Cargando…

Cerebral Perfusion in Hemodialysis Patients: A Feasibility Study

BACKGROUND: Patients on hemodialysis (HD) are known to exhibit low values of regional cerebral oxygenation (rSO2) and impaired cognitive functioning. The etiology of both is currently unknown. OBJECTIVE: To determine the feasibility of serially monitoring rSO2 in patients initiating HD. In addition,...

Descripción completa

Detalles Bibliográficos
Autores principales: Vanderlinden, Jessica Anne, Holden, Rachel Mary, Scott, Stephen Harold, Boyd, John Gordon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114747/
https://www.ncbi.nlm.nih.gov/pubmed/34017595
http://dx.doi.org/10.1177/20543581211010654
_version_ 1783691110167609344
author Vanderlinden, Jessica Anne
Holden, Rachel Mary
Scott, Stephen Harold
Boyd, John Gordon
author_facet Vanderlinden, Jessica Anne
Holden, Rachel Mary
Scott, Stephen Harold
Boyd, John Gordon
author_sort Vanderlinden, Jessica Anne
collection PubMed
description BACKGROUND: Patients on hemodialysis (HD) are known to exhibit low values of regional cerebral oxygenation (rSO2) and impaired cognitive functioning. The etiology of both is currently unknown. OBJECTIVE: To determine the feasibility of serially monitoring rSO2 in patients initiating HD. In addition, we sought to investigate how rSO2 is related to hemodynamic and dialysis parameters. DESIGN: Prospective observational study. SETTING: Single-center tertiary academic teaching hospital in Ontario, Canada. PARTICIPANTS: Six patients initiating HD were enrolled in the study. METHODS: Feasibility was defined as successful study enrollment (>1 patient/month), successful consent rate (>70%), high data capture rates (>90%), and assessment tolerability. Regional cerebral oxygenation monitoring was performed 1 time/wk for the first year of dialysis. A neuropsychological battery was performed 3 times during the study: before dialysis initiation, 3 months, and 1 year after dialysis initiation. The neuropsychological battery included a traditional screening tool: the Repeatable Battery for the Assessment of Neuropsychological Status, and a robot-based assessment: Kinarm. RESULTS: Our overall consent rate was 33%, and our enrollment rate was 0.4 patients/mo. In total 243 rSO2 sessions were recorded, with a data capture rate of 91.4% (222/243) across the 6 patients. Throughout the study, no adverse interactions were reported. Correlations between rSO2 with hemodynamic and dialysis parameters showed individual patient variability. However, at the individual level, all patients demonstrated positive correlations between mean arterial pressure and rSO2. Patients who had more than 3 liters of fluid showed significant negative correlations with rSO2. Less cognitive impairment was detected after initiating dialysis. LIMITATION: This small cohort limits conclusions that can be made between rSO2 and hemodynamic and dialysis parameters. CONCLUSIONS: Prospectively monitoring rSO2 in patients was unfeasible in a single dialysis unit, due to low consent and enrollment rates. However, rSO2 monitoring may provide unique insights into the effects of HD on cerebral oxygenation that should be further investigated. TRIAL REGISTRATION: Due to the feasibility nature of this study, no trial registration was performed.
format Online
Article
Text
id pubmed-8114747
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-81147472021-05-19 Cerebral Perfusion in Hemodialysis Patients: A Feasibility Study Vanderlinden, Jessica Anne Holden, Rachel Mary Scott, Stephen Harold Boyd, John Gordon Can J Kidney Health Dis Original Clinical Research Qualitative BACKGROUND: Patients on hemodialysis (HD) are known to exhibit low values of regional cerebral oxygenation (rSO2) and impaired cognitive functioning. The etiology of both is currently unknown. OBJECTIVE: To determine the feasibility of serially monitoring rSO2 in patients initiating HD. In addition, we sought to investigate how rSO2 is related to hemodynamic and dialysis parameters. DESIGN: Prospective observational study. SETTING: Single-center tertiary academic teaching hospital in Ontario, Canada. PARTICIPANTS: Six patients initiating HD were enrolled in the study. METHODS: Feasibility was defined as successful study enrollment (>1 patient/month), successful consent rate (>70%), high data capture rates (>90%), and assessment tolerability. Regional cerebral oxygenation monitoring was performed 1 time/wk for the first year of dialysis. A neuropsychological battery was performed 3 times during the study: before dialysis initiation, 3 months, and 1 year after dialysis initiation. The neuropsychological battery included a traditional screening tool: the Repeatable Battery for the Assessment of Neuropsychological Status, and a robot-based assessment: Kinarm. RESULTS: Our overall consent rate was 33%, and our enrollment rate was 0.4 patients/mo. In total 243 rSO2 sessions were recorded, with a data capture rate of 91.4% (222/243) across the 6 patients. Throughout the study, no adverse interactions were reported. Correlations between rSO2 with hemodynamic and dialysis parameters showed individual patient variability. However, at the individual level, all patients demonstrated positive correlations between mean arterial pressure and rSO2. Patients who had more than 3 liters of fluid showed significant negative correlations with rSO2. Less cognitive impairment was detected after initiating dialysis. LIMITATION: This small cohort limits conclusions that can be made between rSO2 and hemodynamic and dialysis parameters. CONCLUSIONS: Prospectively monitoring rSO2 in patients was unfeasible in a single dialysis unit, due to low consent and enrollment rates. However, rSO2 monitoring may provide unique insights into the effects of HD on cerebral oxygenation that should be further investigated. TRIAL REGISTRATION: Due to the feasibility nature of this study, no trial registration was performed. SAGE Publications 2021-05-06 /pmc/articles/PMC8114747/ /pubmed/34017595 http://dx.doi.org/10.1177/20543581211010654 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Clinical Research Qualitative
Vanderlinden, Jessica Anne
Holden, Rachel Mary
Scott, Stephen Harold
Boyd, John Gordon
Cerebral Perfusion in Hemodialysis Patients: A Feasibility Study
title Cerebral Perfusion in Hemodialysis Patients: A Feasibility Study
title_full Cerebral Perfusion in Hemodialysis Patients: A Feasibility Study
title_fullStr Cerebral Perfusion in Hemodialysis Patients: A Feasibility Study
title_full_unstemmed Cerebral Perfusion in Hemodialysis Patients: A Feasibility Study
title_short Cerebral Perfusion in Hemodialysis Patients: A Feasibility Study
title_sort cerebral perfusion in hemodialysis patients: a feasibility study
topic Original Clinical Research Qualitative
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114747/
https://www.ncbi.nlm.nih.gov/pubmed/34017595
http://dx.doi.org/10.1177/20543581211010654
work_keys_str_mv AT vanderlindenjessicaanne cerebralperfusioninhemodialysispatientsafeasibilitystudy
AT holdenrachelmary cerebralperfusioninhemodialysispatientsafeasibilitystudy
AT scottstephenharold cerebralperfusioninhemodialysispatientsafeasibilitystudy
AT boydjohngordon cerebralperfusioninhemodialysispatientsafeasibilitystudy