Diplomat of the American Board of Psychiatry and Neurology,
Marcellus, NY
To the Editor:
The report of Chiu et al1 showed that a single university
hospital and 2 community hospitals could achieve results comparable to
those of the recent NINDS rt-PA Study. Thirty patients were treated
from a possible 267 patients appearing in the 3 emergency rooms.
Thirty-seven percent of the remaining 237 patients were rejected
because the time limit for treatment was exceeded. This
group accounts for nearly 3 times the number of patients actually
treated. No mention in the paper was made of how these people fared or
whether there was any attempt at follow-up. An age- and sex-matched
control for those who were selected for treatment ought to be buried in
this group of nearly 90 patients; the only distinguishing variable
would be the time of onset.
It would be of great interest to know whether this control group had a
worse outcome than the people receiving therapy. The report's authors
already may have the data or could obtain it. For most neurologists in
practice over 10 years, their first experience with
thrombolytic therapy was being called to the ICU after
intracerebral hemorrhage when the therapy had
been used for myocardial infarction. They next read the 4 negative
studies on thrombolytic therapy before the NINDS Study.
Their subsequent experience is likely to have been intense pressure
from the media and academic powers-that-be to ignore the first 4
studies and to apply the therapy, along with pressure from hospitals in
competition with others to use the latest (if not
Department of Neurology,
Baylor College of Medicine,
The Methodist Hospital,
Houston, Texas
© 1998 American Heart Association, Inc.
Letters to the Editor
Ischemic Strokes Arriving Too Late for tPA Are an Ideal and Ethical Control Group for Continuing Studies of tPA Efficacy
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