Avalia??o de marcadores cl?nicos e imunol?gicos de idosos e portadores de artrite reumat?ide na pandemia da COVID-19

Detalhes bibliográficos
Ano de defesa: 2023
Autor(a) principal: Rabelo, Cristina Ferreira lattes
Orientador(a): Sato, Douglas kazutoshi lattes
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Pontif?cia Universidade Cat?lica do Rio Grande do Sul
Programa de Pós-Graduação: Programa de P?s-Gradua??o em Medicina e Ci?ncias da Sa?de
Departamento: Escola de Medicina
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://tede2.pucrs.br/tede2/handle/tede/11122
Resumo: INTRODUCTION: The COVID-19 pandemic, known as coronavirus disease 2019, is an infectious disease caused by a novel coronavirus called SARS-CoV-2. This virus, derived from the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), leads to a highly contagious disease capable of inducing pneumonia and severe acute respiratory syndromes (SARS). Certain populations, particularly the elderly, are more susceptible to developing severe manifestations of the disease. OBJECTIVE: Investigate clinical and immunological characteristics of elderly patients with Rheumatoid Arthritis (RA) during COVID-19 pandemic and compare these findings with elderly individuals without autoimmune diseases and without the use of immunosuppressive agents (control group). METHODOLOGY: The study involved the participation of 23 elderly individuals with RA and 21 elderly individuals without autoimmune diseases or the use of immunosuppressive medications. This research followed a cross-sectional, controlled design, where clinical and immunological markers were investigated and compared between the two groups. The study population consisted of patients over 60 years of age receiving care at the outpatient clinics of Hospital S?o Lucas (HSL) affiliated with the Pontifical Catholic University of Rio Grande do Sul (PUCRS) and at the PUCRS Clinical Center. Clinical assessments were conducted through presencial appointment which included physical examinations and standardized questionnaires. The analysis of hematological, biochemical, and systemic inflammation markers followed the established protocols of the clinical analysis laboratory at HSL. Flow cytometry was employed for immunophenotyping and the identification of subpopulations of peripheral blood mononuclear cells (PBMCs). The recruitment of participants occurred between June 2021 and May 2023. RESULTS: The mean age of patients with RA was 70.6 years (? 4.7) and that of controls was 77.0 years (? 10.8). The observed disparity in age between these two groups was determined to be statistically significant, and this discrepancy was taken into consideration in the comparative analyses conducted.. Other clinical characteristics, such as the presence of comorbidities, depression, and frailty assessment rates, were found to be similar across both groups. It is worth noting that all individuals diagnosed with RA were utilizing immunosuppressants. Elderly individuals with RA exhibited lower adherence to social isolation measures and the use of masks at this point in the pandemic. However, but they had greater exposure to booster doses of anti-SARS-CoV2 vaccines, and the clinical events related to the COVID-19 pandemic were comparable between the RA and control groups. Importantly, patients with RA did not necessitate additional hospital care, medical consultations, or intensive care unit management. Moreover, there were no disparities in the reports of acute flu syndrome in the month preceding the interviews. The groups demonstrated homogeneity in terms of lipid profile, renal function, glycated hemoglobin levels, as well as absolute lymphocyte and neutrophil counts. Furthermore, it was observed that RA patients had lower albumin levels in comparison to the control group. Notably, higher frequencies of certain CD4+ T Lymphocyte (LT) subpopulations, including CD3+CD4+CD25+, CD4+CTLA4+, and CD4+PD1+CTLA4+, were identified in individuals with RA. However, no distinctions were found between the total CD4+ LT, total CD8+ LT, NKT LT (known as NKT cells), monocytes, or total B Lymphocyte (LB) populations. Interestingly, the transitional LB subpopulation, characterized by CD19+CD27-CD38hi, was found to be reduced in individuals with RA. In conclusion, this study sheds light on various aspects of elderly individuals with RA in the context of the COVID-19 pandemic and provides insights into immune checkpoints, activated T lymphocytes, and transitional B lymphocytes. CONCLUSIONS: From a clinical standpoint, patients with RA did not experience a worsened condition during this stage of the pandemic and within the outpatient setting, even thoughRA patients exhibited a more activated and more exhausted TL profilein comparison to elderly individuals without of RA. The population of transitional BL was reduced in the RA group , which may suggest that treatment of the disease can influence the immune response to vaccines via this route. RA and the use of immunosuppressive drugs have the potential to alter lymphocyte subpopulations.
id P_RS_adc8bf3acf1a7c59d25d52af2e15c9e9
oai_identifier_str oai:tede2.pucrs.br:tede/11122
network_acronym_str P_RS
network_name_str Biblioteca Digital de Teses e Dissertações da PUC_RS
repository_id_str
spelling Sato, Douglas kazutoshihttp://lattes.cnpq.br/1138053643046606http://lattes.cnpq.br/0877292856605674Rabelo, Cristina Ferreira2024-03-20T18:07:21Z2023-11-27https://tede2.pucrs.br/tede2/handle/tede/11122INTRODUCTION: The COVID-19 pandemic, known as coronavirus disease 2019, is an infectious disease caused by a novel coronavirus called SARS-CoV-2. This virus, derived from the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), leads to a highly contagious disease capable of inducing pneumonia and severe acute respiratory syndromes (SARS). Certain populations, particularly the elderly, are more susceptible to developing severe manifestations of the disease. OBJECTIVE: Investigate clinical and immunological characteristics of elderly patients with Rheumatoid Arthritis (RA) during COVID-19 pandemic and compare these findings with elderly individuals without autoimmune diseases and without the use of immunosuppressive agents (control group). METHODOLOGY: The study involved the participation of 23 elderly individuals with RA and 21 elderly individuals without autoimmune diseases or the use of immunosuppressive medications. This research followed a cross-sectional, controlled design, where clinical and immunological markers were investigated and compared between the two groups. The study population consisted of patients over 60 years of age receiving care at the outpatient clinics of Hospital S?o Lucas (HSL) affiliated with the Pontifical Catholic University of Rio Grande do Sul (PUCRS) and at the PUCRS Clinical Center. Clinical assessments were conducted through presencial appointment which included physical examinations and standardized questionnaires. The analysis of hematological, biochemical, and systemic inflammation markers followed the established protocols of the clinical analysis laboratory at HSL. Flow cytometry was employed for immunophenotyping and the identification of subpopulations of peripheral blood mononuclear cells (PBMCs). The recruitment of participants occurred between June 2021 and May 2023. RESULTS: The mean age of patients with RA was 70.6 years (? 4.7) and that of controls was 77.0 years (? 10.8). The observed disparity in age between these two groups was determined to be statistically significant, and this discrepancy was taken into consideration in the comparative analyses conducted.. Other clinical characteristics, such as the presence of comorbidities, depression, and frailty assessment rates, were found to be similar across both groups. It is worth noting that all individuals diagnosed with RA were utilizing immunosuppressants. Elderly individuals with RA exhibited lower adherence to social isolation measures and the use of masks at this point in the pandemic. However, but they had greater exposure to booster doses of anti-SARS-CoV2 vaccines, and the clinical events related to the COVID-19 pandemic were comparable between the RA and control groups. Importantly, patients with RA did not necessitate additional hospital care, medical consultations, or intensive care unit management. Moreover, there were no disparities in the reports of acute flu syndrome in the month preceding the interviews. The groups demonstrated homogeneity in terms of lipid profile, renal function, glycated hemoglobin levels, as well as absolute lymphocyte and neutrophil counts. Furthermore, it was observed that RA patients had lower albumin levels in comparison to the control group. Notably, higher frequencies of certain CD4+ T Lymphocyte (LT) subpopulations, including CD3+CD4+CD25+, CD4+CTLA4+, and CD4+PD1+CTLA4+, were identified in individuals with RA. However, no distinctions were found between the total CD4+ LT, total CD8+ LT, NKT LT (known as NKT cells), monocytes, or total B Lymphocyte (LB) populations. Interestingly, the transitional LB subpopulation, characterized by CD19+CD27-CD38hi, was found to be reduced in individuals with RA. In conclusion, this study sheds light on various aspects of elderly individuals with RA in the context of the COVID-19 pandemic and provides insights into immune checkpoints, activated T lymphocytes, and transitional B lymphocytes. CONCLUSIONS: From a clinical standpoint, patients with RA did not experience a worsened condition during this stage of the pandemic and within the outpatient setting, even thoughRA patients exhibited a more activated and more exhausted TL profilein comparison to elderly individuals without of RA. The population of transitional BL was reduced in the RA group , which may suggest that treatment of the disease can influence the immune response to vaccines via this route. RA and the use of immunosuppressive drugs have the potential to alter lymphocyte subpopulations.INTRODU??O: A pandemia da COVID-19 (que significa doen?a pelo coronav?rus 2019) ? uma infec??o causada um novo tipo de coronav?rus nomeado SARS-CoV-2, do ingl?s severe acute respiratory syndrome coronavirus 2. O v?rus causou uma doen?a com r?pida dissemina??o , com capacidade de causar pneumonia e s?ndromes respirat?rias agudas graves (SRAG). Existem grupos vulner?veis ? doen?a, como os idosos, que possuem uma maior probabilidade de desenvolver a forma grave. OBJETIVO: Investigar caracter?sticas cl?nicas e imunol?gicas de idosos com Artrite Reumat?ide (AR) durante a pandemia da COVID-19 e comparar estes dados com idosos sem doen?a autoimune e sem uso de imunossupressores (grupo controle). METODOLOGIA: 23 idosos com AR e 21 idosos sem doen?a autoimune e sem uso de medicamentos imunossupressores participaram da pesquisa. Este foi um estudo transversal, controlado, que investigou e comparou entre os grupos os marcadores cl?nicos e imunol?gicos de pacientes com idade acima de 60 anos em atendimento nos ambulat?rios do Hospital S?o Lucas (HSL) da Pontif?cia Universidade Cat?lica do Rio Grande do Sul (PUCRS) e no Centro Cl?nico da PUCRS. A an?lise cl?nica foi realizada atrav?s de exame f?sico em consulta presencial e atrav?s de question?rios padronizados. A avalia??o laboratorial hematol?gica, bioqu?mica e de marcadores de inflama??o sist?mica respeitou as normas padronizadas do laborat?rio de an?lises cl?nicas do HSL. A imunofenotipagem e identifica??o das subpopula??es de c?lulas mononucleares de sangue perif?rico (CMSP) foi realizada por citmetria de fluxo. O recrutamento da amostra ocorreu entre junho de 2021 e maio de 2023. RESULTADOS: A m?dia de idade dos pacientes com AR foi de 70,6 anos (? 4,7) e dos controles de 77,0 anos (? 10,8). A diferen?a de idade foi estatisticamente significativa e foi ajustada para as an?lises comparativas entre os grupos. Outras caracter?sticas cl?nicas como a presen?a de comorbidades e os ?ndices de avalia??o de depress?o e fragilidade foram semelhantes entre os grupos. Todos os indiv?dulos com AR estavam usando imunossupressores. O idosos com AR foram menos aderentes ao isolamento social e ao uso de m?scara neste momento da pandemia, mas apresentavam uma maior exposi??o a doses de vacinas anti-SARS-CoV2 e os eventos cl?nicos relacionados ? pandemia da COVID-19 foram homog?neos entre os grupos. Pacientes portadores de AR n?o necessitaram de mais atendimentos hospitalares, consultas m?dicas, necessidade de manejo em unidade de terapia intensiva. Tamb?m n?o houve disparidades nos relatos de s?ndrome gripal aguda no m?s anterior ? entrevista. Os grupos estavam homog?neos em rela??o ao perfil lip?dico, fun??o renal, hemoglobina glicada e a contagem absoluta de linf?citos e neutr?filos. Os n?veis de albumina estavam inferiores nos pacientes com AR em rela??o aos controles. Foram observadas frequ?ncias mais elevadas de algumas subpopula??es de Linf?cito T (LT) CD4+ na AR: CD3+CD4+CD25+, CD4+CTLA4+, e CD4+PD1+CTLA4+. N?o foramencontradas diferencas entre as popula??es LT CD4+totais, LT CD8+totais,LT NKT (conhecidas como c?lulas NKT ),mon?citos ouLinf?citos B (LB) totais. A subpopula??o de LB CD19+CD27-CD38hi (transicional) estava reduzida nos indiv?duos com AR.Suban?lises no grupo com AR: pacientes em uso de cortic?ide exibiram valores significativamente maiores de CD3+CD8+CD57+ em compara??o com aqueles que n?o estavam usando cortic?ide; quanto maior a frequ?ncia de CD3+CD8+CD28-CD27- maiores os n?veis de PCR (prote?na C reativa); quanto maior os frequ?ncia de CD3+CD8+CD57+, maior foi o tempo de doen?a. CONCLUS?ES:Os pacientes com AR n?o apresentaram pior evolu??o cl?nica durante esta fase da pandemia e no contexto de seguimento ambulatorial, apesar do grupo AR exibir perfil de LT mais ativado e mais exausto em compara??o aos idosos sem AR. A popula??o de LB transicional est? reduzida no grupo com AR, o que pode sugerir que o tratamento da doen?a pode influenciar a resposta imune ?s vacinas por esta via. A AR e as medica??es usadas no seu tratamento, podem modificar subpopula??es de LT e LB.Submitted by PPG Medicina e Ci?ncias da Sa?de (medicina-pg@pucrs.br) on 2024-01-31T11:38:04Z No. of bitstreams: 1 TESE COVID & AR (VersaoFinal).pdf: 1645590 bytes, checksum: a14bd2cf6bcb5e56ee6c06d7584d0c04 (MD5)Approved for entry into archive by Sarajane Pan (sarajane.pan@pucrs.br) on 2024-03-20T17:49:31Z (GMT) No. of bitstreams: 1 TESE COVID & AR (VersaoFinal).pdf: 1645590 bytes, checksum: a14bd2cf6bcb5e56ee6c06d7584d0c04 (MD5)Made available in DSpace on 2024-03-20T18:07:21Z (GMT). No. of bitstreams: 1 TESE COVID & AR (VersaoFinal).pdf: 1645590 bytes, checksum: a14bd2cf6bcb5e56ee6c06d7584d0c04 (MD5) Previous issue date: 2023-11-27Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPESapplication/pdfhttps://tede2.pucrs.br/tede2/retrieve/190005/TES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdf.jpgporPontif?cia Universidade Cat?lica do Rio Grande do SulPrograma de P?s-Gradua??o em Medicina e Ci?ncias da Sa?dePUCRSBrasilEscola de MedicinaCOVID-19IdososArtrite Reumat?idePerfil Imunol?gicoCOVID-19ElderlyRheumatoid ArthritisImmune ProfileCIENCIAS DA SAUDE::MEDICINAAvalia??o de marcadores cl?nicos e imunol?gicos de idosos e portadores de artrite reumat?ide na pandemia da COVID-19info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisTrabalho ser? publicado como artigo ou livro60 meses19/03/2029-721401722658532398500500500600-224747486637135387-9693694523087866273590462550136975366info:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da PUC_RSinstname:Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)instacron:PUC_RSTHUMBNAILTES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdf.jpgTES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdf.jpgimage/jpeg4075https://tede2.pucrs.br/tede2/bitstream/tede/11122/4/TES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdf.jpgab92a1ca82f686dd42b55ae006211a16MD54TEXTTES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdf.txtTES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdf.txttext/plain1286https://tede2.pucrs.br/tede2/bitstream/tede/11122/3/TES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdf.txt148b07b8be3f7ca897b13ceb18bf826bMD53ORIGINALTES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdfTES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdfapplication/pdf520467https://tede2.pucrs.br/tede2/bitstream/tede/11122/2/TES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdfc6afc2d6339dc44b5f9c4edb8a4a3e86MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-8590https://tede2.pucrs.br/tede2/bitstream/tede/11122/1/license.txt220e11f2d3ba5354f917c7035aadef24MD51tede/111222024-03-20 20:00:16.547oai:tede2.pucrs.br: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Biblioteca Digital de Teses e Dissertaçõeshttp://tede2.pucrs.br/tede2/PRIhttps://tede2.pucrs.br/oai/requestbiblioteca.central@pucrs.br||opendoar:2024-03-20T23:00:16Biblioteca Digital de Teses e Dissertações da PUC_RS - Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)false
dc.title.por.fl_str_mv Avalia??o de marcadores cl?nicos e imunol?gicos de idosos e portadores de artrite reumat?ide na pandemia da COVID-19
title Avalia??o de marcadores cl?nicos e imunol?gicos de idosos e portadores de artrite reumat?ide na pandemia da COVID-19
spellingShingle Avalia??o de marcadores cl?nicos e imunol?gicos de idosos e portadores de artrite reumat?ide na pandemia da COVID-19
Rabelo, Cristina Ferreira
COVID-19
Idosos
Artrite Reumat?ide
Perfil Imunol?gico
COVID-19
Elderly
Rheumatoid Arthritis
Immune Profile
CIENCIAS DA SAUDE::MEDICINA
title_short Avalia??o de marcadores cl?nicos e imunol?gicos de idosos e portadores de artrite reumat?ide na pandemia da COVID-19
title_full Avalia??o de marcadores cl?nicos e imunol?gicos de idosos e portadores de artrite reumat?ide na pandemia da COVID-19
title_fullStr Avalia??o de marcadores cl?nicos e imunol?gicos de idosos e portadores de artrite reumat?ide na pandemia da COVID-19
title_full_unstemmed Avalia??o de marcadores cl?nicos e imunol?gicos de idosos e portadores de artrite reumat?ide na pandemia da COVID-19
title_sort Avalia??o de marcadores cl?nicos e imunol?gicos de idosos e portadores de artrite reumat?ide na pandemia da COVID-19
author Rabelo, Cristina Ferreira
author_facet Rabelo, Cristina Ferreira
author_role author
dc.contributor.advisor1.fl_str_mv Sato, Douglas kazutoshi
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/1138053643046606
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/0877292856605674
dc.contributor.author.fl_str_mv Rabelo, Cristina Ferreira
contributor_str_mv Sato, Douglas kazutoshi
dc.subject.por.fl_str_mv COVID-19
Idosos
Artrite Reumat?ide
Perfil Imunol?gico
topic COVID-19
Idosos
Artrite Reumat?ide
Perfil Imunol?gico
COVID-19
Elderly
Rheumatoid Arthritis
Immune Profile
CIENCIAS DA SAUDE::MEDICINA
dc.subject.eng.fl_str_mv COVID-19
Elderly
Rheumatoid Arthritis
Immune Profile
dc.subject.cnpq.fl_str_mv CIENCIAS DA SAUDE::MEDICINA
description INTRODUCTION: The COVID-19 pandemic, known as coronavirus disease 2019, is an infectious disease caused by a novel coronavirus called SARS-CoV-2. This virus, derived from the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), leads to a highly contagious disease capable of inducing pneumonia and severe acute respiratory syndromes (SARS). Certain populations, particularly the elderly, are more susceptible to developing severe manifestations of the disease. OBJECTIVE: Investigate clinical and immunological characteristics of elderly patients with Rheumatoid Arthritis (RA) during COVID-19 pandemic and compare these findings with elderly individuals without autoimmune diseases and without the use of immunosuppressive agents (control group). METHODOLOGY: The study involved the participation of 23 elderly individuals with RA and 21 elderly individuals without autoimmune diseases or the use of immunosuppressive medications. This research followed a cross-sectional, controlled design, where clinical and immunological markers were investigated and compared between the two groups. The study population consisted of patients over 60 years of age receiving care at the outpatient clinics of Hospital S?o Lucas (HSL) affiliated with the Pontifical Catholic University of Rio Grande do Sul (PUCRS) and at the PUCRS Clinical Center. Clinical assessments were conducted through presencial appointment which included physical examinations and standardized questionnaires. The analysis of hematological, biochemical, and systemic inflammation markers followed the established protocols of the clinical analysis laboratory at HSL. Flow cytometry was employed for immunophenotyping and the identification of subpopulations of peripheral blood mononuclear cells (PBMCs). The recruitment of participants occurred between June 2021 and May 2023. RESULTS: The mean age of patients with RA was 70.6 years (? 4.7) and that of controls was 77.0 years (? 