SCOPE: Emergency evaluation and management of spinal epidural abscess in adults. Covers the classic triad (back pain, fever, neurologic deficit), emergent MRI, surgical drainage vs. medical management decision-making, empiric and targeted antibiotic therapy, and neurologic monitoring. Includes associated vertebral osteomyelitis and discitis. Excludes brain abscess (separate template), subdural empyema, and post-operative wound infections (partially overlaps).
PRIORITY KEY: STAT = Immediate | URGENT = Within hours | ROUTINE = Standard | EXT = Extended/atypical cases | - = Not applicable to this setting
Blood cultures (x2 sets, before antibiotics) (CPT 87040)
STAT
STAT
-
STAT
CRITICAL: Positive in 60-70%; identifies organism for targeted therapy; guides antibiotic duration; S. aureus most common (60-70%); draw from 2 separate sites
Positive → organism identification; S. aureus (MRSA vs. MSSA) most common; also Streptococci, gram-negatives, anaerobes
CBC with differential (CPT 85025)
STAT
STAT
ROUTINE
STAT
Leukocytosis (WBC >12,000 in 60-80%); left shift; bandemia; baseline for monitoring; thrombocytopenia may indicate DIC/sepsis
Leukocytosis (66%); normal WBC does NOT exclude SEA (20-40% have normal WBC); leukopenia concerning for overwhelming sepsis
CMP (BMP + LFTs) (CPT 80053)
STAT
STAT
ROUTINE
STAT
Renal function (antibiotic dosing, contrast); electrolytes; hepatic function; glucose (diabetes is major risk factor)
Normal or abnormal; elevated glucose → diabetes workup; renal dysfunction affects antibiotic choice
ESR (erythrocyte sedimentation rate) (CPT 85652)
STAT
STAT
ROUTINE
STAT
Highly sensitive (>94%); ESR >20 mm/hr in nearly all cases of SEA; ESR >30-50 typical; useful for monitoring treatment response
ESR >20 mm/hr (sensitivity 94%); mean ESR is typically 50-80 mm/hr; if normal → SEA very unlikely
CRP (C-reactive protein) (CPT 86140)
STAT
STAT
ROUTINE
STAT
Elevated in >90% of SEA; more responsive to treatment changes than ESR; useful for monitoring
Elevated (typically >10 mg/dL); declines faster than ESR with successful treatment
Procalcitonin (CPT 84145)
STAT
STAT
-
STAT
More specific for bacterial infection than CRP; helps distinguish bacterial from non-infectious inflammation; prognostic
>0.5 ng/mL suggests bacterial infection; >2.0 ng/mL concerning for sepsis; useful in atypical presentations
Blood glucose / HbA1c (CPT 82947+83036)
STAT
STAT
ROUTINE
STAT
Diabetes is a major risk factor (30-50% of SEA patients); undiagnosed diabetes common; affects wound healing and immune function
Gold standard for organism identification; culture of abscess material at surgery; sensitivity higher than blood cultures; also send for Gram stain and histopathology
MRI entire spine with and without contrast (gadolinium) (CPT 72156+72157+72158)
STAT
STAT
URGENT
STAT
GOLD STANDARD — within 4 hours of ED presentation if neurologic deficit; within 24h if no deficit; contrast essential for abscess characterization; image ENTIRE spine (multifocal in 15-20%)
Epidural collection with ring enhancement; T1 hypointense, T2 hyperintense; restricted diffusion (DWI bright, ADC dark within abscess); vertebral body involvement (osteomyelitis); disc involvement (discitis); cord compression; degree of canal compromise
MRI-incompatible implants; severe claustrophobia (sedate — do NOT delay); GFR <30 (gadolinium risk — but benefit outweighs risk in emergency)
Plain radiographs (spine)
STAT
STAT
-
STAT
Immediate while awaiting MRI; identifies vertebral body destruction, disc space narrowing, alignment abnormality; LOW sensitivity for early SEA
Disc space narrowing; vertebral body destruction (late finding — takes 2-4 weeks to appear); alignment; pathologic fracture
Pregnancy (shield)
CT spine without contrast (CPT 72125/72128/72131)
STAT
STAT
-
STAT
If MRI unavailable or contraindicated; inferior to MRI for soft tissue and epidural collection; shows bone destruction better than MRI
Bone destruction; disc space narrowing; paraspinal soft tissue mass; canal compromise; less sensitive than MRI for epidural abscess extent
CT chest/abdomen/pelvis with contrast (CPT 71260+74178)
-
URGENT
ROUTINE
URGENT
Source identification if not obvious; look for primary infection (lung abscess, intra-abdominal abscess, psoas abscess); staging for concurrent infection
Only if MRI absolutely contraindicated; intrathecal contrast via LP followed by CT; demonstrates level of compression; risk of meningitis seeding with LP
Complete or partial block; level of compression; intradural vs. extradural
Infection at LP site (SEA itself may preclude LP at involved level); coagulopathy
Nuclear medicine bone scan (Tc-99m)
-
-
EXT
-
If MRI unavailable; can identify osteomyelitis; may show uptake before radiographic changes; less specific than MRI
Increased uptake at infection site(s); may identify multifocal disease
Pregnancy; limited specificity
Gallium-67 or Indium-111 WBC scan
-
-
EXT
-
Chronic/subacute infection; differentiating active infection from degenerative changes; research use
Increased uptake at infection site
Limited availability; time-consuming; replaced largely by MRI
If diagnosis uncertain; culture acquisition for non-surgical management; distinguish abscess from tumor or hematoma
Organism identification; Gram stain; histopathology confirming infection vs. other pathology
Coagulopathy; inaccessible location; very small collection
PET/CT (FDG) (CPT 78816)
-
-
EXT
-
Chronic/recurrent infection; assess treatment response; identify additional sites of infection; research use
Increased FDG uptake at infection site; may identify occult primary source
Uncontrolled diabetes (glucose >200); pregnancy
Repeat MRI (during treatment)
-
ROUTINE
ROUTINE
-
At 2-4 weeks or if clinical worsening; assess treatment response; monitor for abscess expansion; may appear worse before better on imaging
Stable or decreasing collection size; resolving edema; NOTE: Imaging may lag behind clinical improvement (may appear worse at 2 weeks even with successful treatment)
Same as initial MRI
Post-treatment MRI
-
ROUTINE
ROUTINE
-
At end of antibiotic course (6-8 weeks); baseline for comparison; assess for residual disease
Resolution or significant improvement of collection; healed osteomyelitis; residual enhancement may persist for months (does not necessarily indicate active infection)
LP is generally CONTRAINDICATED in suspected SEA; risk of seeding infection into subarachnoid space → meningitis/spinal subdural empyema; imaging (MRI) is diagnostic modality of choice
N/A
AVOID LP if SEA suspected — LP may spread infection into intradural space; if meningitis suspected concurrently, discuss with neurosurgery/ID before LP
25-30 mg/kg :: IV :: q12h :: Start IMMEDIATELY after blood cultures drawn — do NOT delay for MRI or organism identification; First-line empiric: Vancomycin 25-30 mg/kg IV load (max 2g), then 15-20 mg/kg IV q8-12h (target trough 15-20 mcg/mL) PLUS Ceftriaxone 2g IV q12h OR Cefepime 2g IV q8h; Alternative for β-lactam allergy: Vancomycin + aztreonam 2g IV q8h OR Vancomycin + fluoroquinolone (levofloxacin 750 mg daily); If Pseudomonas risk (IVDU, immunocompromised): Add anti-pseudomonal coverage with cefepime or piperacillin-tazobactam 4.5g IV q6h; Adjust to culture results when available
-
Vancomycin covers MRSA (most important cause); ceftriaxone/cefepime covers MSSA, streptococci, gram-negatives; early antibiotics are associated with better outcomes; every hour of delay increases mortality in sepsis
STAT
STAT
-
STAT
