Os múltiplos benefícios dos inibidores do SGLT2

Detalhes bibliográficos
Autor(a) principal: Cabral, Ana Júlia Marinho
Data de Publicação: 2022
Tipo de documento: Trabalho de conclusão de curso
Idioma: por
Título da fonte: Repositório do Centro Universitário Braz Cubas
Texto Completo: https://repositorio.cruzeirodosul.edu.br/handle/123456789/4143
Resumo: Sodium-Glucose Cotransporter 2 (iSG2) Inhibitors (dapagliflozin, empaglifozin and canaglifozin) are used in the treatment of type 2 Diabetes Mellitus (DM2) but, recently, these are being used in the treatment of cardiovascular and renal drugs, adapting to the growing scientific evidence of clinical and laboratory benefits. The general objective of this study was to describe in an integrative way the importance of using SGT2 inhibitors in glycemic control and cardiovascular and renal outcomes. This is an integrative literature review, using the following databases: BVS, Pubmed and ScienceDirect during the period from March 2022 to April 2022. For the selection of articles, the following health descriptors (decs.bvs. br )” Glucose Drug Transport 2 Inhibitors”, Heart Failure”, “Chronic Kidney Disease”, “death” combined with Boolean operators “AND”. On outcomes, the 13 articles included are cohort and primary and secondary studies of multicenter, double-blind, placebo-controlled, randomized clinical trials testing the iSGT2 in different population samples. It was identified that the use of lower iSGLT2 when compared with the dipeptidyl peptidase-4 (DDP4i) inhibitor group was associated with risks of congestive heart failure (CHF), Relative Risk (RR): 0.66; 95% CI 0.49-0.89; p = 0.0062, or amputation, RR: 0.43; IC 95% 0.30-0.62; p < 0.0001 and cardiovascular death RR: 0.67; 95% CI 0.49-0.90; p = 0.0089. Another study, presented in a population with cardiac function, a study for cardiovascular death or hospitalization for heart failure, 0.75; 95% CI, 0.65 to 0.86; P<0.001. In patients with less severe renal decline, the RR is the composite of a sick patient estimated to have at least 50% decline in end-stage renal disease or death from renal causes (95% CI, 0.45 to 0.68 P< 0.001), and the risk to ratio for the composite of death from cardiovascular or cardiaccauses from cardiac dysfunction was 0.71; (95% CI, 0.5 to 0.92 P = 0.009). Completion Risk and Completion Risk Management LT2 researchers supported Completion Risk and Completion Risk Management data. In addition, the sample reduction in all-cause mortality, the delay in the loss of renal function, and also the reduction in the risk of renal compound. These are probably the SGLT2 inhibitors that are likely to play an important role in the treatment of cardiovascular and renal endocrine diseases.
id CUB_ad8a15b19a3c20fd99bfb946d7ffa27e
oai_identifier_str oai:repositorio.cruzeirodosul.edu.br:123456789/4143
network_acronym_str CUB
network_name_str Repositório do Centro Universitário Braz Cubas
repository_id_str
spelling Os múltiplos benefícios dos inibidores do SGLT2iSGLT2diabetesinsuficiência cardíacainsuficiência renal crônicaCNPQ::CIENCIAS DA SAUDE::MEDICINASodium-Glucose Cotransporter 2 (iSG2) Inhibitors (dapagliflozin, empaglifozin and canaglifozin) are used in the treatment of type 2 Diabetes Mellitus (DM2) but, recently, these are being used in the treatment of cardiovascular and renal drugs, adapting to the growing scientific evidence of clinical and laboratory benefits. The general objective of this study was to describe in an integrative way the importance of using SGT2 inhibitors in glycemic control and cardiovascular and renal outcomes. This is an integrative literature review, using the following databases: BVS, Pubmed and ScienceDirect during the period from March 2022 to April 2022. For the selection of articles, the following health descriptors (decs.bvs. br )” Glucose Drug Transport 2 Inhibitors”, Heart Failure”, “Chronic Kidney Disease”, “death” combined with Boolean operators “AND”. On outcomes, the 13 articles included are cohort and primary and secondary studies of multicenter, double-blind, placebo-controlled, randomized clinical