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胍法辛治疗住院谵妄患者的疗效和安全性:一项范围综述。

Efficacy and safety of guanfacine in hospitalized patients with delirium: A scoping review.

作者信息

Pattamin Nuttapol, Phongphithakchai Atthaphong, Spano Sofia, Maeda Akinori, Chaba Anis, Hikasa Yukiko, Bellomo Rinaldo

机构信息

Department of Intensive Care, Austin Hospital, Heidelberg, Victoria, Australia.

Department of Internal Medicine, Bhumibol Adulyadej Hospital, Royal Thai Air Force, Bangkok, Thailand.

出版信息

Crit Care Resusc. 2024 Nov 24;26(4):286-294. doi: 10.1016/j.ccrj.2024.08.009. eCollection 2024 Dec.

Abstract

OBJECTIVE

To assess current evidence regarding guanfacine use in hospitalized patients with delirium.

INTRODUCTION

Delirium is a common and important complication of critical illness. Central alpha-2 agonists are often used for symptomatic management. Guanfacine is an enteral central alpha-2 agonist approved for the treatment of attention deficit hyperactivity disorders. However, its use for delirium treatment has not been systematically assessed.

INCLUSION CRITERIA

All studies of guanfacine to treat patients with delirium during hospitalization. We excluded reviews, letters, commentaries, correspondence, conference abstracts, expert opinions or editorials.

METHODS

We performed a systematic search of the literature using: MEDLINE (Ovid), Embase (Ovid), CENTRAL and SCOPUS (Elsevier) from inception until 29 February, 2024. Two independent reviewers assessed the identified citations and abstracts. Data on study and patient characteristics, as well as efficacy and safety outcomes, were extracted. Efficacy was defined by guanfacine's ability to relieve delirium and improve clinical outcomes, including intensive care unit (ICU) length of stay (LOS), hospital LOS, and mortality. Safety was assessed for hemodynamic stability or other reported side effects.

RESULTS

We screened 908 articles and included two case reports, one case series, two retrospective descriptive cohorts, and one retrospective analytic cohort. Guanfacine therapy was associated with delirium attenuation and a reduction in the use of sedative agents. Median dosage was 1.5 mg daily, with a median time to delirium improvement of 3 days. However, guanfacine therapy was not associated with decreased ICU or hospital LOS. The most frequently reported adverse events were mild hypotension and bradycardia.

CONCLUSION

There is limited data on the efficacy of guanfacine for the treatment of delirium. However, given its pharmacologic properties and its available safety data, controlled investigations may be justified.

摘要

目的

评估目前关于胍法辛用于住院谵妄患者的证据。

引言

谵妄是危重病常见且重要的并发症。中枢α-2激动剂常用于症状管理。胍法辛是一种经肠道给药的中枢α-2激动剂,被批准用于治疗注意力缺陷多动障碍。然而,其用于谵妄治疗尚未得到系统评估。

纳入标准

所有关于胍法辛治疗住院期间谵妄患者的研究。我们排除了综述、信件、评论、通信、会议摘要、专家意见或社论。

方法

我们使用MEDLINE(Ovid)、Embase(Ovid)、CENTRAL和SCOPUS(爱思唯尔)对文献进行了系统检索,检索时间从数据库建库至2024年2月29日。两名独立评审员评估了检索到的文献和摘要。提取了关于研究和患者特征以及疗效和安全性结果的数据。疗效通过胍法辛缓解谵妄和改善临床结局的能力来定义,包括重症监护病房(ICU)住院时间(LOS)、医院住院时间和死亡率。评估安全性以观察血流动力学稳定性或其他报告的副作用。

结果

我们筛选了908篇文章,纳入了两篇病例报告、一篇病例系列、两篇回顾性描述性队列研究和一篇回顾性分析性队列研究。胍法辛治疗与谵妄减轻和镇静剂使用减少相关。中位剂量为每日1.5毫克,谵妄改善的中位时间为3天。然而,胍法辛治疗与ICU或医院住院时间缩短无关。最常报告的不良事件是轻度低血压和心动过缓。

结论

关于胍法辛治疗谵妄疗效的数据有限。然而,鉴于其药理特性和现有的安全性数据,进行对照研究可能是合理的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/028f/11704153/01da55e31348/gr1.jpg

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