Sharifiaghdas Farzaneh, Sharifiaghdas Sepideh, Taheri Maryam
Urology and Nephrology Research Center (UNRC), Department of Urology, Shahid Labbafinejad Medical Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Torfeh General Hospital, Department of Pediatrics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Urology. 2016 Jul;93:170-4. doi: 10.1016/j.urology.2016.02.013. Epub 2016 Mar 23.
To evaluate the clinical results of monotherapy with combination therapy in treatment of primary monosymptomatic nocturnal enuresis (PMNE) in children.
Between December 2008 and May 2013, we reviewed the records of 176 children with PMNE. The monotherapy group received 120 micrograms of desmopressin melt whereas the combination therapy group received 120 micrograms of desmopressin melt plus 1-2 mg oral tablet of tolterodine. The degree of response was evaluated at 1-3 months during the treatment and 6 months after complete cessation of treatment protocol.
Between 176 children, 84 and 92 patients received monotherapy and combination therapy, respectively. There were no statistical differences in gender, age, or baseline monthly frequency of PMNE between the two groups. At baseline, patients had an overall mean of 23.6 ± 5.6 wet nights per month, which decreased to 10.8 ± 5.6 and 7.3 ± 5.3 in monotherapy group and 8.9 ± 9.5 and 3.3 ± 4.9 in combination therapy group at 1 and 3 months after treatment. The rates of Complete plus Partial Response to treatment at 1 and 3 months for monotherapy and combination therapy group were 63.1% and 73.9% vs 72.5% and 93.47% (P value .12 vs .006). The relapse of PMNE 6 months after complete cessation of treatment was 16.39% and 9.09% for monotherapy vs combination therapy group.
This study supports the efficacy of combination therapy with desmopressin melt plus oral tolterodine over monotherapy with desmopressin melt in the first-line treatment of PMNE in children.
评估单一疗法与联合疗法治疗儿童原发性单症状性夜间遗尿症(PMNE)的临床效果。
2008年12月至2013年5月期间,我们回顾了176例PMNE患儿的记录。单一疗法组接受120微克去氨加压素溶片,而联合疗法组接受120微克去氨加压素溶片加1 - 2毫克口服托特罗定片。在治疗的1 - 3个月期间以及治疗方案完全停止后6个月评估反应程度。
176例患儿中,分别有84例和92例接受单一疗法和联合疗法。两组在性别、年龄或PMNE的基线月发作频率方面无统计学差异。基线时,患者每月总体平均尿床23.6 ± 5.6次,治疗后1个月和3个月时,单一疗法组分别降至10.8 ± 5.6次和7.3 ± 5.3次,联合疗法组分别降至8.9 ± 9.5次和3.3 ± 4.9次。单一疗法组和联合疗法组在治疗1个月和3个月时的完全缓解加部分缓解率分别为63.1%和73.9%,对比72.5%和93.47%(P值分别为0.12和0.006)。治疗方案完全停止后6个月,单一疗法组与联合疗法组的PMNE复发率分别为16.39%和9.09%。
本研究支持在儿童PMNE的一线治疗中,去氨加压素溶片联合口服托特罗定的联合疗法比单一使用去氨加压素溶片更有效。