Reposting Links To And Excerpts From the 2018 “Guidelines on the management of abnormal liver blood tests” From The British Society of Gastroenterology

The single best resource on the evaluation of liver blood test abnormalities is the article referenced and excerpted in my post, Excerpts From The 2017 Guidelines On The Evaluation Of Abnormal Liver Tests From The ACG, posted on April 26, 2019 by Tom Wade MD.

Basically, though, the above American guideline like the British guideline of this post are the same. Order a bunch of liver tests and then consider referring the patient to a GI doctor or even better, to a liverspecialist .*

*Here is recommendation 10 from the British Society of Gastroenterology:

  • Recommendation 10: Adults with abnormal liver blood
    tests, even with a negative extended liver aetiology screen and no risk factors for NAFLD, should be referred/discussed to a gastroenterologist with an interest in liver disease/hepatologist for further evaluation (figure 1). (level 4, grade C)

This post contains links to and excerpts from Resource (1) below, 2018 Guidelines on the management of abnormal liver blood tests [PubMed Abstract], from the British Society of Gastroenterology.

Here are the excerpts:

Recommendations list

  • Recommendation 1: Initial investigation for
    potential liver disease should include bilirubin,
    albumin, alanine aminotransferase (ALT), alkaline phosphatase (ALP) and γ-glutamyltransferase (GGT), together with a full blood count
    if not already performed within the previous 12
    months. (level 2b, grade B)
    ► Research Recommendation 1: Further evidence
    is required to establish the cost-effectiveness
    of case finding for non-alcoholic fatty liver
    disease (NAFLD) in high-risk groups before it
    can be recommended. (level 5, grade D)Recommendation
  • 2: Abnormal liver bloodtest results should only be interpreted after review of the previous results, past medicalhistory and current medical condition. (level 5,
    grade D)
  • Recommendation 3: The extent of liver blood
    test abnormality is not necessarily a guide to
    clinical significance. This is determined by the
    specific analyte which is abnormal (outside the
    reference range) and the clinical context. (level
    5, grade D)
  • Recommendation 4: Patients with abnormal
    liver blood tests should be considered for
    investigation with a liver aetiology screen irrespective of level and duration of abnormality.
    Abnormal refers to an analyte which is outside
    the laboratory reference range (level 2b,
    grade B)
  • Recommendation 5: In adults a standard liver
    aetiology screen should include abdominal
    ultrasound scan (USS), hepatitis B surface
    antigen, hepatitis C antibody (with follow-on
    polymerase chain reaction (PCR) if positive),
    anti-mitochondrial antibody, anti-smooth
    muscle antibody, antinuclear antibody, serum
    immunoglobulins, simultaneous serum
    ferritin and transferrin saturation. (level 2b,
    grade C)
  • Recommendation 6: In children, ferritin and
    transferrin saturation may not be indicated,
    but autoantibody panel should include antiliver kidney microsomal antibody and coeliac
    antibodies. Alpha-1-antitrypsin level and caeruloplasmin (age >3 years) should be included,
    and abnormalities discussed with an appropriate inherited metabolic disease specialist.
    (level 2b, grade C)
  • Recommendation 7: Adults with NAFLD
    should undergo risk stratification to determine
    the extent of their liver fibrosis (figures 1 and 2).
    – First-line testing should use either fibrosis-4
    (FIB-4) or NAFLD Fibrosis Score (NFS)
    – see table 3 (level 2b, grade B). Calculation facilities for FIB-4 and NFS should be incorporated in all primary care computer systems. (level 5, grade D)
    – Second-line testing requires a quantitative assessment of fibrosis with tests such as serum enhanced liver fibrosis (ELF) measurements or Fibroscan/acoustic radiation force
    impulse (ARFI) elastography. (level 2b, grade B)
    – We recommend that hepatologists at a local level champion this idea and discuss it with commissioners of health to deal with the burden of liver disease in their area
  • Recommendation 8: Consider referral to alcohol services for all adults with alcohol-related liver disease (ARLD) with evidence of alcohol dependency as defined by an AUDIT score of >19. (level 3b, grade C)
  • Recommendation 9: Harmful drinkers should undergo risk stratification with clinical assessment and Fibroscan/ARFI elastography. Adults should be referred to secondary care if there is evidence of advanced liver disease (features of cirrhosis or portal hypertension on imaging or from blood tests) and/or Fibroscan reading is >16kPa (if available).
    (level 2b, grade B)
  • Research Recommendation 2: Further evidence is required to establish the most cost-effective approach to identify patients with ARLD and NAFLD at risk of having advanced liver fibrosis.
  • Recommendation 10: Adults with abnormal liver blood
    tests, even with a negative extended liver aetiology screen and no risk factors for NAFLD, should be referred/discussed to a gastroenterologist with an interest in liver disease/hepatologist for further evaluation (figure 1). (level 4, grade C)

 

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Resources

(1) Guidelines on the management of abnormal liver blood tests [PubMed Abstract] [Full Text HTML] [Full Text PDF].  2018 Jan;67(1):6-19. doi: 10.1136/gutjnl-2017-314924. Epub 2017 Nov 9.

(2) ACG Clinical Guideline: Evaluation of Abnormal Liver Chemistries [PubMed Abstract] [Full Text PDF] Am J Gastroenterol. 2017 Jan;112(1):18-35. doi: 10.1038/ajg.2016.517. Epub 2016 Dec 20.

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