Hydrocephalus.pdf

This presentation will help the reader develop clinical skills that will enable them to quickly diagnose and effectively manage Hydrocephalus

1. PAEDIATRICS AND CHILD HEALTH
•Paediatrics and Child Health
•Hydrocephalus
Dr.ChongoShapi(BSc.HB, MBChB)
-Medical Doctor
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4. Hydrocephalus
•Is the disturbance of CSF formation, flow or
absorption leading to an abnormal accumulation of
CSF in the ventricles of the brain
•Is classified according to its underlying pathology
•It can be classified into:
1.Communicating hydrocephalus (non-obstructive):
no obstruction
2.Non-communicating (obstructive) hydrocephalus:
where there is obstruction
-Can also be classified into congenital or acquired
hydrocephalus
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5. Communicating hydrocephalus
-No reabsorption of CSF into the duralvenous
sinuses
-Can occur with subarachnoid haemorrhage (SAH)
or congenital absence of arachnoidalgranulation
-This results in accumulation of CSF within the
subarachnoid spacecausing compression of the
brain tissue within the cranial cavity
-This leads to brain atrophy and long-term mental
retardation
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6. CT scan
See the progression
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7. Non-communicating Hydrocephalus
•There is usually blockage within the ventricular
system
•This results in accumulation of CSF within the
ventricular system
•The brain matter therefore is pushed outwards
against the skull
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8. Causes of Non-Communicating Hydrocephalus
1.TORCHES
2.Mass lesions: abscess, haematoma, tumours
3.Aqueductalstenosis
4.Dandy Walker Malformation (DWM):
-Prominent occiput due to cystic expansion of the 4
th
ventriclein the posterior cranial fossa and midline
cerebellar hypoplasia resulting from developmental
failure of the 4
th
ventricle during embryogenesis
5. AnoldChiariMalformation type II (ACM-II):
-For-shortened occiput where portions of the
cerebellum and brainstem herniate into the cervical
spinal canalblocking CSF flow to posterior cranial
fossa
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9. Causes of Communicating Hydrocephalus
1.Meningitis (TB)
2.Subarachnoid haemorrhage (SAH)
3.Meningeal malignancy
4.Absence of arachnoid granulations
5.Choroid plexus papilloma
6.Basilar impression
7.Achondroplasia(due to increased duralvenous
sinus pressure)
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10. Questions to Establish Diagnosis
Perinatal:
-Was the child born at term or preterm?
-Did the child cry immediately after birth?
-What was the head circumferenceat birth?
-Any abnormality of the spine?
Post-natal:
•At what agedid the caregiver notice the head getting
bigger?
•Did the child have any fever before the head started getting
big?
•What treatment was given and for how long?
•Any history of convulsions?
•Any similar illness in the siblings?
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11. Clinical Presentation
SYMPTOMS
•Infants:
-Poor feeding
-Irritability
-Reduced activity
-Vomiting
•Children and adults include the
following:
-Cognitive deterioration
-Headaches (initially in the morning)
-Neck pain, suggesting tonsillarherniation
-Vomiting, more significant in the morning
-Blurred vision: A consequence of
papilledema and, later, of optic atrophy
-Double vision: Related to unilateral or
bilateral sixth nerve palsy
-Difficulty in walking due to spasticity:
more in lower limbs because the
periventricular pyramidal tract is
stretched by the hydrocephalus
-Drowsiness
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12. SIGNS
Infants:
•Head enlargement (head circumference ≥98th
percentile for age)
•Separation (dysjunction) of sutures
•Dilated scalp veins
•Delayed closure of anterior fontanelleand will be
tense
•Sun-setting eye sign:
-Characteristic of increased intracranial pressure (ICP);
downward deviation of ocular globes, retracted
upper lids, visible white scleraeabove iris
-Increased limb tone (spasticity preferentially affects
the lower limbs)
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15. Children and adults:
•Papilledema
•Failure of upward gaze
•Unsteady gait
•Large head
•Unilateral or bilateral sixth nerve palsy (secondary
to increased ICP)
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16. Work UP
•Lab
-No specific blood tests are recommended
-Genetic testing and counselling when X-linked
hydrocephalus is suspected
-Evaluate CSF in post-hemorrhagicand post-meningitic
hydrocephalus to exclude residual infection
•Imaging
-Skull X-ray (calcifications, thin skull bones, separation
of sutures, beaten copper appearance (BCA))
-CT/MRI head
-EEG when seizures
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17. Beaten copper appearance
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18. Treatment
•Surgery is the mainstay of treatment
•Medical
-Use is controversial
-As temporal measure to treat post-hemorrhagicor
post-meningitichydrocephalus in neonates to delay
surgical intervention
-Medications:
a. Decreasing CSF secretion by the choroid plexus
-Acetazolamide
-Furosemide
b. Increasing CSF reabsorption
-Isosorbide(effectiveness is questionable)
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19. Surgical Treatment
•Surgical treatment is the preferred therapeutic
option
•Options:
a. Shunting
-Ventriculoperitoneal(VP)
-Ventriculoatrial(VA)
-Lumboperitoneal
-Ventriculopleural
-Torkildsenshunt
b. Endoscopic third ventriculostomy(ETV)
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20. Shunting
•The principle of shunting
is to establish a
communication between
the CSF (ventricular or
lumbar) and a drainage
cavity (peritoneum, right
atrium, pleural cavity)
•Shunts are not perfect
•All alternatives to
shunting should be
considered first
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21. VP shunt
•Is used most commonly
•The lateral ventricle is the
usual proximal location
•The advantage of this shunt
is that the need to lengthen
the catheter with growth
may be obviated by using a
long peritoneal catheter
•This reduces repeated
lengthening in a growing
child
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22. VA shunt
•Also called a "vascular shunt.“
•It shunts the cerebral ventricles
through the jugular vein and
superior vena cava into the right
cardiac atrium
•It is used when the patient has
abdominal abnormalities:
-Peritonitis
-Morbid obesity
-After extensive abdominal surgery
•This shunt requires repeated
lengthening in a growing child
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23. LumboperitonealShunt
•Used only for:
-Communicating
hydrocephalus
-CSF fistula
-Pseudotumorcerebri
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24. Torkildsenshunt
•Used rarely
•It shunts the ventricle to
cisternalspace
•Effective only in acquired
obstructive
hydrocephalus
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25. Ventriculopleuralshunt
•A ventriculopleuralshunt
is considered second line
due to fear of breathing
difficulties
•Used if other shunt types
are contraindicated
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26. Complications of Shunting
1.Risk of infection
2.Blockage of the shunt
3.Patient outgrows the shunt
4.Shunt dislodgement
5.Shunt nephritis
6.Subdural haematoma
7.Pseudocyst
8.Slit ventricalsyndrome due to overdrainage
(CT/MRI shows very small “slit-like” collapsed
ventricles)
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27. ETV
•Is a surgical procedure in which an opening
(ostomy) is created in the floor of the 3
rd
ventricle
using an endoscopeplaced within the ventricular
system through a burr hole (trephine)
•This allows the CSF to flow directly to the basal
cisterns,thereby shortcutting any obstruction
•It is used as an alternative to a cerebral shuntto
treat certain forms of obstructive hydrocephalus,
such as aqueductalstenosis
•Complications include subarachnoid haemorrhage,
basilar artery injury and hypothalamic or pituitary
injury
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28. ETV
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29. Thanks
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