Efficacy of different dosing schedules of etidronate for stress shielding after cementless total hip arthroplasty

被引:30
作者
Yamaguchi, K
Masuhara, K
Yamasaki, S
Fuji, T
机构
[1] Kaizuka City Hosp, Dept Orthopaed Surg, Kaizuka 5970015, Japan
[2] Osaka Koseinenkin Hosp, Dept Orthopaed Surg, Osaka, Japan
关键词
etidronate; dose-response relationship; bone mineral density; stress shielding; cementless total hip arthroplasty;
D O I
10.1007/s00776-004-0854-8
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Forty-four women who had undergone cementless total hip arthroplasty (THA) were selected for determination of the optimum dosage of etidronate in the treatment of stress shielding after surgery. Patients were 55-86 years of age. The patients were randomized into three groups. The control group (n = 17) was not treated with osteoactive drugs. The low-dose group (n = 12) and the high-dose group (n = 15) received 200mg or 400mg etidronate daily for 2 weeks, followed by 12 weeks of calcium supplementation of 500 mg/day. These patients received four cycles of therapy over 1 year postoperatively. Periprosthetic bone mineral density (BMD) was measured with dual-energy X-ray absorptiometry at 3 weeks, 6 months, and 12 months. At 12 months, bone loss in the low-dose and high-dose groups was significantly lower compared with the control group in Gruen zones 1 and 7. There were additional significant differences with regard to bone loss between the control group and the high-dose group in zones 2, 4, and 6. Our data suggest that high dosages are more effective in reducing postoperative bone loss after cementless THA.
引用
收藏
页码:32 / 36
页数:5
相关论文
共 21 条
[1]
[Anonymous], 1979, CLIN ORTHOP RELAT RE
[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]
Comparative efficacy and safety study of etidronate and alendronate in postmenopausal osteoporosis.: Effect of adding hormone replacement therapy [J].
Cortet, B ;
Béra-Louville, A ;
Gauthier, P ;
Gauthier, A ;
Marchandise, X ;
Delcambre, B .
JOINT BONE SPINE, 2001, 68 (05) :410-415
[4]
Effect of alendronate on risk of fracture in women with low bone density but without vertebral fractures - Results from the fracture intervention trial [J].
Cummings, SR ;
Black, DM ;
Thompson, DE ;
Applegate, WB ;
Barrett-Connor, E ;
Musliner, TA ;
Palermo, L ;
Prineas, R ;
Rubin, SM ;
Scott, JC ;
Vogt, T ;
Wallace, R ;
Yates, AJ ;
LaCroix, AZ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (24) :2077-2082
[5]
Oral alendronate induces progressive increases in bone mass of the spine, hip, and total body over 3 years in postmenopausal women with osteoporosis [J].
Devogelaer, JP ;
Broll, H ;
CorreaRotter, R ;
Cumming, DC ;
DeDeuxchaisnes, CN ;
Geusens, P ;
Hosking, D ;
Jaeger, P ;
Kaufman, JM ;
Leite, M ;
Leon, J ;
Liberman, U ;
Menkes, CJ ;
Meunier, PJ ;
Reid, I ;
Rodriguez, J ;
Romanowicz, A ;
Seeman, E ;
Vermeulen, A ;
Hirsch, LJ ;
Lombardi, A ;
Plezia, K ;
Santora, AC ;
Yates, AJ ;
Yuan, W .
BONE, 1996, 18 (02) :141-150
[6]
FUJITA T, 1994, KISO RINSHO, V28, P447
[7]
4-YEAR STUDY OF INTERMITTENT CYCLIC ETIDRONATE TREATMENT OF POSTMENOPAUSAL OSTEOPOROSIS - 3 YEARS OF BLINDED THERAPY FOLLOWED BY ONE-YEAR OF OPEN THERAPY [J].
HARRIS, ST ;
WATTS, NB ;
JACKSON, RD ;
GENANT, HK ;
WASNICH, RD ;
ROSS, P ;
MILLER, PD ;
LICATA, AA ;
CHESNUT, CH .
AMERICAN JOURNAL OF MEDICINE, 1993, 95 (06) :557-567
[8]
Kiratli BJ, 1996, J ARTHROPLASTY, V11, P184
[9]
Massari Leo, 1996, Bulletin Hospital for Joint Diseases, V54, P206
[10]
The metal-cancellous cementless Lubeck total hip arthroplasty - Five-to-nine-year results [J].
Matsui, M ;
Nakata, K ;
Masuhara, K ;
Ohzono, K ;
Sugano, N ;
Ochi, T .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1998, 80B (03) :404-410