Whooping Cough
Whooping cough (pertussis) is caused by Bordetella pertussis and characterised by paroxysmal cough with inspiratory whoop. It is particularly dangerous in young infants. Vaccination (prenatal and childhood) is the most effective prevention.
Key Facts
Bordetella pertussis: Gram-negative coccobacillus; highly infectious (attack rate 80-90% in household contacts) Classic presentation: Paroxysmal cough with inspiratory whoop, post-tussive vomiting; '100-day cough' Infants <3 months are at highest risk of severe disease — apnoea may be the only feature; 90% of deaths occur in this age group Maternal vaccination (from 16 weeks gestation) protects neonates via transplacental antibody transfer — ~90% effective UK pertussis resurgences occur in ~3-4 year cycles; major outbreaks in 2012 and 2024 Diagnosis: Nasal swab PCR (best in first 2-3 weeks) or anti-pertussis toxin IgG (after 2 weeks) Treatment: Azithromycin 10mg/kg OD for 3 days (or clarithromycin) — reduces infectivity if given in catarrhal phase but does NOT shorten paroxysmal phase Exclusion from school: Until 48 hours of appropriate antibiotic treatment or 21 days from onset of symptoms
Overview
Key Facts
Pertussis remains an important cause of morbidity and mortality in young infants despite vaccination. The UK maternal vaccination programme, introduced in 2012 following a major outbreak, has been highly effective in reducing neonatal disease.
Epidemiology
Pertussis notifications in England: typically 5,000-10,000 per year with cyclical peaks every 3-4 years. Incidence is highest in infants <3 months (too young to be vaccinated). ~90% of pertussis deaths occur in infants <3 months. Adolescents and adults are an important reservoir of infection (waning immunity).
Aetiology
- Bordetella pertussis: Primary pathogen
- Bordetella parapertussis: Milder illness; not prevented by pertussis vaccine
- Transmission: Respiratory droplets; highly contagious; incubation 7-21 days
Pathophysiology
B. pertussis attaches to ciliated respiratory epithelium via filamentous haemagglutinin and pertactin. It produces pertussis toxin (ADP-ribosylating exotoxin) which impairs immune cell function, increases insulin secretion (causing lymphocytosis), and sensitises the cough reflex. Tracheal cytotoxin causes ciliated cell damage and mucus hypersecretion. The paroxysmal cough is mediated by sensitisation of cough receptors and persists for weeks after the organism is cleared.
Clinical Presentation
Three Phases
Catarrhal phase (1-2 weeks):
- Coryzal symptoms, mild cough, low-grade fever
- MOST INFECTIOUS period
Paroxysmal phase (2-8 weeks):
- Paroxysms of intense cough (10-30 coughs in a row)
- Inspiratory 'whoop' between paroxysms
- Post-tussive vomiting
- Facial congestion/cyanosis during paroxysms
- May be well between paroxysms
Convalescent phase (weeks to months):
- Gradual resolution; cough may persist for months ('100-day cough')
- Paroxysms may recur with subsequent viral infections
Infants <3 Months
- May NOT whoop — too small to generate whoop
- Apnoea may be the ONLY feature
- Cyanotic episodes, feeding difficulty
- High risk of complications: Pneumonia, seizures, encephalopathy, death
Red Flags
- Apnoea in young infant — admit for monitoring
- Marked lymphocytosis (>20 × 10⁹/L) with leucocytosis — correlates with severe disease in infants
- Pulmonary hypertension — rare but can be fatal in infants with hyperleucocytosis
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Pertussis | Paroxysmal cough, whoop, post-tussive vomiting | PCR nasal swab, anti-PT IgG |
| Viral URTI with cough | Shorter duration, no whoop | Clinical |
| Bronchiolitis | <12 months, wheeze + crackles, RSV season | NPA |
| Foreign body | Sudden onset, no prodrome | CXR, bronchoscopy |
| Mycoplasma pneumonia | School-age, dry cough, extrapulmonary features | Serology, PCR |
| TB | Chronic cough, weight loss, contact history | CXR, Mantoux, sputum |
Diagnosis / Investigation
Bedside
- SpO2: During paroxysms
- Video of paroxysm: Helpful if not witnessed by clinician
Bloods
- FBC: Marked lymphocytosis (>10 × 10⁹/L in >50% of cases; >20 correlates with severity)
- Anti-pertussis toxin IgG: Oral fluid or serum — diagnostic after 2 weeks of symptoms
Microbiology
- Nasal swab PCR: Best in first 2-3 weeks; specificity >95%
- Culture: Gold standard but slow (takes 7 days); sensitivity lower than PCR
Imaging
- CXR: If pneumonia suspected; may show perihilar infiltrates or consolidation
Management
Pharmacological
- Azithromycin: 10mg/kg OD for 3 days (first-line) — reduces infectivity; does NOT shorten paroxysmal phase if already established
- Clarithromycin: Alternative (7.5mg/kg BD for 7 days)
- Most effective if given during catarrhal phase
- Antibiotics for household contacts (post-exposure prophylaxis) — especially if vulnerable contacts (pregnant women, young infants)
Non-pharmacological
- Admission: Infants <6 months (especially <3 months); apnoeas; severe paroxysms; feeding difficulty
- Monitoring: Continuous SpO2 and apnoea monitoring for young infants
- Supportive care: Small frequent feeds, minimal stimulation, oxygen if needed
- Suction: Gentle nasal suction if needed
Prevention
- Childhood vaccination: 6-in-1 (DTaP) at 8, 12, 16 weeks + pre-school booster at 3yr 4mo
- Maternal vaccination: Pertussis-containing vaccine (dTaP/IPV) from 16 weeks gestation — ~90% effective at preventing infant disease
- Post-exposure prophylaxis: Azithromycin for household contacts
- School exclusion: 48 hours after starting antibiotics or 21 days from symptom onset if untreated
Referral Criteria
- All infants <3 months with suspected pertussis — admission
- Apnoeas or cyanotic episodes — PICU assessment
- Severe lymphocytosis in infant — haematology/PICU (exchange transfusion in extreme cases)
Prognosis
- Overall mortality: <0.5% in developed countries; higher in unvaccinated infants <3 months
- Infant mortality: ~1% in hospitalised infants <3 months; most deaths from pulmonary hypertension/hyperleucocytosis
- Duration: Paroxysmal cough lasts 2-8 weeks; total illness 6-12 weeks ('100-day cough')
- Post-pertussis bronchiectasis: Rare with modern management
- Maternal vaccination: Has reduced infant pertussis deaths by ~90% since introduction
Other Relevant Information
Pertussis Phases
| Phase | Duration | Features | Infectivity |
|---|---|---|---|
| Catarrhal | 1-2 weeks | Coryzal, mild cough | HIGHEST |
| Paroxysmal | 2-8 weeks | Paroxysms, whoop, vomiting | Decreasing |
| Convalescent | Weeks-months | Gradual resolution | Minimal |
When to Notify and Test
| Situation | Action |
|---|---|
| Clinical suspicion of pertussis | Notify PHE; send nasal PCR |
| Cough >2 weeks with paroxysms | Test (PCR <3 weeks; serology >2 weeks) |
| Household contact is pregnant/infant | Post-exposure prophylaxis with azithromycin |