September 1, 2006 myADHD.com News
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September 1, 2006 |
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Dear Harvey Parker,
Welcome to this issue of myADHD.com News.
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| Medical Practice Updates |
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How to Choose a Medicine for Adult ADHD by
Richard Rubin, MD Clinical Associate
Professor, University of Vermont College of Medicine
At a recent Baptist Hospital of South Florida
Continuing Medical Education program, I presented a
systematic approach for applying newer knowledge to
the treatment of adults. Three variables should be
considered: - characteristics of each
patient,
- differences among
medicines, and
- findings from research
studies.
Characteristics of Each Patient People
bring multiple questions, concerns, preferences, and
experiences to their ADHD treatment expectations. It
is valuable to initially review these for a clear,
up to date planning start. Social, cultural, and
family attitudes can influence acceptance of any and
all medicines. Prior exposure to medicine can
introduce adverse experiences, such as side effects
to be avoided. A certain type of benefit may be
anticipated, such as the immediate effects typical
of the stimulants, versus gradual onset as with the
non-stimulants. People taking medicine for the first
time may respond differently from those with prior
exposure, both positive with greater benefit, and
negative with more side effects. Sometimes people
have had beneficial but only partial response, and
would benefit from addition of another medicine with
complementary actions. The goals for each person’s
treatment plan influence medicine choice. Is rapid
rescue from behavioral problems needed, or ongoing
maintenance? Is performance strengthening for
limited duration each day required, or continuous
symptom stabilizing? Does the patient have other
medical or mental health problems that specific
medicines may improve or worsen? There are different
effects on blood pressure and anxiety, for example.
Substance abuse/misuse is another consideration.
Differences Among Medicines While adult
medicine guidance used to be derived from childhood
practice, we now have an adult ADHD FDA approved
choice in each major category: - the
norepinephrine non-stimulant atomoxetine
(Strattera),
- extended release mixed amphetamine
salts (Adderall XR), and
- dexmethylphenidate
(Focalin XR).
The package insert safety and efficacy information
supporting these approvals provides the informed
consent foundation for each doctor and patient
medicine decision. In addition, doctors have
experience with child approved medicines used
extensively with adults, such as OROS
methylphenidate (Concerta) and short acting
stimulants (Ritalin, Dexedrine, etc.) The main
antidepressant with current practice and research
support for adult ADHD is once a day bupropion
(Wellbutrin XL). The older tricyclics, such as
desipramine, have higher toxicity risks. In addition
to safety and tolerability considerations, the
effectiveness of the medicines vary, both in the
degree of core ADHD symptom reduction, and time
limited versus continuous duration of medicine
effects. The costs and ongoing access to the
medicine, including out of pocket, insured, sample,
and refill options, will influence initial
acceptance and ongoing adherence.
Research Findings The evidence base for
each medicine varies, including both the clinical
trials for FDA approval and other published research
studies. While useful information is provided, the
limitations of trials and studies should be
recognized in applying the results to patient
treatment practice. Assessing the amount of change,
sometimes expressed by the statistic called effect
size, requires the same measurement instrument for
valid comparison. While efficacy approval is based
on significant change compared to placebo, this does
not necessarily mean all symptoms will be improved
to remission in practice. Studies may be limited to
core symptom measurement only, while treatment in
practice requires consideration of impairments also.
The population included in a study will greatly
influence both the effectiveness and safety
conclusions. Clinical trials tend to limit
co-existing psychiatric disorders, medical risk
factors, and social problems that complicate the
outcomes seen in community practice. Lastly, head to
head comparison studies should be interpreted
carefully, due to differences from practice in
dosing, duration, and patient risk exclusions. RL
Rubin MD, 2006
Dr. Rubin practices Child and Adult Psychiatry,
directs The Clinical Study Center in Burlington
Vermont, and serves as Clinical Associate Professor
at the University of Vermont College of Medicine.
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Call (646) 519-5883 Pin 2648 at 8:30 pm on
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