Radaelli G, de Souza Santos F, Borelli WV, Pisani L, Nunes
ML, Scorza FA, da Costa JC. Causes of mortality in early infantile epileptic
encephalopathy: A systematic review. Epilepsy Behav. 2018 Aug;85:32-36
Abstract
INTRODUCTION:
Early infantile epileptic encephalopathy syndrome (EIEE),
also known as Ohtahara syndrome, is an age-dependent epileptic encephalopathy
syndrome defined by clinical features and electroencephalographic findings.
Epileptic disorders with refractory seizures beginning in the neonatal period
and/or early infancy have a potential risk of premature mortality, including
sudden death. We aimed to identify the causes of death in EIEE and conducted a
literature survey of fatal outcomes.
METHODS:
We performed a literature search in MEDLINE, EMBASE, and Web
of Science for data from inception until September 2017. The terms "death
sudden," "unexplained death," "SUDEP,"
"lethal," and "fatal" and the medical subject heading terms
"epileptic encephalopathy," "mortality," "death,"
"sudden infant death syndrome," and "human" were used in
the search strategy. The EIEE case report studies reporting mortality were
included.
RESULTS:
The search yielded 1360 articles. After screening for titles
and abstracts and removing duplicate entries, full texts of 15 articles were
reviewed. After reading full texts, 11 articles met the inclusion criteria (9
articles in English and 2 in Japanese, dated from 1976 to 2015). The review
comprised 38 unique cases of EIEE, 17 of which had death as an outcome. In all
cases, the suppression-burst pattern on electroencephalographies (EEGs) was
common. Most cases (55%) involved male infants. The mean (standard deviation
[SD]) age at onset of seizure was 19.6 ± 33 days. The mean (SD) age at death
was 12.9 ± 14.1 months. Most infants (58.8%) survived less than one year. The
cause of death was described only in eight (47%) patients; the cause was
pneumonia/respiratory illness or sudden unexpected death in epilepsy (SUDEP).
DISCUSSION:
The results show EIEE as a severe disease associated with a
premature mortality, evidenced by a very young age at death. Increasing
interest in the detection of new molecular bases of EIEE is leading us to a
better understanding of this severe disease, but well-reported data are lacking
to clarify EIEE-related causes of death.
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