A European, multicentre, retrospective, non-interventional study (EU-TREAT) of the effectiveness of insulin degludec after switching basal insulin in a population with type 1 or type 2 diabetes

被引:49
作者
Siegmund, Thorsten [1 ]
Tentolouris, Nikolaos [2 ]
Knudsen, Soren T. [3 ]
Lapolla, Annunziata [4 ]
Prager, Rudolf [5 ]
Phan, Tra-Mi [6 ]
Wolden, Michael L. [7 ]
Schultes, Bernd [8 ]
机构
[1] ISAR Klinikum Munchen GmbH, Dept Endocrinol Diabet & Metab, Sonnenstr 24-26, D-80331 Munich, Germany
[2] Univ Athens, Dept Propaedeut & Internal Med 1, Med Sch, Athens, Greece
[3] Aarhus Univ Hosp, Med Dept MEA Diabet & Endocrinol, Aarhus, Denmark
[4] Padova Univ, Dept Med, Padua, Italy
[5] Hietzing Hosp, Dept Metab Disorders & Nephrol, Vienna, Austria
[6] Novo Nordisk Reg Europe AS, Copenhagen, Denmark
[7] Novo Nordisk AS, Copenhagen, Denmark
[8] Swiss Med & Surg Ctr, St Gallen, Switzerland
关键词
basal insulin; hypoglycaemia; insulin analogues; observational study; GLARGINE U100; HYPOGLYCEMIA; VARIABILITY; MANAGEMENT; EFFICACY; TRIALS; SAFETY;
D O I
10.1111/dom.13149
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimsTo evaluate the clinical effectiveness of switching to insulin degludec (IDeg) in insulin-treated patients with either type 1 diabetes (T1DM) or type 2 diabetes (T2DM) under conditions of routine clinical care. Materials and MethodsThis was a multicentre, retrospective, chart review study. In all patients, basal insulin was switched to IDeg at least 6months before the start of data collection. Baseline was defined as the most recent recording during the 3-month period before first prescription of IDeg. Values are presented as mean [95%CI]. ResultsT1DM (n=1717): HbA1c decreased by -2.2 [-2.6; -2.0] mmol/mol (-0.20 [-0.24; -0.17]%) at 6months vs baseline (P<.001). Rate ratio of overall (0.79 [0.69; 0.89]), non-severe nocturnal (0.54 [0.42; 0.69]) and severe (0.15 [0.09; 0.24]) hypoglycaemia was significantly lower in the 6-month post-switch period vs the pre-switch period (P<.001 for all). Total daily insulin dose decreased by -4.88 [-5.52; -4.24] U (-11%) at 6months vs baseline (P<.001). T2DM (n=833): HbA1c decreased by -5.6 [-6.3; -4.7] mmol/mol (-0.51 [-0.58; -0.43] %) at 6months vs baseline (P<.001). Rate ratio of overall (0.39 [0.27; 0.58], P<.001), non-severe nocturnal (0.10 [0.06; 0.16], P<.001) and severe (0.075 [0.01; 0.43], P=.004) hypoglycaemia was significantly lower in the 6-month post-switch period vs the pre-switch period. Total daily insulin dose decreased by -2.48 [-4.24; -0.71] U (-3%) at 6months vs baseline (P=.006). Clinical outcomes for T1DM and T2DM at 12months were consistent with results at 6months. ConclusionsThis study demonstrates that switching patients to IDeg from other basal insulins improves glycaemic control and significantly reduces the risk of hypoglycaemia in routine clinical practice.
引用
收藏
页码:689 / 697
页数:9
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