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Pertussis
(Whooping
cough)
Dr. Shubhangi Kshirsagar
Assistant Professor
Department of Swasthavritta & Yoga
drssksagar@gmail.com
Pertussis
 An acute infectious disease, usually of
young children, caused by B. pertussis.
 It is clinically characterized by an insidious
onset with mild fever and an irritating cough,
gradually becoming paroxysmal with the
characteristic "whoop" (loud crowing
inspiration) often with cyanosis and
vomiting.
 The Chinese call it a “Hundred Day Cough”
Agent factors
a. Agent
 Large proportion of cases - B. pertussis
 Less than 5 % cases - B. parapertussis
 B. Pertussis elaborates an exotoxin and
endotoxin.
 The bacterium survives only for very short
periods outside the human body.
b. Source of infection - Case of pertussis (mild,
missed and unrecognized cases)
c. Infective material - Nasopharyngeal and
bronchial secretions
d. Infective period - infectious during
catarrhal stage
e. Secondary attack rate - 90 per cent in
unimmunized household contacts
Host factors
a. Age
 Highest incidence below 5 years
 Whooping cough is primarily a disease of
infants and pre-school children.
 Infants below 6 months have the highest
mortality.
 In older children, adolescents and adults,
pertussis is often unrecognized because of
its atypical course.
 However, older age groups represent an
important source of infection for susceptible
c. Immunity
 Recovery from whooping cough or adequate
immunization is followed by immunity.
 Second attacks may occur in persons with
declining immunity, but these are usually
mild.
 Infants are susceptible to infection from birth
because maternal antibody does not appear
to give them protection.
Environmental factors
 Pertussis occurs throughout the year.
 But it shows a seasonal trend with more
cases occurring during winter and spring
months due to overcrowding.
 Socioeconomic conditions and ways of life
also play a role in the epidemiology of the
disease.
 Thus, the risk of exposure is greater in the
lower social classes living in overcrowded
conditions.
Mode of transmission
 Droplet infection
 Direct contact
 Most children contract infection from their
playmates who are in the early stages of the
disease.
Incubation period
Usually 7 to 14 days, but not more than 3
weeks
Clinical features
 B. pertussis produces a local infection, the
organism is not invasive.
 It multiplies on the surface epithelium of the
respiratory tract and causes inflammation
and necrosis of the mucosa leading to
secondary bacterial invasion.
 Clinical course of the disease –
1. Catarrhal stage
2. Paroxymal stage
3. Convalescent stage
1. Catarrhal stage
 Lasts for 10 days
 It is characterized by its insidious onset,
lacrimation, sneezing and coryza, anorexia
and malaise, and a hacking night cough that
becomes diurnal.
2. Paroxysmal stage
 Last for 2-4 weeks.
 It is characterized by bursts of rapid,
consecutive coughs followed by a deep, high-
pitched inspiration (whoop).
 It is usually followed by vomiting.
 In young infants it may cause cyanosis and
apnoea.
 In adults and adolescents, uncharacteristic,
persistent cough may be the only
manifestation of the disease.
3. Convalescent stage
 Last for 1-2 weeks
 The illness generally lasts 6 to 8
weeks.
Complications
 Complications occur in 5-6 per cent of cases,
most
frequently in infants aged less than 6
months.
 The chief complications of pertussis are
 Bronchitis
 Bronchopneumonia
 Bronchiectasis
 The violence of the paroxysms may
precipitate subconjunctival haemorrhages,
epistaxis, haemoptysis and punctate cerebral
Control of pertussis
1. Case and contacts
2. Active immunization
3. Passive immunization
Control of pertusis
1. Case & contacts
a. Case
1. Early diagnosis – bacteriological exam of throat
and nose secretion.
2. Isolation
3. Treatment – Antibiotics - Erythromycin 30-
50mg/kg body weight in 4 divided doses for 10
days
Alternate antibiotics- Ampicillin, Tetracycline
b. Contacts
 Infant & young children should keep away from
cases.
 Those who are in contact with whooping cough
case give prophylactic antibiotics
(Azithromycin/Ampicillin for 10 days)
 Booster dose of DPT/DT to their siblings
2. Active immunization
 Combined DPT/Pentavalent vaccine 0.5ml IM
at one month interval starting at the age of 6
weeks (3 dose- 6, 10, 14 weeks)
 A Booster dose at 18-24 month
3. Passive immunization
 The merit of hyperimmune globulin in
pertussis
prophylaxis has yet to be established.
 So far, there is no evidence of its efficacy in
Thank You!

