Digoxin
| Order Code: | DIG |
| Order Form: | Laboratory Requisition |
Specimen:
Plasma
Collection Medium:
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| Plasma Separator Tube |
Alternate
Collection Media:
Call laboratory for additional acceptable specimen collection containers.
Minimum:
3 mL whole blood in light green top tube or TWO microtainers. Do not
draw before 6 hours after dose.
Testing
Schedule:
24 hrs/day, 7 days a week, including holidays.
Analytic Time:
2 hours (upon receipt in laboratory)
Reference Range:
Therapeutic: <2.1 ng/mL at 6 hours after dose in adults.
Critical value: >2.1 ng/mL (adults)
Comments:
Digibind (fab fragment) interferes with digoxin assay. Call lab for
details.
Please print, complete and submit the Advance Beneficiary
Notice
(ABN) along with the Laboratory Requisition before shipping the
specimen.
Test
Limitations:
The assay is unaffected by icterus (bilirubin is less than 65 mg/dL),
hemolysis (Hb is less than 100 mg/dL), lipemia (Intralipid is less than
1500 mg/dL), and biotin is less than 100 ng/mL (criterion: recovery
within plus or minus 0.15 ng/mL at digoxin is less than 1.5 ng/mL, or
within plus or minus 10% at digoxin levels is greater than 1.5 ng/mL).
No interference was observed from rheumatoid factor (RF is less than
1630 IU/mL). In patients receiving therapy with high biotin doses
(i.e. is greater than 5 mg/day) no sample should be taken until at
least 8 hours after the last biotin administration.
In vitro tests were performed on 69 commonly used pharmaceuticals. No
interference with the assay was found.
Digoxin-like immunoreactive substances (DLIS) have been identified in
blood from patients in renal failure, liver failure, and pregnant women
in their third trimester. Studies have shown that the presence of DLIS
in a sample can result in a false elevation of digoxin when assayed by
commercially available immunoassay.(1-3)
The manufacturer of Digoxin Immune FAb (antibody fragment therapy) has
stated that no immunoassay technique is suitable for quantitating
digoxin in serum from patients undergoing this treatment.(4)
Uzara and Nabumetone may cause falsely elevated digoxin results.
As with all tests containing monoclonal mouse antibodies, erroneous
findings may be obtained from samples taken from patients who have been
treated with monoclonal mouse antibodies or have received them for
diagnostic purposes. Digoxin contains additives which minimize these
effects. In rare cases, interference due to extremely high titers of
antibodies of streptavidin can occur.
(1) Keys PW, Stafford RW. In: Taylor WJ, Finn AL, eds. Individualizing
Drug Therapy: Practical Applications of Drug Monitoring. New York,
Gross, Townsend, Frank, Inc; 1981;vol 3:1-21.
(2) Valdes R Jr.: Clin Chem. 1985;31:1525-1532
(3) Valdiva R, Hornig Y, Gross S, Khayam-Bashi H: Digoxin-like
Immunoreactive Factor Cross-reactivity in the CEDIA Digoxin R Assay
on the RA-1000. Clin. Chem. 1990;36(6):1111
(4) Digibind Product Information. Burroughs Wellcome Co. Research
Triangle Park. NC 1990
Methodology:
Competition Principle
Sample
Processing:
Centrifuge at 3000 RPM for 10 minutes.
Label transport tube with two patient identifiers, date and time of collection.
Label transport tube with two patient identifiers, date and time of collection.
Sample
Storage:
Refrigerate.
Transport
Instructions:
Place requisition into outside pocket of bag.
Place specimen into zip-lock type bag, seal bag.
Transport in cooler with refrigerated coolant packs.
Place specimen into zip-lock type bag, seal bag.
Transport in cooler with refrigerated coolant packs.
CPT Code:
80162
See Additional Information:
Chemistry Critical Lab Values
Chemistry Critical Lab Values
