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Kidney function and mortality post-liver transplant in the Model for End-Stage Liver Disease era
The Model for End-Stage Liver Disease (MELD) score incorporates serum creatinine and was introduced to facilitate allocation of orthotopic liver transplantation (LT). The objective is to determine the impact of MELD and kidney function on all-cause mortality. Among LTs performed in a tertiary referr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234151/ https://www.ncbi.nlm.nih.gov/pubmed/22163170 http://dx.doi.org/10.2147/IJNRD.S24812 |
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author | Sethi, Aastha Estrella, Michelle M Ugarte, Richard Atta, Mohamed G |
author_facet | Sethi, Aastha Estrella, Michelle M Ugarte, Richard Atta, Mohamed G |
author_sort | Sethi, Aastha |
collection | PubMed |
description | The Model for End-Stage Liver Disease (MELD) score incorporates serum creatinine and was introduced to facilitate allocation of orthotopic liver transplantation (LT). The objective is to determine the impact of MELD and kidney function on all-cause mortality. Among LTs performed in a tertiary referral hospital between 1995 and 2009, 419 cases were studied. Cox proportional hazards models were constructed to estimate the hazard ratios (HR) and 95% confidence intervals (CI) for death. Over mean follow-ups of 8.4 and 3.1 years during the pre-MELD and MELD era, 57 and 63 deaths were observed, respectively. Those transplanted during the MELD era had a higher likelihood of hepatorenal syndrome (8% vs 2%, P < 0.01), lower kidney function (median estimated glomerular filtration rate [eGFR] 77.8 vs 92.6 mL/ min/1.73 m(2), P < 0.01), and more pretransplantation renal replacement therapy (RRT) (5% vs 1%; P < 0.01). All-cause mortality risk was similar in the MELD vs the pre-MELD era (HR: 0.98, 95% CI: 0.58–1.65). The risk of death, however, was nearly 3-fold greater (95% CI: 1.14–6.60) among those requiring pre- transplant RRT. Similarly, eGFR < 60 mL/min/1.73 m(2) post-transplant was associated with a 2.5-fold higher mortality (95% CI: 1.48–4.11). The study suggests that MELD implementation had no impact on all-cause mortality post-LT. However, the need for pre-transplant RRT and post-transplant kidney dysfunction was associated with a more than 2-fold greater risk of subsequent death. |
format | Online Article Text |
id | pubmed-3234151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32341512011-12-12 Kidney function and mortality post-liver transplant in the Model for End-Stage Liver Disease era Sethi, Aastha Estrella, Michelle M Ugarte, Richard Atta, Mohamed G Int J Nephrol Renovasc Dis Original Research The Model for End-Stage Liver Disease (MELD) score incorporates serum creatinine and was introduced to facilitate allocation of orthotopic liver transplantation (LT). The objective is to determine the impact of MELD and kidney function on all-cause mortality. Among LTs performed in a tertiary referral hospital between 1995 and 2009, 419 cases were studied. Cox proportional hazards models were constructed to estimate the hazard ratios (HR) and 95% confidence intervals (CI) for death. Over mean follow-ups of 8.4 and 3.1 years during the pre-MELD and MELD era, 57 and 63 deaths were observed, respectively. Those transplanted during the MELD era had a higher likelihood of hepatorenal syndrome (8% vs 2%, P < 0.01), lower kidney function (median estimated glomerular filtration rate [eGFR] 77.8 vs 92.6 mL/ min/1.73 m(2), P < 0.01), and more pretransplantation renal replacement therapy (RRT) (5% vs 1%; P < 0.01). All-cause mortality risk was similar in the MELD vs the pre-MELD era (HR: 0.98, 95% CI: 0.58–1.65). The risk of death, however, was nearly 3-fold greater (95% CI: 1.14–6.60) among those requiring pre- transplant RRT. Similarly, eGFR < 60 mL/min/1.73 m(2) post-transplant was associated with a 2.5-fold higher mortality (95% CI: 1.48–4.11). The study suggests that MELD implementation had no impact on all-cause mortality post-LT. However, the need for pre-transplant RRT and post-transplant kidney dysfunction was associated with a more than 2-fold greater risk of subsequent death. Dove Medical Press 2011-11-03 /pmc/articles/PMC3234151/ /pubmed/22163170 http://dx.doi.org/10.2147/IJNRD.S24812 Text en © 2011 Sethi et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Sethi, Aastha Estrella, Michelle M Ugarte, Richard Atta, Mohamed G Kidney function and mortality post-liver transplant in the Model for End-Stage Liver Disease era |
title | Kidney function and mortality post-liver transplant in the Model for End-Stage Liver Disease era |
title_full | Kidney function and mortality post-liver transplant in the Model for End-Stage Liver Disease era |
title_fullStr | Kidney function and mortality post-liver transplant in the Model for End-Stage Liver Disease era |
title_full_unstemmed | Kidney function and mortality post-liver transplant in the Model for End-Stage Liver Disease era |
title_short | Kidney function and mortality post-liver transplant in the Model for End-Stage Liver Disease era |
title_sort | kidney function and mortality post-liver transplant in the model for end-stage liver disease era |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234151/ https://www.ncbi.nlm.nih.gov/pubmed/22163170 http://dx.doi.org/10.2147/IJNRD.S24812 |
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