Bacteria
Whooping Cough
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Whooping Cough
, Bordetella pertussis, Pertussis
See Also
Bacterial Pneumonia
Tetanus Diptheria Acellular Pertussis Vaccine
(
Tdap
)
Diphtheria Tetanus Acellular Pertussis Vaccine
(
DTaP
)
Bordetella Pertussis Test
Epidemiology
Incidence
Worldwide: 30-50 million cases/year with 300,000 deaths/year
U.S.
Gene
ral Population
Peak (2012): 48,277 cases in U.S. (>8.5 cases per 100,000)
In 2018, there were 15,609 reported cases in U.S.
Infants: 88.7 per 100,000 in 2012
Mortality: 18 deaths (mostly infants) in 2012
Pertussis still affects children more than adults
Infants younger than 6 months represent 38% of U.S. cases
Children under age 5 years represent 71% of U.S. cases
Pertussis is a common cause of adult
Chronic Cough
Pertussis is responsible for 20% of adults and teens with severe cough >2 weeks presenting to ED
Senzilet (2001) Clin Infect Dis 32:1691-7 [PubMed]
Most cases in children occur in over age 10 years
With waning
Immunity
, teens and adults are reservoir
Immunity
wanes by as much as 42% per year since last
DTaP
Klein (2012) N Engl J Med 367(11): 1012-9 [PubMed]
Infants are infected by adults
Infants account for most of Pertussis-related mortality (especially under age 3 months)
Infant
Immunity
<1 year is incomplete
Infants comprise >50% of all childhood infections
Infection most severe in infants including apnea,
Pneumonia
,
Seizure
s and death
Causes
Bordetella pertussis (most common)
Bordetella parapertussis
Bordatella
Bronchi
septica
Pathophysiology
Extremely contagious with 80-100% secondary attack rate in those susceptible
Droplet spread with inhalation into airways
Pertussis releases toxins that damage the respiratory epithelium and result in mucosal injury
Incubation Period
: 7 to 10 days (incubation may be as long as 3 weeks)
Contrast with most
Viral Infection
s which incubate for a few days
Toxins (4)
Pertussis Toxin
B-Binding Subunit attaches to
Target Cell
s
A-Action Subunit
Toxin binds membrane G
Protein
s which activate membrane bound adenylate cyclase
Results in increased cAMP, with secondary inhibition of
Macrophage
and neutrophil
Phagocytosis
Extracytoplasmic adenylate cyclase
Suppresses inflammatory cell chemotaxis and
Phagocytosis
Filamentous Hemagglutinin
Binds ciliated epithelial cells
Tracheal Cytotoxin
Attacks respiratory epithelial cell
Findings
Signs and Symptoms
Gene
ral Findings
Variable severity based on age and
Immunity
Pertussis without classic
Paroxysmal cough
ing spasms is common
Especially in teens and adults with prolonged cough (>30% of Pertussis cases)
Exam is often normal (although fine rales may be present)
Catarrhal Stage (1-2 weeks, may be as short as a few days in infants <3 month)
Indistinguishable from a
Common Cold
(but highly contagious)
Low grade fever or afebrile
Malaise
Mild
Conjunctivitis
Mild dry cough
Pharyngitis
Rhinorrhea
or
Rhinitis
Sneezing
Lacrimation
Paroxysmal cough
Stage (2-4 weeks with peak at 2 weeks, may persist up to 10 weeks)
Infants under age 6 months
Apnea (mortality risk)
Cyanosis
Bradycardia
Persistent cough (not in spasms, and whooping is uncommon)
Decreased oral intake
Choking
or gagging
Gasping
Face reddened and flailing limbs with coughing spasms
Older infants, children and adults
Gradually progressive cough in spasms to severe,
Staccato Cough
ing fits
Starts as a dry, intermittent cough before progressing to a
Paroxysmal cough
Cough
ing spasms result from difficult clearing thick mucus in the trachea and
Bronchi
Patient feels as if cannot breath during coughing fit
Sensation
of
Strangulation
or suffocation can be significantly anxiety provoking
Post-tussive
Emesis
may occur
Typically breathing is unencumbered between
Coughing Fits
May be asymptomatic between coughing episodes
Inspiratory whoop
Most common in young children
Uncommon under age 6 months, and in teens and adults
High pitched whooping sound triggered by gasping after a severe coughing spell
Occurs when a deep breath is taken against a closed glottis
Associated secondary conditions (from severe coughing spells)
Subconjunctival Hemorrhage
Back Pain
Post-tussive
Emesis
Mallory Weiss Tear
Cyanosis
Cough Syncope
Cough fracture
(
Rib Fracture
)
Petechiae
(face and trunk)
Pneuomothorax
Pneumomediastinum
Abdominal Hernia
or
Inguinal Hernia
Urinary Incontinence
Rectal Prolapse
Convalescent Stage (2-3 weeks, may last months in young infants)
Bacteria
clear within 3-4 weeks of infection onset
Respiratory epithelium remains damaged following acute infection
Prolonged recovery represents healing time
Cough
ing spasms resolve over 1-3 months ("80 day cough")
Differential Diagnosis
Catarrhal stage
Viral
Upper Respiratory Infection
(e.g.
