Skoog S J, Stokes A, Turner K L
Division of Urology, Oregon Health Sciences University, Portland 97201-3098, USA.
J Urol. 1997 Sep;158(3 Pt 2):1035-40.
Desmopressin nasal spray has proved to be efficacious treatment of primary nocturnal enuresis. Oral desmopressin tablets would be a more easily used, convenient vehicle for our patients and their parents. We evaluated the effectiveness of oral desmopressin in decreasing the number of wet nights in patients with primary nocturnal enuresis.
We performed a double-blind, placebo controlled, parallel group trial of oral desmopressin in 141 children 5 to 17 years old with documented primary nocturnal enuresis at 14 sites. Patients were screened for number of wet nights for 2 weeks before study entry. A minimum of 3 wet nights weekly for 2 consecutive weeks was required for study entry. Patients were randomized to receive 200, 400 or 600 mcg. desmopressin or placebo before bedtime. Fluids were restricted 2 hours before bedtime based on body weight. The primary efficacy variable was mean decrease in the number of wet nights recorded during the last 2-week treatment period. The percentage of responding patients and mean decrease from baseline in number of wet nights at 2, 4 and 6 weeks were also assessed.
The decrease in wet nights was 9, 20, 30 and 36% for placebo, and 200, 400, and 600 mcg. desmopressin orally per day, respectively. The 600 mcg. dose of oral desmopressin daily was statistically significantly different (p < 0.05) from placebo in decreasing wet nights. A complete or near complete response (0 to 2 wet nights) was noted in 3, 18, 33 and 24% of the patients who received placebo, and 200, 400 and 600 mcg. oral desmopressin daily, respectively. The 400 and 600 mcg. treatment groups were statistically significantly different (p < 0.05) from placebo. A less than 50% decrease in wet nights was noted in 83, 79, 64 and 61% of the patients who received placebo, and 200, 400 and 600 mcg. oral desmopressin daily, respectively. Oral desmopressin exhibited a dose response in the treatment of primary nocturnal enuresis. The linear trend for the decrease in wet nights was statistically significant (p < 0.05).
A dose of 600 mcg. oral desmopressin daily significantly decreased the mean number of wet nights when administered for 6 weeks. A higher dose may be necessary for an improved response.
去氨加压素鼻喷雾剂已被证明是治疗原发性夜间遗尿症的有效方法。口服去氨加压素片对我们的患者及其家长来说将是一种更易于使用、方便的药物。我们评估了口服去氨加压素减少原发性夜间遗尿症患者尿床次数的有效性。
我们在14个地点对141名5至17岁有原发性夜间遗尿症记录的儿童进行了口服去氨加压素的双盲、安慰剂对照、平行组试验。在研究开始前对患者进行了2周尿床次数的筛查。研究入选要求连续2周每周至少有3个尿床夜。患者被随机分为接受200、400或600微克去氨加压素或安慰剂。睡前2小时根据体重限制饮水。主要疗效变量是在最后2周治疗期间记录的尿床夜数的平均减少量。还评估了有反应患者的百分比以及在2、4和6周时尿床夜数相对于基线的平均减少量。
安慰剂组、每日口服200、400和600微克去氨加压素组的尿床夜数减少率分别为9%、20%、30%和36%。每日600微克口服去氨加压素剂量在减少尿床夜数方面与安慰剂相比有统计学显著差异(p<0.05)。接受安慰剂、每日200、400和600微克口服去氨加压素的患者中,分别有3%、18%、33%和24%出现完全或近乎完全反应(0至2个尿床夜)。400和600微克治疗组与安慰剂相比有统计学显著差异(p<0.05)。接受安慰剂、每日200、400和600微克口服去氨加压素的患者中,分别有83%、79%、64%和61%的尿床夜数减少不到50%。口服去氨加压素在原发性夜间遗尿症治疗中呈现剂量反应。尿床夜数减少的线性趋势有统计学显著意义(p<0.05)。
每日600微克口服去氨加压素给药6周可显著减少尿床夜数的平均值。可能需要更高剂量以获得更好的反应。