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Case Reports |
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A Case of “Double” Depression
Under Outpatient Treatment Conditions
Leszek Tomasz Ros |
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| The author has encountered in his professional
practice the coexistence of “major
depression” with psychic depressive attacks (dysthymic attacks) of the
so called temporal epilepsy. Apart from major depression of medium intensity,
other manifestations developed. These were, independent of the time of the day,
suddenly occurring within several seconds, developing without any cause, attacks
of very strong dejection, sadness, breakdown, feeling of lacking sense and hopelessness
of life with slight obnubilation of consciousness and strong groundless fear.
Detailed psychiatric examinations, observations of the patient during such attacks
and EEG records confirmed the diagnosis of dysthymic attacks of temporal epilepsy.
The author has treated the patient with sertraline starting from low doses, up
to 100 mg daily - administered orally once daily in morning hours, clonazepam
(Rivotril) in oral doses 1 mg in morning hours, 1 mg during lunchtime, 2 mg in
evening hours, carbamazepine (Tegretol) 0.2 g tablets from low doses to 0.4 mg
administered once daily in evening hours. Complete remission of major depression
and complete regression of dysthymic attacks of “temporal epilepsy” were
obtained. |
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| Introduction |
The concept of “double” depression
was used here by the author conventionally. Sometimes the
author has encountered in his professional practice the coexistence
of “major depression” with psychic depressive
attacks (dysthymic attacks) of the so called temporal epilepsy.
Dysthymic attacks occur without convulsions and loss of consciousness.
Sometimes they are accompanied by slight obnubilation of
consciousness occurring without autopsychic and allopsychic
orientation disturbances. The treatment in such cases is
a rather difficult problem for the doctor, since completely
different pharmacotherapy is used in “major depression” than
in dysthymic attacks of “temporal epilepsy”.
In treating a patient, the doctor should consider in detail
what interactions between administered drugs could develop.
Besides that, it should be kept in mind that typical tricyclic
antidepressants still very useful in the treatment of major
depression can even trigger dysthymic attacks of “temporal
epilepsy”. Therefore, treating major depression, one
should administer drugs that are safe, well tolerated and
not entering into interactions with pharmaceuticals used
in dysthymic attacks of temporal epilpsy. The same criteria
should be accepted in selecting drugs for treatment of dysthymic
attacks of temporal epilepsy.
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| Case Report |
Female patient SA aged 39 never received any
psychiatric treatment. The patient was born after normal pregnancy
but by forceps delivery. In spite of that, during labour the
head of the patient was not damaged so immediately after delivery
she obtained 10 pts in Apgar scale. Her childhood was very
succesful. Her mother was warm, quiet, very affective, caring
and hard working. The father was quiet, very hard working,
very caring about home and family, extremely responsible, affective,
without addictions. The patient has one sister, two years older.
The sister is quiet, well brought up, but sometimes peremptory,
despotic, not tolerating objection, entering into conflicts,
self-assured, slightly conceited. Despite that, the patient
has constantly good familial relations with her sister. Both
parents unfortunately are dead. The mother died suddenly of
lung oedema in the course of acute left ventricular failure.
The father died of lung cancer with multiple metastases to
other organs. The patient got married at the age of 24. Her
marriage has been good. In primary and secondary schoolsshe
achieved very good results. Then she graduated from the Faculty
of Polish Philology at the University where she achieved good
results. Apart from death of her parents, the most terrible
experience in her life was death of her first baby, one hour
after labour. Then she gave birth to another child who lives
and causes no major health or upbringing problems. No mental
diseases occurred in the patient’s family. She denied
any head trauma and loss of consciousness. She gave no history
of major somatic diseases. The manifestations of major depression
and depressive dysthymic attacks began simultaneously five
months before starting treatment by the author. She used to
work as teacher in primary school. Her job has been her passion.
The disease started with extreme reluctance to her occupational
work. Formal and emotional contacts were very good. Logical,
normal current of thoughts, constant mood depression of medium
intensity. Constant groundless anxiety. General feeling of
helplessness - she had constantly a feeling intensity. Constant
groundless anxiety. General feeling of helplessness - she had
constantly a feeling that she could not cope with her occupational
and home duties. Constant psychic stress, restlessness and
psychomotor agitation. Strong fears that something tragic could
happen to the health of a child during her lessons. Similarly
panic fear that her own child would die of a sudden disease
or due to traffic accident. Lack of appetite, insomnia of early
awakening in the morning with impossible falling asleep again.
