Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Am J Obstet Gynecol. 2020 Dec;223(6):894.e1-894.e9. doi: 10.1016/j.ajog.2020.07.004. Epub 2020 Jul 9.
There is an opioid epidemic in the United States with a contributing factor of opioids being prescribed for postoperative pain after surgery.
Among women who underwent stress urinary incontinence and pelvic organ prolapse surgeries, our primary objective was to determine the proportion of women who filled perioperative opioid prescriptions and to compare factors associated with these opioid prescriptions. We also sought to assess the risk of prolonged opioid use through 1 year after stress urinary incontinence and pelvic organ prolapse surgeries.
Using a population-based cohort of commercially insured individuals in the 2005-2015 IBM MarketScan databases, we identified opioid-naive women ≥18 years who underwent stress urinary incontinence and/or pelvic organ prolapse procedures based on Current Procedural Terminology codes. We defined the perioperative period as the window beginning 30 days before surgery extending until 7 days after surgery. Any filled opioid prescription in this window was considered a perioperative prescription. For our primary outcome, we reported the proportion of opioid-naive women who filled a perioperative opioid prescription and reported the median quantity dispensed in the perioperative period. We also assessed demographic and perioperative factors associated with perioperative opioid prescription fills. Previous studies have defined prolonged use as the proportion of women who fill an opioid prescription between 90 and 180 days after surgery. We report this estimate as well as continuous opioid use, defined as the proportion of women with ongoing monthly opioid prescriptions filled through 1 year after stress urinary incontinence and/or pelvic organ prolapse surgery.
Among the 217,460 opioid-naive women who underwent urogynecologic surgery, 61,025 (28.1%) had pelvic organ prolapse and stress urinary incontinence surgeries, 85,575 (39.4%) had stress urinary incontinence surgery without pelvic organ prolapse surgery, and 70,860 (32.6%) had pelvic organ prolapse surgery without stress urinary incontinence surgery. Overall, 167,354 (77.0%) filled a perioperative opioid prescription, and the median quantity was 30 pills (interquartile range, 20-30). In a multivariate regression model, younger age, pelvic organ prolapse surgery with or without stress urinary incontinence surgery, abdominal route, hysterectomy, and mesh use remained significantly associated with opioid prescriptions filled. Among those with a filled perioperative opioid prescription, the risk of prolonged use defined as an opioid prescription filled between 90 and 180 days was 7.5% (95% confidence interval, 7.3-7.6). However, the risk of prolonged use defined as continuous use with at least 1 monthly opioid prescription filled after surgery was significantly lower: 1.2% (1.13-1.24), 0.32% (0.29-0.35), 0.06% (0.05-0.08), and 0.04% (0.02-0.05) at 60, 90, 180, and 360 days after surgery, respectively.
Among privately insured, opioid-naive women undergoing stress urinary incontinence and/or pelvic organ prolapse surgery, 77% of women filled an opioid prescription with a median of 30 opioid pills prescribed. For prolonged use, 7.5% (95% confidence interval, 7.3-7.6) filled an opioid prescription within 90 to 180 days after surgery, but the rates of continuously filled opioid prescriptions were significantly lower at 0.06% (95% confidence interval, 0.05-0.08) at 180 days and 0.04% (95% confidence interval, 0.02-0.05) at 1 year after surgery.
美国正面临阿片类药物泛滥的问题,其中一个促成因素是手术后开具阿片类药物用于缓解术后疼痛。
在接受压力性尿失禁和盆腔器官脱垂手术的女性中,我们的主要目的是确定填写围手术期阿片类药物处方的女性比例,并比较与这些阿片类药物处方相关的因素。我们还试图评估通过压力性尿失禁和盆腔器官脱垂手术后 1 年,长期使用阿片类药物的风险。
我们使用基于 2005-2015 年 IBM MarketScan 数据库的商业保险人群进行了一项基于人群的队列研究,纳入了基于当前操作术语代码接受压力性尿失禁和/或盆腔器官脱垂手术的阿片类药物初治女性,年龄≥18 岁。我们将围手术期定义为手术前 30 天至手术后 7 天的窗口。该窗口内开具的任何阿片类药物处方都被视为围手术期处方。对于我们的主要结局,我们报告了阿片类药物初治女性中填写围手术期阿片类药物处方的比例,并报告了围手术期开具的中位数数量。我们还评估了与围手术期阿片类药物处方填写相关的人口统计学和围手术期因素。先前的研究将长期使用定义为手术后 90-180 天内填写阿片类药物处方的女性比例。我们报告了这个估计值,以及连续使用阿片类药物的比例,定义为通过压力性尿失禁和/或盆腔器官脱垂手术后 1 年持续每月开具阿片类药物处方的女性比例。
在 217460 名接受妇科手术的阿片类药物初治女性中,61025 名(28.1%)患有盆腔器官脱垂和压力性尿失禁手术,85575 名(39.4%)患有单纯压力性尿失禁手术,70860 名(32.6%)患有单纯盆腔器官脱垂手术。总体而言,167354 名(77.0%)女性填写了围手术期阿片类药物处方,中位数数量为 30 片(四分位距 20-30)。在多变量回归模型中,年龄较小、盆腔器官脱垂手术伴或不伴压力性尿失禁手术、腹部入路、子宫切除术和使用网片仍然与阿片类药物处方的开具显著相关。在那些填写了围手术期阿片类药物处方的患者中,定义为手术后 90-180 天内开具阿片类药物处方的长期使用的风险为 7.5%(95%置信区间,7.3-7.6)。然而,定义为手术后至少有 1 个月开具阿片类药物处方的连续使用的长期使用风险显著较低:分别在手术后 60、90、180 和 360 天时,风险为 1.2%(1.13-1.24)、0.32%(0.29-0.35)、0.06%(0.05-0.08)和 0.04%(0.02-0.05)。
在接受压力性尿失禁和/或盆腔器官脱垂手术的私立保险、阿片类药物初治女性中,77%的女性开具了阿片类药物处方,中位数数量为 30 片阿片类药物。对于长期使用,7.5%(95%置信区间,7.3-7.6)在手术后 90-180 天内开具了阿片类药物处方,但在手术后 180 天和 1 年内持续开具阿片类药物处方的比例分别显著下降至 0.06%(95%置信区间,0.05-0.08)和 0.04%(95%置信区间,0.02-0.05)。