Literature DB >> 28984349

Quality of life and comorbidities associated with Dravet syndrome severity: a multinational cohort survey.

Lieven Lagae1, Isabella Brambilla2, Ana Mingorance2, Eddie Gibson3, Alysia Battersby3.   

Abstract

AIM: To test the hypothesis that higher seizure burden in Dravet syndrome is associated with increased comorbidities and lower quality of life (QoL) in a large cohort of patients with Dravet syndrome and their caregivers in Europe.
METHOD: An extensive survey of caregivers of patients with Dravet syndrome on experiences of diagnosis, seizure burden, management, social and financial impact, and health services use was administered online in 10 languages.
RESULTS: The survey received 584 unique responses from caregivers of paediatric (83%) and adult (17%) patients with Dravet syndrome (aged <1-48y). Despite broadly following current treatment guidance, less than 10% of patients were seizure free in the previous 3 months. Nearly all (99.6%) patients aged 5 years or older experienced at least one or more motor, speech, learning, or behavioural impairment. High seizure frequency was related to more reports of emergency treatment, comorbidities, and a lower QoL (as measured by the standardized instrument EQ-5D-5L). If not diagnosed at the first instance, the majority (83%) of adults, but less than 20% of 6- to 11-year-olds were diagnosed after 4 or more years.
INTERPRETATION: Patients with Dravet syndrome with the highest current seizure frequency suffer from more comorbidities and have a lower QoL. Therefore, more effective antiepileptic treatments are needed. WHAT THIS PAPER ADDS: The survey captured about 15% of all patients with Dravet syndrome in Europe. Less than 10% of patients had current seizure freedom. Patients with a high current seizure burden have more comorbidities and lower quality of life.
© 2017 The Authors. Developmental Medicine & Child Neurology published by John Wiley & Sons Ltd on behalf of Mac Keith Press.

Entities:  

Mesh:

Year:  2017        PMID: 28984349     DOI: 10.1111/dmcn.13591

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  23 in total

Review 1.  Dravet Syndrome: Novel Approaches for the Most Common Genetic Epilepsy.

Authors:  Lori L Isom; Kelly G Knupp
Journal:  Neurotherapeutics       Date:  2021-08-10       Impact factor: 6.088

Review 2.  Recent Advances in the Drug Treatment of Dravet Syndrome.

Authors:  Elaine C Wirrell; Rima Nabbout
Journal:  CNS Drugs       Date:  2019-09       Impact factor: 5.749

3.  Dravet Syndrome-The Polish Family's Perspective Study.

Authors:  Justyna Paprocka; Anita Lewandowska; Piotr Zieliński; Bartłomiej Kurczab; Ewa Emich-Widera; Tomasz Mazurczak
Journal:  J Clin Med       Date:  2021-04-28       Impact factor: 4.241

Review 4.  Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening.

Authors:  Aliesha Griffin; Kyla R Hamling; SoonGweon Hong; Mana Anvar; Luke P Lee; Scott C Baraban
Journal:  Front Pharmacol       Date:  2018-06-04       Impact factor: 5.810

5.  Seizure burden in severe early-life epilepsy: Perspectives from parents.

Authors:  Anne T Berg; Karen Kaiser; Tracy Dixon-Salazar; Andi Elliot; Nancy McNamara; Mary Anne Meskis; Emily Golbeck; Priya Tatachar; Linda Laux; Carrie Raia; Janice Stanley; April Luna; Christian Rozek
Journal:  Epilepsia Open       Date:  2019-04-14

6.  In vivo, in vitro and in silico correlations of four de novo SCN1A missense mutations.

Authors:  Andreea Nissenkorn; Yael Almog; Inbar Adler; Mary Safrin; Marina Brusel; Milit Marom; Shayel Bercovich; Daniel Yakubovich; Michal Tzadok; Bruria Ben-Zeev; Moran Rubinstein
Journal:  PLoS One       Date:  2019-02-08       Impact factor: 3.240

7.  Fenfluramine in the successful treatment of super-refractory status epilepticus in a patient with Dravet syndrome.

Authors:  David Millett; Suzanne Pach
Journal:  Epilepsy Behav Rep       Date:  2021-05-31

8.  Improving early diagnosis of rare diseases using Natural Language Processing in unstructured medical records: an illustration from Dravet syndrome.

Authors:  Tommaso Lo Barco; Mathieu Kuchenbuch; Nicolas Garcelon; Antoine Neuraz; Rima Nabbout
Journal:  Orphanet J Rare Dis       Date:  2021-07-13       Impact factor: 4.123

9.  Genetic epilepsies and COVID-19 pandemic: Lessons from the caregiver perspective.

Authors:  Ángel Aledo-Serrano; Ana Mingorance; Adolfo Jiménez-Huete; Rafael Toledano; Irene García-Morales; Carla Anciones; Antonio Gil-Nagel
Journal:  Epilepsia       Date:  2020-05-18       Impact factor: 6.740

10.  Dose-Ranging Effect of Adjunctive Oral Cannabidiol vs Placebo on Convulsive Seizure Frequency in Dravet Syndrome: A Randomized Clinical Trial.

Authors:  Ian Miller; Ingrid E Scheffer; Boudewijn Gunning; Rocio Sanchez-Carpintero; Antonio Gil-Nagel; M Scott Perry; Russell P Saneto; Daniel Checketts; Eduardo Dunayevich; Volker Knappertz
Journal:  JAMA Neurol       Date:  2020-05-01       Impact factor: 18.302

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.