demyelinating
epilepsy
headache
infectious
neuromuscular
Acute Myelopathy Evaluation
VERSION: 1.0
CREATED: January 27, 2026
STATUS: Approved
DIAGNOSIS: Acute Myelopathy Evaluation
ICD-10: G95.9 (Disease of spinal cord, unspecified), G95.89 (Other specified diseases of spinal cord), G37.3 (Acute transverse myelitis in demyelinating disease), G04.91 (Myelitis, unspecified)
CPT CODES: 85025 (CBC with differential), 80053 (CMP (BMP + LFTs)), 85652 (ESR), 86140 (CRP), 87040 (Blood cultures x2), 82947 (Blood glucose), 81003 (Urinalysis), 86900 (Type and screen), 84145 (Procalcitonin), 86255 (AQP4-IgG (aquaporin-4 antibody, serum) β cell-based assay), 82607 (B12, methylmalonic acid), 82390 (Copper and ceruloplasmin), 87389 (HIV 1/2 antigen/antibody), 86592 (RPR/VDRL), 86235 (Anti-SSA (Ro), anti-SSB (La)), 82164 (ACE level (serum)), 86334 (Serum protein electrophoresis (SPEP)), 70553 (MRI brain with and without contrast), 71046 (Chest X-ray), 78816 (PET-CT (whole body)), 95925 (Somatosensory evoked potentials (SSEPs)), 62270 (LUMBAR PUNCTURE), 89051 (Cell count with differential (tubes 1 and 4)), 84157 (Protein), 82945 (Glucose with paired serum), 83916 (Oligoclonal bands (paired with serum)), 86327 (IgG index), 88104 (Cytology), 96365 (IV methylprednisolone (empiric β inflammatory myelitis)), 36514 (Plasma exchange (PLEX))
SYNONYMS: Acute myelopathy, transverse myelitis, TM, spinal cord inflammation, myelitis, NMOSD myelitis, spinal cord lesion, spinal cord syndrome, cord compression, spinal cord injury
SCOPE: Acute or subacute spinal cord dysfunction β broad differential approach. Covers urgent MRI, LP, and comprehensive workup to differentiate compressive (epidural abscess, tumor, disc herniation, hematoma) from non-compressive causes (inflammatory/demyelinating, vascular, infectious). Compressive myelopathy is a surgical emergency. Excludes chronic cervical spondylotic myelopathy, cauda equina syndrome (separate template), and isolated radiculopathy.
PRIORITY KEY: STAT = Immediate | URGENT = Within hours | ROUTINE = Standard | EXT = Extended/atypical cases | - = Not applicable to this setting
βββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
SECTION A: ACTION ITEMS
βββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
1. LABORATORY WORKUP
1A. Essential/Core Labs
Test
ED
HOSP
OPD
ICU
Rationale
Target Finding
CBC with differential (CPT 85025)
STAT
STAT
ROUTINE
STAT
Infection screen (epidural abscess); baseline; leukocytosis
Normal
CMP (BMP + LFTs) (CPT 80053)
STAT
STAT
ROUTINE
STAT
Renal/hepatic function for contrast and medication dosing; electrolytes
Normal
ESR (CPT 85652)
STAT
STAT
ROUTINE
STAT
Markedly elevated in epidural abscess (>20 in ~95%); elevated in inflammatory/autoimmune
Normal; >20 raises concern for abscess/infection
CRP (CPT 86140)
STAT
STAT
ROUTINE
STAT
Elevated in infection, inflammation; useful for monitoring treatment response
Normal
Blood cultures x2 (CPT 87040)
STAT
STAT
-
STAT
If epidural abscess or infection suspected; S. aureus most common
No growth
PT/INR, aPTT (CPT 85610, 85730)
STAT
STAT
-
STAT
Coagulopathy causing epidural hematoma; pre-LP; pre-surgical assessment
Normal
Blood glucose (CPT 82947)
STAT
STAT
ROUTINE
STAT
Diabetic risk factor for epidural abscess; baseline
Normal
Urinalysis (CPT 81003)
STAT
ROUTINE
ROUTINE
STAT
UTI as source for epidural abscess; baseline bladder function
Normal
Type and screen (CPT 86900)
STAT
ROUTINE
-
STAT
Potential surgical intervention
On file
Procalcitonin (CPT 84145)
URGENT
ROUTINE
-
URGENT
Bacterial infection differentiation
<0.5 ng/mL
1B. Extended Workup (Second-line)
Test
ED
HOSP
OPD
ICU
Rationale
Target Finding
AQP4-IgG (aquaporin-4 antibody, serum) β cell-based assay (CPT 86255)
-
STAT
ROUTINE
STAT
NMOSD β longitudinally extensive transverse myelitis (β₯3 segments); affects treatment (avoid interferon-beta, fingolimod)
