[EFFICACY AND SAFETY OF INITIAL DESMOPRESSIN DOSE OF 50 μg IN ELDERLY MALE PATIENTS WITH NOCTURNAL POLYURIA].

Hirofumi Kurose, Keisuke Komiya, Naoyuki Ogasawara, Kosuke Ueda, Katsuaki Chikui, Kiyoaki Nishihara, Makoto Nakiri, Mitsunori Matsuo, Shigetaka Suekane, Tsukasa Igawa
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Abstract

(Introduction) Low-dose desmopressin is now available for the treatment of nocturia associated with nocturnal polyuria in men, and its usefulness in a dose-dependent manner has been reported. Since side effects such as hyponatremia have reported frequently, the initial dose has been set at 25 μg in many cases considering age and other factors. In the present study, we investigated the efficacy and safety of an initial dose of 50 μg in elderly patients. (Subjects and methods) At Chikugo city hospital, 45 patients were started on desmopressin at an initial dose of 50 μg for nocturia with nocturnal polyuria. Efficacy and safety after one and four weeks were evaluated based on bladder (micturition) diary. The investigated parameters included frequency of nocturnal urination, nocturnal polyuria index, time to first nocturnal void, first nocturnal urine volume, nocturnal urine volume, International Prostate Symptom Score (IPSS), Overactive Bladder Symptom Score (OABSS), and Athens Insomnia Scale. Physical examinations were also carried out, along with blood tests. (Results) The mean age of the patients was 78.3 years, which was higher than that reported in prior studies. After one week of treatment, there was a significant decrease in the frequency of nocturnal urination and nocturnal urine volume, as well as a prolongation of the time to first nocturnal void, improvement in nocturnal polyuria index, and improvement in IPSS, IPSS-QOL, OABSS, and Athens Insomnia Scale. In terms of safety, adverse events were observed in eight patients (17.8%), and hyponatremia was observed in seven patients (15.6%), which was comparable to the findings of prior reports. (Conclusion) Good therapeutic results were obtained in elderly patients at an initial desmopressin dose of 50 μg, indicating that the drug could be safely administered to elderly patients with regular follow-ups and appropriate withdrawal and dose reductions.

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[首次给药50μg降压素治疗老年男性隐性多尿症的有效性和安全性]。
(简介)低剂量去氨加压素目前可用于治疗与男性夜间多尿相关的夜尿症,其作用具有剂量依赖性。由于低钠血症等副作用经常被报道,在许多情况下,考虑到年龄和其他因素,初始剂量被设定为25μg。在本研究中,我们调查了50μg初始剂量对老年患者的疗效和安全性。(受试者和方法)在七股市医院,45名患者开始服用去氨加压素,初始剂量为50μg,用于治疗夜间多尿的夜尿。根据膀胱(排尿)日记评估一周和四周后的疗效和安全性。研究参数包括夜间排尿次数、夜间多尿指数、首次夜间排尿时间、首次夜间尿量、夜间尿量,国际前列腺症状评分(IPSS)、膀胱过度活动症状评分(OABSS)和雅典失眠量表。还进行了身体检查和血液检查。(结果)患者的平均年龄为78.3岁,高于以往研究报告的年龄。治疗一周后,夜间排尿次数和夜间尿量显著减少,首次夜间排尿时间延长,夜间多尿指数改善,IPSS、IPSS-QOL、OABSS和雅典失眠量表改善。就安全性而言,8名患者(17.8%)出现不良事件,7名患者(15.6%)出现低钠血症,这与先前报告的结果相当。(结论)在老年患者中,初始去氨加压素剂量为50μg时获得了良好的治疗效果,表明该药物可以安全地用于老年患者,并定期随访,适当地停药和减少剂量。
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