Adenovirus
)
High fever suggests alternative diagnosis
Paroxysmal stage
See
Cough
Causes
Mycoplasma pneumoniae
Chlamydia pneumoniae
(
TWAR
, typically in older adults)
Neonatal Chlamydia Pneumonia
(
Chlamydia trachomatis
)
RSV Bronchiolitis
(esp. infants)
Convalescent stage with persistent cough
See
Chronic Cough
Asthma
Gastroesophageal Reflux
Acute Sinusitis
with post nasal drainage
Diagnosis
See
Bordetella Pertussis Test
Cough
for less than one week is typically of viral origin
Consider Pertussis when cough persists for longer than 2 weeks, especially when worsens over time or
During local outbreaks or known Pertussis contact
Clinical suspicion criteria (CDC clinical case definition)
Major Criteria: Acute cough for 14 days
Minor criteria (requires one)
Paroxysmal cough
Post-tussive
Emesis
Inspiratory Whoop
Pertussis outbreak
Precaution
Requiring minor criteria misses a significant number of Pertussis cases
Do not rely solely on CDC clinical case definition for
Pertussis Diagnosis
(esp. minor criteria)
Cornia (2010) JAMA 304(8): 890-6 [PubMed]
Factors most predictive of Pertussis
Inspiratory Whooping (esp. in children LR+ 2.9 vs adults LR+ 1.2)
Posttussive
Emesis
(LR+ 1.7)
Paroxysmal cough
(adults LR+ 1.2)
Labs
Specific Bordatella Testing
See
Bordetella Pertussis Test
Bordatella PCR
(preferred first-line)
Sample obtained with nasopharyngeal
Dacron
or nylon swab with results back in 1-2 days
Efficacy
Sufficient accuracy alone (
Pertussis Culture
was previously recommended for confirmation)
Test Sensitivity
: 77 to 97%
Much better
Test Sensitivity
than
Pertussis Culture
Test Sensitivity
best in first 3-4 weeks (wanes after 3-4 weeks)
Test Specificity
: 88 to 97%
False Negative
s after 4 weeks of cough
Lower
Test Specificity
than culture (higher
False Positive Rate
)
Bordatella
Pertussis Culture
Indicated during Pertussis outbreaks and for strain identification
Sample obtained with nasopharyngeal
Dacron
or nylon swab
Requires special transport media and culture conditions
Results are delayed 7-10 days
Efficacy
Test Sensitivity
: 20 to 80%
Low
Test Sensitivity
(best in first two weeks)
False Negative
s occur at >2 weeks from cough onset (esp. if after
Antibiotic
s started)
Test Specificity
: 100%
Pertussis
Serology
Indicated in late presentation from onset of cough (4-12 weeks)
Efficacy
Test Sensitivity
: 65%
Test Specificity
: 92%
False Positive
s in recently vaccinated patients (within last year)
False Positive
s in infants age <6 months (maternal antibodies)
Avoid unhelpful tests
Direct fluorescent
Antibody
assays
Low
Test Sensitivity
and
Test Specificity
Labs
Other
Complete Blood Count
Significant
Leukocytosis
during the paroxysmal stage
Leukocytosis
(esp.
Lymphocytosis
) from 15,000 to as high as 100,000
Leukocytosis
>20,000 with >50%
Lymphocyte
s is highly suggestive of Pertussis in infants <3 months
Higher
White Blood Cell Count
s are associated with worse course (consider hospitalization)
Imaging
Chest XRay
Indications
Pneumonia in Children
suspected (
Dyspnea
,
Tachypnea
,
Hypoxia
)
Findings
Normal in most cases
Right heart border may appear "shaggy"
Secondary
Pneumonia
with other
Bacteria
complicates 20% of cases
Echocardiogram
indications
Pulmonary Hypertension
suspected in severely ill children
Management
Gene
ral
Pertussis is a clinical diagnosis (see diagnosis above)
Classic paroxysms of cough and the associated whoop, are often absent in adults
Consider Pertussis in any patient with
Chronic Cough
, especially with suspected waning
Immunity
Hospital Admission Indications
All infants <4 months (and consider ICU admission)
High risk of apnea and death
Infants older than 4 months with severe symptoms, apnea,
Cyanosis
Children with serious comorbidity
Cardiopulmonary disease
Neurologic or muscular disorders
Very high
White Blood Cell Count
s (associated with worse prognosis)
Severe Pertussis with
Hyperleukocytosis
,
Pulmonary Hypertension
(typically infants and young children)
Exchange Transfusion
Improved survival in severe Pertussis and severe
Leukocytosis
Kuperman (2014) Transfusion 54(6): 1630-3 [PubMed]
Extracorporeal Membrane Oxygenation
(
ECMO
)
Indicated in severe
Pulmonary Hypertension
or
Critical Illness
(but poor outcomes)
De Barry (2005) Pediatr Surg Int 21(8): 692-4 [PubMed]
Treatment and reporting are based on clinical suspicion
Test and treat empirically at time of testing if clinically suspect
Do not delay
Antibiotic
s for test confirmation
Test will return about the time a 5 day
Antibiotic
course is completed
Early treatment within 1-2 weeks has the best efficacy in preventing spread to contacts
Effective in reducing disease spread if started in the first 21 days of onset
Antibiotic
s do not however otherwise alter course, complication rate or mortality
Antibiotic
s eradicate B. Pertussis from nasopharynx (hence decreasing spread)
Altunaiji (2007) Cochrane Database Syst Rev (3): CD004404 [PubMed]
Antibiotic
indications (for Pertussis treatment)
Age <12 months: Within 6 weeks of onset of cough
Age >12 months: Within 3 weeks of onset of cough
Quarantine at time of diagnosis for 5 full days on
Antibiotic
s
Or more if longer than three weeks since symptom onset
Treat close contacts (asymptomic contacts need not be quarantined)
Report clinically suspected cases before confirmation
Other measures
Corticosteroid
s have not been found effective in reducing cough or hospitalization length of stay
Antibiotic
dosing
Azithromycin
(preferred first line option)
Avoid shorter 3 day courses due to lack of supporting evidence
Child: 10 mg/kg orally on day 1 and then 5 mg/kg daily for days 2-5
Adult: 500 mg orally on day 1 and then 250 mg daily for days 2-5
Other
Macrolide
s
Clarithromycin
Child: 7.5 mg/kg twice daily for 7 days
Adult: 500 mg orally twice daily for 7 days
Erythromycin
delayed release tablet
Child: 40-60 mg/kg/day divided three to four times daily orally for 14 days
Use with caution in young infants (risk of
Hypertrophic Pyloric Stenosis
)
Adults: 666 mg orally three times daily orally for 14 days
Other agents with some efficacy against Pertussis (not as effective as
Macrolide
s)
Trimethoprim/sulfamethoxazole (
Bactrim
,
Septra
)
Indicated for
Macrolide
allergy or gastrointestinal intolerance (or
Macrolide
resistance)
Do not use in pregnancy,
Lactation
, age <2 months
Dosing
Child: 8/40 mg/kg trimethoprim/sulfamethoxazole divided twice daily for 14 days
Adult:
Bactrim
DS (160/800) one tablet twice daily for 14 days
Clindamycin
Avoid unless unable to use
Macrolide
s or
Bactrim
`
