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Toxicology

  Code Test Description
* Indicates send out test
  * S16055 Arsenic
  Specimen 5 ml urine, 0.5 grams liver, stomach contents, hair, 0.5 grams kidney or 1 ml whole blood or serum
  Method AAS
  Schedule 7–10 days
  Indication Suspicion of arsenic toxicity
  Interpretive
  Guidelines
Levels above baseline are consistent with arsenic toxicity.
  T730 Bromide
  Specimen 1 ml serum (Do Not Use SST)
  Method Gold trichloride
  Schedule 1–3 days
  Indication To monitor anti-convulsant therapy
  Interpretive
  Guidelines
Low levels suggestive of inadequate anti-covulsant doses. High levels suggest toxicity.
  T235 Cholinesterase
  Specimen 1 ml serum or plasma
  Schedule 3–7 days
  Indication Diagnosis of organophosphate toxicity
  Interpretive
  Guidelines
Cholinesterase is irreversibly inhibited by organophosphate-containing pesticides, but reversibly inhibited by carbamate insecticides. Low levels (< 25% of the normal range) support exposure.
  * S16210 Copper
  Specimen 1 ml serum or plasma
  Method Atomic absorption or ICP spectroscopy.
  Schedule 5–10 days
  Indication To detect exposure to excessive copper levels or deficiencies.
  Comments Tissue levels are more useful for the diagnosis of storage disease. For dry weight copper levels request code S16215.
  * S16215 Copper Storage Disease (Tissue Dry Weight)
  Specimen 0.5 grams liver in fresh saline, fixed in 10% formalin or in paraffin block.
  Method Atomic absorption or ICP spectroscopy.
  Schedule 7–10 days
  Indication To detect exposure to excessive copper levels or deficiencies.
  S18702 Cyclosporine, baseline or post dose
  Specimen 1 ml EDTA or heparinized whole blood. Draw post samples 6 hours following administration.
  Schedule 7–10 days
  T735 Digoxin, baseline or post dose
  Specimen 1 ml serum (Do Not Use SST) Draw post samples 6 hours following administration
  Method RIA / TDX (fluorescent)
  Schedule 1–2 days
  Indication To monitor digoxin therapy
  Interpretive
  Guidelines
Therapeutic serum digoxin concentrations should be monitored once a steady state is achieved (at least 6 days after commencing treatment). The optimal therapeutic range for Digoxin levels is 0.8 to 2.0 ng/ml at 6 to 8 hours post-administration. Digoxin levels > 2.5 ng/ml are commonly associated with toxic signs
  Comments 1) The administration of diuretic or angiotensin converting enzyme (ACE) inhibitors, hypokalemia or azotemia will increase the frequency of digoxin toxicity; therefore, careful monitoring is necessary.
2) Minimal cross-reactivity for oleander toxicity.
  T745 Lead, Blood
  Specimen 1 LT or GRT
  Method Anodic stripping voltammetry (ASV)
  Schedule 2–5 days
  Indication To detect exposure to lead.
  Interpretive
  Guidelines
Levels > 25 ug/dl indicate lead toxicity.
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