trials testing the iSGT2 in different population samples. It was identified that the use of lower iSGLT2 when compared with the dipeptidyl peptidase-4 (DDP4i) inhibitor group was associated with risks of congestive heart failure (CHF), Relative Risk (RR): 0.66; 95% CI 0.49-0.89; p = 0.0062, or amputation, RR: 0.43; IC 95% 0.30-0.62; p < 0.0001 and cardiovascular death RR: 0.67; 95% CI 0.49-0.90; p = 0.0089. Another study, presented in a population with cardiac function, a study for cardiovascular death or hospitalization for heart failure, 0.75; 95% CI, 0.65 to 0.86; P<0.001. In patients with less severe renal decline, the RR is the composite of a sick patient estimated to have at least 50% decline in end-stage renal disease or death from renal causes (95% CI, 0.45 to 0.68 P< 0.001), and the risk to ratio for the composite of death from cardiovascular or cardiaccauses from cardiac dysfunction was 0.71; (95% CI, 0.5 to 0.92 P = 0.009). Completion Risk and Completion Risk Management LT2 researchers supported Completion Risk and Completion Risk Management data. In addition, the sample reduction in all-cause mortality, the delay in the loss of renal function, and also the reduction in the risk of renal compound. These are probably the SGLT2 inhibitors that are likely to play an important role in the treatment of cardiovascular and renal endocrine diseases.Os Inibidores do Cotransportador Sódio-Glicose 2 (iSGLT2) (dapaglifozina, empaglifozina e canaglifozina) são tradicionalmente utilizados no tratamento de Diabetes Mellitus tipo 2 (DM2) mas, recentemente, esses medicamentos estão sendo utilizados no tratamento de enfermidades cardiovasculares e renais, adequando-se àscrescentes evidências científicas de benefíciosclínicos e laboratoriais desse grupo de medicamentos. O objetivo geral deste trabalho foi descrever de forma integrativa a importância do uso dos Inibidores de SGLT2 nos desfechos endocrinológicos, cardiovasculareserenais. Trata-se de uma revisão integrativa da literatura, utilizando as bases de dados: BVS, Pubmed e ScienceDirect durante o período de março de 2022 abril de 2022.Para a seleção dos artigos foram considerados os seguintes descritores em saúde (decs.bvs.br)” Inibidores do transportador 2 de sódio-glicose”, Insuficiência Cardíaca”, “Doença Renal Crônica”, “morte” combinados com operadores booleanos “AND”. Nos resultados, os13artigos incluidos são estudos coorte e de análises primárias e secundárias de ensaios clínicos randomizadosmulticêntrico, duplo-cego, controlado por placeboque testaram os iSGT2 em diferentes amostras de população.Foiidentificadoqueouso de iSGLT2quando comparadocom o grupo dos inibidores de dipeptidil peptidase-4 (DDP4i) foi associado a menores riscos de insuficiência cardíaca congestiva (ICC), Risco Relativo(RR): 0,66; IC95%0,49-0,89; p = 0,0062, ou amputação, RR: 0,43; IC 95% 0,30-0,62; p < 0,0001e morte cardiovascular RR: 0,67; IC 95% 0,49-0,90; p = 0,0089.Outro estudo, apresentou em uma população com insuficiência cardíaca, um RRpara morte cardiovascular ou hospitalização por insuficiência cardíaca, 0,75; IC 95%, 0,65 a 0,86; P <0,001.Em pacientes doentes renais crônicos,o RR para o composto de um declínio sustentado na TFG estimada de pelo menos 50%, doença renal em estágio terminal ou morte por causas renais foi de 0,56 (IC 95%, 0,45 a 0,68; P <0,001), e o risco a razão para o composto de morte por causas cardiovasculares ou internação por insuficiência cardíaca foi de 0,71 (IC 95%, 0,55 a 0,92; P = 0,009).Conclui-se que os dados disponíveis sugerem que os inibidores de SGLT2 reduzem o risco de desfechos e eventos de insuficiência cardíaca.Além disso, a amostra evidenciou a queda da mortalidade por todas as causas, o retardo daperda da função renal, e também aredução do risco de composto renal. Esses dados sugerem que os inibidores deSGLT2 provavelmente têm um papel importante no tratamento de doenças endocrinológicas cardiovasculares e renais.Centro Universitário de João PessoaBrasilUNIPÊMacedo, Ciberio Landimhttp://lattes.cnpq.br/8478576288526486Cabral, Ana Júlia Marinho2022-11-16T19:00:28Z2022-11-182022-11-16T19:00:28Z2022-06-13info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/bachelorThesisapplication/pdfCABRAL, Ana Júlia Marinho. Os múltiplos benefícios dos inibidores do SGLT2. 