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Renal Dysfunction After Liver Transplantation: Effect of Donor Type
Recipients of donation after circulatory death (DCD) grafts are reportedly at higher risk of developing renal dysfunction after liver transplantation (LT). We compared the development of acute kidney injury (AKI) and chronic kidney disease (CKD) after LT in recipients of DCD versus donation after br...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317208/ https://www.ncbi.nlm.nih.gov/pubmed/32189415 http://dx.doi.org/10.1002/lt.25755 |
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author | Kollmann, Dagmar Neong, Shuet Fong Rosales, Roizar Hansen, Bettina E. Sapisochin, Gonzalo McCluskey, Stuart Bhat, Mamatha Cattral, Mark S. Lilly, Les McGilvray, Ian D. Ghanekar, Anand Grant, David R. Selzner, Markus Wong, Florence S. H. Selzner, Nazia |
author_facet | Kollmann, Dagmar Neong, Shuet Fong Rosales, Roizar Hansen, Bettina E. Sapisochin, Gonzalo McCluskey, Stuart Bhat, Mamatha Cattral, Mark S. Lilly, Les McGilvray, Ian D. Ghanekar, Anand Grant, David R. Selzner, Markus Wong, Florence S. H. Selzner, Nazia |
author_sort | Kollmann, Dagmar |
collection | PubMed |
description | Recipients of donation after circulatory death (DCD) grafts are reportedly at higher risk of developing renal dysfunction after liver transplantation (LT). We compared the development of acute kidney injury (AKI) and chronic kidney disease (CKD) after LT in recipients of DCD versus donation after brain death (DBD) or living donor liver transplantation (LDLT) livers. Adult recipients of DBD, LDLT, and DCD between 2012 and 2016 at Toronto General Hospital were included. AKI was defined as a post‐LT increase of serum creatinine (sCr) ≥26.5 µmol/L within 48 hours or a ≥50% increase from baseline, and CKD was defined as an estimated glomerular filtration rate <60 mL/minute for >3 months. A total of 681 patients (DCD, n = 57; DBD, n = 446; and LDLT, n = 178) with similar baseline comorbidities were included. Perioperative AKI (within the first 7 postoperative days) was observed more frequently in the DCD group (61%; DBD, 40%; and LDLT, 44%; P = 0.01) and was associated with significantly higher peak AST levels (P < 0.001). Additionally, patients in the DCD group had a significantly higher peak sCr (P < 0.001) and a trend toward higher rates of AKI stage 3 (DCD, 33%; DBD, 21%; LDLT, 21%; P = 0.11). The proportions of recovery from AKI (DCD, 77%; DBD, 72%; LDLT, 78%; P = 0.45) and patients developing CKD (DCD, 33%; DBD, 32%; LDLT, 32%; P = 0.99) were similar. Nevertheless, patients who received DCD or DBD LT and required perioperative renal replacement therapy showed significantly lower patient survival in multivariate analysis (hazard ratio, 7.90; 95% confidence interval, 4.51‐13.83; P < 0.001). In conclusion, recipients of DCD liver grafts experience higher rates of short‐term post‐LT renal dysfunction compared with DBD or LDLT. Additional risk factors for the development of severe kidney injury, such as high Model for End‐Stage Liver Disease score, massive transfusions, or donor age ≥60 years should be avoided. |
format | Online Article Text |
id | pubmed-7317208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73172082020-06-30 Renal Dysfunction After Liver Transplantation: Effect of Donor Type Kollmann, Dagmar Neong, Shuet Fong Rosales, Roizar Hansen, Bettina E. Sapisochin, Gonzalo McCluskey, Stuart Bhat, Mamatha Cattral, Mark S. Lilly, Les McGilvray, Ian D. Ghanekar, Anand Grant, David R. Selzner, Markus Wong, Florence S. H. Selzner, Nazia Liver Transpl Original Articles Recipients of donation after circulatory death (DCD) grafts are reportedly at higher risk of developing renal dysfunction after liver transplantation (LT). We compared the development of acute kidney injury (AKI) and chronic kidney disease (CKD) after LT in recipients of DCD versus donation after brain death (DBD) or living donor liver transplantation (LDLT) livers. Adult recipients of DBD, LDLT, and DCD between 2012 and 2016 at Toronto General Hospital were included. AKI was defined as a post‐LT increase of serum creatinine (sCr) ≥26.5 µmol/L within 48 hours or a ≥50% increase from baseline, and CKD was defined as an estimated glomerular filtration rate <60 mL/minute for >3 months. A total of 681 patients (DCD, n = 57; DBD, n = 446; and LDLT, n = 178) with similar baseline comorbidities were included. Perioperative AKI (within the first 7 postoperative days) was observed more frequently in the DCD group (61%; DBD, 40%; and LDLT, 44%; P = 0.01) and was associated with significantly higher peak AST levels (P < 0.001). Additionally, patients in the DCD group had a significantly higher peak sCr (P < 0.001) and a trend toward higher rates of AKI stage 3 (DCD, 33%; DBD, 21%; LDLT, 21%; P = 0.11). The proportions of recovery from AKI (DCD, 77%; DBD, 72%; LDLT, 78%; P = 0.45) and patients developing CKD (DCD, 33%; DBD, 32%; LDLT, 32%; P = 0.99) were similar. Nevertheless, patients who received DCD or DBD LT and required perioperative renal replacement therapy showed significantly lower patient survival in multivariate analysis (hazard ratio, 7.90; 95% confidence interval, 4.51‐13.83; P < 0.001). In conclusion, recipients of DCD liver grafts experience higher rates of short‐term post‐LT renal dysfunction compared with DBD or LDLT. Additional risk factors for the development of severe kidney injury, such as high Model for End‐Stage Liver Disease score, massive transfusions, or donor age ≥60 years should be avoided. John Wiley and Sons Inc. 2020-04-23 2020-06 /pmc/articles/PMC7317208/ /pubmed/32189415 http://dx.doi.org/10.1002/lt.25755 Text en Copyright © 2020 The Authors. Liver Transplantation published by Wiley Periodicals Inc., on behalf of American Association for the Study Liver Diseases. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Kollmann, Dagmar Neong, Shuet Fong Rosales, Roizar Hansen, Bettina E. Sapisochin, Gonzalo McCluskey, Stuart Bhat, Mamatha Cattral, Mark S. Lilly, Les McGilvray, Ian D. Ghanekar, Anand Grant, David R. Selzner, Markus Wong, Florence S. H. Selzner, Nazia Renal Dysfunction After Liver Transplantation: Effect of Donor Type |
title | Renal Dysfunction After Liver Transplantation: Effect of Donor Type |
title_full | Renal Dysfunction After Liver Transplantation: Effect of Donor Type |
title_fullStr | Renal Dysfunction After Liver Transplantation: Effect of Donor Type |
title_full_unstemmed | Renal Dysfunction After Liver Transplantation: Effect of Donor Type |
title_short | Renal Dysfunction After Liver Transplantation: Effect of Donor Type |
title_sort | renal dysfunction after liver transplantation: effect of donor type |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317208/ https://www.ncbi.nlm.nih.gov/pubmed/32189415 http://dx.doi.org/10.1002/lt.25755 |
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