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1.
Am J Kidney Dis ; 33(4): 786-9, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10196025

ABSTRACT

A 43-year-old woman took a large amount of depakote (divalproex, a slow-release form of valproate), became comatose, and developed severe hypotension refractory to fluid resuscitation and high-dose vasopressors. The serum valproic acid (VPA) concentration on admission was 1,380 microgram/mL (therapeutic range, 50 to 100 microgram/mL). She also had metabolic acidosis, thrombocytopenia, and normal renal and liver functions. Hemodialysis was initiated 4 hours after presentation. After 6 hours of hemodialysis with a high-flux dialyzer, her serum VPA concentration decreased from 940 microgram/mL to 164 microgram/mL, coincident with improvement in clinical status. The half-life of VPA was reduced to 2.4 hours with hemodialysis, whereas it was 7.2 hours before the procedure. Hemodialysis could be a valuable therapeutic intervention in VPA toxicity.


Subject(s)
Renal Dialysis , Valproic Acid/poisoning , Adult , Drug Overdose , Female , Humans , Hypotension/chemically induced , Poisoning/therapy , Valproic Acid/blood
2.
J Acquir Immune Defic Syndr (1988) ; 6(3): 245-51, 1993 Mar.
Article in English | MEDLINE | ID: mdl-8450399

ABSTRACT

Metabolic and anthropometric changes induced by "pharmacological" versus "physiological" doses (5.0 vs. 2.5 mg, every other day) of recombinant human growth hormone (rhGH) were compared in 10 human immunodeficiency virus-positive patients with AIDS or AIDS-related complex. Five patients were randomly assigned to each treatment schedule in a 3-month prospective, double-blind clinical trial. Three of the 10 patients, none taking zidovudine and all with low initial CD4 counts, were withdrawn during the study due to acute opportunistic infections. During treatment, insulin-like growth factor-1 (IGF-1) levels increased significantly (p < 0.05) in the pharmacological hGH treatment group, whereas no significant change was observed in IGF-1 in the physiological dose rhGH group. In the pharmacological hGH treatment group, weight loss preceding the study was reversed (p < 0.05) in each of the four patients who completed the study. This weight gain was associated with increases (p < 0.05) in lean body mass and total body water, with concomitant decreases in fat mass (p < 0.05) and urinary nitrogen excretion. Muscle power and endurance, as assessed by standardized omnikinetic dynamometry, also improved. All four patients lost weight again (p < 0.05) 6 weeks after completion of the study and termination of rhGH treatment. Minor positive changes in body composition were also observed in the physiologic-dose hGH group. The pharmacological dose of hGH was associated with minor increments (p < 0.05) in fasting plasma glucose, insulin, and C-peptide concentrations, which were of negligible clinical significance.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
AIDS-Related Complex/complications , Acquired Immunodeficiency Syndrome/complications , Body Composition/drug effects , Body Weight/drug effects , Growth Hormone/pharmacology , AIDS-Related Complex/blood , AIDS-Related Complex/immunology , Acquired Immunodeficiency Syndrome/blood , Acquired Immunodeficiency Syndrome/immunology , Adult , Body Water/drug effects , Double-Blind Method , Growth Hormone/administration & dosage , Humans , Insulin-Like Growth Factor I/metabolism , Leukocyte Count/drug effects , Male , Middle Aged , Muscles/drug effects , Muscles/physiology , Prospective Studies , Recombinant Proteins/administration & dosage , Recombinant Proteins/pharmacology , T-Lymphocytes/drug effects , beta 2-Microglobulin/metabolism
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