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Lactic Acid Dehydrogenase (LD), Body Fluid

CPT 83615
Synonyms
  • Lactate Dehydrogenase, Variable
  • LD Variable

Test Details

Methodology

Kinetic

Result Turnaround Time

1 - 2 days

Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.

Related Documents

Use

A fluid LD activity nearly equal to the plasma activity is usually associated with inflammatory processes

Footnotes

1. Hoffman RM, Rogers RM. Serum and lavage lactate dehydrogenase isoenzymes in pulmonary alveolar proteinosis. Am Rev Respir Dis. 1991 Jan; 143(1):42-46. PubMed 1986683
2. Lampl Y, Paniri Y, Eshel Y, Sarova-Pinhas I. Cerebrospinal fluid lactate dehydrogenase levels in early stroke and transient ischemic attacks. Stroke. 1990 Jun; 21(6):854-857. PubMed 2349587

Custom Additional Information

Lactate dehydrogenase (LD) is a normal component of CSF. Increased amounts may occur in association with ischemic necrosis, meningitis, leukemia, metastatic cancer of the CNS, and lymphoma. LDH1 and LDH2 are decreased in lavage fluid in pulmonary alveolar proteinosis.1 One application of LD measurement is the differential diagnosis of intracranial hemorrhage in neonates versus traumatic tap. Lactate dehydrogenase is elevated in proportion to severity of CNS hemorrhage, but unchanged by traumatic tap. CSF LDH is higher in stroke than in transient ischemic attack.2

Specimen Requirements

Specimen

Fluid or cerebrospinal fluid (CSF)

Volume

1 mL fluid or 1 mL CSF

Minimum Volume

0.3 mL

Container

Sterile body fluid container

Stability Requirements

Temperature

Period

Room temperature

14 days

Refrigerated

7 days

Frozen

14 days

Freeze/thaw cycles

Stable x3

Reference Range

• Peritoneal: Not established

• Pleural:

− Transudate: <200 U/L

− Exudate: >200 U/L

• Synovial: <240 U/L

• CSF: Not established

The method performance specifications have not been established for this test in body fluid. The test result should be integrated into the clinical context for interpretation.

Storage Instructions

Room temperature

Causes for Rejection

Improper labeling

LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
100156 LD, Body Fluid 14803-1 100156 LD, Body Fluid IU/L 14803-1
Order Code100156
Order Code NameLD, Body Fluid
Order Loinc14803-1
Result Code100156
Result Code NameLD, Body Fluid
UofMIU/L
Result LOINC14803-1