Arden N K, Earl S, Fisher D J, Cooper C, Carruthers S, Goater M
MRC Epidemiology Resource Centre, University of Southampton, Southampton General Hospital, Southampton, SO16 6YD, UK.
Osteoporos Int. 2006;17(11):1626-9. doi: 10.1007/s00198-006-0171-5. Epub 2006 Jul 6.
The objective of this paper was to determine the persistence with teriparatide at 12 months in all patients in the UK who were prescribed the treatment since its launch.
Virtually all patients prescribed teriparatide in the UK receive treatment through Healthcare at Home, Basingstoke, UK. Data was obtained to assess the start date, discontinuation date and reason for discontinuation in all patients receiving teriparatide since its launch. Persistence was defined as the number of patients continuing treatment.
A total of 1,104 patients were included in the analysis. The median duration of use in all patients was 252 days. Of the 435 patients who were at least 12 months post-initiation of treatment, persistence was 87%. Forty-two patients (3.8%) had discontinued treatment due to adverse events.
This study demonstrates that persistence with teriparatide at 12 months is very high and is probably greater than that of existing oral therapies for osteoporosis. The reasons for the high persistence rates seen with teriparatide are likely to be multi-factorial. The high persistence rates should help to optimise the effectiveness of therapy in this group of high-risk patients.
本文的目的是确定自特立帕肽在英国上市以来,所有接受该治疗的患者在12个月时的持续用药情况。
在英国,几乎所有开具特立帕肽处方的患者都通过英国贝辛斯托克的居家医疗服务接受治疗。获取了自特立帕肽上市以来所有接受该药物治疗患者的开始日期、停药日期及停药原因的数据。持续用药定义为继续接受治疗的患者数量。
共有1104例患者纳入分析。所有患者的中位用药时长为252天。在治疗开始至少12个月的435例患者中,持续用药率为87%。42例患者(3.8%)因不良事件停药。
本研究表明,特立帕肽在12个月时的持续用药率很高,可能高于现有的骨质疏松症口服治疗药物。特立帕肽持续用药率高的原因可能是多方面的。高持续用药率有助于优化该高危患者群体的治疗效果。