Konstantinos Dakis, Petroula Nana, Konstantinos Spanos, George Apostolidis, Christos Karathanos, Athanasios Giannoukas, Christian-Alexander Behrendt, Miltiadis Matsagkas, George Kouvelos
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Studies on humans with an AVG receiving any kind of antithrombotic medication, reporting on primary and secondary patency rates, and bleeding complications were included. Due to data heterogeneity, a descriptive report of the outcomes was undertaken. <i>Results:</i> Twelve studies, including 22,436 patients with end-stage renal disease (ESRD) and AVG were included, with patient recruitment spanning over a 41-year time-period (1982-2023). Antithrombotic factors included acetylsalicylic acid (ASA), clopidogrel, dipyridamole, warfarin, unfractioned heparin (UFH), and direct oral anticoagulants (DOACs). Ten studies reported on primary patency rates, and two on secondary patency rates. Primary and secondary patency rates (PPR, SPR) were reported better in four studies, similar in three and worse in one study, regarding patients receiving any kind of antiplatelet therapy. Anticoagulation therapy was not associated with increased PPR or SPR, except for one study on apixaban. Patients receiving single or combined antiplatelets versus patients receiving no treatment presented higher bleeding risk in two studies and similar bleeding risk in three studies. Anticoagulation therapy, excluding apixaban, was associated with higher bleeding risk in three studies, when compared to no anticoagulation. <i>Conclusions:</i> Data derived from the current literature were equivocal regarding the use of antiplatelet treatment in patients with AVG. Studies on anticoagulation therapy are confined. 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Antithrombotic factors included acetylsalicylic acid (ASA), clopidogrel, dipyridamole, warfarin, unfractioned heparin (UFH), and direct oral anticoagulants (DOACs). Ten studies reported on primary patency rates, and two on secondary patency rates. Primary and secondary patency rates (PPR, SPR) were reported better in four studies, similar in three and worse in one study, regarding patients receiving any kind of antiplatelet therapy. Anticoagulation therapy was not associated with increased PPR or SPR, except for one study on apixaban. Patients receiving single or combined antiplatelets versus patients receiving no treatment presented higher bleeding risk in two studies and similar bleeding risk in three studies. 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引用次数: 0
摘要
背景:对于需要肾脏替代治疗但不适合制造动静脉瘘的患者,动静脉移植(AVG)可能是唯一的救助方案。目前,关于AVG患者抗血栓治疗的有效性和安全性的高水平证据很少。材料和方法:PICO(患者;干预;比较器;在PubMed, SCOPUS, Central Cochrane的英文文献中进行数据检索,直到2023年3月1日(PROSPERO协议号:CRD42023401785)。包括对接受抗血栓药物治疗的房颤患者的研究,报告原发性和继发性通畅率,以及出血并发症。由于数据异质性,对结果进行了描述性报告。结果:纳入了12项研究,包括22,436例终末期肾病(ESRD)和AVG患者,患者招募时间跨度为41年(1982-2023)。抗血栓因子包括乙酰水杨酸(ASA)、氯吡格雷、双嘧达莫、华法林、未分离肝素(UFH)和直接口服抗凝剂(DOACs)。10项研究报道了原发性通畅率,2项研究报道了继发性通畅率。在接受任何抗血小板治疗的患者中,有4项研究报告原发性和继发性通畅率(PPR, SPR)较好,3项研究报告相似,1项研究报告较差。除了一项关于阿哌沙班的研究外,抗凝治疗与PPR或SPR的增加无关。在两项研究中,接受单一或联合抗血小板药物治疗的患者与未接受治疗的患者相比,出血风险更高,在三项研究中,出血风险相似。在三项研究中,抗凝治疗(不包括阿哌沙班)与不进行抗凝治疗相比,出血风险更高。结论:目前文献中关于AVG患者使用抗血小板治疗的数据是模棱两可的,关于抗凝治疗的研究是有限的。混杂因素分层的随机试验对于获得可靠的长期数据仍然至关重要。
Antithrombotic therapy impact on patency and bleeding complications of arteriovenous graft placement in dialysis patients.
Background: Arteriovenous grafts (AVG) can be the only bailout solution for patients who require kidney replacement therapy but are unsuitable for arteriovenous fistula (AVF) creation. Currently, high-level evidence on the effectiveness and safety of antithrombotic therapy in AVG patients is scarce. Materials and methods: Following the PICO (patient; intervention; comparator; outcome) model and the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines, a data search of the English literature in PubMed, SCOPUS, Central Cochrane was conducted, until March 1st, 2023 (PROSPERO Protocol Number: CRD42023401785). Studies on humans with an AVG receiving any kind of antithrombotic medication, reporting on primary and secondary patency rates, and bleeding complications were included. Due to data heterogeneity, a descriptive report of the outcomes was undertaken. Results: Twelve studies, including 22,436 patients with end-stage renal disease (ESRD) and AVG were included, with patient recruitment spanning over a 41-year time-period (1982-2023). Antithrombotic factors included acetylsalicylic acid (ASA), clopidogrel, dipyridamole, warfarin, unfractioned heparin (UFH), and direct oral anticoagulants (DOACs). Ten studies reported on primary patency rates, and two on secondary patency rates. Primary and secondary patency rates (PPR, SPR) were reported better in four studies, similar in three and worse in one study, regarding patients receiving any kind of antiplatelet therapy. Anticoagulation therapy was not associated with increased PPR or SPR, except for one study on apixaban. Patients receiving single or combined antiplatelets versus patients receiving no treatment presented higher bleeding risk in two studies and similar bleeding risk in three studies. Anticoagulation therapy, excluding apixaban, was associated with higher bleeding risk in three studies, when compared to no anticoagulation. Conclusions: Data derived from the current literature were equivocal regarding the use of antiplatelet treatment in patients with AVG. Studies on anticoagulation therapy are confined. Randomized trials with confounder stratification remain crucial for robust long-term data.
期刊介绍:
Vasa is the European journal of vascular medicine. It is the official organ of the German, Swiss, and Slovenian Societies of Angiology.
The journal publishes original research articles, case reports and reviews on vascular biology, epidemiology, prevention, diagnosis, medical treatment and interventions for diseases of the arterial circulation, in the field of phlebology and lymphology including the microcirculation, except the cardiac circulation.
Vasa combines basic science with clinical medicine making it relevant to all physicians interested in the whole vascular field.