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现实生活中,有夜间多尿和无夜间多尿的老年男性对去氨加压素治疗夜尿症反应的比较。

Comparison of nocturia response to desmopressin treatment in elderly men with and without nocturnal polyuria in real-life practice.

作者信息

Chen S-L, Huang Y-H, Hung T-W, Ou Y-C

机构信息

Department of Urology, Chung Shan Medical University Hospital, Taichung, Taiwan.

School of Medicine, Chung Shan Medical University, Taichung, Taiwan.

出版信息

Int J Clin Pract. 2016 May;70(5):372-9. doi: 10.1111/ijcp.12786. Epub 2016 Apr 4.

Abstract

OBJECTIVES

To evaluate the safety and efficacy of low-dose desmopressin in elderly men with and without nocturnal polyuria (NP) in real-life practice.

METHODS

Patients with lower urinary tract symptoms (LUTS)/ benign prostate hyperplasia (BPH) who were≧ 65 years old with refractory nocturia were enrolled in this study. We retrospectively analysed elderly men treated with adding desmopressin to current medications for nocturia according to category of the baseline nocturnal urine volume. The 48-h frequency volume chart (FVC), International Prostate Symptom Score (IPSS) and quality of life (QoL) were initially assessed and re-evaluated 12 weeks later. Serum sodium level was checked 1 week, 4 weeks, and 12 weeks after initiation of desmopressin therapy or suspected hyponatremia event. The mean change in numbers of nocturnal voids was evaluated for efficacy of treatment.

RESULTS

A total of 136 patients were included with 55 in non-NP group and 81 in NP group. Hypertension was more common in NP group in regard of comorbidities. During treatment period, there were significant reductions of nocturnal voids from 4.22 ± 1.38 to 2.31 ± 0.98 (p < 0.001) in non-NP group and from 4.52 ± 1.23 to 2.07 ± 0.89 (p < 0.001) in NP group. The reduction in nocturnal voids was more significant in NP group (2.44 ± 1.15 vs. 1.91 ± 1.48, p = 0.003). The mean decrease in serum sodium levels were 3.89 ± 1.22 mmol/l (p < 0.001) in non-NP group and 4.69 ± 3.5 mmol/l (p < 0.001) in NP group at the extreme value.

CONCLUSIONS

Long-term treatment with low-dose desmopressin is safe and effective for nocturia with or without NP in elderly patients with LUTS/BPH during real-life practice. Patients should be well informed about the disease and are closely followed.

摘要

目的

在实际临床中评估低剂量去氨加压素对伴有和不伴有夜间多尿(NP)的老年男性的安全性和有效性。

方法

纳入年龄≧65岁、难治性夜尿症且患有下尿路症状(LUTS)/良性前列腺增生(BPH)的患者。我们根据基线夜间尿量类别,回顾性分析了在当前治疗夜尿症的药物基础上加用去氨加压素治疗的老年男性。最初评估48小时频率-尿量图表(FVC)、国际前列腺症状评分(IPSS)和生活质量(QoL),并在12周后重新评估。在开始去氨加压素治疗或疑似低钠血症事件后1周、4周和12周检查血清钠水平。评估夜间排尿次数的平均变化以确定治疗效果。

结果

共纳入136例患者,非NP组55例,NP组81例。就合并症而言,高血压在NP组中更常见。治疗期间,非NP组夜间排尿次数从4.22±1.38显著减少至2.31±0.98(p<0.001),NP组从4.52±1.23显著减少至2.07±0.89(p<0.001)。NP组夜间排尿次数的减少更显著(2.44±1.15对1.91±1.48,p = 0.003)。非NP组血清钠水平的平均下降在极值时为3.89±1.22 mmol/l(p<0.001),NP组为4.69±3.5 mmol/l(p<0.001)。

结论

在实际临床中,低剂量去氨加压素长期治疗对患有LUTS/BPH的老年患者伴有或不伴有NP的夜尿症是安全有效的。应让患者充分了解病情并密切随访。

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