Measles
Highly contagious viral infection caused by the measles morbillivirus, characterised by fever, cough, coryza, conjunctivitis, Koplik spots, and a maculopapular rash. Vaccine-preventable (MMR) but re-emerging due to declining vaccination rates. Notifiable disease in the UK.
Key Facts
Prodrome: fever, cough, coryza, conjunctivitis (the 3 Cs + fever) followed by Koplik spots (pathognomonic white spots on buccal mucosa) Rash: maculopapular, starts behind ears/hairline, spreads cephalocaudally — appears day 3–5 of illness Highly contagious: R0 = 12–18; airborne transmission; infectious from 4 days before to 4 days after rash onset MMR vaccine: 2 doses (12–13 months and 3 years 4 months); 97% effective after 2 doses Complications: otitis media (~7%), pneumonia (~6%), encephalitis (~0.1%), SSPE (subacute sclerosing panencephalitis — fatal, years later) Notifiable disease: must notify local health protection team immediately on clinical suspicion Vitamin A supplementation: recommended by WHO in severe measles (200,000 IU for 2 days in children >12 months) UK resurgence: outbreaks in under-vaccinated communities; 2024 had significant outbreaks in Birmingham and London
Overview
Key Facts
Measles is one of the most contagious infectious diseases known. Despite effective vaccination, outbreaks continue to occur in under-vaccinated populations. It remains a leading cause of vaccine-preventable death in children globally.
Epidemiology
- Global: ~9 million cases/year; ~128,000 deaths/year (WHO 2023)
- UK: largely eliminated but periodic outbreaks in under-vaccinated communities
- 2023–2024: significant UK outbreak with >1,000 confirmed cases (primarily unvaccinated children)
- UK MMR uptake: ~85% first dose (below 95% herd immunity threshold)
- Most deaths in children <5 years and immunocompromised
Aetiology
- Measles morbillivirus (family Paramyxoviridae, genus Morbillivirus)
- Single-stranded RNA virus; only one serotype (vaccine highly effective)
- Transmission: airborne (droplet nuclei) — can remain airborne for 2 hours in enclosed spaces
- Incubation: 10–14 days (to rash onset)
Pathophysiology
- Virus enters via respiratory epithelium → replicates in lymphoid tissue → viraemia → widespread dissemination
- Infects dendritic cells, macrophages, T and B lymphocytes → transient but profound immunosuppression (immune amnesia lasting weeks to months)
- Endothelial infection → Warthin-Finkeldey giant cells in lymphoid tissue
- Rash: immune-mediated (T-cell response to infected endothelial cells) — immunocompromised patients may not develop rash
- Complications arise from immunosuppression (secondary bacterial infection) or direct viral damage (encephalitis)
Clinical Presentation
Prodromal Phase (2–4 days)
- High fever (often >40°C)
- Cough (dry), coryza, conjunctivitis (the 3 Cs)
- Koplik spots: bluish-white spots on erythematous buccal mucosa (opposite molars) — pathognomonic, appear 1–2 days before rash
- Malaise, irritability
Exanthem Phase
- Maculopapular rash: starts behind ears and hairline → face → trunk → extremities (cephalocaudal spread)
- Rash becomes confluent, may desquamate
- Fever peaks with rash onset then resolves
- Lymphadenopathy
Complications
- Otitis media: ~7% (most common complication)
- Pneumonia: ~6% (leading cause of measles death)
- Febrile seizures: ~1%
- Encephalitis: ~0.1% (1 in 1,000 cases) — 15% mortality, 25% permanent brain damage
- SSPE: ~1 in 25,000 — occurs 7–10 years post-infection; fatal progressive neurological deterioration
Red Flags
- Respiratory distress (pneumonia)
- Altered consciousness (encephalitis)
- Immunocompromised patient (severe/prolonged disease, absence of rash)
- Pregnancy (increased maternal mortality, preterm delivery)
- Infants <12 months (too young for vaccination)
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Rubella | Milder, postauricular lymphadenopathy, pink rash, arthralgia | Rubella IgM |
