Portuguese-Brazilian Evidence-Based Guideline on the Management of Hyperglycemia in Type 2 Diabetes Mellitus

Detalhes bibliográficos
Autor(a) principal: Bertoluci, M
Data de Publicação: 2020
Outros Autores: Nunes Salles, JE, Silva-Nunes, J, Cordeiro Pedrosa, H, Moreira, R, Calado da Silva Duarte, R, Maurício da Costa Carvalho, D, Trujilho, F, Cancela dos Santos Raposo, JF, Parente, E, Valente, F, Ferreira de Moura, F, Hohl, A, Melo, M, Araújo, F, de Araújo Principe, RM, Kupfer, R, Costa e Forti, A, Valerio, C, Ferreira, HJ, Duarte, JM, Kerr Saraiva, JF, Rodacki, M, Gurgel Castelo, MH, Pereira Monteiro, M, Quadros Branco, P, Patrício de Matos, PM, Pereira de Magalhães, P, Betti, R, Réa, R, Trujilho, T, Ferreira Pinto, L, Bauermann Leitão, C
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.17/3767
Resumo: Background: In current management of type 2 diabetes (T2DM), cardiovascular and renal prevention have become important targets to be achieved. In this context, a joint panel of four endocrinology societies from Brazil and Portugal was established to develop an evidence-based guideline for treatment of hyperglycemia in T2DM. Methods: MEDLINE (via PubMed) was searched for randomized clinical trials, meta-analyses, and observational studies related to diabetes treatment. When there was insufficient high-quality evidence, expert opinion was sought. Updated positions on treatment of T2DM patients with heart failure (HF), atherosclerotic CV disease (ASCVD), chronic kidney disease (CKD), and patients with no vascular complications were developed. The degree of recommendation and the level of evidence were determined using predefined criteria. Results and conclusions: In non-pregnant adults, the recommended HbA1c target is below 7%. Higher levels are recommended in frail older adults and patients at higher risk of hypoglycemia. Lifestyle modification is recommended at all phases of treatment. Metformin is the first choice when HbA1c is 6.5-7.5%. When HbA1c is 7.5-9.0%, dual therapy with metformin plus an SGLT2i and/or GLP-1RA (first-line antidiabetic agents, AD1) is recommended due to cardiovascular and renal benefits. If an AD1 is unaffordable, other antidiabetic drugs (AD) may be used. Triple or quadruple therapy should be considered when HbA1c remains above target. In patients with clinical or subclinical atherosclerosis, the combination of one AD1 plus metformin is the recommended first-line therapy to reduce cardiovascular events and improve blood glucose control. In stable heart failure with low ejection fraction (< 40%) and glomerular filtration rate (eGFR) > 30 mL/min/1.73 m2, metformin plus an SGLT-2i is recommended to reduce cardiovascular mortality and heart failure hospitalizations and improve blood glucose control. In patients with diabetes-associated chronic kidney disease (CKD) (eGFR 30-60 mL/min/1.73 m2 or eGFR 30-90 mL/min/1.73 m2 with albuminuria > 30 mg/g), the combination of metformin and an SGLT2i is recommended to attenuate loss of renal function, reduce albuminuria and improve blood glucose control. In patients with severe renal failure, insulin-based therapy is recommended to improve blood glucose control. Alternatively, GLP-1RA, DPP4i, gliclazide MR and pioglitazone may be considered to reduce albuminuria. In conclusion, the current evidence supports individualizing anti-hyperglycemic treatment for T2DM.
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spelling Portuguese-Brazilian Evidence-Based Guideline on the Management of Hyperglycemia in Type 2 Diabetes MellitusHCC ENDASCVDAtherosclerotic DiseaseCardiovascular RiskChronic Kidney DiseaseDiabetes TreatmentGuidelinesIschemic Heart DiseaseHeart FailureType 2 Diabetes.Background: In current management of type 2 diabetes (T2DM), cardiovascular and renal prevention have become important targets to be achieved. In this context, a joint panel of four endocrinology societies from Brazil and Portugal was established to develop an evidence-based guideline for treatment of hyperglycemia in T2DM. Methods: MEDLINE (via PubMed) was searched for randomized clinical trials, meta-analyses, and observational studies related to diabetes treatment. When there was insufficient high-quality evidence, expert opinion was sought. Updated positions on treatment of T2DM patients with heart failure (HF), atherosclerotic CV disease (ASCVD), chronic kidney disease (CKD), and patients with no vascular complications were developed. The degree of recommendation and the level of evidence were determined using predefined criteria. Results and conclusions: In non-pregnant adults, the recommended HbA1c target is below 7%. Higher levels are recommended in frail older adults and patients at higher risk of hypoglycemia. Lifestyle modification is recommended at all phases of treatment. Metformin is the first choice when HbA1c is 6.5-7.5%. When HbA1c is 7.5-9.0%, dual therapy with metformin plus an SGLT2i and/or GLP-1RA (first-line antidiabetic agents, AD1) is recommended due to cardiovascular and renal benefits. If an AD1 is unaffordable, other antidiabetic drugs (AD) may be used. Triple or quadruple therapy should be considered when HbA1c remains above target. In patients with clinical or subclinical atherosclerosis, the combination of one AD1 plus metformin is the recommended first-line therapy to reduce cardiovascular events and improve blood glucose control. In stable heart failure with low ejection fraction (< 40%) and glomerular filtration rate (eGFR) > 30 mL/min/1.73 m2, metformin plus an SGLT-2i is recommended to reduce cardiovascular mortality and heart failure hospitalizations and improve blood glucose control. In patients with diabetes-associated chronic kidney disease (CKD) (eGFR 30-60 mL/min/1.73 m2 or eGFR 30-90 mL/min/1.73 m2 with albuminuria > 30 mg/g), the combination of metformin and an SGLT2i is recommended to attenuate loss of renal function, reduce albuminuria and improve blood glucose control. In patients with severe renal failure, insulin-based therapy is recommended to improve blood glucose control. Alternatively, GLP-1RA, DPP4i, gliclazide MR and pioglitazone may be considered to reduce albuminuria. In conclusion, the current evidence supports individualizing anti-hyperglycemic treatment for T2DM.BMCRepositório do Centro Hospitalar Universitário de Lisboa Central, EPEBertoluci, MNunes Salles, JESilva-Nunes, JCordeiro Pedrosa, HMoreira, RCalado da Silva Duarte, RMaurício da Costa Carvalho, DTrujilho, FCancela dos Santos Raposo, JFParente, EValente, FFerreira de Moura, FHohl, AMelo, MAraújo, Fde Araújo Principe, RMKupfer, RCosta e Forti, AValerio, CFerreira, HJDuarte, JMKerr Saraiva, JFRodacki, MGurgel Castelo, MHPereira Monteiro, MQuadros Branco, PPatrício de Matos, PMPereira de Magalhães, PBetti, RRéa, RTrujilho, TFerreira Pinto, LBauermann Leitão, C2021-07-15T15:07:04Z20202020-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/3767engDiabetol Metab Syndr. 2020 May 24;12:45.10.1186/s13098-020-00551-1info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-10T09:44:15Zoai:repositorio.chlc.min-saude.pt:10400.17/3767Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:21:05.363922Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Portuguese-Brazilian Evidence-Based Guideline on the Management of Hyperglycemia in Type 2 Diabetes Mellitus
title Portuguese-Brazilian Evidence-Based Guideline on the Management of Hyperglycemia in Type 2 Diabetes Mellitus
spellingShingle Portuguese-Brazilian Evidence-Based Guideline on the Management of Hyperglycemia in Type 2 Diabetes Mellitus
Bertoluci, M
HCC END
ASCVD
Atherosclerotic Disease
Cardiovascular Risk
Chronic Kidney Disease
Diabetes Treatment
Guidelines
Ischemic Heart Disease
Heart Failure
Type 2 Diabetes.
title_short Portuguese-Brazilian Evidence-Based Guideline on the Management of Hyperglycemia in Type 2 Diabetes Mellitus
title_full Portuguese-Brazilian Evidence-Based Guideline on the Management of Hyperglycemia in Type 2 Diabetes Mellitus
title_fullStr Portuguese-Brazilian Evidence-Based Guideline on the Management of Hyperglycemia in Type 2 Diabetes Mellitus
title_full_unstemmed Portuguese-Brazilian Evidence-Based Guideline on the Management of Hyperglycemia in Type 2 Diabetes Mellitus
title_sort Portuguese-Brazilian Evidence-Based Guideline on the Management of Hyperglycemia in Type 2 Diabetes Mellitus
author Bertoluci, M
author_facet Bertoluci, M
Nunes Salles, JE
Silva-Nunes, J
