02866nas a2200253 4500000000100000008004100001100001500042700001800057700001600075700001500091700001500106700001400121700001400135700001400149700001300163700002100176700002100197700001600218245012300234250001500357050001600372520217300388020005102561 2016 d1 aZoungas S.1 aWoodward Mark1 aVisseren F.1 aPoulter N.1 aGrobbee D.1 aMancia G.1 aHarrap S.1 aHeller S.1 aMarre M.1 avan der Leeuw J.1 avan der Graaf Y.1 aChalmers J.00aEstimation of individual beneficial and adverse effects of intensive glucose control for patients with type 2 diabetes a2016/09/03 a[IF]: 6.6713 a
AIMS/HYPOTHESIS: Intensive glucose control reduces the risk of vascular complications while increasing the risk of severe hypoglycaemia at a group level. We sought to estimate individual beneficial and adverse effects of intensive glucose control in patients with type 2 diabetes. METHODS: We performed a post hoc analysis of the Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation (ADVANCE) trial, a randomised controlled trial evaluating standard vs intensive glucose control (HbA1c target 1%, 5 year number-needed-to-benefit [NNTB5] <100) and 1% had a small ARR (<0.5%, NNTB5 >200). Similarly, 36% of patients had a substantial estimated ARI for severe hypoglycaemia (5 year number-needed-to-harm [NNTH5] <100) and 29% had a small ARI (NNTH5 >200). When assigning similar or half the weight to severe hypoglycaemia compared with a major vascular event, net benefit was positive in 85% or 99% of patients, respectively. Limiting intensive treatment to the 85% patient subgroup had no significant effect on the overall incidence of major vascular events and severe hypoglycaemia compared with treating all patients. CONCLUSIONS/INTERPRETATION: Taking account of the effects of intensive glucose control on major micro- and macrovascular events and severe hypoglycaemia for individual patients, the estimated net benefit was positive in the majority of the participants in the ADVANCE trial. The estimated individual effects can inform treatment decisions once individual weights assigned to positive and adverse effects have been specified. TRIAL REGISTRATION: ClinicalTrials.gov NCT00145925.
a1432-0428 (Electronic)