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Embedding assessment of liver fibrosis into routine diabetic review in primary care

BACKGROUND & AIMS: Individuals with type 2 diabetes (T2DM) are at high risk of developing non-alcoholic fatty liver disease (NAFLD) and advanced fibrosis/cirrhosis. Screening patients with T2DM and normal liver enzymes for NAFLD in primary care remains contentious. Our aim was to develop and ass...

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Autores principales: Mansour, Dina, Grapes, Allison, Herscovitz, Marc, Cassidy, Paul, Vernazza, Jonathan, Broad, Andrea, Anstee, Quentin M., McPherson, Stuart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213901/
https://www.ncbi.nlm.nih.gov/pubmed/34179738
http://dx.doi.org/10.1016/j.jhepr.2021.100293
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author Mansour, Dina
Grapes, Allison
Herscovitz, Marc
Cassidy, Paul
Vernazza, Jonathan
Broad, Andrea
Anstee, Quentin M.
McPherson, Stuart
author_facet Mansour, Dina
Grapes, Allison
Herscovitz, Marc
Cassidy, Paul
Vernazza, Jonathan
Broad, Andrea
Anstee, Quentin M.
McPherson, Stuart
author_sort Mansour, Dina
collection PubMed
description BACKGROUND & AIMS: Individuals with type 2 diabetes (T2DM) are at high risk of developing non-alcoholic fatty liver disease (NAFLD) and advanced fibrosis/cirrhosis. Screening patients with T2DM and normal liver enzymes for NAFLD in primary care remains contentious. Our aim was to develop and assess a primary care pathway integrating two-tier (Fib-4 then transient elastography [TE]) liver fibrosis assessment, irrespective of aetiology, into routine annual review of all patients with T2DM. METHODS: All patients aged >35 years with T2DM attending annual review at 2 primary care practices in North East England between April 2018 and September 2019 (n = 467) had Fib-4 requested via the electronic patient record. Those with a Fib-4 score above the ‘high-sensitivity’ threshold (>1.3 for ≤65 years and >2.0 for >65 years) underwent TE and were reviewed in secondary care if the liver stiffness measurement (LSM) was >8 kPa. The number of patients identified with advanced disease, service uptake, and predictors of advanced disease were assessed. RESULTS: A total of 85/467 (18.5%) patients had raised Fib-4; 27/467(5.8%) were excluded as a result of frailty or known cirrhosis. A total of 58/467 (12.2%) were referred for TE. Twenty-five of 58 (43.1%) had an LSM of >8 kPa and 13/58 (22.4%) had an LSM >15 kPa; 4/58 (6.7%) did not attend and 5/58 (9.3%) had an invalid reading. Twenty of 440 (4.5%) patients were found to have advanced liver disease following specialist review, compared to 3 patients previously identified through standard care (odds ratio [OR] 6.71 [2.0–22.7] p = 0.0022). Alcohol (OR 1.05 [1.02–1.08] p = 0.001) and BMI (OR 1.09 [1.01–1.17] p = 0.021) were predictors of advanced disease, particularly drinking >14/21 units/week (p <0.0001) CONCLUSIONS: Incorporating 2-tier assessment of liver fibrosis into routine annual diabetes review in primary care significantly improves identification of advanced liver disease in patients with T2DM. LAY SUMMARY: People with type 2 diabetes are at increased risk of developing non-alcoholic fatty liver disease and developing more significant complications. This study looks at introducing screening for advanced liver disease into the annual diabetes reviews performed routinely in primary care; we found that significantly more people were identified as having significant liver disease through this pathway than with current standard care.
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spelling pubmed-82139012021-06-25 Embedding assessment of liver fibrosis into routine diabetic review in primary care Mansour, Dina Grapes, Allison Herscovitz, Marc Cassidy, Paul Vernazza, Jonathan Broad, Andrea Anstee, Quentin M. McPherson, Stuart JHEP Rep Research Article BACKGROUND & AIMS: Individuals with type 2 diabetes (T2DM) are at high risk of developing non-alcoholic fatty liver disease (NAFLD) and advanced fibrosis/cirrhosis. Screening patients with T2DM and normal liver enzymes for NAFLD in primary care remains contentious. Our aim was to develop and assess a primary care pathway integrating two-tier (Fib-4 then transient elastography [TE]) liver fibrosis assessment, irrespective of aetiology, into routine annual review of all patients with T2DM. METHODS: All patients aged >35 years with T2DM attending annual review at 2 primary care practices in North East England between April 2018 and September 2019 (n = 467) had Fib-4 requested via the electronic patient record. Those with a Fib-4 score above the ‘high-sensitivity’ threshold (>1.3 for ≤65 years and >2.0 for >65 years) underwent TE and were reviewed in secondary care if the liver stiffness measurement (LSM) was >8 kPa. The number of patients identified with advanced disease, service uptake, and predictors of advanced disease were assessed. RESULTS: A total of 85/467 (18.5%) patients had raised Fib-4; 27/467(5.8%) were excluded as a result of frailty or known cirrhosis. A total of 58/467 (12.2%) were referred for TE. Twenty-five of 58 (43.1%) had an LSM of >8 kPa and 13/58 (22.4%) had an LSM >15 kPa; 4/58 (6.7%) did not attend and 5/58 (9.3%) had an invalid reading. Twenty of 440 (4.5%) patients were found to have advanced liver disease following specialist review, compared to 3 patients previously identified through standard care (odds ratio [OR] 6.71 [2.0–22.7] p = 0.0022). Alcohol (OR 1.05 [1.02–1.08] p = 0.001) and BMI (OR 1.09 [1.01–1.17] p = 0.021) were predictors of advanced disease, particularly drinking >14/21 units/week (p <0.0001) CONCLUSIONS: Incorporating 2-tier assessment of liver fibrosis into routine annual diabetes review in primary care significantly improves identification of advanced liver disease in patients with T2DM. LAY SUMMARY: People with type 2 diabetes are at increased risk of developing non-alcoholic fatty liver disease and developing more significant complications. This study looks at introducing screening for advanced liver disease into the annual diabetes reviews performed routinely in primary care; we found that significantly more people were identified as having significant liver disease through this pathway than with current standard care. Elsevier 2021-04-22 /pmc/articles/PMC8213901/ /pubmed/34179738 http://dx.doi.org/10.1016/j.jhepr.2021.100293 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Mansour, Dina
Grapes, Allison
Herscovitz, Marc
Cassidy, Paul
Vernazza, Jonathan
Broad, Andrea
Anstee, Quentin M.
McPherson, Stuart
Embedding assessment of liver fibrosis into routine diabetic review in primary care
title Embedding assessment of liver fibrosis into routine diabetic review in primary care
title_full Embedding assessment of liver fibrosis into routine diabetic review in primary care
title_fullStr Embedding assessment of liver fibrosis into routine diabetic review in primary care
title_full_unstemmed Embedding assessment of liver fibrosis into routine diabetic review in primary care
title_short Embedding assessment of liver fibrosis into routine diabetic review in primary care
title_sort embedding assessment of liver fibrosis into routine diabetic review in primary care
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213901/
https://www.ncbi.nlm.nih.gov/pubmed/34179738
http://dx.doi.org/10.1016/j.jhepr.2021.100293
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