Single dose pharmacokinetic study of lithium in Taiwanese/Chinese bipolar patients.

OBJECTIVE: The purpose of this study is to investigate the single dose pharmacokinetics of lithium in Taiwanese/Chinese bipolar patients for future interracial comparisons. METHOD: Eight bipolar patients took 900 mg of lithium carbonate after overnight fasting. Blood samples of 5 mL were taken after...

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Publicado en:Australian & New Zealand Journal of Psychiatry Vol. 32; no. 1; pp. 133 - 137
Autores principales: Lee CF, Yang YY, Hu OY
Formato: research Journal Article
Publicado: Sage Publications Inc. Feb1998
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Feb1998
      vid: 32
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      pub: Sage Publications Inc.
      place: Thousand Oaks, California
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        atl: Single dose pharmacokinetic study of lithium in Taiwanese/Chinese bipolar patients.
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          Lee CF
          Yang YY
          Hu OY
      sug:
        subj:
          Bipolar Disorder Blood
          Ethnic Groups Psychosocial Factors
          Ethnological Research
          Lithium Carbonate Pharmacokinetics
          Adolescence
          Adult
          Bipolar Disorder Drug Therapy
          Bipolar Disorder Ethnology
          Female
          Lithium Carbonate Adverse Effects
          Lithium Carbonate Therapeutic Use
          Male
          Metabolic Clearance Rate
          Reference Values
          Taiwan
          Time
          Human
          Adolescent: 13-18 years
          Adult: 19-44 years
          Female
          Male
      ab: OBJECTIVE: The purpose of this study is to investigate the single dose pharmacokinetics of lithium in Taiwanese/Chinese bipolar patients for future interracial comparisons. METHOD: Eight bipolar patients took 900 mg of lithium carbonate after overnight fasting. Blood samples of 5 mL were taken after 15 min, 30 min, 45 min, 1 h, 2 h, 3 h, 4 h, 7 h, 9 h, 15 h, 25 h and 31 h after dosing. The computer programs CSTRIP and PCNONLIN were used for pharmacokinetic analysis. RESULTS: The pharmacokinetic parameters obtained were as follows: Cmax, 0.970 +/- 0.170 (SD) mmol/L; Tmax, 1.59 +/- 0.78 h; AUC31 h = 548.9 +/- 135.4 mmol x m/L; AUC to infinity = 722.6 +/- 262.7 mmol x m/L; beta-half-life = 16.3 +/- 7.18 h; kappa-half-life = 0.613 +/- 0.442 h; Cl(oral) = 1.13 +/- 0.39 mL/min/kg; Vd/F = 1.43 +/- 0.387 L/kg. Most of the pharmacokinetic parameters were within the ranges reported in investigations of Caucasian subjects. CONCLUSIONS: This study showed that racial differences in lithium pharmacokinetics might not exist. We suggest that methodological designs, including method of blood sampling, measurement of lithium, and pharmacokinetic and statistical calculations, be standardised if future cross-ethnic comparisons are to be conducted.
      pubtype: Academic Journal
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        research
        Journal Article
      ougenre: Article
    language: English
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