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Diagnosis and Treatment of Renal Artery Stenosis in China in the Era of Donation After Cardiac Death

BACKGROUND: The aim of this study was to investigate the clinical features and treatment strategies of transplant renal artery stenosis (TRAS) with kidneys from donation after cardiac death (DCD). MATERIAL/METHODS: We collected the clinical data of donors and recipients of single-center DCD-induced...

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Autores principales: Wang, Qiang, Li, Xiaoli, Liu, Zhijia, Xu, Junnan, Han, Yong, Yu, Tao, Chen, Song, Tang, Yuzhe, Liu, Yubao, Li, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023544/
https://www.ncbi.nlm.nih.gov/pubmed/32015300
http://dx.doi.org/10.12659/AOT.918076
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author Wang, Qiang
Li, Xiaoli
Liu, Zhijia
Xu, Junnan
Han, Yong
Yu, Tao
Chen, Song
Tang, Yuzhe
Liu, Yubao
Li, Xiang
author_facet Wang, Qiang
Li, Xiaoli
Liu, Zhijia
Xu, Junnan
Han, Yong
Yu, Tao
Chen, Song
Tang, Yuzhe
Liu, Yubao
Li, Xiang
author_sort Wang, Qiang
collection PubMed
description BACKGROUND: The aim of this study was to investigate the clinical features and treatment strategies of transplant renal artery stenosis (TRAS) with kidneys from donation after cardiac death (DCD). MATERIAL/METHODS: We collected the clinical data of donors and recipients of single-center DCD-induced TRAS from January 2015 to June 2017. RESULTS: All the 8 cases of TRAS were from hypertensive cerebrovascular accident DCD-originated kidneys. The mean donor age was 53.5 (45~57) years, with mean BMI 27.8 (26.4~32.3) kg/m(2), atherosclerosis index 5.8 (4.9~7.0), and renal atherosclerotic plaque. Clinical features of TRAS were: refractory hypertension with elevated serum creatinine >50%, and negative urine protein and occult blood. Ultrasound of transplanted kidneys showed renal blood flow index 0.49 (0.43~0.55). Angiography confirmed the diagnosis of renal artery trunk or secondary branch stenosis. There were 2 cases of moderate stenosis and 6 cases of severe stenosis. Six patients underwent stent implantation and 2 patients underwent balloon dilatation. Seven patients had serum creatinine recovery after interventional therapy during follow-up. The transplanted kidney of 1 patient ruptured 6 h after interventional therapy and was then resected. CONCLUSIONS: The incidence of TRAS with hypertensive cerebrovascular accident DCD-originated kidneys is relatively high, which is a warning to kidney transplant physicians. Digital subtraction angiography (DSA) is the most reliable diagnostic means of TRAS and can be performed concurrently with intervention therapy. If the donor has severe atherosclerosis, plaques that are visible to the unaided eye in the renal artery trunk should be removed as completely as possible.
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spelling pubmed-70235442020-03-06 Diagnosis and Treatment of Renal Artery Stenosis in China in the Era of Donation After Cardiac Death Wang, Qiang Li, Xiaoli Liu, Zhijia Xu, Junnan Han, Yong Yu, Tao Chen, Song Tang, Yuzhe Liu, Yubao Li, Xiang Ann Transplant Original Paper BACKGROUND: The aim of this study was to investigate the clinical features and treatment strategies of transplant renal artery stenosis (TRAS) with kidneys from donation after cardiac death (DCD). MATERIAL/METHODS: We collected the clinical data of donors and recipients of single-center DCD-induced TRAS from January 2015 to June 2017. RESULTS: All the 8 cases of TRAS were from hypertensive cerebrovascular accident DCD-originated kidneys. The mean donor age was 53.5 (45~57) years, with mean BMI 27.8 (26.4~32.3) kg/m(2), atherosclerosis index 5.8 (4.9~7.0), and renal atherosclerotic plaque. Clinical features of TRAS were: refractory hypertension with elevated serum creatinine >50%, and negative urine protein and occult blood. Ultrasound of transplanted kidneys showed renal blood flow index 0.49 (0.43~0.55). Angiography confirmed the diagnosis of renal artery trunk or secondary branch stenosis. There were 2 cases of moderate stenosis and 6 cases of severe stenosis. Six patients underwent stent implantation and 2 patients underwent balloon dilatation. Seven patients had serum creatinine recovery after interventional therapy during follow-up. The transplanted kidney of 1 patient ruptured 6 h after interventional therapy and was then resected. CONCLUSIONS: The incidence of TRAS with hypertensive cerebrovascular accident DCD-originated kidneys is relatively high, which is a warning to kidney transplant physicians. Digital subtraction angiography (DSA) is the most reliable diagnostic means of TRAS and can be performed concurrently with intervention therapy. If the donor has severe atherosclerosis, plaques that are visible to the unaided eye in the renal artery trunk should be removed as completely as possible. International Scientific Literature, Inc. 2020-02-04 /pmc/articles/PMC7023544/ /pubmed/32015300 http://dx.doi.org/10.12659/AOT.918076 Text en © Ann Transplant, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Original Paper
Wang, Qiang
Li, Xiaoli
Liu, Zhijia
Xu, Junnan
Han, Yong
Yu, Tao
Chen, Song
Tang, Yuzhe
Liu, Yubao
Li, Xiang
Diagnosis and Treatment of Renal Artery Stenosis in China in the Era of Donation After Cardiac Death
title Diagnosis and Treatment of Renal Artery Stenosis in China in the Era of Donation After Cardiac Death
title_full Diagnosis and Treatment of Renal Artery Stenosis in China in the Era of Donation After Cardiac Death
title_fullStr Diagnosis and Treatment of Renal Artery Stenosis in China in the Era of Donation After Cardiac Death
title_full_unstemmed Diagnosis and Treatment of Renal Artery Stenosis in China in the Era of Donation After Cardiac Death
title_short Diagnosis and Treatment of Renal Artery Stenosis in China in the Era of Donation After Cardiac Death
title_sort diagnosis and treatment of renal artery stenosis in china in the era of donation after cardiac death
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023544/
https://www.ncbi.nlm.nih.gov/pubmed/32015300
http://dx.doi.org/10.12659/AOT.918076
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