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(, Sun 1 Apr 2001, 1:00)
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why did you opt out of the NHS database? All it does is mean that your records are instantly available all over the country.
I don't see any particular problem with confidentiality that isn't already there; and a wholly electronic version that's accessible on a need-to-know basis is probably more secure than what we have now, on the basis that there's fewer links in the chain... (It's not as if every Tom, Dick and Harry has access to your records now; why would that change?)
EDIT: I know several people who think that participation in medical research is a moral duty. I don't think that that's obviously correct - though it might be right, the arguments presented don't seem watertight - but I'm willing to accept that it's hugely admirable. It's possible that participation in Biobank is one way to discharge that duty (or near-duty).
(, Sat 1 May 2010, 9:11, 2 replies, latest was 16 years ago)
Some time back there was a short story/ urban myth going about - you might recall it. (Sorry-can't find web page or source just now.)
Chap mislays a library book while packing to move, and tells the librarian he'll return it at his new local library. She logs this into the computer system -'N.Phledge to return 'Kidnapped, R.L.Stevenson, to Tunbridge Wells'. Through a broken linkage of misunderstandings and transferred data this ends up as a police hunt chasing a fleeing kidnapper: the chap who is moving house.
Whatever the intended aim of the story it became another prop to the 'Any organisation of hacker could get my details and misuse it' argument against national databases.
It's a hard argument to beat that - one that has no substance to thrust against.
(, Sat 1 May 2010, 9:59, Reply)
Generally GPs don't seem very keen on it, and various organisations are raising concerns too.
www.guardian.co.uk/commentisfree/henryporter/2010/mar/02/nhs-spine-database-opting-out probably made my mind up.
I'm going to read more on Biobank but I reckon I'll end up doing it.
(, Sat 1 May 2010, 10:26, Reply)
I don't buy the point the article's making. First up, it seems to pander to the false belief that most people's medical records are very interesting indeed, and worth leaking. Second, worries about the database smuggle in the assumption that the current system is more secure than the proposed one. Third, the idea that the number of people who has access is, in its own terms, important is bunk: I don't see why that should be at all. If I'm in Glasgow when I brake my arm or have a heart attack, I'd want more people - specifically, the people in the hospital - to have access to my records. Fourth: the stuff about "government agencies" - tinfoil hat, much? Fifth, the doctors' questionnaire mentioned is misleading, because, as described, it suggests that the choice is between information being kept confidential with the GP, or a national system with no confidentiality. The reality is that there's a third option, which is a confidential national system - which is, by coincidence, what the new one would be (and would have to be under the DPA, and quite possibly as part of your Article 8 rights). Sixth, there's a confusion of privacy and confidentiality; I'm not sure that that makes much of a difference overall here, but they shouldn't be run together anyway.
... and breathe!
Righty-ho. I'm off until tomorrow. See y'all then!
(, Sat 1 May 2010, 11:00, Reply)
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