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儿童先天性神经性膀胱的肾功能。

Renal function in children with congenital neurogenic bladder.

机构信息

Instituto da Criança, Hospital das Clinicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.

出版信息

Clinics (Sao Paulo). 2011;66(2):189-95. doi: 10.1590/s1807-59322011000200002.

DOI:10.1590/s1807-59322011000200002
PMID:21484032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3059879/
Abstract

AIMS

Preservation of renal function in children with congenital neurogenic bladder is an important goal of treatment for the disease. This study analyzed the evolution of renal function in patients with congenital neurogenic bladder.

METHODS

We reviewed the records of 58 pediatric patients with respect to the following attributes: gender, age, etiology of neurogenic bladder, reason for referral, medical/surgical management, episodes of treated urinary tract infections, urodynamics, DMSA scintigraphy, weight, height, blood pressure, glomerular filtration rate, microalbuminuria and metabolic acidosis. Statistical analysis was performed, adopting the 5% significance level.

RESULTS

The mean age at presentation was 4.2 ± 3.5 years. Myelomeningocele was the most frequent etiology (71.4%). Recurrent urinary tract infection was the reason for referral in 82.8% of the patients. Recurrent urinary tract infections were diagnosed in 84.5% of the patients initially; 83.7% of those patients experienced improvement during follow-up. The initial mean glomerular filtration rate was 146.7 ± 70.1 mL/1.73 m²/min, and the final mean was 193.6 ± 93.6 mL/1.73 m²/min, p = 0.0004. Microalbuminuria was diagnosed in 54.1% of the patients initially and in 69% in the final evaluation. Metabolic acidosis was present in 19% of the patients initially and in 32.8% in the final assessment.

CONCLUSIONS

Patient referral to a pediatric nephrologist was late. A reduction in the number of urinary tract infections was observed with adequate treatment, but microalbuminuria and metabolic acidosis occurred frequently despite adequate management.

摘要

目的

保护患有先天性神经性膀胱的儿童的肾功能是治疗该病的重要目标。本研究分析了先天性神经性膀胱患者肾功能的演变情况。

方法

我们回顾了 58 名儿科患者的记录,内容包括:性别、年龄、神经性膀胱的病因、转诊原因、医疗/手术管理、治疗过的尿路感染发作、尿动力学、DMSA 闪烁扫描、体重、身高、血压、肾小球滤过率、微量白蛋白尿和代谢性酸中毒。采用 5%的显著性水平进行了统计分析。

结果

就诊时的平均年龄为 4.2±3.5 岁。最常见的病因是脊髓脊膜膨出(71.4%)。复发性尿路感染是 82.8%患者转诊的原因。最初,84.5%的患者被诊断为复发性尿路感染;83.7%的患者在随访中有所改善。初始平均肾小球滤过率为 146.7±70.1 mL/1.73 m²/min,最终平均为 193.6±93.6 mL/1.73 m²/min,p=0.0004。最初有 54.1%的患者被诊断为微量白蛋白尿,最终评估时有 69%的患者被诊断为微量白蛋白尿。最初有 19%的患者存在代谢性酸中毒,最终评估时有 32.8%的患者存在代谢性酸中毒。

结论

患者向儿科肾病医生转诊较晚。尽管进行了充分的治疗,但尿路感染的数量有所减少,但尽管进行了充分的管理,仍经常出现微量白蛋白尿和代谢性酸中毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/805d/3059879/4ae867dc4f80/cln-66-02-189-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/805d/3059879/3c2c36bf3ea6/cln-66-02-189-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/805d/3059879/4ae867dc4f80/cln-66-02-189-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/805d/3059879/3c2c36bf3ea6/cln-66-02-189-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/805d/3059879/4ae867dc4f80/cln-66-02-189-g002.jpg

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