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Portuguese-Brazilian evidence-based guideline on the management of hyperglycemia in type 2 diabetes mellitus.
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.
Afiliación
  • Bertoluci MC; Internal Medicine Department, School of Medicine, Universidade Federal do Rio Grande do Sul (UFRGS), Rua Ramiro Barcelos, 2350, 4º Andar, Porto Alegre, RS 90035-007 Brazil.
  • Salles JEN; Endocrinology Unit, Hospital de Clínicas de Porto Alegre (HCPA-UFRGS), Rua Ramiro Barcelos, 2350, 4º Andar, Porto Alegre, RS 90035-007 Brazil.
  • Silva-Nunes J; Department of Internal Medicine, Discipline of Endocrinology, Faculdade de Ciências Médicas da Santa Casa de São Paulo (FCMSCSP), Rua Dr. Cesário Mota Junior, 61, São Paulo, SP 01221-020 Brazil.
  • Pedrosa HC; Department of Endocrinology, Diabetes and Metabolism/Centro Hospitalar, Universitário de Lisboa Central (CHULC), Rua da Beneficência, 8, 1069-166 Lisbon, Portugal.
  • Moreira RO; NOVA Medical School (NMS)/Faculdade de Ciências Médicas (FCM) da Universidade Nova de Lisboa, Rua da Beneficência, 8, 1069-166 Lisbon, Portugal.
  • da Silva Duarte RMC; Health and Technology Research Center/Escola Superior de Tecnologia da Saúde de Lisboa, Rua da Beneficência, 8, 1069-166 Lisbon, Portugal.
  • da Costa Carvalho DM; Hospital Curry Cabral, Rua da Beneficência, 8, 1069-166 Lisbon, Portugal.
  • Trujilho FR; Endocrinology Unit and Research Centre, Hospital Regional de Taguatinga, Área Especial Nº 24, Setor C Norte, Taguatinga Norte, Brasília, DF 72115-920 Brazil.
  • Dos Santos Raposo JFC; Instituto Estadual de Diabetes e Endocrinologia Luiz Capriglione (IEDE), Rua Moncorvo Filho, 90, Rio de Janeiro, RJ 20211-340 Brazil.
  • Parente EB; Faculdade de Medicina, Universidade Presidente Antônio Carlos (UNIPAC), Juiz de Fora, MG Brazil.
  • Valente F; Centro Universitário de Valença (UNIFAA), Rua Moncorvo Filho, 90, Rio de Janeiro, RJ 20211-340 Brazil.
  • de Moura FF; Associação Protetora dos Diabéticos de Portugal (APDP), Rua Rodrigo da Fonseca 1, 1250-189 Lisbon, Portugal.
  • Hohl A; Department of Endorinology, Diabetes and Metabolism, Centro Hospitalar S. João, Porto, Portugal.
  • Melo M; Faculty of Medicine, i3S, Universidade do Porto, Porto, Portugal.
  • Araujo FGP; Department of Obesity, Sociedade Brasileira de Endocrinologia e Metabologia, Av. Antonio Carlos Magalhães, s/n, Parque Bela Vista, Salvador, BA 40275-350 Brazil.
  • de Araújo Principe RMMC; NOVA Medical School (NMS), Faculdade de Ciências Médicas (FCM), Universidade Nova de Lisboa, Rua Salitre, 118, 1250-203 Lisbon, Portugal.
  • Kupfer R; Associação Protetora dos Diabéticos de Portugal (APDP), Rua Salitre, 118, 1250-203 Lisbon, Portugal.
  • Costa E Forti A; Sociedade Portuguesa de Diabetologia (SPD), Rua Salitre, 118, 1250-203 Lisbon, Portugal.
  • Valerio CM; Department of Endocrinology, Faculdade de Ciências Médicas da Santa Casa de São Paulo (FCMSCSP), Rua Dr. Cesario Mota Jr., 112, São Paulo, SP 01221-010 Brazil.
  • Ferreira HJ; Endocrinology Division, Department of Internal Medicine, Faculdade de Medicina do ABC, Av. Lauro Gomes, 2000, Santo André, SP Brazil.
  • Duarte JMS; Department of Endocrinology, Universidade de Pernambuco (UPE), Rua Arnobio Marques, 310, Recife, PE 50100-130 Brazil.
  • Saraiva JFK; Endocrinology Service, Instituto de Medicina de Pernambuco (IMIP), Rua Arnobio Marques, 310, Recife, PE 50100-130 Brazil.
  • Rodacki M; Department of Endocrinology and Metabolism/Department of Internal Medicine, Universidade Federal de Santa Catarina (UFSC), Rua Professora Maria Flora Pausewang, s/n, Florianópolis, SC 88036-800 Brazil.
  • Castelo MHCG; Hospital Universitário Polydoro Ernani de São Thiago, Campus Universitário, Rua Professora Maria Flora Pausewang, s/n, Florianópolis, SC 88036-800 Brazil.
  • Monteiro MP; Department of Endocrinology, Diabetes and Metabolism, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
  • Branco PQ; Medical Faculty, University of Coimbra, Praceta Mota Pinto, 3000-075 Coimbra, Portugal.
  • de Matos PMP; Serviço de Medicina, Hospital Beatriz Angelo, Loures, Portugal.
  • de Melo Pereira de Magalhães PC; Endocrinology Service, Hospital Pedro Hispano, Unidade Local de Saúde de Matosinhos, Rua Dr. Eduardo Torres, 4464/513 Senhora da Hora, Portugal.
  • Betti RTB; Department of Diabetes, Instituto Estadual de Diabetes e Endocrinologia Luiz Capriglione (IEDE), Rua Moncorvo Filho, 90, Rio de Janeiro, RJ 20211-340 Brazil.
  • Réa RR; Department of Internal Medicine, School of Medicine, Universidade Federal do Ceará (UFC), Rua Capitão Francisco Pedro, 1290, Fortaleza, CE 60430-375 Brazil.
  • Trujilho TDG; Instituto Estadual de Diabetes e Endocrinologia Luiz Capriglione (IEDE), Rua Moncorvo Filho, 90, Rio de Janeiro, RJ 20211-340 Brazil.
  • Pinto LCF; Unidade de Saúde Familiar Coimbra Celas, Administração Regional de Saúde do Centro, Av. D. Afonso Henriques, 141, 3000-011 Coimbra, Portugal.
  • Leitão CB; Endocrinology Service, Hospital Egas Moniz, Rua Junqueira, 126, 1349-019 Lisbon, Portugal.
Diabetol Metab Syndr ; 12: 45, 2020.
Article en En | MEDLINE | ID: mdl-32489427
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.
Palabras clave

Texto completo: 1 Colección: 01-internacional Tipo de estudio: Clinical_trials / Guideline / Observational_studies País/Región como asunto: America do sul / Brasil Idioma: En Revista: Diabetol Metab Syndr Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Tipo de estudio: Clinical_trials / Guideline / Observational_studies País/Región como asunto: America do sul / Brasil Idioma: En Revista: Diabetol Metab Syndr Año: 2020 Tipo del documento: Article