| Scarlet fever | Sandpaper rash, strawberry tongue, preceding pharyngitis | Throat swab, ASO titre |
| Parvovirus B19 | Slapped cheek, lacy reticular rash, arthropathy | Parvovirus IgM |
| Roseola (HHV-6) | High fever then rash on defervescence, infants | Clinical, HHV-6 PCR |
| Kawasaki disease | Persistent fever, conjunctivitis, strawberry tongue, desquamation | Clinical criteria, echo |
| Drug eruption | Temporal relationship with medication | Drug history |
| Infectious mononucleosis | Pharyngitis, lymphadenopathy, rash with amoxicillin | Monospot, EBV serology |
Diagnosis / Investigation
Bedside
- Clinical diagnosis: prodrome + Koplik spots + characteristic rash is usually sufficient
- Observations: temperature, SpO2
Bloods
- Measles IgM: positive from rash onset (send within 5 days of rash for UKHSA confirmation)
- Oral fluid swab (salivary IgM): preferred sample for UKHSA confirmation in UK
- Measles RNA PCR: throat swab, nasopharyngeal swab, or urine — for genotyping and confirmation
- FBC: leucopenia, lymphopenia (characteristic)
- LFTs: transaminitis in complicated cases
Imaging
- CXR: if pneumonia suspected (interstitial infiltrates or secondary bacterial consolidation)
- CT head: if encephalitis suspected
Special Tests
- Lumbar puncture: if encephalitis — lymphocytic CSF, elevated protein, measles PCR/IgM in CSF
- UKHSA notification: mandatory notification on clinical suspicion; send confirmation samples
Management
Non-pharmacological
- Isolation: airborne precautions; infectious from 4 days before to 4 days after rash onset
- Supportive care: rest, fluids, antipyretics (paracetamol)
- Notification: immediately notify local health protection team on clinical suspicion
- Contact tracing: identify susceptible contacts; offer MMR within 72 hours of exposure (post-exposure prophylaxis)
Pharmacological
- Vitamin A: WHO recommends for all children with measles — 200,000 IU for age >12 months (50,000 IU for 6–11 months) for 2 consecutive days
- Antibiotics: only for secondary bacterial complications (otitis media, pneumonia)
- Human normal immunoglobulin (HNIG): post-exposure prophylaxis for immunocompromised, pregnant, or infants <6 months if exposed — within 6 days of exposure
- Ribavirin: considered in severe/immunocompromised cases (evidence limited)
Post-exposure prophylaxis:
- MMR vaccine within 72 hours of exposure: for unvaccinated contacts aged ≥6 months
- HNIG: for immunocompromised, pregnant, infants <6 months who cannot receive MMR
Surgical/Interventional
- Not applicable
Referral Criteria
- Hospital admission: pneumonia, encephalitis, immunocompromised, severe dehydration, pregnancy
- Public health: all cases (statutory notification)
- Paediatrics: infants, complicated cases
Prognosis
- Uncomplicated measles: full recovery in 7–10 days
- Overall case-fatality rate: 0.1–0.3% in developed countries; up to 5–10% in developing countries
- Pneumonia: leading cause of measles death (~60% of fatalities)
- Encephalitis: 15% mortality, 25% permanent neurological sequelae
- SSPE: universally fatal (onset 7–10 years post-infection)
- Immunocompromised patients: mortality up to 30%
- Measles in pregnancy: increased risk of spontaneous abortion, preterm birth, maternal pneumonia
- Immune amnesia: measles infection resets immune memory — increased susceptibility to other infections for months
Other Relevant Information
UK MMR Vaccination Schedule
| Dose | Age | Vaccine |
|---|---|---|
| 1st | 12–13 months | MMR |
| 2nd | 3 years 4 months | MMR |
| Catch-up | Any age (if missed) | 2 doses, 1 month apart |
Measles Complications by Frequency
| Complication | Incidence |
|---|---|
| Otitis media | ~7% |
| Pneumonia | ~6% |
| Diarrhoea | ~8% |
| Febrile seizures | ~1% |
| Encephalitis | ~0.1% (1 in 1,000) |
| Death | ~0.1–0.3% (developed countries) |
| SSPE | ~1 in 25,000 (years later) |