Total Live Articles: 442

Spinal Cord Compression and Cauda Equina Syndrome

NICE guideline [NG234] Spinal metastases and metastatic spinal cord compression. Published: Sep 2023.

NICE CKS Sciatica (lumbar radiculopathy). Last revised: Jan 2025.

Spinal Cord Compression and Cauda Equina Syndrome

Spinal cord compression is a neurological emergency caused by compression of the spinal cord, commonly due to trauma, metastatic disease, epidural abscess or epidural haematoma. Cauda equina syndrome affects the lumbosacral nerve roots rather than the spinal cord.

Relevant Anatomy

In adults, the spinal cord usually ends at around the L1-L2 vertebral level, forming the conus medullaris.

Below this, the spinal canal contains the descending lumbosacral nerve roots, known as the cauda equina (Latin for “horse’s tail”).

Causes

There are 4 main causes of spinal cord compression: [Ref]

Cause category Description
Traumatic injury Acute spinal trauma can cause compression due to disc herniation, vertebral fracture with bone fragments pushed posteriorly into the spinal canal, or vertebral subluxation/dislocation narrowing the spinal canal.
Metastatic spinal cord compression Metastases to the vertebral column can extend into the epidural space, producing a mass effect on the spinal cord or cauda equina.
Epidural abscess Bacterial infection in the spinal epidural space can form an abscess, causing compression by mass effect.

Neurological injury may also occur due to inflammation, oedema and vascular compromise.

Epidural haematoma Bleeding into the spinal epidural space can form an expanding haematoma, causing acute compression of the spinal cord or cauda equina.

Clinical Features

Note: Cauda equina syndrome is not true spinal cord compression anatomically, as it affects the lumbosacral nerve roots rather than the spinal cord.

Importantly, cauda equina syndrome causes LMN signs because it affects the lumbosacral peripheral nerve roots rather than the spinal cord. In contrast, “true” spinal cord compression usually causes UMN signs below the level of the lesion.

Upper motor neuron (UMN) signs Lower motor neuron (LMN) signs
  • ↑ Tone (hypertonia)
  • Spastic weakness
  • Brisk reflex / hyperreflexia / exaggerated jaw jerk
  • Ankle clonus
  • Babinski sign (extensor plantar responses) or Hoffmann’s sign
  • ↓ Tone (hypotonia)
  • Flaccid weakness
  • Hyporeflexia / areflexia
  • Fasciculations

Cauda Equina Syndrome

Key red flag features for cauda equina syndrome:

  • Sudden onset bilateral sciatica (or unilateral sciatica progressing to bilateral)
  • Severe or progressive bilateral lower limb neurological deficit (e.g. major motor weakness with knee extension, ankle eversion, foot dorsiflexion)
  • Difficulty walking / gait disturbance
  • Saddle anaesthesiaparaesthesia (sensory loss in the perianal, perineal, genital regions)
  • Reduced anal sphincter tone (laxity)
  • Erectile dysfunction
  • Urinary dysfunction: impaired sensation of urinary flow / difficulty initiating micturition
  • Bowel dysfunction: loss of sensation of rectal fullness

Late, advanced features include:

  • Urinary retention with overflow urinary incontinence
  • Faecal incontinence

Spinal Cord Compression

General features of spinal cord compression: [Ref]

  • Localised neck or back pain
  • Symmetrical limb paralysis
  • Sensory level – a clear level on the trunk below which sensation is reduced or altered
  • UMN signs below the level of the lesion +/- LMN signs at the level of the lesion
  • Urinary retention or incontinence

In acute spinal cord compression (e.g. traumatic spinal cord compression), patients may develop spinal shock, with temporary loss of spinal cord function below the level of the lesion.

This can initially cause LMN-like features (e.g. hypotonia, areflexia) and reduced autonomic function (e.g. hypotension). As spinal shock resolves, UMN signs may become evident, such as spasticity, hyperreflexia and an extensor plantar response.

Clinical features as per cord syndromes (the affected anatomical areas of the spinal cord):

Syndrome Clinical presentation
Complete transverse myelopathy Everything below the lesion is affected:

  • Bilateral paralysis
  • Bilateral sensory loss (all modalities)
  • Bladder / bowel dysfunction
Brown-Séquard syndrome (hemisection syndrome)
  • Corticospinal tract involvement → ipsilateral weakness / paralysis
  • Dorsal column involvement → ipsilateral loss of vibration and proprioception
  • Spinothalamic tract involvement → contralateral loss of pain and temperature sensation

The classic ‘crossed findings’ in Brown-Séquard are closely related to the spinal tract decussation concept

Anterior cord syndrome
  • Corticospinal tract involvement → bilateral weakness / paralysis
  • Spinothalamic tract involvement → bilateral loss of pain and temperature sensation

Dorsal columns (situated posteriorly) are spared, thus vibration / proprioception

Posterior cord syndrome
  • Dorsal column involvement → loss of vibration and proprioception

Corticospinal and spinothalamic tract (situated anteriorly) are spared, thus motor function, pain and temperature sensation.

