Interesting to see the infected blood scandal in the news today:
https://www.bbc.co.uk/news/health-68831061
The true scale of the number of medical trials using infected blood products on children in the 1970s and 80s has been revealed by documents seen by BBC News.
They reveal a secret world of unsafe clinical testing involving children in the UK, as doctors placed research goals ahead of patients' needs.
They continued for more than 15 years, involved hundreds of people, and infected most with hepatitis C and HIV.
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Luke O'Shea-Phillips, 42, has mild haemophilia - a blood clotting disorder that means he bruises and bleeds more easily than most.
He caught the potentially lethal viral infection hepatitis C while being treated at the Middlesex Hospital, in central London, which was administered because of a small cut to his mouth, aged three, in 1985.
Documents seen by the BBC suggest he was deliberately given the blood product - which his doctor knew might have been infected - so he could be enrolled in a clinical trial.
The doctor wanted to find out how likely patients were to catch diseases from a new version of heat-treated Factor VIII. Though he had never been treated for his condition before, Luke was given heat-treated Factor VIII to stop his mouth bleeding.
A letter from Luke's doctor, Samuel Machin, to another expert in haemophilia, was submitted in evidence to the public inquiry into the infected blood scandal.
Writing to Peter Kernoff, at London's Royal Free Hospital, Dr Machin detailed the treatment of Luke and another boy, asking: "I hope they will be suitable for your heat-treated trial."
Months earlier, Dr Kernoff had called on fellow doctors in the field to identify patients suitable for clinical trials. Specifically, he said, they had to be "previously untreated patients", known as "PUPs" in the medical community.
They were also nicknamed "virgin haemophiliacs" - a term written on Luke's medical record by Dr Machin.
"I was a guinea pig in clinical trials that could have killed me," Luke told the BBC.
"There is no other way to explain it - my treatment was changed so I could be enrolled in clinical trials. This change in medication gave me a fatal disease - hepatitis C - yet my mother was never even told."
"To the scientific world, it was an incredible benefit being a virgin haemophiliac," he added. "To be a clean petri dish to understand science through, I was without question a part of that."
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Before he died, Dr Machin gave evidence to the public inquiry, when he confirmed that Luke had been recruited to Dr Kernoff's study.
He denied this had been done without Luke's mother's knowledge. "This would have been discussed with his mother, although I acknowledge that standards of consent in the 1980's was quite different to what it is now," Dr Machin said.
However, Mrs O'Shea told the inquiry she was "absolutely not" told about the trial. "With an innocent child of three and a half I would not have considered such an action. I would never ever have allowed my child to be part of a trial - never," she added.
Documents reveal doctors knew Luke had contracted hepatitis C as early as 1993, but he was not told until 1997. One medical record states a positive test result and says: "Have not discussed with patient or family."
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However, evidence of the clinical trials have raised wider concerns.
"A patient should always be given the best possible treatment and they should always have given informed consent - if those two factors haven't been achieved then a trial would be seen as very problematic," says Professor Emma Cave, Professor of Healthcare Law at Durham University.
Professor Edward Tuddenham, who was a haemophilia doctor at the Royal Free Hospital in the 1980s, confirmed these fears. When asked if he thought ethical standards had been met during clinical trials in the 1980s, he simply answered: "No."
The BBC's investigation has revealed that Dr Machin and Dr Kernoff were among a community of doctors with similar research ambitions.
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A specialist school near Alton, in Hampshire, was attended by a large cohort of haemophiliac boys. The school for disabled children had an NHS haemophilia unit on site, so boys who had bleeds could be treated quickly and then return to lessons.
Their doctor, Dr Anthony Aronstam - who has also since died - used his "unique" cohort of boys for extensive clinical trials. One series of experiments considered whether using three to four times more Factor VIII than normally required by a child would help to reduce the number of bleeds he had.
This was preventative treatment, know as prophylaxis, and involved repeated injections with infected Factor VIII products and follow-up blood tests. The high concentrations of infected blood products were administered to the boys without their - or their parents' - consent.
Of the122 pupils attending Treloar's College between 1974-1987, 75 have so far died of HIV and hepatitis C infections.
"Despite knowing the product was riddled with hepatitis, they started a trial that required us to have way more of it than we needed," says Gary Webster, who was unknowingly enrolled.
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Dr Kernoff's pursuit of clinical advancement through research was rigorous, as was his hunt for suitable subjects for trials - PUPs and virgin haemophiliacs - which led to those involved getting young and younger. A four-month-old baby was involved in a trial.