Division of Nephrology, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
PLoS One. 2018 Oct 18;13(10):e0206011. doi: 10.1371/journal.pone.0206011. eCollection 2018.
In this study, we evaluated the effects of various medications on the patency of vascular access (VA) for hemodialysis.
We analyzed data from the Longitudinal Health Insurance Database of Taiwan. We adopted a case-control study design within a cohort of patients who had received regular hemodialysis between 2002 and 2012; 34,354 patients with first VA failure were identified, and the duration from VA creation date to the first VA failure date was calculated. We then classified these patients into two groups, namely arteriovenous fistula (AVF, n = 25,933) and arteriovenous graft (AVG, n = 8,421). Each group was further divided into two subgroups, namely short-term (<1 year) and long-term (≥1 year) patency.
The risk factors for early VA failure were age ≥65 years, diabetes mellitus, hyperlipidemia, cerebral vascular disease, congestive heart failure, peripheral artery disease, and sepsis. Male sex, hypertension, cancer, and peptic ulcer were associated with early AVF failure. Antiplatelet therapy increased the AVF and AVG patency times with adjusted odds ratios of 0.748 (95% confidence interval [CI]: 0.703-0.796, p < 0.0001) and 0.810 (95% CI: 0.728-0.901, p = 0.0001), respectively. A significant decrease in the VA failure risk was observed with an increase in the cumulative defined daily dose of antiplatelet agents.
This nationwide study demonstrated that some risk factors were associated with early VA failure and that the use of antiplatelet agents prevented the loss of VA patency in a dose-response manner. Thus, antiplatelet drugs should be routinely administered to high-risk patients receiving dialysis.
本研究旨在评估各种药物对血液透析血管通路通畅率的影响。
我们分析了来自台湾地区纵向健康保险数据库的数据。我们采用病例对照研究设计,对 2002 年至 2012 年间接受常规血液透析的患者队列进行了分析;共确定了 34354 例首次血管通路失败的患者,并计算了从血管通路创建日期到首次血管通路失败日期的时间。然后,我们将这些患者分为两组:动静脉瘘(AVF,n = 25933)和动静脉移植物(AVG,n = 8421)。每组进一步分为短期(<1 年)和长期(≥1 年)通畅率亚组。
血管早期失败的危险因素包括年龄≥65 岁、糖尿病、血脂异常、脑血管疾病、充血性心力衰竭、外周动脉疾病和脓毒症。男性、高血压、癌症和消化性溃疡与早期 AVF 失败有关。抗血小板治疗增加了 AVF 和 AVG 的通畅时间,调整后的优势比分别为 0.748(95%置信区间[CI]:0.703-0.796,p < 0.0001)和 0.810(95%CI:0.728-0.901,p = 0.0001)。随着抗血小板药物累积定义日剂量的增加,VA 失败风险显著降低。
这项全国性研究表明,一些危险因素与早期血管通路失败有关,而抗血小板药物的使用以剂量反应的方式防止了血管通路通畅率的丧失。因此,应常规给予接受透析的高危患者抗血小板药物。