Compliance and persistence to oral bisphosphonate therapy following initiation within a secondary fracture prevention program: a randomised controlled trial of specialist vs. non-specialist management

被引:49
作者
Ganda, K. [1 ,2 ]
Schaffer, A. [3 ]
Pearson, S. [3 ]
Seibel, M. J. [1 ,2 ]
机构
[1] Univ Sydney, ANZAC Res Inst, Bone Res Program, Concord, NSW 2139, Australia
[2] Concord Repatriat Gen Hosp, Dept Endocrinol & Metab, Concord, NSW 2139, Australia
[3] Univ Sydney, Sydney Med Sch, Pharmacoepidemiol & Pharmaceut Policy Res Grp, Fac Pharm,Sch Publ Hlth, Sydney, NSW 2006, Australia
关键词
Compliance; Osteoporosis; Persistence; Pharmaceutical claims data; Secondary fracture prevention program; Treatment; BONE TURNOVER MARKERS; OSTEOPOROTIC FRACTURE; MEDICATION ADHERENCE; SUBSEQUENT FRACTURE; FRAGILITY FRACTURE; TRAUMA FRACTURE; RISK; WOMEN; MEN; RISEDRONATE;
D O I
10.1007/s00198-013-2610-4
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Following initiation of oral bisphosphonate therapy through a secondary fracture prevention program, 2-year treatment compliance and persistence remained high and were similar in patients randomised to follow-up by either the program or primary care physician. Thus, community-based and specialist management are equally effective in supporting compliance and persistence with anti-osteoporotic treatments. The purpose of this study was to determine whether management by a secondary fracture prevention (SFP) program (aka "fracture liaison service") results in better compliance and persistence to oral bisphosphonate therapy than follow-up by the primary care physician, after initiation within an SFP program. This prospective RCT included 102 patients with incident osteoporotic fractures referred to a SFP program in Sydney, Australia. Following oral bisphosphonate therapy initiation, patients were randomised to either 6-monthly follow-up with the SFP program (group A) or referral to their primary care physician with a single SFP program visit at 24 months (group B). Compliance and persistence to treatment were measured using pharmaceutical claims data. Predictors of compliance and persistence and associations between compliance and persistence, and changes in bone mineral density (BMD) or bone resorption marker, urinary deoxypyridinoline over 24 months were analysed. The median medication possession ratio at 24 months was 0.78 (IQR, 0.50-0.93) in group A and 0.79 (IQR, 0.48-0.96) in group B (p = 0.68). Persistence at 24 months was also similar in both groups (64 vs. 61 %, respectively; p = 0.75). After adjusting for confounders, patients in group A were not more likely to be compliant (OR, 1.06; 95 % CI, 0.46-2.47) or persistent (HR, 0.83; 95 % CI, 0.27-1.67) than those randomised to group B. Time-based changes in BMD or bone turnover were not associated with compliance or persistence. Compliance and persistence to oral bisphosphonate therapy remain high amongst patients initiated within an SFP program, with community-based and SFP program management being equally effective in maintaining therapeutic compliance and persistence over 2 years. These results indicate that one of the main functions of an SFP program may be the initiation of therapy rather than continuous patient monitoring.
引用
收藏
页码:1345 / 1355
页数:11
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