Emergent surgical decompression + drainage
-
-
N/A :: - :: once :: INDICATIONS (Surgery preferred): (1) Neurologic deficit (any weakness, bowel/bladder dysfunction), (2) Sepsis/hemodynamic instability not improving with antibiotics, (3) Significant cord compression on imaging, (4) Failure of medical therapy (no improvement at 48-72h, worsening at any time), (5) Unknown organism (need tissue diagnosis); Procedure: Posterior laminectomy with abscess drainage; cultures from abscess; débridement of infected tissue; may need instrumentation if instability; Timing: Within 24h of diagnosis; emergent (within hours) if progressive deficit
-
Darouiche (2006): Surgical outcomes better than medical management in patients with neurologic deficit; earlier surgery (within 24h) associated with better neurologic recovery; pre-operative neurologic status is #1 predictor of outcome
-
STAT
-
-
DVT prophylaxis
SC
-
40 mg :: SC :: daily :: SCDs immediately; pharmacologic prophylaxis: enoxaparin 40 mg SQ daily — timing is nuanced: may start within 24h of admission if no imminent surgery; post-operatively start 12-24h after surgery per surgeon; high VTE risk population
-
Immobile + infection + inflammatory state = very high DVT risk; mechanical prophylaxis universal; pharmacologic prophylaxis as soon as surgically safe
STAT
STAT
-
STAT
Pain management
IV
-
650-1000 mg :: IV :: q6h :: Back pain often severe; acetaminophen 650-1000 mg q6h (scheduled) + opioids (morphine 2-4 mg IV q3h PRN or hydromorphone 0.5-1 mg IV q3h PRN); NSAIDs: use cautiously (renal function, surgical bleeding) — some ID physicians avoid NSAIDs in active infection; neuropathic agents (gabapentin) if radicular component
-
Severe pain is hallmark of SEA; adequate analgesia is essential; balance with need for neurologic monitoring
STAT
STAT
ROUTINE
STAT
Sepsis resuscitation (if septic)
IV
-
30 mL/kg :: IV :: - :: Surviving Sepsis guidelines: lactate measurement; blood cultures before antibiotics; IV crystalloid 30 mL/kg for hypotension or lactate ≥4 mmol/L; vasopressors (norepinephrine first-line) if MAP <65 despite fluids; reassess volume status; repeat lactate if initially elevated
-
Sepsis from SEA has high mortality; early aggressive resuscitation improves outcomes
STAT
STAT
-
STAT
Glucose control
IV
-
180 mg :: IV :: once :: Target glucose <180 mg/dL; insulin infusion if critically ill; sliding scale or basal-bolus for non-ICU patients; diabetes is major risk factor — optimize control
-
Hyperglycemia impairs immune function and wound healing; tight glucose control improves infection outcomes
Targeted IV antibiotic therapy (based on culture results)
IV
-
2g :: IV :: q4h :: Tailor to organism and sensitivities; typical regimens: — MSSA: Nafcillin 2g IV q4h OR cefazolin 2g IV q8h (preferred for tolerability); duration 6-8 weeks; — MRSA: Vancomycin 15-20 mg/kg IV q8-12h (trough 15-20) for 6-8 weeks; alternatives: daptomycin 6-8 mg/kg IV daily (avoid if pneumonia), linezolid 600 mg IV/PO q12h (monitor for toxicity if >2 weeks); — Streptococci: Penicillin G 4 million units IV q4h or ceftriaxone 2g IV q12h x 6 weeks; — Enterococcus: Ampicillin 2g IV q4h (if susceptible) ± gentamicin synergy; vancomycin if ampicillin-resistant; — Gram-negatives: Ceftriaxone 2g IV q12h or cefepime 2g IV q8h or ciprofloxacin 400 mg IV q8h x 6 weeks depending on sensitivities; — Pseudomonas: Cefepime 2g IV q8h or meropenem 2g IV q8h x 6 weeks
-
IV antibiotics are standard for SEA/osteomyelitis; oral transition data emerging (OVIVA trial) but traditionally 6-8 weeks IV; de-escalate from empiric coverage once cultures return
-
STAT
ROUTINE
STAT
Duration of antibiotics
IV
-
