The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Enlargement of human cerebral ischemic lesion volumes measured by diffusion‐weighted magnetic resonance imaging
Abstract
We aimed to determine the frequency and time course of the enlargement of ischemic cerebral lesions following human stroke and to study the effect of the state of perfusion on lesion enlargement. Acute lesion volumes were measured on diffusion‐weighted magnetic resonance images and compared with lesion volumes measured on T2‐weighted images at 7 days or later. Forty‐four measurements were performed between 2 and 53 hours after stroke onset in 28 patients. Thirteen patients also had magnetic resonance perfusion imaging performed. In 12 (43%) of 28 patients the initial lesion volume increased by 20% or more. The number of studies showing enlargement of the ischemic lesion volume ranged from 12 (43%) of 28 at or after 2 hours to 10 (38%) of 26 at or after 6 hours, 5 (33%) of 15 at or after 24 hours, and 2 (33%) of 6 at or after 48 hours. In 7 of the 10 patients in whom the hypoperfusion volume acutely exceeded the volume of the abnormality on diffusion‐weighted images, lesion volume increased by 20% or more. This study provided evidence that substantial enlargement of human cerebral ischemic lesion volumes can occur beyond the first 6, 12 or 24 hours after onset. A mismatch acutely between the region of hypoperfusion (larger) and the region of diffusion abnormality (smaller) may be predictive of ischemic lesion enlargement.
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Citations
Cites
Tissue Plasminogen Activator for Acute Ischemic Stroke
(1995) · New England Journal of Medicine · doi:10.1056/nejm199512143332401 · Cited by 11,654
Adhesion receptors of the immune system
Springer, T. A. (1990) · Nature · doi:10.1038/346425a0 · Cited by 6,477
Viability thresholds and the penumbra of focal ischemia
Hossmann, K. (1994) · Annals of Neurology · doi:10.1002/ana.410360404 · Cited by 1,370
Fast magnetic resonance diffusion-weighted imaging of acute human stroke
Warach, S., Chien, D., Li, W., Ronthal, M., & Edelman, R. R. (1992) · Neurology · doi:10.1212/wnl.42.9.1717 · Cited by 881
Self-citation
Cited by
Pathobiology of ischaemic stroke: an integrated view
Dirnagl, U., Iadecola, C., & Moskowitz, M. A. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01401-0 · Cited by 3,943
Higashida, R. T., & Furlan, A. J. (2003) · Stroke · doi:10.1161/01.str.0000082721.62796.09 · Cited by 1,543
Diffusion-weighted MR Imaging of the Brain
Schaefer, P. W., Grant, P. E., & Gonzalez, R. G. (2000) · Radiology · doi:10.1148/radiology.217.2.r00nv24331 · Cited by 1,052
Cerebral microinfarcts: the invisible lesions
Smith, E. E., Schneider, J. A., Wardlaw, J. M., & Greenberg, S. M. (2012) · The Lancet Neurology · doi:10.1016/s1474-4422(11)70307-6 · Cited by 456
Neuroplasticity of Language Networks in Aphasia: Advances, Updates, and Future Challenges
Kiran, S., & Thompson, C. K. (2019) · Frontiers in Neurology · doi:10.3389/fneur.2019.00295 · Cited by 250
Metadata
- Authors
- Baird, A. E., Benfield, A., Schlaug, G., Siewert, B., Lövblad, K., Edelman, R. R., & Warach, S.
- Venue
- Annals of Neurology
- Publisher
- Wiley
- Published
- 1997-05
- Volume
- 41
- Issue
- 5
- Pages
- 581-589
- ISSN
- 0364-5134 (ISSN-L)
- 1531-8249
- OpenAlex
- W1968324224
- Cited by
- 581
- References
- 4
- FWCI
- 35.43
- Type
- journal article
- Language
- en
- Open access
- closed
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