Literature DB >> 11767263

Estimated blood alcohol levels reached by "binge" and "nonbinge" drinkers: a survey of young adults in Montana.

H W Perkins1, J Linkenbach, W Dejong.   

Abstract

The authors examined estimated blood alcohol concentrations (BACs) reached by so-called "binge drinkers" and "nonbinge drinkers" using a survey of young adults (age 18-24 years) in Montana. One third of drinkers were classified as "binge drinkers" the last time they consumed alcohol, using a gender-specific definition commonly applied to young adults: for men, having 5 or more drinks in a row, and for women, having 4 or more drinks. BAC levels were estimated on the basis of length of drinking episode, gender, weight, and typical alcohol consumption level. Among "binge drinkers," 63% did not reach .10% BAC or higher, 48% did not reach .08% BAC or higher, and 30% did not reach .06% BAC or higher. Of the "nonbinge drinkers," 7% reached .06% BAC or higher and 4% reached .08% BAC or higher. These findings underscore the potential problem of using binge drinking as a description and shorthand measure of drinking to intoxication.

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Year:  2001        PMID: 11767263

Source DB:  PubMed          Journal:  Psychol Addict Behav        ISSN: 0893-164X


  20 in total

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3.  Drinking beyond the binge threshold in a clinical sample of adolescents.

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7.  A new measure of binge drinking: prevalence and correlates in a probability sample of undergraduates.

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8.  Mifepristone pretreatment reduces ethanol withdrawal severity in vivo.

Authors:  Lynda Sharrett-Field; Tracy R Butler; Jennifer N Berry; Anna R Reynolds; Mark A Prendergast
Journal:  Alcohol Clin Exp Res       Date:  2013-03-25       Impact factor: 3.455

9.  Heavy episodic drinking: determining the predictive utility of five or more drinks.

Authors:  Kristina M Jackson
Journal:  Psychol Addict Behav       Date:  2008-03

10.  Intra-cornu ammonis 1 administration of the human immunodeficiency virus-1 protein trans-activator of transcription exacerbates the ethanol withdrawal syndrome in rodents and activates N-methyl-D-aspartate glutamate receptors to produce persisting spatial learning deficits.

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