Medication for Treating Eating
Disorders
The Psychiatrist's Role And Medication
continued
As has been previously stated, the research on BED (including drug
studies) is minimal but growing. However, several investigators believe that
binge eating is less a matter of willpower than brain chemistry. In some
cases, clinicians and researchers are using
SSRIs with binge eating disorder
for the same reasons they use it for bulimia. Serotonin helps us feel full,
so it is theorized that people with binge eating disorders like bulimia
nervosa may want to eat all the time because they have too little of the
neurotransmitter serotonin and thus never feel satisfied (satiated).
Guidelines for When to Use Medications
-
After nutritional rehabilitation has begun
-
After full patient history and medical
evaluation are complete
-
After full family history and evaluation
-
After review of valid, reliable, published
data-based trials
-
After psychoeducation and initiation of
psychotherapy
-
When medication-responsive coexisting
conditions are clearly identified, particularly when they predate the
onset of the eating disorder
Psychotropic Medications Commonly Used in Eating Disorders
Selective Serotonin Reuptake Inhibitors (SSRIs): Used for
obsessive-compulsive behaviors,
depression, and
anxiety disorders like
panic,
social phobia, and post-traumatic stress disorder. Have been shown to
decrease binge/purge behavior when used in higher doses (e.g., 60 mg
Prozac). May diminish obsessive, rigid thinking and ritualistic behavior
traits. Fluoxetine (Prozac) trials have shown that administering the drug
after weight restoration in anorexia nervosa may prevent relapse. Low risk
of suicidal overdoses with these medications.
Cautions: These medications may not be used in pregnancy, particularly
first trimester, unless absolutely necessary. This class of medications is
not addicting, but there may be side effects with abrupt withdrawal of
Paxil,
Zoloft, and
Luvox. A gradual tapering off is recommended. Drug interactions
do occur. It is important for the prescribing doctor to know about all drugs
being taken, including over-the-counter drugs and herbs or homeopathics.
Monoamine oxidase inhibitors (MAOIs) cannot be used within two weeks of
beginning to take SSRIs. MAOIs cannot be started until five to eight weeks
after discontinuation of Prozac.
Most common side effects: anxiety, nervousness, insomnia, agitation,
gastric irritation, fatigue, drowsiness, sweating, tremor, anorexia (loss of
appetite), diarrhea, dizziness, lightheadedness, sexual dysfunction,
decreased libido.
Examples of general dosing:
Prozac (fluoxetine) 10–80 mg a day
Zoloft (sertraline) 25–200 mg a day
Paxil (paroxetine) 10–50 mg a day
Luvox (fluvoxamine) 50–300 mg a day
Celexa (citalopram) 10–60 mg a day
Norepinephrine-Dopamine Reuptake Inhibitor (NDRI): Wellbutrin (Bupropion).
According to the Food and Drug Administration (FDA), this medication should
not be used in patients with active eating disorders because of the higher
risk of seizures.
Serotonin-Norepinephrine Reuptake Inhibitor (SNRI): This new
antidepressant has not yet been studied in eating disorders, but
theoretically it should be helpful. This medication is used for depression
and anxiety disorders, including generalized anxiety disorders. Weight gain
or loss may occur, with corresponding alteration in appetite.
HealthyPlace.com Audio
Managed
Care and Eating Disorders
Patients with chronic conditions like anorexia nervosa which
require expensive treatments are most likely to have
difficulty getting the care they need under managed care
health plans. Anorexics are obsessed with weight gain and
starve themselves. The condition requires long term medical
and psychological treatment for which many insurers are
refusing to pay.
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There is no clear advantage over SSRIs in terms of side effects. It may
have a more stimulating effect and has been known to cause nausea. Overall,
however, this drug does tend to have fewer side effects than the tricyclics.
There is a lower suicide potential for overdose with this drug than there is
with tricyclics, but the potential may be higher than that with SSRIs.
Most common side effects: Nausea and increased blood pressure
(hypertension).
Examples of general dosing:
Effexor (Venlafaxine) 37.5 mg two times a day to 300 mg total (given
in two doses) a day
Serotonin Antagonist Reuptake Inhibitors (SARIs): This is another new
class of antidepressant not yet studied in eating disorders but used in
depression and anxiety disorders. Compared to the SSRIs, the SARIs have the
advantage of not causing or increasing anxiety, insomnia, or sexual
dysfunction.
