2021
DOI: 10.1016/j.diabres.2021.109035
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Comparing medication persistence among patients with type 2 diabetes using sodium-glucose cotransporter 2 inhibitors or glucagon-like peptide-1 receptor agonists in real-world setting

Abstract: Comparing medication persistence among patients with type 2 diabetes using sodium-glucose cotransporter 2 inhibitors or glucagon-like peptide-1 receptor agonists in real-world setting,

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Cited by 19 publications
(16 citation statements)
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“…To preserve privacy, each identification code is automatically anonymized, and the inverse process is only allowed to the regional authority upon request of judicial authorities. Further details on Healthcare Utilization Databases in pharmacoepidemiological studies are available in previous studies ( 15 , 16 ).…”
Section: Methodsmentioning
confidence: 99%
“…To preserve privacy, each identification code is automatically anonymized, and the inverse process is only allowed to the regional authority upon request of judicial authorities. Further details on Healthcare Utilization Databases in pharmacoepidemiological studies are available in previous studies ( 15 , 16 ).…”
Section: Methodsmentioning
confidence: 99%
“…Current type 2 diabetes guidelines to intensify therapy after metformin are largely based on potential added benefits (e.g., weight reduction) or increased risk of side effects (e.g., hypoglycemia). The reduction in MACE with therapy with sodium-glucose co-transport-2 inhibitors (SGLT-2Is) appear to be significantly less in women with diabetes vs. men, while glucagon-like peptide-1 receptor agonists (GLP-1Ras) confer a similar reduction in major adverse cardiac events, irrespective of the gender [ 13 , 14 ].…”
Section: Types Of Diabetes and Gendermentioning
confidence: 99%
“…However, the duration of the treatmentfree period used to define treatment discontinuation, varied across the studies, spanning from 60 to 184 days [23][24][25][26][27] (Table 3). Treatment discontinuation was defined as a change in the type of OAD by Jermendy et al, 24 Rea et al, 25 Strain et al, 23 and Vlacho et al, 26 whereas Wilding et al 27 MPR is defined as the ratio between the number of days a patient is supplied with the given medication and the number of days between each medication refill over a given time span. 28 It expresses the percentage of time that a subject has the medication available 28 and is, thus, a proxy for treatment adherence.…”
Section: Measurement Methodsmentioning
confidence: 99%