Department of Obstetrics and Gynecology, NorthShore University HealthSystem, Evanston, Illinois.
Department of Obstetrics and Gynecology, University of Chicago Pritzker School of Medicine, Chicago, Illinois.
Am J Perinatol. 2021 Jun;38(7):637-642. doi: 10.1055/s-0040-1721075. Epub 2020 Dec 2.
This study aimed to evaluate whether implementation of an enhanced recovery after surgery (ERAS) protocol is associated with lower maternal opioid use after cesarean delivery (CD).
We performed a pre- and postimplementation (PRE and POST, respectively) study of an ERAS protocol for cesarean deliveries. ERAS is a multimodal, multidisciplinary perioperative approach. The four pillars of our protocol include education, pain management, nutrition, and early ambulation. Patients were counseled by their outpatient providers and given an educational booklet. Pain management included gabapentin and acetaminophen immediately prior to spinal anesthesia. Postoperatively patients received scheduled acetaminophen and ibuprofen. Oxycodone was initiated as needed 24 hours after spinal analgesia. Preoperative diet consisted of clear carbohydrate drink consumed 2 hours prior to scheduled operative time with advancement as tolerated immediately postoperation. Women with a body mass index (BMI) <40 kg/m and scheduled CD were eligible for ERAS. PRE patients were randomly selected from repeat cesarean deliveries (RCDs) at a single site from October 2017 to September 2018, BMI <40 kg/m, without trial of labor. The POST cohort included women who participated in ERAS from October 2018 to June 2019. PRE and POST demographic and clinical characteristics were compared. Primary outcome was total postoperative morphine milligram equivalents (MMEs). Secondary outcomes included length of stay (LOS) and maximum postoperative day 2 (POD2) pain score.
All women in PRE ( = 70) had RCD compared with 66.2% (49/74) in POST. Median total postoperative MMEs were 140.0 (interquartile range [IQR]: 87.5-182.5) in PRE compared with 0.0 (IQR: 0.0-72.5) in POST ( < 0.001). Median LOS in PRE was 4.02 days (IQR: 3.26-4.27) compared with 2.37 days (IQR: 2.21-3.26) in POST ( < 0.001). Mean maximum POD2 pain score was 5.28 (standard deviation [SD] = 1.86) in PRE compared with 4.67 (SD = 1.63) in POST ( = 0.04).
ERAS protocol was associated with decreased postoperative opioid use, shorter LOS, and decreased pain after CD.
· ERAS protocol was associated with decreased postoperative opioid use after CD.. · ERAS protocol was associated with shorter length of stay after CD.. · ERAS protocol was associated with decreased postoperative pain after CD..
本研究旨在评估术后强化康复(ERAS)方案的实施是否与剖宫产术后产妇阿片类药物使用减少有关。
我们对剖宫产的 ERAS 方案进行了实施前后(分别为 PRE 和 POST)研究。ERAS 是一种多模式、多学科的围手术期方法。该方案的四个支柱包括教育、疼痛管理、营养和早期活动。患者由门诊医生提供咨询并发放教育手册。在脊髓麻醉前给予加巴喷丁和对乙酰氨基酚。术后患者接受计划内的对乙酰氨基酚和布洛芬。术后 24 小时根据需要给予羟考酮。术前饮食包括在预定手术时间前 2 小时饮用清澈的碳水化合物饮料,并在术后立即耐受的情况下逐渐推进。BMI<40kg/m2且计划行剖宫产的女性有资格接受 ERAS。PRE 患者是从 2017 年 10 月至 2018 年 9 月在一个地点随机选择的重复剖宫产(RCD)患者,BMI<40kg/m2,无试产。POST 队列包括 2018 年 10 月至 2019 年 6 月期间参与 ERAS 的女性。比较 PRE 和 POST 的人口统计学和临床特征。主要结局是术后总吗啡毫克当量(MME)。次要结局包括住院时间(LOS)和术后第 2 天(POD2)最大疼痛评分。
PRE 组(n=70)所有患者均为 RCD,而 POST 组为 66.2%(n=49)。PRE 组术后总 MME 中位数为 140.0(四分位距[IQR]:87.5-182.5),POST 组为 0.0(IQR:0.0-72.5)(<0.001)。PRE 组 LOS 中位数为 4.02 天(IQR:3.26-4.27),POST 组为 2.37 天(IQR:2.21-3.26)(<0.001)。PRE 组术后第 2 天最大疼痛评分平均为 5.28(标准差[SD]:1.86),POST 组为 4.67(SD:1.63)(=0.04)。
ERAS 方案与剖宫产术后阿片类药物使用减少、住院时间缩短和术后疼痛减轻有关。
· ERAS 方案与剖宫产术后阿片类药物使用减少有关。· ERAS 方案与剖宫产术后住院时间缩短有关。· ERAS 方案与剖宫产术后疼痛减轻有关。