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.
Italian report on RARE epilepsies (i-RARE): A consensus on multidisciplinarity / Riva, A.; Coppola, A.; Bisulli, F.; Verrotti, A.; Bagnasco, I.; Elia, M.; Darra, F.; Lattanzi, S.; Meletti, S.; Laneve, A.; Digennaro, G.; Brambilla, I.; Santoro, K.; Prisco, T.; Macari, F.; Gambardella, A.; di Bonaventura, C.; Balestrini, S.; Marini, C.; Pruna, D.; Capovilla, G.; Specchio, N.; Gobbi, G.; Striano, P.; Emanuele, B.; Paolo, B.; Antonella, B.; Eleonora, B.; Laura, C.; Ilaria, D. N.; Francesco, F.; Rosita, G.; Lucio, G.; Alessia, G.; Loretta, G.; Loredana, L.; Anna, L.; Michela, M.; Domenica, M. S.; Mario, M.; Tullio, M.; Eliana, P.; Giuditta, P.; Cinzia, P.; Marta, P.; Nicola, P.; Virginia, P.; Giovanni, P.; Giulia, P.; Patrizia, P.; Francesca, R.; Romana, R.; Eleonora, R.; Rosita, R. M.; Jasenka, S.; Carlotta, S.; Alberto, S.; Gaetano, T.; Antonio, T.; Massimo, V.; Claudio, Z.. - In: EPILEPSIA OPEN. - ISSN 2470-9239. - 9:5(2024), pp. 1857-1867. [10.1002/epi4.13020]
Italian report on RARE epilepsies (i-RARE): A consensus on multidisciplinarity
Meletti S.;
2024
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.File | Dimensione | Formato | |
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Epilepsia Open - 2024 - Riva - Italian report on RARE epilepsies i‐RARE A consensus on multidisciplinarity.pdf
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