PRODUÇÃO ACADÊMICA Repositório Acadêmico da Graduação (RAG) TCC Medicina
Use este identificador para citar ou linkar para este item: https://repositorio.pucgoias.edu.br/jspui/handle/123456789/3011
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Campo DCValorIdioma
dc.creatorLino, Gabriela Maia Almeida Brandão-
dc.creatorPires, Milena Coutinho-
dc.date.accessioned2021-12-16T02:57:30Z-
dc.date.available2021-12-16T02:57:30Z-
dc.date.issued2019-10-18-
dc.identifier.urihttps://repositorio.pucgoias.edu.br/jspui/handle/123456789/3011-
dc.description.abstractPsoriasis is a chronic systemic inflammatory disease with a major impact on patients' quality of life. The most common presentation is plaque psoriasis or psoriasis vulgaris. Mild illnesses are treated initially with topical medications, while moderate/severe conditions may have topical therapy associated with phototherapy and possibly combined with systemic therapy or the option of using immunobiological agents. The use of immunobiologicals has been shown to be a good option for the treatment of moderate/severe psoriasis, presenting better results in reducing the symptoms and improving the quality of life of the patient. Among the immunobiological drugs inhibiting IL-17 are secukinumab, ixekizumab and brodalumab. Objectives: To verify the efficacy of the use of IL-17 inhibitors (secukinumab, brodalumab and ixekizumab) in the treatment of moderate to severe psoriasis. Conclusion: Ixekizumab was considered the most effective immunobiological in the short-term treatment for moderate to severe plaque psoriasis in terms of PASI 75 and PASI 90, followed by Secukinumab and Brodalumab. Although the short-term effects of biological agents on moderate to severe psoriasis are well documented, studies examining long-term efficacy and safety are more limited and need better evaluation.pt_BR
dc.description.sponsorshipNão recebi financiamentopt_BR
dc.languageporpt_BR
dc.publisherPontifícia Universidade Católica de Goiáspt_BR
dc.relationRecursos dos próprios autores.pt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectPsoríasept_BR
dc.subjectTerapia biológicapt_BR
dc.subjectInterleucina-17pt_BR
dc.subjectSecukinumabpt_BR
dc.subjectIxekizumabept_BR
dc.subjectBrodalumabept_BR
dc.titleTerapia imunológica com inibidor da interleucina-17 no tratamento de psoríase vulgarpt_BR
dc.title.alternativeImmunological therapy with interleucin-17 inhibitor in treatment of vulgar psoriasispt_BR
dc.typeTrabalho de Conclusão de Cursopt_BR
dc.contributor.advisor1Rocha Sobrinho, Hermínio Maurício da-
dc.contributor.advisor1IDhttps://orcid.org/0000-0002-7521-3700pt_BR
dc.contributor.advisor1Latteshttp://lattes.cnpq.br/5573574130526137pt_BR
dc.contributor.referee1Costa, Natália Moriya Xavier da-
dc.contributor.referee1Latteshttp://lattes.cnpq.br/1519406580343535pt_BR
dc.contributor.referee2Aveiro, Nayana Chaves-
dc.contributor.referee2Latteshttp://lattes.cnpq.br/5245608418892000pt_BR
dc.description.resumoA psoríase é uma doença inflamatória crônica sistêmica de grande impacto na qualidade de vida dos doentes. Tem como apresentação mais frequente a psoríase em placas ou psoríase vulgar. Quadros leves da doença são tratados inicialmente com medicações tópicas, enquanto quadros moderados/graves podem ter a terapia tópica associada a fototerapia e, eventualmente, combinada a terapia sistêmica, ou ainda opção do uso de imunobiológicos. O uso de imunobiológicos tem se mostrado uma boa opção para o tratamento da psoríase moderada/grave, apresentando melhores resultados na redução dos sintomas e melhora da qualidade de vida do paciente. Entre os medicamentos imunobiológicos inibidores da IL-17 destacam-se o secuquinumabe, ixekizumabe e