25 P. Trabalho de conclusão de curso Medicina - Centro Universitário de João Pessoa – UNIPÊ, João Pessoa, 2022.https://repositorio.cruzeirodosul.edu.br/handle/123456789/4143porAGUIAR, L. K.; et al. Fatores associados à doença renal crônica segundo critérios laboratoriais da Pesquisa Nacional de Saúde. Revista Brasileira de Epidemiologia. São Paulo, v.23, 2020. DOI: https://doi.org/10.1590/1980-549720200101. Disponível em:. Acessoem: 1 Nov de 2021.BERG, D. D. et al. Time to Clinical Benefit of Dapagliflozin and Significance of Prior Heart Failure Hospitalization in Patients with Heart Failure with Reduced Ejection Fraction. JAMA Cardiology, v. 6, n. 5, 2021.Disponível em: https://pubmed.ncbi.nlm.nih.gov/33595593/. Acessoem: 1 Nov de 2021.BOCCHI, E. A. et al. Emerging topics in heart failure: Sodium-glucose co-transporter 2 inhibitors (sglt2i) in hf. Arquivos Brasileiros de Cardiologia, v. 116, n. 2, p. 355–358, 2021.Disponível em: http://old.scielo.br/scielo.php?pid=S0066-782X2021000200355&script=sci_arttext&tlng=en. Acessoem: 1 Nov de 2021.BRASIL. MINISTÉRIO DA SAÚDE. A vigilância, o controle e a prevençao das doenças crônicas não transmissíveis: DCNT no contexto do Sistema Único de Saúde Brasileiro -Situação e Desafios Atuais. Brasília: Organização Pan-Americana da Saúde, p. 80, 2005.Disponível em:https://bvsms.saude.gov.br/bvs/publicacoes/DCNT.pdf . Acessoem: 1 Nov de 2021.BRAUNWALD, E, et al. Tratado de medicina cardiovascular. 10. ed. –Rio de Janeiro: Elsevier, 2018.CHERTOW, G. M. et al. Quételet (body mass) index and effects of dapagliflozin in chronic kidney disease. Diabetes, Obesity and Metabolism, v. 24, n. 5, p. 827–837, 2022.Disponível em: https://pubmed.ncbi.nlm.nih.gov/34984791/. Acessoem: 1 Nov de 2021.DE OLIVEIRA, J. E. P.; MONTENEGRO JUNIOR, R. M.; VENCIO, S; et al.Diretrizesda Sociedade Brasileira deDiabetes: 2017-2018. São Paulo: Editora Clannad: 2017. Disponível em: https://diabetes.org.br/e-book/diretrizes-da-sociedade-brasileira-de-diabetes-2017-2018/. Acesso em: 1 Nov de 2021.FEDERAÇÃO INTERNACIONAL DE DIABETES. IDF Diabetes Atlas. 10 ed.Bruxelas. International Diabetes Federation; 2021. Disponível em: http://www.idf.org/diabetesatlasAcesso em: 5 Nov de 2021.GILMAN, A. G.; et al. Goodman e Gilman: As bases farmacológicas da terapêutica. 10. ed. Riode Janeiro. McGraw-Hill, 2003.GUIMARÃES, C.; et al. Medicina baseada em evidências. Rev Col Bras Cir. Rio de Janeiro, v. 36, n. 5, p. 369-370, 2009. DOI: <https://doi.org/10.1590/S0100-69912009000500002. Disponível em: https://www.scielo.br/j/rcbc/a/cVbkCq8b7TJvGMkrFf7N9Jc/?lang=pt. Acesso em: 2 Dez de 2021.GUYTON, A.C.; et al. Tratado de Fisiologia Médica. 13.ed. Rio de Janeiro: Elsevier, 2017.HEERSPINK, H. J. L. et al. Dapagliflozin in Patients with Chronic Kidney Disease. New England Journal of Medicine, v. 383, n. 15, p. 1436–1446, 2020.Disponível em: https://www.nejm.org/doi/full/10.1056/NEJMoa2024816. Acessoem: 1 Nov de 2021.IDRIS, I. et al. Lower risk of hospitalization for heart failure, kidney disease and death with sodium-glucose co-transporter-2 inhibitors compared with dipeptidyl peptidase-4 inhibitors in type 2 diabetes regardless of prior cardiovascular or kidney disease: A retrospective cohort study in UK primary care. Diabetes, Obesity and Metabolism, v. 23, n. 10, p. 2207–2214, 2021.Disponível em:https://pubmed.ncbi.nlm.nih.gov/33973690/ . Acessoem: 1 Nov de 2021. 