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How should I approach the diagnosis of Gilbert's Syndrome in a patient with isolated unconjugated hyperbilirubinemia?

Answer

Guideline-Aligned (High Confidence)
Generated by iatroX. Developer: Dr Kola Tytler MBBS CertHE MBA MRCGP (General Practitioner).
Last reviewed: 16 August 2025

When approaching the diagnosis of Gilbert's syndrome in a patient presenting with isolated unconjugated hyperbilirubinemia, the primary consideration is the patient's overall well-being 2. While most individuals presenting with jaundice typically require admission or referral to secondary care due to the potential for serious underlying causes, Gilbert's syndrome is an exception 2. If the person is well, Gilbert's syndrome can be diagnosed and managed in primary care 2.

It is crucial to rule out any red flag signs and symptoms that would necessitate urgent admission for same-day secondary care assessment 2. These include a bilirubin level greater than 100 micromol/L, an abnormal clotting profile or signs of coagulopathy, abnormal renal function, suspected paracetamol overdose, or if the patient is frail or has significant co-morbidities 2. If any of these red flags are present, or if the jaundice is unexplained, immediate referral is required 2.

If the patient is well and other serious causes of jaundice have been excluded, a diagnosis of Gilbert's syndrome can be made in primary care 2. Individuals diagnosed with Gilbert's syndrome should be fully reassured, as it is not associated with liver disease or ill health 2.

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This content was generated by iatroX. Always verify information and use clinical judgment.