Evaluation of Arteriovenous Malformations (AVMs)
Primary Imaging Modality
Digital subtraction angiography (DSA) is the gold standard and mandatory imaging modality for pre-treatment assessment of brain AVMs, providing superior spatial and temporal resolution that cannot be matched by non-invasive imaging. 1, 2, 3
- DSA evaluation must include 2D, 3D, and reformatted cross-sectional views to provide comprehensive angioarchitectural information 1, 2
- Pre-treatment DSA must identify all feeding vessels, nidus architecture, and venous drainage patterns to guide treatment planning 3, 4
- Selective and superselective angiography is required to accurately assess the lesion's angioarchitecture 5
Complementary Non-Invasive Imaging
MRI and MRA
- MRI provides essential information about the AVM's relationship to eloquent brain regions and surrounding parenchyma 2
- MRA helps with initial assessment but lacks the spatial and temporal resolution of DSA for detecting small feeding vessels and detailed nidus characteristics 2, 4
- MRI offers superior soft tissue detail for nidus characterization and eloquent cortex localization 3
CT Angiography
- CT demonstrates 90% sensitivity for overall AVM detection and 100% sensitivity for AVMs >3 cm, making it useful for initial assessment 2
- For ruptured AVMs, CT imaging should be performed immediately to confirm hemorrhage and assess hematoma volume 3
- CT angiography can assist with initial evaluation but cannot replace DSA for treatment planning 4
Clinical Assessment Components
Presentation Patterns
- Pediatric patients present with hemorrhage in 75-85% of cases, compared to lower rates in adults 2
- Hemorrhagic events carry a 25% mortality rate in children with brain AVMs 2
- Adult presentations commonly include intracranial hemorrhage, seizures, or incidental findings on neuroimaging 6
Risk Stratification Using Spetzler-Martin Grading
The Spetzler-Martin grading system is the most commonly used scale for risk stratification and treatment planning. 1
The system assigns points based on three factors:
- Size: 1 point for <3 cm, 2 points for 3-6 cm, 3 points for >6 cm 1
- Eloquent location: 1 additional point if in eloquent cortex 1
- Deep venous drainage: 1 additional point if present 1
Hemorrhage Risk Assessment
- Annual rupture risk is 2-4% for unruptured AVMs 3
- Risk increases to 6-18% in the first year following initial hemorrhage 3
- After a second bleed, risk escalates to 25% in the first year 3
- Prior hemorrhage is a strong predictor of future bleeding risk, particularly in children 2
Additional Evaluation Considerations
High-Risk Features to Identify
- Associated aneurysms on feeding vessels or within the nidus 1
- Venous stasis or venous aneurysms that may increase hemorrhagic risk 1
- Deep location (basal ganglia, thalamus) which is more common in pediatric AVMs 2
- Single draining vein, which increases rupture risk 7
Functional Assessment
- Evaluation of eloquent cortex proximity using functional imaging should be incorporated into treatment planning 1
- Assessment of potential neurological deficit impact on quality of life is essential 1
Post-Treatment Surveillance
Intraoperative or immediate postoperative angiography is mandatory to confirm complete obliteration after any intervention. 2, 3
- Long-term imaging follow-up with DSA is essential to detect residual or recurrent AVM 1, 2, 3, 4
- Non-invasive imaging may be used for longitudinal follow-up in stable cases, but DSA remains the gold standard for detecting concerning findings 1, 2
- Recurrence after apparent complete obliteration occurs occasionally and may be more common in children, necessitating lifelong surveillance 2
Common Pitfalls to Avoid
- Relying solely on non-invasive imaging (MRA/CTA) for treatment planning—this will miss critical angioarchitectural details that only DSA can provide 1, 2, 4
- Failing to obtain immediate post-treatment angiography—residual AVM will not be protected from hemorrhage and requires immediate re-intervention 2, 3
- Discontinuing surveillance after initial negative follow-up imaging—AVMs can recur years after apparent cure, particularly in pediatric patients 2