Initial Management of Suspected Acute Bacterial Meningitis
In suspected acute bacterial meningitis, immediately obtain blood cultures and administer empiric antibiotics within 1 hour of hospital arrival—do not delay treatment for imaging or lumbar puncture, as every hour of delay increases mortality and neurological morbidity. 1, 2
Immediate Stabilization and Assessment (First Hour)
Stabilize airway, breathing, and circulation as the absolute first priority. 1
- Document Glasgow Coma Scale score immediately upon arrival for prognostic assessment and to monitor deterioration 1, 3
- Assess for signs of shock: capillary refill >2 seconds, hypotension (mean arterial pressure <65 mmHg), altered mental status, or lactate >2 mmol/L 1
- If shock or rapidly evolving purpuric rash is present, initiate aggressive fluid resuscitation with 500 mL crystalloid bolus immediately and do NOT perform lumbar puncture at this time 1
- Involve intensive care teams immediately if GCS ≤12, cardiovascular instability, hypoxia, or rapidly evolving rash is present 2
Diagnostic Algorithm
Blood Cultures First
Obtain blood cultures within 1 hour of arrival before any antibiotics are given—blood cultures are positive in 71% of cases even when CSF cultures fail, making them critical for diagnosis. 1, 4
Decision Point: CT Scan Before Lumbar Puncture?
Perform urgent head CT before lumbar puncture ONLY if any of these high-risk features are present: 1, 2
- Immunocompromised state (HIV, immunosuppressive drugs, malignancy)
- History of CNS disease (mass lesion, stroke, focal infection)
- New-onset seizure within the past week
- Altered consciousness or inability to follow commands
- Focal neurological deficits (gaze palsy, facial weakness, limb drift, aphasia)
- Papilledema on fundoscopic examination
- GCS ≤12
If NONE of these features are present, proceed directly to lumbar puncture without CT imaging. 1, 2
Lumbar Puncture Timing
In patients without shock or severe sepsis: 1
- Perform LP within 1 hour of arrival if no CT contraindications exist
- Start antibiotics immediately after LP is completed, within the first hour
- If LP cannot be performed within 1 hour, start antibiotics immediately after blood cultures and perform LP as soon as possible thereafter—preferably within 4 hours of antibiotic initiation 1, 5
Critical timing evidence: CSF culture positivity drops dramatically after antibiotics—73% positive if LP done within 4 hours versus only 11% if delayed beyond 4 hours, and zero positivity after 8 hours. 5
In patients with shock, severe sepsis, or rapidly evolving rash: 1
- Give antibiotics immediately after blood cultures
- Do NOT perform LP during acute resuscitation phase
- Defer LP until patient is stabilized
Empiric Antimicrobial Therapy
Standard Adult Regimen (<60 years, immunocompetent)
Administer the following combination immediately: 2, 3
- Ceftriaxone 2g IV every 12 hours OR Cefotaxime 2g IV every 6 hours
- PLUS Vancomycin 15-20 mg/kg IV every 8-12 hours (target serum trough 15-20 µg/mL)
Never use vancomycin alone—it must be combined with a third-generation cephalosporin due to inadequate CSF penetration, especially when dexamethasone is co-administered. 2
Modified Regimen for High-Risk Patients (≥60 years or immunocompromised)
Add Ampicillin 2g IV every 4 hours to the above regimen for Listeria monocytogenes coverage. 2, 3
Risk factors mandating Listeria coverage include: 2
- Age >50-60 years
- Diabetes mellitus
- Immunosuppressive therapy
- Malignancy
- Other immunocompromising conditions
Pediatric Regimens
- Cefotaxime PLUS Ampicillin (or Amoxicillin)
- Do NOT use ceftriaxone in neonates due to risk of fatal calcium-ceftriaxone precipitation 1
- Cefotaxime or Ceftriaxone PLUS Vancomycin
Adjunctive Dexamethasone Therapy
Administer dexamethasone 10 mg IV every 6 hours (or 0.15 mg/kg in children) immediately before or simultaneously with the first antibiotic dose—this reduces mortality from 15% to 7% and unfavorable outcomes from 25% to 15% in adults. 2
Critical timing requirements: 2
- Give 10-20 minutes before antibiotics or at the same time
- Can still be given up to 12 hours after first antibiotic dose, but benefit diminishes
