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Volume 9

Journal of Neurology and Neuroscience

ISSN: 2171-6625

Page 62

JOINT EVENT

July 23-24, 2018 Birmingham, UK

&

24

th

International Conference on

Neuroscience and Neurochemistry

26

th

Edition of International Conference on

Clinical Psychology and Neuroscience

Efficacy and safety of clobazam in a pediatric refractory epilepsy population less than two years of age

Ersida Buraniqi

1, 2

, Xiaofan Wang

1

, Fatemeh Mohammadpour Touserkani

1

, Kush Kapur

1

and

Tobias Loddenkemper

1

1

Harvard Medical School, USA

2

Mayo Clinic, Rochester, USA

Aim:

To describe our experience with the efficacy and safety of clobazam in refractory epilepsy in a large population of children

less than two years of age.

Methods:

We retrospectively reviewed all patients between 0 and 2 years of age at Boston Children’s Hospital from October

2011 to December 2016. We included patients who were treated with clobazam for refractory epilepsy, and who had a follow-

up visit at least one month after starting clobazam. Response to clobazam was defined as >50% reduction in seizure frequency

at the time of last follow-up visit as compared to baseline.

Results:

155 patients received clobazam, of which 116 [median age 12 months, IQR (p25-p75) 8-16 months] had full follow-

up data ≥1 month after starting clobazam. Median follow-up age was 14 months [IQR (p25-p75) 9-18 months]. At the time of

clobazam initiation, 31/116 (27%) patients were on one antiepileptic drug (AED), 52/116 (45%) patients were on two AEDs,

and 26/116 (22%) patients were on 3 or more AEDs. 7/116 (6%) patients received clobazam monotherapy. Overall response

rate was 33% (38/116) with a median seizure reduction of 75%. 18 (16%) patients had ≤50% reduction, 14 (12%) had no

change and 16 (14%) had worsening of seizure frequency. 30 (26%) patients became seizure free. 8 (7%) patients discontinued

clobazam.

Conclusions:

Clobazam is both well tolerated and effective in reducing seizure frequency in pediatric patients less than two

years of age with refractory epilepsy.

ersidaunivers@gmail.com

J Neurol Neurosci 2018, Volume 9

DOI: 10.21767/2171-6625-C2-012