LACTATE CSF
General Information
HLAB/HOL Code: LACCSF
UPHSM LIS Test #:
Schedule: DAILY
Testing Time: 10-14 Days
Testing Lab: LabCorp
UPHSM LIS Test #:
Schedule: DAILY
Testing Time: 10-14 Days
Testing Lab: LabCorp
Specimen Info
Only 1 specimen type required, unless otherwise specified
Volume: 1.0 mL
Temperature: Frozen
Tube Type: Cerebrospinal fluid (CSF)
Collection Info:
Container: Sterile screw capped vial
Collection: Collect entire sample into a single sterile tube.
Storage Instructions: Freeze as soon as possible after collection.
Temperature: Frozen
Tube Type: Cerebrospinal fluid (CSF)
Collection Info:
Container: Sterile screw capped vial
Collection: Collect entire sample into a single sterile tube.
Storage Instructions: Freeze as soon as possible after collection.
Specimen Acceptability
Cause for Rejection:
Bloody CSF; Received thawed
Bloody CSF; Received thawed
Methods
Enzyme/UV
Clinical Utilities
CSF Lactate is useful for investigating possible disorders of mitochondrial metabolims, when used in conjenction with cerebrospinal fluid pyruvate collected at the same time to determine the Lactate:Pyruvate ratio. The CSF Lactate:Pyruvate ratio is considered a helpful (not diagnostic) tool in the evaluation of patients with possible disorders of mitochondrial metabolism, especially in patients with neurolofic dysfunction and normal blood Lactate:Pyruvate ratios. Pyruvic acid levels alone have little clinical utility. The Lactate:Pyruvate ratio is elevated in several, but not all, mitochondrial disorders vary widely in presentation and age of onset. Many mitochondral disorders have neurologic and myopathic features and may involve multiple organ systems. Determination of lactate, pyruvate, and L:P ratio in cerebrospinal fluid is helpful in directing attention toward a possible mitochondrial disorder in cases with predominately neurologic dysfunction and normal blood lactate levels. An elevated Lactate:Pyruvate ratio may indicate inherited disorders of the respiratory chain complex, tricarboxylic acide cycle disorders and pyruvate carboxylase deficiency. Respiratory chain defects usually result in Lactate:Pyruvate ratios >20. A low Lactate:Pyruvate raio (disproportionately elevated pyruvic acid) may indicate an inherited disorder of pyruvate metabolism. Defects of the pyruvate dehydrogenase complex result in Lactate:Pyruvate ratios <10. The Lactate:Pyruvate ratio is characteristically normal in other patients. An artifactually high ratio can be found in acutely ill patients.
CPT Codes
83605
* The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding
is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.