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Pertusis ( Whooping Cough)

  • 1. Pertussis (Whooping cough) Dr. Shubhangi Kshirsagar Assistant Professor Department of Swasthavritta & Yoga drssksagar@gmail.com
  • 2. Pertussis  An acute infectious disease, usually of young children, caused by B. pertussis.  It is clinically characterized by an insidious onset with mild fever and an irritating cough, gradually becoming paroxysmal with the characteristic "whoop" (loud crowing inspiration) often with cyanosis and vomiting.  The Chinese call it a “Hundred Day Cough”
  • 3. Agent factors a. Agent  Large proportion of cases - B. pertussis  Less than 5 % cases - B. parapertussis  B. Pertussis elaborates an exotoxin and endotoxin.  The bacterium survives only for very short periods outside the human body. b. Source of infection - Case of pertussis (mild, missed and unrecognized cases) c. Infective material - Nasopharyngeal and bronchial secretions
  • 4. d. Infective period - infectious during catarrhal stage e. Secondary attack rate - 90 per cent in unimmunized household contacts
  • 5. Host factors a. Age  Highest incidence below 5 years  Whooping cough is primarily a disease of infants and pre-school children.  Infants below 6 months have the highest mortality.  In older children, adolescents and adults, pertussis is often unrecognized because of its atypical course.  However, older age groups represent an important source of infection for susceptible
  • 6. c. Immunity  Recovery from whooping cough or adequate immunization is followed by immunity.  Second attacks may occur in persons with declining immunity, but these are usually mild.  Infants are susceptible to infection from birth because maternal antibody does not appear to give them protection.
  • 7. Environmental factors  Pertussis occurs throughout the year.  But it shows a seasonal trend with more cases occurring during winter and spring months due to overcrowding.  Socioeconomic conditions and ways of life also play a role in the epidemiology of the disease.  Thus, the risk of exposure is greater in the lower social classes living in overcrowded conditions.
  • 8. Mode of transmission  Droplet infection  Direct contact  Most children contract infection from their playmates who are in the early stages of the disease.
  • 9. Incubation period Usually 7 to 14 days, but not more than 3 weeks
  • 10. Clinical features  B. pertussis produces a local infection, the organism is not invasive.  It multiplies on the surface epithelium of the respiratory tract and causes inflammation and necrosis of the mucosa leading to secondary bacterial invasion.  Clinical course of the disease – 1. Catarrhal stage 2. Paroxymal stage 3. Convalescent stage
  • 11. 1. Catarrhal stage  Lasts for 10 days  It is characterized by its insidious onset, lacrimation, sneezing and coryza, anorexia and malaise, and a hacking night cough that becomes diurnal.
  • 12. 2. Paroxysmal stage  Last for 2-4 weeks.  It is characterized by bursts of rapid, consecutive coughs followed by a deep, high- pitched inspiration (whoop).  It is usually followed by vomiting.  In young infants it may cause cyanosis and apnoea.  In adults and adolescents, uncharacteristic, persistent cough may be the only manifestation of the disease.
  • 13. 3. Convalescent stage  Last for 1-2 weeks  The illness generally lasts 6 to 8 weeks.
  • 14. Complications  Complications occur in 5-6 per cent of cases, most frequently in infants aged less than 6 months.  The chief complications of pertussis are  Bronchitis  Bronchopneumonia  Bronchiectasis  The violence of the paroxysms may precipitate subconjunctival haemorrhages, epistaxis, haemoptysis and punctate cerebral
  • 15. Control of pertussis 1. Case and contacts 2. Active immunization 3. Passive immunization
  • 16. Control of pertusis 1. Case & contacts a. Case 1. Early diagnosis – bacteriological exam of throat and nose secretion. 2. Isolation 3. Treatment – Antibiotics - Erythromycin 30- 50mg/kg body weight in 4 divided doses for 10 days Alternate antibiotics- Ampicillin, Tetracycline
  • 17. b. Contacts  Infant & young children should keep away from cases.  Those who are in contact with whooping cough case give prophylactic antibiotics (Azithromycin/Ampicillin for 10 days)  Booster dose of DPT/DT to their siblings
  • 18. 2. Active immunization  Combined DPT/Pentavalent vaccine 0.5ml IM at one month interval starting at the age of 6 weeks (3 dose- 6, 10, 14 weeks)  A Booster dose at 18-24 month 3. Passive immunization  The merit of hyperimmune globulin in pertussis prophylaxis has yet to be established.  So far, there is no evidence of its efficacy in