The landscape of vitiligo in Latin America: a call to action
Autor: | Angela Londoño-Garcia, Andrea Arango Salgado, María de la Luz Orozco-Covarrubias, Angela Marie Jansen, Mariana Rico-Restrepo, María Cecilia Riviti, Margarita María Velásquez-Lopera, Carla Castro |
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Jazyk: | angličtina |
Rok vydání: | 2023 |
Předmět: | |
Zdroj: | Journal of Dermatological Treatment, Vol 34, Iss 1 (2023) |
Druh dokumentu: | article |
ISSN: | 0954-6634 1471-1753 09546634 |
DOI: | 10.1080/09546634.2022.2164171 |
Popis: | Vitiligo is a chronic pigmentary condition and severely impacts patient quality of life (QoL). It is an underrecognized burden for patients, healthcare systems, and society in Latin America (LA). This paper examines the journey of a vitiligo patient in LA and assesses the disease landscape. Americas Health Foundation (AHF) assembled a panel of six Argentine, Brazilian, Colombian, and Mexican vitiligo experts. On 10–12 May 2022, they met in a virtual meeting. Each panelist wrote a short paper on barriers to vitiligo diagnosis and treatment in LA before the meeting. AHF staff moderated as the panel reviewed and modified each paper over three days. The panel approved the recommendations based on research, professional opinion, and personal experience. The panel agreed that lack of disease awareness and research, social ostracization, and limited therapeutic options hinder patients in their quest for diagnosis and treatment. In addition to the medical and psychological difficulties associated with vitiligo, problems connected to the Latin American healthcare system may negatively impact diagnosis, prognosis, and treatment. Access to timely diagnosis and treatment is crucial for improving outcomes. Governments, medical societies, academics, patient organizations, industry, and the public must unite to eliminate these challenges. |
Databáze: | Directory of Open Access Journals |
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