Statistical analyses were conducted by Michael Mlynash, MD, MS; Stanford Stroke Center.
Yield of CT perfusion for the evaluation of transient ischaemic attack
Article first published online: 11 DEC 2012
© 2012 The Authors. International Journal of Stroke © 2012 World Stroke Organization
International Journal of Stroke
How to Cite
Kleinman, J. T., Mlynash, M., Zaharchuk, G., Ogdie, A. A., Straka, M., Lansberg, M. G., Schwartz, N. E., Singh, P., Kemp, S., Bammer, R., Albers, G. W. and Olivot, J.-M. (2012), Yield of CT perfusion for the evaluation of transient ischaemic attack. International Journal of Stroke. doi: 10.1111/j.1747-4949.2012.00941.x
Conflicts of interest: None declared.
Funding: J. T. K. is supported by the Stanford School of Medicine Medical Scholars program.
- Article first published online: 11 DEC 2012
- Stanford School of Medicine Medical Scholars program
- CT perfusion;
- magnetic resonance imaging;
- MR perfusion;
- transient ischaemic attack
Magnetic resonance diffusion-weighted imaging and perfusion-weighted imaging are able to identify ischaemic ‘footprints’ in transient ischaemic attack. Computed tomography perfusion (CTP) may be useful for patient triage and subsequent management. To date, less than 100 cases have been reported, and none have compared computed tomography perfusion to perfusion-weighted imaging (PWI). We sought to define the yield of computed tomography perfusion for the evaluation of transient ischaemic attack.
Consecutive patients with a discharge diagnosis of possible or definite transient ischaemic event who underwent computed tomography perfusion were included in this study. The presence of an ischaemic lesion was assessed on noncontrast computed tomography, automatically deconvolved CTPTMax (Time till the residue function reaches its maximum), and when available on diffusion-weighted imaging and PWITMax maps.
Thirty-four patients were included and 17 underwent magnetic resonance imaging. Median delay between onset and computed tomography perfusion was 4·4 h (Interquartile range [IQR]: 1·9–9·6), and between computed tomography perfusion and magnetic resonance imaging was 11 h (Interquartile range: 3·8–22). Noncontrast computed tomography was negative in all cases, while CTPTMax identified an ischaemic lesion in 12/34 patients (35%). In the subgroup of patients with multimodal magnetic resonance imaging, an ischaemic lesion was found in six (35%) patients using CTPTMax versus nine (53%) on magnetic resonance imaging (five diffusion-weighted imaging, nine perfusion-weighted imaging). The additional yield of CTPTMax over computed tomography angiography was significant in the evaluation of transient ischaemic attack (12 vs. 3, McNemar, P = 0·004).
CTPTMax found an ischaemic lesion in one-third of acute transient ischaemic attack patients. Computed tomography perfusion may be an acceptable substitute when magnetic resonance imaging is unavailable or contraindicated, and has additional yield over computed tomography angiography. Further studies evaluating the outcome of patients with computed tomography perfusion lesions in transient ischaemic attack are justified at this time.