N/A :: IV :: per protocol :: SEA without osteomyelitis: 4-6 weeks IV; SEA with vertebral osteomyelitis (most cases): 6-8 weeks IV; SEA with endocarditis: 6 weeks minimum from first negative blood culture; duration guided by clinical response, inflammatory markers (ESR, CRP), repeat imaging; may extend if slow response
-
IDSA guidelines: 6 weeks for vertebral osteomyelitis; 4-6 weeks for epidural abscess alone; endocarditis requires 6-week minimum; individualized based on response
-
STAT
ROUTINE
STAT
Oral antibiotic transition (selected cases)
IV
-
750 mg :: IV :: daily :: OVIVA trial (2019): Oral antibiotics non-inferior to IV for bone/joint infections after initial 2 weeks IV in stable patients; Candidates: Clinically improving; afebrile; tolerating PO; CRP trending down; adherent; close follow-up available; Oral options: Fluoroquinolone (levofloxacin 750 mg daily or ciprofloxacin 750 mg BID) + rifampin 300 mg BID (NOT monotherapy); linezolid 600 mg BID (monitor CBC, neuropathy); TMP-SMX DS 2 tabs BID (for MRSA); NOT for: Endocarditis, undrained abscess, persistent bacteremia, non-adherent patient
-
OVIVA trial showed oral switch after 2 weeks IV is non-inferior for bone/joint infections; reduces costs, IV complications, hospital stay; requires careful patient selection and close monitoring; NOT standard for all SEA cases
-
-
ROUTINE
-
Surgical drainage (if not done emergently)
-
-
N/A :: - :: once :: If initial medical management: Re-evaluate need for surgery at 48-72h; indications for delayed surgery: failure to improve, neurologic deterioration, persistent fever/bacteremia, abscess enlargement on imaging; Procedure: Laminectomy + drainage; send cultures even if already on antibiotics (may still grow organism); instrumented fusion if instability/destruction
-
Surgery provides source control, tissue diagnosis, and decompression; delayed surgery for medical failure still beneficial if performed before complete paralysis
-
URGENT
-
-
Medical management alone (selected cases)
-
-
N/A :: - :: q2-4h :: Candidates for medical management without surgery: (1) No neurologic deficit, (2) Organism identified (blood cultures positive), (3) Small abscess (<3 cm collection), (4) Poor surgical candidate (extreme comorbidities), (5) Panspinal disease (multiple levels — surgery impractical); Requirements: Very close neurologic monitoring (q2-4h initially); repeat MRI at 48-72h and weekly; immediate surgery if any deterioration; adherent patient
-
Observational studies: ~40% of SEA can be managed medically if no neurologic deficit and criteria met; HOWEVER, 10-20% will fail medical therapy and require surgery; early surgery generally preferred if feasible
N/A :: IV :: once :: If prolonged IV antibiotics planned (6-8 weeks); enables outpatient IV therapy (OPAT); placed once stabilized and duration confirmed; confirm tip position with X-ray
-
Required for OPAT; reduces peripheral IV complications; monitor for PICC-associated infection
-
URGENT
ROUTINE
-
Outpatient parenteral antibiotic therapy (OPAT)
PO
-
N/A :: PO :: once :: Once clinically stable (afebrile, pain controlled, neurologically stable, adequate PO intake, safe home environment); PICC in place; infusion teaching completed; close ID follow-up (weekly visits); VNA nursing for line care
-
Reduces hospital stay; comparable outcomes to inpatient therapy in appropriate patients; weekly ID visits with labs (CBC, CMP, drug levels, CRP)
-
ROUTINE
ROUTINE
-
Rifampin (adjunctive)
PO
-
300 mg :: PO :: BID :: For staphylococcal osteomyelitis (vertebral involvement); enhances bone penetration; prevents biofilm; ONLY as adjunctive therapy — never monotherapy (rapid resistance); Rifampin 300 mg PO BID added to primary anti-staphylococcal agent; check interactions (CYP3A4 inducer — reduces warfarin, HIV meds, oral contraceptives, etc.)
