Delivery of biannual ultrasound surveillance for individuals with cirrhosis and cured hepatitis C in the UK

Author:

Hamill Victoria12,Gelson Will3,MacDonald Douglas4,Richardson Paul5,Ryder Stephen D.6,Aldersley Mark7,McPherson Stuart8ORCID,Verma Sumita910ORCID,Sharma Rohini11ORCID,Hutchinson Sharon12,Benselin Jennifer6,Barnes Eleanor12,Guha Indra Neil613,Irving William L.6,Innes Hamish1214ORCID

Affiliation:

1. School of Health and Life Sciences Glasgow Caledonian University Glasgow UK

2. Public Health Scotland Glasgow UK

3. Cambridge Liver Unit Cambridge University Hospitals NHS Foundation Trust Cambridge UK

4. Gastroenteology and Hepatology Royal Free London NHS Foundation Trust London UK

5. Royal Liverpool and Broadgreen University Hospitals NHS Trust Liverpool UK

6. NIHR Nottingham Biomedical Research Centre Nottingham University Hospitals NHS Trust and the University of Nottingham UK

7. Leeds Liver Unit St James's University Hospital Leeds UK

8. Newcastle Liver Unit Freeman Hospital Newcastle upon Tyne UK

9. Department of Clinical and Experimental Medicine Brighton and Sussex Medical School Brighton UK

10. Department of Gastroenterology and Hepatology University Hospital Sussex NHS Foundation Trust Brighton UK

11. Imperial College London London UK

12. Nuffield Department of Medicine and the Oxford NIHR Biomedical Research Centre University of Oxford Oxford UK

13. Nottingham Digestive Diseases Centre, School of Medicine University of Nottingham Nottingham UK

14. Division of Epidemiology and Public Health University of Nottingham Nottingham UK

Abstract

AbstractBackgroundPrevious studies show the uptake of biannual ultrasound (US) surveillance in patients with cirrhosis is suboptimal. Here, our goal was to understand in broader terms how surveillance is being delivered to cirrhosis patients with cured hepatitis C in the UK.MethodsHepatitis C cirrhosis patients achieving a sustained viral response (SVR) to antiviral therapies were identified from the national Hepatitis‐C‐Research‐UK resource. Data on (i) liver/abdominal US examinations, (ii) HCC diagnoses, and (iii) HCC curative treatment were obtained through record‐linkage to national health registries. The rate of US uptake was calculated by dividing the number of US episodes by follow‐up time.ResultsA total of 1908 cirrhosis patients from 31 liver centres were followed for 3.8 (IQR: 3.4–4.9) years. Overall, 10 396 liver/abdominal USs were identified. The proportion with biannual US was 19% in the first 3 years after SVR and 9% for all follow‐up years. Higher uptake of biannual US was associated with attending a liver transplant centre; older age and cirrhosis decompensation. Funnel plot analysis indicated significant inter‐centre variability in biannual US uptake, with 6/29 centres outside control limits. Incident HCC occurred in 133 patients, of which 49/133 (37%) were treated with curative intent. The number of US episodes in the two years prior to HCC diagnosis was significantly associated with higher odds of curative‐intent treatment (aOR: 1.53; 95% CI: 1.12–2,09; p = .007).ConclusionsThis study provides novel data on the cascade of care for HCC in the UK. Our findings suggest biannual US is poorly targeted, inefficient and is not being delivered equitably to all patients.

Funder

Cancer Research UK

Medical Research Council

Medical Research Foundation

Publisher

Wiley

Subject

Hepatology

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