Management
Prevention of spread
Quarantine
Pertussis patients are off work and out of school
May return after 5 days on
Antibiotic
s or sooner if 3 weeks after paroxysmal stage ends
Post-exposure Prophyaxis
Indications: Exposure to source patient within 21 days of cough onset
Household exposures
Other close contacts (including healthcare workers who did not wear masks)
Infants under 6 months, pregnant women in third trimester or
Immunocompromised
Protocol
Contacts are typically asymptomatic and need not be quarantined
Use same
Antibiotic
course as above
Monitor contacts for 3 weeks for onset of symptoms
Post-exposure
Vaccination
indications
Age <7 years, if four doses of
DTaP
have not been completed
Age 4 to 6 years, if fifth
DTaP
has not yet been given
Prevention
Precautions
Adults are often the vector of Pertussis transmission to unimmunized or underimmunized children
Adults tend to have subclinical persentations that are often missed
Vaccine
Antigen
deficient strains (escape mutants) have become more common
Vaccine
Antigen
s include Pertussis toxin, fimbriae 2, 3, filamentous hemagglutinin, Pertussis toxin
Pertactin (a key
Immunization
component) is absent in some U.S. Pertussis strains as of 2013
May result in decreased
Immunization
efficacy if pertactin-negative strains become more common
Queenan (2013) N Engl J Med 368(6): 583-4 [PubMed]
Immunity
wanes 2-4 years (even as early as 1 year) after each acellular Pertussis
Vaccine
Repeated pertussis
Vaccination
in adults has poor efficacy in preventing childhood Pertussis
Vaccinated patients have reduced severity of illness, but may still become infected and the transmit the infection
Infants too young to vaccinate are responsible for 85% of Pertussis deaths
Resulted in recommendation as of 2012 to repeat pertussis
Vaccination
in third trimester of all pregnancies
Passive
Immunity
in the first 3 months of life is a key current strategy for young infant protection
Diphtheria Tetanus Acellular Pertussis Vaccine
(
DTaP
)
Primary Series
for 5 doses by age 5 years
Tdap
(
Boostrix
,
Adacel
)
Age 7-10 years old for single catch-up dose if
Primary Series
with <5
DTaP
doses or unknown status
Age 11-18 years old: Single dose pimary series booster
Age 18-64 years old: Single
Tdap
to replace any of the every 10 year
Tetanus
boosters
Pregnant women in third trimester between 27 and 36 weeks (repeat with each pregnancy)
Complications
Infants
Hospitalization
Apnea (50% of infants)
Superimposed
Bacterial Pneumonia
(20% of infants, with high mortality rate)
Dehydration
Encephalopathy (may present with
Seizure
s)
Death (rate has been rising for infants)
Teens and adults
See Findings
Prolonged cough (up to 6 weeks)
Weight loss (33%)
Urinary Incontinence
(28%)
Syncope
(6%)
Severe coughing spasm complications
Cough fracture
(4%,
Rib Fracture
associated with severe coughing spells)
Pneumothorax
Subdural Hemorrhage
Epistaxis
Subconjunctival Hemorrhage
Hernia
Rectal Prolapse
Infectious complications
Otitis Media
(most common infectious complication)
Secondary
Bacterial Pneumonia
(2-4%)
Resources
CDC Pertussis
http://www.cdc.gov/pertussis/
References
Aldeen and Rosenbaum (2017) 1200 Questions Emergency Medicine Boards, 3rd ed, Wolters Kluwer, Baltimore, p. 121
Coffman (2005) Hospital Physician
Gilbert (2001) Sanford Antimicrobial, p. 25
Harrison and Ruttan (2019) Crit Dec Emerg Med 33(7): 3-12
Harrison and Ruttan (2023) Crit Dec Emerg Med 38(2): 23-31
Takhar and Herbert in Majoewsky (2013) EM:Rap 13(4): 2-3
Birkebaek (1999) Clin Infect Dis 29:1239-42 [PubMed]
Gregory (2006) Am Fam Physician 74:420-7 [PubMed]
Kline (2013) Am Fam Physician 88(8): 507-14 [PubMed]
Kline (2021) Am Fam Physician 104(2): 186-92 [PubMed]
Tiwari (2005) MMWR Recomm Rep 54(RR-14): 1-16 [PubMed]
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