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Raeburn B Forbes a Department of Neurology, Ninewells Hospital and
Medical School, Dundee DD1 9SY, b Argyll and Clyde Health
Board, Paisley PA2 7BN, c Scottish Health Purchasing Information Centre, Aberdeen AB15 6RE
Correspondence to: R B Forbes, Department of Neurology, Royal
Victoria Hospital, Belfast BT12 6BA
raeburn.forbes{at}royalhospitals.n-i-nhs.uk
Objective:
To evaluate the cost utility of interferon beta-1b in secondary progressive multiple sclerosis.
Design:
Population based cost utility model
(healthcare perspective). Data on use of health services were obtained
from case records and routine morbidity data and utility values from a
EuroQol survey. Local and published costs were used. Effectiveness was
modelled using data on relative risk reductions from a randomised trial
of interferon beta-1b.
Setting:
Tayside region, 1993-5.
Subjects:
132 ambulatory people with secondary
progressive multiple sclerosis.
Main outcome measures:
Cost per quality adjusted life
year (QALY) gained. Rate of relapse and proportion becoming wheelchair
dependent over three years.
Results:
The number needed to treat for 30 months to delay time to wheelchair dependence in one person by nine months was 18 (95% confidence interval 5 to 26). For every 18 people treated for 30 months, six relapses would be prevented, gaining 0.397 discounted
QALYs. The cost per QALY gained was £1 024 667 (£276 466 to
£1 485 499). If treatment was restricted to patients attending
neurology services, the number needed to treat was 14 (cost per QALY
gained £833 514 (£161 358 to
)). The cost per QALY gained was
not sensitive to changes in cost which took account of a societal perspective.
Conclusions:
The cost per QALY gained from interferon
beta is high because of the high drug cost and modest clinical effect. Resources could be used more efficiently elsewhere.
.
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