Kokan Aamir A, Sheth Sahil, Rogers Katie
Anne Arundel Medical Center, Department of Pharmacy Services, Annapolis, Maryland.
Innov Pharm. 2021 Sep 22;12(4). doi: 10.24926/iip.v12i4.3969. eCollection 2021.
Postoperative ileus is a transient cessation of bowel motility, occurring after bowel resection, characterized by abdominal distension and pain, nausea, vomiting, and an accumulation of gas/fluids in the bowel. It is associated with a greater incidence of postoperative morbidity and increased length of stay or readmission. Alvimopan, a novel peripheral mu receptor antagonist, is indicated for preventing postoperative ileus in patients undergoing intra-abdominal surgery or bowel resection. The objective of this study was to assess the impact of alvimopan use in laparoscopic abdominal surgeries. To assess alvimopan use's impact in laparoscopic abdominal surgeries. A retrospective chart review was conducted of 84 patients who underwent laparoscopic procedures that received alvimopan (September 1, 2018 to October 31, 2018) and compared to patients that did not receive alvimopan (May 1, 2018 to June 30, 2018, due to a national shortage of the medication). The primary outcome was the rate of postoperative ileus. Secondary outcomes included rate of 30-day readmission, length of stay (LOS), postoperative opioid and laxative use, time to initiation of oral diet, and return of bowel function (ROBF) as demonstrated by recorded bowel movement. There was no statistical difference observed in primary outcome of postoperative ileus between alvimopan and no alvimopan groups (2.7% vs 4.3%, p=1). Secondary outcomes such as length of stay (5.4 days vs 5.4 days, p=0.49), length of postoperative stay (5 vs 4.9, p=0.44), days to oral diet (0.9 vs 0.4, p=0.16), time to BM (1.8 vs 2.2, p=0.32), and 30-day readmission were also similar between the two groups. The similar outcome profiles in all primary and secondary outcomes do not support the use of alvimopan in the setting of laparoscopic intra-abdominal surgery.
术后肠梗阻是肠道蠕动的短暂停止,发生在肠道切除术后,其特征为腹胀、腹痛、恶心、呕吐以及肠道内气体/液体积聚。它与术后发病率的增加以及住院时间延长或再次入院有关。阿维莫潘是一种新型外周μ受体拮抗剂,适用于预防接受腹腔内手术或肠道切除术的患者发生术后肠梗阻。本研究的目的是评估阿维莫潘在腹腔镜腹部手术中的应用效果。为评估阿维莫潘在腹腔镜腹部手术中的应用效果,对84例接受腹腔镜手术并使用阿维莫潘的患者(2018年9月1日至2018年10月31日)进行了回顾性病历审查,并与未使用阿维莫潘的患者(由于全国性药物短缺,为2018年5月1日至2018年6月30日)进行比较。主要结局是术后肠梗阻的发生率。次要结局包括30天再入院率、住院时间、术后阿片类药物和泻药的使用情况、开始经口饮食的时间以及通过记录的排便情况证明的肠道功能恢复情况。阿维莫潘组和未使用阿维莫潘组在术后肠梗阻的主要结局方面未观察到统计学差异(2.7%对4.3%,p = 1)。两组在次要结局如住院时间(5.4天对5.4天,p = 0.49)、术后住院时间(5天对4.9天,p = 0.44)、开始经口饮食的天数(0.9天对0.4天,p = 0.16)、排便时间(1.8天对2.2天,p = 0.32)以及30天再入院率方面也相似。所有主要和次要结局中相似的结果并不支持在腹腔镜腹腔内手术中使用阿维莫潘。