Treatment/Prognosis Flashcards

1
Q

What are the 3 Tx options for AVMs?

A

Sg, radiosurgery, and endovascular embolization

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2
Q

When is Tx indicated?

A

An Hx of previous rupture is the most important consideration; other factors include pts with an estimated elevated risk of future hemorrhage d/t younger age, AVM location, size, or other vascular features.

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3
Q

What is a simple way to approximate the risk of recurrence?

A

Lifetime risk of hemorrhage = 105 – pt age in yrs.

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4
Q

What is the goal of Tx with AVMs? Why?

A

Complete obliteration is the goal, there is no benefit or decreased risk of bleed if the obliteration is partial.

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5
Q

Is Tx of unruptured AVMs beneficial?

A

Possibly. The ARUBA trial is the only RCT to address this issue and compared medical management alone to medical management +interventional therapy (neurosurgery, SRS, or embolization). It was stopped early when the risk of death or stroke was found to be significantly lower in the medical management group (HR 0.27; 95% CI 0.14–0.54). (Mohr JP et al., Lancet 2014) However, in those pts who had imaging evidence of obliteration, an 85% risk reduction of stroke was noted (HR 0.15; CI 0.02–0.53; p = 0.002). (Hanakita S et al., Stroke 2016)

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6
Q

Which lesions are most amenable to Sg?

A

Those with low (I–III) Spetzler–Martin scores are most amenable to Sg.

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7
Q

What is frequently done for grade III lesions before Sg?

A

Embolization can be performed for grade III lesions before Sg.

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8
Q

What is the main advantage of Sg?

A

Immediate cure and reduction in the risk of hemorrhage

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9
Q

For what AVM lesions is SRS preferred?

A

Radiosurgery is preferred for lesions <3 cm that are located in deep or eloquent regions of the brain.

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10
Q

What is the main disadvantage of SRS for AVMs?

A

The main disadvantage of SRS is the lag time of 1–3 yrs to complete obliteration (i.e., continued bleeding risk).

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11
Q

How does RT lead to AVM obliteration?

A

Vascular wall thickening (fibrointimal hyperplasia) and luminal thrombosis from RT effect result in obliteration of the AVM.

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12
Q

Is the bleeding risk completely eliminated after SRS?

A

No. It is reduced by ∼54% during latency period and 88% after obliteration but not eliminated. (Maruyama K et al., NEJM 2005; Yen CP et al., Stroke 2011)

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13
Q

On what do SRS cure rates for AVMs primarily depend?

A

Size of AVM: 81%–91% if <3 cm, lower if >3 cm (Maruyama K et al., NEJM 2005)

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14
Q

What can be done for high-grade AVMs (IV–V) not amenable for Sg?

A

Staged SRS (different components targeted at separate sessions) (Sirin S et al., Neurosurg 2006)

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15
Q

For which AVMs can embolization be curative?

A

AVMs <1 cm that are fed by a single artery can be cured by embolization alone.

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16
Q

How are AVMs with feeding artery aneurysms managed?

A

If the aneurysm is >7 mm in diameter, clip or coil the aneurysm 1st, then treat the AVM. The aneurysm is at greater risk for rupture if the AVM is treated 1st.

17
Q

What SRS doses are commonly used for AVMs?

A

Lesions <3 cm: 21–22 Gy to 50% IDL. If the lesion is in the brainstem, lower the dose to ≤16 Gy.

Lesions >3 cm: 16–18 Gy to 50% IDL.