Most common side effects: Sedation and nausea.
Example of general dosing:
Serzone (Nefazodone) 100–600 mg a day
Tricyclics: Reduce depression and panic attacks and may diminish bingeing
and purging behaviors. Generally cause increased appetite and weight gain.
Generally cause more sedation than SSRIs. Much lower threshold for
successful suicide, as they signif- icantly affect heart function in higher
doses; commonly used in overdose attempts. Rapidly absorbed from the
stomach. Have more side effects than SSRIs. Certain medications may increase
blood levels without an actual increase in dose. This may place the person
taking the medication at increased risk for side effects or inadvertent
overdose. Can see side effects with abrupt discontinuation. Tapering is
recommended, just as with SSRIs. Don't use with MAOIs. Thera-peutic blood
levels can be beneficial.
Common side effects: Constipation, blurry vision, urinary hesitancy,
possible affect on cardiac function, weight gain, increased appetite,
possible decrease in libido.
Examples of general dosing:
Desipramine 100–300 mg a day
Imipramine 100–300 mg a day
Notriptyline 50–150 mg a day
Mood Stabilizers
Used primarily for mood stabilization in bipolar (manic-depressive)
disorder or mood swings. May help stabilize mood instability in persons with
borderline personality organization and various disorders of brain function.
Can sometimes be used as augmentors in individuals who are not responding to
antidepressants.
Depakote/valproic acid derivatives: Primary use is as anticonvulsant. May
cause liver failure as more severe side effect. Can be fatal. General dosage
range 500–2,000 mg. Causes less weight gain than lithium, but more than Tegretol. Blood serum levels must be checked. Gastrointestinal side effects
may occur. Toxic levels can be fatal.
Carbamazepine (Tegretol): Anticonvulsant and mood stabilizer. Worse side
effect aplastic anemia. Can be fatal, but rare (1 in 50,000).
Gastrointestinal side effects do occur. Blood levels must be checked. Causes
less weight gain than lithium and Depakote. Toxic levels can be fatal. Dose
range 200–2,000 mg.
Lithium salt: May cause weight gain, acne, retention of water,
hypothyroidism, excessive secretion of urine, excessive thirst. Replacement
of water loss is essential, or toxicity will occur. Toxic levels will kill
and are more likely with decreased potassium. Patients generally will not
use if aware of risk of weight gain. Dose range 600–3,000 mg in eating
disordered clients. Probably should be avoided in eating disorders due to
lithium toxicity associated with low potassium and dehydration.
Lamictal (lamotragine): A newer anticonvulsant showing promise as a mood
stabilizer. No blood levels necessary.
Antianxiety Medications
Generally benign in regard to side effects, but have significant effects
in overdose. Most important concern is addiction potential. Short-term use
is acceptable and long-term use sometimes necessary in severe anxiety
disorders not responsive to SSRIs. In order of most to least addicting:
Ativan, Klonopin (most commonly used for long-term treatment).
Examples of general dosing:
Ativan 009;.5–2.0 mg two to four times per day Klonopin .25–1.0 mg
two to four times per day
Buspirone (Buspar): A new nonaddictive antianxiety drug that works
differently than the benzodiazepines (e.g., Xanax, Valium). Used in
generalized anxiety and as an adjunct to antidepressants for refractory
depression and obsessive-compulsive disorder.
This chapter has been devoted mainly to the use of psychotropic
medications. Eating disordered individuals have coexisting medical
conditions and symptoms that also benefit from medication.
The use of other types of medication in the treatment of eating disorders
is certainly indicated for various medical complications that arise, but
proper precautions must be taken. For example, prescribing hormone
replacement therapy for an anorexic who has stopped menstruating may be a
viable choice, with the precaution that there is no proof that the
medication will prevent osteoporosis and taking it might even foster a false
sense of security by masking the return of normal menstrual function.
Another example would be prescribing laxatives for a bulimic complaining
of constipation. On the one hand, this might be contraindicated, but with
another individual it may be necessary, particularly if the person has
become laxative dependent and requires a slow and gradual weaning. The
following chapter discusses these and other topics in the medical management
of eating disorders, particularly anorexia and bulimia.
pages 1 2
3
By Carolyn
Costin, MA, M.Ed., MFCC - Medical Reference from "The Eating Disorders
Sourcebook"
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