Cordeiro Pedrosa, H
Moreira, R
Calado da Silva Duarte, R
Maurício da Costa Carvalho, D
Trujilho, F
Cancela dos Santos Raposo, JF
Parente, E
Valente, F
Ferreira de Moura, F
Hohl, A
Melo, M
Araújo, F
de Araújo Principe, RM
Kupfer, R
Costa e Forti, A
Valerio, C
Ferreira, HJ
Duarte, JM
Kerr Saraiva, JF
Rodacki, M
Gurgel Castelo, MH
Pereira Monteiro, M
Quadros Branco, P
Patrício de Matos, PM
Pereira de Magalhães, P
Betti, R
Réa, R
Trujilho, T
Ferreira Pinto, L
Bauermann Leitão, C
author_role author
author2 Nunes Salles, JE
Silva-Nunes, J
Cordeiro Pedrosa, H
Moreira, R
Calado da Silva Duarte, R
Maurício da Costa Carvalho, D
Trujilho, F
Cancela dos Santos Raposo, JF
Parente, E
Valente, F
Ferreira de Moura, F
Hohl, A
Melo, M
Araújo, F
de Araújo Principe, RM
Kupfer, R
Costa e Forti, A
Valerio, C
Ferreira, HJ
Duarte, JM
Kerr Saraiva, JF
Rodacki, M
Gurgel Castelo, MH
Pereira Monteiro, M
Quadros Branco, P
Patrício de Matos, PM
Pereira de Magalhães, P
Betti, R
Réa, R
Trujilho, T
Ferreira Pinto, L
Bauermann Leitão, C
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE
dc.contributor.author.fl_str_mv Bertoluci, M
Nunes Salles, JE
Silva-Nunes, J
Cordeiro Pedrosa, H
Moreira, R
Calado da Silva Duarte, R
Maurício da Costa Carvalho, D
Trujilho, F
Cancela dos Santos Raposo, JF
Parente, E
Valente, F
Ferreira de Moura, F
Hohl, A
Melo, M
Araújo, F
de Araújo Principe, RM
Kupfer, R
Costa e Forti, A
Valerio, C
Ferreira, HJ
Duarte, JM
Kerr Saraiva, JF
Rodacki, M
Gurgel Castelo, MH
Pereira Monteiro, M
Quadros Branco, P
Patrício de Matos, PM
Pereira de Magalhães, P
Betti, R
Réa, R
Trujilho, T
Ferreira Pinto, L
Bauermann Leitão, C
dc.subject.por.fl_str_mv HCC END
ASCVD
Atherosclerotic Disease
Cardiovascular Risk
Chronic Kidney Disease
Diabetes Treatment
Guidelines
Ischemic Heart Disease
Heart Failure
Type 2 Diabetes.
topic HCC END
ASCVD
Atherosclerotic Disease
Cardiovascular Risk
Chronic Kidney Disease
Diabetes Treatment
Guidelines
Ischemic Heart Disease
Heart Failure
Type 2 Diabetes.
description Background: In current management of type 2 diabetes (T2DM), cardiovascular and renal prevention have become important targets to be achieved. In this context, a joint panel of four endocrinology societies from Brazil and Portugal was established to develop an evidence-based guideline for treatment of hyperglycemia in T2DM. Methods: MEDLINE (via PubMed) was searched for randomized clinical trials, meta-analyses, and observational studies related to diabetes treatment. When there was insufficient high-quality evidence, expert opinion was sought. Updated positions on treatment of T2DM patients with heart failure (HF), atherosclerotic CV disease (ASCVD), chronic kidney disease (CKD), and patients with no vascular complications were developed. The degree of recommendation and the level of evidence were determined using predefined criteria. Results and conclusions: In non-pregnant adults, the recommended HbA1c target is below 7%. Higher levels are recommended in frail older adults and patients at higher risk of hypoglycemia. Lifestyle modification is recommended at all phases of treatment. Metformin is the first choice when HbA1c is 6.5-7.5%. When HbA1c is 7.5-9.0%, dual therapy with metformin plus an SGLT2i and/or GLP-1RA (first-line antidiabetic agents, AD1) is recommended due to cardiovascular and renal benefits. If an AD1 is unaffordable, other antidiabetic drugs (AD) may be used. Triple or quadruple therapy should be considered when HbA1c remains above target. In patients with clinical or subclinical atherosclerosis, the combination of one AD1 plus metformin is the recommended first-line therapy to reduce cardiovascular events and improve blood glucose control. In stable heart failure with low ejection fraction (< 40%) and glomerular filtration rate (eGFR) > 30 mL/min/1.73 m2, metformin plus an SGLT-2i is recommended to reduce cardiovascular mortality and heart failure hospitalizations and improve blood glucose control. In patients with diabetes-associated chronic kidney disease (CKD) (eGFR 30-60 mL/min/1.73 m2 or eGFR 30-90 mL/min/1.73 m2 with albuminuria > 30 mg/g), the combination of metformin and an SGLT2i is recommended to attenuate loss of renal function, reduce albuminuria and improve blood glucose control. In patients with severe renal failure, insulin-based therapy is recommended to improve blood glucose control. Alternatively, GLP-1RA, DPP4i, gliclazide MR and pioglitazone may be considered to reduce albuminuria. In conclusion, the current evidence supports individualizing anti-hyperglycemic treatment for T2DM.
publishDate 2020
dc.date.none.fl_str_mv 2020
2020-01-01T00:00:00Z
2021-07-15T15:07:04Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.17/3767
url http://hdl.handle.net/10400.17/3767
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Diabetol Metab Syndr. 2020 May 24;12:45.
10.1186/s13098-020-00551-1
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 BMC
publisher.none.fl_str_mv BMC
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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