接受侵入性机械通气的急性呼吸衰竭患者的阿片类药物应用实践模式。

Q4 Medicine
Critical care explorations Pub Date : 2024-07-17 eCollection Date: 2024-07-01 DOI:10.1097/CCE.0000000000001123
Laura C Myers, Nicholas A Bosch, Lauren Soltesz, Kathleen A Daly, Cynthia I Campbell, Emma Schwager, Emmanuele Salvati, Jennifer P Stevens, Hannah Wunsch, Justin M Rucci, S Reza Jafarzadeh, Vincent X Liu, Allan J Walkey
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引用次数: 0

摘要

重要性:阿片类药物危机正影响着全国各地的人们,为遏制阿片类药物相关死亡人数的上升,这一问题值得关注:评估接受有创机械通气的急性呼吸衰竭患者阿片类药物输注管理和剂量的实践模式:设计:回顾性队列研究:来自北加州凯撒医疗集团 21 家医院和飞利浦电子 ICU 研究所 96 家医院的患者:我们对患者是否接受阿片类药物输注以及输注剂量进行了评估:我们确定了诊断为急性呼吸衰竭并开始接受有创机械通气的患者。我们确定了每位患者是否接受了阿片类药物输注,并确定了接受阿片类药物输注者的芬太尼每日输注剂量中位数。我们使用分层回归模型来量化各家医院在阿片类药物输注使用和芬太尼当量日剂量中位数方面的差异。我们将 13140 名患者纳入 KPNC 队列,将 52033 名患者纳入 eRI 队列。在 KPNC 和 eRI 队列中,分别有 7023 名(53.4%)和 16311 名(31.1%)患者在机械通气的前 21 天接受了阿片类药物输注。在考虑了患者和医院层面的固定效应后,患者入院的医院分别解释了 KPNC 和 eRI 队列中阿片类药物输注使用变化的 7% (95% CI, 3-11%) 和 39% (95% CI, 28-49%)。在接受阿片类药物输注的患者中,KPNC队列和eRI队列的每日芬太尼等效剂量中位数分别为692微克(四分位距[IQR]为129-1341微克)和200微克(四分位距[IQR]为0-1050微克)。在KPNC队列和eRI队列中,医院分别解释了4%(95% CI,1-7%)和20%(95% CI,15-26%)的每日芬太尼当量中位剂量变化:在努力限制医疗相关阿片类药物暴露的背景下,我们的研究结果突显了伴随机械通气而来的大量阿片类药物暴露,并表明可能存在镇痛治疗不足或过度的情况。我们的研究结果有助于将医院的镇痛措施与风险调整后的平均值进行比较,并可用于镇痛和镇静临床试验的常规护理对照组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Opioid Administration Practice Patterns in Patients With Acute Respiratory Failure Who Undergo Invasive Mechanical Ventilation.

Importance: The opioid crisis is impacting people across the country and deserves attention to be able to curb the rise in opioid-related deaths.

Objectives: To evaluate practice patterns in opioid infusion administration and dosing for patients with acute respiratory failure receiving invasive mechanical ventilation.

Design: Retrospective cohort study.

Setting and participants: Patients from 21 hospitals in Kaiser Permanente Northern California and 96 hospitals in Philips electronic ICU Research Institute.

Main outcomes and measures: We assessed whether patients received opioid infusion and the dose of said opioid infusion.

Results: We identified patients with a diagnosis of acute respiratory failure who were initiated on invasive mechanical ventilation. From each patient, we determined if opioid infusions were administered and, among those who received an opioid infusion, the median daily dose of fentanyl infusion. We used hierarchical regression models to quantify variation in opioid infusion use and the median daily dose of fentanyl equivalents across hospitals. We included 13,140 patients in the KPNC cohort and 52,033 patients in the eRI cohort. A total of 7,023 (53.4%) and 16,311 (31.1%) patients received an opioid infusion in the first 21 days of mechanical ventilation in the KPNC and eRI cohorts, respectively. After accounting for patient- and hospital-level fixed effects, the hospital that a patient was admitted to explained 7% (95% CI, 3-11%) and 39% (95% CI, 28-49%) of the variation in opioid infusion use in the KPNC and eRI cohorts, respectively. Among patients who received an opioid infusion, the median daily fentanyl equivalent dose was 692 µg (interquartile range [IQR], 129-1341 µg) in the KPNC cohort and 200 µg (IQR, 0-1050 µg) in the eRI cohort. Hospital explained 4% (95% CI, 1-7%) and 20% (95% CI, 15-26%) of the variation in median daily fentanyl equivalent dose in the KPNC and eRI cohorts, respectively.

Conclusions and relevance: In the context of efforts to limit healthcare-associated opioid exposure, our findings highlight the considerable opioid exposure that accompanies mechanical ventilation and suggest potential under and over-treatment with analgesia. Our results facilitate benchmarking of hospitals' analgesia practices against risk-adjusted averages and can be used to inform usual care control arms of analgesia and sedation clinical trials.

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