Fixed-Dose Combinations for Treatment of Type 2 Diabetes Mellitus

被引:48
|
作者
Blonde, Lawrence [1 ]
San Juan, Zinnia T. [2 ]
机构
[1] Ochsner Med Ctr, Dept Endocrinol Diabet & Metab Dis, New Orleans, LA 70121 USA
[2] Texas Tech Univ Hlth Sci Ctr, Dept Internal Med, Div Endocrinol, El Paso, TX USA
关键词
adherence; bioavailability; cost; efficacy; FDC; fixed-dose combination; glycemic control; tolerability; type 2 diabetes mellitus; GLYCEMIC CONTROL; PHARMACOLOGICAL-TREATMENT; MEDICATION NONADHERENCE; PATIENT COMPLIANCE; INITIAL TREATMENT; DUAL THERAPY; ADHERENCE; METFORMIN; MONOTHERAPY; COSTS;
D O I
10.1007/s12325-011-0094-1
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Combining antihyperglycemic agents with complementary mechanisms of action is a cornerstone of type 2 diabetes mellitus (T2DM) management. Although several fixed-dose combinations (FDCs) are available, representing standard types of combination therapy in T2DM, use of these products has been limited. To address the likely concerns of prescribers and patients regarding the use of FDCs in the treatment of T2DM, literature searches were performed to ascertain the bioavailability, efficacy, tolerability, and cost-effectiveness of the currently approved FDCs compared with their individual component drugs given as separate pills in combination. Additionally, data were collected on rates of adherence, clinical outcomes, and overall treatment costs with FDCs versus dual therapy with the same constituent drugs. Bioavailability is equivalent for FDCs and dual therapy used in T2DM. Efficacy and tolerability also appear to be at least as good with FDCs as with dual therapy. Retrospective analyses have suggested that FDCs can enhance adherence to therapy, presumably as a result of the reduction in pill burden, and improved adherence may result in improved glycemic control and reduced disease management costs. In addition, because currently available FDCs come in two or more dose-strength formulations, they also afford some measure of dosing flexibility. The available evidence supports the wider use of FDCs in the treatment of patients with T2DM.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 50 条
  • [1] Fixed-Dose Combinations for Treatment of Type 2 Diabetes Mellitus
    Lawrence Blonde
    Zinnia T. San Juan
    Advances in Therapy, 2012, 29 : 1 - 13
  • [2] Erratum to: Fixed-Dose Combinations for Treatment of Type 2 Diabetes Mellitus
    Lawrence Blonde
    Zinnia T. San Juan
    Advances in Therapy, 2013, 30 : 306 - 307
  • [3] Fixed-Dose Combinations for Treatment of Type 2 Diabetes Mellitus (vol 29, pg 1, 2012)
    Blonde, Lawrence
    San Juan, Zinnia T.
    ADVANCES IN THERAPY, 2013, 30 (03) : 306 - 307
  • [4] Adequacy of clinical trial evidence of metformin fixed-dose combinations for the treatment of type 2 diabetes mellitus in India
    Evans, Valerie
    Roderick, Peter
    Pollock, Allyson M.
    BMJ GLOBAL HEALTH, 2018, 3 (02):
  • [5] FIXED-DOSE COMBINATION THERAPY IN TYPE 2 DIABETES MELLITUS
    Blonde, Lawrence
    Juan, Zinnia T. San
    Bolton, Peggy
    ENDOCRINE PRACTICE, 2014, 20 (12) : 1322 - 1332
  • [6] The power of two: an update on fixed-dose combinations for type 2 diabetes
    Harris, Stewart B.
    EXPERT REVIEW OF CLINICAL PHARMACOLOGY, 2016, 9 (11) : 1453 - 1462
  • [7] EXPLORING THE PERCEIVED VALUE OF FIXED-DOSE COMBINATIONS IN TYPE 2 DIABETES MELLITUS IN THE EU4 AND THE UK
    Arrioja, Cruz J. C.
    Zaniboni, B.
    Yeoh, L.
    Reinert, M.
    Naser, R.
    Mos, J.
    Gulotta, G.
    VALUE IN HEALTH, 2023, 26 (12) : S143 - S143
  • [8] Fixed-dose combinations in type 2 diabetes - role of the canagliflozin metformin combination
    Fleming, Joshua W.
    Fleming, Laurie W.
    Davis, Courtney S.
    DIABETES METABOLIC SYNDROME AND OBESITY-TARGETS AND THERAPY, 2015, 8 : 287 - 294
  • [9] Fixed-dose combinations for treatment of diabetes unsafe, finds study
    Nischal, P. M.
    NATIONAL MEDICAL JOURNAL OF INDIA, 2018, 31 (03): : 191 - 191
  • [10] Sitagliptin/Metformin Fixed-Dose CombinationIn Patients with Type 2 Diabetes Mellitus
    Claudine M. Chwieduk
    Drugs, 2011, 71 : 349 - 361