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日本每日一次特立帕肽的依从性和持续性:一项回顾性处方数据库队列研究。

Adherence and persistence with once-daily teriparatide in Japan: a retrospective, prescription database, cohort study.

作者信息

Tanaka Ikuko, Sato Masayo, Sugihara Tomoko, Faries Douglas E, Nojiri Shuko, Graham-Clarke Peita, Flynn Jennifer A, Burge Russel T

机构信息

Nagoya Rheumatology Clinic/Initiative for Rheumatology and Osteoporosis, Nagoya 4500002, Japan.

Lilly Research Laboratories Japan, Eli Lilly Japan K.K., 7-1-5 Isogami dori, Chuoku, Kobe 6510086, Japan.

出版信息

J Osteoporos. 2013;2013:654218. doi: 10.1155/2013/654218. Epub 2013 Dec 12.

Abstract

Adherence and persistence with osteoporosis treatments are essential for reducing fracture risk. Once-daily teriparatide is available in Japan for treating osteoporosis in patients with a high risk of fracture. The study objective was to describe real-world adherence and persistence with once-daily teriparatide 20 μg during the first year of treatment for patients who started treatment during the first eight months of availability in Japan. This prescription database study involved patients with an index date (first claim) between October 2010 and May 2011, a preindex period ≥6 months, and a postindex period ≥12 months and who were aged >45 years. Adherence (medication possession ratio (MPR)) and persistence (time from the start of treatment to discontinuation; a 60-day gap in supply) were calculated. A total of 287 patients started treatment during the specified time period; 123 (42.9%) were eligible for inclusion. Overall mean (standard deviation) adherence was 0.702 (0.366), with 61.0% of patients having high adherence (MPR > 0.8). The percentage of patients remaining on treatment was 65.9% at 180 days and 61.0% at 365 days. Our findings suggest that real-world adherence and persistence with once-daily teriparatide in Japan are similar to that with once-daily teriparatide in other countries and with other osteoporosis medications.

摘要

坚持和持续使用骨质疏松症治疗药物对于降低骨折风险至关重要。在日本,每日一次的特立帕肽可用于治疗骨折高风险患者的骨质疏松症。本研究的目的是描述在日本特立帕肽上市的前八个月开始治疗的患者在治疗的第一年中每日一次使用20μg特立帕肽的真实世界中的依从性和持续性。这项处方数据库研究纳入了索引日期(首次索赔)在2010年10月至2011年5月之间、索引前期≥6个月、索引后期≥12个月且年龄>45岁的患者。计算了依从性(药物持有率(MPR))和持续性(从治疗开始到停药的时间;供应中断60天)。共有287名患者在指定时间段内开始治疗;123名(42.9%)符合纳入条件。总体平均(标准差)依从性为0.702(0.366),61.0%的患者具有高依从性(MPR>0.8)。在180天时仍在接受治疗的患者百分比为65.9%,在365天时为61.0%。我们的研究结果表明,在日本每日一次使用特立帕肽的真实世界中的依从性和持续性与其他国家每日一次使用特立帕肽以及其他骨质疏松症药物的情况相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a5e/3876673/9757669ba052/JOSTEO2013-654218.001.jpg

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