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CMAJ : Canadian Medical Association Journal logoLink to CMAJ : Canadian Medical Association Journal
. 2004 Mar 30;170(7):1087. doi: 10.1503/cmaj.1040368

UK patient first to contract vCJD via blood transfusion

Barbara Sibbald 1
PMCID: PMC374209  PMID: 15051685

The death of a patient in the UK from variant CreutzfeldtJakob disease (vCJD) is very likely the first documented transfusion-related transmission, The Lancet has reported.

The unidentified patient received blood during surgery in 1997, showed symptoms of vCJD in late 2003 and died in December. The donor of the blood fell ill with the brain-wasting disease in 1999 and died soon afterwards.

Although it is possible both individuals acquired the disease separately, The Lancet reports that it is unlikely (2004;363:417-21). The transfused patient was much older than the average person who dies of vCJD: 69 versus 30. This, and an examination of blood donation records, led the researchers to conclude that the odds of the disease not being acquired via a transfusion were about 1 in 30 000.

In another study (The Lancet 2004;363:422-8), the department of medical research at the French Atomic Energy Commission reported that the macaque monkey can be infected with bovine spongiform encephalopathy (BSE) orally or intravenously.

They concluded that blood transfusion should be regarded as a “likely route of contamination for vCJD patients with a medical history involving a transfusion during the period of risk [1980 to 1996].”

Variant CJD is an incurable, degenerative brain disorder normally associated with eating meat infected with BSE.

The news of the transfusion case “created quite a stir” at Canadian Blood Services (CBS), said Medical Director Dr. Heather Hume. However, CBS has stringent donor exclusion measures in place that “we believe are sufficient,” said Hume.

First introduced in 1999, CBS travel exclusions now rule out potential donors who have spent 3 months or more cumulatively in the UK or France, or 5 years or more in Western Europe since 1980. In addition, donors who have received a blood transfusion in the UK since 1980 are barred from donating.

As a result of these restrictions, CBS has lost 5%–6% of its donors. “There aren't any additional measures we could take, in the absence of a test,” said Hume.

The US Food and Drug Administration (FDA) has similar donor criteria while Héma-Québec's rules are even more stringent, excluding donors who have spent 30 days in the UK or France; or 6 months in Western Europe.

The US Office of Blood Research and Review announced in February that it would re-evaluate its donor policy, even though current measures now eliminate 90% of the overall risk.

“The new case in England has caused shock waves around the globe,” noted FDA spokesperson Lester Crawford. — Barbara Sibbald, CMAJ


Articles from CMAJ : Canadian Medical Association Journal are provided here courtesy of Canadian Medical Association

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