冠心病 PCI 无回流风险因素分析及相关预测模型的构建。

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
American journal of translational research Pub Date : 2024-08-15 eCollection Date: 2024-01-01 DOI:10.62347/ECNI6080
Liang Zhang, Jun Lin, Lintao Luo, Bin Liu, Xiaojuan Zeng
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引用次数: 0

摘要

目的分析冠心病(CHD)患者经皮冠状动脉介入治疗(PCI)无回流的风险因素,并构建预测性提名图模型:该回顾性研究纳入了2022年1月至2023年12月在重庆医科大学附属第三医院接受PCI治疗的260例冠心病患者。根据心肌梗死溶栓治疗(TIMI)血流分级将受试者分为 PCI 无回流组(n = 86)和正常回流组(n = 174)。收集了患者的一般数据、PCI 相关数据和实验室指标。采用逻辑回归分析冠心病患者PCI术后无血流回流的风险因素。根据回归分析中的重要变量,使用 R 语言构建了一个提名图预测模型。通过接收者操作特征曲线(ROC)和校准曲线评估了模型的准确性,并绘制了决策曲线以明确模型的临床实用性。模型的性能指标包括曲线下面积(AUC)、准确性、灵敏度和特异性:多变量逻辑回归分析表明,高血压、胱抑素C(Cys-C)、超敏c反应蛋白(hs-CRP)和血小板与淋巴细胞比值(PLR)是导致CHD患者PCI术后无再流的危险因素(OR>1,P<0.001),而ADAM金属肽酶与凝血酶原1型基序13(ADAMTS-13)和淋巴细胞(LYM)是保护因素(OR<1,P<0.001)。基于上述风险因素的提名图预测模型显示出良好的预测价值。在训练集中,提名图预测模型的AUC为0.967(95% CI:0.946-0.989),特异性为0.923,灵敏度为0.908。在验证集中,AUC 为 0.894(95% CI:0.817-0.971),特异性为 0.807,灵敏度为 0.857。校准曲线显示预测概率与实际概率之间的一致性很好,决策曲线显示在训练集和验证集的阈值概率范围内(0.0-0.99)都有临床益处:结论:影响冠心病患者PCI术后无复流的风险因素包括高血压、血清Cys-C、hs-CRP、PLR、ADAMTS-13和LYM水平。基于上述因素的提名图风险预测模型对识别 PCI 后无复流高风险患者很有价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of risk factors for PCI no-reflow in coronary heart disease and construction of related prediction models.

Objective: To analyze the risk factors of percutaneous coronary intervention (PCI) no-reflow in patients with coronary heart disease (CHD) and construct a predictive nomogram model.

Methods: This retrospective study included 260 patients with CHD who underwent PCI in the Third Affiliated Hospital of Chongqing Medical University from January 2022 to December 2023. The subjects were divided into a PCI no-reflow group (n = 86) and normal reflow group (n = 174) based on thrombolysis in myocardial infarction (TIMI) blood flow grading. General data, PCI related data and laboratory indexes of patients were collected. Logistic regression was used to analyze the risk factors of no-reflow after PCI in CHD patients. Based on the significant variables from regression analysis, a nomogram prediction model was constructed by using R language. The accuracy of the model was evaluated by receiver operating characteristic (ROC) curve and calibration curve, and the decision curve was drawn to clarify the clinical utility of the model. Model performance metrics included area under the curve (AUC), accuracy, sensitivity and specificity.

Results: Multivariate logistic regression analysis showed that hypertension, cystatin C (Cys-C), hypersensitive c-reactive protein (hs-CRP) and platelet-to-lymphocyte ratio (PLR) were risk factors for no-reflow after PCI in CHD patients (OR > 1, P < 0.001), while ADAM metallopeptidase with thrombospondin type 1 motif 13 (ADAMTS-13) and lymphocyte (LYM) were protective factors (OR < 1, P < 0.001). The nomogram prediction model based on the above risk factors showed good predictive value. The AUC of the nomogram prediction model in the training set was 0.967 (95% CI: 0.946-0.989), with a specificity of 0.923 and a sensitivity of 0.908. In the validation set, the AUC was 0.894 (95% CI: 0.817-0.971), with a specificity of 0.807 and a sensitivity of 0.857. The calibration curve indicated good agreement between the predicted and actual probabilities, and the decision curve showed clinical benefit across a range of threshold probabilities in both the training and validation sets (0.0-0.99).

Conclusion: The risk factors affecting the occurrence of no-reflow after PCI in patients with CHD include hypertension, serum Cys-C, hs-CRP, PLR, ADAMTS-13 and LYM levels. The nomogram risk prediction model based on the above factors is valuable for identifying patients with high risk of no-reflow after PCI.

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American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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