Negative (positive = NMOSD)
MOG-IgG antibody (serum) β cell-based assay (CPT 86255)
-
STAT
ROUTINE
STAT
MOGAD β often presents as myelitis; treatment implications differ from MS and NMOSD
Negative (positive = MOGAD)
B12, methylmalonic acid (CPT 82607)
-
ROUTINE
ROUTINE
-
Subacute combined degeneration (posterior columns + corticospinal tracts)
Normal
Copper and ceruloplasmin (CPT 82390)
-
ROUTINE
ROUTINE
-
Copper deficiency myelopathy (mimics B12 deficiency pattern)
Normal
Zinc level
-
ROUTINE
ROUTINE
-
Zinc excess causes copper deficiency
Normal
HIV 1/2 antigen/antibody (CPT 87389)
-
ROUTINE
ROUTINE
-
HIV-associated vacuolar myelopathy; opportunistic infections
Negative
HTLV-1/2 antibody
-
ROUTINE
ROUTINE
-
HTLV-associated myelopathy/tropical spastic paraparesis (HAM/TSP)
Negative
RPR/VDRL (CPT 86592)
-
ROUTINE
ROUTINE
-
Syphilitic myelitis (tabes dorsalis = posterior columns)
Non-reactive
ANA, dsDNA (CPT 86235, 86225)
-
ROUTINE
ROUTINE
-
Lupus myelitis
Negative
Anti-SSA (Ro), anti-SSB (La) (CPT 86235)
-
ROUTINE
ROUTINE
-
SjΓΆgren syndrome myelitis
Negative
ACE level (serum) (CPT 82164)
-
ROUTINE
ROUTINE
-
Neurosarcoidosis (spinal cord granulomas)
Normal
QuantiFERON-TB Gold
-
ROUTINE
ROUTINE
-
Spinal TB (Pott disease, TB myelitis)
Negative
Anti-thyroid antibodies (TPO, thyroglobulin)
-
ROUTINE
ROUTINE
-
Hashimoto encephalopathy/myelopathy
Negative
1C. Rare/Specialized (Refractory or Atypical)
Test
ED
HOSP
OPD
ICU
Rationale
Target Finding
Paraneoplastic panel (serum) β ANNA-1, CRMP-5, amphiphysin
-
ROUTINE
ROUTINE
-
Paraneoplastic myelitis (lung, breast, lymphoma); amphiphysin is classic for stiff-person / paraneoplastic myelopathy
Negative
Anti-GFAP antibody (serum and CSF)
-
EXT
EXT
-
GFAP astrocytopathy β autoimmune meningoencephalomyelitis
Negative
Antiphospholipid antibodies (lupus anticoagulant, anticardiolipin, Ξ²2-glycoprotein I)
-
ROUTINE
ROUTINE
-
Spinal cord infarction from hypercoagulable state
Negative
Serum protein electrophoresis (SPEP) (CPT 86334)
-
ROUTINE
ROUTINE
-
Multiple myeloma (spinal cord compression from plasmacytoma); POEMS
Normal
Lyme antibody (ELISA, Western blot)
-
ROUTINE
ROUTINE
-
Lyme myelitis (endemic areas)
Negative
CMV PCR (blood)
-
EXT
-
EXT
CMV myelitis (immunocompromised)
Negative
VZV IgM, VZV PCR (blood)
-
EXT
-
EXT
VZV myelitis (may follow shingles)
Negative
Sickle cell screen
-
EXT
EXT
-
Spinal cord infarction in sickle cell disease
Normal
2. DIAGNOSTIC IMAGING & STUDIES
2A. Essential/First-line
Study
ED
HOSP
OPD
ICU
Timing
Target Finding
Contraindications
MRI entire spine (cervical, thoracic, lumbar) with and without gadolinium contrast (CPT 72156+72157+72158)
STAT
STAT
URGENT
STAT
IMMEDIATELY β within 4 hours of presentation maximum; faster if progressive deficit. Entire spine because multifocal lesions change differential (NMOSD, metastatic)
Compressive: epidural mass (abscess, tumor, hematoma), disc herniation. Non-compressive: cord signal change (T2 hyperintensity), enhancement pattern, longitudinal extent, location within cord cross-section
GFR <30 (give contrast anyway if emergent); gadolinium allergy (premedicate); pacemaker
MRI brain with and without contrast (CPT 70553)
URGENT
URGENT
ROUTINE
URGENT
Within 24h (same session if possible)
MS (periventricular/juxtacortical lesions), NMOSD (area postrema, hypothalamic), ADEM (multifocal white matter), metastatic disease, leptomeningeal enhancement
Same as spine MRI
CT spine (without contrast)
STAT
STAT
-
STAT
ONLY if MRI unavailable or contraindicated; far less sensitive for cord pathology
Fracture, bony compression, large epidural mass, disc herniation
Pregnancy (relative)
Chest X-ray (CPT 71046)
URGENT
ROUTINE
-
URGENT
Baseline; lung malignancy screening (metastatic cord compression); sarcoidosis (hilar adenopathy)
Normal
CRITICAL: If MRI shows compressive myelopathy β NEUROSURGERY STAT. Do not delay for additional workup.