She was weeping frequently. She was feeling worse than others
and deserving contempt and condemnation. The patient denied
other depressive delusions. She reported worst general feeling
in morning hours, slightly better during day an best in evening
hours. Feeling of lack of sense and hopelessness of life of
medium intensity. She denied any suicidal ideation. Apart from
major depression of medium intensity, the diagnosis of which
was confirmed by detailed psychiatric examination, tests by
Hamilton scale, Montgomery - Asberg scale, Beck’s Depression
Self - assessment Inventory, ICD-10 scale and DSM III and DSM
IV scales, other manifestations developed. These were, independent
of the time of the day, suddenly occurring within several seconds,
developing without any cause, attacks of very strong dejection,
sadness, breakdown, feeling of lacking sense and hopelessness
of life with slight obnubilation of consciousness and strong
groundless fear. The above mentioned attacks occurred 2-3 times
a week on the average and lasted for several minutes to several
hours. They produced extremely strong sufferings for the patients
and were just unbearable. Detailed psychiatric examinations,
observations of the patient during such attacks and EEG records
confirmed the diagnosis of dysthymic attacks of temporal epilepsy.
Laboratory tests : -Basic laboratory blood and urine analyses
gave normal results
-Chest radiogram was normal,
-ECG record was normal,
-EEG record at the beginning of the treatment : Record with predominating
irregular alpha wave activity of 35 µV amplitude. Besided that, series
of beta waves were visible. Against this background in both temporal regions
many times developed short series of waves of sharp shape, and sometimes
5.5 - 7 Hz theta waves with sharp waves of amplitude up to 50 µV
with a tendency to generalized synchronization. Arrest reaction - marked.
Hyperventilation - unchanged. Opinion : record with moderately intense
pathological changes in both temporal regions. EEG record after one-year
treatment. In the record rapid activity predominated of 20-40 µV
amplitude (probably drug-induced). In posterior parts of the brain groups
of alpha waves occur, of 10-12 HZ frequency and 40-60 µV amplitude.
In both temporal regions isolated theta waves occur. Arrest reaction -
marked.
Hyperventilation - without influence on the record. Photostimulation -
causes following rhythm. Opinion : record normal.
-eye fundus examination: normal,
-neurological examination: no focal and meningeal symptoms,
-physical examination was normal,
-cranial computed tomography : normal
The author has treated the patient with sertraline starting from low doses,
up to 100 mg daily - administered orally once daily in morning hours, clonazepam
(Rivotril) in oral doses 1 mg in morning hours, 1 mg during lunchtime,
2 mg in evening hours, carbamazepine (Tegretol) 0.2 g tablets from low
doses to 0.4 mg administered once daily in evening hours. Complete remission
of major depression and complete regression of dysthymic attacks of “temporal
epilepsy” were obtained. |
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| Discussion |
| The author selecting sertraline for treatment
of major depression as typical selective central serotonin
reuptake inhibitor took many factors into account. Sertraline
is a very safe, well tolerated and effective drug in the treatment
of endogenous depression.1-13 Many authors believe14 that initial
50 mg sertraline daily dose is usually an effective therapeutic
dose and simultaneously an optimal dose in the treatment of
major depression, taking into account both effectiveness and
tolerance in the case of most patients. These authors14 think
that in the case of absent appropriate reaction during 24 days,
sertraline dose can be increased at one-week intervals by 50
mg daily up to 200 mg daily dose. These authors14 believe that
sertraline should be administered most frequently once daily
and the hour of the day is without importance. The author of
this paper administered the drug once daily. The drug was given
always in morning hours in order that the interval between
sertraline and carbamazepine administration was longest possible
(carbamazepine was administered always once daily in evening
hours) to avoid unnecessary interactions between these drugs.
