Diagnostic Requirements for Rhabdomyolysis
The diagnostic threshold for rhabdomyolysis is a serum creatine kinase (CK) level at least 10 times the upper limit of normal, typically accompanied by clinical symptoms including muscle pain, weakness, and dark urine. 1, 2
Primary Diagnostic Criteria
Serum Creatine Kinase (CK) Elevation:
Urinalysis Findings:
- Myoglobinuria (tea/cola-colored urine)
- Positive for blood on dipstick
- Negative for RBCs on microscopy 1
Supporting Laboratory Tests
Plasma myoglobin:
- Confirms muscle breakdown
- Rises earlier than CK but has shorter half-life (2-3 hours)
- May return to normal while CK remains elevated 1
Additional Laboratory Abnormalities:
- Elevated AST/ALT (due to muscle breakdown rather than primary liver disease)
- Electrolyte disturbances (hyperkalemia, hypocalcemia, hyperphosphatemia)
- Metabolic acidosis
- Signs of acute kidney injury (elevated BUN, creatinine) 1
Clinical Presentation
- Muscle pain and tenderness
- Muscle weakness
- Dark urine (tea or cola-colored)
- Swelling of affected muscle groups 2, 3
Important Considerations
- Timing of Testing: Single CK measurements may miss peak values, so serial monitoring is essential 1
- Severity Assessment: CK levels correlate with severity and risk of complications
- Compartment Syndrome: Consider measuring compartment pressure if clinical signs present (pain, tension, paresthesia, paresis) 1
- Acute Kidney Injury: The most significant complication, occurring in 13-50% of cases 4
Pitfalls to Avoid
- Delayed Diagnosis: CK may not peak until 24-72 hours after the initial muscle injury
- Missed Underlying Causes: Always investigate potential triggers (trauma, exertion, medications, infections)
- Inadequate Monitoring: Single CK measurements may miss the diagnosis; serial monitoring is crucial
- Overlooking Complications: Particularly acute kidney injury, electrolyte abnormalities, and compartment syndrome
Special Considerations
- In exertional rhabdomyolysis, consider underlying muscle diseases if symptoms are disproportionate to exertion or if there's a family history of muscle disorders 5
- For recurrent episodes, consider metabolic myopathies, glycogen storage disorders, or fatty acid oxidation disorders 1
- Drug-induced cases should prompt evaluation for statin-associated autoimmune myopathy if symptoms persist after drug discontinuation 1
Once diagnosed, immediate aggressive fluid resuscitation is crucial, targeting a urine output >300 mL/hour to prevent acute kidney injury 1, 2.