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

DiagnosisKey FeaturesInvestigation
RubellaMilder, postauricular lymphadenopathy, pink rash, arthralgiaRubella IgM
Scarlet feverSandpaper rash, strawberry tongue, preceding pharyngitisThroat swab, ASO titre
Parvovirus B19Slapped cheek, lacy reticular rash, arthropathyParvovirus IgM
Roseola (HHV-6)High fever then rash on defervescence, infantsClinical, HHV-6 PCR
Kawasaki diseasePersistent fever, conjunctivitis, strawberry tongue, desquamationClinical criteria, echo
Drug eruptionTemporal relationship with medicationDrug history
Infectious mononucleosisPharyngitis, lymphadenopathy, rash with amoxicillinMonospot, 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

DoseAgeVaccine
1st12–13 monthsMMR
2nd3 years 4 monthsMMR
Catch-upAny age (if missed)2 doses, 1 month apart

Measles Complications by Frequency

ComplicationIncidence
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)