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Recombinant human DNase (rhDNase) in cystic fibrosis: is it cost effective?
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Introduction |
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Almost simultaneously with a request to prescribe any novel
treatment for our patients, the bellowing voices of the Mr Bumbles, to
be found inhabiting our drug and therapeutic committees and our local
family health services authorities, will be heard to exclaim, `More!
after he has prescribed the drugs already allotted by the
pharmacy!'1 Thus those of us committed to the care of patients with cystic fibrosis should not have been surprised to encounter a wall of resistance to the introduction of recombinant human
DNase (rhDNase) at an estimated cost of £7500 per patient per year.
Even after multicentre, international studies conducted by most
respected colleagues we were asked to make the case again, and to prove
its efficacy and cost effectiveness.
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What is cost effectiveness in cystic fibrosis? |
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The concept of cost effectiveness is fraught with difficulties for
clinicians committed to the care of patients with cystic fibrosis.
There is no easily defined starting point and no
This article has been cited by other articles:
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Doull, I. J M
(2001). Recent advances: Recent advances in cystic fibrosis. Arch. Dis. Child.
85: 62-66
[Abstract] [Full Text]
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