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Question answered:04/03/08
ATTRACT cannot comment directly on whether isolated raised bilirubin is sufficient to diagnose gilbert’s syndrome. At ATTRACT we simply report the evidence we find and leave any interpretation down to the health professional.
GP notebook contains a chapter on raised bilirubin (1), within this there is suggested protocol for investigation of a slightly raised isolated bilirubin in an asymptomatic patient in primary care. This states:
“Recommended investigation for isolated raised bilirubin in primary care (1):
values <1.5 times upper limit of normal (ULN)
suggested that should retest LFTs in 1-3 months unless clinical suspicion of disease
values >1.5 ULN:
it is suggested that confirm proportion of indirect (unconjugated) bilirubin
Gilbert's syndrome is probable if >70%, unconjugated: no further testing needed if non-progessive on interval retesting, unless clinical suspicion of haemolysis
if bilirubin is increasing on restesting
then consider haemolysis and test haptoglobin, LDH and blood count with reticulocyte count
values > 3 x ULN:
it is probable that raised bilirubin is a result of disease process
further investigation required
consider ultrasound (conjugated >50%) or haemolysis (unconjugated >70%)
Notes:
values up to 20% over ULN are likely to be statistical rather than clinical 'abnormals'
referral to secondary care is indicated if bilirubin is raised > 2 ULN (unexplained by laboratory tests)”
The NLH Q&A service answered the following question in 2005, “is an isolated raised bilirubin level sufficient to make a diagnosis of gilbert's syndrome in an otherwise well patient in primary care? if not what other investigations need doing to make the diagnosis in primary care” (2). The answer to this question can be viewed in full at: http://www.clinicalanswers.nhs.uk/index.cfm?question=945
1.http://www.gpnotebook.co.uk/simplepage.cfm?ID=x20070406183836295600&linkID=70009&cook=yes
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