scholarly journals PG11 THE DEVELOPMENT AND PERFORMANCE OF MODELS TO PREDICT RISK OF LIVER DISEASE DIAGNOSIS FOLLOWING LIVER FUNCTION TESTING IN PRIMARY CARE

2008 ◽  
Vol 11 (6) ◽  
pp. A518
Author(s):  
DJ McLernon ◽  
JF Dillon ◽  
FM Sullivan ◽  
PT Donnan
2019 ◽  
Vol 71 (4) ◽  
pp. 699-706 ◽  
Author(s):  
John F. Dillon ◽  
Michael H. Miller ◽  
Emma M. Robinson ◽  
Adrian Hapca ◽  
Mohsen Rezaeihemami ◽  
...  

2009 ◽  
Vol 26 (4) ◽  
pp. 251-259 ◽  
Author(s):  
David J McLernon ◽  
Peter T Donnan ◽  
Stephen Ryder ◽  
Paul Roderick ◽  
Frank M Sullivan ◽  
...  

2020 ◽  
Vol 5 (5) ◽  
pp. 1090-1100
Author(s):  
Iain Macpherson ◽  
Jennifer H Nobes ◽  
Eleanor Dow ◽  
Elizabeth Furrie ◽  
Michael H Miller ◽  
...  

Abstract Chronic liver disease (CLD) is a significant health problem affecting millions of people worldwide. In Scotland, CLD is a major cause of premature mortality. Liver function tests (LFTs) are a panel of frequently requested blood tests which may indicate liver disease. However, LFTs commonly contain at least one abnormal result, and abnormalities are rarely investigated to the extent recommended by national guidelines. The intelligent Liver Function Testing (iLFT) pathway is a novel, automated system designed to improve early diagnosis of liver disease. Initial abnormal LFT results trigger a cascade of reflexive testing to help identify the cause of any liver dysfunction. Algorithms combine these results with demographic and clinical data (such as patient age, body mass index, and alcohol intake) and fibrosis estimates to produce an electronic diagnosis and management plan. The pilot trial demonstrated that iLFT increased diagnosis of liver disease whilst remaining cost-effective. As such, iLFT has been fully operational across our region (NHS Tayside, Scotland) since August 2018. In the first year, iLFT generated over 2000 diagnoses from 1824 patient samples with an abnormality in the initial LFTs. The majority of these patients could be safely managed in primary care. iLFT allows maximal value to be obtained from liver blood tests across biochemistry, virology, immunology, and hematology with only minor changes to working practices. ‘Intelligent’, algorithm-led testing pathways break down the barrier between clinical and laboratory medicine and offer solutions to many of the challenges experienced in modern healthcare systems.


2018 ◽  
Author(s):  
John F Dillon ◽  
Michael H Miller ◽  
Dr Emma M Robinson ◽  
Adrian Hapca ◽  
Mohsen Rezaeihemami ◽  
...  

2017 ◽  
Vol 67 (656) ◽  
pp. e194-e200 ◽  
Author(s):  
Kate Homer ◽  
John Robson ◽  
Susannah Solaiman ◽  
Abigail Davis ◽  
Saima Zubeda Khan ◽  
...  

BackgroundCurrent liver function testing for statin monitoring is largely unnecessary and costly. Statins do not cause liver disease. Both reduction in test frequency and use of a single alanine transaminase (ALT) rather than a full seven analyte liver function test (LFT) array would reduce cost and may benefit patients.AimTo assess LFT testing in relation to statin use and evaluate an intervention to reduce full-array LFTs ordered by GPs for statin monitoring.Design and settingTwo-year cross-sectional time series in two east London clinical commissioning groups (CCGs) with 650 000 patients. One CCG received the intervention; the other did not.MethodThe intervention comprised local guidance on LFTs for statin monitoring and access to a single ALT rather than full LFT array.ResultsOf the total population, 17.6% were on statins, accounting for 43.2% of total LFTs. In the population without liver disease, liver function tests were 3.6 times higher for those on statins compared with those who were not. Following intervention there was a significant reduction in the full LFT array per 1000 people on statins, from 70.3 (95% confidence interval [CI] = 66.3 to 74.6) in the pre-intervention year, to 58.1 (95% CI = 55.5 to 60.7) in the post-intervention year (P<0.001). In the final month, March 2016, the rate was 53.2, a 24.3% reduction on the pre-intervention rate.ConclusionThis simple and generalisable intervention, enabling ordering of a single ALT combined with information recommending prudent rather than periodic testing, reduced full LFT testing by 24.3% in people on statins. This is likely to have patient benefit at reduced cost.


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