神经源性膀胱儿童膀胱增强成形术后的代谢后果和小管功能。

Jei-Wen Chang, Hui-Hsin Yang, Tzu-Ching Lin, Fang-Cheng Kuo, Yu-Hua Fan, Hsin-Hung Chen, Ling-Yu Yang, Chin-Su Liu, Hsin-Lin Tsai
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引用次数: 0

摘要

背景:许多研究报道了增强膀胱成形术(AC)后的肾脏结局和代谢后果,但很少有研究讨论肾小管功能的变化。本研究的目的是确定代谢紊乱的患病率,评估肾小管功能和24小时尿液化学,以评估代谢改变与尿石症之间的关系。方法:我们调查了2000年1月至2020年12月期间接受AC手术的儿童的血清生化、血气和24小时尿代谢谱。评估的结果包括代谢并发症、肾小管功能和镁状态。还分析了24小时尿液化学物质与尿石症形成之间的关系。结果:共纳入25例患者,平均随访时间为13.8±5.7年。AC的平均年龄为7.5±4.4岁,分别有22例和3例患者通过回肠和结肠进行AC。血清钠、钾、氯、钙均无异常。1例(4.0%)患者被诊断为低镁血症(镁)。结论:AC对儿童是安全的,对代谢谱没有明显的负面影响,尽管24小时尿镁排泄量< 88 mg/1.73 m2的发生率很高。本研究强调了纵向随访肾小管功能和24小时尿液代谢特征,特别是镁状态的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolic consequences and tubular function after augmentation cystoplasty in children with neurogenic bladder.

Background: While many studies have reported the renal outcomes and metabolic consequences of augmentation cystoplasty (AC), few have focused on changes in renal tubular function. This study investigated the prevalence of metabolic disturbances, renal tubular function, and 24-hour urine chemistry, aiming to evaluate the association between metabolic alterations and urolithiasis after AC.

Methods: We investigated serum biochemistry, blood gas, and 24-hour urinary metabolic profile of children who underwent AC between January 2000 and December 2020. The assessed outcomes included metabolic complications, tubular function, and magnesium status. Associations between 24-hour urinary metabolic parameters and urolithiasis formation were also examined.

Results: A total of 25 patients with a mean follow-up period of 13.8 ± 5.7 years were enrolled. The mean age at AC was 7.5 ± 4.4 years, and 22 and 3 patients underwent AC using the ileum and colon, respectively. There were no abnormalities in serum levels of sodium, potassium, chloride, and calcium. Hypomagnesemia (magnesium <1.7 mg/dL) due to renal loss was observed in one patient (4.0%). Six (24.0%) patients had increased urinary β2-microglobulin levels and normal serum levels. The ratio of the maximum rate of tubular phosphate reabsorption to the glomerular filtration rate was low in three (12.0%) patients. Four (16.0%) patients had normal serum magnesium levels but urinary magnesium excretion <40 mg/d. Urolithiasis occurred in 11 patients (44.0%). The most common 24-hour urine metabolic abnormality was hypomagnesiuria (72.0%). No urinary metabolic parameters or daily protein intake were associated with urolithiasis.

Conclusion: AC for children is safe and does not significantly impact the metabolic profile. Excretions of 24-hour urinary calcium, uric acid, magnesium, and the sodium-to-potassium ratio were not associated with urolithiasis. However, a high prevalence of 24-hour urine magnesium excretion <88 mg/1.73 m 2 was noted. Further prospective studies are needed to investigate longitudinal changes in renal tubular function and 24-hour urine metabolic profiles, particularly magnesium status.

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