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随机尿渗透压、年龄和膀胱容量作为夜间遗尿症患者对去氨加压素反应的预测指标。

Spot urine osmolality, age and bladder capacity as predictors of response to desmopressin in nocturnal enuresis.

作者信息

Eller D A, Homsy Y L, Austin P F, Tanguay S, Cantor A

机构信息

Division of Pediatric Urology, Tampa General Hospital Children's Medical Center, University of South Florida, USA.

出版信息

Scand J Urol Nephrol Suppl. 1997;183:41-5.

PMID:9165605
Abstract

The objective of the current study was to find a cost-effective way of correlating spot urine osmolalities, bladder capacity and age in patients with monosymptomatic nocturnal enuresis with response to treatment with desmopressin (Minirin, DDAVP). A total of 35 children fulfilled the entry criteria and were included in the study. Constipation was eliminated in these children by appropriate enema treatment and diet adjustment prior to enrollment. Urine samples were collected at home at times that would best reflect fluctuations in plasma vasopressin levels (08:00, 16:00 and 22:00) over three consecutive 24-hour periods. Maximal functional bladder capacity was determined from the largest voided volume. A 2-week dose-titration treatment period with intranasal desmopressin was then conducted. With doses of desmopressin being increased by 10 micrograms every 3 days. Response to desmopressin treatment was then assessed and factors that were observed to be markers of a favourable response were noted. Of the 35 children, 27 demonstrated a complete response to desmopressin treatment, at doses of 10-30 micrograms. Spot urine osmolalities were not predictive of the response to desmopressin (P > 0.1). In contrast, there was a significant correlation between a high maximum functional bladder capacity and response to desmopressin (P = 0.006). Age was also predictive of a good response to desmopressin treatment (P = 0.008).

摘要

本研究的目的是找到一种经济有效的方法,来关联单纯性夜间遗尿症患者的随机尿渗透压、膀胱容量和年龄,以及他们对去氨加压素(弥凝,DDAVP)治疗的反应。共有35名儿童符合入选标准并纳入研究。在入组前,通过适当的灌肠治疗和饮食调整消除了这些儿童的便秘问题。在连续三个24小时期间,于最能反映血浆血管加压素水平波动的时间(08:00、16:00和22:00)在家中采集尿液样本。根据最大排尿量确定最大功能性膀胱容量。然后进行为期2周的鼻内去氨加压素剂量滴定治疗期,每3天增加10微克去氨加压素剂量。随后评估去氨加压素治疗的反应,并记录观察到的作为良好反应标志物的因素。在这35名儿童中,27名在10 - 30微克剂量下对去氨加压素治疗表现出完全反应。随机尿渗透压不能预测对去氨加压素的反应(P > 0.1)。相比之下,高最大功能性膀胱容量与对去氨加压素的反应之间存在显著相关性(P = 0.006)。年龄也是去氨加压素治疗良好反应的预测指标(P = 0.008)。

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