Portuguese-Brazilian evidence-based guideline on the management of hyperglycemia in type 2 diabetes mellitus
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/218614 |
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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Bertoluci, Marcello CasacciaLeitão, Cristiane Bauermann2021-03-11T04:23:52Z20201758-5996http://hdl.handle.net/10183/218614001122777Background: 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.application/pdfengDiabetology & metabolic syndrome. London. vol. 12 (2020), 45, 30 f.Diabetes mellitus tipo 2HiperglicemiaDiabetes treatmentType 2 diabetesCardiovascular riskGuidelinesHeart failureChronic kidney diseaseIschemic heart diseaseASCVDAtherosclerotic diseasePortuguese-Brazilian evidence-based guideline on the management of hyperglycemia in type 2 diabetes mellitusEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001122777.pdf.txt001122777.pdf.txtExtracted Texttext/plain138585http://www.lume.ufrgs.br/bitstream/10183/218614/2/001122777.pdf.txtf1100d4f2601ccb8c67e50823d5ea740MD52ORIGINAL001122777.pdfTexto completo (inglês)application/pdf1670135http://www.lume.ufrgs.br/bitstream/10183/218614/1/001122777.pdf9574819dc659fcf486d589899033bf47MD5110183/2186142021-05-07 04:53:51.057714oai:www.lume.ufrgs.br:10183/218614Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-05-07T07:53:51Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.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, Marcello Casaccia Diabetes mellitus tipo 2 Hiperglicemia Diabetes treatment Type 2 diabetes Cardiovascular risk Guidelines Heart failure Chronic kidney disease Ischemic heart disease ASCVD Atherosclerotic disease |
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, Marcello Casaccia |
author_facet |
Bertoluci, Marcello Casaccia Leitão, Cristiane Bauermann |
author_role |
author |
author2 |
Leitão, Cristiane Bauermann |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Bertoluci, Marcello Casaccia Leitão, Cristiane Bauermann |
dc.subject.por.fl_str_mv |
Diabetes mellitus tipo 2 Hiperglicemia |
topic |
Diabetes mellitus tipo 2 Hiperglicemia Diabetes treatment Type 2 diabetes Cardiovascular risk Guidelines Heart failure Chronic kidney disease Ischemic heart disease ASCVD Atherosclerotic disease |
dc.subject.eng.fl_str_mv |
Diabetes treatment Type 2 diabetes Cardiovascular risk Guidelines Heart failure Chronic kidney disease Ischemic heart disease ASCVD Atherosclerotic disease |
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.issued.fl_str_mv |
2020 |
dc.date.accessioned.fl_str_mv |
2021-03-11T04:23:52Z |
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Diabetology & metabolic syndrome. London. vol. 12 (2020), 45, 30 f. |
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