Moride Y, Ducruet T, Rochon S, Lavoie F
Faculty of Pharmacy, Universityof Montréal and Centre for Clinical Epidemiology and Community Studies, SMBD Jewish General Hospital, Montreal, Quebec, Canada.
Rheumatology (Oxford). 2003 Nov;42 Suppl 3:iii17-22. doi: 10.1093/rheumatology/keg494.
The effectiveness of pharmacological therapies is dependent in part on patient persistency with the prescribed therapeutic regimen. In the case of non-specific non-steroidal anti-inflammatory drugs (NSAIDs), effectiveness is often compromised by undesirable side-effects, poor compliance or discontinuation of therapy. While patterns of utilization of non-specific NSAIDs have been investigated, few data are available on the patterns of persistency for cyclooxygenase (COX)-2-specific inhibitors. This study used a provincial health-care system database in Quebec, Canada, to determine the duration of treatment in new users of COX-2-specific inhibitors and non-specific NSAIDs over the first 3 months of treatment, and to characterize the factors associated with treatment persistency. Results demonstrate that the median duration of treatment was longer among patients initially prescribed COX-2-specific inhibitors (30 days and 23 days for celecoxib and rofecoxib respectively) than in those prescribed non-selective NSAIDs (10 days). Although the percentage of patients remaining on COX-2-specific drugs declined over the course of treatment, few patients on either celecoxib or rofecoxib switched drugs, either to the other COX-2-specific inhibitor or to non-specific NSAIDs. Factors associated with persistent drug use were: COX-2-specific inhibitors, age, and the use of gastroprotective agents either at treatment initiation or during follow-up. Dosage, chronic disease score and prescriber's specialty were only marginally associated with persistency. Prior use of gastroprotective agents was associated with lower persistency. Although the limitations of this study, which included lack of information on the indication for the prescription and the reason for switch or discontinuation, preclude definite conclusions regarding patterns of use of these drugs, the data suggest that the use of COX-2-specific inhibitors may result in increased persistency with treatment.
药物治疗的有效性部分取决于患者对规定治疗方案的依从性。就非特异性非甾体抗炎药(NSAIDs)而言,有效性常常因不良副作用、依从性差或治疗中断而受到影响。虽然已经对非特异性NSAIDs的使用模式进行了研究,但关于环氧化酶(COX)-2特异性抑制剂的依从模式的数据却很少。本研究利用加拿大魁北克省的一个省级医疗保健系统数据库,来确定COX-2特异性抑制剂和非特异性NSAIDs新使用者在治疗的前3个月内的治疗持续时间,并对与治疗依从性相关的因素进行描述。结果表明,最初开具COX-2特异性抑制剂处方的患者(塞来昔布和罗非昔布的治疗持续时间中位数分别为30天和23天)的治疗持续时间长于开具非选择性NSAIDs处方的患者(10天)。尽管继续使用COX-2特异性药物的患者百分比在治疗过程中有所下降,但使用塞来昔布或罗非昔布的患者很少换药,既没有换用另一种COX-2特异性抑制剂,也没有换用非特异性NSAIDs。与持续用药相关的因素有:COX-2特异性抑制剂、年龄,以及在治疗开始时或随访期间使用胃保护剂。剂量、慢性病评分和开处方者的专业与依从性仅有微弱关联。先前使用胃保护剂与较低的依从性相关。尽管本研究存在局限性,包括缺乏关于处方适应证以及换药或停药原因的信息,无法就这些药物的使用模式得出明确结论,但数据表明,使用COX-2特异性抑制剂可能会提高治疗的依从性。