Key result
The microconcentrator-based urine myoglobin assay demonstrated a clinically inadequate sensitivity of 26.4% for the detection of severe rhabdomyolysis.
Why the study?
Does the microconcentrator qualitative assay for urine myoglobin accurately detect severe rhabdomyolysis in patients evaluated for the condition?
Observational (n=673)
Does the microconcentrator qualitative assay for urine myoglobin accurately detect severe rhabdomyolysis in patients evaluated for the condition?
The microconcentrator-based urine myoglobin assay has poor sensitivity and is clinically inadequate for screening or diagnosing severe rhabdomyolysis.
Answers are grounded in this paper and cite their sources.
Do not rely on this assay to detect severe rhabdomyolysis; leaves open need for sensitive alternatives in prospective studies.
BACKGROUND: In the diagnosis of rhabdomyolysis, the microconcentrator qualitative assay for urine myoglobin (uMb) is often used as a screening tool. The accuracy and clinical utility of this assay in screening patients with rhabdomyolysis have not been examined. METHODS: We conducted a retrospective analysis of the relationship between creatine kinase (CK), serum myoglobin (sMb), the urine qualitative assay for myoglobin and the semi-quantitative assay for urine haem pigments (uH) in patients evaluated for rhabdomyolysis. RESULTS: There were 673 patients with CK and uMb recorded on the same day. The uMb assay had a sensitivity of only 26.4% [95% confidence interval (CI): 23.1-29.7%] and specificity of 96.8% (95% CI: 95.5-98.1%) for the detection of severe rhabdomyolysis, defined as a CK >10 000 U/l. SMb and CK measured simultaneously in 83 patients were highly correlated (R(2) = 0.72 for log-transformed values), suggesting that the negative uMb test was not a result of the absence of sMb. In 241 patients who had CK, uMb and uH measured on the same day, the presence of 'moderate' or 'large' uH in the absence of haematuria, indicating presence of myoglobinuria, had a sensitivity of 81% (95% CI: 76-86%) for the detection of CK >10 000 U/l vs a sensitivity of 22% (95% CI: 17-27%) for the uMb assay. CONCLUSIONS: The microconcentrator-based uMb assay has a poor and clinically inadequate sensitivity in the detection and diagnosis of rhabdomyolysis.
No takes yet. Share an insight, caveat, or question.
Grover et al. (2004) conducted an observational in Rhabdomyolysis (n=673). Microconcentrator qualitative assay for urine myoglobin vs. Creatine kinase >10,000 U/l (reference standard) was evaluated on Sensitivity for the detection of severe rhabdomyolysis (CK >10 000 U/l) (95% CI 23.1-29.7). The microconcentrator-based urine myoglobin assay demonstrated a clinically inadequate sensitivity of 26.4% for the detection of severe rhabdomyolysis.
Synapse has enriched 10 related papers. Consider them for comparative context: