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Investigating clinical predictors of arteriovenous fistula functional patency in a European cohort

BACKGROUND: Arteriovenous fistula (AVF) failure to mature (FTM) rates contribute to excessive dependence on central venous catheters for haemodialysis. Choosing the most appropriate vascular access site for an individual patient is guided largely by their age, co-morbidities and clinical examination...

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Autores principales: Masengu, Agnes, Maxwell, Alexander P., Hanko, Jennifer B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720209/
https://www.ncbi.nlm.nih.gov/pubmed/26798475
http://dx.doi.org/10.1093/ckj/sfv131
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author Masengu, Agnes
Maxwell, Alexander P.
Hanko, Jennifer B.
author_facet Masengu, Agnes
Maxwell, Alexander P.
Hanko, Jennifer B.
author_sort Masengu, Agnes
collection PubMed
description BACKGROUND: Arteriovenous fistula (AVF) failure to mature (FTM) rates contribute to excessive dependence on central venous catheters for haemodialysis. Choosing the most appropriate vascular access site for an individual patient is guided largely by their age, co-morbidities and clinical examination. We investigated the clinical predictors of AVF FTM in a European cohort of patients and applied an existing clinical risk prediction model for AVF FTM to this population. METHODS: A prospective cohort study was designed that included all patients undergoing AVF creation between January 2009 and December 2014 in a single centre (Belfast City Hospital) who had a functional AVF outcome observed by March 2015. RESULTS: A total of 525 patients had a functional AVF outcome recorded and were included in the FTM analysis. In this cohort, 309 (59%) patients achieved functional AVF patency and 216 (41%) patients had FTM. Female gender [P < 0.001, odds ratio (OR) 2.03 (CI 1.37–3.02)] and lower-arm AVF [P < 0.001, OR 4.07 (CI 2.77–5.92)] were associated with AVF FTM. The Lok model did not predict FTM outcomes based on the associated risk stratification in our population. CONCLUSIONS: In this European study, female gender was associated with twice the risk of AVF FTM and a lower-arm AVF with four times the risk of FTM. The FTM risk prediction model was not found to be discriminative in this population. Clinical risk factors for AVF FTM vary between populations; we would recommend that units investigate their own clinical predictors of FTM to maximize AVF functional patency and ultimately survival in dialysis patients. Clinical predictors of AVF FTM may not be sufficient on their own to improve vascular access functional patency rates.
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spelling pubmed-47202092016-01-21 Investigating clinical predictors of arteriovenous fistula functional patency in a European cohort Masengu, Agnes Maxwell, Alexander P. Hanko, Jennifer B. Clin Kidney J Dialysis BACKGROUND: Arteriovenous fistula (AVF) failure to mature (FTM) rates contribute to excessive dependence on central venous catheters for haemodialysis. Choosing the most appropriate vascular access site for an individual patient is guided largely by their age, co-morbidities and clinical examination. We investigated the clinical predictors of AVF FTM in a European cohort of patients and applied an existing clinical risk prediction model for AVF FTM to this population. METHODS: A prospective cohort study was designed that included all patients undergoing AVF creation between January 2009 and December 2014 in a single centre (Belfast City Hospital) who had a functional AVF outcome observed by March 2015. RESULTS: A total of 525 patients had a functional AVF outcome recorded and were included in the FTM analysis. In this cohort, 309 (59%) patients achieved functional AVF patency and 216 (41%) patients had FTM. Female gender [P < 0.001, odds ratio (OR) 2.03 (CI 1.37–3.02)] and lower-arm AVF [P < 0.001, OR 4.07 (CI 2.77–5.92)] were associated with AVF FTM. The Lok model did not predict FTM outcomes based on the associated risk stratification in our population. CONCLUSIONS: In this European study, female gender was associated with twice the risk of AVF FTM and a lower-arm AVF with four times the risk of FTM. The FTM risk prediction model was not found to be discriminative in this population. Clinical risk factors for AVF FTM vary between populations; we would recommend that units investigate their own clinical predictors of FTM to maximize AVF functional patency and ultimately survival in dialysis patients. Clinical predictors of AVF FTM may not be sufficient on their own to improve vascular access functional patency rates. Oxford University Press 2016-02 2015-12-13 /pmc/articles/PMC4720209/ /pubmed/26798475 http://dx.doi.org/10.1093/ckj/sfv131 Text en © The Author 2015. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Dialysis
Masengu, Agnes
Maxwell, Alexander P.
Hanko, Jennifer B.
Investigating clinical predictors of arteriovenous fistula functional patency in a European cohort
title Investigating clinical predictors of arteriovenous fistula functional patency in a European cohort
title_full Investigating clinical predictors of arteriovenous fistula functional patency in a European cohort
title_fullStr Investigating clinical predictors of arteriovenous fistula functional patency in a European cohort
title_full_unstemmed Investigating clinical predictors of arteriovenous fistula functional patency in a European cohort
title_short Investigating clinical predictors of arteriovenous fistula functional patency in a European cohort
title_sort investigating clinical predictors of arteriovenous fistula functional patency in a european cohort
topic Dialysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720209/
https://www.ncbi.nlm.nih.gov/pubmed/26798475
http://dx.doi.org/10.1093/ckj/sfv131
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