Your browser doesn't support javascript.
loading
Italian report on RARE epilepsies (i-RARE): A consensus on multidisciplinarity.
Riva, Antonella; Coppola, Antonietta; Bisulli, Francesca; Verrotti, Alberto; Bagnasco, Irene; Elia, Maurizio; Darra, Francesca; Lattanzi, Simona; Meletti, Stefano; La Neve, Angela; Di Gennaro, Giancarlo; Brambilla, Isabella; Santoro, Katia; Prisco, Tommaso; Macari, Francesca; Gambardella, Antonio; di Bonaventura, Carlo; Balestrini, Simona; Marini, Carla; Pruna, Dario; Capovilla, Giuseppe; Specchio, Nicola; Gobbi, Giuseppe; Striano, Pasquale.
Affiliation
  • Riva A; Department of Neurosciences Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
  • Coppola A; Epilepsy Center, Department of Neuroscience, Odontostomatology and Reproductive Sciences, Federico II University of Naples, Naples, Italy.
  • Bisulli F; IRCCS Istituto Delle Scienze Neurologiche di Bologna, Full Member of the ERN EpiCARE, Bologna, Italy.
  • Verrotti A; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
  • Bagnasco I; Department of Pediatrics, University of Perugia, Perugia, Italy.
  • Elia M; Division of Neuropsychiatry, Epilepsy Center for Children, Martini Hospital, Turin, Italy.
  • Darra F; Unit of Neurology and Clinical Neurophysiopathology, Oasi Research Institute-IRCCS, Troina, Italy.
  • Lattanzi S; Unit of Child Neuropsychiatry, Department of Engineering for Innovation Medicine, University of Verona, Full Member of the ERN EpiCARE Verona, Verona, Italy.
  • Meletti S; Neurological Clinic, Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy.
  • La Neve A; Neurophysiology Unit and Epilepsy Centre, OCB Hospital, AOU Modena, Modena, Italy.
  • Di Gennaro G; Department of Biomedical, Metabolic and Neural Science, University of Modena and Reggio Emilia, Modena, Italy.
  • Brambilla I; Department of Basic Medical Sciences, Neurosciences and Sense Organs, University of Bari, Bari, Italy.
  • Santoro K; IRCCS NEUROMED, Pozzilli, Isernia, Italy.
  • Prisco T; Dravet Italia Onlus, Verona, Italy.
  • Macari F; Epag ERN EpiCare, Verona, Italy.
  • Gambardella A; Research Center For Pediatric Epilepsies (CREP), Department of Surgery, Dentistry, Paediatrics and Gynecology, University of Verona, Verona, Italy.
  • di Bonaventura C; Alleanza Epilessie Rare e Complesse, Italy.
  • Balestrini S; Associazione Famiglie LGS Italia, Correggio, Italy.
  • Marini C; Or.S.A, Treviso, Italy.
  • Pruna D; Associazione Sclerosi Tuberosa, Rome, Italy.
  • Capovilla G; Department of Precision Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
  • Specchio N; Department of Human Neurosciences, Policlinico Umberto I, Sapienza University of Rome, Rome, Italy.
  • Gobbi G; Neuroscience Department, Meyer Children's Hospital, Florence, Italy.
  • Striano P; University of Florence, Florence, Italy.
Epilepsia Open ; 2024 Aug 23.
Article in En | MEDLINE | ID: mdl-39176980
ABSTRACT

OBJECTIVE:

Rare and complex epilepsies encompass a diverse range of disorders characterized by seizures. We aimed to establish a consensus on key issues related to these conditions through collaboration among experienced neurologists, neuropediatricians, and patient advocacy representatives.

METHODS:

Employing a modified Delphi method, a scientific board comprising 20 physicians and 4 patient advocacy representatives synthesized existing literature with their expertise to formulate statements on contentious topics. A final 32-member expert panel, representing diverse regions of Italy, validated these statements through a two-round voting process, with consensus defined as an average score ≥7.

RESULTS:

Sixteen statements reached a consensus, emphasizing the necessity for epidemiological studies to ascertain the true prevalence of rare epilepsies. Etiology emerged as a crucial factor influencing therapeutic strategies and outcome prediction, with particular concern regarding prolonged and tonic-clonic seizures. The importance of early implementation of specific drugs and non-pharmacological interventions in the treatment algorithm for developmental and epileptic encephalopathies (DEEs) was underscored. Multidisciplinary care involving experts with diverse skills was deemed essential, emphasizing non-seizure outcomes in adolescence and adulthood.

SIGNIFICANCE:

This national consensus underscores the imperative for personalized, comprehensive, and multidisciplinary management of rare epilepsies/DEEs. It advocates for increased research, particularly in epidemiology and therapeutic approaches, to inform clinical decision-making and healthcare policies, ultimately enhancing patients' outcomes. PLAIN LANGUAGE

SUMMARY:

The modified Delphi method is broadly used to evaluate debated topics. In this work, we sought the consensus on integrated and social care in epilepsy management. Both representatives of high-level epilepsy centers and patients' caregivers were directly involved.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Epilepsia Open Year: 2024 Document type: Article Affiliation country: Italy Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Epilepsia Open Year: 2024 Document type: Article Affiliation country: Italy Country of publication: United States