Effect of alendronate on limited-activity days and bed-disability days caused by back pain in postmenopausal women with existing vertebral fractures

被引:151
作者
Nevitt, MC
Thompson, DE
Black, DM
Rubin, SR
Ensrud, K
Yates, AJ
Cummings, SR
机构
[1] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[3] Merck & Co Inc, Sci Commun Grp, Rahway, NJ 07065 USA
[4] Merck & Co Inc, Clin Res, Rahway, NJ 07065 USA
[5] Univ Minnesota, Vet Affairs Med Ctr, Dept Med, Minneapolis, MN USA
关键词
D O I
10.1001/archinte.160.1.77
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Women with new vertebral fractures have an increased risk of back pain and functional limitation because of back pain. Alendronate sodium treatment reduces the risk of new vertebral fracture by 50% in postmenopausal women with osteoporosis. Objective: To determine the effect of alendronate therapy on days affected by back pain in postmenopausal women with existing vertebral fractures. Design: Three-year, placebo-controlled, randomized, double-blind study. Setting: Fifteen university-based research clinics in the United States. Participants: A total of 2027 postmenopausal women aged 55 to 81 years with low femoral neck bone density and a preexisting vertebral fracture. Intervention: Alendronate sodium (5 mg/d for 2 years and 10 mg/d for the third year) or placebo. Main Outcome Measures: Occurrence and severity of back pain, number of days with back pain, and number of days of bed rest or limited activity because of back pain during 3 years of follow-up. Results: Irrespective of treatment assignment, women with new, clinically recognized vertebral fractures during follow-up had an increased risk of days of bed disability and days of limited activity because of back pain after the fracture. Women receiving alendronate reported an average of 3.2 fewer days of bed rest (P =.001) and 11.4 fewer days of limited activity (not including days of bed rest) because of back pain (P =.04) during follow-up than those receiving placebo. In the alendronate group, relative to the placebo group, there was a reduced risk of 1 or more bed-rest days (relative risk, 0.68; 95% confidence interval, 0.53-0.87), of 7 or more bedrest days (0.44; 0.30-0.64), and of 7 or more limited activity days (0.87; 0.76-0.99). There were no statistically significant differences between treatment groups in the frequency of days of back pain or increases in back-related disability between baseline and study end. Conclusion: In postmenopausal women with preexisting vertebral fracture, alendronate therapy for 3 years reduced the number of days of bed disability and days of limited activity caused by back pain.
引用
收藏
页码:77 / 85
页数:9
相关论文
共 29 条
[1]  
BLACK DM, 1995, J BONE MINER RES, V10, P890
[2]   Randomised trial of effect of alendronate on risk of fracture in women with existing vertebral fractures [J].
Black, DM ;
Cummings, SR ;
Karpf, DB ;
Cauley, JA ;
Thompson, DE ;
Nevitt, MC ;
Bauer, DC ;
Genant, HK ;
Haskell, WL ;
Marcus, R ;
Ott, SM ;
Torner, JC ;
Quandt, SA ;
Reiss, TF ;
Ensrud, KE .
LANCET, 1996, 348 (9041) :1535-1541
[3]  
BLACK DM, 1993, OSTEOPOROSIS INT, V3, P29
[4]   QUALITY-OF-LIFE ISSUES IN WOMEN WITH VERTEBRAL FRACTURES DUE TO OSTEOPOROSIS [J].
COOK, DJ ;
GUYATT, GH ;
ADACHI, JD ;
CLIFTON, J ;
GRIFFITH, LE ;
EPSTEIN, RS ;
JUNIPER, EF .
ARTHRITIS AND RHEUMATISM, 1993, 36 (06) :750-756
[5]   COVARIANCE ANALYSIS OF HEART-TRANSPLANT SURVIVAL DATA [J].
CROWLEY, J ;
HU, M .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1977, 72 (357) :27-36
[6]  
CUMMINGS SR, 1995, VERTEBRAL FRACTURE O, P3
[7]  
Dolan AL, 1996, BRIT J RHEUMATOL, V35, P1269
[8]  
ETTINGER B, 1992, J BONE MINER RES, V7, P449
[9]   Personal experience in managing acute compression fractures, their aftermath, and the bone pain syndrome, in osteoporosis [J].
Frost, HM .
OSTEOPOROSIS INTERNATIONAL, 1998, 8 (01) :13-15
[10]   VERTEBRAL FRACTURE ASSESSMENT USING A SEMIQUANTITATIVE TECHNIQUE [J].
GENANT, HK ;
WU, CY ;
VANKUIJK, C ;
NEVITT, MC .
JOURNAL OF BONE AND MINERAL RESEARCH, 1993, 8 (09) :1137-1148