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Submitted on May 31, 2006
Accepted on August 22, 2006
New Mexico Clinical Research & Osteoporosis Center, Albuquerque, NM; Arthritis & Osteoporosis Consultants of the Carolinas, Charlotte, NC
* To whom correspondence should be addressed. E-mail: LEWIECKI{at}aol.com.
Context: Vertebral fracture (VF) is the most common type of fragility fracture, yet most VFs are not clinically apparent. VFs are associated with a significant increase in morbidity, mortality, and risk of future fracture. Many patients with VFs do not have T-scores classified as osteoporosis. Knowledge of VFs may change diagnostic classification, estimation of future fracture risk, and clinical management. Vertebral fracture assessment (VFA) by dual-energy x-ray absorptiometry (DXA) is a method for imaging the spine to diagnose VFs.
Evidence Acquisition: Background information and medical evidence on the technology and clinical applications of VFA was acquired by electronic searching of PubMed for appropriate terms that included vertebral fracture, imaging, diagnosis, DXA, and cost-effectiveness. Matches with the highest levels of medical evidence were selected for review, recognizing that the new and evolving nature of the field required inclusion of some material that relied partly on expert opinion.
Evidence Synthesis: The sensitivity and specificity of VFA compares favorably to spine radiographs in its ability to diagnose Grade 2 and Grade 3 VFs. VFA involves less radiation, lower cost, and often greater patient convenience than spine radiography. Cost-effectiveness modeling suggests that imaging of the spine in selected patients provides essential diagnostic and therapeutic information at a nominal cost. Patients with T-scores that are classified as low bone mass (osteopenia) who are selected for pharmacological therapy based on the presence of a VF benefit by reduction in fracture risk. Guidelines for the clinical application of VFA have been developed by the International Society for Clinical Densitometry (ISCD).
Conclusions: VFA is a technology for diagnosing VFs that may alter diagnostic classification, improve fracture risk stratification, and identify patients likely to benefit from pharmacological therapy who otherwise might not be treated.
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