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The rigid cranial vault contains:
 Brain Tissue (1400g/80%)
 Blood (75ml/10%)
 Cerebrospinal fluid (75ml/10%)

The volume and pressure of these three components are
usually in the state of equilibrium and produce the ICP.
ICP is usually measured in the lateral ventricles, with
normal pressure being 10-20mmHg.
CSF is produced by the Choroid Plexuses, specialized
structures made of ependymal cells which are located in
the ventricles.
CSF fills the brain ventricles, the central canal of the spinal
cord and the subarachnoid space.
CSF bathes the brain and spinal cord , providing a
protective cushion around the CNS.

CSF should be clear and transparent in appearance.
1. CSF IS PRODUCED BY THE CHOROID PLEXUS IN EACH
OF THE FOUR VENTRICLES.
 LATERAL VENTRICLE





Anterior Horn
Inferior Horn
Posterior Horn

2. CSF FROM THE LATERAL VENTRICLES FLOWS TO THE
THIRD VENTRICLE.
3. CSF FLOWS FROM THE THIRD VENTRICLE THROUGH
THE CEREBRAL AQUEDUCT TO THE FOURTH
VENTRICLE.
4. CSF EXITS THE FOURTH VENTRICLE THROUGH OPENING
IN THE WALL OF THE FOURTH VENTRICLES AND ENTERS
THE SUBARACHNOID SPACE. SOME ENTERS THE CENTRAL
CANAL OF THE SPINAL CORD.
5. CSF FLOWS THROUGH THE SUBARACHNOID SPACE TO
THE ARACHNOID GRANULATION IN THE SUPERIOR
SAGITAL SINUS, WHERE IT ENTERS THE VENOUS
CIRCULATION
States that, because of the limited space for
expansion within the skull, an increase in any one
components causes a change in the volume of the
others.
______________________________________
Because the brain tissue has limited space to expand, compensation
typically is accomplished by displacing or shifting CSF, increasing the
absorption or diminishing the production, or decreasing the cerebral
blood volume. Without such changes, ICP will begin to rise. Under
normal circumstances, minor changes in blood volume and CSF volume
occur constantly due to alterations in intrathoracic pressure, posture, bp
and systemic O2 and CO2 levels.
ICP OF MORE THAN 20 MMHG.
 Ischemia in early stages stimulates vasomotor center






causing systemic pressure to rise to maintain cerebral
blood flow.
Blood pressure, pulse and respirations are suggestive of
increase in ICP.
Increase in PaCO2 in blood and brain tissue causes
cerebral vasodilation leading to inrease CBF AND ICP.
Decrease in PaCO2 has a vasoconstrictive effect, limiting
blood flow to the brain.
Decreased venous flow may also increase Cerebral blood
volume, thus incresing in ICP
 Abnormal accumulation of fluid in intracellular,

extracellular or interstitial space or both. As
braintissue swells within the rigid skull several
mechanisms attempt to compensate for Increase in
ICP, it includes:
 Autoregulation-brains ability to change the diameter
of its blood vessels automatically to maintain a
constant CBF during alterations in Systemic Blood
Pressure.
 Arterial Systemic Blood Pressure is 50-150mmHg.

ICP changes are closely linked with Cerebral
Perfusion Pressure and ICP is less than
40mmhg.Normal CPP is 70-100mmHg.
 Patients with less than 50 mmHg CPP experience
irreversible neurologic damage therefore CPP must
be maintained at 70-80mmHg to ensure adequate
blood flow.
 CBF decreases significantly causing a Cushing
Response/Reflex.
 Is present when Ischemic, the vasomotor center

triggers an increase in arterial pressure in an effort
to overcome Increase in ICP. A Sympathetically
mediated response cause an increase in the systolic
blood pressure with the widening of the pulse
pressure and cardiac slowing.
 Increase in Systolic Blood Pressure, widening of
pulse pressure and reflex slowing of the heart rate.
Head Injury

