Ampath Chats

Bordetella pertussis: Whooping Cough

Ampath Chats
Bordetella pertussis: Whooping Cough
Read Document

PATHCHAT Edition No. 50
December 2018
Please contact your local Ampath pathologist for more information.

Authors: Dr. Kathy-Anne Strydom (Clinical Microbiologist) & Dr. Marcelle Myburgh (Clinical Virologist)

Introduction

What is Pertussis?

  • Pertussis (whooping cough) is a highly infectious respiratory disease caused by Bordetella pertussis.
  • Other Bordetella species (B. parapertussis, B. holmesii) may cause milder forms of the disease.

Transmission & Infectious Period:

  • Spread via respiratory droplets.
  • High secondary attack rate (up to 90%) in susceptible contacts.
  • Incubation period: 5–21 days (average: 7–10 days).
  • Most infectious during the early (catarrhal) phase but can transmit for up to 3 weeks if untreated.

📌 Despite high vaccine coverage, pertussis outbreaks occur in epidemic cycles every 2–5 years.

Epidemiology

🔹 Global & Local Trends:

  • Pertussis is endemic worldwide.
  • Recent resurgence despite vaccination efforts.
  • South Africa has seen increased cases, especially in infants under 6 months.
  • Growing incidence in adolescents and adults.

📌 Neonates and young infants have the highest morbidity and mortality from pertussis.

Clinical Presentation

Classic Pertussis Stages (Most Common in Unvaccinated Children):

1. Catarrhal Stage (1–2 weeks):

  • Nonspecific symptoms (cough, coryza, sneezing).
  • Most infectious stage.

2. Paroxysmal Stage (2–8 weeks):

  • Severe paroxysmal coughing fits.
  • Inspiratory "whoop" after coughing spells.
  • Post-tussive vomiting.
  • Highest risk of complications (e.g., pneumonia, encephalopathy, seizures).

3. Convalescent Stage (1–2 weeks):

  • Cough gradually resolves.

Atypical Presentations:

  • Neonates may present with apnoea, seizures, or pneumonia instead of classic cough.
  • Vaccinated individuals and adults may have only a prolonged cough (no whooping).

📌 Atypical presentations delay diagnosis, increasing transmission risk and mortality.

Diagnosis of Bordetella Pertussis

Diagnostic Methods:

  • Polymerase Chain Reaction (PCR) (Preferred).
  • Serology (Anti-pertussis toxin IgG).
  • Culture (Not routinely performed).

🔹 Comparison of Diagnostic Methods:

PCR Testing (Most Sensitive, Rapid Result):

  • Sensitivity: 70–99%
  • Specificity: 86–100%
  • Specimen: Nasopharyngeal swab/aspirate or sputum
  • Best performed in the catarrhal or early paroxysmal stage (before antibiotics).
  • Single-copy gene targets have lower sensitivity but higher specificity than multi-copy targets.

Serology (Useful for Late Presentations):

  • Sensitivity: 50–99%
  • Specificity: >90%
  • Specimen: Blood
  • Requires paired serum samples (acute and convalescent phases).
  • Affected by recent vaccination or maternal antibodies in neonates.

Culture (Not Routinely Used):

  • Sensitivity: 12–60%
  • Specificity: 100%
  • Specimen: Nasopharyngeal swab/aspirate or sputum
  • Requires specialized transport media for viability.

📌 Negative PCR does NOT rule out pertussis—results should be correlated with clinical suspicion.

Treatment of Pertussis

Management is Primarily Supportive:

  • Monitor for respiratory distress, especially in infants.
  • Adequate hydration & nutrition support.
  • Hospitalization for high-risk infants (age <3 months, severe disease, apnoea).

🔹 Antibiotic Therapy (Reduces Transmission, Not Disease Course):

First-Line (Macrolides):

  • Azithromycin (preferred in infants <1 month).
  • Clarithromycin or erythromycin.

Alternative:

  • Trimethoprim-sulfamethoxazole (if macrolides are contraindicated).

📌 Antibiotics are most effective if given within 2 weeks of symptom onset.

Prevention of Pertussis

Primary Prevention: Vaccination

  • Acellular pertussis (aP) vaccine is part of the South African Expanded Programme on Immunisation (EPI).
  • Immunity wanes after ~5 years, requiring booster doses.

🔹 Recommended Booster Schedule:

  • Every 4–6 years (Tdap or TdaP vaccine).
  • During each pregnancy (27–36 weeks gestation), regardless of prior vaccination.
  • Healthcare workers & household contacts of neonates should be vaccinated.

📌 Maternal vaccination provides passive immunity to newborns and reduces pertussis-related infant mortality.

Post-Exposure Prophylaxis (PEP) for Close Contacts

Who Should Receive PEP?

  • Household contacts and family members.
  • Infants <2 months old.
  • Infants <1 year if not fully vaccinated.
  • Pregnant women in their third trimester.
  • Healthcare workers and caregivers in contact with infants.

PEP Regimen:

  • Macrolides (same as treatment).
  • Start within 21 days of index case symptom onset.

📌 PEP is essential to prevent transmission, especially in households with young infants.

Key Takeaways for Clinicians

Pertussis is highly contagious and remains a global health concern despite vaccination efforts.
PCR is the preferred diagnostic test due to high sensitivity and rapid turnaround time.
Atypical presentations occur in neonates, vaccinated individuals, and adults, often delaying diagnosis.
Macrolides reduce transmission but have limited impact on disease course.
Booster vaccinations are essential, especially in pregnant women and high-risk contacts.
Post-exposure prophylaxis should be given to close contacts, particularly infants and pregnant women.

📌 Early recognition and prevention strategies are crucial to controlling pertussis outbreaks.