-
Rifampin improves outcomes in staphylococcal bone infections; biofilm activity; excellent bone penetration; drug interactions are significant
-
ROUTINE
ROUTINE
-
Bracing / spinal orthosis
-
-
N/A :: - :: continuous :: If spinal instability (vertebral body destruction, kyphosis, instrumentation); TLSO for thoracolumbar; cervical collar for cervical; duration: typically 6-12 weeks or until radiographic healing
-
External stabilization; pain relief; prevents pathologic fracture progression; may allow non-operative management of mild instability
-
ROUTINE
ROUTINE
-
Nutritional optimization
-
-
1.2-1.5 g/kg :: - :: - :: Protein supplementation (1.2-1.5 g/kg/day); calorie optimization; correct vitamin deficiencies; dietitian consultation; affects wound healing and immune function
-
Malnutrition common in chronic illness; protein essential for wound healing; improves infection outcomes
-
ROUTINE
ROUTINE
-
Diabetes optimization
-
-
180 mg :: PO :: - :: Endocrinology consult if poorly controlled; insulin titration; goal HbA1c <7.5% (individualized); glucose <180 mg/dL during acute illness
-
Diabetes is major risk factor; uncontrolled diabetes impairs healing and immune response
-
STAT
ROUTINE
STAT
Substance abuse counseling (if applicable)
-
-
30% :: - :: - :: IVDU is major risk factor for SEA (20-30% of cases); addiction medicine consultation; harm reduction; hepatitis/HIV screening; reduces recurrence risk
-
IVDU patients at high risk for recurrent infection; addressing substance use reduces future SEA risk
Spine surgery / Neurosurgery consultation — EMERGENT
STAT
STAT
-
STAT
Consult IMMEDIATELY on suspicion — before or concurrent with MRI; surgery vs. medical management decision; ALL patients with SEA need spine surgery evaluation even if medical management is planned (contingency for neurologic deterioration)
Infectious disease consultation
STAT
STAT
ROUTINE
STAT
Antibiotic selection; duration; OPAT planning; monitoring plan; repeat imaging decisions; often co-manage with surgery
Neurologic examination — serial monitoring
STAT
STAT
-
STAT
CRITICAL: q2-4h neurologic checks initially; document motor strength (bilateral LE myotomes), sensory level, rectal tone, bladder function; ANY deterioration → STAT surgical evaluation; pre-operative neuro status is the #1 outcome predictor
CRITICAL — positive in 60-70%; draw 2 sets from separate sites; do NOT delay antibiotics if cultures cause delay — draw quickly and start treatment
Fall precautions / mobility assessment
STAT
STAT
ROUTINE
STAT
SEA patients may have weakness, sensory loss, impaired balance; fall risk assessment; assistive devices; PT/OT evaluation
Documentation of timeline
STAT
STAT
-
STAT
Document: time of symptom onset (back pain → radiculopathy → weakness is classic progression over days-weeks), time of presentation, time of MRI, time of surgical consultation, time of antibiotics, neurologic exam at each time point
At 48-72h if medically managed (assess for enlargement); at 2-4 weeks (assess treatment response — NOTE: imaging may appear worse before better); at end of treatment (baseline); PRN if clinical worsening
CT-guided drainage (percutaneous)
-
URGENT
-
-
Alternative to surgery in selected cases (poor surgical candidate, small collection, posterior access); less reliable than surgical drainage; may be repeated if recurrence
Selected cases with retained hardware, incompletely treated osteomyelitis, immunocompromised; oral suppressive therapy (TMP-SMX, doxycycline, or other based on organism) after initial 6-8 week course; indefinite duration in some cases
Spinal fusion (delayed)
-
-
ROUTINE
-
