INVESTIGADORES
D`ALESSIO Luciana
artículos
Título:
Analysis of psychotic disorders in patients with refractory partial epilepsy
Autor/es:
D`ALESSIO LUCIANA, GIAGANTE BRENDA, IBARRA VIVIANA, PAPAYANNIS CRISTINA, ODDO SILVIA, SOLÍS PATRICIA, CONSALVO DAMIÁN, SILVA WALTER, DONNOLI VICENTE, ZIEHER LUIS MARÍA, KOCHEN SILVIA.
Revista:
ACTAS ESPAñOLAS DE PSIQUIATRÃA
Editorial:
Ars medica
Referencias:
Lugar: Barcelona; Año: 2008 vol. 36 p. 138 - 143
ISSN:
1139-9287
Resumen:
Introduction. The association between psychotic disorders
and epilepsy has been controversial. Different subtypes
of psychotic disorders in epilepsy patients have been described
according to temporal relationship with seizures-postictal
(PIP), interictal (IIP) and bimodal (BP) psychoses are
described in literature.
Objectives. Determine clinical characteristics of patients
with refractory partial epilepsy and psychoses and
compare the results with a control group of patients with
refractory partial epilepsy without psychoses.
Methods. A total of 57 patients with refractory partial
epilepsy and psychotic disorders (psychotic group [PG]) and
56 patients with refractory partial epilepsy and without
psychoses (control group [CG]) were evaluated according to
DSM IV criteria and SCID I. All patients underwent complete
neurological, neuroimaging, neuropsychological, and
psychiatric assessment. Clinical, demographic and neuroimaging
data were compared between patients in CG and
PG.
Results. In PG, 15 patients (26%) had criteria for PIP, 29
patients (51%) for IIP and 13 patients (23%) for BP. Epilepsy
time duration and bilateral hippocampal sclerosis were significantly
more frequent in patients in PG (p<0.05). No differences
were found between psychoses subtypes.
Conclusions. Longer evolution of seizures and the presence
of bilateral hippocampal sclerosis may increase propensity
to develop psychoses in patients with refractory
partial epilepsy. Longer evolution of seizures and the presence
of bilateral hippocampal sclerosis may increase propensity
to develop psychoses in patients with refractory
partial epilepsy.