Blake K V
Nemours Children's Clinic, Jacksonville, FL 32207, USA.
Ann Pharmacother. 1999 Dec;33(12):1299-314. doi: 10.1345/aph.18430.
To review the pharmacology, pharmacokinetics, clinical efficacy, and adverse effects of montelukast, a leukotriene receptor antagonist used to treat asthma, and to discuss the therapeutic role of montelukast as long-term medication and difficulties associated with the management of asthma.
A MEDLINE search (up to May 1999) was conducted to identify relevant English-language publications, including preclinical studies, clinical trials, and recent reviews.
All available published reports of controlled, clinical trials of montelukast in adults and children with asthma were summarized, including pharmacokinetic and pharmacologic effects of montelukast.
Information on the safety and efficacy of montelukast was evaluated on the basis of patient selection, study design, methodology, and statistical significance as compared with placebo or inhaled corticosteroid treatment.
Montelukast is approved for the prophylaxis and chronic treatment of asthma at a dose of 10 mg once daily for adolescents (> or =15 y) and adults and 5 mg once daily for children (6-14 y). In placebo-controlled clinical trials, montelukast significantly improved pulmonary lung function (as measured by forced expiratory volume in 1 sec), significantly reduced beta2-agonist use, and significantly improved patient-reported end points in adults and children (> or =6 y) with chronic asthma. In adults, a similar magnitude of improvement in lung function is seen with or without inhaled corticosteroid use; the effects of montelukast may be additive to those of inhaled corticosteroids and permit the reduction of the required dose of inhaled corticosteroids. In cases of exercise-induced asthma (adults and children), montelukast treatment attenuates the fall in pulmonary function following exercise. It attenuates both the early- and late-phase responses of asthma after allergen inhalation. Improvements in asthma control are similar in asthmatic patients who are aspirin-sensitive or not aspirin-sensitive and can be seen within one day of treatment. Tolerance does not develop, and the adverse events do not differ from those of placebo.
Montelukast is indicated for the prophylaxis of chronic asthma in adults and children (> or =6 y). It may be considered for use as first-line therapy in patients with mild persistent asthma or for additional control in patients who are still symptomatic while receiving treatment with inhaled corticosteroids. It may also be used for additional control in aspirin-sensitive asthmatic patients. Consideration may be given for using montelukast to allow tapering of the dose of inhaled corticosteroids while maintaining clinical stability. Chronic treatment with montelukast can provide additional control of symptoms during exercise, but inhaled beta2-agonists remain first-line therapy for prophylaxis and treatment.
综述用于治疗哮喘的白三烯受体拮抗剂孟鲁司特的药理学、药代动力学、临床疗效及不良反应,并探讨孟鲁司特作为长期用药的治疗作用以及哮喘管理中存在的困难。
进行了MEDLINE检索(截至1999年5月)以识别相关英文出版物,包括临床前研究、临床试验及近期综述。
总结了所有已发表的关于孟鲁司特在成人及儿童哮喘患者中进行的对照临床试验报告,包括孟鲁司特的药代动力学和药理作用。
根据患者选择、研究设计、方法以及与安慰剂或吸入性糖皮质激素治疗相比的统计学意义,评估孟鲁司特的安全性和疗效信息。
孟鲁司特已被批准用于哮喘的预防和慢性治疗,青少年(≥15岁)及成人剂量为每日1次,每次10mg;儿童(6 - 14岁)剂量为每日1次,每次5mg。在安慰剂对照临床试验中,孟鲁司特显著改善肺功能(以1秒用力呼气量衡量),显著减少β2受体激动剂的使用,并显著改善慢性哮喘成人及儿童(≥6岁)患者报告的终点指标。在成人中,无论是否使用吸入性糖皮质激素,肺功能改善程度相似;孟鲁司特的作用可能与吸入性糖皮质激素相加,并允许减少所需的吸入性糖皮质激素剂量。在运动诱发性哮喘(成人和儿童)病例中,孟鲁司特治疗可减轻运动后肺功能下降。它可减轻变应原吸入后哮喘的早期和晚期反应。在阿司匹林敏感或不敏感的哮喘患者中,哮喘控制的改善相似,且在治疗1天内即可显现。不会产生耐受性,不良事件与安慰剂无异。
孟鲁司特适用于成人及儿童(≥6岁)慢性哮喘的预防。对于轻度持续性哮喘患者,可考虑将其作为一线治疗药物;对于在接受吸入性糖皮质激素治疗时仍有症状的患者,可考虑用于进一步控制症状。它也可用于阿司匹林敏感哮喘患者的进一步控制。可考虑使用孟鲁司特在维持临床稳定性的同时逐渐减少吸入性糖皮质激素的剂量。孟鲁司特的长期治疗可在运动期间提供额外的症状控制,但吸入性β2受体激动剂仍然是预防和治疗的一线药物。