Katelyn Jauregui, Shania Liu, Asad Patanwala, David Begley, Kok Eng Khor, Bernadette Bugeja, Ian Fong, Joanne Rimington, Jonathan Penm
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The secondary objective was to analyze the effect of this guideline on the provision of an analgesic discharge plan.</p><p><strong>Design: </strong>A retrospective historical control cohort study.</p><p><strong>Setting: </strong>A tertiary metropolitan hospital.</p><p><strong>Interventions: </strong>A discharge analgesia guideline recommending the supply of opioid analgesics on discharge based on patient use in the 24 hours prior to discharge and the supply of an analgesic discharge plan.</p><p><strong>Main outcome measure(s): </strong>The primary outcome measure was the number of days' supply of opioids. The secondary outcome measure was the proportion of patients receiving an analgesic discharge plan.</p><p><strong>Results: </strong>There was no change in the number of days' supply of opioids provided on discharge (median, interquartile range: 5, 3-9.75 vs 6, 4-10; p = 0.107) and in the proportion of patients receiving an analgesic discharge plan (26 percent vs 22.2 percent; p = 0.604). 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引用次数: 0
摘要
研究目的本研究的主要目的是评估出院镇痛指南对手术患者出院时阿片类镇痛药供应天数的影响。次要目标是分析该指南对提供出院镇痛计划的影响:设计:回顾性历史对照队列研究:干预措施:干预措施:出院镇痛指南,根据患者在出院前24小时内的用药情况建议出院时阿片类镇痛药的供应量,以及镇痛药出院计划的供应量:主要结果测量指标:主要结果测量指标是阿片类药物的供应天数。次要结果指标是接受出院镇痛计划的患者比例:结果:出院时阿片类药物的供应天数(中位数,四分位数间距:5,3-9.75 vs 6,4-10;p = 0.107)和接受出院镇痛计划的患者比例(26% vs 22.2%;p = 0.604)均无变化。在调整了混杂变量后,阿片类药物供应天数(调整后发病率比,95% 置信区间[CI]:1.1,0.9-1.2)和提供镇痛出院计划(调整后几率比,95% 置信区间:0.6,0.2-1.4)没有变化:总体而言,我们的研究发现,在实施出院镇痛指南后,出院时阿片类药物的供应天数和提供出院镇痛计划的情况没有发生变化,但我们也发现,在实施指南之前,处方做法已经与指南保持一致。
Effectiveness of a discharge analgesia guideline on discharge opioid prescribing after a surgical procedure from a tertiary metropolitan hospital.
Objective: The primary objective of this study was to evaluate the effectiveness of a discharge analgesia guideline on the number of days' supply of opioid analgesics provided among surgical patients upon hospital discharge. The secondary objective was to analyze the effect of this guideline on the provision of an analgesic discharge plan.
Design: A retrospective historical control cohort study.
Setting: A tertiary metropolitan hospital.
Interventions: A discharge analgesia guideline recommending the supply of opioid analgesics on discharge based on patient use in the 24 hours prior to discharge and the supply of an analgesic discharge plan.
Main outcome measure(s): The primary outcome measure was the number of days' supply of opioids. The secondary outcome measure was the proportion of patients receiving an analgesic discharge plan.
Results: There was no change in the number of days' supply of opioids provided on discharge (median, interquartile range: 5, 3-9.75 vs 6, 4-10; p = 0.107) and in the proportion of patients receiving an analgesic discharge plan (26 percent vs 22.2 percent; p = 0.604). The results of two multivariable regression models showed no change in the number of days' supply of opioids (adjusted incidence rate ratio, 95 percent confidence interval [CI]: 1.1, 0.9-1.2) and the provision of an analgesic discharge plan (adjusted odds ratio, 95 percent CI: 0.6, 0.2-1.4) after adjusting for confounding variables.
Conclusion: Overall, our study found no change in the number of days' supply of opioids provided on discharge and the provision of an analgesic discharge plan after implementation of a discharge analgesia guideline, but we also found that prescribing practices already aligned with the guideline before its implementation.
期刊介绍:
The Journal of Opioid Management deals with all aspects of opioids. From basic science, pre-clinical, clinical, abuse, compliance and addiction medicine, the journal provides and unbiased forum for researchers and clinicians to explore and manage the complexities of opioid prescription.