10.8). The observed disparity in age between these two groups was determined to be statistically significant, and this discrepancy was taken into consideration in the comparative analyses conducted.. Other clinical characteristics, such as the presence of comorbidities, depression, and frailty assessment rates, were found to be similar across both groups. It is worth noting that all individuals diagnosed with RA were utilizing immunosuppressants. Elderly individuals with RA exhibited lower adherence to social isolation measures and the use of masks at this point in the pandemic. However, but they had greater exposure to booster doses of anti-SARS-CoV2 vaccines, and the clinical events related to the COVID-19 pandemic were comparable between the RA and control groups. Importantly, patients with RA did not necessitate additional hospital care, medical consultations, or intensive care unit management. Moreover, there were no disparities in the reports of acute flu syndrome in the month preceding the interviews. The groups demonstrated homogeneity in terms of lipid profile, renal function, glycated hemoglobin levels, as well as absolute lymphocyte and neutrophil counts. Furthermore, it was observed that RA patients had lower albumin levels in comparison to the control group. Notably, higher frequencies of certain CD4+ T Lymphocyte (LT) subpopulations, including CD3+CD4+CD25+, CD4+CTLA4+, and CD4+PD1+CTLA4+, were identified in individuals with RA. However, no distinctions were found between the total CD4+ LT, total CD8+ LT, NKT LT (known as NKT cells), monocytes, or total B Lymphocyte (LB) populations. Interestingly, the transitional LB subpopulation, characterized by CD19+CD27-CD38hi, was found to be reduced in individuals with RA. In conclusion, this study sheds light on various aspects of elderly individuals with RA in the context of the COVID-19 pandemic and provides insights into immune checkpoints, activated T lymphocytes, and transitional B lymphocytes. CONCLUSIONS: From a clinical standpoint, patients with RA did not experience a worsened condition during this stage of the pandemic and within the outpatient setting, even thoughRA patients exhibited a more activated and more exhausted TL profilein comparison to elderly individuals without of RA. The population of transitional BL was reduced in the RA group , which may suggest that treatment of the disease can influence the immune response to vaccines via this route. RA and the use of immunosuppressive drugs have the potential to alter lymphocyte subpopulations.
publishDate 2023
dc.date.issued.fl_str_mv 2023-11-27
dc.date.accessioned.fl_str_mv 2024-03-20T18:07:21Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://tede2.pucrs.br/tede2/handle/tede/11122
url https://tede2.pucrs.br/tede2/handle/tede/11122
dc.language.iso.fl_str_mv por
language por
dc.relation.program.fl_str_mv -721401722658532398
dc.relation.confidence.fl_str_mv 500
500
500
600
dc.relation.department.fl_str_mv -224747486637135387
dc.relation.cnpq.fl_str_mv -969369452308786627
dc.relation.sponsorship.fl_str_mv 3590462550136975366
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Pontif?cia Universidade Cat?lica do Rio Grande do Sul
dc.publisher.program.fl_str_mv Programa de P?s-Gradua??o em Medicina e Ci?ncias da Sa?de
dc.publisher.initials.fl_str_mv PUCRS
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Escola de Medicina
publisher.none.fl_str_mv Pontif?cia Universidade Cat?lica do Rio Grande do Sul
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da PUC_RS
instname:Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
instacron:PUC_RS
instname_str Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
instacron_str PUC_RS
institution PUC_RS
reponame_str Biblioteca Digital de Teses e Dissertações da PUC_RS
collection Biblioteca Digital de Teses e Dissertações da PUC_RS
bitstream.url.fl_str_mv https://tede2.pucrs.br/tede2/bitstream/tede/11122/4/TES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdf.jpg
https://tede2.pucrs.br/tede2/bitstream/tede/11122/3/TES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdf.txt
https://tede2.pucrs.br/tede2/bitstream/tede/11122/2/TES_CRISTINA_FERREIRA_RABELO_CONFIDENCIAL.pdf
https://tede2.pucrs.br/tede2/bitstream/tede/11122/1/license.txt
bitstream.checksum.fl_str_mv ab92a1ca82f686dd42b55ae006211a16
148b07b8be3f7ca897b13ceb18bf826b
c6afc2d6339dc44b5f9c4edb8a4a3e86
220e11f2d3ba5354f917c7035aadef24
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
MD5
repository.name.fl_str_mv Biblioteca Digital de Teses e Dissertações da PUC_RS - Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
repository.mail.fl_str_mv biblioteca.central@pucrs.br||
_version_ 1796793263573696512