2B. Extended
Study
ED
HOSP
OPD
ICU
Timing
Target Finding
Contraindications
CT chest/abdomen/pelvis with contrast (CPT 71260, 74178)
-
ROUTINE
ROUTINE
-
If metastatic cord compression or sarcoidosis suspected
Primary malignancy; lymphadenopathy
Contrast allergy, renal impairment
CT angiography (CTA) of aorta
-
URGENT
-
URGENT
If spinal cord infarction suspected (especially post-aortic surgery)
Aortic dissection, aortic aneurysm, occlusion of artery of Adamkiewicz
Same as CT contrast
MR angiography (MRA) of spinal vessels
-
EXT
EXT
-
Spinal dural arteriovenous fistula (dAVF); spinal AVM
Abnormal vascular flow voids; fistula identification
Same as MRI
Conventional spinal angiography (DSA)
-
EXT
EXT
-
Gold standard for spinal dAVF/AVM; if MRA suggestive
Fistula or AVM identification and localization for treatment
Contrast allergy; coagulopathy
PET-CT (whole body) (CPT 78816)
-
EXT
ROUTINE
-
Occult malignancy search
Primary tumor
Pregnancy; uncontrolled diabetes
Repeat MRI spine
-
ROUTINE
ROUTINE
-
At 2-4 weeks for treatment response; earlier if clinical worsening
Improving signal; resolving enhancement
Same as initial
NCS/EMG (CPT 95907-95913, 95886)
-
ROUTINE
ROUTINE
-
If concomitant peripheral neuropathy suspected (e.g., GBS mimicking myelopathy)
Peripheral nerve involvement vs pure cord
None significant
2C. Rare/Specialized
Study
ED
HOSP
OPD
ICU
Timing
Target Finding
Contraindications
Somatosensory evoked potentials (SSEPs) (CPT 95925)
-
ROUTINE
ROUTINE
-
Assess dorsal column function; prognosis
Delayed or absent cortical potentials
None
Motor evoked potentials (MEPs)
-
EXT
EXT
-
Corticospinal tract assessment
Delayed or absent
Epilepsy (relative); implanted devices
Spinal cord biopsy
-
-
EXT
-
Extremely rare; only for diagnostic uncertainty when all other testing inconclusive and progressive decline
Tumor, vasculitis, infection, sarcoidosis
High morbidity; neurosurgical decision
LUMBAR PUNCTURE (CPT 62270)
Indication: ALL non-compressive myelopathies require LP. Perform AFTER MRI (need to exclude compressive cause and epidural abscess β LP through an abscess risks seeding meningitis).
Timing: URGENT β after MRI confirms non-compressive etiology.
Volume Required: 20-25 mL (many studies needed)
Study
ED
HOSP
OPD
Rationale
Target Finding
Opening pressure
URGENT
ROUTINE
ROUTINE
Elevated in some inflammatory conditions
Normal (10-20 cm H2O)
Cell count with differential (tubes 1 and 4) (CPT 89051)
URGENT
ROUTINE
ROUTINE
Pleocytosis: infection, inflammation. MS: mild. NMOSD: moderate with neutrophils. Infection: marked
Variable by etiology
Protein (CPT 84157)
URGENT
ROUTINE
ROUTINE
Elevated in GBS, infection, NMOSD, cord compression
Variable
Glucose with paired serum (CPT 82945)
URGENT
ROUTINE
ROUTINE
Low in TB, bacterial, fungal, leptomeningeal malignancy
Normal in most inflammatory causes
Oligoclonal bands (paired with serum) (CPT 83916)
-
ROUTINE
ROUTINE
Positive in MS (>90%); may be positive in NMOSD, sarcoidosis
Positive bands in CSF only = intrathecal synthesis (MS)
IgG index (CPT 86327)
-
ROUTINE
ROUTINE
Elevated in MS and other inflammatory conditions
Normal <0.7
AQP4-IgG (CSF)
-
ROUTINE
ROUTINE
NMOSD confirmation (serum is more sensitive; CSF adds specificity)
Negative
MOG-IgG (CSF)
-
ROUTINE
ROUTINE
MOGAD confirmation
Negative
Autoimmune encephalitis panel (CSF)
-
ROUTINE
ROUTINE
GFAP, NMDAR (rare spinal involvement)
Negative
Cytology (CPT 88104)
-
ROUTINE
ROUTINE
Leptomeningeal carcinomatosis, lymphoma
Negative
Flow cytometry
-
ROUTINE
ROUTINE
CNS lymphoma
Normal
VDRL (CSF)
-
ROUTINE
ROUTINE
Neurosyphilis
Non-reactive
ACE level (CSF)
-
ROUTINE
ROUTINE
Neurosarcoidosis
Normal
HSV 1/2 PCR
-
ROUTINE
ROUTINE
HSV myelitis (rare)
Negative
VZV PCR
-
ROUTINE
ROUTINE
VZV myelitis (may follow shingles)
