巴西 MG 省 Uberlândia 的溶血性尿毒症。

ISRN pediatrics Pub Date : 2011-01-01 Epub Date: 2011-12-01 DOI:10.5402/2011/651749
V Bonetti, C M F Mangia, J M F Zuza, M O Barcelos, M M S Fonseca, S P Nery, J T A Carvalhaes, M C Andrade
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摘要

目的分析巴西 MG 省乌贝兰迪亚市溶血性尿毒症 (HUS) 的流行病学、临床和实验室特征。方法对一家提供全面服务的医院的儿科肾脏内科从 1994 年 1 月至 2004 年 1 月的十年间进行了历史队列研究,分析了人口统计学因素、诱发因素、住院时间、支持疗法和疾病进展。研究结果研究对象为 27 名 5 至 99 个月大(中位数为 14 个月大)的儿童,其中 70.4% 为男性。在 27 名患者中,77.8% 来自城市地区,18.5% 来自农村地区。据报告,其中八名患者(29.6%)饮用生牛奶,81.5%的病例出现临床腹泻。最常见的症状和体征是发热和呕吐(85.1%)、无尿(63.0%)、抽搐(33.0%)、心脏受累(11.0%)和急性肺水肿(7.4%)。20名患者(74%)进行了透析。平均住院时间为 24 天(13 至 36 天不等)。在对患者进行监测期间,2 人死亡(7.4%),3 人发展为慢性肾病(11.0%),21 人(77.8%)发展为高血压。结论我们的研究结果表明,典型(腹泻后)和非典型的 HUS 均可诊断为儿童肾功能衰竭的病因,并建议尽可能对病原体进行调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hemolytic-Uremic Syndrome in Uberlândia, MG, Brazil.

Purpose. To analyze the epidemiological, clinical, and laboratory characteristics of hemolytic-uremic syndrome (HUS) in Uberlandia, MG, Brazil. Methods. A historical cohort study was performed encompassing a ten-year period from January 1994 to January 2004 in the Department of Pediatric Nephrology at a full-service hospital; demographic factors, triggering factors, time of hospitalization, supportive therapy, and disease progression were analyzed. Results. Twenty-seven children aged 5 to 99 months (median age of 14 months) were studied; 70.4% were male. Of the 27 patients, 77.8% were from urban areas and 18.5% were from rural areas. Eight of the patients (29.6%) were reported to drink raw milk, and clinical diarrhea was reported in 81.5% of cases. The most common signs and symptoms were fever and vomiting (85.1%), anuria (63.0%), seizure (33.0%), cardiac involvement (11.0%), and acute pulmonary edema (7.4%). Dialysis was performed on 20 patients (74%). The mean hospital stay was 24 days (range: 13 to 36 days). While monitoring the patients, 2 died (7.4%), 3 developed chronic kidney disease (11.0%), and 21 (77.8%) developed hypertension. Conclusion. Our results emphasize the possibility of diagnosing HUS as a cause of renal failure in childhood in both typical (postdiarrheal) and atypical forms and suggest that an investigation of the etiological agent should be made whenever possible.

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