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Important changes include: (1) the decision to treat high-risk individuals with a glucagon-like-peptide 1 (GLP-1) receptor agonist or sodiumglucose cotransporter 2 (SGLT2) inhibitor to reduce major adverse cardiovascular events (MACE), hospitalisation for heart failure (hHF), cardiovascular death or chronic kidney disease (CKD) progression should be considered independently of baseline HbA1c or individualised HbA1c target

The incidence of MBSH ranged significantly across different diagnostic methods: 2.666.4% (self-report), 6.661.8% (oral glucose tolerance test), 29.478.6% (mixed-meal tolerance test), and 5075% (continuous glucose monitoring)

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