Adina Alazraki, MD, FAAP Assistant Professor, Radiology and Pediatrics Emory University School of Medicine Children s Healthcare of Atlanta

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Transcription:

Adina Alazraki, MD, FAAP Assistant Professor, Radiology and Pediatrics Emory University School of Medicine

Technical: Patient positioning Performance of the scan Analysis of the data Theoretical: Identification of a suitable control population Interpretation of normal for growing skeleton

Systemic long-term steroids Chronic inflammatory conditions Hypogonadism Prolonged immobilization Osteogenesis imperfecta Idiopathic juvenile osteoporosis Recurrent low trauma fractures Apparent osteopenia on radiographs

Relies on the absorption of x-rays of 2 different energy levels Low energy: 30-50 kev- bone attenuation>soft tissue High energy: >70 kev- bone is similar to soft tissue Quantification in grams

The diagnosis of osteoporosis in children and adolescents should NOT be made on the basis of densitometric criteria alone. Osteoporosis requires both a clinically significant fracture history and low bone mineral content or bone mineral density Clinically significant fracture history is one or more of the following: long bone fracture of the lower extremities vertebral compression fracture two or more long bone fractures of the upper extremities Low bone mineral content or bone mineral density = BMC or areal BMD Z-score < or = 2.0, adjusted for age, gender and body size, as appropriate

More specific terminology Perhaps pet peaves

DXA is an areal rather than a volumetric density measurement DXA-derived BMD is based on the two-dimensional projected area of a three-dimensional structure The third dimension, depth cannot be accounted for because it is in the same direction as the xray beam. Results in inherent error

PA lumbar spine and TBLH are most accurate and reproducible Soft tissue measures may help in systemic diseases Hip is not reliable during growth

Positioning and ROI selection Lumbar spine: straight and centered; last rib pair and upper sacrum visualized Whole body ROIs are generated automatically using edge-detection software for L1 to L4 Artifact can falsely elevate abmd BMC not affected by artifact

Small child Very low bone mineral density (OI) Makes for difficult anatomic delineation

Posterior spinal fusion hardware makes accuracy difficult Attempt to mask the hardware has limited value Trend may be more helpful as long as masking is similar

Z-score of zero is equivalent to the mean T-score is a measure of bone density loss since early adulthood NA to peds It is recommended that the phrase low bone density be used in DXA reports Age, gender, ethnicity, and physiologic maturity level are included in most current normative datasets Binkovitz, Larry A., and Maria J. Henwood. Pediatric DXA: Technique and Interpretation. Pediatric Radiology 37.1 (2007): 21 31. PMC. Web. 17 Mar. 2016.

Baseline DXA reports should contain the following information: DXA manufacturer, model and software version referring physician patient age, gender, race/ethnicity, weight, and height relevant medical history including previous fractures indication for study bone age results, if available technical quality BMC and areal BMD BMC and areal BMD Z-score source of reference data for Z-score calculations adjustments made for growth and maturation interpretation recommendations for the necessity and timing of the next DXA study are optional

Total body less head BMD Body composition data: Total BMC Lean body mass Fat mass/fat percentage Height-for-age AP spine BMD

Serial DXA reports should include the same information as for baseline testing, but additionally include: indications for follow-up scan comparability of studies interval changes in height, weight BMC and areal BMD Z-scores adjusted or unadjusted for height or other adjustments percentage change in BMC and areal BMD and interval change in Z- scores recommendations for the necessity and timing of the next BMD study are optional.

Reporting the trend TOTAL BODY LESS HEAD: Bone mineral density is 0.816 g/cm2. This is 81 percent of age-matched controls and yields a Z score of -2.3. There has been 9% improvement from the previous.

Must have accurate patient info (age, height, wt, sex, ethnicity) Use appropriate control reference data Pay attention to terminology Z-score not T-score Make sure the clinicians who refer know the capabilities of your software