Real-world use of cardioprotective glucose-lowering drugs in patients with type 2 diabetes and cardiovascular disease: A Danish nationwide cohort study, 2012 to 2019.
Real-world use of cardioprotective glucose-lowering drugs in patients with type 2 diabetes and cardiovascular disease: A Danish nationwide cohort study, 2012 to 2019.
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DOI:
10.1111/dom.14245
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发表时间:
2021-03
期刊:
影响因子:
--
通讯作者:
Grove EL
中科院分区:
文献类型:
--
作者:
Funck KL;Knudsen JS;Hansen TK;Thomsen RW;Grove EL
To investigate temporal trends in time to initiation of sodium‐glucose co‐transporter‐2 inhibitors and glucagon‐like peptide 1 analogues (cardioprotective glucose‐lowering drugs [GLDs]) in patients with a new dual diagnosis of type 2 diabetes (T2DM) and cardiovascular disease (CVD). In a cohort study, we identified patients with a new dual diagnosis of T2DM and CVD using linked healthcare data from nationwide registries on drug prescriptions and diagnosis codes. For each calendar year between 2012 and 2018, we examined time to initiation and cumulative user proportions (CUPs) for cardioprotective GLD use 1 and 2 years after the dual diagnosis. Among all individuals living in Denmark in the period 2012 to 2018, 41 733 patients with a new dual diagnosis of T2DM and CVD were identified (median [interquartile range] age 71 [64–79] years, 61% male, and 57% with CVD as the latest diagnosis). Incidence curve slopes and 1‐ and 2‐year CUPs for cardioprotective GLDs increased during the study period (1‐year CUP 4.0%, 95% confidence interval [CI] 3.6–4.5) in 2012 to 14.7, 95% CI 13.7–15.7, in 2018; 2‐year CUP 5.5, 95% CI 5.0–6.1, in 2012 to 16.7, 95% CI 15.8–17.7, in 2017). T2DM patients with CVD as the second (latest) diagnosis had higher 1‐year CUPs than CVD patients with T2DM as the latest diagnosis: 2012: 7.0 (95% CI 6.2–8.0) versus 1.4 (95% CI 1.0–1.8); 2018: 18.1 (95% CI 16.8–19.6) versus 10.0 (95% CI 8.8‐11.3). In patients with T2DM and CVD, the incidence of cardioprotective GLD initiation increased between 2012 and 2018, however, within 2 years of dual diagnosis, it remained low.
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影响因子:
2.6
作者:
Heald, Adrian H.;Livingston, Mark;Stedman, Mike
通讯作者:
Stedman, Mike
影响因子:
9.3
作者:
Pantalone KM;Misra-Hebert AD;Hobbs TM;Ji X;Kong SX;Milinovich A;Weng W;Bauman J;Ganguly R;Burguera B;Kattan MW;Zimmerman RS
通讯作者:
Zimmerman RS
DOI:
10.1056/nejmoa1603827
发表时间:
2016-07-28
期刊:
The New England journal of medicine
影响因子:
--
作者:
Marso SP;Daniels GH;Brown-Frandsen K;Kristensen P;Mann JF;Nauck MA;Nissen SE;Pocock S;Poulter NR;Ravn LS;Steinberg WM;Stockner M;Zinman B;Bergenstal RM;Buse JB;LEADER Steering Committee;LEADER Trial Investigators
通讯作者:
LEADER Trial Investigators
影响因子:
8.2
作者:
Buse, John B.;Wexler, Deborah J.;Davies, Melanie J.
通讯作者:
Davies, Melanie J.
影响因子:
3.8
作者:
Nicolucci, Antonio;Candido, Riccardo;Manicardi, Valeria
通讯作者:
Manicardi, Valeria