How representative of a general type 2 diabetes population are patients included in cardiovascular outcome trials with SGLT2 inhibitors? A large European observational study

被引:63
作者
Birkeland, Kare I. [1 ,2 ]
Bodegard, Johan [3 ]
Norhammar, Anna [4 ]
Kuiper, Josephina G. [5 ]
Georgiado, Elena [6 ]
Beekman-Hendriks, Wendy L. [7 ]
Thuresson, Marcus [8 ]
Pignot, Marc [9 ]
Herings, Ron M. C. [5 ,10 ]
Kooy, Adriaan [11 ,12 ]
机构
[1] Oslo Univ Hosp, Div Surg Inflammatory Med & Transplantat, Dept Transplantat Med, Oslo, Norway
[2] Univ Oslo, Oslo, Norway
[3] AstraZeneca Nord Balt, Fredrik Selmersvei 6, N-0601 Oslo, Norway
[4] Karolinska Inst, Karolinska Univ Hosp, Stockholm, Sweden
[5] PHARMO Inst Drug Outcomes Res, Utrecht, Netherlands
[6] Team Gesundheit GmbH, Essen, Germany
[7] AstraZeneca, The Hague, Netherlands
[8] Statisticon AB, Uppsala, Sweden
[9] Kantar Hlth GmbH, Munich, Germany
[10] Vrije Univ Amsterdam Med Ctr, Dept Epidemiol & Biostat, Amsterdam, Netherlands
[11] Univ Med Ctr Groningen, Groningen, Netherlands
[12] Bethesda Diabet Res Ctr, Groningen, Netherlands
关键词
cardiovascular disease; cardiovascular outcome trial; observational study; representativeness; SGLT2; inhibitors; GLUCOSE-LOWERING DRUGS; HEART-FAILURE; CVD-REAL; MORTALITY; DAPAGLIFLOZIN; DIAGNOSIS; ACCURACY; VALIDITY; DESIGN; RISK;
D O I
10.1111/dom.13612
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Enrollment criteria vary substantially among cardiovascular outcome trials (CVOTs) of sodium-glucose cotransporter-2 inhibitors (SGLT-2is), which impacts the relationship between a trial population and the general type 2 diabetes (T2D) population. The aim of this study was to evaluate the representativeness of four SGLT-2i CVOTs of a general T2D population. Methods T2D patients from Germany, The Netherlands, Norway and Sweden were included in the study. Given the available data per country, key inclusion and exclusion criteria were defined by diagnoses, procedures and drug treatments to facilitate comparability among countries. Representativeness was determined by dividing the number of patients fulfilling the key enrolment criteria of each CVOT (CANVAS, DECLARE-TIMI 58, EMPA-REG OUTCOME, VERTIS-CV) by the total T2D population. Results In 2015, a total T2D population of 803 836 patients was identified in Germany (n = 239 485), in The Netherlands (n = 36 213), in Norway (n = 149 782) and in Sweden (n = 378 356). These populations showed a 25% to 44% cardiovascular (CV) disease baseline prevalence and high CV-preventive drug use (>80%). The general T2D population had less prevalent CV disease and patients were slightly older than those included in the CVOTs. The DECLARE-TIMI 58 trial had the highest representativeness, 59% compared to the general T2D population, and this representativeness was almost 2-, 3- and 4-fold higher compared to the CANVAS (34%), EMPA-REG OUTCOME (21%) and VERTIS-CV (17%) trials, respectively. Conclusions In large T2D populations within Europe, consistent patterns of representativeness of CVOTs were found when applying the main enrolment criteria. The DECLARE-TMI 58 trial had the highest representativeness, indicating that it included and examined patients who are most representative of the general T2D patients in the studied countries.
引用
收藏
页码:968 / 974
页数:7
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