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Biomedical subjects

Mario Siebler

Publications and source records attributed to Mario Siebler.

22 records · Page 2Linked to original sources

MR imaging in acute stroke: diffusion-weighted and perfusion imaging parameters for predicting infarct size.

PURPOSE: To investigate the predictive value of the ischemic lesion size, as depicted in the acute stroke phase on diffusion-weighted magnetic resonance (MR) images and time-to-peak (TTP) maps of tissue perfusion imaging, for infarct size, as derived from T2-weighted imaging in the postacute phase. MATERIALS AND METHODS: Fifty patients who underwent diffusion-weighted and perfusion imaging within 1-24 hours after stroke onset and a follow-up T2-weighted investigation after about 8 days were included. Lesion volumes were evaluated by using a semiautomatic thresholding technique. Volumetric results of acute diffusion-weighted and perfusion imaging were analyzed in comparison with follow-up T2-weighted images and in terms of the time difference between symptom onset and initial MR imaging. RESULTS: At diffusion-weighted imaging, the acute lesion defined by a signal intensity increase of more than 20%, compared with the contralateral side, showed the best correlation with the infarct size after 1 week. At perfusion imaging, the best predictor relative to the contralateral side was a delay of more than 6 seconds on TTP maps. Temporal analysis of volumetric results, which depended on the time difference between symptom onset and examination, revealed two patient subgroups. CONCLUSION: Diffusion-weighted imaging helped to predict the size of the lesion on T2-weighted images obtained after about 8 days in patients with a symptom onset of more than 4 hours (r = 0.96), while in patients with a symptom onset of less than 4 hours, perfusion imaging provided important additional information about brain tissue with impaired perfusion.

Acute Disease↗

Diffusion-weighted imaging in acute stroke--a tool of uncertain value?

The concept of a mismatch between the lesion volume in diffusion- and perfusion-weighted magnetic resonance imaging (MRI) indicating 'tissue at risk of infarction' is based on the assumption that tissue with diffusion slowing in diffusion-weighted MRI (DWI) or decreased values of the apparent diffusion coefficient represents irreversibly damaged tissue. Recent experimental as well as clinical studies, however, have shown that tissue with diffusion slowing may well normalize if the hypoperfusion is moderate or transient. We will interpret these findings in the light of experimental data and suggest a way for the interpretation of different time courses of lesion development in DWI within a clinical MRI protocol. MR stroke imaging delivers important information in acute stroke, particularly in defining the 'tissue at risk of infarction'.

Brain Ischemia↗

Virtual arterial endoscopy as a diagnostic aid in a patient with basilar artery fenestration and thromboembolic pontine infarct.

Focal signal intensity loss of the basilar artery on MR angiograms obtained in a 69-year-old man was considered to be caused by an embolus, and thrombolytic therapy was initiated. On the follow-up MR angiograms, the same oval signal intensity loss of the basilar artery was observed. On the basis of a virtual endoscopic look into the basilar artery, the diagnosis of a rare vascular anomaly--a fenestration of the basilar artery--was confirmed and the presence of a thrombus at the site of the signal intensity loss was excluded.

Aged↗

Microembolism in Carotid Artery Disease.

Abnormal high intensity transient signals detectable with transcranial Doppler (TCD) sonography have been associated with formed cerebral microembolism. Using long-term TCD monitoring, these clinically silent microembolic events can be observed in patients with cerebrovascular disease. Downstream of high grade internal carotid artery (ICA) stenosis, they occur significantly more frequently in neurologically symptomatic than in asymptomatic patients. Although the occurrence of microemboli is random, the individual rate underlies circadian fluctuations and seems to decline within the first weeks after an ischemic event. Pathoanatomic work suggests that luminal ulcer and thrombosis of the stenosed ICA are the major sources of microemboli. Thus, by tapping into an important pathomechanism, the detection of clinically silent cerebral microembolism appears to provide paraclinical evidence of "unstable carotid artery disease" and may help to evaluate more specific treatment strategies. (ECHOCARDIOGRAPHY, Volume 13, September 1996)

Journal Article↗