Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/105885
Title: Portuguese-Brazilian evidence-based guideline on the management of hyperglycemia in type 2 diabetes mellitus
Authors: Bertoluci, Marcello Casaccia
Salles, João Eduardo Nunes
Silva-Nunes, José
Pedrosa, Hermelinda Cordeiro
Moreira, Rodrigo Oliveira
da Silva Duarte, Rui Manuel Calado
da Costa Carvalho, Davide Mauricio
Trujilho, Fábio Rogério
Dos Santos Raposo, João Filipe Cancela
Parente, Erika Bezerra
Valente, Fernando
de Moura, Fábio Ferreira
Hohl, Alexandre
Melo, Miguel 
Araujo, Francisco Garcia Pestana
de Araújo Principe, Rosa Maria Monteiro Castro
Kupfer, Rosane
Costa E Forti, Adriana
Valerio, Cynthia Melissa
Ferreira, Hélder José
Duarte, João Manuel Sequeira
Saraiva, José Francisco Kerr
Rodacki, Melanie
Castelo, Maria Helane Costa Gurgel
Monteiro, Mariana Pereira
Branco, Patrícia Quadros
de Matos, Pedro Manuel Patricio
de Melo Pereira de Magalhães, Pedro Carneiro
Betti, Roberto Tadeu Barcellos
Réa, Rosângela Roginski
Trujilho, Thaisa Dourado Guedes
Pinto, Lana Catani Ferreira
Leitão, Cristiane Bauermann
Keywords: Diabetes treatment; Type 2 diabetes; Cardiovascular risk; Guidelines; Heart failure; Chronic kidney disease; Ischemic heart disease; ASCVD; Atherosclerotic disease
Issue Date: 2020
Publisher: Springer Nature
Project: Sociedade Brasileira de Diabetes (SBD 
Serial title, monograph or event: Diabetology and Metabolic Syndrome
Volume: 12
Issue: 1
Abstract: 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.
URI: https://hdl.handle.net/10316/105885
ISSN: 1758-5996
DOI: 10.1186/s13098-020-00551-1
Rights: openAccess
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais

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