Qiangqiang Zhou, Hongyu Xu, Shengrong Long, Wei Wei, Xiang Li
{"title":"缺血性卒中合并急性肾损伤患者联合抗血小板治疗的死亡风险分析:MIMIC-IV数据库的回顾性队列分析","authors":"Qiangqiang Zhou, Hongyu Xu, Shengrong Long, Wei Wei, Xiang Li","doi":"10.3390/diseases13050141","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Ischemic stroke (IS), a major cerebrovascular disease, is associated with high disability and mortality rates. Acute kidney injury (AKI) often complicates IS and increases in-hospital mortality. While antiplatelet agents are commonly used for IS treatment, their effectiveness in IS patients with AKI is unclear.</p><p><strong>Methods: </strong>This study, using data from the MIMIC-IV database, divided patients into non-combination (clopidogrel or ticagrelor alone) and combination (with aspirin) groups. The primary outcome was 28-day mortality, with secondary outcomes including 90-day, 1-year, and in-hospital mortality. Multivariable Cox and logistic regression models were used to analyze the relationship between antiplatelet regimens and mortality. Subgroup analyses and interaction tests were conducted.</p><p><strong>Results: </strong>Results showed the combination group had lower 28-day, 90-day, 1-year, and in-hospital mortality risks than the non-combination group (all <i>p</i> < 0.001). Subgroup analysis revealed an interaction effect by AKI stage, with combination therapy not significantly reducing mortality in severe AKI (stages 2 and 3, <i>p</i> = 0.743, <i>p</i> = 0.244).</p><p><strong>Conclusions: </strong>This study demonstrates that combination antiplatelet therapy significantly reduces 28-day, 90-day, 1-year, and in-hospital mortality risks of IS patients with AKI, suggesting its potential benefits in improving both short- and long-term clinical outcomes. However, this does not apply to patients with severe AKI, indicating heterogeneous survival benefits of combination therapy across AKI severity. Clinical decision-making should incorporate AKI stage stratification to evaluate the applicability of combination antiplatelet therapy. Further research is needed to explore the impact of AKI staging on antiplatelet therapy in IS patients.</p>","PeriodicalId":72832,"journal":{"name":"Diseases (Basel, Switzerland)","volume":"13 5","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12110695/pdf/","citationCount":"0","resultStr":"{\"title\":\"Mortality Risk Analysis of Combination Antiplatelet Therapy in Patients with Ischemic Stroke and Acute Kidney Injury: A Retrospective Cohort Analysis of the MIMIC-IV Database.\",\"authors\":\"Qiangqiang Zhou, Hongyu Xu, Shengrong Long, Wei Wei, Xiang Li\",\"doi\":\"10.3390/diseases13050141\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Ischemic stroke (IS), a major cerebrovascular disease, is associated with high disability and mortality rates. Acute kidney injury (AKI) often complicates IS and increases in-hospital mortality. While antiplatelet agents are commonly used for IS treatment, their effectiveness in IS patients with AKI is unclear.</p><p><strong>Methods: </strong>This study, using data from the MIMIC-IV database, divided patients into non-combination (clopidogrel or ticagrelor alone) and combination (with aspirin) groups. The primary outcome was 28-day mortality, with secondary outcomes including 90-day, 1-year, and in-hospital mortality. Multivariable Cox and logistic regression models were used to analyze the relationship between antiplatelet regimens and mortality. Subgroup analyses and interaction tests were conducted.</p><p><strong>Results: </strong>Results showed the combination group had lower 28-day, 90-day, 1-year, and in-hospital mortality risks than the non-combination group (all <i>p</i> < 0.001). Subgroup analysis revealed an interaction effect by AKI stage, with combination therapy not significantly reducing mortality in severe AKI (stages 2 and 3, <i>p</i> = 0.743, <i>p</i> = 0.244).</p><p><strong>Conclusions: </strong>This study demonstrates that combination antiplatelet therapy significantly reduces 28-day, 90-day, 1-year, and in-hospital mortality risks of IS patients with AKI, suggesting its potential benefits in improving both short- and long-term clinical outcomes. However, this does not apply to patients with severe AKI, indicating heterogeneous survival benefits of combination therapy across AKI severity. Clinical decision-making should incorporate AKI stage stratification to evaluate the applicability of combination antiplatelet therapy. 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引用次数: 0
摘要
背景:缺血性脑卒中是一种主要的脑血管疾病,具有高致残率和高死亡率。急性肾损伤(AKI)常使IS并发症并增加住院死亡率。虽然抗血小板药物通常用于IS治疗,但其在合并AKI的IS患者中的有效性尚不清楚。方法:本研究使用MIMIC-IV数据库的数据,将患者分为非联用组(氯吡格雷或替格瑞洛单独用药)和联用组(与阿司匹林联合用药)。主要结局是28天死亡率,次要结局包括90天、1年和住院死亡率。采用多变量Cox和logistic回归模型分析抗血小板方案与死亡率的关系。进行亚组分析和交互作用试验。结果:联合用药组28天、90天、1年及院内死亡风险均低于非联合用药组(p < 0.001)。亚组分析显示AKI分期的相互作用,联合治疗不能显著降低严重AKI(2期和3期,p = 0.743, p = 0.244)的死亡率。结论:本研究表明,联合抗血小板治疗可显著降低IS合并AKI患者28天、90天、1年和住院死亡风险,提示其在改善短期和长期临床结果方面具有潜在益处。然而,这并不适用于严重AKI患者,这表明不同AKI严重程度的联合治疗的生存益处是不同的。临床决策应结合AKI分期分层来评估联合抗血小板治疗的适用性。AKI分期对is患者抗血小板治疗的影响有待进一步研究。
Mortality Risk Analysis of Combination Antiplatelet Therapy in Patients with Ischemic Stroke and Acute Kidney Injury: A Retrospective Cohort Analysis of the MIMIC-IV Database.
Background: Ischemic stroke (IS), a major cerebrovascular disease, is associated with high disability and mortality rates. Acute kidney injury (AKI) often complicates IS and increases in-hospital mortality. While antiplatelet agents are commonly used for IS treatment, their effectiveness in IS patients with AKI is unclear.
Methods: This study, using data from the MIMIC-IV database, divided patients into non-combination (clopidogrel or ticagrelor alone) and combination (with aspirin) groups. The primary outcome was 28-day mortality, with secondary outcomes including 90-day, 1-year, and in-hospital mortality. Multivariable Cox and logistic regression models were used to analyze the relationship between antiplatelet regimens and mortality. Subgroup analyses and interaction tests were conducted.
Results: Results showed the combination group had lower 28-day, 90-day, 1-year, and in-hospital mortality risks than the non-combination group (all p < 0.001). Subgroup analysis revealed an interaction effect by AKI stage, with combination therapy not significantly reducing mortality in severe AKI (stages 2 and 3, p = 0.743, p = 0.244).
Conclusions: This study demonstrates that combination antiplatelet therapy significantly reduces 28-day, 90-day, 1-year, and in-hospital mortality risks of IS patients with AKI, suggesting its potential benefits in improving both short- and long-term clinical outcomes. However, this does not apply to patients with severe AKI, indicating heterogeneous survival benefits of combination therapy across AKI severity. Clinical decision-making should incorporate AKI stage stratification to evaluate the applicability of combination antiplatelet therapy. Further research is needed to explore the impact of AKI staging on antiplatelet therapy in IS patients.