24KIDNEY DISEASE: IMPROVING GLOBAL OUTCOMES (KDIGO) CKD Work Group. KDIGO 2020Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Int (Suppl) 2013;3:1-150. Disponível em:https://www.scielo.br/j/ress/a/8PrkGvDL5tTRhyJkNLkxD5k/?lang=pt. Acessoem: 1 mai de 2022.LEE, H. F. et al. Major adverse cardiovascular and limb events in patients with diabetes and concomitant peripheral artery disease treated with sodium glucose cotransporter 2 inhibitor versus dipeptidyl peptidase-4 inhibitor. Cardiovascular Diabetology, v. 19, n. 1, p. 1–12, 2020.Disponível em:https://pubmed.ncbi.nlm.nih.gov/32998736/ . Acessoem: 1 Nov de 2021.LEVIN, A. et al. Empagliflozin and cardiovascular and kidney outcomes across KDIGO risk categories: Post hoc analysis of a randomized, double-blind, placebo-controlled, multinational trial. Clinical Journal of the American Society of Nephrology, v. 15, n. 10, p. 1433–1444, 2020. Disponível em:https://pubmed.ncbi.nlm.nih.gov/32994159/ . Acessoem: 1 Nov de 2021.MAHAFFEY, K. W. et al. Canagliflozin and Cardiovascular and Renal Outcomes in Type 2 Diabetes Mellitus and Chronic Kidney Disease in Primary and Secondary Cardiovascular Prevention Groups: Results from the Randomized CREDENCE Trial. Circulation, v. 140, n. 9, p. 739–750, 2019. Disponível em: https://pubmed.ncbi.nlm.nih.gov/31291786/ Acesso em 16 abr de 2022.MCMURRAY, J. J. V. et al. Effects of Dapagliflozin in Patients With Kidney Disease, With and Without Heart Failure. JACC: Heart Failure, v. 9, n. 11, p. 807–820, 2021. Disponível em: https://pubmed.ncbi.nlm.nih.gov/34446370/. Acesso em: 1 Nov de 2021.NEUEN, B. L. et al. Relative and Absolute Risk Reductions in Cardiovascular and Kidney Outcomes With Canagliflozin Across KDIGO Risk Categories: Findings From the CANVAS Program. American Journal of Kidney Diseases, v. 77, n. 1, p. 23-34.e1, 2021.Disponível em:https://pubmed.ncbi.nlm.nih.gov/32971190/. Acessoem: 1 Nov de 2021.OSHIMA, M. et al. Early change in albuminuria with canagliflozin predicts kidney and cardiovascular outcomes: A post hoc analysis from the Credence trial. Journal of the American Society of Nephrology, v. 31, n. 12, p. 2925–2936, 2020. Disponível em:https://jasn.asnjournals.org/content/31/12/2925. Acessoem: 1 Nov de 2021.PACKER, M. et al. Cardiovascular and Renal Outcomes with Empagliflozin in Heart Failure. New England Journal of Medicine, v. 383,n. 15, p. 1413–1424, 2020.Disponível em:https://www.nejm.org/doi/full/10.1056/NEJMoa2022190. Acessoem: 1 Nov de 2021.PAGE, M. J. et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71. doi: 10.1136/bmj.n Disponível em: http://prisma-statement.org/documents/PRISMA%202020%20flow%20diagram%20EUROPEAN%20PORTUGUESE.pdf Acesso em: 22 mai de 2022.PERKOVIC, V. et al. Canagliflozin and Renal Outcomes in Type 2 Diabetes and Nephropathy. New England Journal of Medicine, v. 380, n. 24, p. 2295–2306, 2019.Disponível em:https://www.nejm.org/doi/full/10.1056/nejmoa1811744. Acessoem: 1 Nov de 2021.POULSEN, S. B.; FENTON, R. A.; RIEG, T.; Sodium-glucose cotransport. Curr Opin Nephrol Hypertens. London, vol. 24, n. 5, p. 463-469, 2015. DOI:10.1097/MNH.0000000000000152. Disponível em: https://pubmed.ncbi.nlm.nih.gov/26125647/. Acesso em: 10 Out de 2021. RIEG, T.; VALLON V. Development of SGLT1 and SGLT2 inhibitors.Diabetologia. 2018; vol. 61, n. 10, p. 2079-2086. doi:10.1007/s00125-018-4654-7. Disponível em: https://pubmed.ncbi.nlm.nih.gov/30132033/. Acesso em: 10 Abri de 2022. 25RIELLA, M.C. Princípios de Nefrologia e Distúrbios Hidroeletrolíticos. 4 ed. Rio de Janeiro: Guanabara Koogan, 2003.ROHDE,L. E. P.;MONTERA,M. W.;BOCCHI,E. A.;et al. Diretriz Brasileira de Insuficiência Cardíaca Crônica e Aguda.Arq. Bras. Cardiol, Rio de Janeiro, v. 111, n. 3, p. 436-539, 2018. Disponível em: https://abccardiol.org/article/diretriz-brasileira-de-insuficiencia-cardiaca-cronica-eaguda/Acesso em: 5 Out de 2021.TAVARES, N. U. L. et al. Uso de medicamentos para tratamento de doenças crônicas não transmissíveis no Brasil: resultados da Pesquisa Nacional de Saúde, 2013. Epidemiologia e Serviços de Saúde, v. 24, n. 2, p. 315–323, 2015.Disponível em:. Acessoem: 1 Nov de 2021.VERMA, S. et al. Empagliflozin reduces cardiovascular events, mortality and renal events in participants with type 2 diabetes after coronary artery bypass graft surgery: subanalysis of the EMPA-REG OUTCOME® randomised trial. Diabetologia, v. 61, n. 8, p. 1712–1723, 2018.Disponível em: https://pubmed.ncbi.nlm.nih.gov/29777264/. Acessoem: 1 Nov de 2021.VILAR,L; et al.Endocrinologia clínica. 6. ed. Rio de Janeiro: Guanabara Koogan, 2013.ZHANG, R. et al. Lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals. BMC Medicine, v. 20, n. 1, p. 1–11, 2022.Disponível em: https://pesquisa.bvsalud.org/global-literature-on-novel-coronavirus-2019-ncov/resource/pt/covidwho-1699213. Acessoem: 1 Nov de 2021.info:eu-repo/semantics/openAccessreponame:Repositório do Centro Universitário Braz Cubasinstname:Centro Universitário Braz Cubas (CUB)instacron:CUB2022-11-16T19:29:42Zoai:repositorio.cruzeirodosul.edu.br:123456789/4143Repositório InstitucionalPUBhttps://repositorio.brazcubas.edu.br/oai/requestbibli@brazcubas.edu.bropendoar:2022-11-16T19:29:42Repositório do Centro Universitário Braz Cubas - Centro Universitário Braz Cubas (CUB)false
dc.title.none.fl_str_mv Os múltiplos benefícios dos inibidores do SGLT2
title Os múltiplos benefícios dos inibidores do SGLT2
spellingShingle Os múltiplos benefícios dos inibidores do SGLT2
Cabral, Ana Júlia Marinho
iSGLT2
diabetes
insuficiência cardíaca
insuficiência renal crônica
CNPQ::CIENCIAS DA SAUDE::MEDICINA
title_short Os múltiplos benefícios dos inibidores do SGLT2
title_full Os múltiplos benefícios dos inibidores do SGLT2
title_fullStr Os múltiplos benefícios dos inibidores do SGLT2
title_full_unstemmed Os múltiplos benefícios dos inibidores do SGLT2
title_sort Os múltiplos benefícios dos inibidores do SGLT2
author Cabral, Ana Júlia Marinho
author_facet Cabral, Ana Júlia Marinho
author_role author
dc.contributor.none.fl_str_mv Macedo, Ciberio Landim
http://lattes.cnpq.br/8478576288526486
dc.contributor.author.fl_str_mv Cabral, Ana Júlia Marinho
dc.subject.por.fl_str_mv iSGLT2
diabetes
insuficiência cardíaca
insuficiência renal crônica
CNPQ::CIENCIAS DA SAUDE::MEDICINA
topic iSGLT2
diabetes
insuficiência cardíaca
insuficiência renal crônica
CNPQ::CIENCIAS DA SAUDE::MEDICINA
description Sodium-Glucose Cotransporter 2 (iSG2) Inhibitors (dapagliflozin, empaglifozin and canaglifozin) are used in the treatment of type 2 Diabetes Mellitus (DM2) but, recently, these are being used in the treatment of cardiovascular and renal drugs, adapting to the growing scientific evidence of clinical and laboratory benefits. The general objective of this study was to describe in an integrative way the importance of using SGT2 inhibitors in glycemic control and cardiovascular and renal outcomes. This is an integrative literature review, using the following databases: BVS, Pubmed and ScienceDirect during the period from March 2022 to April 2022. For the selection of articles, the following health descriptors (decs.bvs. br )” Glucose Drug Transport 2 Inhibitors”, Heart Failure”, “Chronic Kidney Disease”, “death” combined with Boolean operators “AND”. On outcomes, the 13 articles included are cohort and primary and secondary studies of multicenter, double-blind, placebo-controlled, randomized clinical trials testing the iSGT2 in different population samples. It was identified that the use of lower iSGLT2 when compared with the dipeptidyl peptidase-4 (DDP4i) inhibitor group was associated with risks of congestive heart failure (CHF), Relative Risk (RR): 0.66; 95% CI 0.49-0.89; p = 0.0062, or amputation, RR: 0.43; IC 95% 0.30-0.62; p < 0.0001 and cardiovascular death RR: 0.67; 95% CI 0.49-0.90; p = 0.0089. Another study, presented in a population with cardiac function, a study for cardiovascular death or hospitalization for heart failure, 0.75; 95% CI, 0.65 to 0.86; P<0.001. In patients with less severe renal decline, the RR is the composite of a sick patient estimated to have at least 50% decline in end-stage renal disease or death from renal causes (95% CI, 0.45 to 0.68 P< 0.001), and the risk to ratio for the composite of death from cardiovascular or cardiaccauses from cardiac dysfunction was 0.71; (95% CI, 0.5 to 0.92 P = 0.009). Completion Risk and Completion Risk Management LT2 researchers supported Completion Risk and Completion Risk Management data. In addition, the sample reduction in all-cause mortality, the delay in the loss of renal function, and also the reduction in the risk of renal compound. These are probably the SGLT2 inhibitors that are likely to play an important role in the treatment of cardiovascular and renal endocrine diseases.
