首页> 外文期刊>Journal of Thoracic Disease >Novel risk model for predicting acute adverse drug reactions following cardiac catheterization from TRUST study (The Safety and toleRability of UltraviSt in Patients Undergoing Cardiac CaTheterization)
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Novel risk model for predicting acute adverse drug reactions following cardiac catheterization from TRUST study (The Safety and toleRability of UltraviSt in Patients Undergoing Cardiac CaTheterization)

机译:一种新的风险模型,可通过TRUST研究预测心脏导管插入后的急性药物不良反应(接受心脏导管插入术的患者的UltraviSt的安全性和耐受性)

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Background: Acute drug reactions (ADRs) are common complications of contrast administration following cardiac catheterization. Serious reactions may be life threatening. However, few risk models for predicting ADRs exist. The study aims to develop a novel tool for predicting the risk of ADRs [occurring within 1 hour in patients undergoing coronary angiography or percutaneous coronary intervention (PCI)]. Methods: A total of 17,139 consecutive patients included in the TRUST study were randomly (2:1) assigned to a development data set (n=11,426) or a validation data set (n=5,713). Multivariate logistic regression was applied to identify independent predictors of contrast-induced nephropathy (CIN), including age, contrast dose, premedication, and prehydration. The performance of our model was assessed using the c-statistic for discrimination and the Hosmer-Lemeshow test for calibration. Results: The overall incidence of ADRs was 42 (0.37%) in the development data set: 0.09% in the low-risk category (score: 0–2), 0.36% in the moderate-risk category (score: 3–4), and 1.78% in the high-risk category (score ≥5). The risk score across the subgroup of the study population exhibited good discrimination and predictive ability for ADRs (c-statistic: 0.694). Meanwhile, the calibration was also demonstrated to be accurate by the Hosmer-Lemeshow goodness-of-fit test (P=0.305). Conclusions: Our data showed that our simple risk model showed good discrimination and predictive ability of ADRs following cardiac catheterization.
机译:背景:急性药物反应(ADR)是心脏导管插入术后对比剂给药的常见并发症。严重的反应可能会危及生命。但是,几乎没有用于预测ADR的风险模型。这项研究旨在开发一种新的工具来预测ADR的风险[在接受冠状动脉造影或经皮冠状动脉介入治疗(PCI)的患者1小时内发生]。方法:将TRUST研究中包括的17,139名连续患者随机(2:1)分配至发展数据集(n = 11,426)或验证数据集(n = 5,713)。应用多因素logistic回归来确定造影剂诱发的肾病(CIN)的独立预测因子,包括年龄,造影剂剂量,用药前和水合。使用c统计量进行判别,并使用Hosmer-Lemeshow检验进行校准,评估模型的性能。结果:在发展数据集中,ADR的总发生率为42(0.37%):低风险类别(得分:0-2)为0.09%,中风险类别(得分:3-4)为0.36% ,高危类别(得分≥5)为1.78%。研究人群亚组的风险评分显示出良好的区分性和对ADR的预测能力(c统计:0.694)。同时,Hosmer-Lemeshow拟合优度检验也证明校准是准确的(P = 0.305)。结论:我们的数据表明,我们简单的风险模型显示出良好的辨别力和心脏导管术后ADR的预测能力。

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