Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Symptom Research, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Int J Gynecol Cancer. 2021 Jul;31(7):1052-1060. doi: 10.1136/ijgc-2021-002674. Epub 2021 Jun 16.
To compare discharge opioid refills, prescribed morphine equivalent dose and quantity, and longitudinal patient-reported outcomes before and after implementation of a tiered opioid prescribing algorithm among women undergoing open gynecologic surgery within an enhanced recovery after surgery program.
We compared opioid prescriptions, clinical outcomes, and patient-reported outcomes among 273 women. Post-discharge symptom burden was collected up to 42 days after discharge using the validated 27-item MD Anderson Symptom Inventory and analyzed using linear mixed effects models and Kaplan-Meier curves for symptom recovery.
Among 113 pre-implementation and 160 post-implementation patients there was no difference in opioid refills (9.7% vs 11.3%, p=0.84). The post-implementation cohort had a significant reduction in median morphine equivalent dose (112.5 mg vs 225 mg, p<0.01), with no difference in median hospital length of stay (3 days vs 3 days, p=1.0) or 30-day readmission rate (9.4% vs 7.1%, p=0.66). There was no difference in patient-reported pain between the pre- and post-implementation cohorts on the day of discharge (severity 4.93 vs 5.14, p=0.53) or in any patient-reported symptoms, interference measures, or composite scores by post-discharge day 7. The median recovery time for most symptoms was 7 days, except for pain (14 days), fatigue (18 days), and physical interference (21 days), with no differences between cohorts.
After implementation of a tiered opioid prescribing algorithm, the quantity and dose of discharge opioids prescribed decreased with no change in post-operative refills and without negatively impacting patient-reported symptom burden or interference, which can be used to educate and reassure patients and providers.
比较强化康复术后计划中接受开腹妇科手术的女性在实施分级阿片类药物处方算法前后出院时阿片类药物的补充、规定的吗啡等效剂量和数量,以及纵向患者报告的结果。
我们比较了 273 名女性的阿片类药物处方、临床结果和患者报告的结果。使用经过验证的 27 项 MD 安德森症状量表(MD Anderson Symptom Inventory),在出院后长达 42 天内收集出院后的症状负担,并使用线性混合效应模型和 Kaplan-Meier 曲线进行分析,以了解症状的恢复情况。
在 113 名实施前患者和 160 名实施后患者中,阿片类药物补充剂无差异(9.7%比 11.3%,p=0.84)。实施后队列的中位数吗啡等效剂量显著降低(112.5mg比 225mg,p<0.01),但中位住院时间无差异(3 天比 3 天,p=1.0)或 30 天再入院率(9.4%比 7.1%,p=0.66)。实施前后队列在出院当天的患者报告疼痛无差异(严重程度 4.93 比 5.14,p=0.53),或在出院后第 7 天的任何患者报告症状、干扰措施或综合评分中无差异。大多数症状的中位数恢复时间为 7 天,除疼痛(14 天)、疲劳(18 天)和身体干扰(21 天)外,队列之间无差异。
在实施分级阿片类药物处方算法后,开具的出院阿片类药物的数量和剂量减少,而术后补充剂没有变化,且不会对患者报告的症状负担或干扰产生负面影响,这可用于教育和安抚患者和提供者。