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Liver blood marker testing in UK primary care: a UK wide cohort study, 2004–2016

OBJECTIVE: We aimed to determine (1) the temporal trends of liver enzyme testing in UK general practice and (2) how these vary among different subgroups at risk of chronic liver disease (CLD). DESIGN: Retrospective cohort study. SETTING: UK primary care database (Clinical Practice Research Datalink...

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Autores principales: Scutt, Polly, Ban, Lu, Card, Tim, Crooks, Colin John, Guha, Neil, West, Joe, Morling, Joanne R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516205/
https://www.ncbi.nlm.nih.gov/pubmed/36167394
http://dx.doi.org/10.1136/bmjopen-2021-058967
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author Scutt, Polly
Ban, Lu
Card, Tim
Crooks, Colin John
Guha, Neil
West, Joe
Morling, Joanne R
author_facet Scutt, Polly
Ban, Lu
Card, Tim
Crooks, Colin John
Guha, Neil
West, Joe
Morling, Joanne R
author_sort Scutt, Polly
collection PubMed
description OBJECTIVE: We aimed to determine (1) the temporal trends of liver enzyme testing in UK general practice and (2) how these vary among different subgroups at risk of chronic liver disease (CLD). DESIGN: Retrospective cohort study. SETTING: UK primary care database (Clinical Practice Research Datalink (CPRD)), 2004–2016. PARTICIPANTS: Patients aged 18 years or over, registered in the CPRD from 1 January 2004 to 31 December 2016. OUTCOME MEASURES: The frequency of testing recorded within the study period in general practice was calculated for: alanine aminotransferase (ALT); aspartate aminotransferase (AST); gamma glutamyl transferase (GGT); alkaline phosphatase (ALP); bilirubin and platelets. Analyses were conducted in subgroups of patients at high risk of developing liver disease. RESULTS: The study cohort included 2 912 066 individuals with median follow-up of 3.2 years. The proportion of patients with at least one measurement for ALT, ALP, bilirubin or platelet test gradually increased over the course of the study period and fell for AST and GGT. By 2016, the proportion of the population receiving one of more tests in that year was: platelet count 28.0%, ALP 26.2%, bilirubin 25.6%, ALT 23.7%, GGT 5.1% and AST 2.2%. Those patients with risk factors for CLD had higher proportions receiving liver marker assessments than those without risk factors. CONCLUSIONS: The striking finding that AST is now only measured in a fraction of the population has significant implications for routine guidance which frequently expects it. A more nuanced approach where non-invasive markers are targeted towards individuals with risk factors for CLD may be a solution.
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spelling pubmed-95162052022-09-29 Liver blood marker testing in UK primary care: a UK wide cohort study, 2004–2016 Scutt, Polly Ban, Lu Card, Tim Crooks, Colin John Guha, Neil West, Joe Morling, Joanne R BMJ Open Gastroenterology and Hepatology OBJECTIVE: We aimed to determine (1) the temporal trends of liver enzyme testing in UK general practice and (2) how these vary among different subgroups at risk of chronic liver disease (CLD). DESIGN: Retrospective cohort study. SETTING: UK primary care database (Clinical Practice Research Datalink (CPRD)), 2004–2016. PARTICIPANTS: Patients aged 18 years or over, registered in the CPRD from 1 January 2004 to 31 December 2016. OUTCOME MEASURES: The frequency of testing recorded within the study period in general practice was calculated for: alanine aminotransferase (ALT); aspartate aminotransferase (AST); gamma glutamyl transferase (GGT); alkaline phosphatase (ALP); bilirubin and platelets. Analyses were conducted in subgroups of patients at high risk of developing liver disease. RESULTS: The study cohort included 2 912 066 individuals with median follow-up of 3.2 years. The proportion of patients with at least one measurement for ALT, ALP, bilirubin or platelet test gradually increased over the course of the study period and fell for AST and GGT. By 2016, the proportion of the population receiving one of more tests in that year was: platelet count 28.0%, ALP 26.2%, bilirubin 25.6%, ALT 23.7%, GGT 5.1% and AST 2.2%. Those patients with risk factors for CLD had higher proportions receiving liver marker assessments than those without risk factors. CONCLUSIONS: The striking finding that AST is now only measured in a fraction of the population has significant implications for routine guidance which frequently expects it. A more nuanced approach where non-invasive markers are targeted towards individuals with risk factors for CLD may be a solution. BMJ Publishing Group 2022-09-26 /pmc/articles/PMC9516205/ /pubmed/36167394 http://dx.doi.org/10.1136/bmjopen-2021-058967 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Gastroenterology and Hepatology
Scutt, Polly
Ban, Lu
Card, Tim
Crooks, Colin John
Guha, Neil
West, Joe
Morling, Joanne R
Liver blood marker testing in UK primary care: a UK wide cohort study, 2004–2016
title Liver blood marker testing in UK primary care: a UK wide cohort study, 2004–2016
title_full Liver blood marker testing in UK primary care: a UK wide cohort study, 2004–2016
title_fullStr Liver blood marker testing in UK primary care: a UK wide cohort study, 2004–2016
title_full_unstemmed Liver blood marker testing in UK primary care: a UK wide cohort study, 2004–2016
title_short Liver blood marker testing in UK primary care: a UK wide cohort study, 2004–2016
title_sort liver blood marker testing in uk primary care: a uk wide cohort study, 2004–2016
topic Gastroenterology and Hepatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516205/
https://www.ncbi.nlm.nih.gov/pubmed/36167394
http://dx.doi.org/10.1136/bmjopen-2021-058967
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