Bordetella pertussis: Difference between revisions

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Bordetella pertussis
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== Microbiology ==
+
== Background ==
   
  +
===Microbiology===
* Small, Gram-negative coccobacillus
 
* Fastidious, slow-growing, and strictly aerobic
 
* Catalase positive non-fermentative
 
* Pertussis toxin helps it to evade the host defenses
 
   
  +
*Small, Gram-negative coccobacillus
== Pathophysiology ==
 
  +
*Fastidious, slow-growing, and strictly aerobic
  +
*Catalase positive non-fermentative
  +
*Pertussis toxin helps it to evade the host defenses
   
  +
===Pathophysiology===
* Four steps to infection: attachment, evasion of host defenses, local damage, and systemic manifestations
 
* Virulence determined by filamentous hemagglutinin (FHA) and fimbriae (FIM) adhesins
 
** Required for tracheal colonization
 
** Pertussis toxin (PT) also plays a role
 
* Adenylate cyclase toxin (ACT) and PT allow it to evade host defenses
 
** ACT inhibits macrophages by catalysing ATP to cAMP
 
** PT delays neutrophil recruitment by suppressing G protein signaling pathways
 
* Tracheal cytotoxin (TCT) produces NO and damages the tracheal epitheleal cells
 
* Few systemic manifestations because it doesn't enter circulation
 
   
  +
*Four steps to infection: attachment, evasion of host defenses, local damage, and systemic manifestations
== Pertussis ==
 
  +
*Virulence determined by filamentous hemagglutinin (FHA) and fimbriae (FIM) adhesins
  +
**Required for tracheal colonization
  +
**Pertussis toxin (PT) also plays a role
  +
*Adenylate cyclase toxin (ACT) and PT allow it to evade host defenses
  +
**ACT inhibits macrophages by catalysing ATP to cAMP
  +
**PT delays neutrophil recruitment by suppressing G protein signaling pathways
  +
*Tracheal cytotoxin (TCT) produces NO and damages the tracheal epitheleal cells
  +
*Few systemic manifestations because it doesn't enter circulation
   
  +
==Pertussis==
=== Presentation ===
 
   
  +
===Presentation===
* Presents with cough lasting 14 days or more, with paroxysms of coughing, an inspiratory whoop, and post-tussive vomiting
 
* Incubation period or 7 to 10 days on average (range 5 to 21 days)
 
   
  +
*Presents with cough lasting 14 days or more, with paroxysms of coughing, an inspiratory whoop, and post-tussive vomiting
=== Young Children ===
 
  +
*Incubation period or 7 to 10 days on average (range 5 to 21 days)
   
  +
===Young Children===
* Three stages:
 
*# '''Catarrhal stage''', with rhinorrhea, nonpurulent conjuctivitis, occasional cough, and a low-grade fever; lasts 1 to 2 weeks.
 
*# '''Paroxysmal stage''', with fits of coughing and an inspiratory whoop; lasts 1 to 6 weeks. Occasionally associated with hyperinsulinemia and hypoglycemia in infants.
 
*# '''Convalescent stage''', with the cough slowly resolving over 1 to 6 weeks, occasionally up to 8 weeks.
 
   
  +
*Three stages:
=== Adults ===
 
  +
*#'''Catarrhal stage''', with rhinorrhea, nonpurulent conjuctivitis, occasional cough, and a low-grade fever; lasts 1 to 2 weeks.
  +
*#'''Paroxysmal stage''', with fits of coughing and an inspiratory whoop; lasts 1 to 6 weeks. Occasionally associated with hyperinsulinemia and hypoglycemia in infants.
  +
*#'''Convalescent stage''', with the cough slowly resolving over 1 to 6 weeks, occasionally up to 8 weeks.
   
  +
===Adults===
* Can present atypically, with less whooping and less post-tussive vomiting
 
* Coughing is seen in most patients, lasting longer than 21 days
 
** Mean duration 36 to 48 days
 
* Post-tussive vomiting is suggestive of pertussis
 
   
  +
*Can present atypically, with less whooping and less post-tussive vomiting
=== Diagnosis ===
 
  +
*Coughing is seen in most patients, lasting longer than 21 days
  +
**Mean duration 36 to 48 days
  +
*Post-tussive vomiting is suggestive of pertussis
   
  +
===Diagnosis===
* Nasopharyngeal swab/aspirate culture
 
** Sensitivity 15 to 80%
 
* PCR
 
* Serology
 
** Antibodies (IgG and IgA) against GHA, agglutinogen, or PT
 
*** IgG rises 2 to 3 weeks after infection or immunization (1 week after booster)
 
*** Look for a two-fold increase in IgG to diagnose acute infection
 
** Antigens including PT
 
   
  +
*Nasopharyngeal swab/aspirate culture
=== Management ===
 
  +
**Sensitivity 15 to 80%
  +
*PCR
  +
*Serology
  +
**Antibodies (IgG and IgA) against GHA, agglutinogen, or PT
  +
***IgG rises 2 to 3 weeks after infection or immunization (1 week after booster)
  +
***Look for a two-fold increase in IgG to diagnose acute infection
  +
**Antigens including PT
   
