Robson W L M, Leung A K C, Norgaard J P
Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada.
J Urol. 2007 Jul;178(1):24-30. doi: 10.1016/j.juro.2007.03.015. Epub 2007 May 11.
Desmopressin is a well established and effective therapy for nocturnal enuresis. Water intoxication leading to hyponatremia is an infrequent but serious adverse event associated with desmopressin. We assessed the safety of desmopressin in children 18 years or younger with nocturnal enuresis with a focus on the relative safety of the oral compared with the intranasal formulation.
Published data (MEDLINE) from December 1972 to August 2006 and post-marketing safety data from December 1972 to June 2005 were analyzed.
A total of 21 clinical trials on desmopressin use in children with nocturnal enuresis were identified. There were no reports of hyponatremia. A total of 21 publications were identified that included 48 case reports of hyponatremia in children with nocturnal enuresis. In all case reports patients were treated with intranasal desmopressin. Post-marketing safety data included 151 cases of hyponatremia in children with nocturnal enuresis, of whom 145 were treated with intranasal desmopressin and 6 were treated with the tablet formulation. Prodromal symptoms of hyponatremia were identified as headache, nausea and vomiting.
Data suggest that there is a decreased risk of hyponatremia with oral desmopressin compared with intranasal desmopressin. Identifiable and preventable risk factors for hyponatremia are inappropriately high fluid intake, administration of a larger than recommended dose, young age (less than 6 years) and concomitant administration of another medication. When desmopressin is prescribed, patients should be instructed to avoid high fluid intake when the medication is ingested, not ingest a higher than recommended dose and promptly discontinue the medication and seek assessment if headache, nausea or vomiting develops.
去氨加压素是治疗夜间遗尿症的一种成熟且有效的疗法。导致低钠血症的水中毒是与去氨加压素相关的一种罕见但严重的不良事件。我们评估了去氨加压素在18岁及以下夜间遗尿症儿童中的安全性,重点关注口服制剂与鼻内制剂相比的相对安全性。
分析了1972年12月至2006年8月发表的数据(MEDLINE)以及1972年12月至2005年6月的上市后安全性数据。
共确定了21项关于去氨加压素用于夜间遗尿症儿童的临床试验。没有低钠血症的报告。共确定了21篇出版物,其中包括48例夜间遗尿症儿童低钠血症的病例报告。在所有病例报告中,患者均接受鼻内去氨加压素治疗。上市后安全性数据包括151例夜间遗尿症儿童低钠血症病例,其中145例接受鼻内去氨加压素治疗,6例接受片剂制剂治疗。低钠血症的前驱症状被确定为头痛、恶心和呕吐。
数据表明,与鼻内去氨加压素相比,口服去氨加压素导致低钠血症的风险降低。低钠血症可识别和可预防的风险因素包括液体摄入量过高、给药剂量大于推荐剂量、年龄小(小于6岁)以及同时服用另一种药物。开具去氨加压素处方时,应告知患者在服药时避免大量饮水。不要摄入高于推荐剂量的药物,如果出现头痛、恶心或呕吐,应立即停药并寻求评估。