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Risk of percutaneous renal biopsy of native kidneys in the evaluation of acute kidney injury

BACKGROUND: Percutaneous renal biopsy (PRB) of native kidneys (NKs) to better understand and treat acute kidney injury (AKI) is being advocated, but little is known about the risk of complications. METHODS: We performed a retrospective study of PRB of NKs in 955 adults from 1991 to 2015 at an academ...

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Autores principales: Korbet, Stephen M, Gashti, Casey N, Evans, Joni K, Whittier, William L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165762/
https://www.ncbi.nlm.nih.gov/pubmed/30289129
http://dx.doi.org/10.1093/ckj/sfy048
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author Korbet, Stephen M
Gashti, Casey N
Evans, Joni K
Whittier, William L
author_facet Korbet, Stephen M
Gashti, Casey N
Evans, Joni K
Whittier, William L
author_sort Korbet, Stephen M
collection PubMed
description BACKGROUND: Percutaneous renal biopsy (PRB) of native kidneys (NKs) to better understand and treat acute kidney injury (AKI) is being advocated, but little is known about the risk of complications. METHODS: We performed a retrospective study of PRB of NKs in 955 adults from 1991 to 2015 at an academic medical center with real-time ultrasound and automated biopsy needles. Patients undergoing PRB for evaluation of AKI (n = 160) were compared with 795 patients biopsied for other reasons (not-AKI) for postbiopsy complications [need for transfusion of packed red blood cells (PRBCs), an interventional radiologic or surgical procedure, readmission or death]. RESULTS: Patients biopsied for AKI were older (58 ± 16 versus 44 ± 16 years; P < 0.0001), with a higher serum creatinine (SCr) (4.5 ± 2.7 versus 1.8 ± 1.6 mg/dL; P < 0.0001) and lower hemoglobin (Hgb) (10.4 ± 1.7 versus 12.1 ± 2.1; P < 0.0001) and a greater proportion had an abnormal bleeding time (12.5% versus 7.4%, P 0.04), partial thromboplastin time (15.2% versus 5.3%, P < 0.0001) and/or prothrombin time (27.0% versus 12.8%; P < 0.0001) compared with not-AKI patients. Complications post-PRB were significantly greater in patients biopsied for AKI {11.3% versus 6.7%; P=0.04; odds ratio [OR] 1.78 [95% confidence interval (CI) 1.01–3.12]} with patients biopsied for AKI requiring more blood transfusions (10.0% versus 5.3%; P 0.02; OR 2.04 (95% CI 1.12–3.74)]. By multivariate analysis, baseline features predictive of a complication were increased SCr and decreased Hgb level, as well as female gender and increased systolic blood pressure. CONCLUSION: Patients biopsied for evaluation of AKI are at greater risk of complications due to increased risk factors.
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spelling pubmed-61657622018-10-04 Risk of percutaneous renal biopsy of native kidneys in the evaluation of acute kidney injury Korbet, Stephen M Gashti, Casey N Evans, Joni K Whittier, William L Clin Kidney J Diagnostic Tests BACKGROUND: Percutaneous renal biopsy (PRB) of native kidneys (NKs) to better understand and treat acute kidney injury (AKI) is being advocated, but little is known about the risk of complications. METHODS: We performed a retrospective study of PRB of NKs in 955 adults from 1991 to 2015 at an academic medical center with real-time ultrasound and automated biopsy needles. Patients undergoing PRB for evaluation of AKI (n = 160) were compared with 795 patients biopsied for other reasons (not-AKI) for postbiopsy complications [need for transfusion of packed red blood cells (PRBCs), an interventional radiologic or surgical procedure, readmission or death]. RESULTS: Patients biopsied for AKI were older (58 ± 16 versus 44 ± 16 years; P < 0.0001), with a higher serum creatinine (SCr) (4.5 ± 2.7 versus 1.8 ± 1.6 mg/dL; P < 0.0001) and lower hemoglobin (Hgb) (10.4 ± 1.7 versus 12.1 ± 2.1; P < 0.0001) and a greater proportion had an abnormal bleeding time (12.5% versus 7.4%, P 0.04), partial thromboplastin time (15.2% versus 5.3%, P < 0.0001) and/or prothrombin time (27.0% versus 12.8%; P < 0.0001) compared with not-AKI patients. Complications post-PRB were significantly greater in patients biopsied for AKI {11.3% versus 6.7%; P=0.04; odds ratio [OR] 1.78 [95% confidence interval (CI) 1.01–3.12]} with patients biopsied for AKI requiring more blood transfusions (10.0% versus 5.3%; P 0.02; OR 2.04 (95% CI 1.12–3.74)]. By multivariate analysis, baseline features predictive of a complication were increased SCr and decreased Hgb level, as well as female gender and increased systolic blood pressure. CONCLUSION: Patients biopsied for evaluation of AKI are at greater risk of complications due to increased risk factors. Oxford University Press 2018-10 2018-07-02 /pmc/articles/PMC6165762/ /pubmed/30289129 http://dx.doi.org/10.1093/ckj/sfy048 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Diagnostic Tests
Korbet, Stephen M
Gashti, Casey N
Evans, Joni K
Whittier, William L
Risk of percutaneous renal biopsy of native kidneys in the evaluation of acute kidney injury
title Risk of percutaneous renal biopsy of native kidneys in the evaluation of acute kidney injury
title_full Risk of percutaneous renal biopsy of native kidneys in the evaluation of acute kidney injury
title_fullStr Risk of percutaneous renal biopsy of native kidneys in the evaluation of acute kidney injury
title_full_unstemmed Risk of percutaneous renal biopsy of native kidneys in the evaluation of acute kidney injury
title_short Risk of percutaneous renal biopsy of native kidneys in the evaluation of acute kidney injury
title_sort risk of percutaneous renal biopsy of native kidneys in the evaluation of acute kidney injury
topic Diagnostic Tests
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165762/
https://www.ncbi.nlm.nih.gov/pubmed/30289129
http://dx.doi.org/10.1093/ckj/sfy048
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