Peds Flashcards

1
Q

Treatment Options for Triventricular Hydrocephalus

A

VP Shunt
ETV
ETV with Choroid Plexus Cauterization

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2
Q

ETV Procedure Steps

A

Stereotactic Navigation
Peelaway sheath
Insert Scope into lateral Ventricle
Identify ventricular anatomy and pass into 3V (often need to find the choroid plexus and follow anteriorly to foramen of monroe)
Floor of 3V… Mammillary bodies, pituitary recess, and TUBER CINEREUM (floor of 3V)
Make hole with blunt end of stealth probe, and then dilate with 5mm fogarty balloon catheter

Optional -> leave a ventricular catheter behind connected to a reservoir.

Follow up 1mo, 3mo, 6mo (MRI), then annually or q2y

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3
Q

ETV Pearls

A

Preop images with high res T2 (FIESTA or CISS) is essential to determine if anatomy is well suited for ETV

Prepontine membranes have been reported as a predictor of postop ETV failure. Typically more than 2mm of space is needed between the basilar artery and clivus to safely perform ETV

More than 90% of choroid needs to be coagulated to improve results of ETV.

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4
Q

Normal Volume of CSF in adult ventricles, and subarachnoid Space

A

100 to 150 mL

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5
Q

Rate of CSF Production

A

0.3 to 0.4 mL CSF per minute…

400 to 500 mL per day

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6
Q

Shunt failure rate at 2 years

A

60% still working

40% had some issue/revision

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7
Q

Shunt infection rate at 1 year

A

4 to 10%

Reduced with antibiotic impregnated catheters

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8
Q

Common Causes of Hydrocephalus

Peds

A
22% Prematurity and IVH
16% Myelomengocele
11% P Fossa brain tumor
8% Aqueductal Stenosis
8% Congenital Communicating
8% Other brain tumors
5% Head Injury

Less Common
intracranial cysts, nonpremature ICH, encephalocele, craniosynostosis

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9
Q

ETV Success

A

ETV Higher Success Rates…

  • older children (>1 year)
  • adults
  • previously unshunted patients
  • specific etiologies such as aqueductal stenosis, tectal glioma, P F Tumors

ETV Success Score helps estimate success rates

For neonates and young infants, ETV success rates are low (20-45%)

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10
Q

Arachnoid Cyst Facts

A

1) Most likely Asymptomatic and Don’t Grow
80% Stable over time
20% Change (10% GROW, 10% SHRINK)

2) Children with arachnoid cysts have an increased risk of ICH/SDH
- lifetime risk of 4-9%

3) Fenestration may relieve HA

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11
Q

Surgery for Arachnoid Cysts

A

Controversial
Most are followed.
Case by case basis… surgery if there is growth, symptoms of elevated ICP, hemorrhage, etc

Shunt and Fenestration
Debate as to which is best

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12
Q

Main Determinant of Surgery for Pediatric Gliomas

A

LOCATION

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13
Q

Glioma Categories

A
LOW GRADE
Pilocytic astrocytoma
pleomorphic xanthoastrocytoma
gangioglioma
dysembryoplastic neuroepithelial tumor
WHO II Astrocytoma
WHO II Oligodendroglioma

HIGH GRADE
Anaplastic Astrocytoma
Glioblastoma

BRAINSTEM GLIOMAS
diffuse intrinsic pontine glioma
exophytic meduallary glioma
midbrain tectal glioma

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14
Q

Imaging Findings

Oligodendroglioma and WHO II astrocytoma

A

hypointense T1
hyperintense T2
do not enhance

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15
Q

Imaging Findings

PXA
Gangioglioma
Pilocytic Astrocytoma

A

Cystic and solid components
May have mural nodule (possibly with enhancement)

PXA and GG often in TEMPORAL LOBE

Pilocytic Astrocytoma in CEREBELLUM 60% of the time

DNETs often in frontal or temporal lobe with hypo intense T1 and multilobulated hyper intense appearance on T2, no enhancement

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16
Q

Pediatric Glioma Pearls

A

All tumors that can be safely resected (with acceptable risk) should undergo GTR

Chemo for LGG can delay need for XRT, and in combo with XRT for HGG can improve survival

OS and PFS are most significantly associated with extent of surgical resection AS WELL AS histological grade

17
Q

Pediatric Low Grade Glioma Survival

A

10 year PFS

85% with GTR