Health equity, care access and quality in headache - part 1
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Citações na Scopus
4
Tipo de produção
article
Data de publicação
2024
Título da Revista
ISSN da Revista
Título do Volume
Editora
BMC
Autores
TANA, Claudio
RAFFAELLI, Bianca
TORRE, Elena Ruiz de la
MASSI, Daniel Gams
KISANI, Najib
GARCIA-AZORIN, David
WALISZEWSKA-PROSOL, Marta
Citação
JOURNAL OF HEADACHE AND PAIN, v.25, n.1, article ID 12, 12p, 2024
Resumo
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.
Palavras-chave
Migraine, Health equity, Care access, Stigma, Clinical governance, COVID-19
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