Negative
CMV PCR
-
ROUTINE
ROUTINE
CMV myelitis (immunocompromised)
Negative
EBV PCR
-
ROUTINE
ROUTINE
EBV-associated lymphoma/myelitis
Negative
HTLV-1 antibody (CSF)
-
ROUTINE
ROUTINE
HAM/TSP confirmation
Negative
AFB smear and culture
-
ROUTINE
ROUTINE
Spinal TB
Negative
Bacterial culture
-
ROUTINE
ROUTINE
Bacterial myelitis (rare)
No growth
Cryptococcal antigen
-
ROUTINE
ROUTINE
Cryptococcal myelitis (immunocompromised)
Negative
3. TREATMENT
3A. Acute/Emergent
Treatment
Route
Indication
Dosing
Contraindications
Monitoring
ED
HOSP
OPD
ICU
IV methylprednisolone (empiric β inflammatory myelitis) (CPT 96365)
IV
-
1000 mg :: IV :: daily :: 1000 mg IV daily x 3-5 days (infuse over 1-2h). Start empirically if inflammatory myelitis suspected (non-compressive cord lesion on MRI). Do NOT wait for antibody results
Active untreated infection (relative β treat infection concurrently if needed); uncontrolled diabetes
Glucose q6h; BP; GI prophylaxis (PPI); insomnia; psychosis (rare); weight; taper plan
-
STAT
-
STAT
Emergent surgical decompression
-
-
N/A :: - :: once :: For compressive myelopathy: epidural abscess, tumor with cord compression, acute disc herniation with myelopathy, epidural hematoma. Earlier decompression = better neurologic outcome. Within 24h is critical; within 12h is ideal
Medically unstable for surgery (optimize first)
Post-op neurologic exam; wound care; DVT prophylaxis
STAT
STAT
-
STAT
Empiric IV antibiotics (if epidural abscess suspected)
IV
-
15-20 mg/kg :: IV :: q12h :: Vancomycin 15-20 mg/kg IV q8-12h + ceftriaxone 2g IV q12h (or cefepime 2g IV q8h). Start BEFORE surgery. S. aureus is most common organism
See individual agents
Cultures; vancomycin trough; renal function
STAT
STAT
-
STAT
DVT prophylaxis: Enoxaparin
SC
-
40 mg :: SC :: daily :: 40 mg SC daily (start post-operatively or when not bleeding; within 24-48h)
Active bleeding; post-surgical (timing per surgeon); coagulopathy
Platelets q3 days
-
ROUTINE
-
ROUTINE
Pneumatic compression devices
-
-
N/A :: - :: continuous :: Apply bilaterally immediately β spinal cord injury patients are HIGH risk for DVT/PE
Acute DVT
Skin checks
STAT
STAT
-
STAT
Bladder management
-
-
200 mL :: - :: - :: Foley catheter if urinary retention (very common in myelopathy); measure post-void residual if not catheterized; intermittent catheterization if PVR >200 mL
N/A
I/O; bladder scan; transition to intermittent cath when possible
STAT
STAT
-
STAT
Bowel management
-
-
N/A :: - :: per protocol :: Bowel program: docusate + senna; digital stimulation if neurogenic bowel; avoid impaction
Bowel obstruction
Bowel function daily
-
ROUTINE
-
ROUTINE
3B. Second-line / Specific Treatments
Treatment
Route
Indication
Dosing
Contraindications
Monitoring
ED
HOSP
OPD
ICU
Plasma exchange (PLEX) (CPT 36514)
-
Steroid-refractory inflammatory myelitis; NMOSD exacerbation; severe transverse myelitis
N/A :: - :: once :: 5-7 exchanges over 10-14 days (every other day); 1-1.5 plasma volumes per exchange
Hemodynamic instability; sepsis
BP; electrolytes; Ca2+; fibrinogen
-
URGENT
-
URGENT
IVIG (CPT 96365)
-
Alternative to PLEX if PLEX unavailable; MOGAD (may be preferred); steroid-refractory
0.4 g/kg :: - :: daily x 5 days :: 0.4 g/kg/day x 5 days (total 2 g/kg)
IgA deficiency; renal failure
Renal function; headache; thrombosis
-
URGENT
-
URGENT
Oral prednisone taper (after IV pulse)
IV
Inflammatory myelitis; NMOSD
1 mg/kg :: PO :: - :: 1 mg/kg/day (max 60-80 mg) tapered over 4-8 weeks for first episode; longer taper for NMOSD/MOGAD
See steroid contraindications
Glucose; BP; bone health
-
ROUTINE
ROUTINE
-
Gabapentin
PO
Neuropathic pain, spasticity
300 mg :: PO :: qHS :: 300 mg PO qHS β titrate to 900-1800 mg TID
Severe renal impairment
Sedation; dizziness
-
ROUTINE
ROUTINE
ROUTINE
