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Articles |
1
Departments of Pathology
2
Medical & Research Technology, University of
Maryland School of Medicine, Baltimore, MD 21201.
3
RushPresbyterianSt. Lukes Medical Center,
Chicago, IL 60612.
4
Hospital of the University of Pennsylvania,
Philadelphia, PA 19104.
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New England Medical Center, Boston, MA 02111.
6
Abbott Laboratories, Abbott North Park, IL 60064.
a Address correspondence to this author, at: University of Maryland Medical Center, Clinical Pathology, 22 South Greene St., Baltimore, MD 21201; Fax (410) 328-5880; e-mail hazzazy{at}umabnet.ab.umd.edu
Performance characteristics of the Abbott nonpretreatment AxSYM® Digoxin II assay were evaluated for quantification of digoxin at four independent sites. Correlation of digoxin measurements with the Abbott pretreatment AxSYM®, Baxter Stratus® II, Abbott TDx/TDxFLx II®, Abbott IMx®, Emit® 2000, and Beckman Synchron CX® digoxin assays showed acceptable agreement, as indicated by: slope values >0.84, r >0.90, y-intercepts for all comparisons at or below the assay detection limit, and Sy|x ranging between 7.5% and 15.4% of the average digoxin value. Susceptibility to interference from digoxin-like immunoreactive factors (DLIFs) was examined in 233 samples from renal patients, liver disease patients, cord blood, and third-trimester pregnancies; the AxSYM Digoxin II assay demonstrated the least DLIFs interference. DLIF susceptibility for four of the methods was significantly greater (P <0.05) than in the AxSYM Digoxin II assay; susceptibilities of the Stratus II and Emit 2000 methods were similar to the AxSYM Digoxin II assay.
The following articles in journals at HighWire Press have cited this article:
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W. Steimer, C. Muller, and B. Eber Digoxin Assays: Frequent, Substantial, and Potentially Dangerous Interference by Spironolactone, Canrenone, and Other Steroids Clin. Chem., March 1, 2002; 48(3): 507 - 516. [Abstract] [Full Text] [PDF] |
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