INDICATIONS

Diagnosis

Suspected SAH

  • Perform LP only if scan negative in face of reasonable clinical suspicion, and at least 12 hr after onset of symptoms (e.g. headache)
  • Tests
    • CSF xanthochromia, glucose and protein plus
    • Blood test for LFT’s, glucose and protein

Myelopathies and suspected multiple sclerosis


If spinal cord compression suspected, do not perform LP
  • Tests
    • protein, IgG or gammaglobulin,
    • oligoclonal bands
    • N.B. take paired blood sample

Acute or demyelinating peripheral neuropathies

  • e.g. Guillain-Barré syndrome
  • Tests
    • cells, protein

Infections of CNS

  • e.g. bacterial meningitis, tuberculosis, acute and subacute encephalitides, neurosyphilis, viral, fungal, and protozoal meningitis
  • Tests
    • gram stain, cells, protein, treponemal serology
    • glucose, culture, special stains, and antibodies

Meningeal infiltration

  • Tests
    • cytology

Suspected idiopathic intracranial hypertension

  • Tests
    • opening CSF pressure

Introduction of contrast media

Introduction of chemotherapeutic agents

  • e.g. in leukaemia

CONTRAINDICATIONS

  • Raised intracranial pressure. Request CT scan
    • indicated by morning or postural headache, vomiting, and papilloedema
    • in patients with acute headache and reduced conscious level, a normal CT scan result can be falsely reassuring – see Community-acquired meningitis guideline
    • danger is of fatal transtentorial or cerebellar ‘coning’
  • Suspected spinal cord compression. MR scan is investigation of choice
    • diagnostic LP does not distinguish intrinsic lesion (e.g. multiple sclerosis) from extrinsic compression by disc or tumour
  • Local sepsis
    • puncture through infected skin carries risk of meningitis
  • Coagulopathy

EQUIPMENT

  • Sterile gloves
  • Green sterile towel and drapes
  • Dressing pack with cotton balls, gauze swabs, gallipot
  • Skin antiseptic
  • Lidocaine 2% plain injection in 5 mL syringe with orange (25 G) and green (21 G) needles
  • LP needles (22 G): 3 and 3.5 inches long
    • prefer atraumatic needle for elective LP
  • Manometer
  • Specimen containers (3 clear glass, 1 grey top plastic) for microscopy/culture, protein, other tests (if indicated), and glucose, respectively. See SPECIMENS
    • if further investigations may be required over the next few days, take an extra container(s) to send to microbiology and virology with a request to ‘please store sample’
  • Adhesive dressing

PROCEDURE

  • If not competent in procedure, organise supervision by a clinician experienced in the procedure 

Preparation

  • Appoint and brief assistant
  • Number the 3 (or more, see above) clear glass bottles (1, 2, 3) 

Consent

  • Explain procedure, inform patient of symptoms that may follow procedure, and reassure
  • Obtain and record written consent – see Consent guideline

Position of patient and puncture

  • Place patient on left side with back against edge of bed, neck slightly flexed, and both legs drawn up towards chest
    • consider placing pillow between patient’s legs to ensure that back is perpendicular to bed, and raise bed to comfortable height
  • Palpate anterior superior iliac crest. L3–4 interspace is apparent as a palpable gap lying perpendicularly beneath it, but L2–3 or L4–5 are equally acceptable sites
  • Mark skin over chosen interspace about 1 cm inferior to tip of adjacent spinous process

Aseptic technique

  • Wash hands and put on gloves
  • Cleanse patient’s skin and position sterile drapes
  • Assistant opens all packs including syringes and needle, shaking sterile contents onto sterile towel
  • Check all equipment fits
  • Draw up lidocaine while assistant holds lidocaine bottle
  • Stretch patient’s skin evenly over interspace, infiltrate skin and deeper tissues with lidocaine (orange needle for skin and green needle for deeper tissues)
    • allow at least 1 min for lidocaine to work
  • Introduce LP needle at 90° to back, with bevel in sagittal plane (to minimise size of hole) and pointing slightly towards head
  • Push through resistance of superficial supraspinous ligament and negotiate interspinous ligament to meet firmer resistance of ligamentum flavum at about 4–7 cm
  • An extra push results in a popping sensation as dura is breached and needle enters subarachnoid space
  • Withdraw stylet and clear colourless fluid should drip out
  • Measure CSF pressure, then collect CSF specimens with assistant holding CSF bottles
  • After CSF collected and while still sterile, replace LP stylet into introducer and withdraw LP needle

