Gmehlin Cameron G, Nemet Marko, Rizwan Zeeshan M, Ahmad Sumera, Gajic Ognjen, Tekin Aysun
Department of Internal Medicine, Mayo Clinic, Rochester, MN.
Department of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN.
Crit Care Explor. 2025 May 14;7(5):e1263. doi: 10.1097/CCE.0000000000001263. eCollection 2025 May 1.
Patients admitted to the ICU often experience gastrointestinal complications. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have become increasingly prevalent in the treatment of type 2 diabetes mellitus and obesity, and there is evidence that their use may be associated with an increased risk of clinically significant gastrointestinal events. However, their impact on critically ill patients admitted to the medical ICU is unknown.
This study examined whether pre-ICU use of GLP-1RAs was associated with increased incidence of gastrointestinal complications and hospitalization outcomes.
DESIGN, SETTING AND PARTICIPANTS: Multicenter, retrospective cohort study of critically ill patients admitted to academic and community hospitals of Mayo Clinic Health System from January 1, 2018, to December 31, 2023. Patients who were admitted to surgical ICUs and those who were exposed to GLP-1RA medications before but did not have an active prescription within 30 days of admission were excluded. Patients exposed to GLP-1RA were matched with those nonexposed in a 1:1 fashion based on demographic factors, factors affecting gastrointestinal motility, overall illness burden, and clinical acuity.
Outcomes of interest were the development of gastrointestinal dysfunction, ICU- and hospital-free days, and mortality.
A total of 31,327 patients with diabetes or obesity were identified of whom these, 631 were exposed to GLP-1RA before admission. In the matched cohort of 1262 patients, baseline variables were evenly distributed between the two groups. There were no significant differences in the odds of developing nausea/vomiting, constipation, ileus, obstruction, impaction, or aspiration pneumonia between the GLP-1RA exposed and unexposed groups. Similarly, ICU and hospital mortality rates were comparable across the two groups. However, GLP-1RA exposed patients had significantly more hospital-free days compared with unexposed patients (estimate, 1.19; 95% CI, 0.38-2.0; p = 0.004).
GLP-1RA exposure was not associated with increased odds of clinically significant gastrointestinal complications in nonsurgical critically ill patients. Increased hospital-free days observed among GLP-1RA exposed patients requires further study.
入住重症监护病房(ICU)的患者常出现胃肠道并发症。胰高血糖素样肽-1受体激动剂(GLP-1RAs)在2型糖尿病和肥胖症的治疗中越来越普遍,有证据表明其使用可能与临床上显著的胃肠道事件风险增加有关。然而,它们对入住内科ICU的重症患者的影响尚不清楚。
本研究调查了ICU前使用GLP-1RAs是否与胃肠道并发症发生率增加及住院结局相关。
设计、设置和参与者:对2018年1月1日至2023年12月31日入住梅奥诊所医疗系统学术和社区医院的重症患者进行多中心回顾性队列研究。排除入住外科ICU的患者以及那些在入院前30天内曾接触过GLP-1RA药物但入院时没有有效处方的患者。根据人口统计学因素、影响胃肠动力的因素、总体疾病负担和临床严重程度,将接触GLP-1RA的患者与未接触者按1:1的比例进行匹配。
关注的结局是胃肠道功能障碍的发生、无ICU和无医院天数以及死亡率。
共确定了31327例糖尿病或肥胖患者,其中631例在入院前接触过GLP-1RA。在1262例患者的匹配队列中,两组间基线变量分布均匀。GLP-1RA暴露组和未暴露组在发生恶心/呕吐、便秘、肠梗阻、阻塞、粪嵌塞或吸入性肺炎的几率上无显著差异。同样,两组间ICU和医院死亡率相当。然而,与未暴露患者相比,GLP-1RA暴露患者的无医院天数显著更多(估计值为1.19;95%置信区间为0.38 - 2.0;p = 0.004)。
在非手术重症患者中,接触GLP-1RA与临床上显著的胃肠道并发症几率增加无关。GLP-1RA暴露患者中观察到的无医院天数增加需要进一步研究。