酒精戒断综合征:一项回顾性、开放性研究。
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Thiamine Substitution in Alcohol Use Disorder: A Narrative Review of Medical Guidelines.硫胺素替代治疗酒精使用障碍:医学指南的叙述性综述。
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Alcohol Biomarkers in Clinical and Forensic Contexts.临床与法医背景下的酒精生物标志物。
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Adjunct Ketamine Use in the Management of Severe Ethanol Withdrawal.辅助氯胺酮在严重乙醇戒断治疗中的应用。
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酒精戒断综合征的围手术期管理

Perioperative Management of Alcohol Withdrawal Syndrome.

作者信息

Ungur Alexander Lavinius, Neumann Tim, Borchers Friedrich, Spies Claudia

机构信息

Department of Anesthesiology and Intensive Care Medicine, Campus Charité Mitte and Campus Virchow-Klinikum, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Department of Anesthesiology and Intensive Care Medicine, Campus Benjamin Franklin, Charité - Universitätsmedizin Berlin, Berlin, Germany.

出版信息

Visc Med. 2020 Jun;36(3):160-166. doi: 10.1159/000507595. Epub 2020 Jun 9.

DOI:10.1159/000507595
PMID:32775345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7383285/
Abstract

BACKGROUND

In the perioperative course, alcohol withdrawal syndrome (AWS) can occur in any setting, especially in aero-digestive and acute trauma surgery. Challenging issues are the overlap of other forms of delirium in perioperative and intensive care settings as well as general anesthesia masking the onset of withdrawal symptoms. In contrast to other etiologies of delirium, the pathophysiology and thus treatment strategy of AWS is different: the key point is the tolerance to GABAergic molecules of alcohol-dependent subjects resulting in central nervous hyperactivity once the effect of alcohol or other GABA-stimulating agents is decreased.

SUMMARY

Despite limitations due to insufficient accuracy of self-reporting questionnaires and limited feasibility in emergency settings, the AUDIT and the shortened AUDIT-C are the standard tools for detection of alcohol use disorders (AUD), as well as predicting AWS risk and severity in approximately half of these AUD patients. The most important risk factors for AWS are a high blood alcohol concentration at hospital admission, AWS episodes in medical history, and lack of control of alcohol use. Patients considered at risk for severe AWS must be treated with prophylactic medication before the onset of symptoms. Thiamine supplementation is required for all malnourished alcohol-dependent patients. Writing down alcohol-related diagnoses in the medical records requires the patient's presumed consent after shared decision-making. These reports should remain strictly confidential if the patient desires. Psychological support for the perioperative period as well as the following course should be offered to all AUD patients including support in short- and long-term detoxification. Alternative diagnoses must be ruled out with no timely delay, especially if fever and coma are the leading symptoms. The backbone of AWS therapy is the symptom-triggered administration of intravenous benzodiazepines (BZO) in escalating doses until the aimed revised Clinical Institute Withdrawal Assessment for Alcohol Scale (CIWA-Ar) or Richmond Agitation-Sedation Scale (RASS) score is achieved. Clonidine, dexmedetomidine, baclofen, ketamine, and neuroleptics may be used as symptom-orientated adjuncts. The therapeutic administration of ethanol or clomethiazole is considered to be harmful in critically ill patients after the onset of AWS. General supportive and intensive care including high-dose thiamine supplementation are mandatory in severe AWS cases. The timely differential diagnosis of delirium is important - and AWS is a diagnosis of exclusion - because BZO are strongly recommended for AWS patients but may not be the treatment of choice in other etiologies of delirium.

KEY MESSAGES

Screening for AWS risk factors should be integrated in the preoperative and emergency assessment. Other severe diagnoses must be ruled out before the diagnosis of AWS can be established. Preventive treatment should be given to high-risk patients scoring positive for AUD and for patients with a lack of alcohol use control. The principles of AWS therapy are symptom-orientated doses of BZO and as adjuncts α-agonists, neuroleptics, and others guided by repeated reassessment with validated tools and thiamine administration. Length of stay and morbidity are reduced if AWS therapy is symptom-orientated and protocol-based.

摘要

背景

在围手术期过程中,酒精戒断综合征(AWS)可发生于任何情况下,尤其是在航空消化道和急性创伤手术中。具有挑战性的问题是围手术期和重症监护环境中其他形式谵妄的重叠,以及全身麻醉掩盖戒断症状的发作。与其他谵妄病因不同,AWS的病理生理学及相应治疗策略有所不同:关键在于酒精依赖者对γ-氨基丁酸(GABA)能分子产生耐受性,一旦酒精或其他GABA刺激剂的作用减弱,就会导致中枢神经系统活动亢进。

总结

尽管由于自我报告问卷的准确性不足以及在紧急情况下可行性有限存在局限性,但酒精使用障碍识别测试(AUDIT)和缩短版的AUDIT-C仍是检测酒精使用障碍(AUD)以及预测约半数此类AUD患者AWS风险和严重程度的标准工具。AWS最重要的危险因素是入院时血液酒精浓度高、病史中有AWS发作以及酒精使用失控。被认为有严重AWS风险的患者必须在症状发作前接受预防性药物治疗。所有营养不良的酒精依赖患者都需要补充硫胺素。在共同决策后,若患者假定同意,应将与酒精相关的诊断记录在病历中。如果患者希望,这些报告应严格保密。应为所有AUD患者提供围手术期及后续过程的心理支持,包括短期和长期戒酒支持。必须及时排除其他诊断,特别是当发热和昏迷为主要症状时。AWS治疗的核心是根据症状静脉注射苯二氮䓬类药物(BZO),剂量逐步增加,直至达到目标修订版酒精戒断临床评估量表(CIWA-Ar)或里士满躁动-镇静量表(RASS)评分。可乐定、右美托咪定、巴氯芬、氯胺酮和抗精神病药物可作为针对症状的辅助药物。在AWS发作后,对重症患者进行乙醇或氯美噻唑的治疗性给药被认为是有害的。严重AWS病例必须进行一般支持治疗和重症监护,包括补充大剂量硫胺素。及时进行谵妄的鉴别诊断很重要——AWS是一种排除性诊断——因为强烈建议为AWS患者使用BZO,但在其他谵妄病因中可能并非首选治疗方法。

关键信息

应将AWS危险因素筛查纳入术前和急诊评估。在确立AWS诊断之前,必须排除其他严重诊断。应对AUD筛查呈阳性且酒精使用失控的高危患者进行预防性治疗。AWS治疗原则是以症状为导向给予BZO剂量,并以α-激动剂、抗精神病药物等作为辅助药物,通过使用经过验证的工具进行反复重新评估和给予硫胺素进行指导。如果AWS治疗以症状为导向且基于方案,则住院时间和发病率会降低。