Clinical Pharmacology and Pharmacy, Department of Public Health, University of Southern Denmark, Odense, Denmark.
Department of Clinical Biochemistry & Pharmacology, Odense University Hospital, Odense, Denmark.
Basic Clin Pharmacol Toxicol. 2018 Jul;123(1):78-83. doi: 10.1111/bcpt.12986. Epub 2018 Mar 30.
Montelukast, a leukotriene receptor antagonist, was marketed in 1998 as an oral supplementary treatment to patients with mild to moderate asthma. The aim of this study was to describe the early discontinuation pattern among montelukast users in Denmark in the period of 1 March 1998 to 31 December 2016, and to identify demographic characteristics possibly associated with early discontinuation. This nationwide drug utilization study was based on data collected from three nationwide Danish registers. All montelukast users who redeemed at least one prescription in the study period were identified. Early discontinuation was defined as failing to fill a second prescription for montelukast within at least a year after the initial montelukast prescription. Among 135,271 included montelukast users, 47,480 (35%) discontinued the use of montelukast after a single redeemed prescription. The trend in early discontinuation increased throughout the years. The most predominant demographic risk factors for early discontinuation were prescription for only nasal topical anti-allergic treatment up to a year prior to montelukast initiation [adjusted odds ratio (OR) 2.25; 95% confidence interval (CI) 2.13-2.38], as well as suspected off-label use (adjusted OR 2.02; 95% CI 1.97-2.08). Several risk factors were associated with a decreased risk of early discontinuation; most pronounced was a prescription of inhaled corticosteroids within a year up to montelukast initiation [adjusted OR 0.47 (95% CI 0.46-0.49)]. Early discontinuation was more pronounced after patent expiry in 2012 [adjusted OR 1.42 (95% CI 1.38-1.45)]. In conclusion, we found that early montelukast discontinuation increased during the last 19 years. Appropriateness of the treatment indication as estimated by concomitant prescription of adequate inhalation therapy was associated with a low risk of early discontinuation. A more pronounced early discontinuation was observed after patent expiry in 2012, which could reflect a more liberal approach to montelukast prescription.
孟鲁司特,一种白三烯受体拮抗剂,于 1998 年作为一种口服补充疗法上市,用于治疗轻度至中度哮喘患者。本研究的目的是描述 1998 年 3 月 1 日至 2016 年 12 月 31 日期间丹麦孟鲁司特使用者的早期停药模式,并确定可能与早期停药相关的人口统计学特征。这项全国性药物利用研究基于从三个全国性丹麦登记处收集的数据。所有在研究期间至少开出一张处方的孟鲁司特使用者都被确定为研究对象。早期停药定义为在初始孟鲁司特处方后至少一年内未能开出第二张孟鲁司特处方。在纳入的 135271 名孟鲁司特使用者中,有 47480 人(35%)在单次处方后停止使用孟鲁司特。早期停药的趋势随着时间的推移而增加。早期停药的主要人口统计学危险因素是在开始孟鲁司特治疗前一年内仅开具鼻用局部抗过敏治疗的处方[调整后的优势比(OR)2.25;95%置信区间(CI)2.13-2.38],以及疑似超适应证使用(调整后的 OR 2.02;95%CI 1.97-2.08)。有几个危险因素与早期停药的风险降低相关;最显著的是在开始孟鲁司特治疗前一年内开具吸入皮质类固醇的处方[调整后的 OR 0.47(95%CI 0.46-0.49)]。在 2012 年专利期满后,早期停药更为明显[调整后的 OR 1.42(95%CI 1.38-1.45)]。总之,我们发现,在过去的 19 年里,孟鲁司特的早期停药率增加了。治疗适应证的适当性,如估计同时开具适当的吸入治疗,与早期停药的低风险相关。在 2012 年专利期满后,早期停药更为明显,这可能反映了孟鲁司特处方更为宽松。