Effects of Bivalirudin and Unfractionated Heparin on Liver and Renal Function in Chinese Patients with Coronary Artery Disease Undergoing Coronary Angiography with/without Percutaneous Coronary Intervention

Unfractionated heparin (UFH) and bivalirudin are widely used as anticoagulants in cardiovascular medicine, including for thrombosis prevention during coronary angiography (CAG) and percutaneous coronary intervention (PCI). Little is known of the effects of UFH and bivalirudin on liver and kidney fun...

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Published inJournal of clinical and translational hepatology Vol. 9; no. 4; pp. 477 - 483
Main Authors Jia, Qiaowei, Hu, Jia, Ji, Wenfeng, Wang, Liansheng, Jia, Enzhi
Format Journal Article
LanguageEnglish
Published United States XIA & HE Publishing Inc 28.08.2021
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Summary:Unfractionated heparin (UFH) and bivalirudin are widely used as anticoagulants in cardiovascular medicine, including for thrombosis prevention during coronary angiography (CAG) and percutaneous coronary intervention (PCI). Little is known of the effects of UFH and bivalirudin on liver and kidney function in patients subjected to these procedures. This study compared the effects of bivalirudin and UFH on liver/renal function in patients with coronary artery disease who underwent CAG, with or without PCI. The study comprised 134 consecutive patients (40-89 years-old), who underwent CAG (or CAG and PCI); among them, 66 and 68 patients were subject to, respectively, bivalirudin or UFH. The following indicators of liver/renal function were measured before and after the procedures: plasma alanine aminotransferase (ALT), aspartate aminotransferase (AST), blood urea nitrogen, estimated glomerular filtration rate (eGFR), creatinine clearance, and serum creatinine. Patients were further stratified by severity of chronic kidney disease (CKD), based on original eGFR. Relative to baseline, in the bivalirudin group, ALT and AST were higher after CAG ( =0.005, 0.025), while blood urea nitrogen and serum creatinine were lower ( =0.049, <0.001). In the UFH group, ALT, AST, eGFR, and creatinine clearance were lower after CAG ( ≤0.001, all). Patients given bivalirudin with moderate or severe CKD, but not those with mild CKD, gained significant improvement in kidney function. Relative to UFH, bivalirudin may better safeguard the renal function of patients with coronary artery disease who undergo CAG, especially patients with moderate-to-severe renal insufficiency. UFH may cause less liver damage than bivalirudin.
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These authors contributed equally to this work.
The authors have no conflict of interests related to this publication.
This study received support from the National Natural Science Foundations of China (No. 81970302).
Guarantor (EJ), conception of the study (EJ), initial drafting of the paper (QJ), enrollment of participants and collection of data (JH), supervision of the enrollment of patients and collection of data (EJ), and data analysis and review of the manuscript for important intellectual content (EJ, QJ, JH).
ISSN:2225-0719
2310-8819
DOI:10.14218/JCTH.2020.00150