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Methods to Purify the Supply were ignored

In the Eighties as the World used blood testing of ALTs and HBcAb (antibodies to Hepatitis B) to remove HCV from the supply we failed to

Penrose 27 87 The Lancet in July 1981 
When non-A non-B hepatitis was first recognised, many British workers seemed to regard it as a purely American problem. Lately, non-A non-B hepatitis has been accepted in the U.K. as a serious hazard of treatment with factor VIII and factor IX concentrates, but no-one has paid much attention to this type of hepatitis in the patient who receives a few units of blood or platelets. In a UK prospective study of post-transfusion hepatitis,[124] frank hepatitis developed in 1%, there were sustained increases of alanine aminotransaminase (ALT) in 4.5%, and the ALT was raised at some time after transfusion in 20%. Although only a small proportion of these cases of hepatitis and "transaminitis" seemed to be due to hepatitis B virus, nothing has been done to assess the value of preventive methods other than hepatitis B screening.
American workers have been less complacent.

Penrose Inquiry 27.113 
Dr Edward Follett and Dr Brian Dow,[164] reporting on a study of NANB Hepatitis in the West of Scotland in 1984, wrote: Evidence from USA would suggest that if ALT/SGPT testing is performed on all blood donations and those with high levels excluded, around 29-40% of non-A, non-B PTH cases could be prevented with the loss of around 3% of blood donations.

Penrose Inquiry 27.117 
After an outbreak of post-transfusion NANB Hepatitis following the use of certain BPL immunoglobulin concentrates,[168] Professor Andrew Lever, Professor Howard Thomas[169] and others contrasted the lack of tests for the NANB Hepatitis virus(es) with tests for other viruses, at the end of 1984:
Sensitive radioimmunoassays for hepatitis B surface antigen and IgM anti-HB-core allow identification of cases of post-transfusion hepatitis caused by the hepatitis B virus, and similar assays exist for the diagnosis of hepatitis A, cytomegalovirus, and Epstein-Barr virus infections which are rarer causes. Most post-transfusion hepatitis, however, is caused by a group of unidentified viruses designated non-A, non-B

There were deluded figures running the Blood Supply that fought against purifying it

Penrose Inquiry 27.132 
Again, the SNBTS Directors were aware of developments in the USA. In a letter to Dr Fraser on 28 August 1986 on the question of surrogate testing, Professor Cash stated, 'I have a feeling that as the drums are beating louder and louder in other parts of the world on this topic the Brits remain fast asleep'.[194] While he noted that the suggestion of a UK prospective trial had been raised at the recent NBTS meeting and 'went down like the proverbial lead balloon',

Penrose Inquiry 27.156 
On 26 January 1987, Dr Forrester produced a note, 'Material for PMO Report'. He made the following comments on blood transfusion and NANB Hepatitis: This "hepatitis" is a residual rag-bag when Hepatitis B and Hepatitis A are excluded, and consequently no specific test can detect it. It is relatively benign. But U.S. blood banks have noted that the combination of a liver function test and a test for the core (not the surface) antigen of Hepatitis B distinguishes perhaps a third of blood donations which would convey [NANB Hepatitis] and allows them to be excluded.
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