publishDate 2022
dc.date.none.fl_str_mv 2022-11-16T19:00:28Z
2022-11-18
2022-11-16T19:00:28Z
2022-06-13
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/bachelorThesis
format bachelorThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv CABRAL, Ana Júlia Marinho. Os múltiplos benefícios dos inibidores do SGLT2. 25 P. Trabalho de conclusão de curso Medicina - Centro Universitário de João Pessoa – UNIPÊ, João Pessoa, 2022.
https://repositorio.cruzeirodosul.edu.br/handle/123456789/4143
identifier_str_mv CABRAL, Ana Júlia Marinho. Os múltiplos benefícios dos inibidores do SGLT2. 25 P. Trabalho de conclusão de curso Medicina - Centro Universitário de João Pessoa – UNIPÊ, João Pessoa, 2022.
url https://repositorio.cruzeirodosul.edu.br/handle/123456789/4143
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv AGUIAR, L. K.; et al. Fatores associados à doença renal crônica segundo critérios laboratoriais da Pesquisa Nacional de Saúde. Revista Brasileira de Epidemiologia. São Paulo, v.23, 2020. DOI: https://doi.org/10.1590/1980-549720200101. Disponível em:. Acessoem: 1 Nov de 2021.BERG, D. D. et al. Time to Clinical Benefit of Dapagliflozin and Significance of Prior Heart Failure Hospitalization in Patients with Heart Failure with Reduced Ejection Fraction. JAMA Cardiology, v. 6, n. 5, 2021.Disponível em: https://pubmed.ncbi.nlm.nih.gov/33595593/. Acessoem: 1 Nov de 2021.BOCCHI, E. A. et al. Emerging topics in heart failure: Sodium-glucose co-transporter 2 inhibitors (sglt2i) in hf. Arquivos Brasileiros de Cardiologia, v. 116, n. 2, p. 355–358, 2021.Disponível em: http://old.scielo.br/scielo.php?pid=S0066-782X2021000200355&script=sci_arttext&tlng=en. Acessoem: 1 Nov de 2021.BRASIL. MINISTÉRIO DA SAÚDE. A vigilância, o controle e a prevençao das doenças crônicas não transmissíveis: DCNT no contexto do Sistema Único de Saúde Brasileiro -Situação e Desafios Atuais. Brasília: Organização Pan-Americana da Saúde, p. 80, 2005.Disponível em:https://bvsms.saude.gov.br/bvs/publicacoes/DCNT.pdf . Acessoem: 1 Nov de 2021.BRAUNWALD, E, et al. Tratado de medicina cardiovascular. 10. ed. –Rio de Janeiro: Elsevier, 2018.CHERTOW, G. M. et al. Quételet (body mass) index and effects of dapagliflozin in chronic kidney disease. Diabetes, Obesity and Metabolism, v. 24, n. 5, p. 827–837, 2022.Disponível em: https://pubmed.ncbi.nlm.nih.gov/34984791/. Acessoem: 1 Nov de 2021.DE OLIVEIRA, J. E. P.; MONTENEGRO JUNIOR, R. M.; VENCIO, S; et al.Diretrizesda Sociedade Brasileira deDiabetes: 2017-2018. São Paulo: Editora Clannad: 2017. Disponível em: https://diabetes.org.br/e-book/diretrizes-da-sociedade-brasileira-de-diabetes-2017-2018/. Acesso em: 1 Nov de 2021.FEDERAÇÃO INTERNACIONAL DE DIABETES. IDF Diabetes Atlas. 10 ed.Bruxelas. International Diabetes Federation; 2021. Disponível em: http://www.idf.org/diabetesatlasAcesso em: 5 Nov de 2021.GILMAN, A. G.; et al. Goodman e Gilman: As bases farmacológicas da terapêutica. 10. ed. Riode Janeiro. McGraw-Hill, 2003.GUIMARÃES, C.; et al. Medicina baseada em evidências. Rev Col Bras Cir. Rio de Janeiro, v. 36, n. 5, p. 369-370, 2009. DOI: <https://doi.org/10.1590/S0100-69912009000500002. Disponível em: https://www.scielo.br/j/rcbc/a/cVbkCq8b7TJvGMkrFf7N9Jc/?lang=pt. Acesso em: 2 Dez de 2021.GUYTON, A.C.; et al. Tratado de Fisiologia Médica. 