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Respiratory System

Pertussis (Whooping Cough)

A highly contagious acute bacterial respiratory infection caused by Bordetella pertussis. Characterized by distinct phases, including a paroxysmal stage with severe coughing fits often followed by an inspiratory 'whoop' and vomiting. Most severe in infants.

Also known as: Whooping Cough, 100-day cough

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Referral and warning signs

When to refer

Hospital admission (H/RR) required for: All infants <3-6 months with suspected pertussis. Patients with severe paroxysms, apnea, cyanosis, seizures. Patients with pneumonia or other significant complications. Patients unable to maintain hydration/nutrition orally.

Red flags

  • Apneic episodes
  • Cyanosis during or after coughing fits
  • Seizures
  • Signs of pneumonia (persistent fever, tachypnea between paroxysms, focal chest signs)
  • Inability to feed / Dehydration
  • Age < 3-6 months

Signs and symptoms

  • Incubation period: 7-10 days.
  • Stage 1: Catarrhal Phase (1-2 weeks): Resembles common cold - mild cough, rhinorrhea, low-grade fever, sneezing. Highly infectious stage.
  • Stage 2: Paroxysmal Phase (1-6 weeks, can be longer): Severe, repetitive coughing fits (paroxysms) occurring in bursts. Inspiratory 'whoop' sound often follows paroxysm as patient gasps for air (may be absent in infants <6mo and adults). Post-tussive vomiting common. Cyanosis, apnea, exhaustion may occur during/after paroxysms, especially in infants. Conjunctival haemorrhages, facial petechiae from coughing.
  • Stage 3: Convalescent Phase (Weeks to months): Gradual reduction in frequency and severity of coughing paroxysms. Cough may persist or recur with subsequent URTI.

Risk factors

  • Incomplete or lack of pertussis vaccination (DPT/Pentavalent/Tdap).
  • Infancy (<1 year), especially <6 months (highest risk of severe disease/death).
  • Exposure to an infected individual (household contact, school).
  • Waning immunity in adolescents and adults (who can transmit to infants).

Diagnosis

Clinical assessment

Clinical suspicion based on characteristic cough (paroxysmal, whoop, post-tussive vomiting) lasting ≥2 weeks, especially during an outbreak or with known exposure. Diagnosis often made clinically. Differential diagnosis: Other causes of prolonged cough (viral bronchitis, Mycoplasma/Chlamydia pneumonia, asthma, GERD, foreign body, TB), Croup (barking cough, stridor), Bronchiolitis (wheeze, younger infants).

Investigations

  • Nasopharyngeal Swab/Aspirate:
  • - Culture for Bordetella pertussis: Gold standard but sensitivity decreases after first 2 weeks of cough and after antibiotics. Requires specific media.
  • - PCR for B. pertussis DNA: Highly sensitive and specific, preferred method, useful up to 3-4 weeks after cough onset.
  • Blood: Complete Blood Count (CBC) may show marked lymphocytosis (high lymphocyte count), especially in infants/young children.
  • Serology (Antibody testing): Useful later in illness (>2-3 weeks cough), requires paired sera or specific IgM/IgA interpretation. Less useful for acute diagnosis.
  • Chest X-ray: Usually normal or may show peribronchial thickening; used to exclude pneumonia.

Diagnostic criteria

Clinical diagnosis based on characteristic cough illness ≥2 weeks, OR laboratory confirmation (positive culture or PCR).

Management

Non-pharmacological management

  • Supportive Care:
  • - Maintain hydration and nutrition (small, frequent feeds may be better tolerated).
  • - Gentle suctioning of secretions if needed.
  • - Oxygen therapy if hypoxic.
  • - Minimize stimuli that trigger coughing paroxysms.
  • Hospitalization: Required for infants (<3-6 months), severe cases with apnea/cyanosis/pneumonia/seizures, or inability to feed.
  • Infection Control:
  • - Droplet precautions for hospitalized patients until 5 days of effective antibiotic therapy completed.
  • - Exclude cases from school/daycare until 5 days of antibiotics completed.
  • - Reportable disease.

Pharmacological treatment

  • Antibiotics: Primarily given to reduce infectivity (limit spread) and may shorten duration/severity if started early (within first 1-2 weeks of cough - catarrhal/early paroxysmal phase). Less effective if started later but still recommended to decrease transmission.
  • - Macrolides are preferred:
  • - Azithromycin: Child <6mo: 10mg/kg/day OD x 5 days. Child ≥6mo: 10mg/kg (max 500mg) OD on Day 1, then 5mg/kg (max 250mg) OD on Days 2-5. Adult: 500mg OD Day 1, then 250mg OD Days 2-5.
  • - Erythromycin: 40-50 mg/kg/day divided QID (Adult 500mg QID) for 7-14 days (UCG 2023 specifically mentions 7 days). (More side effects, longer course).
  • - Clarithromycin: Alternative macrolide.
  • - Alternative if macrolide allergic/intolerant: Trimethoprim-Sulfamethoxazole (TMP-SMX) - Contraindicated in infants <2 months.
  • Cough suppressants, antihistamines, mucolytics: NOT effective and NOT recommended.
  • Corticosteroids: No proven benefit.

Monitoring

  • Monitor respiratory status (frequency/severity of paroxysms, apnea, cyanosis).
  • Monitor feeding and hydration.
  • Monitor for complications (pneumonia, seizures).

Complications

  • Apnea (especially infants)
  • Pneumonia (secondary bacterial)
  • Seizures (due to hypoxia or encephalopathy)
  • Encephalopathy
  • Weight loss / Malnutrition
  • Dehydration
  • Otitis media
  • Subconjunctival haemorrhage, petechiae
  • Pneumothorax, subcutaneous emphysema (from forceful coughing)
  • Hernias (inguinal, umbilical), rectal prolapse
  • Death (highest risk in young infants)

Prevention

  • Vaccination: Routine childhood immunization with DTaP/Pentavalent vaccine. Adolescent and adult booster doses (Tdap) recommended to maintain immunity and reduce transmission to infants.
  • Vaccination during pregnancy (Tdap) protects newborn.
  • Post-exposure Prophylaxis (PEP): Antibiotics (usually macrolide) recommended for close contacts (household, daycare) especially if high-risk individuals (infants, pregnant women) are exposed, regardless of vaccination status.

Patient education

  • Explain the stages of pertussis and prolonged nature of cough.
  • Purpose of antibiotics (reduce spread, may lessen severity if early).
  • Importance of completing antibiotic course.
  • Need for supportive care (fluids, nutrition).
  • How to manage paroxysms (minimize triggers).
  • Signs of complications and when to seek urgent care.
  • Importance of vaccination for prevention (childhood series, boosters).
  • Need for antibiotic prophylaxis for close contacts.

Uganda-specific notes

Included in Pentavalent vaccine schedule. Diagnosis often clinical. Erythromycin is the antibiotic listed in UCG 2023. High mortality in young, unvaccinated infants. Post-exposure prophylaxis for contacts important.

References

  • Uganda Clinical Guidelines (UCG) 2023

    Chapter 5, Section 5.2.8

For learning and professional reference. Use current local guidance and clinical judgement.

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