Secondary effect in Brain Tumors,
Subarachnoid Hemorrhage and toxic and
viral Encephalopathies

Increase in Intracranial Pressure

Decrease Cerebral Perfusion

A-ltered respiration (cheyne
stroke)
P-rojectile vomiting
R-restlessness
I-rritability
L-evel of consciousness
B-bradycardia

Cerebral ischemia and cell death
Stimulates further swelling

Autoregulation
Restlessness without apparent cause
Confusion or increasing drowsiness

May shift brain tissue
through openings in the
rigid dura or presses
down on the brain stem

Cessation of blood flow to the
brain leading to irreversible
brain anoxia and brain death
HERNIATION

Becomes stuporous
Neurologic functioning deteriorates
Commatose---Decortication
---Decerebration
Medical Management
 Maintain Cerebral Oxygenation
 Decrease Intracranial Pressure
 Cerebral Perfusion
 Hyperventilation
 Prevent Complication
 Monitor ICP
 Prevent Intracranial Pressure
Mannitol
 Classification: Diagnostic agent, Osmotic

diuretics, Urinary irrigant
 Indication: reduction of intracranial pressure and

treatment of cerebral edema.
 Contraindication: contraindicated with anuria

due to severe renal disease.
Mannitol
 Precautions: use cautiously with pulmonary

congestion, active intracranial bleeding (except
during craniotomy), dehydration, renal disease,
heart failure, pregnancy, lactation.
 Availability: given in bolus doses
 Side Effects: increased urination, GI upset, dry

mouth, headache, blurred vision.
Mannitol
NURSING RESPONSIBILITIES:
 Assess patient’s history of pulmonary congestion,
active intracranial bleeding, dehydration, renal
disease, heart failure, pregnancy, lactation.
 Assess skin color, lesions, edema, hydration,
orientation, muscle strength, reflexes, pupils,
pulses, BP, perfusion, RR patterns, adventitious
sounds, urinary output patterns, S. electrolytes,
urinalysis, renal function test.
 Do not expose solutions to low temperatures,

crystallization may occur.
 Monitor serum electrolytes periodically with
prolonged therapy.
 Inform patient that he/she may experience side
effects.
 Encourage to report difficulty breathing and chest
pain.
PHENYTOIN
 Classification: antiarrhythmic, group 1b;

antiepileptic; hydantoin
 Indication: prevention of siezures.
 Contraindication: hypersensitivity to

hydantoins, sinus bradycardia, sinoatrial block,
strokes-adams syndrome, pregnancy, lactation.
PHENYTOIN
 Precautions: use cautiously with acute

intermittent porphyria, hypotension, severe
myocardial insufficiency, DM, hyperglycemia.
 Side effects: drowsiness, dizziness, confusion,

blurred vision, GI upset.
PHENYTOIN
 Nursing Responsibilities:
 Monitor injection sites carefully, drug solutions are

very alkaline and irritating.
 Give oral drug with or without food in consistent
manner.
 Monitor hepatic function periodically during longterm therapy; monitor bld. Counts and urinalysis
monthly.
 Monitor bld. urine sugar of patients with DM

regularly.
 Monitor bld. proteins to detect early malfunction of
the immune system.
 Inform client that he/she may experience side
effects.
 Encourage to report rash, severe nausea and
vomiting, drowsiness, slurred speech, impaired
coordination (ataxia), swollen glands, bleeding,
swollen and tender gums, yellowish discoloration
of the skin and eyes, joint pain, unexplained fever,
sore throat, persistent headache, malaise.
PENTOBARBITAL
 Classification: antiepileptic; barbiturate;

hypnotic; sedative or hypnotic
 Indication: sedative
 Contraindication: contraindicated with
hypersensitivity to barbiturates, manifest or latent
porphyria, marked liver impairment, nephritis,
severe respiratory distress, previous addiction to
sedative-hypnotic drugs, pregnancy.
PENTOBARBITAL
 Precautions: use cautiously with acute or chronic

