Xu Feiyi, Gong Xun, Chen Wei, Dong Xiaomin, Li Jiang
Department of Pharmacy, Affiliated Hospital of Guilin Medical University, Guilin, Guangxi, China.
University of Pharmacy, Guilin Medical University, Guilin, Guangxi, China.
Front Pharmacol. 2024 Dec 16;15:1511545. doi: 10.3389/fphar.2024.1511545. eCollection 2024.
Ondansetron is widely used for prophylaxis of postoperative nausea and vomiting (PONV) after general anesthesia. While previous studies have emphasized its early use, the effects of ondansetron in intensive care unit (ICU) patients following cardiac surgery remain unclear. This study investigates the association between postoperative ondansetron exposure and the risk of mortality, acute kidney injury (AKI), and postoperative atrial fibrillation (POAF) in ICU patients after cardiac surgery.
We conducted a retrospective cohort study utilizing data from the MIMIC-IV database. Adult patients who underwent cardiac surgery and were subsequently admitted to the ICU were included. Cox proportional hazards models were employed to assess the effect of ondansetron exposure on ICU and 28-day mortality. Multivariable logistic regression analyses examined the associations between ondansetron exposure and the incidence of AKI (2-day and 7-day) and POAF. Sensitivity analyses included Propensity Score Matching (PSM) and the inclusion of patients with ICU stays of less than 24 h to ensure robustness of results. Subgroup analyses explored the effects of age and other clinical factors, with interaction tests to examine differential impacts.
A total of 7,170 were included. The incidence of AKI was 74.4% at 2 days and 76.7% at 7 days post-surgery. The 28-day postoperative mortality rate was 1.4%, while the ICU mortality rate was 1.0%. POAF occurred in 17.4% of the patients. Ondansetron exposure was not associated with 28-day mortality or ICU mortality ( > 0.05). However, after PSM, ondansetron exposure was significantly associated with an elevated risk of AKI at 2 days (OR 1.28, 95% CI 1.13-1.45, < 0.001] and 7 days (OR 1.25, 95% CI 1.15-1.45, < 0.001), as well as POAF (OR 1.20, 95% CI 1.04-1.39, = 0.014).Subgroup analysis revealed a stronger association in patients aged over 65 years, where ondansetron was linked to an increased risk of 7-day AKI (OR 1.51, 95% CI 1.29-1.78, < 0.001) and POAF (OR 1.31, 95% CI 1.12-1.53, = 0.001). Interaction tests showed a significant interaction between ondansetron exposure and age (P for interaction = 0.018 for AKI and P for interaction = 0.02 for POAF). Sensitivity analyses, including patients with ICU stays of less than 24 h, confirmed the robustness of these findings.
In ICU patients following cardiac surgery, postoperative use of ondansetron is associated with an increased risk of both 7-day AKI and POAF, particularly in patients aged 65 years and older. These findings suggest that the use of ondansetron in this population should be approached with caution, especially in elderly patients who may be more susceptible to these complications. Further research is needed to explore the mechanisms underlying the association between ondansetron and these adverse outcomes.
昂丹司琼广泛用于全身麻醉后预防术后恶心和呕吐(PONV)。虽然先前的研究强调其早期使用,但昂丹司琼在心脏手术后重症监护病房(ICU)患者中的作用仍不清楚。本研究调查了心脏手术后ICU患者术后使用昂丹司琼与死亡率、急性肾损伤(AKI)和术后房颤(POAF)风险之间的关联。
我们利用MIMIC-IV数据库的数据进行了一项回顾性队列研究。纳入接受心脏手术并随后入住ICU的成年患者。采用Cox比例风险模型评估昂丹司琼暴露对ICU和28天死亡率的影响。多变量逻辑回归分析检查了昂丹司琼暴露与AKI(2天和7天)和POAF发生率之间的关联。敏感性分析包括倾向评分匹配(PSM)以及纳入ICU住院时间少于24小时的患者以确保结果的稳健性。亚组分析探讨了年龄和其他临床因素的影响,并进行交互检验以检查差异影响。
共纳入7170例患者。术后2天AKI发生率为74.4%,术后7天为76.7%。术后28天死亡率为1.4%,而ICU死亡率为1.0%。17.4% 的患者发生了POAF。昂丹司琼暴露与28天死亡率或ICU死亡率无关(P>0.05)。然而,PSM后,昂丹司琼暴露与术后2天(OR 1.28, 95% CI 1.13 - 1.45, P<0.001)和7天(OR 1.25, 95% CI 1.15 - 1.45, P<0.001)AKI风险升高以及POAF(OR 1.20, 95% CI 1.04 - 1.39, P = 0.014)显著相关。亚组分析显示,在65岁以上患者中关联更强,其中昂丹司琼与术后7天AKI风险增加(OR 1.51, 95% CI 1.29 - 1.78, P<0.001)和POAF(OR 1.31,95% CI 1.12 - 1.53, P = 0.001)相关。交互检验显示昂丹司琼暴露与年龄之间存在显著交互作用(AKI交互作用P值 = 0.018,POAF交互作用P值 = 0.02)。包括ICU住院时间少于24小时患者的敏感性分析证实了这些发现的稳健性。
在心脏手术后的ICU患者中,术后使用昂丹司琼与术后7天AKI和POAF风险增加相关,尤其是在65岁及以上患者中。这些发现表明,在该人群中使用昂丹司琼应谨慎,特别是在可能更容易发生这些并发症的老年患者中。需要进一步研究以探索昂丹司琼与这些不良结局之间关联的潜在机制。