Baclofen
PO
Spasticity
5 mg :: PO :: TID :: 5 mg PO TID; increase by 5 mg/dose q3 days; max 80 mg/day
Seizure history (lowers threshold); abrupt withdrawal causes seizures
Sedation; falls; do NOT stop abruptly
-
ROUTINE
ROUTINE
-
Tizanidine
PO
Spasticity (alternative)
2 mg :: PO :: TID :: 2 mg PO TID; max 36 mg/day
Hepatic impairment; concurrent CYP1A2 inhibitors (ciprofloxacin)
LFTs; sedation; hypotension
-
ROUTINE
ROUTINE
-
Oxybutynin
PO
Neurogenic bladder (overactive)
5 mg :: PO :: BID :: 5 mg PO BID-TID
Urinary retention; angle-closure glaucoma
Anticholinergic side effects; PVR
-
ROUTINE
ROUTINE
-
Acetaminophen
PO
Pain
650-1000 mg :: PO :: q6h :: 650-1000 mg PO q6h; max 4g/day
Hepatic disease
LFTs
STAT
ROUTINE
ROUTINE
STAT
3C. Disease-Modifying Therapy (Once Diagnosis Established)
Treatment
Route
Indication
Dosing
Pre-Treatment Requirements
Contraindications
Monitoring
ED
HOSP
OPD
ICU
MS disease-modifying therapy
-
-
N/A :: - :: per protocol :: Per MS-specific template; high-efficacy preferred if myelitis presentation
-
-
Per agent
-
-
-
-
Rituximab
PO
-
375 mg/m2 :: PO :: - :: 375 mg/m2 weekly x 4 weeks OR 1000 mg x 2 (14 days apart); maintenance q6 months
-
-
CD19/20; immunoglobulins; infection
-
-
-
-
Eculizumab
IV
-
900 mg :: IV :: - :: 900 mg IV weekly x 4 β 1200 mg q2 weeks
-
-
Meningococcal vaccination (β₯2 weeks before); complement levels; infection
-
-
-
-
Inebilizumab
IV
-
300 mg :: IV :: - :: 300 mg IV x 2 (14 days apart); then 300 mg q6 months
-
-
CD19; infection
-
-
-
-
Satralizumab
SC
-
120 mg :: SC :: - :: 120 mg SC at weeks 0, 2, 4, then q4 weeks
-
-
LFTs; infection
-
-
-
-
Azathioprine
PO
-
2-3 mg/kg :: PO :: - :: 2-3 mg/kg/day PO
-
-
TPMT genotype; CBC weekly x 4, then biweekly, then monthly; LFTs
-
-
-
-
Mycophenolate mofetil
PO
-
1000-1500 mg :: PO :: BID :: 1000-1500 mg PO BID
-
-
CBC; LFTs; pregnancy test (teratogenic)
-
-
-
-
Anti-TB therapy
-
-
N/A :: - :: per protocol :: RIPE x 12-18 months
-
-
LFTs; visual acuity
-
-
-
-
IV penicillin G
IV
-
18-24 million units :: IV :: daily :: 18-24 MU/day IV x 14 days
-
-
RPR q3-6 months
-
-
-
-
Radiation + surgery + steroids
IV
-
10 mg :: IV :: q6h :: Per oncology; dexamethasone 10 mg IV load β 4 mg IV q6h while radiation planned
-
-
Glucose; GI prophylaxis
-
-
-
-
4. OTHER RECOMMENDATIONS
4A. Referrals & Consults
Recommendation
ED
HOSP
OPD
ICU
Indication
Neurology (neuro-immunology if available)
STAT
STAT
STAT
STAT
All myelopathy; diagnostic workup direction; immunotherapy decisions
Neurosurgery
STAT
STAT
-
STAT
Compressive myelopathy (abscess, tumor, hematoma, disc); surgical timing critical
Spine surgery (orthopedic)
STAT
STAT
-
STAT
Alternative for compressive causes where neurosurgery unavailable
Radiation oncology
-
URGENT
-
-
Metastatic cord compression; radiation planning
Oncology
-
ROUTINE
ROUTINE
-
Newly diagnosed malignancy; systemic treatment
Infectious disease
-
ROUTINE
ROUTINE
-
Epidural abscess management; TB; HIV; unusual infections
Urology
-
ROUTINE
ROUTINE
-
Neurogenic bladder management; intermittent catheterization training; urodynamics
Physical therapy (PT)
-
STAT
ROUTINE
URGENT
Mobility assessment; strengthening; gait training; transfer training; wheelchair assessment
Occupational therapy (OT)
-
STAT
ROUTINE
URGENT
ADL assessment; hand function; adaptive equipment; home modifications
Rehabilitation medicine (physiatry)
-
ROUTINE
ROUTINE
-
Rehabilitation planning; SCI rehabilitation protocols; disposition
Speech-language pathology
-
ROUTINE
ROUTINE
-
If cervical myelopathy affecting swallowing
Respiratory therapy
-
URGENT
-
STAT
If cervical myelopathy affecting respiratory muscles; FVC monitoring
Social work
-
ROUTINE
ROUTINE
-
Discharge planning; DME; caregiver support; disability
Psychology
-
ROUTINE
ROUTINE
