Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

Effects of Prandial Versus Fasting Glycemia on Cardiovascular Outcomes in Type 2 Diabetes: The HEART2D trial (CROSBI ID 163027)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Raz, Itamar ; Wilson, Peter ; Strojek, Krzysztof ; Kowalska, Irina ; Božikov, Velimir ; Gitt, Anselm ; Jermendy, György ; Campaigne, Barbara ; Kerr, Lisa ; Miličević, Zvonko et al. Effects of Prandial Versus Fasting Glycemia on Cardiovascular Outcomes in Type 2 Diabetes: The HEART2D trial // Diabetes care, 32 (2009), 3; 381-386. doi: 10.2337/dc08-1671

Podaci o odgovornosti

Raz, Itamar ; Wilson, Peter ; Strojek, Krzysztof ; Kowalska, Irina ; Božikov, Velimir ; Gitt, Anselm ; Jermendy, György ; Campaigne, Barbara ; Kerr, Lisa ; Miličević, Zvonko ; Jacober, Scott

engleski

Effects of Prandial Versus Fasting Glycemia on Cardiovascular Outcomes in Type 2 Diabetes: The HEART2D trial

Hyperglycemia and Its Effect After Acute Myocardial Infarction on Cardiovascular Outcomes in Patients With Type 2 Diabetes Mellitus (HEART2D) is a multinational, randomized, controlled trial designed to compare the effects of prandial versus fasting glycemic control on risk for cardiovascular outcomes in patients with type 2 diabetes after acute myocardial infarction (AMI). Patients (type 2 diabetes, aged 30–75 years) were randomly assigned within 21 days after AMI to the 1) prandial strategy (PRANDIAL) (three premeal doses of insulin lispro targeting 2-h postprandial blood glucose <7.5 mmol/l) or the 2) basal strategy (BASAL) (NPH twice daily or insulin glargine once daily targeting fasting/premeal blood glucose <6.7 mmol/l). A total of 1, 115 patients were randomly assigned (PRANDIAL n = 557 ; BASAL n = 558), and the mean patient participation after randomization was 963 days (range 1–1, 687 days). The trial was stopped for lack of efficacy. Risks of first combined adjudicated primary cardiovascular events in the PRANDIAL (n = 174, 31.2%) and BASAL (n = 181, 32.4%) groups were similar (hazard ratio 0.98 [95% CI 0.8–1.21]). Mean A1C did not differ between the PRANDIAL and BASAL groups (7.7 ± 0.1 vs. 7.8 ± 0.1% ; P = 0.4) during the study. The PRANDIAL group showed a lower daily mean postprandial blood glucose (7.8 vs. 8.6 mmol/l ; P < 0.01) and 2-h postprandial blood glucose excursion (0.1 vs. 1.3 mmol/l ; P < 0.001) versus the BASAL group. The BASAL group showed lower mean fasting blood glucose (7.0 vs. 8.1 mmol/l ; P < 0.001) and similar daily fasting/premeal blood glucose (7.7 vs. 7.3 mmol/l ; P = 0.233) versus the PRANDIAL group. Treating diabetic survivors of AMI with prandial versus basal strategies achieved differences in fasting blood glucose, less-than-expected differences in postprandial blood glucose, similar levels of A1C, and no difference in risk for future cardiovascular event rates.

hypergycemia; acute miocardial infarction; diabetes type 2

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

32 (3)

2009.

381-386

objavljeno

0149-5992

10.2337/dc08-1671

Povezanost rada

Kliničke medicinske znanosti

Poveznice
Indeksiranost