brodalumabe. Objetivos: Abordar a eficácia do uso de imunobiológicos inibidores da IL-17 (secukinumab, brodalumabe e ixekizumab) no tratamento da Psoríase moderada a grave. Conclusão: O Ixekizumab foi considerado o imunobiológico mais eficaz no tratamento a curto prazo para psoríase em placas moderada a grave em termos de PASI 75 e PASI 90, seguido por Secukinumab e Brodalumab. Embora os efeitos a curto prazo dos agentes biológicos na psoríase moderada a grave estejam bem documentados, estudos que examinam a eficácia e a segurança a longo prazo são mais limitados e carecem de melhores avaliações.pt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.departmentEscola de Ciências Médicas, Farmacêuticas e Biomédicaspt_BR
dc.publisher.initialsPUC Goiáspt_BR
dc.subject.cnpqCNPQ::CIENCIAS DA SAUDE::MEDICINA::CLINICA MEDICA::ALERGOLOGIA E IMUNOLOGIA CLINICApt_BR
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Drug survival of biological therapy is showing class effect: updated results from Slovenian National Registry of psoriasis. Int J Dermatol, v. 58, n.6, p. 631-641, 2019. MADDUR, M. et al. Th17 cells: biology, pathogenesis of autoimmune and inflammatory diseases, and therapeutic strategies. Am J Pathol, v. 1, p.181:8-18, 2012. MAIA, C. P. A. et al. Sociedade Brasileira de Dermatologia. Consenso Brasileiro de Psoríase 2012 - Guias de tratamento Sociedade Brasileira de Dermatologia, 2012. MANSOURI, M. et al.The potential role of Th17 lymphocytes in patients with psoriasis. An Bras Dermatol, v. 93, n. 1, p. 63-6, 2018. MARINONI, B. et al. The Th17 axis in psoriatic disease: pathogenetic and therapeutic implications. Auto Immun Highlights, v. 5, p. 9-19, 2014. MARTI, L. et al. Alterations in cytokine profile and dendritic cells subsets in peripheral blood of rheumatoid arthritis patients before and after biologic therapy. Ann N Y Acad Sci, v.1173, p. 334-42, 2009. MELINDA, G. et al. Interleukin-17 (IL-17) inhibitors in the treatment of plaque psoriasis: a review. Skin Therapy Lett, v. 20, n. 1, p. 1-5, 2015. MROWIETZ, U. Implementing treatment goals for successful long-term management of psoriasis. J Eur Acad Dermatol Venereol, v. 26, (Suppl 2), p. 12–20, 2012. NAST, A. et al. EuropeanS3-Guidelines on the systemic treatment of psoriasis vulgaris - Update 2015 - Short version - EDF in cooperation with EADV and IPC. J Eur Acad Dermatol Venereol, v. 29, p. 2277-94, 2015. PATHIRANA, D. et al. "European S3‐Guidelines on the systemic treatment of psoriasis vulgaris: Supported by the EDF/EADV/IPC." Journal of the European Academy of Dermatology and Venereology, v. 23, p. 1-70, 2009. ROMAN, M.; CHIU, M.W. Spotlight on brodalumab in the treatment of moderate-to-severe plaque psoriasis: design, development, and potential place in therapy. Drug Design, Development and Therapy; v.11, p. 2065-2075, 2017 SILVA, M. et al. Psoriasis: correlation between clinical severity (PASI) and quality of life index (DLQI) in patients assessed before and after systemic treatment. An Bras Dermatol, v. 88, n. 5, p.760-3, 2013. TORRES, T.; FILIPE, P. Interleukin-17 as a therapeutic target in psoriasis. Acta Med Port, v. 27, n. 2, p. 252-8, 2014. VIDE, J; MAGINA, S. Moderate to severe psoriasis treatment challenges through the era of biological drugs. An. Bras. Dermatol., Rio de Janeiro, v. 92, n. 5, p. 668-674, 2017. WCISLO-DZIADECKA, D. et al. Are new variants of psoriasis therapy (IL-17 inhibitors) safe? Int J Dermatol. 2019. doi: 10.1111/ijd.14509 YAJIMA et al. Alopecia Diffusa while Using Interleukin-17 Inhibitors against Psoriasis Vulgaris. Case Rep Dermatol, v.11, p. 82–85, 2019.pt_BR
dc.degree.graduationMedicina-
dc.degree.levelGraduação-
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