-
Adjustment disorder; depression; coping with disability
Pain management
-
ROUTINE
ROUTINE
-
Neuropathic pain refractory to standard agents
Wound care (if pressure injury)
-
ROUTINE
ROUTINE
ROUTINE
Immobile patients at high risk for pressure ulcers
4B. Patient Instructions
Recommendation
ED
HOSP
OPD
Return to ED immediately if: new weakness, worsening numbness, loss of bowel/bladder function, inability to walk, difficulty breathing
STAT
STAT
ROUTINE
Spinal cord injury can improve with treatment β recovery varies by cause (inflammatory often recovers well; vascular and compressive recovery depends on timing)
-
ROUTINE
ROUTINE
Bladder management is critical: perform intermittent catheterization as instructed; report urinary retention or incontinence
-
ROUTINE
ROUTINE
Bowel program compliance: maintain regular schedule; adequate fiber and fluids
-
ROUTINE
ROUTINE
Skin checks daily: pressure injury prevention (reposition every 2h if immobile; use pressure-relieving mattress)
-
ROUTINE
ROUTINE
Physical therapy exercises between sessions as instructed
-
ROUTINE
ROUTINE
Do NOT drive until cleared by neurology
-
ROUTINE
ROUTINE
Follow-up with neurology in 1-2 weeks; repeat MRI at 2-4 weeks
-
ROUTINE
ROUTINE
4C. Lifestyle & Prevention
Recommendation
ED
HOSP
OPD
Pressure injury prevention (positioning, specialized mattress, skin checks)
-
ROUTINE
ROUTINE
Fall prevention (assistive devices, home modifications)
-
ROUTINE
ROUTINE
DVT prevention (compression stockings long-term; anticoagulation per protocol)
-
ROUTINE
ROUTINE
Autonomic dysreflexia awareness (if thoracic/cervical injury: sudden hypertension, headache, flushing above level β emergency)
-
ROUTINE
ROUTINE
Bladder health (adequate fluid intake; catheterization technique; UTI prevention)
-
ROUTINE
ROUTINE
Mental health support (spinal cord injury carries high depression/anxiety rates)
-
ROUTINE
ROUTINE
Vaccination (if starting immunosuppression: complete vaccines before rituximab/eculizumab)
-
ROUTINE
ROUTINE
Smoking cessation
-
ROUTINE
ROUTINE
βββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
SECTION B: REFERENCE (Expand as Needed)
βββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
5. DIFFERENTIAL DIAGNOSIS
Alternative Diagnosis
Key Distinguishing Features
Tests to Differentiate
Epidural abscess
Back pain + fever + neurologic deficit (triad in 10-15%); IVDU, diabetes, spinal procedure risk factors; ESR/CRP very elevated
MRI with contrast (ring-enhancing epidural collection); blood cultures; ESR >20
Metastatic cord compression
Known malignancy; progressive back pain (often worse at night); bony destruction
MRI (enhancing epidural mass with bony changes); CT body for primary; PET-CT
Disc herniation (acute)
Sudden onset; radiculopathy predominant initially; may progress to myelopathy
MRI (disc protrusion with cord compression)
Epidural hematoma
Anticoagulation; post-procedure; coagulopathy; sudden onset
MRI (epidural collection; T1 signal depends on age of blood); coagulation panel
Transverse myelitis (idiopathic)
Non-compressive; T2 cord signal change; may be partial or complete; often thoracic
MRI (T2 hyperintensity <3 segments); LP (pleocytosis); diagnose after excluding MS, NMOSD, MOGAD
MS (spinal cord relapse)
Partial myelitis (<3 segments); brain lesions present; prior episodes; young adult
MRI brain (periventricular/juxtacortical lesions); oligoclonal bands; short segment cord lesion
NMOSD
Longitudinally extensive transverse myelitis (LETM β₯3 segments); severe; often central cord/gray matter
AQP4-IgG antibody; MRI (LETM, central cord pattern); brain MRI (area postrema lesion)
MOGAD
LETM possible; conus/lower cord predilection; may have bilateral optic neuritis
MOG-IgG antibody; MRI pattern; generally better recovery than NMOSD
