Bordetella pertussis: Clinical manifestations and diagnosis

Bordetella pertussis: Clinical manifestations and diagnosis


Introduction

  • Whooping cough is caused by B. pertussis.
  • < 5% cases it is caused by B. parapertussis.
  • No cross immunity of B. pertussis with B. parapertussis:
  • antibodies against B. Pertussis do not protect against B. parapertussis.
  • More cases occur during winter and spring month, due to overcrowding.

Source of infection:

  • Case of pertussis (not carrier).
  • There is no subclinical case
  • Chronic carrier state does not exist.

Infective period:

  • Catarrhal stage.
  • The infective period extends from a week after exposure to about 3 weeks after the onset of the paroxysmal stage.

Secondary attack rate :

  • High, i.e. 90%.

Age group:

  • Disease of infants and young children (< 5 years of age).
  • Infants are susceptible to infection from birth because maternal antibody does not give them protection.
  • Mean age of infection is between 2 0- 3 0 months.
  • However, it can also affect, though less commonly, older children, adolescents and adults.

Sex predisposition in pertussis:

  • Incidence and fatality are more among female than male children.

Infective material:

  • The infective bacilli occur abundantly in the nasopharyngeal and bronchial secretions.
  • Objects freshly contaminated by such discharges are also infective.

Mode of transmission:

  • By droplet infection and direct contact.
  • The role of fomites in the spread of infection appears to be very small, unless they are freshly contaminated.
lncubation period:
7 – 14 days.

Clinical features

  • After an incubation period of about 1-2 weeks
  • Disease takes a protracted course comprising three stages”
  • Catarrhal, paroxysmal and Convalescent
  • each lasting approximately two weeks. 

Catarrhal stage:

  •  Infectivity is maximum.

Paroxysmal stage: –

  • Post-tussive vomiting
  • Mucus Plug.
  • Vomiting with cough.
  • Episodes are often worsened at night and interfere with sleep.
  • Most complication occur during paroxymal stage.
  • Paroxysm is precipitated by noise, eating and physical contact
  • Leukocytosis due to absolute lymphocytosis is characteristic in late catarrhal or paraoxysmal stage

Convalescent stage

Complications of Pertussis

  • Respiratory –
  • Patchy Atelatasis
  • Subcutaneous emphysema
  • Neurological-
  • Persistent seizures
  • Paraplegia 
  • Ataxia: Not of cerebellar origin. There is no involvement of the cerebellum in Pertusis
  • Gastro Intestinal manifestation-
  • Hernia & Rectal Prolapse

Hemorrhagic-

  • Subconjunctival haemorrhage, Intracranial haemorrhage
  • Severe malnutrition
Diagnosis:
  • Presence of recurrent bouts of severe cough followed by an audible whoop suggests a diagnosis of pertusis.
  • Culture of nasopharyngeal secretions remains the gold standard of diagnosis.
  • Best specimen is collected by nasopharyngeal aspiration.
  • An alternative to the aspirate is a Dacron or rayon nasopharyngeal swab. 
  • DNA detection by polymerase chain reaction (PCR) increased sensitivity and quicker results.

Lymphocytosis

  • A peculiar feature of Bordetella infection is “lymphocytosis” (lymphocytosis is unusual in bacterial infections).
  • M bordetella an absolute lymphocyte count of >10 x 109/L is common among young children
  • Manifests in the blood as a mature lymphocytosis. 
  • Lymphocytes often have a weird “clefted” appearance”
Exam Question
 

Introduction

  • Whooping cough is caused by B. pertussis.
  • < 5% cases it is caused by B. parapertussis.

Source of infection:

  • Case of pertussis (not carrier).

Secondary attack rate :

  • High, i.e. 90%.

Age group:

  • Disease of infants and young children (< 5 years of age).
  • Infants are susceptible to infection from birth because maternal antibody does not give them protection.

Mode of transmission:

  • By droplet infection and direct contact.
  • The role of fomites in the spread of infection appears to be very small, unless they are freshly contaminated.
 lncubation period:
7 – 14 days.

Clinical features 

Catarrhal stage:

  •  Infectivity is maximum .

Paroxysmal stage: –

  •  Post-tussive vomiting
  • Mucus Plug.
  • Vomiting with cough.
  • Episodes are often worsen at night and interfere with sleep.
  • Most complication occur during paroxymal stage.
  • Paroxysm is precipitated by noise, eating and physical contact
  • Leukocytosis due to absolute lymphocytosis is characteristic in late catarrhal or paraoxysmal stage

Convalescent stage

Complications of Pertussis

Respiratory –

  • Patchy Atelectasis
  • Subcutaneous emphysema

Neurological-

  • Persistent seizures
  • Paraplegia 
  • Ataxia: Not of cerebellar origin. There is no involvement of the cerebellum in Pertusis
Diagnosis:
  • Presence of recurrent bouts of severe cough followed by an audible whoop suggests a diagnosis of pertusis.
  • Culture of nasopharyngeal secretions remains the gold standard of diagnosis.
  • Best specimen is collected by nasopharyngeal aspiration.

DNA detection by polymerase chain reaction (PCR) increased sensitivity and quicker results.

Lymphocytosis

  • Lymphocytes often have a weird “clefted” appearance”
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