Treatment patterns and associated factors in 14 668 people with type 2 diabetes initiating a second-line therapy: Results from the global DISCOVER study programme.
Adult
Aged
Diabetes Mellitus, Type 2
/ drug therapy
Dipeptidyl-Peptidase IV Inhibitors
/ therapeutic use
Drug Therapy, Combination
Female
Glycated Hemoglobin
/ analysis
Humans
Hypoglycemic Agents
/ therapeutic use
Insulin
/ therapeutic use
Male
Metformin
/ therapeutic use
Middle Aged
Practice Patterns, Physicians'
/ statistics & numerical data
Prospective Studies
antidiabetic drug
population study
type 2 diabetes
Journal
Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645
Informations de publication
Date de publication:
11 2019
11 2019
Historique:
received:
13
03
2019
revised:
28
06
2019
accepted:
04
07
2019
pubmed:
13
7
2019
medline:
29
9
2020
entrez:
13
7
2019
Statut:
ppublish
Résumé
To evaluate treatment data from DISCOVER (NCT02322762 and NCT02226822), a global, prospective, observational study programme of patients with type 2 diabetes initiating a second-line glucose-lowering therapy. Data were collected using a standardized case report form. First- and second-line treatments were assessed in 14 668 patients from 37 countries across six regions. Among patients prescribed first-line metformin monotherapy, Firth logistic regression models were used to assess factors associated with second-line treatment choices. The most common first-line therapies were metformin monotherapy (57.9%) and combinations of metformin with a sulphonylurea (14.6%). The most common second-line therapies were combinations of metformin with other agents (72.2%), including dipeptidyl peptidase-4 (DPP-4) inhibitors (25.1%) or sulphonylureas (21.3%). Among patients prescribed first-line metformin monotherapy, the most common second-line therapies were combinations of metformin with a DPP-4 inhibitor [32.8%; across-region range (ARR): 2.4%-51.3%] or a sulphonylurea (30.0%; ARR: 18.3%-63.6%); only a few patients received combinations of metformin with sodium-glucose co-transporter-2 inhibitors (6.7%; ARR: 0.0%-10.8%) or glucagon-like peptide-1 receptor agonists (1.9%; ARR: 0.1%-4.5%). Both clinical and non-medical factors were associated with choice of second-line therapy after metformin monotherapy. Fewer patients than expected received metformin monotherapy at first line, and the use of newer therapies at second line was uncommon in some regions of the world. Patients' socioeconomic status was associated with treatment patterns, suggesting that therapy choices are influenced by cost and access.
Identifiants
pubmed: 31297947
doi: 10.1111/dom.13830
pmc: PMC6852520
doi:
Substances chimiques
Dipeptidyl-Peptidase IV Inhibitors
0
Glycated Hemoglobin A
0
Hypoglycemic Agents
0
Insulin
0
hemoglobin A1c protein, human
0
Metformin
9100L32L2N
Banques de données
ClinicalTrials.gov
['NCT02322762', 'NCT02226822']
Types de publication
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2474-2485Informations de copyright
© 2019 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.
Références
Inform Prim Care. 2011;19(4):251-5
pubmed: 22828580
Lancet Diabetes Endocrinol. 2018 Oct;6(10):798-808
pubmed: 30170949
J Diabetes Investig. 2018 Mar 26;:
pubmed: 29582574
N Engl J Med. 2017 Aug 17;377(7):644-657
pubmed: 28605608
Diabetes Obes Metab. 2018 Aug;20(8):1983-1987
pubmed: 29569378
Diabetes Obes Metab. 2019 Nov;21(11):2474-2485
pubmed: 31297947
Int J Clin Pharmacol Ther. 2009 Oct;47(10):617-26
pubmed: 19825325
J Diabetes Complications. 2017 Jul;31(7):1188-1196
pubmed: 28499961
N Engl J Med. 2016 Jul 28;375(4):311-22
pubmed: 27295427
Br J Clin Pharmacol. 2010 Jan;69(1):4-14
pubmed: 20078607
Clin Ther. 2017 Apr;39(4):759-770
pubmed: 28342563
Endocr Pract. 2018 Jan;24(1):91-120
pubmed: 29368965
BMJ. 2018 Jul 18;362:k2693
pubmed: 30021781
Diabetes Res Clin Pract. 2019 May;151:20-32
pubmed: 30904743
Diabetes Care. 2018 Dec;41(12):2669-2701
pubmed: 30291106
Circulation. 2017 Jul 18;136(3):249-259
pubmed: 28522450
Diabetes Ther. 2018 Jun;9(3):1185-1199
pubmed: 29696567
Diabetes Ther. 2018 Feb;9(1):165-175
pubmed: 29260460
N Engl J Med. 2006 Dec 7;355(23):2427-43
pubmed: 17145742
Ann Intern Med. 2017 Feb 21;166(4):279-290
pubmed: 28055075
Ann Intern Med. 2018 Sep 18;169(6):394-397
pubmed: 30178023
N Engl J Med. 2016 Nov 10;375(19):1834-1844
pubmed: 27633186
Diabetes Care. 2016 Jul;39(7):e99-e101
pubmed: 27222504
N Engl J Med. 2015 Nov 26;373(22):2117-28
pubmed: 26378978
Lancet Diabetes Endocrinol. 2018 Feb;6(2):105-113
pubmed: 29221659
J Diabetes Complications. 2018 Nov;32(11):1035-1039
pubmed: 30177468
Circ Heart Fail. 2019 Jun;12(6):e005855
pubmed: 31129998
Diabetologia. 2013 May;56(5):973-84
pubmed: 23494446
Cardiovasc Diabetol. 2018 Jun 5;17(1):79
pubmed: 29871636