volume 66 issue 4 pages 1110-1118

Fenfluramine treatment for Dravet syndrome: Long term real‐world analysis demonstrates safety and reduced health care burden

Alessandra Boncristiano 1
Simona Balestrini 1, 2
Viola Doccini 1
N. Specchio 3, 4
Nicola Pietrafusa 3
Marina Trivisano 3
F. Darra 5, 6
Alberto Cossu 6
Domenica Battaglia 7
Michela Quintiliani 7
M. Luigia Gambardella 7
Eliana Parente 8
Rita Monni 9
Sara Matricardi 10, 11
C. Marini 11
Francesca Ragona 12
T. Granata 12
P. Striano 13, 14
Antonella Riva 13, 14
Renzo Guerrini 1, 2
9
 
Neuropsychiatry Department ASST Mantova Mantova Italy
10
 
Department of Pediatrics University of Chieti Chieti Italy
11
 
Child Neurology and Psychiatry Unit “G. Salesi” Children's Hospital, Azienda Ospedaliero Universitaria Delle Marche Ancona Italy
Publication typeJournal Article
Publication date2024-12-30
scimago Q1
wos Q1
SJR2.371
CiteScore11.4
Impact factor6.6
ISSN00139580, 15281167, 15281157
PubMed ID:  39740232
Abstract
Objective

Fenfluramine (FFA), stiripentol (STP), and cannabidiol (CBD) are approved add‐on therapies for seizures in Dravet syndrome (DS). We report on the long‐term safety and health care resource utilization (HCRU) of patients with DS treated with FFA under an expanded access program (EAP).

Methods

A cohort of 124 patients received FFA for a median of 2.8 years (34.4 months). We compared data on safety and HCRU during FFA treatment with those from a same pre‐treatment period. Echocardiography was conducted every 6 months. Information collected included gender, age, and auxological parameters (height, weight, and body mass index [BMI]) at the start (T0) and follow‐up (T1); FFA treatment details (start, withdrawal, dosage); adverse events (AEs); and HCRU data including hospital admissions, status epilepticus (SE) episodes, and rescue medication use. We grouped patients by weight: ≤37.4 kg (n = 68, 54.8%) and ≥37.5 kg (n = 56; 45.1%), with FFA dosing adjusted accordingly. Statistical analyses included paired t test, Wilcoxon signed‐rank test, Kaplan–Meier analysis, and Bonferroni correction to adjust for multiple testing.

Results

Mean age was 47 months at clinical diagnosis and 81 months at T0. The last follow‐up average FFA dose was .5 mg/kg/day, with a median of .4 mg/kg/day. FFA led to a 9.5% reduction in prior treatment load. At last follow‐up, 118 of 124 (91.5%) remained on FFA. Rescue medication use decreased significantly from 4.5 to 1, hospitalizations from 1 to 0, and SE episodes from 0–240 to 0–180 (p < .001 for all). Seizure freedom was achieved in 9 of 118 patients (7.6%). AEs occurred in 39 of 124 patients (31.5%), with no cardiac issues or deaths. There was an overall mean reduction in BMI, with no statistical significance, and never requiring FFA withdrawal.

Significance

FFA is well tolerated, without cardiac toxicity, and reduces treatment load and HCRU, suggesting improved patient management. BMI reduction in young children highlights the need for growth and nutritional monitoring.

Found 
Found 

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Boncristiano A. et al. Fenfluramine treatment for Dravet syndrome: Long term real‐world analysis demonstrates safety and reduced health care burden // Epilepsia. 2024. Vol. 66. No. 4. pp. 1110-1118.
GOST all authors (up to 50) Copy
Boncristiano A., Balestrini S., Doccini V., Specchio N., Pietrafusa N., Trivisano M., Darra F., Cossu A., Battaglia D., Quintiliani M., Gambardella M. L., Parente E., Monni R., Matricardi S., Marini C., Ragona F., Granata T., Striano P., Riva A., Guerrini R. Fenfluramine treatment for Dravet syndrome: Long term real‐world analysis demonstrates safety and reduced health care burden // Epilepsia. 2024. Vol. 66. No. 4. pp. 1110-1118.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1111/epi.18241
UR - https://onlinelibrary.wiley.com/doi/10.1111/epi.18241
TI - Fenfluramine treatment for Dravet syndrome: Long term real‐world analysis demonstrates safety and reduced health care burden
T2 - Epilepsia
AU - Boncristiano, Alessandra
AU - Balestrini, Simona
AU - Doccini, Viola
AU - Specchio, N.
AU - Pietrafusa, Nicola
AU - Trivisano, Marina
AU - Darra, F.
AU - Cossu, Alberto
AU - Battaglia, Domenica
AU - Quintiliani, Michela
AU - Gambardella, M. Luigia
AU - Parente, Eliana
AU - Monni, Rita
AU - Matricardi, Sara
AU - Marini, C.
AU - Ragona, Francesca
AU - Granata, T.
AU - Striano, P.
AU - Riva, Antonella
AU - Guerrini, Renzo
PY - 2024
DA - 2024/12/30
PB - Wiley
SP - 1110-1118
IS - 4
VL - 66
PMID - 39740232
SN - 0013-9580
SN - 1528-1167
SN - 1528-1157
ER -
BibTex |
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BibTex (up to 50 authors) Copy
@article{2024_Boncristiano,
author = {Alessandra Boncristiano and Simona Balestrini and Viola Doccini and N. Specchio and Nicola Pietrafusa and Marina Trivisano and F. Darra and Alberto Cossu and Domenica Battaglia and Michela Quintiliani and M. Luigia Gambardella and Eliana Parente and Rita Monni and Sara Matricardi and C. Marini and Francesca Ragona and T. Granata and P. Striano and Antonella Riva and Renzo Guerrini},
title = {Fenfluramine treatment for Dravet syndrome: Long term real‐world analysis demonstrates safety and reduced health care burden},
journal = {Epilepsia},
year = {2024},
volume = {66},
publisher = {Wiley},
month = {dec},
url = {https://onlinelibrary.wiley.com/doi/10.1111/epi.18241},
number = {4},
pages = {1110--1118},
doi = {10.1111/epi.18241}
}
MLA
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MLA Copy
Boncristiano, Alessandra, et al. “Fenfluramine treatment for Dravet syndrome: Long term real‐world analysis demonstrates safety and reduced health care burden.” Epilepsia, vol. 66, no. 4, Dec. 2024, pp. 1110-1118. https://onlinelibrary.wiley.com/doi/10.1111/epi.18241.