Optimization of insulin therapy in patients with Type 2 diabetes mellitus: beyond basal insulin

被引:39
作者
Blak, B. T. [1 ]
Smith, H. T. [2 ]
Hards, M. [1 ]
Curtis, B. H. [3 ]
Ivanyi, T. [4 ]
机构
[1] Cegedim Strateg Data Med Res Ltd, London NW1 0QG, England
[2] Lilly UK, Erl Wood Manor, Windlesham, Surrey, England
[3] Lilly USA, Indianapolis, IN USA
[4] Lilly Hungary, Budapest, Hungary
关键词
basal insulin; prandial insulin; premixed insulin; Type; 2; diabetes; UK General Practice; GENERAL-PRACTICE; GLYCEMIC CONTROL; ORAL-THERAPY; INTENSIFICATION; INITIATION; PREVALENCE; ALGORITHM; GLARGINE; TARGET; TRIAL;
D O I
10.1111/j.1464-5491.2012.03586.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabet. Med. 29, e13e20 (2012) Abstract Aims To describe patients with Type 2 diabetes mellitus treated with basal insulin, with or without oral antidiabetics in UK primary care, and evaluate insulin treatment patterns and factors explaining changes in therapy. Methods Retrospective analysis of patients with Type 2 diabetes within The Health Improvement Network UK primary care database. Patients receiving basal insulin between January and June 2006 were followed until July 2009. Results Analysis included 3185 patients, mean age 65.6 years [standard deviation (SD) 12.4], 50.9% men, median diabetes duration 9.6 years, median basal insulin use 1.3 years, 86.5% had received oral antidiabetics in the previous 12 months. Mean follow-up was 2.9 years (SD 1.0), 59.8% patients maintained basal insulin throughout follow-up with a mean HbA1C of 69 mmol/mol (SD 19; 8.4%, SD 1.7) at baseline and 65 mmol/mol (SD 17; 8.1%, SD 1.6) during follow-up. During follow-up, 6.9% of patients discontinued, 19.3% intensified with and 14.1% switched to prandial or premixed insulin. Patients who intensified (prandial) had a mean HbA1c of 77 mmol/mol (SD 18; 9.2%, SD 1.6) before change and a mean HbA1c of 71 mmol/mol (SD 21; 8.6%, SD 2.0) at the end of the study. Those switching to premixed insulin had a mean HbA1c of 80 mmol/mol (SD 18; 9.5%, SD 1.7) before change and a mean HbA1c of 69 mmol/mol (SD 17; 8.5%, SD 1.5) at the end of the study. Increasing HbA1c and longer diabetes duration explained intensification and switch. Conclusions The majority of patients had HbA1c above the 53 mmol/mol (< 7%) target at baseline and post-intensification/switch. The HbA1c levels were reduced by intensification/switch suggesting that insulin changes did have some impact. Most patients did not change insulin treatment despite having higher than recommended HbA1c levels. Reasons for not changing treatment in face of unsatisfactory clinical outcomes are unclear. Further research is warranted to explore barriers towards therapy change.
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页码:E13 / E20
页数:8
相关论文
共 20 条
[1]  
[Anonymous], 2009, TYP 2 DIAB NEW AG BL
[2]  
[Anonymous], 2003, NAT SERV FRAM DIAB D
[3]   HOW DOES THE HEALTH IMPROVEMENT NETWORK (THIN) DATA ON PREVALENCE OF CHRONIC DISEASES COMPARE WITH NATIONAL FIGURES? [J].
Blak, B. T. ;
Thompson, M. .
VALUE IN HEALTH, 2009, 12 (07) :A253-A253
[4]   The Audit Commission review of diabetes services in England and Wales, 1998-2001 [J].
Fitzsimons, B ;
Wilton, L ;
Lamont, T ;
McCulloch, L ;
Boyce, J .
DIABETIC MEDICINE, 2002, 19 :73-78
[5]   Prevalence of inadequate glycemic control among patients with type 2 diabetes in the United Kingdom general practice research database: A series of retrospective analyses of data from 1998 through 2002 [J].
Fox, KM ;
Gerber, RA ;
Bolinder, B ;
Chen, J ;
Kumar, S .
CLINICAL THERAPEUTICS, 2006, 28 (03) :388-395
[6]   Intensification to biphasic insulin aspart 30/70 (BIAsp 30, NovoMix® 30) can improve glycaemic control in patients treated with basal insulins: a subgroup analysis of the IMPROVE™ observational study [J].
Gumprecht, J. ;
Benroubi, M. ;
Borzi, V. ;
Kawamori, R. ;
Shaban, J. ;
Shah, S. ;
Shestakova, M. ;
Wenying, Y. ;
Ligthelm, R. ;
Valensi, P. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2009, 63 (06) :966-972
[7]   Performance of the QRISK cardiovascular risk prediction algorithm in an independent UK sample of patients from general practice: a validation study [J].
Hippisley-Cox, J. ;
Coupland, C. ;
Vinogradova, Y. ;
Robson, J. ;
Brindle, P. .
HEART, 2008, 94 (01) :34-39
[8]   Addition of biphasic, prandial, or basal insulin to oral therapy in type 2 diabetes [J].
Holman, Rury R. ;
Thorne, Kerensa I. ;
Farmer, Andrew J. ;
Davies, Melanie J. ;
Keenan, Joanne F. ;
Paul, Sanjoy ;
Levy, Jonathan C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (17) :1716-1730
[9]   Insulin initiation in Type 2 diabetes: the implications of the 4-T study [J].
Holt, R. I. G. .
DIABETIC MEDICINE, 2010, 27 (01) :1-3
[10]  
Jones S, 2009, CURR MED RES OPIN, V25, P691, DOI [10.1185/03007990902739669, 10.1185/03007990902739669 ]