National trends in osteoporosis visits and osteoporosis treatment, 1988-2003

被引:100
作者
Stafford, RS [1 ]
Drieling, RL [1 ]
Hersh, AL [1 ]
机构
[1] Stanford Univ, Stanford Prevent Res Ctr, Palo Alto, CA 94304 USA
关键词
D O I
10.1001/archinte.164.14.1525
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Research is limited on physicians' prescribing practices for osteoporosis treatment. We investigated patterns of pharmacotherapy from 1988 to 2003 and the impact of new medications on identification and treatment of patients with osteoporosis. Methods: We tracked trends from 1988 through 2003 in the frequency of osteoporosis visits and patterns of pharmacotherapy associated with these visits using nationally representative data on prescribing patterns by office-based US physicians from the IMS HEALTH National Disease and Therapeutic Index. Results: The number of physician visits for osteoporosis increased 4-fold between 1994 (1.3 million visits) and 003 (6.3 million visits), whereas it had remained stable in prior years. This increase coincided with the availability of oral daily bisphosphonates and the selective estrogen receptor modulator raloxifene. The annualized percentage of osteoporosis visits where medications were prescribed increased from 82% in 1988 to 97% by 2003. Prior to 1994, the leading choices for osteoporosis therapy were calcium and estrogens, with lesser roles played by calcitonins and bisphosphonates. Between 1994 and 2003, the percentage of visits where bisphosphonates and raloxifene were prescribed increased from 14% to 73% and from 0% to 12%, respectively, while prescriptions for other medications declined. Conclusions: New medications for osteoporosis offering improved efficacy and convenient dosing were associated with increased frequency of patient visits and treatment. This finding suggests that new drug therapy contributed to increased disease recognition and treatment.
引用
收藏
页码:1525 / 1530
页数:6
相关论文
共 42 条
[31]   Osteoporosis recognition: Correcting Gehlbach et al. [J].
Probst, JC ;
Moore, CG ;
Baxley, EG ;
Shinogle, JA .
AMERICAN JOURNAL OF PUBLIC HEALTH, 2002, 92 (12) :1885-1885
[32]   Alendronate and estrogen-progestin in the long-term prevention of bone loss: Four-year results from the early postmenopausal intervention cohort study - A randomized, controlled trial [J].
Ravn, P ;
Bidstrup, M ;
Wasnich, RD ;
Davis, JW ;
McClung, MR ;
Balske, A ;
Coupland, C ;
Sahota, O ;
Kaur, A ;
Daley, M ;
Cizza, G .
ANNALS OF INTERNAL MEDICINE, 1999, 131 (12) :935-+
[33]   Medical expenditures for the treatment of osteoporotic fractures in the United States in 1995: Report from the national osteoporosis foundation [J].
Ray, NF ;
Chan, JK ;
Thamer, M ;
Melton, LJ .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (01) :24-35
[34]   Drug therapy: Selective estrogen-receptor modulators - Mechanisms of action and application to clinical practice [J].
Riggs, BL ;
Hartmann, LC .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (07) :618-629
[35]   Risks and benefits of estrogen plus progestin in healthy postmenopausal women - Principal results from the Women's Health Initiative randomized controlled trial [J].
Rossouw, JE ;
Anderson, GL ;
Prentice, RL ;
LaCroix, AZ ;
Kooperberg, C ;
Stefanick, ML ;
Jackson, RD ;
Beresford, SAA ;
Howard, BV ;
Johnson, KC ;
Kotchen, JM ;
Ockene, J .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (03) :321-333
[36]   Identification and fracture outcomes of undiagnosed low bone mineral density in postmenopausal women - Results from the National Osteoporosis Risk Assessment [J].
Siris, ES ;
Miller, PD ;
Barrett-Connor, E ;
Faulkner, KG ;
Wehren, LE ;
Abbott, TA ;
Berger, ML ;
Santora, AC ;
Sherwood, LM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (22) :2815-2822
[37]   The comparative effect on bone density, endometrium, and lipids of continuous hormones as replacement therapy (CHART study) - A randomized controlled trial [J].
Speroff, L ;
Rowan, J ;
Symons, J ;
Genant, H ;
Wilborn, W .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (17) :1397-1403
[38]  
*US CENS BUR POP D, PROJ TOT RES POP 5 Y
[39]  
*US CENS BUR POP D, 2000, RES POP EST US AG SE
[40]   Treatment of osteoporosis with bisphosphonates [J].
Watts, NB .
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA, 2001, 27 (01) :197-+