右美托咪定对非插管重症监护患者复苏镇痛剂需求的影响

IF 1.1 Q4 PHARMACOLOGY & PHARMACY
Sophie E Andrei, Wenxin Zhuo, Kellie N Shiekh, Justin P Reinert
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引用次数: 0

摘要

背景:右美托咪定是一种中枢作用的α-2-肾上腺素受体激动剂,通常用于重症监护室(ICU),具有镇静、镇痛和抗焦虑的作用。研究表明右美托咪定可以作为一种有效的辅助镇痛剂,但这些研究非常有限,而且通常使用的是插管患者。为了更好地评估右美托咪定在成人重症监护病房中的作用,需要收集更多有关其镇痛效果及其在非插管患者中的实用性的信息:本研究是一项回顾性队列分析,研究对象为 2022 年 10 月 1 日至 2023 年 8 月 31 日期间入住一家拥有 302 张病床的三级学术医疗中心、使用右美托咪定的成人非插管 ICU 患者和未使用右美托咪定的成人非插管 ICU 患者。纳入标准为:有必要的阿片类药物医嘱,并有相应的疼痛评分和至少一项其他疼痛评估,无症状性心动过缓病史,入院时也不能有症状性心动过缓。研究的主要目的是评估 ICU 入院时同时输注右美托咪定的吗啡毫克当量 (MME) 量。次要结果包括首次使用阿片类药物镇痛的时间和重症监护室的住院时间:结果:共纳入 38 名患者。各组间的基线人口统计学差异不大。右美托咪定组接受的 MMEs 总量明显少于对照组(P < 0.001)。右美托咪定组首次抢救镇痛用药时间明显更长(P = 0.025),谵妄发生率明显增加(P < 0.001)。结论:右美托咪定可显著降低镇痛剂的剂量:结论:右美托咪定可明显降低非插管 ICU 患者的 MME 需求量,并延长首次抢救镇痛剂量的用药时间,同时不会增加不良反应,但会增加谵妄的发生率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Dexmedetomidine on Rescue Analgesic Needs in Non-intubated Intensive Care Patients.

Background: Dexmedetomidine is a centrally acting alpha-2-adrenoceptor agonist that is usually used in the intensive care unit (ICU) for its sedative, analgesic, and anxiolytic properties. Studies have shown that dexmedetomidine can be an effective adjunct analgesic, but they are limited and usually use a population of intubated patients. To better evaluate the role of dexmedetomidine use in the adult ICU, more information needs to be gathered on its analgesic effect and its utility in non-intubated patients.

Methods: This study was a retrospective cohort analysis between adult non-intubated ICU patients on dexmedetomidine and non-intubated ICU patients not on dexmedetomidine who were admitted to a 302-bed tertiary academic medical center between October 1, 2022, and August 31, 2023. Inclusion criteria necessitated an as-needed opioid order with a corresponding pain score and at least 1 other pain assessment and no history of symptomatic bradycardia, nor could it be present on admission. The primary study objective was to assess the amount of morphine milligram equivalents (MMEs) received during ICU admission with concomitant dexmedetomidine infusion. Secondary outcomes included the time to first dose of rescue opioid analgesia and ICU length of stay.

Results: A total of 38 patients were included. Baseline demographics did not differ significantly between groups. There was a significant statistical difference in the total amount of MMEs received, with the dexmedetomidine group having significantly less than the control group (P < 0.001). The dexmedetomidine group also had a significantly longer time to first rescue analgesia dose (P = 0.025) and a significantly increased incidence of delirium (P < 0.001). There was no difference in other adverse events between groups.

Conclusion: Dexmedetomidine significantly decreased MME requirements and increased time to first rescue analgesia dose in non-intubated ICU patients without increasing adverse effects but was associated with an increased incidence of delirium.

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来源期刊
Journal of Pharmacy Technology
Journal of Pharmacy Technology PHARMACOLOGY & PHARMACY-
CiteScore
1.50
自引率
0.00%
发文量
49
期刊介绍: For both pharmacists and technicians, jPT provides valuable information for those interested in the entire body of pharmacy practice. jPT covers new drugs, products, and equipment; therapeutic trends; organizational, legal, and educational activities; drug distribution and administration; and includes continuing education articles.
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