TY - JOUR
T1 - Effect of endogenous digoxin-like substances on the interpretation of high concentrations of digoxin in children
AU - Stone, Judy
AU - Bentur, Yedidia
AU - Zalstein, Eli
AU - Soldin, Steven
AU - Giesbrecht, Esther
AU - Koren, Gideon
N1 - Funding Information:
Because of the narrow margin of safety of digoxin and the large interpatient variability in its pharmacokinetics and pharmacodynamics, serious toxic effects may occur even when the drug is used in recommended doses. Since the introduction of immunoassays for digoxin, measurement of serum concentrations of the glycoside has been the standard Supported by grant No. MA 8544, from the Medical Research Council of Canada, and by a grant from the Heart and Stroke Foundation of Canada. Dr. Koren is a Career Scientist of the Ontario Ministry of Health. Submitted for publication Jan. 26, 1990; accepted March 20, 1990. Reprint requests: Gideon Koren, MD, Division of Clinical Pharmacology, Hospital for Sick Children, 555 University Ave., Toronto, Ontario M5G 1XS, Canada. 9/25/20990 means of monitoring to avoid toxic effects, l However, it has become apparent that endogenous substances, commonly referred to as "endogenous digoxin-like substances," cross-react with many of the available radioimmunoassays. 2 Falsely positive concentrations of digoxin have been docu-
PY - 1990/8
Y1 - 1990/8
N2 - The objective of this study was to assess the effect of endogenous digoxin-like substances on the interpretation of excessive concentrations of digoxin in children. After the development of a high-pressure liquid chromatography (HPLC) method for digoxin in our laboratories, we analyzed sera of children in whom the fluorescence polarization immunoassay identified potentially toxic concentrations of the glycoside (greater than 3 nmol/L; 2.3 ng/ml). Sixteen of them were receiving long-term digoxin therapy, and one had an accidental overdose. The immunoassay yielded significantly higher concentrations (4.1±1.2 nmol/L; 3.2±0.9 ng/ml) than the HPLC method (3.3±1.6 nmol/L; 2.6±1.2 ng/ml; p<0.01). In five cases (30%) these differences were clinically significant because administration of digoxin had been discontinued in the presence of true digoxin concentrations within the therapeutic range and the lack of clinical toxic effects. These data suggest that therapeutic drug monitoring using immunoassays of digoxin may be too inaccurate to detect potential toxic effects, and that much more weight should be focused on clinical monitoring. The HPLC method for assay of digoxin is extremely meticulous and will not become clinically available; therefore the development of better immunoassays should be encouraged.
AB - The objective of this study was to assess the effect of endogenous digoxin-like substances on the interpretation of excessive concentrations of digoxin in children. After the development of a high-pressure liquid chromatography (HPLC) method for digoxin in our laboratories, we analyzed sera of children in whom the fluorescence polarization immunoassay identified potentially toxic concentrations of the glycoside (greater than 3 nmol/L; 2.3 ng/ml). Sixteen of them were receiving long-term digoxin therapy, and one had an accidental overdose. The immunoassay yielded significantly higher concentrations (4.1±1.2 nmol/L; 3.2±0.9 ng/ml) than the HPLC method (3.3±1.6 nmol/L; 2.6±1.2 ng/ml; p<0.01). In five cases (30%) these differences were clinically significant because administration of digoxin had been discontinued in the presence of true digoxin concentrations within the therapeutic range and the lack of clinical toxic effects. These data suggest that therapeutic drug monitoring using immunoassays of digoxin may be too inaccurate to detect potential toxic effects, and that much more weight should be focused on clinical monitoring. The HPLC method for assay of digoxin is extremely meticulous and will not become clinically available; therefore the development of better immunoassays should be encouraged.
UR - http://www.scopus.com/inward/record.url?scp=0025358785&partnerID=8YFLogxK
U2 - 10.1016/S0022-3476(05)80555-4
DO - 10.1016/S0022-3476(05)80555-4
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 2166153
AN - SCOPUS:0025358785
SN - 0022-3476
VL - 117
SP - 321
EP - 325
JO - Journal of Pediatrics
JF - Journal of Pediatrics
IS - 2 PART 1
ER -