Gressler Laura E, Sze Christina, Punyala Ananth, Martinez-Diaz Susana, Bhojani Naeem, Zorn Kevin C, Elterman Dean, Chughtai Bilal
Division of Pharmaceutical Evaluation and Policy, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, AR, United States.
Department of Urology, Weill Cornell Medicine, New York Presbyterian Hospital, New York, NY, United States.
Can Urol Assoc J. 2025 May;19(5):E160-E165. doi: 10.5489/cuaj.8958.
This study aimed to analyze opioid prescribing behavior following surgical interventions for benign prostatic hyperplasia (BPH), focusing on differences in postoperative opioid prescribing practices between patients who undergo surgical procedures in operative room (OR) settings vs. non-operative room (non-OR) settings.
A retrospective cohort study was conducted using a 10% random sample of the IQVIA PharMetrics Plus for Academics database, including men who underwent surgical interventions for BPH from 2015-2020. Propensity score analysis and inverse probability treatment weighting were employed to adjust for potential confounders. Primary outcomes included opioid receipt, cumulative days of opioid use, and morphine equivalent daily dose (MEDD).
Among the included men (n=6022), those undergoing procedures in OR settings were more likely to receive opioid prescriptions postoperatively compared to those in non-OR settings (42.78% vs. 28.00%, p<0.001). While cumulative days and MEDD of opioid prescriptions did not significantly differ between groups, there was a statistically significant difference in the distribution of opioid receipt duration (p=0.0128). The adjusted model showed significantly higher odds of opioid prescription for men undergoing OR procedures (odds ratio 1.922, 95% confidence interval 1.690-2.185).
Men undergoing BPH surgeries in OR settings were more likely to receive opioid prescriptions postoperatively, suggesting potential overprescription. Despite similar cumulative opioid use, differences in prescription rates indicate a need for improved postoperative pain management strategies, possibly using non-opioid alternatives. Future research should focus on optimizing pain control, characterizing actual opioid consumption, and considering patient-specific factors in surgical decision-making.
本研究旨在分析良性前列腺增生(BPH)手术干预后的阿片类药物处方行为,重点关注在手术室(OR)环境与非手术室(非OR)环境中接受手术的患者术后阿片类药物处方实践的差异。
使用IQVIA PharMetrics Plus for Academics数据库10%的随机样本进行回顾性队列研究,纳入2015年至2020年接受BPH手术干预的男性。采用倾向评分分析和逆概率治疗加权法来调整潜在混杂因素。主要结局包括阿片类药物的使用、阿片类药物使用的累计天数以及吗啡当量日剂量(MEDD)。
在纳入的男性(n = 6022)中,与非OR环境中的患者相比,在OR环境中接受手术的患者术后更有可能接受阿片类药物处方(42.78%对28.00%,p < 0.001)。虽然阿片类药物处方的累计天数和MEDD在组间无显著差异,但阿片类药物使用持续时间的分布存在统计学显著差异(p = 0.0128)。调整后的模型显示,接受OR手术的男性开具阿片类药物处方的几率显著更高(优势比1.922,95%置信区间1.690 - 2.185)。
在OR环境中接受BPH手术的男性术后更有可能接受阿片类药物处方,提示可能存在过度处方。尽管阿片类药物的累计使用量相似,但处方率的差异表明需要改进术后疼痛管理策略,可能使用非阿片类替代药物。未来的研究应侧重于优化疼痛控制、描述实际阿片类药物消费量,并在手术决策中考虑患者特定因素。