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Modafinil-Induced Reversible Hyperkinetic Nondystonic Movement Disorder
in a Patient With Major Depressive Disorder
Alexander Luborzewski, M.D., Francesca Regen, M.D., Frank Schindler,
M.D. and Ion Anghelescu, M.D., Department of Psychiatry and Psychotherapy,
Charité - University Medicine Berlin, Campus Benjamin Franklin,
Berlin, Germany
Fatigue, lack of energy, and lassitude are commonly reported symptoms
in major depressive disorder and are likely to persist as residual conditions
in patients with partial response to antidepressant therapy. Modafinil,
a newer psychostimulant, has been used as an augmentation strategy to
treat persistent fatigue and sleepiness in patients with major depression
who are partial responders to antidepressant treatment(1). Furthermore,
modafinil may fasten the onset and degree of resolution of symptoms of
depression with fatigue when combined with selective serotonin reuptake
inhibitor treatment(2). Modafinil seems to be generally well tolerated;
frequent adverse events include headaches, nausea and nervousness, which
are transient in most cases.
Case Report
A 76-year-old female patient with a history of major depressive disorder
(DSM-IV), was admitted to the psychiatric department with a severe major
depressive episode (Hamilton Depression Rating Scale) in August 2003.
After partial response with venlafaxine 150 mg/d and concomitant treatment
with zopiclone 7.5 mg/d for insomnia, she still suffered from severe lack
of energy, persistent fatigue and lassitude. Modafinil 200 mg/d was then
administered as augmentation to ongoing antidepressant therapy with rapid
improvement of residual symptoms and full remission from depression after
2 weeks of treatment (Hamilton Depression Rating Scale). The patient was
discharged with venlafaxine 150 mg/d and modafinil 200 mg/d and subsequently
was followed at our outpatient clinic. After 4 months of continuous treatment,
the patient presented with bothersome, nondystonic, hyperkinetic, involuntary
movements affecting the orofacial region and the lower limbs, which had
developed over the past 4 days. After discontinuation of modafinil, the
drug-induced movement disorder improved and then finally disappeared completely
within 4 days.
Comment
The authors report a case of a severe and disabling, but reversible,
orofacial and lower limb hyperkinetic, nondystonic, modafinil-induced
movement disorder. No such movement disorders have been observed in patients
treated with modafinil for daytime sleepiness or narcolepsy even in large-scale
trials(3). Neither have there been any reports on those disorders in depressed
patients receiving modafinil as an augmentation strategy. A causal relationship
between the intake of modafinil and the movement disorder described seems
probable, because the movement disorder developed within a timeframe of
4 months of continuous treatment with modafinil, which is in line with
a case report on orofacial dyskinesias following a 10-month period of
treatment with the modafinil derivative adrafinil(4). Furthermore, the
movement disorder completely resolved within 4 days after discontinuation
of modafinil. This case report supports further evidence that, like in
the case of antipsychotics(5) elderly patients might have a greater risk
for developing hyperkinetic movement disorders.
REFERENCES
1. Fava M, Thase ME, DeBattista C: A multicenter, placebo-controlled
study of modafinil augmentation in partial responders to selective serotonin
reuptake inhibitors with persistent fatigue and sleepiness. J Clin Psychiatry
2005; 66:85–93[Medline]
2. Ninan PT, Hassman HA, Glass SJ, et al: Adjunctive modafinil at initiation
of treatment with a selective serotonin reuptake inhibitor enhances the
degree and onset of therapeutic effects in patients with major depressive
disorder and fatigue. J Clin Psychiatry 2004; 65:414–420[Medline]
3. US Modafinil Multicenter Study Group: Randomized trial of modafinil
as a treatment for the excessive daytime somnolence of narcolepsy. Neurology
2000; 54(5): 1166-1175
4. Thobois S, Xie J, Mollion H, et al: Adrafinil-induced orofacial dyskinesia.
Mov Disord 2004 Aug; 19(8):965-966
5. Kane JM, Woerner M, Lieberman J: Tardive dyskinesia: prevalence, incidence,
and risk factors. Psychopharmacology (Berl) Suppl 1985; 2:72–78
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