Myasthenia Gravis/Lambert-Eaton Myasthenic Syndrome Evaluation
Synonyms |
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Cerner Name |
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Clinical Info |
Confirming the autoimmune basis of a defect in neuromuscular transmission (eg, myasthenia gravis [MG], Lambert-Eaton myasthenic syndrome [LEMS]) Distinguishing LEMS from autoimmune forms of MG Providing a quantitative autoantibody baseline for future comparisons in monitoring a patient's clinical course and response to immunomodulatory treatment |
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Specimen Sources |
Blood, Arterial Blood, Capillary Blood, Central Line Blood, Venous |
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Specimen Types |
Blood |
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Container |
Red Top Tube |
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Collection Instructions |
Container/Tube: Red top tube or Gold Top Tube |
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Specimen Volume |
3 mL serum ( 2 mL min) |
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Transport Instructions |
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Specimen Stability |
72 Hours Room Temperature |
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Methodology |
ARBI, CCPQ, MUSK: Radioimmunoassay (RIA)ACMFS: Flow Cytometry |
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Days Performed |
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Performing Laboratory |
Mayo Medical Laboratories |
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CPT |
83519 x 2 |
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PDM |
5910940 |
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Only Orderable at Locations: |
Orderable Everywhere |
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Results |
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Result Interpretation
MG Lambert-Eaton Interpretation, S Interpretation NA
ACh Receptor (Muscle) Binding Ab Radioimmunoassay (RIA) < or =0.02 nmol/L P/Q-Type Calcium Channel Ab RIA < or =0.02 nmol/L |
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Forms |
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