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Vascular Multiplicity Should Not Be a Contra-Indication for Live Kidney Donation and Transplantation
BACKGROUND: Whether vascular multiplicity should be considered as contraindication and therefore ‘extended donor criterion’ is still under debate. METHODS: Data from all live kidney donors from 2006–2013 (n = 951) was retrospectively reviewed. Vascular anatomy as imaged by MRA, CTA or other modaliti...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831799/ https://www.ncbi.nlm.nih.gov/pubmed/27077904 http://dx.doi.org/10.1371/journal.pone.0153460 |
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author | Lafranca, Jeffrey A. van Bruggen, Mark Kimenai, Hendrikus J. A. N. Tran, Thi C. K. Terkivatan, Türkan Betjes, Michiel G. H. IJzermans, Jan N. M. Dor, Frank J. M. F. |
author_facet | Lafranca, Jeffrey A. van Bruggen, Mark Kimenai, Hendrikus J. A. N. Tran, Thi C. K. Terkivatan, Türkan Betjes, Michiel G. H. IJzermans, Jan N. M. Dor, Frank J. M. F. |
author_sort | Lafranca, Jeffrey A. |
collection | PubMed |
description | BACKGROUND: Whether vascular multiplicity should be considered as contraindication and therefore ‘extended donor criterion’ is still under debate. METHODS: Data from all live kidney donors from 2006–2013 (n = 951) was retrospectively reviewed. Vascular anatomy as imaged by MRA, CTA or other modalities was compared with intraoperative findings. Furthermore, the influence of vascular multiplicity on outcome of donors and recipients was studied. RESULTS: In 237 out of 951 donors (25%), vascular multiplicity was present. CTA had the highest accuracy levels regarding vascular anatomy assessment. Regarding outcome of donors with vascular multiplicity, warm ischemia time (WIT) and skin-to-skin time were significantly longer if arterial multiplicity (AM) was present (5.1 vs. 4.0 mins and 202 vs. 178 mins). Skin-to-skin time was significantly longer, and complication rates were higher in donors with venous multiplicity (203 vs. 180 mins and 17.2% vs. 8.4%). Outcome of renal transplant recipients showed a significantly increased WIT (30 vs. 26.7 minutes), higher rate of DGF (13.9% vs. 6.9%) and lower rate of BPAR (6.9% vs. 13.9%) in patients receiving a kidney with AM compared to kidneys with singular anatomy. CONCLUSIONS: We conclude that vascular multiplicity should not be a contra-indication, since it has little impact on clinical outcome in the donor as well as in renal transplant recipients. |
format | Online Article Text |
id | pubmed-4831799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48317992016-04-22 Vascular Multiplicity Should Not Be a Contra-Indication for Live Kidney Donation and Transplantation Lafranca, Jeffrey A. van Bruggen, Mark Kimenai, Hendrikus J. A. N. Tran, Thi C. K. Terkivatan, Türkan Betjes, Michiel G. H. IJzermans, Jan N. M. Dor, Frank J. M. F. PLoS One Research Article BACKGROUND: Whether vascular multiplicity should be considered as contraindication and therefore ‘extended donor criterion’ is still under debate. METHODS: Data from all live kidney donors from 2006–2013 (n = 951) was retrospectively reviewed. Vascular anatomy as imaged by MRA, CTA or other modalities was compared with intraoperative findings. Furthermore, the influence of vascular multiplicity on outcome of donors and recipients was studied. RESULTS: In 237 out of 951 donors (25%), vascular multiplicity was present. CTA had the highest accuracy levels regarding vascular anatomy assessment. Regarding outcome of donors with vascular multiplicity, warm ischemia time (WIT) and skin-to-skin time were significantly longer if arterial multiplicity (AM) was present (5.1 vs. 4.0 mins and 202 vs. 178 mins). Skin-to-skin time was significantly longer, and complication rates were higher in donors with venous multiplicity (203 vs. 180 mins and 17.2% vs. 8.4%). Outcome of renal transplant recipients showed a significantly increased WIT (30 vs. 26.7 minutes), higher rate of DGF (13.9% vs. 6.9%) and lower rate of BPAR (6.9% vs. 13.9%) in patients receiving a kidney with AM compared to kidneys with singular anatomy. CONCLUSIONS: We conclude that vascular multiplicity should not be a contra-indication, since it has little impact on clinical outcome in the donor as well as in renal transplant recipients. Public Library of Science 2016-04-14 /pmc/articles/PMC4831799/ /pubmed/27077904 http://dx.doi.org/10.1371/journal.pone.0153460 Text en © 2016 Lafranca et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lafranca, Jeffrey A. van Bruggen, Mark Kimenai, Hendrikus J. A. N. Tran, Thi C. K. Terkivatan, Türkan Betjes, Michiel G. H. IJzermans, Jan N. M. Dor, Frank J. M. F. Vascular Multiplicity Should Not Be a Contra-Indication for Live Kidney Donation and Transplantation |
title | Vascular Multiplicity Should Not Be a Contra-Indication for Live Kidney Donation and Transplantation |
title_full | Vascular Multiplicity Should Not Be a Contra-Indication for Live Kidney Donation and Transplantation |
title_fullStr | Vascular Multiplicity Should Not Be a Contra-Indication for Live Kidney Donation and Transplantation |
title_full_unstemmed | Vascular Multiplicity Should Not Be a Contra-Indication for Live Kidney Donation and Transplantation |
title_short | Vascular Multiplicity Should Not Be a Contra-Indication for Live Kidney Donation and Transplantation |
title_sort | vascular multiplicity should not be a contra-indication for live kidney donation and transplantation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831799/ https://www.ncbi.nlm.nih.gov/pubmed/27077904 http://dx.doi.org/10.1371/journal.pone.0153460 |
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