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CECILIA CAMARDA

Clinical features, disease progression and use of healthcare resources in a large sample of 866 patients from 24 headache centers: A real-life perspective from the Italian chROnic migraiNe (IRON) project

  • Authors: Barbanti, Piero; Fofi, Luisa; Grazzi, Licia; Vernieri, Fabrizio; Camarda, Cecilia; Torelli, Paola; Cevoli, Sabina; Russo, Antonio; Bono, Francesco; Finocchi, Cinzia; Rao, Renata; Messina, Stefano; De Simone, Roberto; Vanacore, Nicola; Bonassi, Stefano
  • Publication year: 2021
  • Type: Articolo in rivista
  • OA Link: http://hdl.handle.net/10447/566102

Abstract

Objective: To develop a dedicated Italian chronic migraine (CM) database (IRON project) to overcome disease misconceptions, improve clinical administration, reduce patients' burden, and rationalize economic resource allotment.Background: Proper CM management requires a comprehensive appraisal of its full clinical, social, and economic complexity.Methods: In this cross-sectional study, CM patients were screened in 24 certified headache centers with face-to-face interviews. Information on sociodemographic factors, medical history, characteristics of CM, and of prior episodic migraine (EM), and healthcare resource use was gathered using a semistructured web-based questionnaire.Results: A total of 866 CM patients were enrolled. CM started similar to 20 years after EM onset (age at EM onset 17.4 +/- 9.1 vs. age at CM onset 35.3 +/- 12.5 [mean +/- SD]). CM prophylaxis, used by 430/866 (49.6%) of the patients, was often ineffective, not tolerated, and prematurely discontinued. Medications and diagnostic workup, frequently inappropriate, were mostly subsidized by the Italian national health service. CM patients with >= 25 headache days/month revealed substantial clinical differences and heavier disability and economic burden compared with those with <25 headache days/month.Conclusions: CM is a heterogeneous headache disorder deserving more in-depth clinical characterization, sharper diagnostic criteria, and tailored treatments. CM registries are expected to improve clinical management, resulting in increased disease awareness, better healthcare resource allocation, and reduced economic burden.