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Early hospital readmissions after ABO- or HLA- incompatible living donor kidney transplantation
Early hospital readmission (EHR) after kidney transplantation (KT) is associated with adverse outcomes and significant healthcare costs. Despite survival benefits, ABO- and HLA-incompatible (ABOi and HLAi) KTs require desensitization and potent immunosuppression that increase risk of EHR. However, l...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397202/ https://www.ncbi.nlm.nih.gov/pubmed/30824777 http://dx.doi.org/10.1038/s41598-019-39841-8 |
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author | Lee, Juhan Kim, Deok Gie Kim, Beom Seok Kim, Myoung Soo Il Kim, Soon Kim, Yu Seun Huh, Kyu Ha |
author_facet | Lee, Juhan Kim, Deok Gie Kim, Beom Seok Kim, Myoung Soo Il Kim, Soon Kim, Yu Seun Huh, Kyu Ha |
author_sort | Lee, Juhan |
collection | PubMed |
description | Early hospital readmission (EHR) after kidney transplantation (KT) is associated with adverse outcomes and significant healthcare costs. Despite survival benefits, ABO- and HLA-incompatible (ABOi and HLAi) KTs require desensitization and potent immunosuppression that increase risk of EHR. However, little data exist regarding EHR after incompatible KT. We defined EHR as admission for any reason within 30 days of discharge from the index hospitalization. Patients who underwent living donor KT from 2010–2017 were classified into one of three groups (control, ABOi KT, or HLAi KT). Our study included 732 patients, 96 (13.1%) of who experienced EHR. HLAi KT patients had a significantly higher incidence of EHR than other groups (26.6%; P < 0.001). In addition, HLAi KT (HR, 2.26; 95% CI, 1.35–3.77; P = 0.002) and advanced age (≥60 years) (HR, 1.93; 95% CI, 1.20–3.12; P = 0.007) were independent risk factors for EHR. Patients with EHR showed 1.5 times and 3 times greater risk of late hospital readmission and death-censored graft loss, respectively, and consistently exhibited inferior renal function compared to those without EHR, regardless of immunologic incompatibilities. We recommend that KT recipients experiencing EHR or its risk factors be managed with extreme care due to their increased susceptibility to adverse outcomes. |
format | Online Article Text |
id | pubmed-6397202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63972022019-03-05 Early hospital readmissions after ABO- or HLA- incompatible living donor kidney transplantation Lee, Juhan Kim, Deok Gie Kim, Beom Seok Kim, Myoung Soo Il Kim, Soon Kim, Yu Seun Huh, Kyu Ha Sci Rep Article Early hospital readmission (EHR) after kidney transplantation (KT) is associated with adverse outcomes and significant healthcare costs. Despite survival benefits, ABO- and HLA-incompatible (ABOi and HLAi) KTs require desensitization and potent immunosuppression that increase risk of EHR. However, little data exist regarding EHR after incompatible KT. We defined EHR as admission for any reason within 30 days of discharge from the index hospitalization. Patients who underwent living donor KT from 2010–2017 were classified into one of three groups (control, ABOi KT, or HLAi KT). Our study included 732 patients, 96 (13.1%) of who experienced EHR. HLAi KT patients had a significantly higher incidence of EHR than other groups (26.6%; P < 0.001). In addition, HLAi KT (HR, 2.26; 95% CI, 1.35–3.77; P = 0.002) and advanced age (≥60 years) (HR, 1.93; 95% CI, 1.20–3.12; P = 0.007) were independent risk factors for EHR. Patients with EHR showed 1.5 times and 3 times greater risk of late hospital readmission and death-censored graft loss, respectively, and consistently exhibited inferior renal function compared to those without EHR, regardless of immunologic incompatibilities. We recommend that KT recipients experiencing EHR or its risk factors be managed with extreme care due to their increased susceptibility to adverse outcomes. Nature Publishing Group UK 2019-03-01 /pmc/articles/PMC6397202/ /pubmed/30824777 http://dx.doi.org/10.1038/s41598-019-39841-8 Text en © The Author(s) 2019 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 Lee, Juhan Kim, Deok Gie Kim, Beom Seok Kim, Myoung Soo Il Kim, Soon Kim, Yu Seun Huh, Kyu Ha Early hospital readmissions after ABO- or HLA- incompatible living donor kidney transplantation |
title | Early hospital readmissions after ABO- or HLA- incompatible living donor kidney transplantation |
title_full | Early hospital readmissions after ABO- or HLA- incompatible living donor kidney transplantation |
title_fullStr | Early hospital readmissions after ABO- or HLA- incompatible living donor kidney transplantation |
title_full_unstemmed | Early hospital readmissions after ABO- or HLA- incompatible living donor kidney transplantation |
title_short | Early hospital readmissions after ABO- or HLA- incompatible living donor kidney transplantation |
title_sort | early hospital readmissions after abo- or hla- incompatible living donor kidney transplantation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397202/ https://www.ncbi.nlm.nih.gov/pubmed/30824777 http://dx.doi.org/10.1038/s41598-019-39841-8 |
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