EPOCH-MAKING THERAPY IN PROLONGED ALCOHOL WITHDRAWAL SYNDROME

  • EGAMI Hideaki
    Principal Investigator
    SCHOOL OF MEDICINE,KURUME UNIVERSITY ASSISTANT

About This Project

Japan Grant Number
JP08671115 (JGN)
Funding Program
Grants-in-Aid for Scientific Research
Funding Organization
Japan Society for the Promotion of Science

Kakenhi Information

Project/Area Number
08671115
Research Category
Grant-in-Aid for Scientific Research (C)
Allocation Type
  • Single-year Grants
Review Section / Research Field
  • Medicine > 内科 > Psychiatric science
Research Institution
  • KURUME UNIVERSITY
Project Period (FY)
1996 〜 1998
Project Status
Completed
Budget Amount*help
1,700,000 Yen (Direct Cost: 1,700,000 Yen)

Research Abstract

In our preliminary study, acute alcohol produced phase-shifts in the circadian rhythms of locomotor activity and body temperature, while chronic alcohol treatment induced changes in the periods of free-running rhythms in mammals. These data suggest that chronic administration of alcohol may cause disordered circadian rhythms in humans, for example, insomnia, secondary depression, alcohol withdrawal and prolonged alcohol withdrawal in alcoholism. In this study, we investigated that 81 (54%) of 150 inpatients with alcoholism had been treated under a diagnosis of alcohol withdrawal (delirium tremens) and 11 of these 81 cases (13.6%) had been diagnosed with prolonged alcohol withdrawal (prolonged delirium tremens). The clinical efficacy of specific benzodiazepine antagonist flumazenil for hepatic coma and prolonged delirium tremens was studied. Methods were as follows : 1) The level of hepatic coma was assessed by the stage of hepatic coma, alcohol withdrawal was assessed with CIWA and each subject was examined byelectroencephalogram(EEG) before and after flumazenil injection. Flumazenil was given as an iv infusion and continuously given as an 24-hr iv drip injection for a few days. As a result, all unconscious patients were clearly reversed in a few minutes, and EEG returned to normal ranges of alpha dominant activities at occipital sites and normal ranges persisted thereafter. Additionally, this may provide a clue to elucidating the theory that there may be abnormalities of the benzodiazepine receptor, or a possible inverse agonist ligand in alcohol withdrawal. We conclude that this clinical study may be very important to discovering a new therapy for prolonged alcohol withdrawal (prolonged delirium tremens) and for preventing transition to dementia associated with alcohol.

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