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Published on: August 11, 2014
Hepatitis B in the Cambridge dialysis and transplant unit 1966-1983
Insights
Hepatitis B surveillance in Cambridge dialysis and transplant units revealed a 6.44% prevalence of anti-HBc in haemodialysis patients. No unit cross-infection occurred, with one staff infection from an outpatient.
Area of Science:
- Hepatology
- Infectious Diseases
- Nephrology
Background:
- Hepatitis B virus (HBV) poses a significant risk in healthcare settings, particularly for immunocompromised patients.
- Dialysis and transplant patients are at increased risk of HBV infection due to their clinical status and frequent healthcare interactions.
Purpose of the Study:
- To report the results of hepatitis B surveillance in Cambridge dialysis and transplant units.
- To assess the prevalence of hepatitis B infection markers in haemodialysis patients.
- To identify sources and transmission routes of hepatitis B within the units.
Main Methods:
- Surveillance of hepatitis B markers (anti-HBc, HBsAg) in patients and staff.
- Review of patient admission and transplantation data.
- Exclusion of pre-existing carriers through preadmission screening.
Main Results:
- 34/528 (6.44%) of haemodialysis patients had anti-HBc on admission.
- 19 HBsAg carrier patients and 2 carrier staff were excluded by preadmission screening.
- Eight patients became antigenaemic post-admission; two others were identified post-transplantation.
- Of the newly infected patients, seven had asymptomatic carriage and one had acute hepatitis during haemodialysis.
- No cross-infection was observed within the dialysis or transplant units.
- One staff member acquired infection accidentally from an outpatient.
Conclusions:
- Hepatitis B surveillance is crucial in dialysis and transplant units.
- While no unit cross-infection occurred, vigilance is needed to prevent transmission.
- External sources, like outpatients, can pose a risk to healthcare staff.
Abstract:
The results of hepatitis B surveillance of the Cambridge dialysis and transplant units from June 1969 to July 1983 are reported. On admission 34/528 (6.44%) haemodialysis patients had anti-HBc. Preadmission screening excluded 19 HBs Ag carrier patients and two carrier staff. Eight patients became antigenaemic after admission and two others were found to be antigenaemic post-transplantation but pretransplant sera were not available from them. These two had active hepatitis and of the others, seven had asymptomatic carriage and one had acute hepatitis during haemodialysis. Two infected patients were admitted temporarily and one antigenaemic organ donor identified retrospectively. No cross infection occurred on the unit and the only instance of accidental infection of a member of staff was from an outpatient.
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