Ikeda Hirokazu, Watanabe Tsuneki, Isoyama Keiichi
Department of Pediatrics, Showa University Fujigaoka Hospital, Yokohama, Kanagawa, Japan.
Department of Pediatrics, Showa University, Tokyo, Japan.
Int J Urol. 2017 Sep;24(9):698-702. doi: 10.1111/iju.13394. Epub 2017 Jun 21.
To investigate renal concentrating ability after long-term fast-melting oral desmopressin lyophilisate treatment in children with monosymptomatic nocturnal enuresis.
The present retrospective study involved 58 children (43 boys, 15 girls; aged 6-12 years) with nocturnal enuresis receiving oral desmopressin lyophilisate. After treatment for 4 weeks with a complete response, patients were placed on a reduced dose of 120 μg on alternate days. Moring urine osmolality was measured using urine samples obtained after medication and non-medication dry nights. Patients who experienced ≥1 wet nights/month during alternate-day oral desmopressin lyophilisate treatment or within 6 months after its cessation were assigned to the relapse group, whereas those who experienced <1 wet night/month were assigned to the continued success group.
The continued success and relapse groups included 41 and 17 patients, respectively. The mean duration of treatment was 18.5 and 18.3 months in the continued success group and relapse group, respectively. There was no significant difference in morning urine osmolality after medication nights between the continued success and relapse groups; however, morning urine osmolality after non-medication nights was significantly higher in the continued success group than in the relapse group (P < 0.0001). Similarly, nocturnal urine volume was significantly higher in the relapse group than in the continued success group (P = 0.046).
These results suggest that patients receiving long-term oral desmopressin lyophilisate treatment develop increased nocturnal renal concentrating ability, which results in sustained dryness even after treatment cessation.
探讨在单症状性夜间遗尿症儿童中,长期服用速溶口服去氨加压素冻干制剂治疗后的肾脏浓缩能力。
本回顾性研究纳入了58例接受口服去氨加压素冻干制剂治疗的夜间遗尿症儿童(43例男孩,15例女孩;年龄6 - 12岁)。在经过4周治疗且完全缓解后,患者改为隔日服用120μg的减量剂量。使用服药及未服药干燥夜间后的尿液样本测量晨尿渗透压。在隔日口服去氨加压素冻干制剂治疗期间或停药后6个月内,每月经历≥1次尿床的患者被分配至复发组,而每月经历<1次尿床的患者被分配至持续成功组。
持续成功组和复发组分别包括41例和17例患者。持续成功组和复发组的平均治疗时长分别为18.5个月和18.3个月。持续成功组和复发组服药夜间后的晨尿渗透压无显著差异;然而,持续成功组未服药夜间后的晨尿渗透压显著高于复发组(P < 0.0001)。同样,复发组的夜间尿量显著高于持续成功组(P = 0.046)。
这些结果表明,接受长期口服去氨加压素冻干制剂治疗的患者夜间肾脏浓缩能力增强,即使在停药后也能保持持续干爽。