TY - JOUR
T1 - Tricyclic Antidepressants in Red Cells and Plasma
T2 - Correlation with Impaired Intraventricular Conduction in Acute Overdose
AU - Amitai, Yona
AU - Erickson, Timothy
AU - Kennedy, Eugenia J.
AU - Leikin, Jerrold B.
AU - Hryhorczuk, Danial O.
AU - Noble, Jerrold
AU - Hanashiro, Paul K.
AU - Frischer, Henri
PY - 1993/8
Y1 - 1993/8
N2 - Tricyclic antidepressant levels in red blood cells and plasma in acute overdose and their association with cardiotoxicity were studied. This was a prospective study in 15 patients with acute tricyclic antidepressant overdose. Tricyclic antidepressant parent compounds and metabolites were measured in red blood cells and plasma, and tricyclic antidepressant levels were correlated with ECG indexes of toxicity. Plasma levels of the parent compounds were higher than their red blood cell levels on admission (mean ± SD, 691 ± 409 and 337 ± 220 ng/ml, respectively). Admission metabolite levels were higher in red blood cells than in plasma (264 ± 180 and 190 ± 164 ng/ml, respectively). QRS duration and the red blood cell levels of the metabolites were significantly correlated at the time of admission (r = 0.77, p < 0.01), as well as at 6 to 10 hours (r = 0.74, p < 0.01). Clinical Pharmacology and Therapeutics (1993) 54, 219–227; doi:
AB - Tricyclic antidepressant levels in red blood cells and plasma in acute overdose and their association with cardiotoxicity were studied. This was a prospective study in 15 patients with acute tricyclic antidepressant overdose. Tricyclic antidepressant parent compounds and metabolites were measured in red blood cells and plasma, and tricyclic antidepressant levels were correlated with ECG indexes of toxicity. Plasma levels of the parent compounds were higher than their red blood cell levels on admission (mean ± SD, 691 ± 409 and 337 ± 220 ng/ml, respectively). Admission metabolite levels were higher in red blood cells than in plasma (264 ± 180 and 190 ± 164 ng/ml, respectively). QRS duration and the red blood cell levels of the metabolites were significantly correlated at the time of admission (r = 0.77, p < 0.01), as well as at 6 to 10 hours (r = 0.74, p < 0.01). Clinical Pharmacology and Therapeutics (1993) 54, 219–227; doi:
UR - http://www.scopus.com/inward/record.url?scp=0027301540&partnerID=8YFLogxK
U2 - 10.1038/clpt.1993.133
DO - 10.1038/clpt.1993.133
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C2 - 8354029
AN - SCOPUS:0027301540
SN - 0009-9236
VL - 54
SP - 219
EP - 227
JO - Clinical Pharmacology and Therapeutics
JF - Clinical Pharmacology and Therapeutics
IS - 2
ER -