冠状动脉造影和经皮冠状动脉介入治疗后放射性造影剂引起的急性肾损伤:一项回顾性队列研究

Van Bui Pham, Quang Dung Nguyen, Nghia Huynh Thi Nguyen, Thanh Phuong Pham Nguyen, Thanh Liem Vo, Minh Cuong Duong
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引用次数: 0

摘要

尽管冠状动脉造影(CA)/经皮冠状动脉介入治疗(PCI)在诊断和治疗冠状动脉疾病方面取得了显著的技术进步,但造影剂诱导的急性肾损伤(CI-AKI)一直是医院获得性AKI的重要原因。越南大多数当地CI-AKI研究样本量小,CA或PCI干预后仅24-48小时的短期随访,导致结论存在争议。我们对2014年1月至2015年3月在越南胡志明市Nguyen Tri Phuong大学公立医院和Tam Duc私立心脏病学中心接受CA/ PCI的成年患者在较长随访期间的CI-AKI发生率和相关危险因素进行了研究。这两家医院的所有320例CA/PCI患者被纳入回顾性队列研究。从患者记录中收集有关人口统计数据、治疗和实验室检测结果的信息。CA/PCI术后24、48、72和≥72小时CI-AKI总累积发生率分别为6.7%、12%、14%和16.9%。CI-AKI的预后因素包括干预前清除率肌酐升高1 ml/min/1,73m²(P = 0.006,风险比(HR) = 0.970, 95%CI 0.949 ~ 0.991),射血分数升高1% (P = 0.023, HR = 0.984, 95%CI 0.970 ~ 0.998)。CA/PCI干预后迟发性CI-AKI并不罕见。因此,干预后较长时间内监测血清肌酐,及时发现CI-AKI至关重要。此外,诸如紧急干预、慢性肾脏疾病和射血分数< 45%等危险因素的信息可以帮助预测CI-AKI的发展。
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Radiocontrast-Induced Acute Kidney Injury Following Coronary Angiography and Percutaneous Coronary Intervention: A Retrospective Cohort Study
Despite the remarkable technological advances in coronary angiography (CA)/percutaneous coronary intervention (PCI) for diagnosis and treatment of coronary artery disease, the contrast-induced acute kidney injury (CI-AKI) is always an important cause of hospital-acquired AKI. Most local CI-AKI studies in Vietnam had small sample sizes and short-term follow-up of only 24-48 hours following CA or PCI intervention, resulting in controversial conclusions. We conducted a study of the incidence of CI-AKI during a longer follow-up time period and associated risk factors among adult patients undergoing CA/ PCI at Nguyen Tri Phuong University Public Hospital and Tam Duc Private Cardiology Center in Ho Chi Minh City, Vietnam between January 2014 and March 2015. All 320 patients with CA/PCI at the two hospitals were enrolled in a retrospective cohort study. Information on demographic data, treatment, and laboratory test results was collected from the patients’ records. The total cumulative incidence of CI-AKI at 24, 48, 72 and ≥72 hours following CA/PCI was 6.7%, 12%, 14% and 16.9% respectively. Prognostic factors for CI-AKI included an increase by 1 ml/min/1,73m² in clearance creatinine before the intervention (P = 0.006, Hazard Ratio (HR) = 0.970, 95%CI 0.949 – 0.991) and an increase by 1% in ejection fraction (P = 0.023, HR = 0.984, 95%CI 0.970 – 0.998). Delayed CI-AKI was not rare after CA/PCI intervention. Therefore, it is pivotal to monitor serum creatinine in a longer time after the intervention to timely detect CI-AKI. Also, information on risk factors such as emergency interventions, chronic kidney disease, and ejection fraction < 45% could assist in predicting CI-AKI development.
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