PERTUSSIS
“WHOOPING COUGH”
Dr Ubaid N P JR Community Medicine Pariyaram Medical College
▪ Acute infectious disease caused by Bordetella
pertussis
▪ Hundred day cough
▪ Important cause of death in infants
▪ Insidious onset, mild fever, irritating cough
whoop(loud crowing inspiration)
EPIDEMIOLOGICAL DETERMINANTS
▪ AGENT
– Causative agent is B.pertussis
– <5% - B.parapertussis
– Encapsulated, phase 1 strains
– Carries 3 major agglutinogens 1 2&3
– Survive only short period outside human body
• SOURCEOF INFECTION
B.Pertussis infects only man
Source is a case of pertussis
No c/c carrier state
▪ INFECTIVE MATERIAL
Nasopharyngeal and bronchial secretion
▪ INFECTIVE PERIOD
Most infective during catarrhal stage. One week after
exposure to 3 weeks after onset of paroxysmal stage
▪ SECONDARY ATTACK RATE
Averages 90% in unimmunized household contacts
HOST FACTORS
▪ AGE
Primarily disease of infants and preschool children
 SEX
Incidence and fatality more among females
 IMMUNITY
Recovery from whooping cough & immunization
 ENVIORNMENTAL FACTORS
occur through out year more in winter and spring
Low socioeconomic group
▪ MODE OFTRANSMISSION
Droplet infection and direct contact
▪ INCUBATION PERIOD
7 to 14 days
▪ CLINICAL COURSE
It produces local infection
Organism not invasive
Multiplies on epithelium of resp tract
Cause inflammation necrosis of mucosa
(a)Catarrhal stage
lasting for 10 days. Insidious onset lacrimation,sneezing
coryza, malaise, hacking night cough
(b)Paroxysmal stage
2-4 weeks
Characterized by burst of rapid consecutive cough followed
by deep high pitched inspiration[whoop],vomiting
In infants, cyanosis apnoea
(c)Convalescent stage
Lasting for 1-2 weeks
3 stages of clinical course
COMPLICATIONS:
▪ Bronchitis,bronchopneumonia,bronchectasis,
▪ Subconjunctival haemorrhage
▪ Haemoptysis
▪ Epistaxis,
▪ Punctate cerebral haemorrhage-convulsion and coma
▪ Pertussis- associated encephalopathy
CONTROL OF WHOOPING COUGH
▪ CASES AND CONTACTS
Early dx by bacteriological exmn of secretions
Fluorescent antibody technique
Erythromycin is doc 30-50 mg/kg bwt 4 divided
doses for 10 days
▪ CONTACTS
Prophylactic erythromycin or ampicillin for 10 days
▪ Active immunisation
DPT 3 DOSES 0.5 ML 6,10 14WEEKS BOOSTER
18-24 mnths
UNTOWARD REACTION
Local reacns: at injection site,mild fever,irritability
Rare reacns:inconsolable screaming,
seizures,hypotonic hyporesponsive
episodes,anaphylactic reaction,encephalopathy.
▪ CONTRAINDICATIONS
Anaphylaxis ,encephalopathy,epilepsy,febrile
episodes, reaction to previous vaccination
THANKYOU

Pertusis

  • 1.
    PERTUSSIS “WHOOPING COUGH” Dr UbaidN P JR Community Medicine Pariyaram Medical College
  • 2.
    ▪ Acute infectiousdisease caused by Bordetella pertussis ▪ Hundred day cough ▪ Important cause of death in infants ▪ Insidious onset, mild fever, irritating cough whoop(loud crowing inspiration)
  • 3.
    EPIDEMIOLOGICAL DETERMINANTS ▪ AGENT –Causative agent is B.pertussis – <5% - B.parapertussis – Encapsulated, phase 1 strains – Carries 3 major agglutinogens 1 2&3 – Survive only short period outside human body • SOURCEOF INFECTION B.Pertussis infects only man Source is a case of pertussis No c/c carrier state
  • 4.
    ▪ INFECTIVE MATERIAL Nasopharyngealand bronchial secretion ▪ INFECTIVE PERIOD Most infective during catarrhal stage. One week after exposure to 3 weeks after onset of paroxysmal stage ▪ SECONDARY ATTACK RATE Averages 90% in unimmunized household contacts
  • 5.
    HOST FACTORS ▪ AGE Primarilydisease of infants and preschool children  SEX Incidence and fatality more among females  IMMUNITY Recovery from whooping cough & immunization  ENVIORNMENTAL FACTORS occur through out year more in winter and spring Low socioeconomic group
  • 6.
    ▪ MODE OFTRANSMISSION Dropletinfection and direct contact ▪ INCUBATION PERIOD 7 to 14 days ▪ CLINICAL COURSE It produces local infection Organism not invasive Multiplies on epithelium of resp tract Cause inflammation necrosis of mucosa
  • 7.
    (a)Catarrhal stage lasting for10 days. Insidious onset lacrimation,sneezing coryza, malaise, hacking night cough (b)Paroxysmal stage 2-4 weeks Characterized by burst of rapid consecutive cough followed by deep high pitched inspiration[whoop],vomiting In infants, cyanosis apnoea (c)Convalescent stage Lasting for 1-2 weeks 3 stages of clinical course
  • 8.
    COMPLICATIONS: ▪ Bronchitis,bronchopneumonia,bronchectasis, ▪ Subconjunctivalhaemorrhage ▪ Haemoptysis ▪ Epistaxis, ▪ Punctate cerebral haemorrhage-convulsion and coma ▪ Pertussis- associated encephalopathy
  • 9.
    CONTROL OF WHOOPINGCOUGH ▪ CASES AND CONTACTS Early dx by bacteriological exmn of secretions Fluorescent antibody technique Erythromycin is doc 30-50 mg/kg bwt 4 divided doses for 10 days ▪ CONTACTS Prophylactic erythromycin or ampicillin for 10 days
  • 10.
    ▪ Active immunisation DPT3 DOSES 0.5 ML 6,10 14WEEKS BOOSTER 18-24 mnths UNTOWARD REACTION Local reacns: at injection site,mild fever,irritability Rare reacns:inconsolable screaming, seizures,hypotonic hyporesponsive episodes,anaphylactic reaction,encephalopathy.
  • 11.
  • 12.