Dry tap

  • If no fluid emerges or fluid does not flow easily, rotate needle – a flap of dura may be lying against bevel
  • If there is still no fluid, reinsert stylet and cautiously advance, withdrawing stylet after each movement
    • pain radiating down either leg indicates that needle is too lateral and has hit nerve roots. Withdraw needle almost completely, check patient's position, and reinsert in midline
  • If needle meets total obstruction, do not force it: it may be lying against an intervertebral disc and could damage it. Again, withdraw, check position, and reinsert
  • If there is complete failure, move one space up or down depending upon original position
  • Procedure may be easier if patient is sitting up, although this would preclude measurement of CSF pressure
  • Dry tap usually results from faulty technique
    • after 2 or 3 attempts ask someone more experienced for help
    • rare causes of genuine dry tap are arachnoiditis, meningeal infiltration and true low CSF pressure

Manometry

  • When CSF flows freely, connect manometer to needle hub
  • Ask assistant to hold top and record pressure (normal 80–180 mm CSF)
    • height of meniscus should change with respiration

Low pressure

  • Most common cause is poor needle placement
    • if genuine, do not try to aspirate as CSF flow may be obstructed by cerebellar tonsil herniation or spinal block
  • In either case, seek a neurological opinion

Raised pressure

  • Slightly raised CSF pressure in very anxious or obese patient may be ignored
  • Investigate pressures >250 mm as abnormal
    • if greatly raised pressure is discovered in clear fluid, collect CSF from the manometer to provide specimens
    • ask patient to 'uncurl' to see if pressure falls once abdominal compression relieved
    • if still raised despite this manoeuvre, withdraw needle immediately and seek neurological opinion

Bloodstained tap

  • Collect bloodstained fluid in 3 tubes

Traumatic tap

  • Blood forms streams in otherwise clear CSF
  • The first 3 consecutive specimens show clearing of blood and usually become less obviously coloured, with a corresponding fall of the red cell count

Subarachnoid bleeding

  • CSF is usually diffusely bloodstained in all 3 tubes, but the 3-tube test should not be relied upon to exclude SAH

SPECIMENS

  • Requests depend on clinical problem
  • If taking CSF samples for both diagnostic microbiology and suspected SAH, take samples for microbiology first

Diagnostic microbiology

Possible specimens

  • Gram stain, cells, protein, treponemal serology
  • Glucose, culture, special stains, and antibodies
  • For routine bacterial culture, always obtain 1 mL in sterile container
    • if TB meningitis suspected, obtain additional ≥5 mL for TB culture
    • if pre-treated with antimicrobials and meningococcal meningitis suspected, obtain additional 1 mL in separate sterile container for meningococcal PCR
    • if herpes simplex virus meningo-encephalitis suspected, obtain additional 1 mL in separate sterile container for HSV PCR
    • request other CSF PCR tests according to suspected pathogen(s)
  • If further investigations may be required over the next few days, take an extra container(s) and send to virology and microbiology with a request to ‘please store sample’
  • Suspected SAH

    CSF glucose

    • CSF into fluoride oxalate bottle and send to clinical biochemistry

    CSF xanthochromia and protein

    • CSF into 3 plain bottles (minimum volume 1 mL in each bottle)
    • Place last of 3 plain bottles to be filled in dark container (protected from light)

    Blood tests

    • LFT’s, glucose and protein

    Transport and biochemistry

    • Provide following information with sample
      • time between onset of symptoms and LP
      • results of CT scan. Xanthochromia screening will normally be performed only where CT scan is negative
      • date of any previous LP. Xanthochromia screening is misleading after recent LP
    • Send to clinical biochemistry (do not use pneumatic tube system)
    • Contact clinical biochemistry, ask for senior member of staff or bleep duty biochemist
      • explain that CSF sample is being sent for xanthochromia screening

    Myelopathies and suspected multiple sclerosis

    • Protein, IgG or gammaglobulin
    • Oligoclonal bands
    • N.B. take paired blood sample

    Acute or demyelinating peripheral neuropathies

    • Cells, protein 

    Meningeal infiltration

    • Cytology 

    AFTERCARE

    • Headache is best prevented by careful technique, use of a small gauge needle and ensuring adequate fluid intake for first 24 hr
      • lying down after LP does not reduce the incidence of headache

    Postural headache

    • Significantly worsened by sitting and/or standing from supine position and improved by lying
    • Occurs in about 20–30% of patients
    • May be accompanied by vomiting, and may not occur for 3–4 days
    • It usually lasts 36–72 hr, but can occasionally persist for a week

    Management

    • Lie patient flat, bed tilted head down
    • Liberal use of analgesics (paracetamol or codeine phosphate) with
      • anti-emetics – metoclopramide (duration max 5 day) or domperidone (duration max 7 day)

    © 2022 The Bedside Clinical Guidelines Partnership.

    Created by University Hospital North Midlands and Keele University School of Computing and Mathematics.

    Research and development team: James Mitchell, Ed de Quincey, Charles Pantin, Naveed Mustfa