Spinal cord infarction
Hyperacute onset (minutes); anterior spinal artery syndrome (motor + pain/temperature loss, preserved proprioception/vibration); often thoracolumbar
MRI DWI (restricted diffusion, "owl eye" or pencil-like on axial); CTA aorta; vascular risk factors
Spinal dural AV fistula
Older male; progressive myelopathy with flow voids on MRI; dorsal cord; edema disproportionate to enhancement
MRI (flow voids, dorsal cord edema, enhancement); spinal angiography (gold standard)
GBS (axonal variant)
Ascending weakness; areflexia; may mimic acute myelopathy if rapidly progressive; CSF albuminocytologic dissociation
NCS/EMG; LP (elevated protein, normal cells); no cord signal on MRI
Neurosarcoidosis
Dorsal subpial enhancement; trident sign; may have pulmonary sarcoidosis
Chest CT; ACE level; biopsy; characteristic MRI pattern
Spinal TB (Pott disease)
Endemic area; systemic TB; vertebral body destruction with epidural abscess; gibbus deformity
MRI; AFB culture; TB PCR; QuantiFERON; chest X-ray
Neuromyelitis optica spectrum disorder β See NMOSD above
Syphilitic myelitis (tabes dorsalis)
Posterior column dysfunction (proprioception, vibration loss); lightning pains; Argyll Robertson pupils
CSF VDRL; RPR; FTA-ABS
Copper deficiency myelopathy
Posterior column + corticospinal tract (mimics B12 deficiency); gastric surgery, zinc excess
Serum copper and ceruloplasmin; zinc level
Radiation myelopathy
History of radiation; months to years after treatment; progressive; no enhancement (chronic)
Radiation history; MRI (cord atrophy, signal change within radiation field)
Functional neurological disorder
Non-anatomic sensory loss; Hoover sign; give-way weakness; normal MRI
Normal MRI; normal LP; clinical exam findings
6. MONITORING PARAMETERS
Parameter
ED
HOSP
OPD
ICU
Frequency
Target/Threshold
Action if Abnormal
Neurologic exam (strength, sensory level, reflexes, rectal tone)
STAT
STAT
ROUTINE
STAT
q4h x 48h, then q8h; sensory level marking on skin for tracking
Stable or improving; sensory level not ascending
If ascending level or worsening motor: STAT repeat MRI; neurosurgery if compressive
Bladder function (PVR, I/O)
STAT
STAT
ROUTINE
STAT
PVR with each void initially; I/O daily
PVR <200 mL; adequate output
If PVR >200: intermittent catheterization; Foley if >500 or unable to cath
Respiratory function (FVC, NIF) β cervical myelopathy
STAT
STAT
-
STAT
q4-6h if cervical; q2h if declining
FVC >20 mL/kg
If FVC <20: ICU; prepare for intubation
Blood pressure / autonomic function
STAT
STAT
-
STAT
q4h; orthostatic vitals when mobilizing
Stable BP; no orthostatic hypotension >20 mmHg
Volume; midodrine; compression stockings; if hypertensive crisis above level β autonomic dysreflexia β find and remove stimulus (distended bladder, bowel impaction)
Temperature
STAT
STAT
-
STAT
q4h
Afebrile
If febrile: infection workup; wound check; UTI screen
Skin assessment (pressure areas)
-
ROUTINE
ROUTINE
ROUTINE
q shift; at every reposition
Intact skin; no erythema >30 min
Pressure relief; wound care; specialty mattress
ESR / CRP (if infection)
-
ROUTINE
ROUTINE
-
q48-72h during treatment
Declining trend
If not improving: reassess antibiotic coverage; repeat imaging
Post-void residual (PVR)
-
ROUTINE
ROUTINE
-
With each void initially; daily once stable
<200 mL
Intermittent catheterization protocol
MRI response
-
ROUTINE
ROUTINE
-
At 2-4 weeks; 3-6 months; or sooner if worsening
Improving signal and enhancement
Adjust treatment; consider PLEX/escalation
AQP4/MOG antibody titers (if positive)
-
-
ROUTINE
-
At 3-6 months, then annually
Declining or stable
If rising with clinical worsening: relapse; adjust DMT
7. DISPOSITION CRITERIA
Disposition
Criteria
Discharge home
