Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.21/11824
Title: Portuguese-Brazilian evidence-based guideline on the management of hyperglycemia in type 2 diabetes mellitus
Author: Bertoluci, Marcello Casaccia
Salles, João Eduardo
Silva-Nunes, José
Pedrosa, Hermelinda Cordeiro
Moreira, Rodrigo Oliveira
Duarte, Rui Manuel
Carvalho, Davide Mauricio
Trujilho, Fábio Rogério
Raposo, João Filipe
Parente, Erika Bezerra
Valente, Fernando
Moura, Fábio Ferreira de
Hohl, Alexandre
Melo, Miguel
Araujo, Francisco Garcia
Principe, Rosa Maria
Kupfer, Rosane
Costa e Forti, Adriana
Valerio, Cynthia Melissa
Ferreira, Hélder José
Duarte, João Manuel
Saraiva, José Francisco
Rodacki, Melanie
Castelo, Maria Helane
Monteiro, Mariana Pereira
Branco, Patrícia Quadros
Matos, Pedro Manuel
Magalhães, Pedro Carneiro
Betti, Roberto Tadeu
Réa, Rosângela Roginski
Trujilho, Thaisa Dourado
Pinto, Lana Catani
Leitão, Cristiane Bauermann
Keywords: Diabetes
Diabetes treatment
Type 2 diabetes
Cardiovascular risk
Guidelines
Heart failure
Chronic kidney disease
Ischemic heart disease
ASCVD
Atherosclerotic disease
Portugal
Brasil
Issue Date: May-2020
Publisher: BMC
Citation: Bertoluci MC, Salles JE, Silva-Nunes J, Pedrosa HC, Moreira RO, Duarte RM, et al. Portuguese-Brazilian evidence-based guideline on the management of hyperglycemia in type 2 diabetes mellitus. Diabetol Metab Syndr. 2020;12:45.
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 the 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 was 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.
Peer review: yes
URI: http://hdl.handle.net/10400.21/11824
DOI: 10.1186/s13098-020-00551-1
Publisher Version: https://dmsjournal.biomedcentral.com/articles/10.1186/s13098-020-00551-1#citeas
Appears in Collections:ESTeSL - Artigos



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