Transcript week1

BMJ 2002;324:698 ( 23 March )
News extra
Psychologists allowed to prescribe drugs for mental illness
Deborah Josefson Nebraska
New Mexico has become the first US state to allow psychologists to
prescribe drugs.
The American Psychological Association has been lobbying since 1984
to gain legislative support for bills that authorize psychologists to
prescribe psychiatric drugs. The association argues that it is more cost
effective for patients to receive their psychotherapy and drug
treatment from one practitioner.
Before New Mexico’s act, only the US territory of Guam allowed
psychologists to prescribe drugs. Guam lumped psychologists with
physician assistants as allied healthcare specialists with prescribing
privileges in 1998, but to date no psychologists there have taken
advantage of the law.
Louisiana also allows psychologists (2004)
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Some general points to begin……
A bit of history
1. The focus of this course is
pharmacotherapy
2. The practice of pharmacotherapy cannot be
oversimplified (ie one illness - one type of
pill)
3. Many variables impinge on adherence/
compliance and prescriptions can have
tremendous variation for individuals
4. Ways to characterize
drugs
a. chemical structure
b. chemical name -
N-(-4-hydroxyphenyl)
acetamide
c. generic name or nonproprietary name
acetaminophen
- can be useful sometimes because they
give clue to the nature of the drug
ex. bz, local anesthetics
** textbooks, scientific discussions of drug
use generic name
d. Trade nameex. Luvox
Paxil
Namenda
Aricept
Lunesta
fluvoxamine
paroxetine
memantine
donepazil
eszopiclone
What is the trade name for acetaminophen?
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active ingredients - same in trade vs
generic
◦ inactive ingredients may be different
e. New novel compounds Clinicaltrials.gov
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CP 101,606 - traxoprodil
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stroke,
dyskinesias
Parkinson’s Disorder
Postoperative disorder
Alcohol-induced neurotoxicity
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Typical cost for a drug to reach market
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Screening tests using animal models
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ensures that drugs are safe and effective.
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http://www.fda.gov/cder/index.html
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Screening tests using animal models
Phase 1 - assessment of safety and
toxicity
 small n, small dose
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Phase 2 - tested in limited n of patients
 individuals with condition ~ few hundred patients
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Phase 3 - Expanded clinical trials
 usually administered to thousands
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3 phases (or 4)
Phase 1 – early 1800’s –
◦ isolation of morphine from opium in 1805
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early 1800’s –
◦ isolation of morphine from opium in 1805
 1855 – invention of hypodermic needle
 used in agitation, aggression in psychiatric hospitals
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2nd phase
early 1900’s
◦ first barbiturate synthesized in 1903
◦ phenobarbital in 1912
 by 1950’s – 2500 preps and 50 used clinically as
anticonvulsant, sedative-hypnotic,
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insulin◦ introduced to psychiatry in 1920’s to stimulate
appetite and produce
◦ 1930’s – alleviating morphine withdrawal and
treating schizophrenia
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development of barbiturates (first 1/2 of 20th
century)
Lithium’s usefulness in treating bipolar
(1949).
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1950’s to current
◦ introduction of more current psychotropics
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introduction of new drug discovery methods
◦ ability to recreate and determine genetic
components of various neurotransmitter receptor
subtypes