By Douglas S. Goodin, M.D.
ESI Special Topics,
February 2003
Citing URL - http://www.esi-topics.com/fbp/2003/february03-DouglasSGoodin.html
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Douglas S. Goodin, M.D.
answers a
few questions about this month's fast breaking paper in the field of
Neuroscience & Behavior.
From
•>>February 2003
Field: Neuroscience & Behavior
Article Title:
"Disease modifying therapies in multiple sclerosis - Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology and the MS Council for Clinical Practice Guidelines"
Authors: Goodin,
DS;Frohman, EM;Garmany, GP;Halper,
J;Likosky, WH;Lublin, FD;Silberberg, DH;Stuart, WH;van den
Noort, S
Journal: NEUROLOGY
Volume: 58
Page: 169-178
Year: JAN 22 2002
* Amer Acad Neurol, 1080 Montreal Ave, St Paul, MN 55116 USA.
* Amer Acad Neurol, St Paul, MN 55116 USA.
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Why
do you think your paper is highly cited?
I think that this paper is cited because it is a
comprehensive (and hopefully critical) analysis of the role of disease-modifying
therapies in the treatment of MS. The use of these therapies has
been quite controversial and this paper uses an objective
evidence-based approach to understand the value of the different
therapies.
Does
it describe a new discovery or a new methodology that's useful to
others?
It uses an evidence-based approach that is useful to readers
and to practicing physicians. The methodology, however, is not
new .
What
were some of the circumstances that led you to do this research?
It was a topic that was considered very important both to the
American Academy of Neurology and to the MS
Council for Clinical Practice Guidelines. These two
organizations are responsible for producing evidence-based
guidelines relating to various topics in neurology.
Could
you summarize the significance of your paper in layman's terms?
This paper reviews the scientific evidence for the use of
various disease-modifying therapies in the treatment of multiple
sclerosis (MS). These therapies include the immunosuppressant
agents, glucocorticoids (steroids), in addition to newer agents
such as beta-interferon (Avonex, Betaseron, and Rebif)
and glatiramer acetate (Copaxone). It is concluded that
all of the newer agents have good evidence for partial efficacy
(Type A recommendation) with respect for their ability to reduce
the attack rate of MS. There is less evidence for the ability of
these agents to reduce the severity of MS, although the data is
more convincing in this regard for beta-interferon therapy (Type
B Recommendation) than it is for glatiramer acetate (Type C
Recommendation). The evidence in favor of the effectiveness of
immunosuppressant or steroid therapy is, in general, less
compelling than it is for either of these newer agents.
Douglas S. Goodin,
Professor of Neurology, University of California, San
Francisco
Director, UCSF Multiple Sclerosis Center
San Francisco, CA, USA
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ESI Special Topics,
February 2003
Citing URL - http://www.esi-topics.com/fbp/2003/february03-DouglasSGoodin.html
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