Lumbar puncture Flashcards

Doherty, Diagnostic Lumbar Pncture (2014) Wright, Cerebrospinal fluid and lumbar puncture: a practical review (2012) UpToDate

1
Q

Lumbar puncture indicaions

A

A) To investigate or exclude meningitis

Bacterial
Viral
Tuberculous
Cryptococcal
Chemical
Carcinomatous

B) To investigate neurological disorders

Multiple Sclerosis
Sarcoidosis
Guillian Barre, Chronic Inflammatory Demyelinating Polyneuropathy
Mitochondrial Disorders
Leukencephalopathies
Paraneoplastic Syndromes

C) To demonstrate and manage disorders of Intracranial Pressure

Idiopathic Intracranial Hypertension
Spontaneous Intracranial Hypotension

D) To administer therapeutic or diagnostic agents*

Spinal anaesthesia
Intrathecal chemotherapy
Intrathecal antibiotics
Intrathecal baclofen
Contrast media in myelography or cisternography
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2
Q

Lumbar pncture anatomy: which tissues does the needle pierce?

A
The Lumbar Puncture needle pierces in order: 
skin 
subcutaneous tissue 
supraspinous ligament 
interspinous ligament 
ligamentum flavum 
epidural space containing the internal vertebral venous plexus 
dura 
arachnoid
the subarachnoid space
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3
Q

Tests frequently performed on CSF

A
  • Microbiology
    Cell count, culture and sensitivity
  • Biochemistry
    Protein and glucose
  • Xanthochromia
    Spetrophotometry
  • Oligoclonal bands
    Investigation of CNS inflammation
  • Cytology
    Investigation of malignant meningitis
  • Cytospin
    Investigation of CNS lympoma
  • Viral PCR
    PCR for viral DNA
  • ACE
    Investigation of neurosarcoidosis
  • Lactate
    Investigation of neurodegenerative disorders
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4
Q

Post lumbar puncture headache: Incidence, risk factors, symptoms, management

A

Incidence: 32%

Risk Factors:
younger age, female gender, and headache before or at the time of the procedure

Symptoms:
The symptoms of PLPH usually develop within 24 hours of Lumbar Puncture, and the natural history is for symptoms to resolve by about 10 days. The pain is usually diffuse, global or bitemporal headache, which can be accompanied by nausea, altered hearing, tinnitus, photophobia or neck stiffness. Low pressure may produce diplopia due to traction on the fourth or sixth cranial nerve

Management:
Maintaining a supine posture
Oral or intravenous fluids
Symptomatic management with analgesia and antiemetics
There is some evidence for the use of intravenous caffeine or intravenous theophylline
The definitive treatment if conservative management fails is epidural blood patching

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5
Q

Lumbar puncture: complications

A
Local discomfort and radicular pain
Spinal hematoma
Meningitis
Post lumbar puncture headache
Epidermoid tumor
Abducens palsy
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6
Q

Lumbar puncture: Red flags

A

Platelet count <40
International normalized ratio (INR) >1.5
Local skin infection
Local developmental abnormality, e.g., myelomeningocele
Raised intracranial pressure (with a pressure gradient across the CNS compartments)

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7
Q

When is a head CT before LP recommended?

A
Suspicion of raised intracranial pressure
Age >60 years
Immunocompromised patient
Previous CNS disease
Recent seizure
Reduced consciousness
Papilloedema
Abnormal neurological examination
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8
Q

Anticoagulant managemet prior to LP

A
  • There is no clear evidence that low-dose aspirin given
    alone increases hemorrhagic risk following LP
  • It is recommended that thienopyridine derivatives, e.g., clopidogrel and ticlopidine, should be discontinued for 7 and 14 days respectively
  • Discontinuing platelet glycoprotein IIb/IIIa inhibitors for 8 h prior to LP, e.g., tirofiban, has also been suggested.
  • Unfractionated heparin is routinely discontinued for 2–4 h prior to LP
    Post LP, unfractionated heparin should be delayed by at least 1 h to minimize hematoma risk
  • Low-molecular-weight heparin at prophylactic dose is discontinued for 12 h and at therapeutic dose for 24 h to allow normalization of coagulation

**No evidence to guide how long after thrombolysis a LP could be conducted

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9
Q

Lumbar puncture: Risk of CNS herniation pathophysiology

A

CNS herniation occurs if there is a change in the pressure gradient within the CNS compartment sufficient to cause movement of CNS tissue out of its normal position.
This can involve brain, spinal cord, and nerve root tissue, often with devastating and fatal consequences. In these cases, an abnormal pressure gradient already exists, and it is the further transient lowering of pressure, as a result of CSF withdrawal from an LP, which allows the raised pressure compartment above the LP to move along the pressure gradient and consequently move CNS tissue.
This is in contrast to states of uniformly raised intracranial pressure within the whole CNS compartment, e.g., idiopathic intracranial hypertension (IIH), where no internal pressure gradient has developed so is it is safe to perform an LP

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10
Q

Normal Intracranial Pressure in adults

A

10-20 cm

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11
Q

Differential diagnosis
of neurological disease
according to intracranial
pressure: Hypotension

A

A) Primary
- CSF leak
Atraumatic/ spontaneous

B) Secondary 
- CSF leak
Post LP
Post surgical
Trauma
  • Post-coital
- Drugs
Acetazolamide
Bendroflumethiazide
Furosemide
Indometacin
Topiramate
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12
Q

Differential diagnosis
of neurological disease
according to intracranial
pressure: Normotension

A
  • Normal pressure hydrocephalus
  • CNS demyelination
  • Bechet’s syndrome
  • CNS vasculitis
  • Neuropathy
  • Encephalitis
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13
Q

Differential diagnosis
of neurological disease
according to intracranial
pressure: Hypertension

A
  • Idiopathic intracranial hypertension
  • Intracranial hypertension without papilloedema (IWOP)
  • Intracranial space-occupying lesiona
  • Choroid plexus papilloma
  • Arachnoid granulation agenesis
  • Hydrocephalus (communicating and noncommunicating)
- Infective meningitis
Acute bacterial
Cryptococcal
Tuberculosis
Viral
Fungal
  • Cerebral venous sinus thrombosis
  • Acute hemorrhagic leucoencephalitis
  • Neurosarcoidosis
  • Guillian-Barre´ syndrome
  • Malignant meningitis
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14
Q

Which parameter indicates subdural hematoma and how to interpret it correctly

A

Subdural hematoma is indicated by xanthochromia

Xanthochromia is correctly assesed if
• Normal serum bilirubin levels.
• Delaying CSF sampling until the red cells have broken
down to bilirubin (12-h post-event is recommended).
• Using the least blood-stained CSF sample, usually the
last CSF sample collected.
• Transporting the CSF sample in the dark with minimal
agitation.
• Analyzing the sample with spectrophotometry rather
than visual inspection.

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15
Q

Normal CSF Findings

A

Appearance:
Clear

White cells:
0-5

Protein:
<0,5 g/L (23-38 mg d/L)

Glucose
>60-75% of serum glucose

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16
Q

CSF Findings in Viral Infecion

A

Appearance:
Clear/ opaque

White cells:
10-2000

Protein:
0,5-0,9

Glucose:
Normal

17
Q

CSF Findings in Bacterial Infection

A

Appearance:
Turbid

White cells:
100-60000

Protein:
>0,9 (1-5)

Glucose:
<40 % of serum glucose

18
Q

CSF Findings in Fungal Infection

A

Appearance:
Clear

White cells:
20-500

Protein:
>0,5 (0,5-5)

Glucose:
<80% of serum glucose

19
Q

CSF Findings in TB infection

A

Appearance:
Clear/opaque

White cells:
50-5000

Protein:
>1 (1-5)

Glucose:
<50% of serum glucose

20
Q

CSF Findings in GBS and spinal shock

A

Appearance:
Clear

White Cells:
Normal

Protein:
>1

Glucose:
Normal

21
Q

CSF Findings in Multiple Sclerosis

A

Appearance:
Clear

White Cells:
>15 atypical

Protein:
Normal

Glucose:
Normal

22
Q

In which conditions is lactate in CSF increased?

A

Mitochondrial disease

Inborn errors of metabolism (pediatrics)

23
Q

What are oligoclonal bands and in which conditions are present in CSF?

A

Oligoclonal bands are proteins, principally gamma immunoglobulin, thought to represent a local B cell
immune response, but may represent systemic infection or systemic immunoglobulin production

They may be present in:
multiple sclerosis
paraneoplastic disorders
systemic lupus erythematosus 
neurosarcoidosis
cerebral angiitis
CNS infections
24
Q

Which test is a biomarker for Creutzfeld Jacob Disease

A

CSF Protein 14-3-3

25
Q

Which test is a biomarker for narcolepsy

A

Low CSF hypocretin levels

26
Q

Spinal hematoma: Symptoms

A
  • severe, persistent back pain or radicular pain
  • new sensory or motor symptoms
  • sphincter disturbance
  • meningism
27
Q

Causes of Xanthochromia

A
  • Subarachnoid and intracerebral hemorrage
  • Traumatic tap
  • Jaundice
  • Protein >150
  • Hypercarotinemia
  • Malignant meningeal melanoma
28
Q

Causes of elevated CSF protein

A
  • Tumor
  • Bleeding
  • Nerve inflammation
  • Injury
29
Q

Causes of low CSF glucose

A
  • Bacterial meningitis
  • Mycobacterial, Mycoplasmal (M. pneumoniae),
    treponemal, and Fungal CNS infections
  • Leptomeningeal carcinomatosis
  • Leukemia
  • CNS lymphoma
  • Severe subarachnoid hemorrhages
  • Neurosarcoidosis
30
Q

What should you do for accurate CSF glucose interpretation?

A

Blood sample should be taken 2 hours prior to LP or LP should be performed in a fasting state

31
Q

What is albuminocytologic dissociation

A

The pattern of albuminocytologic dissociation
is seen most often in Guillain-Barré syndrome
and consists of an elevated protein, sometimes
extremely elevated, in the absence of an increased cell
count or other abnormalities

32
Q

How long after the entrance of RBC in the subarachnoid spase can xanthochromia be detected

A

2 hours after