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Ocular changes during hemodialysis in patients with end-stage renal disease
BACKGROUND: To explore ocular changes during hemodialysis (HD) in chronic renal failure patients and to determine the effects of different causes of renal failure during HD. METHODS: A total of 90 eyes from 45 end-stage renal disease (ESRD) patients undergoing HD were evaluated in this study. All op...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107936/ https://www.ncbi.nlm.nih.gov/pubmed/30139333 http://dx.doi.org/10.1186/s12886-018-0885-0 |
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author | Chen, Hejun Zhang, Xi Shen, Xi |
author_facet | Chen, Hejun Zhang, Xi Shen, Xi |
author_sort | Chen, Hejun |
collection | PubMed |
description | BACKGROUND: To explore ocular changes during hemodialysis (HD) in chronic renal failure patients and to determine the effects of different causes of renal failure during HD. METHODS: A total of 90 eyes from 45 end-stage renal disease (ESRD) patients undergoing HD were evaluated in this study. All ophthalmological examinations were conducted within 1 h before and after a single HD session. The HD patients were divided into primary kidney disease (KD), hypertensive KD, diabetic KD (DM-KD) and unknown etiology subgroups according to the primary etiology of renal failure. The statistics of 38 eyes from 19 healthy people were set as normal control. RESULTS: Tear break-up time (TBUT) (P = 0.020), Schirmer’s I test results (P = 0.030), anterior chamber depth (ACD) (P = 0.006), lens thickness (LT) (P < 0.001) and choroidal thickness (CHT) (P < 0.001)decreased significantly after a single HD. The retinal nerve fiber layer (RNFL) thickness and average retinal thickness (RT) increased after HD, especially in the nasal inner macula (NIM) subfield (P < 0.001), the inferior inner macula (IIM) subfield (P = 0.004) and the superior outer macula (SOM) subfield (P = 0.012). TBUT, Schirmer’s I test, IOP, RT, and CHT were correlated with one or more parameters. All ESRD patients regardless of etiology had the same trend for most parameters during HD, with the exception of the logMAR of BCVA, central corneal thickness, RNFL thickness and CHT. CONCLUSIONS: HD may affect a range of ocular parameters in ESRD patients. Dry eye parameters, RT and CHT exhibited the most obvious changes. Different etiologies tended to have similar trends in ocular parameter changes during HD. |
format | Online Article Text |
id | pubmed-6107936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61079362018-08-29 Ocular changes during hemodialysis in patients with end-stage renal disease Chen, Hejun Zhang, Xi Shen, Xi BMC Ophthalmol Research Article BACKGROUND: To explore ocular changes during hemodialysis (HD) in chronic renal failure patients and to determine the effects of different causes of renal failure during HD. METHODS: A total of 90 eyes from 45 end-stage renal disease (ESRD) patients undergoing HD were evaluated in this study. All ophthalmological examinations were conducted within 1 h before and after a single HD session. The HD patients were divided into primary kidney disease (KD), hypertensive KD, diabetic KD (DM-KD) and unknown etiology subgroups according to the primary etiology of renal failure. The statistics of 38 eyes from 19 healthy people were set as normal control. RESULTS: Tear break-up time (TBUT) (P = 0.020), Schirmer’s I test results (P = 0.030), anterior chamber depth (ACD) (P = 0.006), lens thickness (LT) (P < 0.001) and choroidal thickness (CHT) (P < 0.001)decreased significantly after a single HD. The retinal nerve fiber layer (RNFL) thickness and average retinal thickness (RT) increased after HD, especially in the nasal inner macula (NIM) subfield (P < 0.001), the inferior inner macula (IIM) subfield (P = 0.004) and the superior outer macula (SOM) subfield (P = 0.012). TBUT, Schirmer’s I test, IOP, RT, and CHT were correlated with one or more parameters. All ESRD patients regardless of etiology had the same trend for most parameters during HD, with the exception of the logMAR of BCVA, central corneal thickness, RNFL thickness and CHT. CONCLUSIONS: HD may affect a range of ocular parameters in ESRD patients. Dry eye parameters, RT and CHT exhibited the most obvious changes. Different etiologies tended to have similar trends in ocular parameter changes during HD. BioMed Central 2018-08-23 /pmc/articles/PMC6107936/ /pubmed/30139333 http://dx.doi.org/10.1186/s12886-018-0885-0 Text en © The Author(s). 2018 Open AccessThis 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 Chen, Hejun Zhang, Xi Shen, Xi Ocular changes during hemodialysis in patients with end-stage renal disease |
title | Ocular changes during hemodialysis in patients with end-stage renal disease |
title_full | Ocular changes during hemodialysis in patients with end-stage renal disease |
title_fullStr | Ocular changes during hemodialysis in patients with end-stage renal disease |
title_full_unstemmed | Ocular changes during hemodialysis in patients with end-stage renal disease |
title_short | Ocular changes during hemodialysis in patients with end-stage renal disease |
title_sort | ocular changes during hemodialysis in patients with end-stage renal disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107936/ https://www.ncbi.nlm.nih.gov/pubmed/30139333 http://dx.doi.org/10.1186/s12886-018-0885-0 |
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