Associations between the 2007 Medicare reimbursement reduction for bone mineral density testing and osteoporosis drug therapy patterns of female Medicare beneficiaries

被引:3
|
作者
Kim, Sun Jung [1 ,2 ]
Lee, Joo Hun [3 ]
Kim, Sulgi [4 ]
Nakagawa, Shunichi [5 ]
Bertelson, Heather [6 ]
Lam, Julia [7 ]
Yoo, Ji Won [6 ,7 ]
机构
[1] Yonsei Univ, Coll Med, Dept Publ Hlth, Seoul, South Korea
[2] Yonsei Univ, Coll Med, Inst Hlth Serv Res, Seoul, South Korea
[3] Hanyang Univ, Coll Social Sci, Dept Media & Commun, Seoul 133791, South Korea
[4] Case Western Reserve Univ, Dept Epidemiol & Biostat, Cleveland, OH 44106 USA
[5] Columbia Univ, Coll Phys & Surg, Dept Med, New York, NY USA
[6] Aurora Hlth Care, Dept Internal Med, Milwaukee, WI USA
[7] Univ Wisconsin, Sch Med & Publ Hlth, Dept Med, Madison, WI USA
来源
关键词
accessibility of health services; drug therapy; osteoporosis; elderly women; OLDER WOMEN; PREDICTION; ADHERENCE; FRACTURES; HIP;
D O I
10.2147/PPA.S62780
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To examine how drug therapy patterns for osteoporosis have changed after the Medicare Physician Fee Schedule (MPFS) reimbursement reduction in 2007, in relation to follow-up bone mineral density (BMD) testing status. Methods: We used a retrospective temporal shift design to examine changes in drug therapy patterns before (Phase 1: January 1, 2005-December 31, 2006) and after (Phase 2: July 1, 2007-June 30, 2009) the MPFS reimbursement reduction in 2007, Cleveland, OH, USA. Participants were osteoporotic older women in Phase 1 (n = 1,340) and Phase 2 (n = 1,437). The main outcomes were a) adherence, b) adjustment, c) occurrence of an extended gap, and d) restarting drug therapy after an extended gap. Follow-up BMD testing status by study phase and location were also analyzed. Results: BMD testing rates at physicians' offices decreased from 64.5% in Phase 1 to 58.4% in Phase 2 (P = 0.02); however, testing rates in hospital outpatient settings increased (from 20.8% to 24.5%). There were also decreases in drug therapy adjustment from 15.9% in Phase 1 to 11.6% in Phase 2 (odds ratio [OR]: 0.73; P < 0.01) and in restarting drug therapy after an extended gap (55.4% in Phase 1 and 43.6% in Phase 2; OR: 0.76; P < 0.01). Conclusion: There were no changes in the overall rate of follow-up BMD testing. The rates of drug adjustments and restarting drug therapy after an extended gap did decrease. These decreases were more evident when follow-up BMD testing was not performed.
引用
收藏
页码:909 / 915
页数:7
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