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(Stroke. 2005;36:2497.)
© 2005 American Heart Association, Inc.
Research Reports |
From the Department of Neurology (E.E.S., A.R.A., W.J.K., L.H.S.), Massachusetts General Hospital, Boston; the Department of Radiological Sciences (I.P.), UCLA, Los Angeles, Calif; and the Department of Internal Medicine (E.R.), Beth Israel-Deaconess Medical Center, Boston, Mass.
Background and Purpose Some patients with mild or improving ischemic stroke symptoms do not receive intravenous tissue plasminogen activator (tPA) because they look "too good to treat" (TGT); however, some have poor outcomes.
Methods We retrospectively analyzed data from a prospective single-center study between 2002 and 2004. TGT patients were those arriving within 3 hours of symptom onset and not treated with intravenous tPA solely because of mild or improving symptoms.
Results Of 128 patients presenting within 3 hours, 41 (34%) were not given tPA because of mild or improving stroke. Of the TGT patients, 11 of 41 (27%) died or were not discharged home because of neurological worsening (n=6) or persistent "mild" neurological deficit (n=5). No single variable at presentation was associated with death or lack of home discharge. There were 10 of 41 TGT patients (24%) who had
4-point improvement in National Institutes of Health Stroke Scale score before tPA decision; these patients were more likely to have subsequent neurological worsening (relative risk, 4.1, 95% CI, 1.1 to 15.4; P=0.05).
Conclusion A substantial minority of patients deemed too good for intravenous tPA were unable to be discharged home. A re-evaluation of the stroke severity criteria for tPA eligibility may be indicated.
Key Words: angiography computed tomography outcome stroke, acute tissue plasminogen activator
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