Chen Shanshan, Liao Dehua, Yang Minghua, Wang Shengfeng
Department of Pharmacy, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan 410013, China.
Postdoctoral Research Station of Clinical Medicine and Department of Pediatrics, The Third Xiangya Hospital, Central South University, Changsha, Hunan 410013, China.
Thromb Res. 2023 Feb;222:20-23. doi: 10.1016/j.thromres.2022.12.002. Epub 2022 Dec 18.
There is a scarcity of data on anticoagulation-related nephropathy (ARN) caused by direct-acting oral anticoagulants (DOACs) in recent years.
We collected literatures on DOACs-induced ARN to October 1, 2022, without language restrictions for retrospective analysis.
Twenty events were included with a median onset time of 28 days among which fourteen were caused by dabigatran. Patients accompanied by chronic kidney disease (85 %) seemed more easily to have an ARN. Clinical symptoms associated with ARN were mostly presented as hematuria and acute decline of renal function (100 %), then abnormal coagulation function (75 %) but only one with an INR over 3. Renal biopsies were performed in 14 patients, with thirteen showing occlusive intratubular red blood cell casts and ten showing acute tubular injury of varying intensity or even tubular necrosis. Extensive changes in interstitial compartment like hemorrhage, fibrosis or inflammation were also presented in eight biopsies. IgA nephropathy as a latent or undiagnosed disease was demonstrated in eight biopsies. Treatments of ARN were mainly supportive with all patients discontinuing DOACs and 35 % initiating dialysis for acute deterioration of renal function. Steroids were used in 9 patients with a severe ARN verified by biopsy. 60 % of patients did not recover baseline renal function and some even deteriorated.
In conclusion, DOACs-induced ARN is a rare but serious adverse reaction. A prompt diagnosis of ARN and supportive treatments are necessary for patients receiving DOACs concurrent with an acute renal injury.
近年来,关于直接口服抗凝剂(DOACs)引起的抗凝相关肾病(ARN)的数据稀缺。
我们收集了截至2022年10月1日关于DOACs诱导的ARN的文献,无语言限制,进行回顾性分析。
纳入20例事件,中位发病时间为28天,其中14例由达比加群引起。伴有慢性肾脏病的患者(85%)似乎更容易发生ARN。与ARN相关的临床症状主要表现为血尿和肾功能急性下降(100%),其次是凝血功能异常(75%),但只有1例国际标准化比值(INR)超过3。14例患者进行了肾活检,13例显示肾小管内红细胞管型阻塞,10例显示不同程度的急性肾小管损伤甚至肾小管坏死。8例活检还出现了间质广泛改变,如出血、纤维化或炎症。8例活检显示IgA肾病为潜在或未确诊疾病。ARN的治疗主要是支持性治疗,所有患者停用DOACs,35%的患者因肾功能急性恶化开始透析。9例经活检证实为严重ARN的患者使用了类固醇。60%的患者肾功能未恢复至基线水平,部分患者甚至病情恶化。
总之,DOACs诱导的ARN是一种罕见但严重的不良反应。对于接受DOACs且并发急性肾损伤的患者,及时诊断ARN并给予支持性治疗是必要的。