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Preoperative Comorbidities and Outcomes of Medically Complex Living Kidney Donors

INTRODUCTION: Recent reports have described an increased risk of renal disease in living kidney donors compared with the general population. However, these reports do not detail the outcomes of medically complex living donors (MCLDs) with preoperative comorbidities (PCs), such as hypertension, dysli...

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Autores principales: Hiramitsu, Takahisa, Tomosugi, Toshihide, Futamura, Kenta, Okada, Manabu, Tsujita, Makoto, Goto, Norihiko, Ichimori, Toshihiro, Narumi, Shunji, Takeda, Asami, Watarai, Yoshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943774/
https://www.ncbi.nlm.nih.gov/pubmed/31922057
http://dx.doi.org/10.1016/j.ekir.2019.10.002
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author Hiramitsu, Takahisa
Tomosugi, Toshihide
Futamura, Kenta
Okada, Manabu
Tsujita, Makoto
Goto, Norihiko
Ichimori, Toshihiro
Narumi, Shunji
Takeda, Asami
Watarai, Yoshihiko
author_facet Hiramitsu, Takahisa
Tomosugi, Toshihide
Futamura, Kenta
Okada, Manabu
Tsujita, Makoto
Goto, Norihiko
Ichimori, Toshihiro
Narumi, Shunji
Takeda, Asami
Watarai, Yoshihiko
author_sort Hiramitsu, Takahisa
collection PubMed
description INTRODUCTION: Recent reports have described an increased risk of renal disease in living kidney donors compared with the general population. However, these reports do not detail the outcomes of medically complex living donors (MCLDs) with preoperative comorbidities (PCs), such as hypertension, dyslipidemia, glucose intolerance, and obesity. Analysis of living donors with end-stage renal disease (ESRD) has shown that these PCs may contribute significantly to the development of ESRD. We aimed to evaluate the effect of PCs on postoperative renal function and mortality in MCLDs. METHODS: Between January 2008 and December 2016, 807 living-donor kidney transplants were performed in our unit. Of these, 802 donors completed postoperative follow-up of >5 months. Donors were stratified into 4 groups based on the number of PCs present: healthy living donors (HLDs) with no PCs (n = 214) or MCLDs with 1 PC (n = 302), 2 PCs (n = 196), or 3 PCs (n = 90) (denoted MCLD [PC 1], MCLD [PC 2], or MCLD [PC 3], respectively). We compared pathology observation data from baseline biopsy, postoperative estimated glomerular filtration rate (eGFR), postoperative urinary protein concentration, and mortality between HLD and MCLD groups. RESULTS: Interstitial fibrosis, tubular atrophy, glomerulosclerosis, and arteriolosclerosis were more frequent in MCLDs (PC 3) than in HLDs. No significant differences were identified between HLDs and MCLDs in terms of postoperative eGFR and short-term mortality. Overt proteinuria and ESRD were not observed. CONCLUSIONS: Appropriate postdonation management of MCLDs with PCs may result in similar outcomes as for HLDs.
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spelling pubmed-69437742020-01-09 Preoperative Comorbidities and Outcomes of Medically Complex Living Kidney Donors Hiramitsu, Takahisa Tomosugi, Toshihide Futamura, Kenta Okada, Manabu Tsujita, Makoto Goto, Norihiko Ichimori, Toshihiro Narumi, Shunji Takeda, Asami Watarai, Yoshihiko Kidney Int Rep Clinical Research INTRODUCTION: Recent reports have described an increased risk of renal disease in living kidney donors compared with the general population. However, these reports do not detail the outcomes of medically complex living donors (MCLDs) with preoperative comorbidities (PCs), such as hypertension, dyslipidemia, glucose intolerance, and obesity. Analysis of living donors with end-stage renal disease (ESRD) has shown that these PCs may contribute significantly to the development of ESRD. We aimed to evaluate the effect of PCs on postoperative renal function and mortality in MCLDs. METHODS: Between January 2008 and December 2016, 807 living-donor kidney transplants were performed in our unit. Of these, 802 donors completed postoperative follow-up of >5 months. Donors were stratified into 4 groups based on the number of PCs present: healthy living donors (HLDs) with no PCs (n = 214) or MCLDs with 1 PC (n = 302), 2 PCs (n = 196), or 3 PCs (n = 90) (denoted MCLD [PC 1], MCLD [PC 2], or MCLD [PC 3], respectively). We compared pathology observation data from baseline biopsy, postoperative estimated glomerular filtration rate (eGFR), postoperative urinary protein concentration, and mortality between HLD and MCLD groups. RESULTS: Interstitial fibrosis, tubular atrophy, glomerulosclerosis, and arteriolosclerosis were more frequent in MCLDs (PC 3) than in HLDs. No significant differences were identified between HLDs and MCLDs in terms of postoperative eGFR and short-term mortality. Overt proteinuria and ESRD were not observed. CONCLUSIONS: Appropriate postdonation management of MCLDs with PCs may result in similar outcomes as for HLDs. Elsevier 2019-10-10 /pmc/articles/PMC6943774/ /pubmed/31922057 http://dx.doi.org/10.1016/j.ekir.2019.10.002 Text en © 2019 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Clinical Research
Hiramitsu, Takahisa
Tomosugi, Toshihide
Futamura, Kenta
Okada, Manabu
Tsujita, Makoto
Goto, Norihiko
Ichimori, Toshihiro
Narumi, Shunji
Takeda, Asami
Watarai, Yoshihiko
Preoperative Comorbidities and Outcomes of Medically Complex Living Kidney Donors
title Preoperative Comorbidities and Outcomes of Medically Complex Living Kidney Donors
title_full Preoperative Comorbidities and Outcomes of Medically Complex Living Kidney Donors
title_fullStr Preoperative Comorbidities and Outcomes of Medically Complex Living Kidney Donors
title_full_unstemmed Preoperative Comorbidities and Outcomes of Medically Complex Living Kidney Donors
title_short Preoperative Comorbidities and Outcomes of Medically Complex Living Kidney Donors
title_sort preoperative comorbidities and outcomes of medically complex living kidney donors
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943774/
https://www.ncbi.nlm.nih.gov/pubmed/31922057
http://dx.doi.org/10.1016/j.ekir.2019.10.002
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