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环孢素相关同种异体移植血栓形成的识别与治疗。

Identification and treatment of cyclosporine-associated allograft thrombosis.

作者信息

Schlanger R E, Henry M L, Sommer B G, Ferguson R M

出版信息

Surgery. 1986 Aug;100(2):329-33.

PMID:3526606
Abstract

Endothelial injury associated with cyclosporine (CSA) therapy in the absence of rejection has resulted in irreversible intrarenal allograft thrombosis and transplant loss. Indium 111 (111In)-labeled platelet scanning is an effective way to identify those transplants that are at risk for acute loss. Two hundred prospective 111In scans were obtained (100 on allografts with normal function and 100 with transplant dysfunction of all causes). 111In scans in patients with dose-dependent CSA nephrotoxicity (N = 58) and biopsy proved acute rejection (N = 22) were negative. Grossly abnormal scans (three to eight times greater than hepatic uptake) were noted in nine recipients identified as having a hemolytic uremic-like syndrome associated with CSA use. Accelerated allograft functional loss was irreversible in six patients despite stopping CSA, systemic anticoagulation, increased steroids and antilymphocyte globulin, and infusion of fresh-frozen plasma. Three patients with grossly positive 111In scans and clinical and laboratory parameters consistent with this syndrome were treated with cessation of CSA and intra-arterial infusion of streptokinase into the renal allograft followed by systemic heparinization. Normal transplant function was regained and continues at 1, 7, and 8 months after transplant. 111In-labeled platelet scanning can noninvasively identify this syndrome of CSA-associated arteriopathy and allow for early therapy to reverse it. Intrarenal arterial streptokinase therapy is a successful way to treat acute CSA-associated arteriopathy.

摘要

在无排斥反应情况下,环孢素(CSA)治疗相关的内皮损伤已导致肾内同种异体移植物不可逆血栓形成及移植失败。铟111(111In)标记的血小板扫描是识别有急性丢失风险的移植物的有效方法。共进行了200次前瞻性111In扫描(100次针对功能正常的同种异体移植物,100次针对各种原因导致移植功能障碍的移植物)。剂量依赖性CSA肾毒性患者(N = 58)和活检证实为急性排斥反应患者(N = 22)的111In扫描均为阴性。在9例被确定患有与CSA使用相关的溶血尿毒综合征样综合征的受者中,发现扫描结果严重异常(比肝脏摄取高3至8倍)。尽管停用CSA、进行全身抗凝、增加类固醇和抗淋巴细胞球蛋白用量以及输注新鲜冷冻血浆,但6例患者的移植物功能加速丧失仍不可逆。3例111In扫描结果明显阳性且临床和实验室参数符合该综合征的患者,通过停用CSA并将链激酶动脉内注入肾同种异体移植物,随后进行全身肝素化治疗。移植后1个月、7个月和8个月时恢复并维持了正常的移植功能。111In标记的血小板扫描可无创识别CSA相关动脉病综合征,并允许早期治疗以逆转该综合征。肾内动脉链激酶治疗是治疗急性CSA相关动脉病的成功方法。

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