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From the Department of Neurology, University of Virginia Health System, Charlottesville, VA.
Address correspondence and reprint requests to Dr. Bradford B. Worrall, Department of Neurology, University of Virginia Health System, Box 800394, Charlottesville, VA; e-mail: 22908bbw9r{at}virginia.edu
A 36-year-old woman without prior medical problems presented 45 minutes after collapsing. Examination revealed coma with asymmetric unreactive pupils, dysconjugate gaze, absent oculocephalic reflex, and minimal reflexive movements. Her initial National Institutes of Health Stroke Scale (NIHSS) score was 24.
Noncontrasted head CT and CT angiogram (figure 1) confirmed basilar artery occlusion (BAO). IV recombinant tissue plasminogen activator (IV rt-PA) was given 2 hours after symptom onset. Posttreatment cerebral angiography revealed a patent basilar artery and MRI demonstrated scattered small infarctions (figure 2). Transesophageal echocardiography revealed a small patent foramen ovale without right-to-left shunt. Hypercoagulable workup showed only slightly low levels of antithrombin III and protein S function. Seventy-two hours later, she walked out of the hospital with minimal neurologic deficits, which included an incomplete left homonymous hemianopsia. Total NIHSS score at discharge was 3.
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Optimal treatment for BAO is controversial. Intra-arterial (IA) rt-PA results in better recanalization rates, but outcomes may not be better than IV rt-PA.1 Young age, short occlusion, and recanalization are associated with increased survival after BAO,2 as evidenced by our patient. The additional time required for IA therapy remains to be justified. Other strategies, including a combined IV/IA bridging regimen, need to be rigorously investigated.
Footnotes
Disclosure: The authors report no conflicts of interest.
Received July 21, 2006. Accepted in final form November 15, 2006.
References
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