Background and Purpose-In acute stroke patients treated with intravenous tissue plasminogen activator (t-PA), early recanalization of occluded arteries can improve the clinical outcome. The magnetic susceptibility effect of deoxygenated hemoglobin in red thrombi can present as hypointense signals on T2*-weighted gradient echo imaging. We investigated whether the gradient echo imaging M1 susceptibility vessel sign (M1 SVS) can predict no early recanalization after t-PA infusion. Methods-Patients with internal carotid artery and M1 occlusion were prospectively studied. MRI studies, including DWI, T2*, and MRA, were performed before and within 30 minutes and 24 hours after t-PA infusion. The NIHSS score was obtained before and 7 days after t-PA administration. The relationship between the presence of the M1 SVS and no early recanalization and patient outcome was examined. Results-A total of 48 patients (29 men; mean age, 74.6 +/- 11.2 years) were enrolled. M1 SVS was present in 13 (27.1%) patients and absent in 35 (72.9%) patients. There were no significant differences in clinical characteristics between the 2 groups. Follow-up MRA within 30 minutes after t-PA infusion revealed that 20 (57.1%) of the 35 patients without the M1 SVS had early recanalization, but that none of the 13 patients with the M1 SVS had early recanalization (P = 0.0002). Seven days after t-PA infusion, dramatic improvement was more frequently observed in patients without the M1 SVS (51.4%) than in those with the M1 SVS (0%, P = 0.0007). Conclusion-The M1 SVS on T2* appears to be a strong predictor for no early recanalization after t-PA therapy. (Stroke. 2009; 40: 3130-3132.)
机构:
Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea
Cho, KH
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Kim, JS
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea
Kim, JS
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Kwon, SU
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea
Kwon, SU
;
Cho, AH
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea
Cho, AH
;
Kang, DW
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea
机构:
Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea
Cho, KH
;
Kim, JS
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea
Kim, JS
;
Kwon, SU
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea
Kwon, SU
;
Cho, AH
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea
Cho, AH
;
Kang, DW
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea