Meningococcal Disease
Invasive infection with Neisseria meningitidis causing meningitis and/or meningococcaemia (septicaemia). A medical emergency with rapidly progressive course. Non-blanching purpuric rash is the hallmark of meningococcal septicaemia. Case-fatality rate ~5–10% even with optimal treatment.
Key Facts
Non-blanching petechial/purpuric rash in unwell febrile patient is meningococcal disease until proven otherwise — glass test IM benzylpenicillin in the community BEFORE hospital transfer: 1.2g (adult), 600mg (child 1–9), 300mg (infant <1) Serogroups: B and W now predominant in UK; MenACWY and MenB vaccines in routine UK immunisation schedule Lumbar puncture: raised WCC (neutrophils), raised protein, low glucose, Gram-negative diplococci — BUT do NOT delay antibiotics for LP IV ceftriaxone 2g BD (adult) or cefotaxime: empirical treatment — start immediately Chemoprophylaxis for contacts: single-dose ciprofloxacin 500mg (adult) or rifampicin 600mg BD for 2 days Notifiable disease: must notify local health protection team immediately — urgent contact tracing Waterhouse-Friderichsen syndrome: bilateral adrenal haemorrhage in fulminant meningococcaemia — DIC, shock, adrenal crisis
Overview
Key Facts
Meningococcal disease is a medical emergency that can progress from initial symptoms to death within hours. Rapid recognition and immediate antibiotic treatment are essential. UK vaccination programmes have significantly reduced incidence.
Epidemiology
- UK: ~500–1,000 cases/year (declining due to vaccination)
- Peak incidence: children <5 years and adolescents 15–19
- Case-fatality rate: ~5–10% (meningitis); ~20–30% (meningococcaemia/septicaemia)
- Winter/spring seasonality
- University freshers: increased risk (close living, social mixing)
Aetiology
- Neisseria meningitidis: Gram-negative diplococcus; polysaccharide capsule determines serogroup
- Serogroups: B (~50% of UK cases), W, Y, C (rare since MenC vaccine)
- Transmission: respiratory droplets, close contact; carriage rate ~10% in adolescents
- Risk factors: asplenia, complement deficiency, crowded living (dormitories, barracks), recent viral URTI
Pathophysiology
- Nasopharyngeal colonisation → bloodstream invasion → bacteraemia
- Endotoxin (LOS — lipooligosaccharide) triggers massive inflammatory response
- Complement activation → DIC → purpura fulminans
- Meningeal inflammation → raised ICP, cerebral oedema
- Adrenal gland haemorrhage → Waterhouse-Friderichsen syndrome
- Rapid progression: can deteriorate from well to critically ill within hours
Clinical Presentation
Meningitis Presentation
- Headache, photophobia, neck stiffness
- Fever, vomiting
- Altered consciousness, irritability
- Kernig sign (unable to extend knee with hip flexed), Brudzinski sign (neck flexion causes hip/knee flexion)
- Bulging fontanelle in infants
Meningococcaemia (Septicaemia)
- Non-blanching petechial/purpuric rash — may start as blanching maculopapular then progress to purpura
- Fever, rigors, myalgia
- Rapid deterioration: tachycardia, hypotension, cold extremities
- Purpura fulminans: large ecchymoses, skin necrosis, DIC
- Shock, multi-organ failure
Red Flags
- Non-blanching rash + fever in child/young person
- Rapidly progressive purpuric rash
- Signs of shock (tachycardia, hypotension, prolonged cap refill)
- Reduced consciousness (GCS <12)
- Neck stiffness + fever + headache
- Infants: bulging fontanelle, high-pitched cry, poor feeding, floppiness
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Viral meningitis | Milder course, lymphocytic CSF, enterovirus common | CSF PCR (enterovirus) |
| Pneumococcal meningitis | Older adults, post-splenectomy, otitis media, Gram-positive diplococci | Blood/CSF culture |
| Haemophilus meningitis | Now rare in UK (Hib vaccine); young children | CSF culture |
| ITP | Non-blanching rash BUT well child, no fever | FBC (isolated thrombocytopenia), blood film |
| HSP (IgA vasculitis) | Purpuric rash on buttocks/legs, arthralgia, abdominal pain | Clinical, urinalysis |
| Sepsis (other) | Same shock presentation, different source | Blood cultures, source investigation |
Diagnosis / Investigation
Bedside
- Glass test: non-blanching rash does not fade under pressure
- Observations: HR, BP, RR, SpO2, GCS, capillary refill, temperature
- Blood glucose: hypoglycaemia
Bloods
- Blood cultures: BEFORE antibiotics (but do NOT delay treatment to obtain)
- Meningococcal PCR: on EDTA blood — can be positive even after antibiotics
- FBC: leucocytosis or leucopenia
- CRP, lactate: severity markers
- Coagulation screen: DIC (prolonged PT/APTT, low fibrinogen, raised D-dimer)
- U&Es, LFTs: organ dysfunction
- Blood gas: metabolic acidosis
Special Tests
- Lumbar puncture (if safe — NO LP if signs of raised ICP, haemodynamic instability, coagulopathy, GCS ≤12):
- CSF: turbid, raised WCC (neutrophils), raised protein (>1 g/L), low glucose (<50% of blood glucose)
- Gram stain: Gram-negative diplococci
- CSF PCR: meningococcal DNA
- CSF culture
Imaging
- CT head: before LP if signs of raised ICP (papilloedema, focal neurology, GCS ≤12)
- CXR: if respiratory compromise
Management
Non-pharmacological
- Do NOT delay antibiotics for any investigation
- Resuscitation: ABC approach, high-flow oxygen, IV access × 2
- IV fluids: 20 ml/kg 0.9% NaCl bolus, reassess, repeat up to 60 ml/kg
- ICU referral: early if septic shock, DIC, or GCS ≤12
Pharmacological
Pre-hospital:
- IM/IV benzylpenicillin: 1.2g adult, 600mg child 1–9, 300mg <1 year — give IMMEDIATELY on clinical suspicion before transfer
In-hospital:
- IV ceftriaxone 2g BD (adult); 80mg/kg in children; continue for 7 days (5 days if confirmed meningococcal)
- OR IV cefotaxime: alternative
- Dexamethasone 0.15mg/kg QDS IV for 4 days: if suspected bacterial meningitis in adults — give with or before first antibiotic dose; NOT if meningococcal septicaemia without meningitis
- DIC management: cryoprecipitate, FFP, platelets as needed
- Vasopressors: noradrenaline if fluid-refractory shock
Close contacts:
- Ciprofloxacin 500mg stat (adult) or rifampicin 600mg BD for 2 days
- Children: rifampicin or ceftriaxone IM
- Offer to household contacts and 'kissing contacts' within 7 days
- MenACWY + MenB vaccine for contacts if outbreak serogroup matches
Referral Criteria
- All cases: infectious diseases, ICU
- Public health: immediate statutory notification; contact tracing
- ENT/neurosurgery: if complications (abscess, hydrocephalus)
- Rehabilitation: for survivors with sequelae
Prognosis
- Overall case-fatality rate: 5–10%
- Meningococcal septicaemia without meningitis: mortality 20–30%
- Meningitis alone (without septicaemia): mortality ~5%
- Purpura fulminans/Waterhouse-Friderichsen: mortality >50%
- Survivors: 10–20% have long-term sequelae (deafness, limb amputation, cognitive impairment, skin scarring)
- Sensorineural deafness: ~5% of survivors
- Limb loss (from gangrene/DIC): ~7% of survivors
- With prompt treatment and intensive care, majority survive
Other Relevant Information
UK Meningococcal Vaccination Schedule
| Vaccine | Age | Protection |
|---|---|---|
| MenB (Bexsero) | 8 weeks, 16 weeks, 12 months | Serogroup B |
| MenACWY | 14 years (school Year 9) + university freshers | Serogroups A, C, W, Y |
| MenC (historical) | Replaced by MenACWY | Serogroup C |
CSF Findings in Meningitis
| Parameter | Bacterial | Viral | TB |
|---|---|---|---|
| Appearance | Turbid | Clear | Fibrinous |
| WCC | Neutrophils ↑↑ | Lymphocytes ↑ | Lymphocytes ↑ |
| Protein | ↑↑ | Normal/↑ | ↑↑↑ |
| Glucose | ↓↓ (<50% blood) | Normal | ↓↓ |
| Gram stain | May show organism | Negative | ZN often negative |