13.ed. Rio de Janeiro: Elsevier, 2017.HEERSPINK, H. J. L. et al. Dapagliflozin in Patients with Chronic Kidney Disease. New England Journal of Medicine, v. 383, n. 15, p. 1436–1446, 2020.Disponível em: https://www.nejm.org/doi/full/10.1056/NEJMoa2024816. Acessoem: 1 Nov de 2021.IDRIS, I. et al. Lower risk of hospitalization for heart failure, kidney disease and death with sodium-glucose co-transporter-2 inhibitors compared with dipeptidyl peptidase-4 inhibitors in type 2 diabetes regardless of prior cardiovascular or kidney disease: A retrospective cohort study in UK primary care. Diabetes, Obesity and Metabolism, v. 23, n. 10, p. 2207–2214, 2021.Disponível em:https://pubmed.ncbi.nlm.nih.gov/33973690/ . Acessoem: 1 Nov de 2021. 24KIDNEY DISEASE: IMPROVING GLOBAL OUTCOMES (KDIGO) CKD Work Group. KDIGO 2020Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Int (Suppl) 2013;3:1-150. Disponível em:https://www.scielo.br/j/ress/a/8PrkGvDL5tTRhyJkNLkxD5k/?lang=pt. Acessoem: 1 mai de 2022.LEE, H. F. et al. Major adverse cardiovascular and limb events in patients with diabetes and concomitant peripheral artery disease treated with sodium glucose cotransporter 2 inhibitor versus dipeptidyl peptidase-4 inhibitor. Cardiovascular Diabetology, v. 19, n. 1, p. 1–12, 2020.Disponível em:https://pubmed.ncbi.nlm.nih.gov/32998736/ . Acessoem: 1 Nov de 2021.LEVIN, A. et al. Empagliflozin and cardiovascular and kidney outcomes across KDIGO risk categories: Post hoc analysis of a randomized, double-blind, placebo-controlled, multinational trial. Clinical Journal of the American Society of Nephrology, v. 15, n. 10, p. 1433–1444, 2020. Disponível em:https://pubmed.ncbi.nlm.nih.gov/32994159/ . Acessoem: 1 Nov de 2021.MAHAFFEY, K. W. et al. Canagliflozin and Cardiovascular and Renal Outcomes in Type 2 Diabetes Mellitus and Chronic Kidney Disease in Primary and Secondary Cardiovascular Prevention Groups: Results from the Randomized CREDENCE Trial. Circulation, v. 140, n. 9, p. 739–750, 2019. Disponível em: https://pubmed.ncbi.nlm.nih.gov/31291786/ Acesso em 16 abr de 2022.MCMURRAY, J. J. V. et al. Effects of Dapagliflozin in Patients With Kidney Disease, With and Without Heart Failure. JACC: Heart Failure, v. 9, n. 11, p. 807–820, 2021. Disponível em: https://pubmed.ncbi.nlm.nih.gov/34446370/. Acesso em: 1 Nov de 2021.NEUEN, B. L. et al. Relative and Absolute Risk Reductions in Cardiovascular and Kidney Outcomes With Canagliflozin Across KDIGO Risk Categories: Findings From the CANVAS Program. American Journal of Kidney Diseases, v. 77, n. 1, p. 23-34.e1, 2021.Disponível em:https://pubmed.ncbi.nlm.nih.gov/32971190/. Acessoem: 1 Nov de 2021.OSHIMA, M. et al. Early change in albuminuria with canagliflozin predicts kidney and cardiovascular outcomes: A post hoc analysis from the Credence trial. Journal of the American Society of Nephrology, v. 31, n. 12, p. 2925–2936, 2020. Disponível em:https://jasn.asnjournals.org/content/31/12/2925. Acessoem: 1 Nov de 2021.PACKER, M. et al. Cardiovascular and Renal Outcomes with Empagliflozin in Heart Failure. New England Journal