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ARTICLES:
L. S. Boylan, L. A. Flint, D. L. Labovitz, S. C. Jackson, K. Starner, and O. Devinsky
Depression but not seizure frequency predicts quality of life in treatment-resistant epilepsy
Neurology 2004; 62: 258-261
[Abstract][Full text][PDF]
ludger_vanelst{at}psyallg.ukl.uni-freiburg.de Ludger Tebartz van Elst, et al.
The interesting article by Boylan et al
examines the treatment of
depressive comorbidity in patients with refractory epilepsy. [1] According to their data, depression measured with the Beck
Depression Inventory (BDI) but not seizure frequency predicts the quality
of life in affected patients. The authors also stress the high
prevalence of depression and the low rate of respective diagnosis and
treatment in this patient sample.
According to our experience, this article
is very relevant as we have found similar rates of depression
in similar patient samples and a severe neglect of this problem in the
treatment of patients with refractory epilepsy. Even when antidepressive
treatment is recommended by liaison psychiatrists, the majority of
cases are not treated in the course of the disease. One
possible reason might be that the presentation of depressive symptoms in
epilepsy is often atypical compared to classic major depression.
Patients with refractory epilepsy often suffer from interictal dysphoric
disorder of epilepsy (IDD) with irritability, anger attacks, mood swings
and other pleiomorphic affective-somatoform symptoms. [2] While specialists
easily recognize IDD, non specialists might interpret these symptoms as
non-pathological reactions to seizures. This psychodynamic interpretation
of psychopathological symptoms might explain the resistance in the
medical profession to treat this condition while also focusing on reducing
seizure frequency.
Furthermore, there is indirect evidence
that chronic and untreated IDD might be associated with psychotic
disorders of epilepsy (POE). [3,4] While a causal relationship between IDD
and POE is unclear, such considerations underline the
need to treat affective symptoms in patients with epilepsy. The paper by
Boylan et al will hopefully increase the awareness of the need to
recognize and treat depression in refractory epilepsy.
References
1. Boylan LS, Flint LA, Labovitz DL, Jackson SC, Starner K, Devinsky
O. Depression but not seizure frequency predicts quality of life in
treatment-resistant epilepsy. Neurology 2004; 62(2):258-261.
2. Blumer D. Dysphoric disorders and paroxysmal affects: recognition
and treatment of epilepsy-related psychiatric disorders. Harvard Review of
Psychiatry 2000; 8:8-17.
3. Tebartz van Elst L, Trimble M. Amygdala pathology in
schizophrenia and psychoses of epilepsy. Current Opinion in Psychiatry
2003; 16:321-326.
4. Tebartz vE, Baeumer D, Lemieux L, Woermann FG, Koepp M,
Krishnamoorthy S et al. Amygdala pathology in psychosis of epilepsy: A
magnetic resonance imaging study in patients with temporal lobe epilepsy.
Brain 2002; 125(Pt 1):140-149.
In reply to van Elst et al
5 March 2004
Laura S. Boylan, Dept of Neurology, New York University 462 First Ave., New York, NY 10016, Daniel L. Labovitz, Lynn A . Flint, Orrin Devinsky
laura.boylan{at}med.nyu.edu Laura S. Boylan, et al.
We thank Tebartz van Elst et al for their comments. They point
out that neurologists frequently disregard recommendations for depression
treatment made by consulting psychiatrists. They go on to suggest that
the reluctance to treat may result from neurologists’ failure to recognize
atypical psychiatric syndromes or a tendency to think their patients’
reactions are ‘normal’ or expected. We agree that these are important
issues. Further, we note that neurologists are sometimes uncomfortable
taking on the management of depression. At the same time, some patients
are averse to seeing a psychiatrist. Neurologists should be willing to
initiate treatment with antidepressants. Educational efforts starting at
least as early as residency could be helpful.
There are more barriers to the treatment of depression
in epilepsy. The time available for neurology encounters is limited. Perhaps use of screening tools to be filled in by
patients while they wait could be helpful. In a recent study by Gilliam
et al, this approach was demonstrated to work to reduce adverse
effects of antiepileptic drugs. [1] We plan to initiate screening with brief
depression and quality of life scales. It is our hope that
routine use of these measures will help promote awareness and diagnosis as
well as followup on progress and outcomes.
References
1. Gilliam FG, Fessler AJ, Baker G, Vahle V, Carter J, Attarian H.
Systematic screening allows reduction of adverse antiepileptic drug
effects: a randomized trial. Neurology 2004: 2(1):23-7.