pain, seizure disorders, fever, hyperthyroidism,
DM, severe anemia, pulmonary or cardiac disease,
status asthmaticus, shock, uremia.
 Availability: injection 50mg/mL
 Side Effects: drowsiness and anxiety
PENTOBARBITAL
 Nursing Responsibilities:
 Do not administer intra-arterially; may produce

arteriospasm, thrombosis, or gangrene.
 Administer IV doses slowly.
 Administer IM doses deep in a muscle mass.
 Do not use parenteral form if solution is discolored
or contains precipitate.
PENTOBARBITAL
 Monitor injection sites carefully for irritation, and

extravasation (IV use); solutions are alkaline and
very irritating to the tissues.
 Monitor BP, Pulse, and respiration carefully during
IV administration.
 Inform client that he/she may feel drowsy and less
anxious.
 Instruct client not to try to get up after receiving
this drug.
Other Drugs that may be used:
 STEROIDS
 HYPERTENSIVE DRUGS
 NEUROMUSCULAR BLOCKING AGENTS
INEFFECTIVE CEREBRAL TISSUE
PERFUSION RELATED TO INCREASED ICP

GOAL: Within 8 hours of nursing interventions
patient will have stable or improving levels of
consciousness.
Nursing Interventions
INDEPENDENT:
 Note customary baseline data (e.g., usual BP, weight,
mentation, ABGs, and other appropriate study
values).
Rationale:
 provide comparison with current findings.
 Determine presence of visual, sensory/motor

changes, headache, dizziness, altered mental
status, personality changes.
Rationale:
 this may indicate presence increased intracranial
pressure.
 Note history of brief/intermittent periods of

confusion/blackout.
Rationale:
 This suggests transient ischemic attacks-TIAs
 Elevate head of the bed 30 degrees and maintain

head/neck in midline or neutral position.
Rationale:
 To promote circulation/venous drainage.
 Assist with/monitor hypothermia therapy.

Rationale:
 Which may be used to decrease metabolic and
oxygen needs.
 Encourage client to quit smoking (if he/she does),

join smoke-out, and other stop-smoking program.
Rationale:
 Smoking causes vasoconstriction and may further
compromise perfusion
 Avoid emotional stress, frequent arousal from sleep, and

environmental stimuli (noise, conversation).

Rationale:
 This may increase ICP.
DEPENDENT:
 Administer medications such as diuretics
(mannitol), anticonvulsant (phenytoin) as ordered.
Rationale:
 These drugs are used to decrease cerebral edema
and prevent seizure.
Ineffective airway clearance related to
neuromuscular dysfunction

GOAL: Within 30 minutes of nursing intervention
interventions client will demonstrate
absence/reduction of congestion, improved oxygen
exchange.
Nursing Interventions
INDEPENDENT:
 Position head midline with flexion appropriate for
age/condition.
Rationale:
 To open or maintain open airway in at-rest or
compromised individual.
 Elevate the head of the bed.

Rationale:
 may aid in clearing secretions as well as improving
venous drainage of the brain.
 Auscultate breath sounds and assess air

movement.
Rationale:
 To ascertain status and note progress.
 Discourage coughing.

Rationale:
 because it increases ICP.
 Suction with care the secretions obstructing the airway

Rationale:
 because transient elevations of ICP occur with suctioning.
 Provide opportunities for rest; limit to level of

respiratory tolerance.
Rationale:
 Prevents/lessens fatigue.
 Maintain a neurologic observation record.

Rationale:
 Repeated assessments of the patient are made frequently
to immediately note improvement or deterioration.
C E R E B R A L A N G I O G R A P H Y
C O M P U T E D T O M O G R A P H Y ( C T )

SCANNING
M A G N E T I C R E S O N A N C E I M A G I N G
P O S I T R O N E M I S S I O N T O M O G R A P H Y
(PET)
T R A N S C R A N I A L D O P P L E R
L U M B A R P U N C T U R E
Cerebral angiography is a procedure that uses a special dye (contrast material) and
x-rays to see how blood flows through the brain.
A computed tomography (CT) scan is an imaging method that uses x-rays
to create pictures of cross-sections of the body.
Magnetic Resonance Imaging is a test that uses a magnetic field and pulses of
radio wave energy to make pictures of organs and structures inside the body.
Positron emission tomography (PET)
 Is a test that uses a special type of camera and a tracer (radioactive

chemical) to look at organs in the body. The tracer usually is a
special form of a substance (such as glucose) that collects in cells
that are using a lot of energy, such as cancer cells.
 During the test, the tracer liquid is put into a vein (intravenous,
or IV) in your arm. The tracer moves through your body, where
much of it collects in the specific organ or tissue. The tracer gives off
tiny positively charged particles (positrons). The camera records the
positrons and turns the recording into pictures on a computer.
 PET scan pictures do not show as much detail as computed
tomography (CT) scans or magnetic resonance imaging
(MRI) because the pictures show only the location of the tracer. The
PET picture may be matched with those from a CT scan to get more
detailed information about where the tracer is located.
 A PET scan is often used to evaluate cancer, check blood flow, or see
how organs are working.
Transcranial Doppler is a test used to measures the velocity of blood flow
through the brains blood vessels
Lumbar Puncture
 Is a diagnostic and at times therapeutic procedure

that is performed to collect a sample of cerebrospinal
fluid for biochemical, microbiological and cytological
analysis.
 Shows that you have high pressure in the
cerebrospinal fulid that sorrounds your brain and
spinal cord.
 Rarely as a treatment (therapeutic lumbar puncture)
to relieve increased intracranial pressure.
Surgical Management
 Shunt Surgery -where a catheter (a thin, flexible tube) is inserted into

the fluid-filled sapace in your brain or spine to divert excess fluid to
another part of the body.
Types
 Lumboperitoneal shunting - Shunting fluid from the spine to the
abdomen
 Ventriculoperitoneal shunting- from the brain to the abdomen
 Ventriculoatrial shunting- from the brain to the heart
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What you should know about Intracranial pressure

  • 1.
  • 2. The rigid cranial vault contains:  Brain Tissue (1400g/80%)  Blood (75ml/10%)  Cerebrospinal fluid (75ml/10%) The volume and pressure of these three components are usually in the state of equilibrium and produce the ICP. ICP is usually measured in the lateral ventricles, with normal pressure being 10-20mmHg.
  • 3. CSF is produced by the Choroid Plexuses, specialized structures made of ependymal cells which are located in the ventricles. CSF fills the brain ventricles, the central canal of the spinal cord and the subarachnoid space. CSF bathes the brain and spinal cord , providing a protective cushion around the CNS. CSF should be clear and transparent in appearance.
  • 4. 1. CSF IS PRODUCED BY THE CHOROID PLEXUS IN EACH OF THE FOUR VENTRICLES.  LATERAL VENTRICLE    Anterior Horn Inferior Horn Posterior Horn 2. CSF FROM THE LATERAL VENTRICLES FLOWS TO THE THIRD VENTRICLE. 3. CSF FLOWS FROM THE THIRD VENTRICLE THROUGH THE CEREBRAL AQUEDUCT TO THE FOURTH VENTRICLE.
  • 5. 4. CSF EXITS THE FOURTH VENTRICLE THROUGH OPENING IN THE WALL OF THE FOURTH VENTRICLES AND ENTERS THE SUBARACHNOID SPACE. SOME ENTERS THE CENTRAL CANAL OF THE SPINAL CORD. 5. CSF FLOWS THROUGH THE SUBARACHNOID SPACE TO THE ARACHNOID GRANULATION IN THE SUPERIOR SAGITAL SINUS, WHERE IT ENTERS THE VENOUS CIRCULATION
  • 6. States that, because of the limited space for expansion within the skull, an increase in any one components causes a change in the volume of the others. ______________________________________ Because the brain tissue has limited space to expand, compensation typically is accomplished by displacing or shifting CSF, increasing the absorption or diminishing the production, or decreasing the cerebral blood volume. Without such changes, ICP will begin to rise. Under normal circumstances, minor changes in blood volume and CSF volume occur constantly due to alterations in intrathoracic pressure, posture, bp and systemic O2 and CO2 levels.
  • 7. ICP OF MORE THAN 20 MMHG.
  • 8.  Ischemia in early stages stimulates vasomotor center     causing systemic pressure to rise to maintain cerebral blood flow. Blood pressure, pulse and respirations are suggestive of increase in ICP. Increase in PaCO2 in blood and brain tissue causes cerebral vasodilation leading to inrease CBF AND ICP. Decrease in PaCO2 has a vasoconstrictive effect, limiting blood flow to the brain. Decreased venous flow may also increase Cerebral blood volume, thus incresing in ICP
  • 9.  Abnormal accumulation of fluid in intracellular, extracellular or interstitial space or both. As braintissue swells within the rigid skull several mechanisms attempt to compensate for Increase in ICP, it includes:  Autoregulation-brains ability to change the diameter of its blood vessels automatically to maintain a constant CBF during alterations in Systemic Blood Pressure.
  • 10.  Arterial Systemic Blood Pressure is 50-150mmHg. ICP changes are closely linked with Cerebral Perfusion Pressure and ICP is less than 40mmhg.Normal CPP is 70-100mmHg.  Patients with less than 50 mmHg CPP experience irreversible neurologic damage therefore CPP must be maintained at 70-80mmHg to ensure adequate blood flow.  CBF decreases significantly causing a Cushing Response/Reflex.
  • 11.  Is present when Ischemic, the vasomotor center triggers an increase in arterial pressure in an effort to overcome Increase in ICP. A Sympathetically mediated response cause an increase in the systolic blood pressure with the widening of the pulse pressure and cardiac slowing.  Increase in Systolic Blood Pressure, widening of pulse pressure and reflex slowing of the heart rate.
  • 12. Head Injury Secondary effect in Brain Tumors, Subarachnoid Hemorrhage and toxic and viral Encephalopathies Increase in Intracranial Pressure Decrease Cerebral Perfusion A-ltered respiration (cheyne stroke) P-rojectile vomiting R-restlessness I-rritability L-evel of consciousness B-bradycardia Cerebral ischemia and cell death
  • 13. Stimulates further swelling Autoregulation Restlessness without apparent cause Confusion or increasing drowsiness May shift brain tissue through openings in the rigid dura or presses down on the brain stem Cessation of blood flow to the brain leading to irreversible brain anoxia and brain death HERNIATION Becomes stuporous Neurologic functioning deteriorates Commatose---Decortication ---Decerebration
  • 14.
  • 15. Medical Management  Maintain Cerebral Oxygenation  Decrease Intracranial Pressure  Cerebral Perfusion  Hyperventilation  Prevent Complication  Monitor ICP  Prevent Intracranial Pressure
  • 16.
  • 17. Mannitol  Classification: Diagnostic agent, Osmotic diuretics, Urinary irrigant  Indication: reduction of intracranial pressure and treatment of cerebral edema.  Contraindication: contraindicated with anuria due to severe renal disease.
  • 18. Mannitol  Precautions: use cautiously with pulmonary congestion, active intracranial bleeding (except during craniotomy), dehydration, renal disease, heart failure, pregnancy, lactation.  Availability: given in bolus doses  Side Effects: increased urination, GI upset, dry mouth, headache, blurred vision.
  • 19. Mannitol NURSING RESPONSIBILITIES:  Assess patient’s history of pulmonary congestion, active intracranial bleeding, dehydration, renal disease, heart failure, pregnancy, lactation.  Assess skin color, lesions, edema, hydration, orientation, muscle strength, reflexes, pupils, pulses, BP, perfusion, RR patterns, adventitious sounds, urinary output patterns, S. electrolytes, urinalysis, renal function test.
  • 20.  Do not expose solutions to low temperatures, crystallization may occur.  Monitor serum electrolytes periodically with prolonged therapy.  Inform patient that he/she may experience side effects.  Encourage to report difficulty breathing and chest pain.
  • 21. PHENYTOIN  Classification: antiarrhythmic, group 1b; antiepileptic; hydantoin  Indication: prevention of siezures.  Contraindication: hypersensitivity to hydantoins, sinus bradycardia, sinoatrial block, strokes-adams syndrome, pregnancy, lactation.
  • 22. PHENYTOIN  Precautions: use cautiously with acute intermittent porphyria, hypotension, severe myocardial insufficiency, DM, hyperglycemia.  Side effects: drowsiness, dizziness, confusion, blurred vision, GI upset.
  • 23. PHENYTOIN  Nursing Responsibilities:  Monitor injection sites carefully, drug solutions are very alkaline and irritating.  Give oral drug with or without food in consistent manner.  Monitor hepatic function periodically during longterm therapy; monitor bld. Counts and urinalysis monthly.
  • 24.  Monitor bld. urine sugar of patients with DM regularly.  Monitor bld. proteins to detect early malfunction of the immune system.  Inform client that he/she may experience side effects.  Encourage to report rash, severe nausea and vomiting, drowsiness, slurred speech, impaired coordination (ataxia), swollen glands, bleeding, swollen and tender gums, yellowish discoloration of the skin and eyes, joint pain, unexplained fever, sore throat, persistent headache, malaise.
  • 25. PENTOBARBITAL  Classification: antiepileptic; barbiturate; hypnotic; sedative or hypnotic  Indication: sedative  Contraindication: contraindicated with hypersensitivity to barbiturates, manifest or latent porphyria, marked liver impairment, nephritis, severe respiratory distress, previous addiction to sedative-hypnotic drugs, pregnancy.
  • 26. PENTOBARBITAL  Precautions: use cautiously with acute or chronic pain, seizure disorders, fever, hyperthyroidism, DM, severe anemia, pulmonary or cardiac disease, status asthmaticus, shock, uremia.  Availability: injection 50mg/mL  Side Effects: drowsiness and anxiety
  • 27. PENTOBARBITAL  Nursing Responsibilities:  Do not administer intra-arterially; may produce arteriospasm, thrombosis, or gangrene.  Administer IV doses slowly.  Administer IM doses deep in a muscle mass.  Do not use parenteral form if solution is discolored or contains precipitate.
  • 28. PENTOBARBITAL  Monitor injection sites carefully for irritation, and extravasation (IV use); solutions are alkaline and very irritating to the tissues.  Monitor BP, Pulse, and respiration carefully during IV administration.  Inform client that he/she may feel drowsy and less anxious.  Instruct client not to try to get up after receiving this drug.
  • 29. Other Drugs that may be used:  STEROIDS  HYPERTENSIVE DRUGS  NEUROMUSCULAR BLOCKING AGENTS
  • 30.
  • 31. INEFFECTIVE CEREBRAL TISSUE PERFUSION RELATED TO INCREASED ICP GOAL: Within 8 hours of nursing interventions patient will have stable or improving levels of consciousness.
  • 32. Nursing Interventions INDEPENDENT:  Note customary baseline data (e.g., usual BP, weight, mentation, ABGs, and other appropriate study values). Rationale:  provide comparison with current findings.
  • 33.  Determine presence of visual, sensory/motor changes, headache, dizziness, altered mental status, personality changes. Rationale:  this may indicate presence increased intracranial pressure.  Note history of brief/intermittent periods of confusion/blackout. Rationale:  This suggests transient ischemic attacks-TIAs
  • 34.  Elevate head of the bed 30 degrees and maintain head/neck in midline or neutral position. Rationale:  To promote circulation/venous drainage.  Assist with/monitor hypothermia therapy. Rationale:  Which may be used to decrease metabolic and oxygen needs.
  • 35.  Encourage client to quit smoking (if he/she does), join smoke-out, and other stop-smoking program. Rationale:  Smoking causes vasoconstriction and may further compromise perfusion  Avoid emotional stress, frequent arousal from sleep, and environmental stimuli (noise, conversation). Rationale:  This may increase ICP.
  • 36. DEPENDENT:  Administer medications such as diuretics (mannitol), anticonvulsant (phenytoin) as ordered. Rationale:  These drugs are used to decrease cerebral edema and prevent seizure.
  • 37. Ineffective airway clearance related to neuromuscular dysfunction GOAL: Within 30 minutes of nursing intervention interventions client will demonstrate absence/reduction of congestion, improved oxygen exchange.
  • 38. Nursing Interventions INDEPENDENT:  Position head midline with flexion appropriate for age/condition. Rationale:  To open or maintain open airway in at-rest or compromised individual.  Elevate the head of the bed. Rationale:  may aid in clearing secretions as well as improving venous drainage of the brain.
  • 39.  Auscultate breath sounds and assess air movement. Rationale:  To ascertain status and note progress.  Discourage coughing. Rationale:  because it increases ICP.  Suction with care the secretions obstructing the airway Rationale:  because transient elevations of ICP occur with suctioning.
  • 40.  Provide opportunities for rest; limit to level of respiratory tolerance. Rationale:  Prevents/lessens fatigue.  Maintain a neurologic observation record. Rationale:  Repeated assessments of the patient are made frequently to immediately note improvement or deterioration.
  • 41. C E R E B R A L A N G I O G R A P H Y C O M P U T E D T O M O G R A P H Y ( C T ) SCANNING M A G N E T I C R E S O N A N C E I M A G I N G P O S I T R O N E M I S S I O N T O M O G R A P H Y (PET) T R A N S C R A N I A L D O P P L E R L U M B A R P U N C T U R E
  • 42. Cerebral angiography is a procedure that uses a special dye (contrast material) and x-rays to see how blood flows through the brain.
  • 43. A computed tomography (CT) scan is an imaging method that uses x-rays to create pictures of cross-sections of the body.
  • 44. Magnetic Resonance Imaging is a test that uses a magnetic field and pulses of radio wave energy to make pictures of organs and structures inside the body.
  • 45. Positron emission tomography (PET)  Is a test that uses a special type of camera and a tracer (radioactive chemical) to look at organs in the body. The tracer usually is a special form of a substance (such as glucose) that collects in cells that are using a lot of energy, such as cancer cells.  During the test, the tracer liquid is put into a vein (intravenous, or IV) in your arm. The tracer moves through your body, where much of it collects in the specific organ or tissue. The tracer gives off tiny positively charged particles (positrons). The camera records the positrons and turns the recording into pictures on a computer.  PET scan pictures do not show as much detail as computed tomography (CT) scans or magnetic resonance imaging (MRI) because the pictures show only the location of the tracer. The PET picture may be matched with those from a CT scan to get more detailed information about where the tracer is located.  A PET scan is often used to evaluate cancer, check blood flow, or see how organs are working.
  • 46.
  • 47. Transcranial Doppler is a test used to measures the velocity of blood flow through the brains blood vessels
  • 48. Lumbar Puncture  Is a diagnostic and at times therapeutic procedure that is performed to collect a sample of cerebrospinal fluid for biochemical, microbiological and cytological analysis.  Shows that you have high pressure in the cerebrospinal fulid that sorrounds your brain and spinal cord.  Rarely as a treatment (therapeutic lumbar puncture) to relieve increased intracranial pressure.
  • 49. Surgical Management  Shunt Surgery -where a catheter (a thin, flexible tube) is inserted into the fluid-filled sapace in your brain or spine to divert excess fluid to another part of the body. Types  Lumboperitoneal shunting - Shunting fluid from the spine to the abdomen  Ventriculoperitoneal shunting- from the brain to the abdomen  Ventriculoatrial shunting- from the brain to the heart
  • 50. THANK YOU for Listening..!