  +
===Management===
* Treat within 21 days of symptom onset (except if <1 mo. old, just treat)
 
* In children
 
** Azithromycin 10 mg/kg on day 1 followed by 5 mg/kg/d for 4 days
 
** Erythomycin 40-50 mg/kg/d divided qid for 7-14 days
 
** Clarithromycin 15 mg/kg/d divided bid for 7 days
 
** Azithromycin for children <1 year
 
* In infants <1 mo, azithromycin 10 mg/kg/d for 5 days
 
* In adults
 
** Azithromycin 500mg followed by 250 mg daily for 4 more days
 
** Erythomycin 500 mg qid for 7-14 days
 
** Clarithromycin 500 mg bid for 7 days
 
* Consider prophylaxis of close contacts, third-trimester pregnancy, infants, and healthcare workers
 
** Azithromycin 500 mg for one day followed by 250 mg for 4 more days
 
** Erythromycin 500 mg qid for 7 to 14 days
 
** Clarithromycin 500 mg bid for 7 days
 
   
  +
*Treat within 21 days of symptom onset (except if <1 mo. old, just treat)
=== Complications ===
 
  +
*In children
  +
**Azithromycin 10 mg/kg on day 1 followed by 5 mg/kg/d for 4 days
  +
**Erythomycin 40-50 mg/kg/d divided qid for 7-14 days
  +
**Clarithromycin 15 mg/kg/d divided bid for 7 days
  +
**Azithromycin for children <1 year
  +
*In infants <1 mo, azithromycin 10 mg/kg/d for 5 days
  +
*In adults
  +
**Azithromycin 500mg followed by 250 mg daily for 4 more days
  +
**Erythomycin 500 mg qid for 7-14 days
  +
**Clarithromycin 500 mg bid for 7 days
  +
*Consider prophylaxis of close contacts, third-trimester pregnancy, infants, and healthcare workers
  +
**Azithromycin 500 mg for one day followed by 250 mg for 4 more days
  +
**Erythromycin 500 mg qid for 7 to 14 days
  +
**Clarithromycin 500 mg bid for 7 days
   
  +
===Complications===
* Case-fatality rate of 1% in children under 6 months
 
* Pnuemonia is the most common complication, either caused by the disease itself for by coinfection (especially RSV)
 
* Encephalopathy is a rare complication, usually in unimmunized children
 
** Begins weeks 2 to 4 after cough, with seizures and focal neurologic deficits
 
* Pulmonary hypertension
 
* Pneumonia and urinary incontinence are common in older patients
 
* The paroxysms of coughing can also cause subconjunctival hemorrhages, syncope, and rib fractures
 
   
  +
*Case-fatality rate of 1% in children under 6 months
=== Infection Control ===
 
  +
*Pnuemonia is the most common complication, either caused by the disease itself for by coinfection (especially RSV)
  +
*Encephalopathy is a rare complication, usually in unimmunized children
  +
**Begins weeks 2 to 4 after cough, with seizures and focal neurologic deficits
  +
*Pulmonary hypertension
  +
*Pneumonia and urinary incontinence are common in older patients
  +
*The paroxysms of coughing can also cause subconjunctival hemorrhages, syncope, and rib fractures
   
  +
===Infection Control===
* Droplet precautions
 
   
  +
*Droplet precautions
== Carrier State ==
 
   
  +
==Carrier State==
* Transient nasopharyngeal carriage in immunized children
 
   
  +
*Transient nasopharyngeal carriage in immunized children
== Vaccination ==
 
   
  +
==Vaccination==
* Options include whole-cell (DTP) and acellular (DTaP or Tdap)
 
  +
** Acellular removed lipopolysaccharide so is less reactive, but is as or more effective than whole cell
 
  +
*Options include whole-cell (DTP) and acellular (DTaP or Tdap)
*** There was a fear of encephalopathy and SIDS with DTP
 
  +
**Acellular removed lipopolysaccharide so is less reactive, but is as or more effective than whole cell
*** Acellular has PT, the two hemagluttinins, and protectin
 
  +
***There was a fear of encephalopathy and SIDS with DTP
** DTaP (diphtheria toxoid, tetanus toxoid, and acellular pertussis, pediatric formula)
 
  +
***Acellular has PT, the two hemagluttinins, and protectin
*** Given at 2, 4, 6, and 18 months, with booster at 4-6 years
 
  +
**DTaP (diphtheria toxoid, tetanus toxoid, and acellular pertussis, pediatric formula)
** Tdap booster once in adulthood, and with every pregnancy for women (third trimester)
 
  +
***Given at 2, 4, 6, and 18 months, with booster at 4-6 years
* None of the vaccines carry life-long immunity; even the immunity from the acellular pertussis vaccine wanes after 4-5 years
 
