Epilepsia Open (Oct 2024)

Italian report on RARE epilepsies (i‐RARE): A consensus on multidisciplinarity

  • Antonella Riva,
  • Antonietta Coppola,
  • Francesca Bisulli,
  • Alberto Verrotti,
  • Irene Bagnasco,
  • Maurizio Elia,
  • Francesca Darra,
  • Simona Lattanzi,
  • Stefano Meletti,
  • Angela La Neve,
  • Giancarlo Di Gennaro,
  • Isabella Brambilla,
  • Katia Santoro,
  • Tommaso Prisco,
  • Francesca Macari,
  • Antonio Gambardella,
  • Carlo diBonaventura,
  • Simona Balestrini,
  • Carla Marini,
  • Dario Pruna,
  • Giuseppe Capovilla,
  • Nicola Specchio,
  • Giuseppe Gobbi,
  • Pasquale Striano,
  • the iRARE Study Group

DOI
https://doi.org/10.1002/epi4.13020
Journal volume & issue
Vol. 9, no. 5
pp. 1857 – 1867

Abstract

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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.

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