If significant vertebral destruction and instability after infection controlled; typically 6-12 weeks after infection resolution; staged reconstruction
Hyperbaric oxygen therapy
-
-
EXT
-
Refractory osteomyelitis; adjunctive to antibiotics and surgery; limited evidence but some centers use for difficult cases
═══════════════════════════════════════════════════════════════
SECTION B: SUPPORTING INFORMATION
═══════════════════════════════════════════════════════════════
Known cancer history; bone destruction without disc involvement (SEA typically involves disc); no fever (usually); no elevated ESR/CRP/WBC (unless concurrent infection); may be painful but not typically as acute; enhances but no ring-enhancement or diffusion restriction
MRI: enhancing epidural mass WITHOUT ring enhancement or restricted diffusion; bone destruction; CT/PET: metastatic staging; tumor markers; biopsy if uncertain; ESR/CRP may be mildly elevated in malignancy but not as high as SEA
Vertebral compression fracture (osteoporotic)
Older patient; osteoporosis history; no fever; acute onset with movement; no neurologic deficit (usually); no elevated inflammatory markers; vertebral body wedging; may have benign edema
MRI: vertebral body edema WITHOUT epidural collection; no ring enhancement; normal ESR/CRP; DEXA: osteoporosis; mechanism (fall, lifting); responds to bracing/pain management
Disc herniation (without infection)
No fever; no elevated inflammatory markers; unilateral radiculopathy (usually); no epidural collection on MRI; common, benign presentation
MRI: disc herniation without epidural enhancement; no T2 hyperintense collection; normal ESR/CRP; normal WBC; unilateral symptoms more common
Spinal epidural hematoma
Anticoagulation; post-procedural (epidural injection, LP, surgery); acute onset; hematoma signal characteristics on MRI (not ring-enhancing); no fever; rapidly progressive
MRI: epidural collection with blood signal (T1 hyperintense in subacute phase); NO ring enhancement; NO restricted diffusion in hematoma (unlike abscess); coagulation studies; anticoagulation history; recent procedure
Transverse myelitis / NMOSD
Intramedullary (within cord) rather than epidural; autoimmune; no fever; no elevated ESR/CRP (or mildly elevated); subacute onset; responds to steroids/PLEX
MRI: intramedullary T2 hyperintensity, NOT epidural collection; AQP4/MOG antibodies; CSF: pleocytosis but sterile; normal inflammatory markers
Degenerative lumbar stenosis
Chronic symptoms (claudication); older patient; no fever; no inflammatory markers; bilateral symptoms with walking; relieved by sitting/flexion; chronic findings on MRI
MRI: chronic stenosis (ligamentum flavum hypertrophy, disc bulging, facet hypertrophy) WITHOUT acute epidural collection; normal ESR/CRP; chronic history
Similar to SEA but NO epidural collection; disc and vertebral body involvement; back pain and fever; elevated inflammatory markers; may progress to SEA
MRI: vertebral body and disc enhancement and edema WITHOUT epidural collection; blood cultures may be positive; requires IV antibiotics but not emergent surgical decompression (unless instability or progression to SEA)
Psoas abscess
Contiguous spread can cause spinal infection; flank/groin pain; hip flexion pain; may track from spine or vice versa; fever; iliopsoas enhancement on imaging
CT/MRI: psoas muscle enlargement with rim-enhancing collection; may extend to spine; blood cultures; percutaneous drainage often possible
NOTE: The classic triad (back pain → radiculopathy → paralysis) is present in only 10-15% of patients at presentation. Most patients present with 1-2 features. Maintain HIGH suspicion in any patient with back pain + fever, especially with risk factors.
