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Toxicology |
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| 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 |
710 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 |
13 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 |
37 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 |
510 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 |
710 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 |
710 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 |
12 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 |
25 days |
 |
| Indication |
To detect exposure to lead. |
 |
Interpretive Guidelines |
Levels > 25 ug/dl indicate lead toxicity. |
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