Adherence in patients transferred from immediate release metformin to a sustained release formulation: a population-based study

被引:54
作者
Donnelly, L. A. [1 ]
Morris, A. D. [2 ,3 ]
Pearson, E. R. [2 ,3 ]
机构
[1] Univ Dundee, Biomed Res Inst, Dundee, Scotland
[2] Univ Dundee, Biomed Res Inst, Dundee DD1 9SY, Scotland
[3] Univ Dundee, Diabet Res Ctr, Dundee DD1 9SY, Scotland
关键词
adherence; glucophage SR; metformin; metformin XL; RETROSPECTIVE COHORT; GLYCEMIC CONTROL; DOUBLE-BLIND; TYPE-2; EFFICACY;
D O I
10.1111/j.1463-1326.2008.00973.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: Metformin is the most commonly prescribed oral agent used in the treatment of type 2 diabetes. It is effective at reducing glycosylated Haemoglobin (HbA1c) and decreasing microvascular and macrovascular disease. However, up to 25% of patients develop gastrointestinal side effects leading to cessation in 5-10% of users. Metformin XL (glucophage SR) is a once a day preparation that delays absorption, leading to decreased peak metformin concentrations. We hypothesised that the XL preparation of metformin would be better tolerated than the standard immediate release (IR) preparation leading to improved adherence to therapy. Methods: In a retrospective observational study, we studied adherence and glycaemic control in patients prescribed metformin IR and XL preparations in Tayside, UK. Results: Metformin XL was used by 137 patients during the study period. Overall adherence was greater in the XL group (80%) compared with the 10 772 patients in the IR group (72%, p = 0.0026). In the 40 patients who changed from metformin IR to metformin XL who had sufficient data to determine adherence, the adherence increased from 62% in the IR group to 81% in the XL group (p < 0.0001). This was associated with an HbA1c reduction from 9.1 to 8.4% (p = 0.0739, n = 29). Conclusions: Metformin XL use is associated with increased adherence compared with the IR preparation, although the mechanism for this cannot be determined from this study. In patients intolerant of metformin IR the XL preparation should be considered.
引用
收藏
页码:338 / 342
页数:5
相关论文
共 15 条
[1]   Gastrointestinal tolerability of extended-release metformin tablets compared to immediaterelease metformin tablets: results of a retrospective cohort study [J].
Blonde, L ;
Dailey, GE ;
Jabbour, SA ;
Reasner, CA ;
Mills, DJ .
CURRENT MEDICAL RESEARCH AND OPINION, 2004, 20 (04) :565-572
[2]  
British Medical Association and Royal Pharmaceutical, 2003, BRIT NAT FORM
[3]   Adherence to prescribed oral hypoglycaemic medication in a population of patients with Type 2 diabetes: a retrospective cohort study [J].
Donnan, PT ;
MacDonald, TM ;
Morris, AD .
DIABETIC MEDICINE, 2002, 19 (04) :279-284
[4]  
Evans J. M. M., 1995, Pharmaceutical Medicine (London), V9, P177
[5]   Efficacy, dose-response relationship and safety of once-daily extended-release metformin (Glucophage® XR) in type 2 diabetic patients with inadequate glycaemic control despite prior treatment with diet and exercise:: results from two double-blind, placebo-controlled studies [J].
Fujioka, K ;
Brazg, RL ;
Raz, I ;
Bruce, S ;
Joyal, S ;
Swanink, R ;
Pans, M .
DIABETES OBESITY & METABOLISM, 2005, 7 (01) :28-39
[6]   Glycemic control in patients with type 2 diabetes Mellitus switched from twice-daily immediate-release metformin to a once-daily extended-release formulation [J].
Fujioka, K ;
Pans, M ;
Joyal, S .
CLINICAL THERAPEUTICS, 2003, 25 (02) :515-529
[7]   The metabolic effects of once daily extended-release metformin in patients with type 2 diabetes: a multicentre study [J].
Gao, H. ;
Xiao, W. ;
Wang, C. ;
Zhang, J. ;
Yang, Y. ;
Yang, J. ;
Yang, W. ;
Hong, T. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2008, 62 (05) :695-700
[8]   Efficacy of metformin in type II diabetes: Results of a double-blind, placebo-controlled, dose-response trial [J].
Garber, AJ ;
Duncan, TG ;
Goodman, AM ;
Mills, DJ ;
Rohlf, JL .
AMERICAN JOURNAL OF MEDICINE, 1997, 103 (06) :491-497
[9]   Glycemic durability of rosiglitazone, metformin, or glyburide monotherapy [J].
Kahn, Steven E. ;
Haffner, Steven M. ;
Heise, Mark A. ;
Herman, William H. ;
Holman, Rury R. ;
Jones, Nigel P. ;
Kravitz, Barbara G. ;
Lachin, John M. ;
O'Neill, M. Colleen ;
Zinman, Bernard ;
Viberti, Giancarlo .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (23) :2427-2443
[10]   The DIACOM study (effect of DosIng frequency of oral Antidiabetic agents on the COMpliance and biochemical control of type 2 diabetes) [J].
Kardas, P .
DIABETES OBESITY & METABOLISM, 2005, 7 (06) :722-728