VanderWielen Beth A, Storm Andrew C, Schroeder Darrel R, Sprung Juraj, Weingarten Toby N
Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, 200 1St Street SW, Rochester, MN, 55905, USA.
Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine and Science, Rochester, MN, USA.
Surg Endosc. 2024 Dec;38(12):7227-7232. doi: 10.1007/s00464-024-11327-3. Epub 2024 Oct 9.
Both the transoral gastric reduction (TORe) and endoscopic sleeve gastroplasty (ESG) procedures are novel endoscopic bariatric and metabolic therapies (EBMT). Our practice has an aggressive approach to prophylaxis of postoperative nausea and vomiting (PONV) for EBMT cases, but there is divergence of practice regarding use of prophylactic neurokinin-1 receptor (NK-1) antagonists (aprepitant, fosaprepitant). Herein, we determined the incidence of PONV and its potential association with NK-1 antagonist administration following EBMT.
We identified and reviewed medical records of patients who underwent EBMT between 2018 and 2023. Patients were divided into those administered or not administered an NK-1 antagonist. We analyzed rates of PONV, which was defined as rescue antiemetics during anesthesia recovery. A propensity score was calculated, and outcomes were assessed using generalized estimating equations with inverse probability of treatment weighting (IPTW).
We identified 404 patients undergoing EBMT (256 [63%] TORe, 148 [37%] ESG), and of these 253 patients developed PONV, (62.6% [95% CI: 57.9% to 67.3%]). NK-1 antagonists were administered to 119 (29.5%) patients. PONV was experienced by 42 (35%) and 211 (74%) of patients who were or were not administered an NK-1 antagonist, respectively (IPTW OR = 0.18, [95%CI: 0.10 to 0.31], P < 0.001).
EBMT has a high incidence of PONV during anesthesia recovery. Administration of a NK-1 antagonist as part of a multiagent PONV prophylaxis regimen dramatically reduces risk for this common adverse event.
经口胃减容术(TORe)和内镜下袖状胃成形术(ESG)均为新型内镜下减肥与代谢治疗(EBMT)方法。我们的医疗团队对EBMT病例的术后恶心呕吐(PONV)预防采取积极措施,但在预防性使用神经激肽-1受体(NK-1)拮抗剂(阿瑞匹坦、福沙匹坦)方面存在实践差异。在此,我们确定了EBMT后PONV的发生率及其与NK-1拮抗剂给药的潜在关联。
我们识别并回顾了2018年至2023年间接受EBMT的患者的病历。患者被分为接受或未接受NK-1拮抗剂治疗的两组。我们分析了PONV的发生率,PONV定义为麻醉恢复期间使用补救性止吐药的情况。计算倾向评分,并使用具有治疗权重逆概率(IPTW)的广义估计方程评估结果。
我们确定了404例接受EBMT的患者(256例[63%]为TORe,148例[37%]为ESG),其中253例患者发生了PONV(62.6%[95%CI:57.9%至67.3%])。119例(29.5%)患者接受了NK-Ⅰ拮抗剂治疗。接受或未接受NK-1拮抗剂治疗的患者中,分别有42例(35%)和211例(74%)发生了PONV(IPTW OR = 0.18,[95%CI:0.10至0.31],P < 0.001)。
EBMT在麻醉恢复期间PONV的发生率较高。作为多药物PONV预防方案的一部分使用NK-1拮抗剂可显著降低这一常见不良事件的风险。