Lottmann H, Froeling F, Alloussi S, El-Radhi A S, Rittig S, Riis A, Persson B-E
Service de Chirurgie Viscerale Pédiatrique, Hôpital, Necker-Enfants Malades, Paris, France.
Int J Clin Pract. 2007 Sep;61(9):1454-60. doi: 10.1111/j.1742-1241.2007.01493.x. Epub 2007 Jul 26.
Desmopressin is a useful treatment for primary nocturnal enuresis (PNE), a common childhood condition that can persist into adolescence. This open-label, randomised, cross-over study evaluated the preference of children and adolescents with PNE for sublingual desmopressin oral lyophilisate (MELT) vs. tablet treatment, and the efficacy, safety, compliance and ease of use associated with each formulation. In total, 221 patients aged 5-15 years who were already receiving desmopressin tablets were randomised 1 : 1 to receive desmopressin treatment in the order MELT/tablet (n = 110) or tablet/MELT (n = 111) for 3 weeks each. Each formulation was administered in bioequivalent doses (0.2/0.4 mg tablets identical with 120/240 microg MELT). Following treatment, patients were questioned regarding treatment preference. Diary card data and 100 mm Visual Analogue Scale scores were also recorded.
Overall, patients preferred the MELT formulation to the tablet (56% vs. 44%; p = 0.112). This preference was age dependent (p = 0.006); patients aged < 12 years had a statistically significant preference for desmopressin MELT (p = 0.0089). Efficacy was similar for both formulations (MELT: 1.88 +/- 1.94 bedwetting episodes/week; tablet: 1.90 +/- 1.85 episodes/week). Ease of use of both formulations was high. Compliance (> or = 80%) was 94.5% for MELT patients vs. 88.9% for the tablet (p = 0.059). No serious/severe adverse events were reported.
There was an overall preference for the MELT, and a statistically significant preference for desmopressin MELT in children aged 5-11 years. Desmopressin MELT had similar levels of efficacy and safety at lower dosing levels than the tablet, and therefore facilitates early initiation of PNE treatment in children aged 5-6 years.
去氨加压素是治疗原发性夜间遗尿症(PNE)的一种有效药物,PNE是一种常见的儿童疾病,可持续至青春期。本开放标签、随机、交叉研究评估了患有PNE的儿童和青少年对舌下含服去氨加压素口服冻干剂(MELT)与片剂治疗的偏好,以及每种剂型的疗效、安全性、依从性和易用性。总共221名年龄在5至15岁且已在服用去氨加压素片剂的患者被随机分为1:1,按MELT/片剂(n = 110)或片剂/MELT(n = 111)的顺序接受去氨加压素治疗,各为期3周。每种剂型均以生物等效剂量给药(0.2/0.4 mg片剂等同于120/240 μg MELT)。治疗后,询问患者对治疗剂型的偏好。还记录了日记卡数据和100 mm视觉模拟量表评分。
总体而言,患者更喜欢MELT剂型而非片剂(56%对44%;p = 0.112)。这种偏好与年龄有关(p = 0.006);12岁以下的患者对去氨加压素MELT有统计学上的显著偏好(p = 0.0089)。两种剂型的疗效相似(MELT:1.88±1.94次/周尿床;片剂:1.90±1.85次/周)。两种剂型的易用性都很高。MELT患者的依从性(≥80%)为94.5%,片剂患者为88.9%(p = 0.059)。未报告严重/重度不良事件。
总体上更倾向于MELT剂型,5至11岁儿童对去氨加压素MELT有统计学上的显著偏好。去氨加压素MELT在较低剂量水平下具有与片剂相似的疗效和安全性水平,因此有助于5至6岁儿童早期开始PNE治疗。