on contrast-enhanced short-time MRI and conventional CT: Comparison of diagnostic parameters in patients with acute neurological symptoms - Ultrafast Brain MRI in Acute Neurological Emergencies: the FAMILIES trial (LMU-RAD00055)
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- I67.88
- Sponsor
- Klinikum der Universität München, Campus Großhadern
- Enrollment
- 150
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
Results: Ninety-three additional intracranial lesions (acute ischemia, n = 21; intracranial hemorrhage/microbleeds, n = 27; edema, n = 2; white matter lesion, n = 38; chronic infarction, n = 3; others, n = 2) were detected by ultrafast-MRI, whereas 101 additional intracranial lesions were detected by the standard-length protocol (acute ischemia, n = 24; intracranial hemorrhage/microbleeds, n = 32; edema, n = 2; white matter lesion, n = 38; chronic infarction, n = 3; others, n = 2). Image quality was equivalent to the standard-length protocol. Ultrafast-MRI demonstrated high diagnostic accuracy (sensitivity, 0.939 [0.881-0.972]; specificity, 1.000 [0.895-1.000]) for the detection of intracranial pathologies. MRI led to a change in patient management in 10% compared with the initial CT. Conclusions: Ultrafast-MRI enables time-optimized diagnostic workup in acute neurological emergencies at high sensitivity and specificity compared with a standard-length protocol, with direct impact on patient management. Ultrafast MRI protocols are a powerful tool in the emergency setting and may be implemented on various scanner types based on the optimization of individual acquisition parameters.
Investigators
Eligibility Criteria
Inclusion Criteria
- •patients of the emergency department of the Ludwig\-Maximilians\-University (LMU) Munich\-Großhadern (minimum age 18 years)
- •\- suspected intracranial pathologies (hemorrhage, ischemia, tumor, signs of inflammation, edema, increased intracranial pressure (ICP))
- •\- insufficient explanation of symptoms after examination using the cranial computed tomography
Exclusion Criteria
- •\- patients with MRI\-incompatible intracorporeal material (e.g. pacemaker, bladder pacemaker, nerve stimulators)
- •\- lacking capability of giving consent
- •\- claustrophobia
- •\- unstable general condition
- •\- pregnancy
- •\- sufficient explanation of symptoms by the cranial computed tomography
Outcomes
Primary Outcomes
Not specified