Central cord syndrome Primarily affects the medial corticospinal tract fibres supplying the upper limbs

  • Motor weakness affecting the UL > LL
  • Classically after cervical hyper-extension injury, esp. in older patients with cervical spondylosis

Conus medullaris syndrome

  • Caused by compression of the terminal spinal cord (called: conus medullaris) at ~L1-L2 vertebral level
  • The conus medullaris sits at the transition between the spinal cord and cauda equina, thus causing mixed UMN and LMN signs
  • Typical presentation
    • Mixed UMN and LMN signs
    • Early bladder / bowel / sexual dysfunction
    • Saddle anaesthesia / paraesthesia

Cause-Specific Clinical Features

[Ref]

Cause of spinal cord compression Clinical clues
Traumatic injury
  • Sudden onset, with preceding traumatic injury
  • Most commonly associated with high-velocity trauma
  • Focal spine pain with midline tenderness is typical
Metastatic spinal cord compression
  • Symptoms develop and progress gradually over days or longer
  • Past or current diagnosis of cancer (e.g. breast / lung / prostate cancer, multiple myeloma)
  • Night-time back pain disturbing sleep – highly characteristic
  • Severe unremitting back pain
  • Mechanical pain (aggravated by standing, sitting or moving)
  • Back pain aggravated by straining (for example, coughing, sneezing or bowel movements)
  • Claudication (muscle pain or cramping in the legs when walking or exercising)
Epidural abscess
  • Variable onset (may be acute, subacute, or gradual)
  • Risk factors
    • Diabetes – most prominent risk factor
    • IVDU
    • Recent spinal surgery / lumbar puncture / epidural or spinal anaesthesia
    • Alcohol abuse
    • Bacteraemia
    • Immunosuppression
  • Often accompanied by fever
Epidural haematoma
  • Sudden onset
  • Risk factors
    • Coagulopathy
    • Patients taking anticoagulation / antiplatelet
    • Recent spinal surgery / lumbar puncture / epidural or spinal anaesthesia

Investigation and Diagnosis

Gold standard / 1st line imaging: MRI [Ref]

  • For suspected metastatic spinal cord compression, MRI of the entire spine should be performed to ensure additional lesions are not missed

Exception: in trauma (i.e. suspected traumatic spinal cord compression), CT is the preferred initial imaging study as it is highly sensitive [Ref]

Additional investigations depending on underlying cause:

  • Epidural abscess → blood cultures and inflammatory markers (WBC, CRP, ESR)
  • Epidural haematoma → clotting profile (including platelet count, INR, aPTT)

Management

Management depends on the specific underlying cause identified during the diagnostic work-up.

Traumatic Spinal Cord Compression

[Ref]

  • Initial medical management
    • Primary focus: BP control (hypotension is associated with poor neurological outcomes)
    • Bladder catheterisation
  • Definitive management: surgery
    • Decompression and reduction
    • Fixation and fusion for long-term stability

Corticosteroids are NOT routinely recommended in traumatic spinal cord compression.

Metastatic Spinal Cord Compression

Immediate Management

Corticosteroid therapy Immediately give oral dexamethasone 16 mg

  • To be continued daily while awaiting definitive management
  • Also offer PPI and monitor blood glucose

If metastatic spinal cord compression is suspected clinically, give corticosteroids immediately without waiting for MRI confirmation.

If subsequent MRI excludes the diagnosis, the corticosteroid can be discontinued.

Pain management Provide prompt analgesia

If conventional analgesia fails in breast cancer / prostate cancer / myeloma → offer bisphosphonates for pain relief and fracture risk reduction

If patients have suspected or confirmed metastatic spinal cord compression and neurological signs of spinal instability → immobilise them in a supine position to minimise weight-bearing on the spine

Definitive Management

1st line: surgical decompression

  • Surgery should be offered ASAP after neurological signs or symptoms appear
  • Also offer surgical stabilisation for those with spinal instability

If the patient is NOT suitable for spinal surgery → urgent radiotherapy

Compression from Epidural Abscess

[Ref]

  • Immediate management: IV antibiotics
  • Definitive management: surgery (surgical evacuation combined with irrigation, biopsy, and culture)

Compression from Epidural Haematoma

[Ref]

  • Immediate management: reverse any anticoagulation or platelet dysfunction
  • Definitive management: surgical evacuation of the blood clot if the haematoma is actively compressing the spinal cord

References

Related Articles

Sciatica and Lumbosacral Radiculopathy

Low Back Pain (LBP)

Share Your Feedback Below

Disclaimer

We’re actively expanding Guideline Genius to cover the full UKMLA content map. Therefore, you may notice some conditions not uploaded yet, or articles that currently focus on diagnosis and management for now.

We are also continuously reviewing and updating existing content to ensure accuracy and alignment with current guidelines. Some earlier articles are undergoing revision as part of this process. Once all content has been fully reviewed, this will be clearly communicated on the platform.

For updates, follow us on Instagram @guidelinegenius.

We welcome any feedback or suggestions via the anonymous feedback box at the bottom of each article and will do our best to respond promptly.

Thank you for your support.
The Guideline Genius Team

UK medical guidelines made easy. From guidelines to genius in minutes!

Quick Links

Cookie Policy

Social Media

© 2026 GUIDELINE GENIUS LTD

Stay Updated withGuideline Genius

Sign up to be notified when our newsletter launches, covering major guideline updates, article updates, and future UKMLA resources.