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Distillation
Alcohol vapors are released from the mash at high
temperatures
Proof
Measure of the percent alcohol
intestines
Increases rate of alcohol absorption
related injuries
Patients with a BAC >0.08 are 3.2 times more likely
Alcohol poisoning Consuming large amounts of alcohol in short period of time can be lethal Alcohol alone or mixed with another drug responsible for more deaths due to toxic overdose than any other substance Death caused by either central nervous system and respiratory depression or by inhalation of vomit or fluid into the lungs Signs include inibility to be roused, weak and rapid pulse, unusual breathing pattern, and cool, damp, pale or bluish skin If wait to call for help until person is unconscious, risk of death increases tenfold
Risk of contracting STI or unplanned pregnancy increases among those who drink heavily
Cirrhosis
Alcoholic hepatitis
Cancer Chronic inflammation of pancreas
lipase, UDS, UA, pregnancy test) PPD CXR EKG Acetaminophen and salicilate level as indicated
Sites include stomach, small intestine, and colon Dependent on gastric emptying time Metabolized primarily in the liver by oxidation Alcohol dehydrogenase exhibits zero-order kinetics
(15 mg/dl/hr) Proportional to body weight Microsomal ethanol oxidizing system (MEOS) Alcohol inhibits cytochrome P-450
Alcohol
ADH
Acetaldehyde
ALDH
Acetic acid and water
20-99mg% loss of muscular coordination, change in behavior 100-199mg% ataxia, mental impairment 200-299mg% obvious intoxication, nausea and vomiting 300-399mg% severe dysarthria and amnesia
obtundation, often fatal Important to remember the role of tolerance in all these categories
pressure and maintain airway Intravenous fluids (Banana Bag-NS, thiamine, MVI, Folate, B-12) Assess for other drug use especially benzos or opioids as antagonists can be used Closely monitor until withdrawal begins and then start treatment
MSSA (Modified Selective Severity Assessment) CIWA-A (Clinical Institute Withdrawal Assessment for Alcohol) Advantage for personnel to monitor progress and treat accordingly Disadvantage is cookbook approach
Most people abstain or drink moderately placing them at low risk for alcohol use disorders. In general, Moderate Drinking is up to 2 drinks/day for men; up to 1 drink/day for women
ONE DRINK-12 OUNCE CAN OR BOTTLE OF BEER OR WINE COOLER/ONE 5 OUNCE GLASS OF WINE
Women:
A binge is a pattern of drinking alcohol that brings blood alcohol concentration (BAC) to 0.08 gm% or above. For the typical adult, this pattern corresponds to consuming 5 or more drinks (male) or 4 or more drinks (female) in about 2 hours. Binge drinking is clearly dangerous for the drinker and for society
GENES : 60% addictive,both alcohol specificand non specific Enviroment : 40% both shared and non shared
Drinker type
Men Moderate Less than 21 Women Less than 14
Hazardous
Harmful
21 50
50+
14 35
35+
Disorder Odds
Anxiety Disorder Mood Disorders (especially Major Depression) Personality Disorders Antisocial Personality Disorder Drug Dependence Nicotine Dependence
2.6x
Alcohol use, abuse, and dependence are complex behavioral traits influenced by many factors:
genetic and biological responses
environmental influences
adulthood
Due to its interaction with the enzyme dopamine-betahydroxylase , which breaks down doapmine, Antabuse adverse affects when combined with drugs affecting the release and re-uptake of dopamine (Such as Ritalin, Adderall, and Cocaine). Metabolism of other drugs may be inhibited by Antabuse (such as Benzodiazepines, morphine, and barbituates). Extremely important to take under consideration when someone is undergoing other medical treatment along with the treatment for alcohol addiction.
Naltrexone is
metabolized in the liver into a variety of metabolites, with the 6-naltrexol being the metabolite useful in treating alcoholism. The mechanism of action is not quite fully understood. Approved for use in the treatment of alcoholism in April of 2006.
Alcohol inhibits the activity of receptors known as NMethy-D-aspartate receptors (or NMDARs), causing the brain to create more NMDARs Absence of alcohol, or no inhibition of the receptor, causes these receptors to be overly active and cause symptoms such as delirium tremens (DT). Acamprosate is thought to reduce glutamate surges that excite NMDARs. This property makes Acamprosate useful in treating the withdrawal symptoms in alcoholics. Acamprosate has also been shown in some studies to act as a neuro-protectant and protect neurons from damage caused by alcohol withdrawal
Cognitive behavioral therapy tries to understand how an individual's learning has occurred. A therapist using CBT will, firstly, attempt to help you understand the reasons for your 'bad' behavior and why you developed such a negative response to certain 'triggers'. more important goal of CBT, is to identify and learn better responses, or coping strategies, for the triggers.
You, for example, may suffer from stress. In order to unwind after a bad day you have a drink which relaxes you. You learn that alcohol relieves stress. Over time you become dependent on this drink to relax, before long you are having two, three, a bottle. Your wife complains you are drinking too much, the relationship suffers. Hangovers become common and you get into trouble at work ultimately being made redundant. This causes more friction with your wife and so on.
A therapist , using your testimony, will help you identify the reasons for your drinking; you learned that alcohol relieved stress, and every time you drank to ease the stress, the idea that drink relieved stress was reinforced. However, over time drink no longer fulfilled this function, in fact it created more stress. Despite this you continued with the behavior becuase of the'maladaptive learning process'.
Having identified the reason for the behavior you and the therapist would then identify coping skills that could be utilized to deal with stress in the future. Skills that didn't involve drinking.