Bordetella pertussis: Difference between revisions
From IDWiki
Bordetella pertussis
(→: moved to own page) |
No edit summary |
||
Line 1: | Line 1: | ||
== |
== 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 15:46, 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:
- 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
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
- Antibodies (IgG and IgA) against GHA, agglutinogen, or 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)
- Acellular removed lipopolysaccharide so is less reactive, but is as or more effective than whole cell
- None of the vaccines carry life-long immunity; even the immunity from the acellular pertussis vaccine wanes after 4-5 years