奎硫平在预防ICU高危老年患者谵妄中的作用。

IF 0.9 Q4 CRITICAL CARE MEDICINE Journal of Critical Care Medicine Pub Date : 2024-10-31 eCollection Date: 2024-10-01 DOI:10.2478/jccm-2024-0032
Walid Y Kamel, Heba Y Kamel, Ibrahim M Elsherif
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引用次数: 0

摘要

背景:本研究的目的是表明奎硫平作为谵妄预防束对老年谵妄多重风险患者的有效性。患者与方法:研究对象为90例60岁以上老年患者。将患者分为Q组(使用喹硫平)和C组(不使用喹硫平)。谵妄的评估采用重症监护谵妄筛查清单(ICDSC)和ICU混淆评估方法(CAM-ICU)。结果:C组谵妄发生率明显高于C组,谵妄严重程度明显高于C组;然而,这在统计学上并不显著。Q组谵妄的主要类型为低活动型,c组谵妄的主要类型为多活动型。CAM-ICU-7与ICDSE的互信度kappa为0.98,表明两者具有良好的相关性。嗜睡是喹硫平最常见的副作用(25%),其次是口干(18%)。结论:预防束中老年人群预防性低剂量喹硫平可降低谵妄的发生率,且主要副作用发生率低,CAM-ICU-7在谵妄的监测和早期诊断方面与ICDSC一样有效。
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Role of Quetiapine in the Prevention of ICU Delirium in Elderly Patients at a High Risk.

Background: The aim of the present study was to denote the effectiveness of Quetiapine as additive to preventive bundle of delirium in elderly patients with multiple risks for delirium.

Patients and methods: The study was performed on 90 elderly patients over 60 years. The patients were divided into Group Q (Quetiapine) and Group C (No Quetiapine). Delirium was assessed using Intensive Care Delirium Screening Checklist (ICDSC) and the Confusion Assessment Method for the ICU (CAM-ICU).

Results: The incidence of delirium was significantly higher in group C. The severity of delirium was higher among group C; however, it was not statistically significant. The dominant type of delirium was hypoactive in group Q whereas hyperactive in group C. The interrater reliability between CAM-ICU-7 and ICDSE showed a kappa 0.98 denoting excellent correlation between the two scores. Somnolence was the most common side effect of Quetiapine (25%) followed by dry mouth (18%).

Conclusions: Prophylactic low dose of Quetiapine in elderly population in the preventive bundle could reduce the incidence of delirium with a low incidence of a major side effect, as well as CAM-ICU-7 is as effective as ICDSC in monitoring and early diagnosis of delirium.

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来源期刊
Journal of Critical Care Medicine
Journal of Critical Care Medicine CRITICAL CARE MEDICINE-
CiteScore
2.00
自引率
9.10%
发文量
21
审稿时长
11 weeks
期刊最新文献
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