Role of DWI, FLAIR, and ADC Sequences in Acute Ischemic Stroke Diagnosis and Management
Diffusion-weighted imaging (DWI) is the most sensitive and specific imaging technique for detecting acute ischemic stroke, with sensitivity of 88-100% and specificity of 95-100%, making it superior to both FLAIR and conventional CT for early stroke detection. 1
Diffusion-Weighted Imaging (DWI)
- DWI detects restricted diffusion as extracellular water moves into the intracellular environment during ischemia, making abnormal areas of ischemia readily visible within minutes of symptom onset 1
- DWI allows precise identification of lesion size, site, and age, which correlates significantly with clinical outcomes and final infarct volume 2, 3
- DWI can detect small cortical lesions and subcortical lesions, including those in the brain stem or cerebellum, areas often poorly visualized with standard MRI sequences and non-enhanced CT (NECT) 1
- DWI can identify subclinical satellite ischemic lesions that provide valuable information on stroke mechanism 1
- In TIA patients, DWI positivity (present in approximately 39% of cases) indicates higher risk for recurrent ischemic events 1, 4
Apparent Diffusion Coefficient (ADC)
- ADC maps are essential companions to DWI as they eliminate T2 "shine-through" effect, greatly increasing the specificity of the technique 1
- ADC values in ischemic lesions are typically 29% lower than in normal-appearing brain tissue 2
- ADC ratios correlate significantly with clinical outcome, making them valuable prognostic indicators 2, 5
- ADC values may help differentiate tissue destined to infarct from potentially salvageable tissue with reperfusion therapy 5
- Early after ischemia onset, the visible diffusion lesion includes both regions of irreversible infarction (with more severe ADC changes) and regions of salvageable penumbra (with less severe ADC changes) 1
Fluid-Attenuated Inversion Recovery (FLAIR)
- Standard FLAIR sequences are relatively insensitive to acute ischemic changes compared to DWI 1
- FLAIR detects approximately 91% of ischemic lesions, while DWI detects 98% 2
- Vascular hyperintensities on FLAIR sequences can indicate slow-flowing blood passing through leptomeningeal collaterals 1
- DWI-FLAIR mismatch (positive DWI with negative FLAIR) can help identify patients within the 4.5-hour treatment window for thrombolysis when time of onset is unknown 6
- FLAIR visibility of lesions increases with longer time from stroke onset, lower patient age, and larger DWI lesion volume 6
Clinical Applications in Stroke Management
- For patients within the 4.5-hour window (IV tPA candidates), either NECT or MRI is recommended to exclude intracranial hemorrhage before IV tPA administration 4
- DWI is superior to conventional imaging in patients with minor strokes and those imaged later after symptom onset 7
- Initial DWI lesion volume is a strong predictor of clinical outcome - in first-ever stroke patients, a lesion volume ≤22 mL predicts good outcome with 75% sensitivity and 100% specificity 2
- The artery susceptibility sign on gradient echo sequences is the MR correlate of the hyperdense MCA seen on NECT, with MRI detecting clot in 82% of cases versus 54% with NECT 1
- In patients beyond 6 hours from symptom onset, multimodal imaging with perfusion assessment (including DWI) is essential for treatment selection 4
Practical Considerations and Pitfalls
- While MRI with DWI is more sensitive than NECT for early detection of ischemic changes, it should not delay treatment if not immediately available 4
- A streamlined MRI protocol including DWI, FLAIR, gradient echo, and MR perfusion can be performed in approximately 10 minutes, making it competitive with CT in terms of acquisition time 1
- The main limitation to routine MRI use in acute stroke is not acquisition time but access to scanners on an emergency basis 1
- Focusing solely on structural imaging without perfusion assessment may miss the opportunity to identify salvageable tissue, especially in patients presenting beyond the standard treatment windows 4
- Magnetic susceptibility imaging (T2*-weighted sequences) can reliably detect intracranial hemorrhage, allowing MRI to be used as the sole initial imaging modality for evaluating acute stroke patients 1