Heterogeneity in renal end points of cardiovascular outcomes trials in Type 2 diabetes

被引:1
作者
Balijepalli, Chakrapani [1 ]
Yan, Kevin [1 ]
Zoratti, Michael [2 ]
Franklin, Meg [3 ]
Druyts, Eric [1 ]
机构
[1] Pharmalytics Grp, Vancouver, BC V6B 2Z4, Canada
[2] McMaster Univ, Dept Hlth Res Methods Evidence & Impact, Hamilton, ON L8S 4L8, Canada
[3] Franklin Pharmaceut Consulting LLC, Rock Hill, SC 29730 USA
关键词
CVOT; DPP-4; inhibitors; GLP-1; analogues; heterogeneity; renal composite; SGLT-2; Type; 2; diabetes; KIDNEY-DISEASE; NETWORK; RISK;
D O I
10.2217/cer-2020-0137
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Composite renal end points and end stage renal disease (ESRD) are frequently included as prespecified secondary end points in the cardiovascular outcomes trials (CVOTs) of diabetes medications. We examined the heterogeneity in the definitions of composite renal end point and ESRD in CVOTs. Five criteria (macroalbuminuria, doubling of serum creatinine, estimated glomerular filtration rate [GFR], ESRD and renal death), were considered for the renal composite end point across the trials. Only three of the 12 trials included all five criteria, whereas the other trials included different combinations of four, three and two criteria. ESRD definition also showed considerable heterogeneity across the trials. Heterogeneity exists in the definitions of renal composite and ESRD end points in CVOTs making it challenging to assess comparative efficacy of the active treatments for reimbursement purposes.
引用
收藏
页码:169 / 173
页数:5
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