OBJECTIVE Immobilization and inadequate nutrition after high-energy trauma result in loss of lean muscle mass. Body composition (percent body fat (%BF), fat mass (FM), fat free mass (FFM)) is traditionally… Click to show full abstract
OBJECTIVE Immobilization and inadequate nutrition after high-energy trauma result in loss of lean muscle mass. Body composition (percent body fat (%BF), fat mass (FM), fat free mass (FFM)) is traditionally quantified with techniques that require expensive equipment and/or ionizing radiation. The purpose of this study was to assess reliability and validity of amplitude-mode (A-mode) ultrasound to quantify body composition for use in a randomized clinical trial assessing interventions to prevent muscle loss in young individuals after high energy musculoskeletal trauma. METHODS 31 volunteer subjects underwent body composition assessments using A-mode ultrasound and air displacement plethysmography (ADP). Independent raters performed 2 serial ultrasound measures. The same raters performed body composition assessment in 12 consecutive subjects that sustained acute musculoskeletal trauma indicated for surgery. Test-retest and interrater reliability were assessed using intraclass correlation coefficient (ICC). Agreement between ultrasound and ADP was assessed with Bland-Altmann analysis. RESULTS Test-retest and interrater reliability was excellent for volunteer subjects, with ICC values (%BF, FM, FFM) of 0.87, 0.90, and 0.99 (rater 1); 0.80, 0.82, and 0.98 (rater 2). FFM measured by US was strongly correlated with ADP measures (r=0.9635, p<0.05). Bland-Altman analysis demonstrated no systematic bias between ultrasound and ADP measures of body composition. In trauma subjects, the interrater reliability was excellent, with ICCs of 0.96, 0.98, and 0.99 for %BF, FM, and FFM respectively. CONCLUSIONS A-mode ultrasound is a relatively low-cost tool that provides reliable estimates of body composition, and is a viable alternative for monitoring body composition in young, healthy patients. LEVEL OF EVIDENCE Diagnostic Level II.
               
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