A new approach to the development of assessment guidelines for osteoporosis

被引:250
|
作者
Kanis, JA
Black, D
Cooper, C
Dargent, P
Dawson-Hughes, B
De Laet, C
Delmas, P
Eisman, J
Johnell, O
Jonsson, B
Melton, L
Oden, A
Papapoulos, S
Pols, H
Rizzoli, R
Silman, A
Tenenhouse, A
机构
[1] Univ Sheffield, WHO Ctr Metab Bone Dis, Sheffield S10 2RX, S Yorkshire, England
[2] Univ Calif San Francisco, Div Clin Epidemiol, San Francisco, CA 94143 USA
[3] Univ Southampton, MRC, Environm Epidemiol Unit, Southampton SO9 5NH, Hants, England
[4] INSERM, Paris, France
[5] Tufts Univ, USDA, Human Res Ctr, Boston, MA 02111 USA
[6] Erasmus MC, Inst Publ Hlth, Rotterdam, Netherlands
[7] Hop Edouard Herriot, INSERM, Res Unit, Lyon, France
[8] St Vincents Hosp, Garvan Inst Med Res, Darlinghurst, NSW 2010, Australia
[9] Malmo Gen Hosp, Dept Orthopaed, Malmo, Sweden
[10] Stockholm Sch Econ, Dept Econ, Stockholm, Sweden
[11] Mayo Clin, Clin Epidemiol Sect, Rochester, MN USA
[12] Leiden Univ, Med Ctr, Dept Endocrinol, NL-2300 RA Leiden, Netherlands
[13] Univ Hosp, Div Bone Dis, Geneva, Switzerland
[14] Univ Manchester, ARC Epidemiol Res Unit, Manchester M13 9PL, Lancs, England
[15] Montreal Gen Hosp, Div Bone Metab, Montreal, PQ, Canada
关键词
D O I
10.1007/s001980200069
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The diagnosis of osteoporosis is made from the measurement of BMD. DXA at the hip is the appropriate diagnostic site. Current clinical guidelines follow the principle that BMD measurements are indicated in individuals with risk factors for fracture and that treatment is recommended in those with a BMD below a critical value. In some countries reimbursement for the costs of treatment depend upon such thresholds for BMD. In Europe the critical value corresponds to a T-score of-2.5 SD, whereas in the USA less stringent criteria are used. It is evident, however, that fracture risk at any given T-score varies markedly according to age and other risk factors. This has led to the view that interventions should be targeted to those at high risk, irrespective of a fixed BMD threshold. In this sense, BMD is utlized as a risk assessment, since in many instances intervention thresholds will be less stringent than the diagnostic threshold. Thus, intervention thresholds need to differ from diagnostic thresholds and be based on fracture probabilities. A 10-year fracture probability appears to be an appropriate time frame. There are a number of problems to be overcome in the development of assessment guidelines. They need to take account of not only the risk of hip fracture but also that of other fractures which contribute significantly to morbidity, particularly in younger individuals. A promising approach is to weight fracture probabilities according to the disutility incurred compared with hip fracture probability. Account also needs to be taken of the large geographic variation in fracture probabilities worldwide. A further challenge for the future will be to identify risk factors that predict fracture with high validity in different regions of the world and their independent contributions, so that models of risk prediction can be constructed and ultimately validated in independent cohorts.
引用
收藏
页码:527 / 536
页数:10
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