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口服甲磺酸卡莫司他对儿童血尿和/或蛋白尿的影响。

Effect of oral camostat mesilate on hematuria and/or proteinuria in children.

作者信息

Asami Tadashi, Tomisawa Shuichi, Uchiyama Makoto

机构信息

Department of Homeostatic Regulation and Development, Division of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

出版信息

Pediatr Nephrol. 2004 Mar;19(3):313-6. doi: 10.1007/s00467-003-1377-9. Epub 2004 Jan 23.

Abstract

The effects of camostat mesilate (CM), a derivative of gabexate mesilate developed for oral use, on primary glomerulonephritis (GN) and chance hematuria and/or proteinuria were evaluated. Fourteen patients (6 males, 8 females) with a mean age of 11 years and 3 months (range 4-16 years) were enrolled. Histological and clinical diagnoses of the 14 patients were as follows: IgA nephropathy 3, non-IgA GN 2, and asymptomatic significant microscopic hematuria [more than 100 red blood cells per high-power field (x400)] with or without proteinuria 9. They were consecutively treated with oral CM (100 mg twice a day) when they were confirmed to have continuous significant microscopic hematuria and/or proteinuria after a few months of observational follow-up. Urinary findings were normalized in 10 of the 14 patients (85.7%) between 1 month 1 week and 10 months (mean 4 months) after administration of CM. Hematuria cleared in 11 of 13 patients, and proteinuria disappeared in 4 of 5 patients. The mean duration of CM administration was 21.7 +/- 9.1 months (range 4-37 months). At present, 3-12 years after discontinuation of CM therapy, their urinary findings remain normal at 9 years 10 months to 26 years 6 months of age. In conclusion, there appears to be an association between the oral use of CM and reduction in significant microscopic hematuria and/or proteinuria. Oral CM therapy could represent a practical primary care approach to chance hematuria and/or proteinuria in children.

摘要

对甲磺酸卡莫司他(CM)(一种开发用于口服的甲磺酸加贝酯衍生物)对原发性肾小球肾炎(GN)以及偶然性血尿和/或蛋白尿的影响进行了评估。纳入了14例患者(6例男性,8例女性),平均年龄为11岁3个月(范围4 - 16岁)。这14例患者的组织学和临床诊断如下:IgA肾病3例,非IgA GN 2例,无症状性显著镜下血尿[每高倍视野(×400)超过100个红细胞]伴或不伴蛋白尿9例。在经过几个月的观察随访确认他们持续存在显著镜下血尿和/或蛋白尿后,连续给予口服CM(每日2次,每次100 mg)。在给予CM后1个月1周和10个月(平均4个月)之间,14例患者中有10例(85.7%)的尿液检查结果恢复正常。13例患者中有11例血尿消失,5例患者中有4例蛋白尿消失。CM给药的平均持续时间为21.7±9.1个月(范围4 - 37个月)。目前,在停止CM治疗3 - 12年后,他们在9岁10个月至26岁6个月时尿液检查结果仍保持正常。总之,口服CM与显著镜下血尿和/或蛋白尿的减少之间似乎存在关联。口服CM治疗可能是儿童偶然性血尿和/或蛋白尿的一种实用的初级保健方法。

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