Bordetella pertussis: Difference between revisions

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Bordetella pertussis
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==Background==
= Microbiology =


===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
== Bordatella species ==
*Fastidious, slow-growing, and strictly aerobic
*Catalase positive non-fermentative
*Pertussis toxin helps it to evade the host defenses


===Pathophysiology===
* ''B. pertussis'', ''B. parapertussis'', and ''B. holmesii'' are the most common species to cause disease in humans
* ''B. bronchiseptica'' causes kenel cough in dogs and cats, with rare human infections in immunocompromised hosts
* Ovine-adapted ''B. parapertussis'' causes respiratory infections in sheep
* ''B. avium'' causes disease in poultry
* ''B. hinzii'' causes disease in poultry and rarely in immunocompromised hosts
* ''B. trematum'' has been found in wounds and otitis media
* ''B. petrii'' causes rare infections in immunocompromised hosts
* ''B. ansorpii'' was isolated from an epidermal cyst and an immunocompromised host


*Four steps to infection: attachment, evasion of host defenses, local damage, and systemic manifestations
= Pathophysiology =
*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


==Clinical Manifestations==
* 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


*Presents with cough lasting 14 days or more, with paroxysms of coughing, an inspiratory whoop, and post-tussive vomiting
= Pertussis =
*Incubation period of [[Usual incubation period::7 to 10 days]] on average (range [[Incubation period range::5 to 21 days]])


== Presentation ==
===Young Children===


*Three stages:
* Presents with cough lasting 14 days or more, with paroxysms of coughing, an inspiratory whoop, and post-tussive vomiting
*#'''Catarrhal stage''', with rhinorrhea, nonpurulent conjuctivitis, occasional cough, and a low-grade fever; lasts 1 to 2 weeks.
* Incubation period or 7 to 10 days on average (range 5 to 21 days)
*#'''Paroxysmal stage''', with fits of coughing and an inspiratory whoop; lasts 1 to 6 weeks. May have post-tussive emesis. 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===
== Young Children ==


*Can present atypically, with less whooping and less post-tussive vomiting
* Three stages:
*Coughing is seen in most patients, lasting longer than 21 days
*# '''Catarrhal stage''', with rhinorrhea, nonpurulent conjuctivitis, occasional cough, and a low-grade fever; lasts 1 to 2 weeks.
**Mean duration 36 to 48 days
*# '''Paroxysmal stage''', with fits of coughing and an inspiratory whoop; lasts 1 to 6 weeks. Occasionally associated with hyperinsulinemia and hypoglycemia in infants.
*Post-tussive vomiting is suggestive of pertussis
*# '''Convalescent stage''', with the cough slowly resolving over 1 to 6 weeks, occasionally up to 8 weeks.


== Adults ==
===Carrier State===


*Transient nasopharyngeal carriage in immunized children
* 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 ==
===Complications===


*Case-fatality rate of 1% in children under 6 months
* Nasopharyngeal swab/aspirate culture
*Pneumonia is the most common complication, either caused by the disease itself for by coinfection (especially RSV)
** Sensitivity 15 to 80%
*Encephalopathy is a rare complication, usually in unimmunized children
* PCR
**Begins weeks 2 to 4 after cough, with seizures and focal neurologic deficits
* Serology
*Pulmonary hypertension
** Antibodies (IgG and IgA) against GHA, agglutinogen, or PT
*Pneumonia and urinary incontinence are common in older patients
*** IgG rises 2 to 3 weeks after infection or immunization (1 week after booster)
*The paroxysms of coughing can also cause subconjunctival hemorrhages, syncope, and rib fractures
*** Look for a two-fold increase in IgG to diagnose acute infection
** Antigens including PT


== Management ==
==Diagnosis==


*Nasopharyngeal swab/aspirate culture
* Treat within 21 days of symptom onset (except if <1 mo. old, just treat)
**Sensitivity 15 to 80%
* In children
*PCR
** Azithromycin 10 mg/kg on day 1 followed by 5 mg/kg/d for 4 days
*Serology
** Erythomycin 40-50 mg/kg/d divided qid for 7-14 days
**Antibodies (IgG and IgA) against GHA, agglutinogen, or PT
** Clarithromycin 15 mg/kg/d divided bid for 7 days
***IgG rises 2 to 3 weeks after infection or immunization (1 week after booster)
** Azithromycin for children <1 year
***Look for a two-fold increase in IgG to diagnose acute infection
* In infants <1 mo, azithromycin 10 mg/kg/d for 5 days
**Antigens including PT
* 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 ==
==Management==


*Treat within 21 days of symptom onset (except if <1 mo. old, treat regardless of duration)
* Case-fatality rate of 1% in children under 6 months
*In children
* Pnuemonia is the most common complication, either caused by the disease itself for by coinfection (especially RSV)
**[[Azithromycin]] 10 mg/kg on day 1 followed by 5 mg/kg/d for 4 days
* Encephalopathy is a rare complication, usually in unimmunized children
**[[Erythomycin]] 40-50 mg/kg/d divided qid for 7-14 days
** Begins weeks 2 to 4 after cough, with seizures and focal neurologic deficits
**[[Clarithromycin]] 15 mg/kg/d divided bid for 7 days
* Pulmonary hypertension
**[[Azithromycin]] for children <1 year
* Pneumonia and urinary incontinence are common in older patients
*In infants <1 mo, [[azithromycin]] 10 mg/kg/d for 5 days
* The paroxysms of coughing can also cause subconjunctival hemorrhages, syncope, and rib fractures
*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


==Prevention==
== Infection Control ==


===Infection Control===
* Droplet precautions


*Droplet precautions
= Carrier State =
*Duration
**Treated: after 5 days of effective treatment
**Untreated: after 3 weeks from onset of paroxysms
*Communicable from onset of catarrhal stage to 3 weeks after onset of coughing or paroxysms


===Post-Exposure Prophylaxis===
* Transient nasopharyngeal carriage in immunized children


*Consider prophylaxis of close contacts (face-to-face within 3 feet), third-trimester pregnancy, infants, and healthcare workers
= Vaccination =
*Should be considered up to 21 days following last contact
*Options include:
**[[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


===Immunization===
* 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


*Options include whole-cell (DTP) and acellular (DTaP or Tdap)
{{DISPLAYTITLE:''Bordatella pertussis''}}
**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

{{DISPLAYTITLE:''Bordetella pertussis''}}
[[Category:Gram-negative coccobacilli]]
[[Category:Gram-negative coccobacilli]]
[[Category:Respiratory infections]]
[[Category:Pediatrics]]

Latest revision as of 20:35, 23 September 2024

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

Clinical Manifestations

  • Presents with cough lasting 14 days or more, with paroxysms of coughing, an inspiratory whoop, and post-tussive vomiting
  • Incubation period of 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. May have post-tussive emesis. 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

Carrier State

  • Transient nasopharyngeal carriage in immunized children

Complications

  • Case-fatality rate of 1% in children under 6 months
  • Pneumonia 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

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, treat regardless of duration)
  • In children
  • In infants <1 mo, azithromycin 10 mg/kg/d for 5 days
  • In adults

Prevention

Infection Control

  • Droplet precautions
  • Duration
    • Treated: after 5 days of effective treatment
    • Untreated: after 3 weeks from onset of paroxysms
  • Communicable from onset of catarrhal stage to 3 weeks after onset of coughing or paroxysms

Post-Exposure Prophylaxis

  • Consider prophylaxis of close contacts (face-to-face within 3 feet), third-trimester pregnancy, infants, and healthcare workers
  • Should be considered up to 21 days following last contact
  • Options include:

Immunization

  • 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