  +
**Tdap booster once in adulthood, and with every pregnancy for women (third trimester)
  +
*None of the vaccines carry life-long immunity; even the immunity from the acellular pertussis vaccine wanes after 4-5 years
   
 
{{DISPLAYTITLE:''Bordatella pertussis''}}
 
{{DISPLAYTITLE:''Bordatella pertussis''}}

Revision as of 11:46, 29 July 2020

Background

Microbiology

  • Small, Gram-negative coccobacillus
  • Fastidious, slow-growing, and strictly aerobic
  • Catalase positive non-fermentative
  • Pertussis toxin helps it to evade the host defenses

Pathophysiology

  • Four steps to infection: attachment, evasion of host defenses, local damage, and systemic manifestations
  • Virulence determined by filamentous hemagglutinin (FHA) and fimbriae (FIM) adhesins
    • Required for tracheal colonization
    • Pertussis toxin (PT) also plays a role
  • Adenylate cyclase toxin (ACT) and PT allow it to evade host defenses
    • ACT inhibits macrophages by catalysing ATP to cAMP
    • PT delays neutrophil recruitment by suppressing G protein signaling pathways
  • Tracheal cytotoxin (TCT) produces NO and damages the tracheal epitheleal cells
  • Few systemic manifestations because it doesn't enter circulation

Pertussis

Presentation

  • Presents with cough lasting 14 days or more, with paroxysms of coughing, an inspiratory whoop, and post-tussive vomiting
  • Incubation period or 7 to 10 days on average (range 5 to 21 days)

Young Children

  • Three stages:
    1. Catarrhal stage, with rhinorrhea, nonpurulent conjuctivitis, occasional cough, and a low-grade fever; lasts 1 to 2 weeks.
    2. Paroxysmal stage, with fits of coughing and an inspiratory whoop; lasts 1 to 6 weeks. Occasionally associated with hyperinsulinemia and hypoglycemia in infants.
    3. Convalescent stage, with the cough slowly resolving over 1 to 6 weeks, occasionally up to 8 weeks.

Adults

  • Can present atypically, with less whooping and less post-tussive vomiting
  • Coughing is seen in most patients, lasting longer than 21 days
    • Mean duration 36 to 48 days
  • Post-tussive vomiting is suggestive of pertussis

Diagnosis

  • Nasopharyngeal swab/aspirate culture
    • Sensitivity 15 to 80%
  • PCR
  • Serology
    • Antibodies (IgG and IgA) against GHA, agglutinogen, or PT
      • IgG rises 2 to 3 weeks after infection or immunization (1 week after booster)
      • Look for a two-fold increase in IgG to diagnose acute infection
    • Antigens including PT

Management

  • Treat within 21 days of symptom onset (except if <1 mo. old, just treat)
  • In children
    • Azithromycin 10 mg/kg on day 1 followed by 5 mg/kg/d for 4 days
    • Erythomycin 40-50 mg/kg/d divided qid for 7-14 days
    • Clarithromycin 15 mg/kg/d divided bid for 7 days
    • Azithromycin for children <1 year
  • In infants <1 mo, azithromycin 10 mg/kg/d for 5 days
  • In adults
    • Azithromycin 500mg followed by 250 mg daily for 4 more days
    • Erythomycin 500 mg qid for 7-14 days
    • Clarithromycin 500 mg bid for 7 days
  • Consider prophylaxis of close contacts, third-trimester pregnancy, infants, and healthcare workers
    • Azithromycin 500 mg for one day followed by 250 mg for 4 more days
    • Erythromycin 500 mg qid for 7 to 14 days
    • Clarithromycin 500 mg bid for 7 days

Complications

  • Case-fatality rate of 1% in children under 6 months
  • Pnuemonia is the most common complication, either caused by the disease itself for by coinfection (especially RSV)
  • Encephalopathy is a rare complication, usually in unimmunized children
    • Begins weeks 2 to 4 after cough, with seizures and focal neurologic deficits
  • Pulmonary hypertension
  • Pneumonia and urinary incontinence are common in older patients
  • The paroxysms of coughing can also cause subconjunctival hemorrhages, syncope, and rib fractures

Infection Control

  • Droplet precautions

Carrier State

  • Transient nasopharyngeal carriage in immunized children

Vaccination

  • Options include whole-cell (DTP) and acellular (DTaP or Tdap)
    • Acellular removed lipopolysaccharide so is less reactive, but is as or more effective than whole cell
      • There was a fear of encephalopathy and SIDS with DTP
      • Acellular has PT, the two hemagluttinins, and protectin
    • DTaP (diphtheria toxoid, tetanus toxoid, and acellular pertussis, pediatric formula)
      • Given at 2, 4, 6, and 18 months, with booster at 4-6 years
    • Tdap booster once in adulthood, and with every pregnancy for women (third trimester)
  • None of the vaccines carry life-long immunity; even the immunity from the acellular pertussis vaccine wanes after 4-5 years