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Serum D-dimer is a potential predictor for thromboembolism complications in patients with renal biopsy

Renal biopsy has been widely recommended in clinic to determine the histological patterns of kidney disease. To prevent bleeding complications, patients should routinely stop anticoagulants prior to renal biopsy. However, patients with kidney disease are susceptible to thromboembolisms, particularly...

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Autores principales: Tan, Xia, Chen, Guochun, Liu, Yu, Zhou, Letian, He, Liyu, Liu, Di, Liu, Yexin, Zhang, Fan, Li, Huiqiong, Liu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500525/
https://www.ncbi.nlm.nih.gov/pubmed/28684778
http://dx.doi.org/10.1038/s41598-017-05210-6
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author Tan, Xia
Chen, Guochun
Liu, Yu
Zhou, Letian
He, Liyu
Liu, Di
Liu, Yexin
Zhang, Fan
Li, Huiqiong
Liu, Hong
author_facet Tan, Xia
Chen, Guochun
Liu, Yu
Zhou, Letian
He, Liyu
Liu, Di
Liu, Yexin
Zhang, Fan
Li, Huiqiong
Liu, Hong
author_sort Tan, Xia
collection PubMed
description Renal biopsy has been widely recommended in clinic to determine the histological patterns of kidney disease. To prevent bleeding complications, patients should routinely stop anticoagulants prior to renal biopsy. However, patients with kidney disease are susceptible to thromboembolisms, particularly in those with severe hypoalbuminemia. This study was designed to investigate the application of serum D-dimer as a predictor for thrombotic events after renal biopsy. 400 consecutive native renal biopsies were prospectively included in this 2-month follow-up study. The overall incidence of bleeding and thrombotic complication is 4%, including hematuria or large perinephric hematoma (2.5%, n = 10) and thrombotic complication (1.5%, n = 6). Compared to low serum D-dimer (<2.00 μg/ml), subjects in the group of high serum D-dimer (≥2.00 μg/ml) were more incline to develop thrombotic complications (9.1% versus 0.3%; RR, 30.33; p < 0.001). D-dimer correlated positively with age (r(s) = 0.258, P < 0.001). Inverse correlations were found for albumin (r(s) = −0.339, P < 0.001). Taken together, patients with high serum D-dimer carry an increased risk of thrombotic complications after renal biopsy. Our findings suggest that serum D-dimer can serve as a potential predictor for thrombotic events in patients with kidney disease. Further cautions should be given to these subjects.
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spelling pubmed-55005252017-07-10 Serum D-dimer is a potential predictor for thromboembolism complications in patients with renal biopsy Tan, Xia Chen, Guochun Liu, Yu Zhou, Letian He, Liyu Liu, Di Liu, Yexin Zhang, Fan Li, Huiqiong Liu, Hong Sci Rep Article Renal biopsy has been widely recommended in clinic to determine the histological patterns of kidney disease. To prevent bleeding complications, patients should routinely stop anticoagulants prior to renal biopsy. However, patients with kidney disease are susceptible to thromboembolisms, particularly in those with severe hypoalbuminemia. This study was designed to investigate the application of serum D-dimer as a predictor for thrombotic events after renal biopsy. 400 consecutive native renal biopsies were prospectively included in this 2-month follow-up study. The overall incidence of bleeding and thrombotic complication is 4%, including hematuria or large perinephric hematoma (2.5%, n = 10) and thrombotic complication (1.5%, n = 6). Compared to low serum D-dimer (<2.00 μg/ml), subjects in the group of high serum D-dimer (≥2.00 μg/ml) were more incline to develop thrombotic complications (9.1% versus 0.3%; RR, 30.33; p < 0.001). D-dimer correlated positively with age (r(s) = 0.258, P < 0.001). Inverse correlations were found for albumin (r(s) = −0.339, P < 0.001). Taken together, patients with high serum D-dimer carry an increased risk of thrombotic complications after renal biopsy. Our findings suggest that serum D-dimer can serve as a potential predictor for thrombotic events in patients with kidney disease. Further cautions should be given to these subjects. Nature Publishing Group UK 2017-07-06 /pmc/articles/PMC5500525/ /pubmed/28684778 http://dx.doi.org/10.1038/s41598-017-05210-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tan, Xia
Chen, Guochun
Liu, Yu
Zhou, Letian
He, Liyu
Liu, Di
Liu, Yexin
Zhang, Fan
Li, Huiqiong
Liu, Hong
Serum D-dimer is a potential predictor for thromboembolism complications in patients with renal biopsy
title Serum D-dimer is a potential predictor for thromboembolism complications in patients with renal biopsy
title_full Serum D-dimer is a potential predictor for thromboembolism complications in patients with renal biopsy
title_fullStr Serum D-dimer is a potential predictor for thromboembolism complications in patients with renal biopsy
title_full_unstemmed Serum D-dimer is a potential predictor for thromboembolism complications in patients with renal biopsy
title_short Serum D-dimer is a potential predictor for thromboembolism complications in patients with renal biopsy
title_sort serum d-dimer is a potential predictor for thromboembolism complications in patients with renal biopsy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500525/
https://www.ncbi.nlm.nih.gov/pubmed/28684778
http://dx.doi.org/10.1038/s41598-017-05210-6
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