Mild myelopathy; stable or improving; ambulatory; independent bladder function; adequate outpatient follow-up; MRI and workup complete or schedulable outpatient
Admit to floor
Non-compressive myelopathy requiring IV steroids; moderate deficits; bladder dysfunction requiring catheterization; incomplete workup
Admit to ICU
Cervical myelopathy with respiratory compromise; post-surgical; ascending myelopathy; autonomic instability
Emergent surgery
Compressive myelopathy: epidural abscess, acute cord compression from tumor/hematoma/disc with neurologic deficit
Transfer to higher level
Need for neurosurgery not available; need for PLEX; MRI not available STAT; spinal cord injury center
Inpatient rehabilitation (SCI rehab)
Significant motor deficits; paraparesis/paraplegia; wheelchair-dependent; bladder/bowel dysfunction; able to participate in 3h/day therapy
Skilled nursing facility
Unable to tolerate intensive rehab; requires skilled nursing; ongoing IV antibiotics
8. EVIDENCE & REFERENCES
Recommendation
Evidence Level
Source
STAT MRI entire spine for acute myelopathy
Class I, Level B
AAN Practice Guideline; Transverse Myelitis Consortium Working Group (2002)
IV methylprednisolone 1g/day x 3-5 days for inflammatory myelitis
Class I, Level B
Consensus; extrapolated from MS relapse data (ONTT) and TM studies
PLEX for steroid-refractory inflammatory myelitis
Class IIa, Level B
Weinshenker et al. (Ann Neurol 1999) ; superior to sham in severe demyelinating attacks
AQP4-IgG (cell-based assay) for NMOSD diagnosis
Class I, Level A
Wingerchuk et al. IPND 2015 criteria
MOG-IgG for MOGAD diagnosis
Class I, Level B
Banwell et al. (Lancet Neurol 2023)
Surgical decompression within 24h for compressive myelopathy
Class I, Level B
Fehlings et al. (2012) ; earlier surgery = better outcomes
Epidural abscess: antibiotics + surgical drainage
Class I, Level B
Darouiche et al. (NEJM 2006)
B12 replacement for subacute combined degeneration
Class I, Level A
Well-established; early treatment may be reversible
Rituximab for NMOSD prevention
Class I, Level A
Multiple trials; standard of care
Eculizumab for NMOSD prevention
Class I, Level A
PREVENT trial (Pittock et al. NEJM 2019)
AQP4-IgG-positive NMOSD: avoid interferon-beta and fingolimod
Class III (Harm)
Case reports of worsening
LP after MRI (not before) in acute myelopathy
Class I, Level C
Risk of seeding infection through abscess; need anatomic diagnosis first
Bladder management with intermittent catheterization
Class I, Level B
Spinal cord injury guidelines; prevents UTI better than indwelling catheter
DVT prophylaxis in acute myelopathy
Class I, Level A
High thrombotic risk in immobilized SCI patients
APPENDIX: MRI PATTERN RECOGNITION IN MYELOPATHY
Pattern
Diagnosis Suggested
Short segment (<3 vertebral segments), eccentric/dorsolateral
MS
Longitudinally extensive (β₯3 segments), central cord/gray matter
NMOSD
Longitudinally extensive, conus/lower cord
MOGAD
Anterior cord (gray matter "owl eyes" on axial)
Spinal cord infarction
Dorsal cord, flow voids, extensive edema
Dural AV fistula
Ring-enhancing epidural collection
Epidural abscess
Enhancing epidural mass with bony destruction
Metastatic tumor
Posterior columns bilateral
B12 deficiency, copper deficiency, syphilis (tabes)
Dorsal subpial enhancement, "trident sign"
Neurosarcoidosis
Central cord, bright/enhancing, expansile
Cord tumor (astrocytoma, ependymoma)
APPENDIX: ANTERIOR SPINAL ARTERY SYNDROME (Spinal Cord Infarction)
Affected
Preserved
Motor function (corticospinal tracts)
Proprioception (dorsal columns)
Pain/temperature sensation (spinothalamic tracts)
Vibration sense (dorsal columns)
Bladder/bowel function (autonomic)
Light touch (partial β dorsal columns)
Classic pattern: bilateral motor weakness + bilateral pain/temperature loss BELOW level + PRESERVED proprioception/vibration