Co-amoxiclav jaundice: clinical and histological features and HLA class II association

O'Donohue, J., Oien, K. , Donaldson, J., Underhill, J., Clare, M., MacSween, R.N.M. and Mills, P.R. (2000) Co-amoxiclav jaundice: clinical and histological features and HLA class II association. Gut, 47(5), pp. 717-720. (doi: 10.1136/gut.47.5.717) (PMID:11034591) (PMCID:PMC1728095)

Full text not currently available from Enlighten.


BACKGROUND AND AIMS Jaundice associated with co-amoxiclav has been increasingly recognised. We aimed to characterise its clinical and histological features and to investigate linkage with human leucocyte antigen class II haplotypes. METHODS We identified cases in the west of Scotland in the period 1991–1997 and performed polymerase chain reaction amplification and oligonucleotide probing on whole blood. RESULTS Twenty two cases were identified (10 male, mean age 59.1 years). Jaundice occurred a median of 17 days after drug commencement, with a median peak bilirubin level of 225 μmol/l (range 84–598) and median duration of jaundice 69 days (range 29–150). Two patients had primary biliary cirrhosis and two other patients had persistently abnormal liver biochemistry on follow up. One death occurred in a frail elderly woman despite resolving jaundice. The frequency of jaundice was 1 in 78 209 co-amoxiclav prescriptions. Liver biopsy, available in 12 patients, showed perivenular bilirubinostasis, accompanying reactive ceroid laden macrophages, and portal inflammation with focal injury to interlobular bile ducts. Fourteen of 20 patients had DRB1*1501 compared with 27 of 134 controls (p<2.5×10–6; odds ratio (OR) 9.25; relative risk (RR) 6.43). Of these, seven patients were homozygous for DRB1*1501(p<10–8; OR 35.54; RR=8.68) compared with two of 134 controls. All patients with DRB1*1501 had the extended haplotype DRB1*1501-DRB5*0101-DQA1*0102-DQB1*0602. There were no clinical or histological differences between genotypes. CONCLUSIONS Co-amoxiclav associated hepatotoxicity may have a genetic basis and be delayed, severe, and prolonged, although complete recovery is usual.

Item Type:Articles
Glasgow Author(s) Enlighten ID:Oien, Professor Karin
Authors: O'Donohue, J., Oien, K., Donaldson, J., Underhill, J., Clare, M., MacSween, R.N.M., and Mills, P.R.
College/School:College of Medical Veterinary and Life Sciences > Institute of Cancer Sciences
Journal Name:Gut
Publisher:B M J Group
ISSN (Online):1468-3288

University Staff: Request a correction | Enlighten Editors: Update this record