pulmonary AVM Flashcards

1
Q

preprocedural steps before pulmonary AVM procedure

A
  1. EKG - to look for Left heart block (since you are going through the right heart for the procedure)
  2. antibiotics
  3. anticoagulation with heparin to prevent pericatheter thrombus
  4. air embolism risk (bubble filter IVs or blood filters)
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2
Q

should pulmonary AVMs less than 3 mm be treated

A

yes

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3
Q

what is the technique used to embolize pAVMs known as

A

anchor technique

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4
Q

common side effect of pAVM embolisation

A

pleurisy

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5
Q

what pattern of inheritance is HHT

A

autosomal dominant

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6
Q

what criteria are used to diagnose HHT

A

The Curaçao criteria

  1. Epistaxis (Nosebleeds): Frequent, spontaneous nosebleeds that start in childhood or adolescence.
  2. Telangiectasia: Presence of multiple telangiectasiason mucous membranes (e.g., inside the mouth) or skin
  3. Arteriovenous Malformations (AVMs): in organs such as the lungs, liver, brain, or GI
  4. Family History: A family history of HHT or a diagnosis of HHT in a close relative.

To diagnose HHT, a patient usually needs to meet at least three of these criteria. If a person meets two of the criteria, a genetic test or further clinical evaluation may be recommended to confirm the diagnosis.

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7
Q

what percentage of adults with HHT have epistaxis

A

90%

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8
Q

what percentage range of patients with a solitary pAVM have HHT

A

65-90%

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9
Q

what are the symptoms of paradoxical emboli 2/2 pAVM

A
  1. migraine
  2. TIA/Stroke
  3. brain abscess
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10
Q

what percentage range of pAVMs are simple

A

80-90%

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11
Q

does anyone know the growth rate of pAVMs

A

NO

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12
Q

what is the diagnostic imaging modality used for screening for pAVM

A

contrast echocardiogram

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13
Q

what lifelong precautions are needed for patients with pAVMs

A

antibiotic prophylaxis for any procedures (including dental) and air embolism/bubble precautions

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14
Q

does paradoxical embolization depend on the size of a pAVM feeding artery

A

no, it can happen with any feeding artery diameter, even less than 3 mm

Shovlin CL, Jackson JE, Bamford KB, et al. Pri-mary determinants of ischaemic stroke/brain ab-scess risks are independent of severity of pulmo-nary arteriovenous malformations in hereditaryhaemorrhagic telangiectasia. Thorax 2008; 63:259–266

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15
Q

what are the predictors of recanalization and reperfusion of a pAMV

A
  1. embolization more than 1 cm from the sacn
  2. single coils used for embolization
  3. coil oversizing (not getting a good packing)
  4. large feeding arteries
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16
Q

if an amplatzer plug is used to embolize a pAVM feeding artery, what can be done to decrease the risk of recanalization

A

placing a coil behind it

17
Q

when is imaging obtained after pAVM embolization

A

6 months after
then 3-5 years if sac involution occurs

18
Q
A