Bisgaard Hans, Skoner David, Boza Maria L, Tozzi Carol A, Newcomb Kathleen, Reiss Theodore F, Knorr Barbara, Noonan Gertrude
Danish Pediatric Asthma Center, Copenhagen University Hospital, Gentofte, Copenhagen, Denmark.
Pediatr Pulmonol. 2009 Jun;44(6):568-79. doi: 10.1002/ppul.21018.
Montelukast is a potent leukotriene-receptor antagonist administered once daily that provides clinical benefit in the treatment of asthma and allergic rhinitis in children and adults. Because of its wide use as a pediatric controller, there is a need for a further review of the safety and tolerability of montelukast in children.
To summarize safety and tolerability data for montelukast from previously reported as well as from unpublished placebo-controlled, double-blind, pediatric studies and their active-controlled open-label extension/extended studies.
These studies evaluated 2,751 pediatric patients 6 months to 14 years of age with persistent asthma, intermittent asthma associated with upper respiratory infection, or allergic rhinitis. These patients were enrolled in seven randomized, placebo-controlled, double-blind registration and post-registration studies and three active-controlled open-label extension/extended studies conducted by Merck Research Laboratories between 1995 and 2004.
Montelukast was well tolerated in all studies. Clinical and laboratory adverse experiences for patients treated with montelukast were generally mild and transient. The most frequent clinical adverse events for all treatments (placebo, montelukast, active control/usual care) in virtually all studies were upper respiratory infection, worsening asthma, pharyngitis, and fever.
The clinical and laboratory safety profile for montelukast was similar to that observed for placebo or active control/usual care therapies. The safety profile of montelukast did not change with long-term use.
孟鲁司特是一种强效白三烯受体拮抗剂,每日服用一次,对儿童和成人哮喘及过敏性鼻炎的治疗具有临床益处。由于其作为儿科控制药物被广泛使用,因此有必要进一步评估孟鲁司特在儿童中的安全性和耐受性。
总结已发表以及未发表的安慰剂对照、双盲儿科研究及其活性对照开放标签扩展/延长研究中孟鲁司特的安全性和耐受性数据。
这些研究评估了2751名6个月至14岁患有持续性哮喘、与上呼吸道感染相关的间歇性哮喘或过敏性鼻炎的儿科患者。这些患者参加了1995年至2004年间默克研究实验室进行的7项随机、安慰剂对照、双盲注册和注册后研究以及3项活性对照开放标签扩展/延长研究。
在所有研究中,孟鲁司特耐受性良好。接受孟鲁司特治疗的患者的临床和实验室不良经历通常较轻且为短暂性。几乎在所有研究中,所有治疗(安慰剂、孟鲁司特、活性对照/常规治疗)最常见的临床不良事件为上呼吸道感染、哮喘恶化、咽炎和发热。
孟鲁司特的临床和实验室安全性概况与安慰剂或活性对照/常规治疗所观察到的相似。孟鲁司特的安全性概况不会因长期使用而改变。