Intraoperative Opioid Waste and Association of Intraoperative Opioid Dose with Postoperative Adverse Outcomes: A Hospital Registry Study.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY Pain and Therapy Pub Date : 2024-04-01 Epub Date: 2024-01-28 DOI:10.1007/s40122-023-00574-2
Simone Redaelli, Aiman Suleiman, Dario von Wedel, Sarah Ashrafian, Ricardo Munoz-Acuna, Guanqing Chen, Mitra Khany, Catriona Stewart, Nikolai Ratajczak, John Hertig, Sarah Nabel, Maximilian S Schaefer, Satya Krishna Ramachandran
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Abstract

Introduction: Perioperative opioid use has been associated with adverse clinical outcomes. Additionally, opioid disposal carries significant costs, due to the waste of pharmaceutical products and the time needed by skilled labor to report the waste. In this study, we aimed to estimate costs and predict factors of opioid-associated intraoperative product waste, as well as to evaluate whether higher intraoperative opioid doses are associated with increased risk of adverse postoperative outcomes.

Methods: We included 170,607 patients undergoing general anesthesia and receiving intraoperative fentanyl, hydromorphone, or morphine at Beth Israel Deaconess Medical Center, Boston, MA, USA, between January 2010 and June 2020. We estimated product waste-associated costs based on various opioid syringe sizes and determined predictors of opioid waste. Further, we evaluated whether higher opioid doses were associated with postoperative adverse events according to the severity-indexed, incident report-based medication error-reporting program classification. The primary outcome included post-extubation desaturation, postoperative nausea or vomiting, or postoperative somnolence or sedation.

Results: The use of the smallest syringe sizes (50 mcg for fentanyl, 0.2 mg for hydromorphone, and 2 mg for morphine) resulted in the lowest product waste-associated costs. The main predictor of opioid waste was the administration of more than one intraoperative opioid (adjusted odds ratio [aOR] = 7.64, 95% CI 7.40-7.89, P < 0.001). Intraoperative doses of fentanyl > 50-100 mcg (aOR = 1.17 [1.10-1.25], P < 0.001, adjusted risk difference [ARD] 2%) and > 100 mcg (aOR = 1.24 [1.16-1.33], P < 0.001, ARD 3%), hydromorphone > 1 mg (aOR = 1.13 [1.06-1.20], P < 0.001, ARD 2%), and morphine > 2-4 mg (aOR = 1.26 [1.02-1.56], P = 0.04, ARD 3%) and > 4 mg (aOR = 1.45 [1.18-1.77], P < 0.001, ARD 5%) were associated with higher risk of the primary outcome.

Conclusion: Smaller syringe sizes of intraoperative opioids may help to reduce product waste and associated costs, as well postoperative adverse events through utilization of lower intraoperative opioid doses.

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术中阿片类药物浪费及术中阿片类药物剂量与术后不良后果的关系:一项医院登记研究。
导言:围手术期阿片类药物的使用与不良临床结果有关。此外,阿片类药物的处理也需要大量成本,这是因为药品的浪费和熟练劳动力报告浪费所需的时间。在这项研究中,我们旨在估算阿片类药物相关术中产品浪费的成本和预测因素,并评估术中阿片类药物剂量增加是否与术后不良预后风险增加有关:我们纳入了 2010 年 1 月至 2020 年 6 月期间在美国马萨诸塞州波士顿贝斯以色列女执事医疗中心接受全身麻醉并在术中使用芬太尼、氢吗啡酮或吗啡的 170,607 名患者。我们根据不同的阿片注射器规格估算了产品浪费相关成本,并确定了阿片浪费的预测因素。此外,我们还根据基于严重程度指数、事故报告的用药错误报告计划分类,评估了较高阿片类药物剂量是否与术后不良事件相关。主要结果包括拔管后不饱和、术后恶心或呕吐、术后嗜睡或镇静:结果:使用最小规格的注射器(芬太尼为 50 微克,氢吗啡酮为 0.2 毫克,吗啡为 2 毫克)产生的产品浪费相关成本最低。阿片类药物浪费的主要预测因素是术中使用一种以上的阿片类药物(调整后的几率比 [aOR] = 7.64,95% CI 7.40-7.89,P 50-100 毫克(aOR = 1.17 [1.10-1.25],P 100 毫克(aOR = 1.24 [1.16-1.33],P 1 毫克(aOR = 1.13 [1.06-1.20],P 2-4 毫克(aOR = 1.26 [1.02-1.56],P = 0.04,ARD 3%)和 > 4 毫克(aOR = 1.45 [1.18-1.77],P 结论:术中阿片类药物的注射器规格越小,可能有助于减少产品浪费和相关成本,并通过使用较低的术中阿片类药物剂量来减少术后不良事件。
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来源期刊
Pain and Therapy
Pain and Therapy CLINICAL NEUROLOGY-
CiteScore
6.60
自引率
5.00%
发文量
110
审稿时长
6 weeks
期刊介绍: Pain and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of pain therapies and pain-related devices. Studies relating to diagnosis, pharmacoeconomics, public health, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, acute pain, cancer pain, chronic pain, headache and migraine, neuropathic pain, opioids, palliative care and pain ethics, peri- and post-operative pain as well as rheumatic pain and fibromyalgia. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports, trial protocols, short communications such as commentaries and editorials, and letters. The journal is read by a global audience and receives submissions from around the world. Pain and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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