Health equity, care access and quality in headache – part 1

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Abstract

Current definitions of migraine that are based mainly on clinical characteristics do not account for other patient’s features such as those related to an impaired quality of life, due to loss of social life and productivity, and the differences related to the geographical distribution of the disease and cultural misconceptions which tend to underestimate migraine as a psychosocial rather than neurobiological disorder. Global differences definition, care access, and health equity for headache disorders, especially migraine are reported in this paper from a collaborative group of the editorial board members of the Journal of Headache and Pain. Other components that affect patients with migraine, in addition to the impact promoted by the migraine symptoms such as stigma and social determinants, are also reported.

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Tana, C., Raffaelli, B., Souza, M. N. P., de la Torre, E. R., Massi, D. G., Kisani, N., … Waliszewska-Prosół, M. (2024, December 1). Health equity, care access and quality in headache – part 1. Journal of Headache and Pain. BioMed Central Ltd. https://doi.org/10.1186/s10194-024-01712-7

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