Sepsis/septic shock; hemodynamic instability; respiratory compromise; post-operative monitoring (surgeon-dependent); severe neurologic deficit with close monitoring needed
General medical/neurosurgery floor
ALL patients with confirmed or suspected SEA require admission; IV antibiotic initiation; neurologic monitoring; surgical evaluation; pre-operative preparation if surgery planned
Observation (NOT appropriate)
SEA is NEVER an observation diagnosis; all patients require admission until diagnosis confirmed/excluded and treatment initiated
6-week IV antibiotic duration for vertebral osteomyelitis; MRI is imaging modality of choice; surgical drainage if neurologic deficit, spinal instability, or failure of medical therapy
Spinal Epidural Abscess Management
AANS/CNS Joint Guidelines
2017
Emergent surgical decompression recommended for patients with neurologic deficit; medical management may be considered for select patients without deficit and with identified organism
Native Vertebral Osteomyelitis
British Infection Association / British Orthopaedic Association
2015
MRI within 24h; blood cultures before antibiotics; echocardiogram for S. aureus bacteremia; 6-week IV antibiotics
Comprehensive review of SEA: S. aureus most common (60-70%); pre-operative neurologic status is #1 predictor of outcome; early surgery associated with better outcomes; medical management reasonable in selected cases without deficit
Established framework for surgical vs. medical management decision-making
915 patients: Surgical treatment associated with better neurologic outcomes than medical management alone; patients presenting with neurologic deficit benefit most from early surgery
Supports surgical decompression as preferred approach, especially with neurologic deficit
6-week IV antibiotic duration for vertebral osteomyelitis; longer for complicated cases (endocarditis, undrained abscess); rifampin adjunct for staphylococcal infections
Standardized antibiotic duration and adjunctive therapy
Peaks early; should begin declining within 1 week; normalize by 3-4 weeks
Rising or plateau after 1 week
Repeat imaging; reassess antibiotic coverage; consider surgery
ESR
May initially rise; begins declining at 2-3 weeks; may not normalize for 6-8 weeks or longer
Rising after 3-4 weeks; failure to decline after 4 weeks
Repeat imaging; ID reassessment; consider treatment failure
WBC
Should normalize within days-1 week
Persistent leukocytosis
Evaluate for secondary site; persistent infection
NOTE: ESR is slow to change and may remain elevated for weeks after successful treatment. CRP is more responsive and useful for early treatment monitoring. Imaging may appear worse at 2-4 weeks despite clinical improvement (this is normal — abscess organization and enhancement may increase before resolution).
Modified MESS Score (Medical vs. Surgical Management)
Consider medical management if ALL of the following:
- [ ] No neurologic deficit
- [ ] Organism identified (blood cultures or biopsy positive)
- [ ] Abscess ≤2.5 cm in maximum dimension
- [ ] No significant spinal instability (SINS <7)
- [ ] Hemodynamically stable (not septic shock)
- [ ] Patient can be monitored closely (serial exams possible)
- [ ] Patient is a poor surgical candidate (relative factor)
If ANY box is unchecked → strongly consider surgical drainage
SINS (Spinal Instability Neoplastic Score) — Also useful for infection
Can be applied to infectious destruction to assess instability (see MSCC template for full scoring details). SINS ≥7 suggests instability requiring surgical stabilization.
Appendix E: Post-Discharge OPAT Monitoring Checklist¶
Monitoring
Frequency
Parameters
ID clinic visit
Weekly
Clinical assessment, review labs, antibiotic tolerance, PICC site
CBC
Weekly
Anemia, thrombocytopenia (linezolid), leukopenia
CMP
Weekly
Renal function (vancomycin, aminoglycosides)
Vancomycin trough
Weekly (more frequent initially)
Target 15-20 mcg/mL
ESR, CRP
Weekly
Declining trend
LFTs
Weekly (if on rifampin or other hepatotoxic drugs)
Transaminases <3x ULN
PICC site assessment
Each VNA visit (2-3x/week)
No erythema, drainage, tenderness
Neurologic exam
Each ID visit; patient self-monitoring daily
Stable; no new weakness/numbness
Temperature
Patient: daily
Afebrile
This template represents the initial build phase (Skill 1) and requires validation through the checker pipeline (Skills 2-6) before clinical deployment.