Very few authors15 report extrapyramidal adverse effects connected
with sertraline administration. A review of literature15 made
possible to identify 13 published cases of extrapyramidal symptoms
induction by sertraline. In the patient treated and described
above, slight extrapyramidal manifestations developed after
sertraline. They were quickly controlled by Rivotril which
was administered by the author of the paper in order to treat
dysthymic attacks of temporal epilepsy and correction of fear
in major depression. Carbamazepine given by the author for
treatment of dysthymic attacks of temporal epilepsy exerted
no adverse effects. |
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| References |
| 1. |
Shapiro PA, Lesperance F,
Frasure-Smith N. An open-label preliminary trial of sertraline
for treatment of major depression after acute myocardial
infarction. Department of Psychiatry, Columbia University
College of Physicians and Surgeons, New York, NY 10032,
USA. |
| 2. |
Finkel SL, Richter EM, Clary CM. Comparative
efficiency and safety of sertraline versus nortriptyline
in major depression in patients 70 and older. International
Psychogeriatrics 1999; 11 (1) : 85-99. |
| 3. |
Luketsos GG, Taragano F, Freisman GJ.
Major depression and its response to sertraline in primary
care vs. Psychiatric office practice patients, results
of an open-label trial in Argentina. Neuropsychiatry
and Memory Group, John Hopkins University, Baltimore,
MD, USA. |
| 4. |
Moller HJ, Gallinat J, Hegerl U. Double-blind,
multicenter comparative study of sertraline and amitriptyline
in hospitalized patients with major depression. Pharmacopsychiatry
1980; 31 (6) : 170-7. |
| 5. |
Kirli S, Caliskan M. A comparative study
of sertraline versus imipramine in postpsychotic depressive
disorder of schizophrenia. Schizophrenia Reserach 1998;
33 (1-2). |
| 6. |
Hirschfeld RM, Russel JM, Delgado PL.
Predictors of response to acute treatment of chronic
and double depression with sertraline or imipramine.
Journal of Clinical Psychiatry 1998; 59 (12) : 669-75. |
| 7. |
Davis SM, Harrison WM, Keller MB. The
treatment of chronic depression, part 3; psychosocial
functioning before and after treatment with sertraline
or imipramine. J Clinical Psychiatry 1998; 59 (11) :
608-19. |
| 8. |
Keller MB, Gelenberg AJ, Hirschfeld RM.
The treatment of chronic depression, part 2 : a double-blind,
randomized trial of sertraline and imipramine. J Clinical
Psychiatry 1998; 59 (11) : 598-607. |
| 9. |
Rush AJ, Koran LM, Keller MB. The treatment
of chronic depression, part 1 : Study design and rationale
for evaluating the comparative efficacy of sertraline
and imipramine as acute, crossover, continuation and
maintenance phase therapies. J Clinical Psychiatry 1998;
59 (11) : 589-97 |
| 10 |
Keller MB, Kocsis JH, Thase M. Maintenance
phase efficacy of sertraline for chronic depression :
a randomized controlled trial. JAMA 1998; 280 (19) :
1665-72. |
| 11. |
Bennie EH, Mullin JM, Martindale JJ. A
double-blind multicenter trial comparing sertraline and
fluoxetine in outpatients with major depression. J Clinical
Psychiatry 1995; 56 (6) : 229-37. |
| 12. |
Aguglia E, Casacchia M, Cassano GB. Double-blind
study of the efficacy and safety of sertraline verus
fluoxetine in major depression. International Clinical
Psychopharmacology Fall 1993; 8 (3) : 197-202. |
| 13. |
Murdoch D, McTavish D. Sertraline. A review
of its pharmacodynamic and pharmacokinetic properties,
and therapeutic potental in depression and obsessive
compulsive disorder (Review) (72 refs) Drugs 1992; 44
(4) : 604-24. |
| 14. |
Preskorm SH, Lane RM. Sertraline 50 mg
daily: the optimal dose in the treatment of depression.
(Review) (55 refs) International Clinical Psychopharmacology
1996; 10 (3) : 129-41. |
| 15. |
Lambert MT, Trutia C, Petty F. Extrapyramidal
adverse effects associated with sertraline. Progress
in Neuro-Psychopharmacology and Biological Psychiatry
1998; 22 (5) : 714-8. |
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