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Cerebrovascular events in hemodialysis patients; a retrospective observational study

BACKGROUND: This study reports findings in subjects who underwent brain imaging for any reason, and examined factors influencing cerebrovascular events (CVEs) in hemodialysis (HD) patients. METHODS: We reviewed the files of patients on HD between January 2015 and January 2018. A total of 432 patient...

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Autores principales: Ozelsancak, Ruya, Micozkadioglu, Hasan, Torun, Dilek, Tekkarismaz, Nihan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909467/
https://www.ncbi.nlm.nih.gov/pubmed/31830923
http://dx.doi.org/10.1186/s12882-019-1629-y
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author Ozelsancak, Ruya
Micozkadioglu, Hasan
Torun, Dilek
Tekkarismaz, Nihan
author_facet Ozelsancak, Ruya
Micozkadioglu, Hasan
Torun, Dilek
Tekkarismaz, Nihan
author_sort Ozelsancak, Ruya
collection PubMed
description BACKGROUND: This study reports findings in subjects who underwent brain imaging for any reason, and examined factors influencing cerebrovascular events (CVEs) in hemodialysis (HD) patients. METHODS: We reviewed the files of patients on HD between January 2015 and January 2018. A total of 432 patients who underwent HD for at least 5 months by the January 2015 and who were older than 18 years were included in the study; 264 had been examined by cerebral computed tomography or magnetic resonance imaging examination within the 3 years. Cerebrovascular pathology was detected in 139 of 264 patients. RESULTS: Of the 139 patients, 65 (24.62%) had ischemic lesions, 25 (9.47%) had hemorrhagic lesions, and 49 (18.56%) had cerebral small vessel disease (CSVD). We compared recorded data and later clinical findings between patients with and those without CVEs. The cause of end-stage renal disease was diabetes in 58.5% of patients with ischemic lesions, 52% in those with hemorrhagic lesions, and 55% in those with CSVD (P < 0.05). Patients with cerebrovascular ischemia were older (P = 0.0001) and had lower serum creatinine (sCr) (P = 0.0001) and higher serum C-reactive protein (CRP) (P = 0.002) levels than normal subjects. Hemorrhagic patients were older (P = 0.003) and had lower sCr (P = 0.003) and serum predialysis potassium (P = 0.003) and parathyroid hormone (PTH) (P = 0.004) levels than normal subjects. Patients with CSVD were older (P < 0.0001) and had lower sCr (P < 0.0001), phosphorus (P < 0.007), and PTH (P < 0.013) and higher CRP (P < 0.002) levels than normal subjects. CONCLUSIONS: HD patients with CVEs are older and typically have diabetes mellitus and lower sCr levels.
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spelling pubmed-69094672019-12-19 Cerebrovascular events in hemodialysis patients; a retrospective observational study Ozelsancak, Ruya Micozkadioglu, Hasan Torun, Dilek Tekkarismaz, Nihan BMC Nephrol Research Article BACKGROUND: This study reports findings in subjects who underwent brain imaging for any reason, and examined factors influencing cerebrovascular events (CVEs) in hemodialysis (HD) patients. METHODS: We reviewed the files of patients on HD between January 2015 and January 2018. A total of 432 patients who underwent HD for at least 5 months by the January 2015 and who were older than 18 years were included in the study; 264 had been examined by cerebral computed tomography or magnetic resonance imaging examination within the 3 years. Cerebrovascular pathology was detected in 139 of 264 patients. RESULTS: Of the 139 patients, 65 (24.62%) had ischemic lesions, 25 (9.47%) had hemorrhagic lesions, and 49 (18.56%) had cerebral small vessel disease (CSVD). We compared recorded data and later clinical findings between patients with and those without CVEs. The cause of end-stage renal disease was diabetes in 58.5% of patients with ischemic lesions, 52% in those with hemorrhagic lesions, and 55% in those with CSVD (P < 0.05). Patients with cerebrovascular ischemia were older (P = 0.0001) and had lower serum creatinine (sCr) (P = 0.0001) and higher serum C-reactive protein (CRP) (P = 0.002) levels than normal subjects. Hemorrhagic patients were older (P = 0.003) and had lower sCr (P = 0.003) and serum predialysis potassium (P = 0.003) and parathyroid hormone (PTH) (P = 0.004) levels than normal subjects. Patients with CSVD were older (P < 0.0001) and had lower sCr (P < 0.0001), phosphorus (P < 0.007), and PTH (P < 0.013) and higher CRP (P < 0.002) levels than normal subjects. CONCLUSIONS: HD patients with CVEs are older and typically have diabetes mellitus and lower sCr levels. BioMed Central 2019-12-12 /pmc/articles/PMC6909467/ /pubmed/31830923 http://dx.doi.org/10.1186/s12882-019-1629-y Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ozelsancak, Ruya
Micozkadioglu, Hasan
Torun, Dilek
Tekkarismaz, Nihan
Cerebrovascular events in hemodialysis patients; a retrospective observational study
title Cerebrovascular events in hemodialysis patients; a retrospective observational study
title_full Cerebrovascular events in hemodialysis patients; a retrospective observational study
title_fullStr Cerebrovascular events in hemodialysis patients; a retrospective observational study
title_full_unstemmed Cerebrovascular events in hemodialysis patients; a retrospective observational study
title_short Cerebrovascular events in hemodialysis patients; a retrospective observational study
title_sort cerebrovascular events in hemodialysis patients; a retrospective observational study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909467/
https://www.ncbi.nlm.nih.gov/pubmed/31830923
http://dx.doi.org/10.1186/s12882-019-1629-y
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