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通过肾内细针测压法检测肾移植排斥反应。

The detection of renal allograft rejection by fine-needle intrarenal manometry.

作者信息

Wilson R G, Taylor R M, Proud G

出版信息

Br J Surg. 1985 Oct;72(10):816-8. doi: 10.1002/bjs.1800721014.

Abstract

The causes of early renal allograft malfunction include rejection, acute tubular necrosis, cyclosporin nephrotoxicity and vascular complications. Fine-needle intrarenal manometry is a potential method of distinguishing rejection from the other causes of malfunction and has been used by Salaman and Griffin in patients' treated with cyclosporin. The technique involves inserting a fine-needle, which is connected to a specially designed manometer, into the substance of the transplant kidney. One hundred and six measurements of intrarenal pressure have been made in 28 patients immunosuppressed with either azathioprine and prednisolone or cyclosporin. Thirteen rejection episodes were identified and confirmed by biopsy. These were treated by pulse steroid (methylprednisolone) therapy. Seven episodes of cyclosporin toxicity were identified and there were fifteen episodes of acute tubular necrosis. The mean intrarenal pressure in the rejecting group was 52.8 mmHg compared with 22.3, 24.1 and 24.3 mmHg for the normal function, acute tubular necrosis and cyclosporin nephrotoxicity groups, respectively (P less than 0.01; Wilcoxon unpaired test). There were no differences within these groups related to the type of immunosuppression used. There were no clinical complications associated with the procedure. Thus in newly transplanted patients, fine-needle intrarenal manometry accurately identified rejection and distinguished it from normal function, acute tubular necrosis and cyclosporin nephrotoxicity in all the patients regardless of the immunosuppressants used.

摘要

早期肾移植移植物功能障碍的原因包括排斥反应、急性肾小管坏死、环孢素肾毒性和血管并发症。细针肾内测压是一种区分排斥反应与其他功能障碍原因的潜在方法,萨拉曼和格里芬已将其用于接受环孢素治疗的患者。该技术包括将一根与特殊设计的压力计相连的细针插入移植肾实质。对28例接受硫唑嘌呤和泼尼松龙或环孢素免疫抑制治疗的患者进行了106次肾内压测量。通过活检确定并证实了13次排斥反应发作。这些发作采用脉冲类固醇(甲泼尼龙)治疗。确定了7次环孢素毒性发作,以及15次急性肾小管坏死发作。排斥反应组的平均肾内压为52.8 mmHg,而正常功能组、急性肾小管坏死组和环孢素肾毒性组分别为22.3 mmHg、24.1 mmHg和24.3 mmHg(P<0.01;Wilcoxon非配对检验)。这些组内与所使用的免疫抑制类型无关。该操作未出现临床并发症。因此,在新移植的患者中,细针肾内测压能准确识别排斥反应,并将其与所有患者的正常功能、急性肾小管坏死和环孢素肾毒性区分开来,无论使用何种免疫抑制剂。

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