Department of Surgery, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Division of Cardiovascular Surgery, Department of Surgery, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan.
Sci Rep. 2020 Jul 22;10(1):12135. doi: 10.1038/s41598-020-69019-6.
While the patency of vascular access is essential for hemodialysis patients, optimal pharmaceutical treatment to maintain arteriovenous fistula (AVF) patency remains lacking. As cardiovascular diseases are highly prevalent in patients with end-stage renal disease, various cardiovascular medications have also been used to maintain AVF patency. However, previous studies revealed inconsistent therapeutic effects and a comprehensive evaluation of this issue is needed. The present retrospective, longitudinal cohort study included patients receiving successful AVF creation. The evaluated cardiovascular medications included antiplatelet agents, antihypertensive agents, nitrates and nitrites, statins, dipyridamole, and pentoxifylline. The outcome was AVF primary patency. All laboratory data and medication profiles were recorded at baseline and followed at 3-month interval, until the end of the 2-year study period. Cox proportional regression model with time-dependent covariates was used to evaluate the risk for AVF patency loss. A total of 349 patients were included in the present study, in which 57% were men and the mean age was 65 ± 14 years. Among the included patients, 40% used antiplatelet agents, 27% used dipyridamole and 36% used statins at baseline. Of all the evaluated cardiovascular medications, only dipyridamole showed significant association with a higher risk for loss of AVF patency. To evaluate the effect of combination of antiplatelet agents and dipyridamole, the patients were classified into four groups, I: combine use of antiplatelet agents and dipyridamole, II: antiplatelet only, III: dipyridamole only; IV: none of both were used. Of the four groups, group IV exhibited highest AVF patency (52.4%), which was followed by group III (42.7%), group II (40%), and group I (28.6%), respectively. Compared with group IV, only group I showed a significantly higher risk for AVF patency loss. None of the cardiovascular medications evaluated in the present study showed a beneficial effect on AVF patency. Furthermore, dipyridamole showed an association with a higher risk of AVF patency loss. We do not suggest a beneficial effect of dipyridamole on maintaining AVF patency, particularly in combination with antiplatelet agents.
虽然血管通路的通畅对于血液透析患者至关重要,但维持动静脉瘘(AVF)通畅的最佳药物治疗仍存在不足。由于心血管疾病在终末期肾病患者中非常普遍,因此也使用了各种心血管药物来维持 AVF 的通畅。然而,先前的研究显示出治疗效果不一致,因此需要对此问题进行全面评估。本回顾性、纵向队列研究纳入了接受成功 AVF 建立的患者。评估的心血管药物包括抗血小板药物、降压药、硝酸盐和亚硝酸盐、他汀类药物、双嘧达莫和己酮可可碱。主要结局为 AVF 初始通畅率。所有实验室数据和药物使用情况均在基线时记录,并在 3 个月的间隔内随访,直至 2 年研究结束。使用具有时间依赖性协变量的 Cox 比例风险回归模型来评估 AVF 通畅丧失的风险。本研究共纳入 349 例患者,其中 57%为男性,平均年龄为 65±14 岁。在纳入的患者中,40%在基线时使用抗血小板药物,27%使用双嘧达莫,36%使用他汀类药物。在所有评估的心血管药物中,只有双嘧达莫与 AVF 通畅丧失的风险增加显著相关。为了评估抗血小板药物和双嘧达莫联合使用的效果,将患者分为四组:I 组:联合使用抗血小板药物和双嘧达莫;II 组:仅使用抗血小板药物;III 组:仅使用双嘧达莫;IV 组:两者均未使用。四组中,AVF 通畅率最高的是 IV 组(52.4%),其次是 III 组(42.7%)、II 组(40%)和 I 组(28.6%)。与 IV 组相比,仅 I 组的 AVF 通畅丧失风险显著增加。本研究评估的心血管药物均未显示对 AVF 通畅有有益作用。此外,双嘧达莫与 AVF 通畅丧失的风险增加相关。我们不建议双嘧达莫对维持 AVF 通畅有有益作用,尤其是与抗血小板药物联合使用时。