Dönmez Esra, Özcan Sevgi, İnce Orhan, Şahin İrfan, Okuyan Ertuğrul
Department of Cardiology, Bagcılar Training and Research Hospital, İstanbul, Türkiye.
Turk Kardiyol Dern Ars. 2023 Mar;51(2):97-103. doi: 10.5543/tkda.2022.46994.
Contrast-induced nephropathy (CIN) is one of the well-known complications of cardiac catheterization and related with in-hospital and long-term morbidity and mortality. We aimed to evaluate if CHA2DS2-VASc score can also be used as a surrogate for CIN development and moreover the relationship between CIN development and in-hospital major adverse cardiac events (MACE) in patients presenting with STEMI and undergoing primary PCI.
All patients presented with STEMI and underwent primary PCI between 2015-2019 in our center were included retrospectively.
A total of 572 patients were included. Age [P = 0.032, β: 0.153, odds ratio (95% CI): 0.014-0.302], diabetes mellitus [(P = 0.023, β: 0.134, odds ratio (95% CI): 0.017-0.217], history of stroke [P = 0.034, β: 0.118, OR (95% CI): 0.017-0.436], volume of contrast medium [P = 0.042, β: 0.155, OR (95% CI): 0.109-0.462], left ventricular ejection fraction [P = 0.003, β: 0.376, OR (95% CI): 0.214-0.517], and CHA2DS2-VASc score [P = 0.001, β: 0.115, OR (95% CI): 0.054-0.177] were detected as independent risk factors associated with contrast-induced nephropathy development. The area under the curve for CHA2DS2-VASc score was 0.809 (95% CI: 0.760-0.857). A cut-off value of 2.5 for CHA2DS2-VASc score was associated with 80.1% sensitivity and 71.4% specificity in the prediction of contrast-induced nephropathy development.
Our current study showed that the CHA2DS2-VASc risk score has an effective discriminating power in determining the contrast-induced nephropathy development and a score ≥2 defines the group at risk in patients presenting with ST-elevation myocardial infarction and underwent primary percutaneous coronary intervention. Moreover, contrast-induced nephropathy development is associated with longer coronary care unit stay and major adverse cardiac events (in-hospital decompensated heart failure, cardiogenic shock, cardiac arrest, and mortality).
造影剂肾病(CIN)是心脏导管插入术常见的并发症之一,与住院期间及长期的发病率和死亡率相关。我们旨在评估CHA2DS2-VASc评分是否也可作为CIN发生的替代指标,以及在ST段抬高型心肌梗死(STEMI)患者接受直接经皮冠状动脉介入治疗(PCI)时CIN发生与住院期间主要不良心脏事件(MACE)之间的关系。
回顾性纳入2015年至2019年在我们中心就诊且接受直接PCI的所有STEMI患者。
共纳入572例患者。年龄[P = 0.032,β:0.153,比值比(95%可信区间):0.014 - 0.302]、糖尿病[(P = 0.023,β:0.134,比值比(95%可信区间):0.017 - 0.217]、卒中史[P = 0.034,β:0.118,OR(95%可信区间):0.017 - 0.436]、造影剂用量[P = 0.042,β:0.155,OR(95%可信区间):0.109 - 0.462]、左心室射血分数[P = 0.003,β:0.376,OR(95%可信区间):0.214 - 0.517]以及CHA2DS2-VASc评分[P = 0.001,β:0.115,OR(95%可信区间):0.054 - 0.177]被检测为与造影剂肾病发生相关的独立危险因素。CHA2DS2-VASc评分的曲线下面积为0.809(95%可信区间:0.760 - 0.857)。CHA2DS2-VASc评分截断值为2.5时,预测造影剂肾病发生的敏感度为80.1%,特异度为71.4%。
我们目前的研究表明,CHA2DS2-VASc风险评分在确定造影剂肾病发生方面具有有效的鉴别能力,评分≥2可定义ST段抬高型心肌梗死且接受直接经皮冠状动脉介入治疗患者中的高危组。此外,造影剂肾病的发生与冠心病监护病房住院时间延长及主要不良心脏事件(住院期间失代偿性心力衰竭、心源性休克、心脏骤停和死亡)相关。