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Chronic liver disease. A case control study of the effect of previous blood transfusion
Insights
This study found no clear evidence that blood transfusions cause chronic liver disease in Britain. The investigation highlighted the need for improved transfusion history recall in patients for future risk assessments.
Area of Science:
- Hepatology
- Infectious Diseases
- Epidemiology
Background:
- Hepatitis NANB virus (HNV) infection transmitted via blood transfusion is a potential cause of chronic liver disease.
- Assessing the role of blood transfusions in chronic liver disease requires accurate patient histories.
Purpose of the Study:
- To investigate blood transfusion as a cause of non-A, non-B hepatitis (NANB) and chronic liver disease in England.
- To evaluate the reliability of patient transfusion histories.
Main Methods:
- A case-control study comparing patients with chronic liver disease to matched controls.
- Detailed medical histories, including operations and blood transfusions within ten years, were collected.
- Hospital records were used to verify transfusion histories.
Main Results:
- No significant difference in transfusion history was found between chronic liver disease patients and controls.
- Male patients with chronic liver disease were more likely to have resided in the Middle or Far East.
- Excluding patients with this travel history did not yield statistically significant differences in transfusion rates.
Conclusions:
- The study found no clear evidence of blood transfusion being a major cause of chronic liver disease in Britain.
- The methodology, focusing on confirmed transfusion histories in newly diagnosed patients, can be adapted for ongoing risk assessment.
Abstract:
A means of assessing hepatitis NANB virus infection, via blood transfusion, as a cause of chronic liver disease was investigated in a hospital in each of two cities in England. Patients with chronic liver disease were matched for age and sex with other patients in the same hospital and histories taken included details of previous operations and blood transfusions; if these were within ten years of the study enquiries were made of hospital records officers. All positive histories were found correct, but about one third of previous transfusions had been omitted by both case and control patients. Sixty-seven male and 35 female patients with chronic liver disease and their controls were included in analyses. The only clear difference which emerged related to residence for more than a year in the Middle or Far East by male case- (40%) or control- (21%) patients (P less than 0.05). The exclusion of patients with this history left only 34 pairs in which five (15%) of the case patients and one (3%) of the control patients had a transfusion history: this difference was not statistically significant. Although the study results have shown no clear evidence of blood transfusion as a major cause of chronic liver disease in Britain, the study method, with sufficient numbers to allow analyses of newly diagnosed patients with confirmed transfusion histories, could be used to provide an ongoing assessment of the risk.
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