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Atopic Dermatitis: Improving Patient Access to Health Care in Dermatology

dc.contributor.authorTorres, T
dc.contributor.authorGonçalo, M
dc.contributor.authorPaiva-Lopes, MJ
dc.contributor.authorClaro, C
dc.contributor.authorVarela, P
dc.contributor.authorSilva, JM
dc.contributor.authorCordeiro, A
dc.contributor.authorMendes-Bastos, P
dc.date.accessioned2024-08-13T10:51:49Z
dc.date.available2024-08-13T10:51:49Z
dc.date.issued2023
dc.description.abstractIntroduction and Objective: The present study on atopic dermatitis (AD) in Portugal aims to characterize patient needs and discuss measures to improve health care in dermatology, particularly in cases of moderate to severe disease. Methods: The study was conducted in three phases–(1) data collection on the patient access to healthcare and subsequent analysis; (2) critical evaluation of the data in individual interviews with dermatologists and one pediatrician; and lastly, (3) data discussion in consensus meetings to validate the existing care capacity in dermatology, to identify gaps in care for patients with AD and to define mitigation strategies. Results: In Portugal, it is estimated that AD affects ~ 360,000 patients, 70,000 of whom have moderate to severe disease. Healthcare capacity analysis confirmed that the private system plays an important role in the management of AD. It is estimated that 30% of patients rely solely on the Portuguese public health service. Nevertheless, patients with moderate to severe disease can only access advanced targeted therapies from public healthcare providers. Analysis of public care capacity in dermatology shows relevant gaps in the referral system, the geographical coverage of specialized centers, the number of specialists and high waiting times for first appointments. Considering the negative impact of the disease on patients’ quality of life, 86% of patients with AD use private settings to better manage their disease. Conclusion: In conclusion, private setting bridges the gaps in public health care capacity in dermatology, and therefore, it is crucial for patients with AD. However, a major limitation is the lack of reimbursement for advanced targeted therapies recommended for moderate to severe AD when they are prescribed in a private setting, thus compromising patient access to these therapies. A possible strategy could be to extend the prescription of these therapies to a private setting based on a reimbursement model similar to that outlined in Act 48/2016 of 22 March.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationPort J Dermatol and Venereol. 2023;81(2):73-81pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4985
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSociedade Portuguesa de Dermatologia e Venereologiapt_PT
dc.subjectHealth equitypt_PT
dc.subjectHealth services accessibilitypt_PT
dc.subjectEssential drugspt_PT
dc.subjectDermatologypt_PT
dc.subjectAtopic dermatitispt_PT
dc.subjectHSAC DERpt_PT
dc.subjectHDE PEDpt_PT
dc.titleAtopic Dermatitis: Improving Patient Access to Health Care in Dermatologypt_PT
dc.title.alternativeDermatite Atópica: Melhorar o Acesso dos Doentes aos Cuidados de Saúde em Dermatologiapt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage81pt_PT
oaire.citation.issue2pt_PT
oaire.citation.startPage73pt_PT
oaire.citation.volume81pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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