Early administration of ketorolac after cardiac surgery and postoperative complications: Analysis of the MIMIC-IV database

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Cts-Clinical and Translational Science Pub Date : 2024-08-05 DOI:10.1111/cts.13907
Yi Liu, Bo Pan, Jie Liu, Jun Zhang
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Abstract

Inflammation may contribute to postoperative cardiac complications and ketorolac, an anti-inflammatory agent inhibiting cyclooxygenase (COX), shows promise in enhancing cardiac graft patency by suppressing endothelial cell proliferation in animal studies. However, the safety of postoperative ketorolac use remains controversial. This study investigates the association between early ketorolac application and complications following cardiac surgery. Data from the Medical Information Mart for Intensive Care-IV (MIMIC-IV) database fueled this retrospective cohort study. The primary outcome is a composite of mortality, pulmonary insufficiency, severe acute kidney injury (AKI), hemorrhage or hematoma, infection, cardiogenic shock, and cerebrovascular infarction postcardiac surgery. Propensity score matching (PSM; 1:1 match, caliper 0.2), multivariate logistic regression, interaction stratification analysis, pairwise algorithmic, and overlap weight model analyses were employed. Following inclusion and exclusion criteria, 7143 patients who underwent valvular surgery or coronary artery bypass grafting (CABG) were included. PSM created a balanced cohort of 3270 individuals (1635 in the ketorolac group). The matched cohort exhibited an 8.1% overall rate of postoperative complications, with a lower composite outcome rate in patients receiving ketorolac within 48 h of surgery compared with those without (PSM, OR 0.70 [95% CI, 0.54–0.90]). Consistent associations were observed in total cohort analyses, sensitivity, and subgroup analyses. Early ketorolac use within 48 h post-CABG or valvular procedures in adults is independently associated with a lower incidence of composite postoperative adverse events. Prospective trials are warranted to assess causality.

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心脏手术后尽早使用酮咯酸与术后并发症:MIMIC-IV 数据库分析。
炎症可能会导致术后心脏并发症,而酮咯酸是一种抑制环氧化酶(COX)的消炎药,在动物实验中,它可以通过抑制内皮细胞增殖来提高心脏移植物的通畅性。然而,术后使用酮咯酸的安全性仍存在争议。本研究调查了早期使用酮咯酸与心脏手术后并发症之间的关系。这项回顾性队列研究的数据来自重症监护医学信息市场-IV(MIMIC-IV)数据库。主要研究结果是心脏手术后死亡率、肺功能不全、严重急性肾损伤(AKI)、出血或血肿、感染、心源性休克和脑血管梗塞的综合结果。研究采用了倾向评分匹配(PSM;1:1 匹配,卡尺 0.2)、多变量逻辑回归、交互分层分析、配对算法和重叠权重模型分析。根据纳入和排除标准,共纳入了 7143 名接受瓣膜手术或冠状动脉旁路移植术(CABG)的患者。PSM 建立了一个由 3270 人组成的平衡队列(酮咯酸组有 1635 人)。匹配队列的术后并发症总发生率为 8.1%,与未接受酮咯酸治疗的患者相比,术后 48 小时内接受酮咯酸治疗的患者的综合结果率较低(PSM,OR 0.70 [95% CI,0.54-0.90])。在总体队列分析、敏感性分析和亚组分析中均观察到了一致的相关性。成人心血管造影术或瓣膜手术后 48 小时内尽早使用酮咯酸可降低术后综合不良事件的发生率。需要进行前瞻性试验来评估因果关系。
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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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