of Medicine, v. 383,n. 15, p. 1413–1424, 2020.Disponível em:https://www.nejm.org/doi/full/10.1056/NEJMoa2022190. Acessoem: 1 Nov de 2021.PAGE, M. J. et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71. doi: 10.1136/bmj.n Disponível em: http://prisma-statement.org/documents/PRISMA%202020%20flow%20diagram%20EUROPEAN%20PORTUGUESE.pdf Acesso em: 22 mai de 2022.PERKOVIC, V. et al. Canagliflozin and Renal Outcomes in Type 2 Diabetes and Nephropathy. New England Journal of Medicine, v. 380, n. 24, p. 2295–2306, 2019.Disponível em:https://www.nejm.org/doi/full/10.1056/nejmoa1811744. Acessoem: 1 Nov de 2021.POULSEN, S. B.; FENTON, R. A.; RIEG, T.; Sodium-glucose cotransport. Curr Opin Nephrol Hypertens. London, vol. 24, n. 5, p. 463-469, 2015. DOI:10.1097/MNH.0000000000000152. Disponível em: https://pubmed.ncbi.nlm.nih.gov/26125647/. Acesso em: 10 Out de 2021. RIEG, T.; VALLON V. Development of SGLT1 and SGLT2 inhibitors.Diabetologia. 2018; vol. 61, n. 10, p. 2079-2086. doi:10.1007/s00125-018-4654-7. Disponível em: https://pubmed.ncbi.nlm.nih.gov/30132033/. Acesso em: 10 Abri de 2022. 25RIELLA, M.C. Princípios de Nefrologia e Distúrbios Hidroeletrolíticos. 4 ed. Rio de Janeiro: Guanabara Koogan, 2003.ROHDE,L. E. P.;MONTERA,M. W.;BOCCHI,E. A.;et al. Diretriz Brasileira de Insuficiência Cardíaca Crônica e Aguda.Arq. Bras. Cardiol, Rio de Janeiro, v. 111, n. 3, p. 436-539, 2018. Disponível em: https://abccardiol.org/article/diretriz-brasileira-de-insuficiencia-cardiaca-cronica-eaguda/Acesso em: 5 Out de 2021.TAVARES, N. U. L. et al. Uso de medicamentos para tratamento de doenças crônicas não transmissíveis no Brasil: resultados da Pesquisa Nacional de Saúde, 2013. Epidemiologia e Serviços de Saúde, v. 24, n. 2, p. 315–323, 2015.Disponível em:. Acessoem: 1 Nov de 2021.VERMA, S. et al. Empagliflozin reduces cardiovascular events, mortality and renal events in participants with type 2 diabetes after coronary artery bypass graft surgery: subanalysis of the EMPA-REG OUTCOME® randomised trial. Diabetologia, v. 61, n. 8, p. 1712–1723, 2018.Disponível em: https://pubmed.ncbi.nlm.nih.gov/29777264/. Acessoem: 1 Nov de 2021.VILAR,L; et al.Endocrinologia clínica. 6. ed. Rio de Janeiro: Guanabara Koogan, 2013.ZHANG, R. et al. Lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals. BMC Medicine, v. 20, n. 1, p. 1–11, 2022.Disponível em: https://pesquisa.bvsalud.org/global-literature-on-novel-coronavirus-2019-ncov/resource/pt/covidwho-1699213. Acessoem: 1 Nov de 2021.
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 Centro Universitário de João Pessoa
Brasil
UNIPÊ
publisher.none.fl_str_mv Centro Universitário de João Pessoa
Brasil
UNIPÊ
dc.source.none.fl_str_mv reponame:Repositório do Centro Universitário Braz Cubas
instname:Centro Universitário Braz Cubas (CUB)
instacron:CUB
instname_str Centro Universitário Braz Cubas (CUB)
instacron_str CUB
institution CUB
reponame_str Repositório do Centro Universitário Braz Cubas
collection Repositório do Centro Universitário Braz Cubas
repository.name.fl_str_mv Repositório do Centro Universitário Braz Cubas - Centro Universitário Braz Cubas (CUB)
repository.mail.fl_str_mv bibli@brazcubas.edu.br
_version_ 1798311337975087104