- Never give dexamethasone more than 12 hours after antibiotics—timing is critical for efficacy
- Continue for 4 days if pneumococcal meningitis is confirmed or highly probable
- Discontinue if alternative etiology (viral, fungal) is identified
- In children with meningococcal meningitis, continue full 4-day course 1
Special consideration with vancomycin: Dexamethasone reduces vancomycin CSF penetration, so consider adding Rifampin 300 mg IV every 12 hours to the regimen in suspected pneumococcal meningitis. 2
Exception—do NOT use dexamethasone: In children with meningococcal septicaemia (shock without meningitis), steroids are not recommended except for inotrope-resistant shock. 1
CSF Interpretation
Expected Findings in Bacterial Meningitis 1, 4
| Parameter | Typical Finding | Clinical Significance |
|---|---|---|
| Opening pressure | 200-500 mm H₂O | Indicates raised ICP |
| WBC count | 1,000-5,000 cells/mm³ (range 100-110,000) | Elevated in virtually all cases |
| Differential | 80-95% neutrophils | ~10% may show lymphocyte predominance |
| Glucose | <40 mg/dL in 50-60% | Hypoglycorrhachia strongly suggests bacterial etiology |
| CSF/serum glucose ratio | <0.4 (children >12 months); <0.6 (neonates) | 80% sensitive, 98% specific |
| Protein | Elevated | Marker of blood-brain barrier disruption |
Gram Stain Diagnostic Yield 1, 4
Overall sensitivity: 60-90% in untreated patients, but drops ~20% if antibiotics given before LP 4
Pathogen-specific positivity rates: 1
- Streptococcus pneumoniae: 90%
- Haemophilus influenzae: 86%
- Neisseria meningitidis: 75%
- Gram-negative bacilli: 50%
- Listeria monocytogenes: 33%
Partially Treated Meningitis
If antibiotics were given before LP, CSF findings remain diagnostically useful: 4
- Elevated WBC, low glucose, and high protein persist despite antibiotic pretreatment
- Order CSF PCR (sensitivity 87-100%, specificity 98-100%)—remains positive even after antibiotics 4
- Blood cultures obtained before antibiotics may be positive even when CSF cultures are negative 4
- Never assume viral meningitis based solely on lymphocyte predominance in CSF—partially treated bacterial meningitis can present this way 4
Supportive Care
Fluid Management
Maintain euvolemic state to preserve normal hemodynamic parameters—do NOT restrict fluids to reduce cerebral edema. 3
In shock: 1
- Administer rapid 500 mL crystalloid boluses (20 mL/kg in children)
- Reassess after each bolus; may require up to 60 mL/kg total
- Use norepinephrine as first-line vasopressor if fluid-resistant shock develops, targeting mean arterial pressure ≥65 mmHg 3
Seizure Management
If continuous or uncontrolled seizures occur, this is a contraindication to immediate LP and requires urgent neuroimaging. 1
ICU Transfer Criteria 2
Transfer to intensive care if:
- GCS ≤12
- Rapidly evolving purpuric rash
- Cardiovascular instability requiring inotropes
- Respiratory failure requiring ventilatory support
- Inotrope-resistant shock (consider vasopressin and stress-dose steroids as rescue)
Common Pitfalls to Avoid
Never delay antibiotics for imaging or LP—treatment must begin within 1 hour regardless of diagnostic testing status. 1, 2
Never send patients for unnecessary CT scans—67% of delays in one study were due to CT scans in patients without contraindications to immediate LP. 5
Never use vancomycin monotherapy—it must be combined with ceftriaxone or cefotaxime. 2
Never omit Listeria coverage in patients ≥50-60 years or immunocompromised—add ampicillin to the empiric regimen. 2
Never use ceftazidime as empiric therapy for community-acquired meningitis—it has inferior pneumococcal coverage and should be reserved for nosocomial or Pseudomonas infections. 2
Never rely solely on negative CSF cultures to exclude bacterial meningitis if antibiotics were given before LP—use clinical parameters, CSF chemistry, and PCR testing. 4
Never assume absence of pleocytosis excludes meningitis—rare cases (124 reported) of culture-proven bacterial meningitis occur without CSF pleocytosis, with 31% mortality; blood cultures are positive in 71% of these cases. 6
Never discontinue empiric therapy based on initial negative Gram stain alone—Gram stain sensitivity is only 60-90% and varies by pathogen. 1, 4