Key Facts
Page Updated 1-2-26
- Agent: Bordetella pertussis, a Gram-negative pleomorphic bacillus
- Reservoir/Source: Humans/Respiratory Droplets
- Identification:
- Symptoms: Classic pertussis has 3 stages:
- Catarrhal Stage: Mild upper respiratory tract symptoms with coryza and cough for 1-2 weeks.
- Paroxysmal Stage: Long series of coughs without inspiration followed by characteristic high-pitched inspiratory “whoop”. It can also be followed by post-tussive emesis. Some cases may not show typical paroxysms or whoop.
- Fever is usually absent or minimal if present.
- Infants often have a shorter catarrhal stage and may present with facial color changes, apnea, leukocytosis, and absence of whoop.
- Most complications occur during paroxysmal stage.
- Convalescent Stage: Cough improves over weeks.
- Differential Diagnosis: A whooping cough syndrome may also be caused by Bordetella parapertussis, Bordetella holmesii, Mycoplasma pneumoniae, Chlamydia trachomatis, Chlamydia pneumoniae, Bordetella bronchiseptica and less commonly some viruses including adenovirus.
- Diagnosis: Clinical syndrome and isolation of B. pertussis from a culture or a positive polymerase chain reaction (PCR) test for B. pertussis confirms the diagnosis. Serological tests are not recommended. See Box 3: Case Definition.
- Complications: Pertussis is most severe in infants younger than the age of 6 months, especially for pre-term and/or unimmunized infants. Infants are at risk for severe coughing spells causing conjunctival hemorrhage, pneumonia, pulmonary hypertension, respiratory failure, and death. Complications in adolescents and adults include syncope, pneumonia, and rib fractures. In adults, complications may increase with age, especially for those over 45 years old.
- Incubation Period: Usually 7 to 10 days but can range from 5 to 21 days.
- Communicability and Transmission: Highly contagious, primarily spread by respiratory droplets (e.g., coughing, sneezing, sharing breathing space for an extended period of time). Indirect spread through articles soiled with bodily fluids is possible but not common. Transmission is highest before the cough begins – i.e., during the initial catarrhal phase, until the third week after onset of paroxysmal cough. Infected people can also spread pertussis until 5 days after the start of appropriate antibiotic treatment. See Table 1: Pertussis Infectious Period by Age Group and Treatment for infectious periods by age group and treatment. See Contact Definition for what constitutes contact with a case.
- Immunity: Immunity is not lifelong. Immunity due to natural infection has been shown to wane in adolescence and adulthood. Immunity conferred by the pertussis component of the DTaP/Tdap vaccine decreases over time, with little or no protection 5 to 10 years following the last dose. Even with full immunization, some exposed people may still develop disease – but they are less likely to develop severe disease requiring hospitalization.
- Specimen Collection/Lab Testing: See Box 1: Pertussis Laboratory Testing.
- Specific Treatment and Post-Exposure Prophylaxis: See Table 2: Recommended Treatment and Postexposure Prophylaxis, by Age Group.
- Recommended Vaccines: DTaP or Tdap. See Box 2: Pertussis Vaccination.
- Reportable Criteria: Report by electronic transmission (including fax or email), telephone or mail within 1 working day from identification to LACDPH.
Investigation of a Suspected Pertussis Case
Investigation of Contacts and Outbreak Management
Multiple Cases & Exposure Settings
Boxes, Tables, & Resources
Box 1: Pertussis Laboratory Testing
The preferred methods for the laboratory diagnosis of pertussis are:
- Positive polymerase chain reaction (PCR) test for B. pertussis OR
- Isolation of B. pertussis from a clinical specimen, although the organism can be difficult to isolate and use of this method is rare.
Note: Serology testing is not recommended.
Best practices for PCR testing:
- Only test patients with signs and symptoms of pertussis. Testing asymptomatic persons increases the likelihood of obtaining false positive results.
- Only test patients during the first 3 weeks of cough when bacterial DNA is still present.
- Do not test patients who have had ≥5 days of antibiotics.
- Optimal specimen collection for PCR testing:
- Specimens for PCR testing should be obtained by aspiration or swabbing of the posterior nasopharynx.
- Specimens collected by nasopharyngeal (NP) aspiration, a saline flush of the posterior nasopharynx, are preferred over specimens collected by NP swab. A specimen collected by NP aspiration will contain a larger quantity of bacteria.
- Specimens collected by NP swab should be obtained using polyester (such as Dacron®), rayon, or nylon-flocked swabs. Cotton-tipped or calcium alginate swabs are not acceptable as residues present in these materials inhibit PCR assays.
- Throat swabs and anterior nasal swabs have unacceptably low rates of DNA recovery and should not be used to rule out pertussis.
For more information on pertussis laboratory testing, see the Pertussis Laboratory Section of the CDPH Pertussis Quicksheet.
| Test | Specimen Collection Tube |
|---|---|
| Pertussis, Qualitative Real-time PCR Specimen: Nasopharyngeal (NP) swab |
Universal Viral Transport Media![]() |
Box 2: Pertussis Vaccination
- The primary DTaP series is essential for reducing severe disease in young infants. During a community outbreak, infants can receive DTaP on an accelerated schedule with the first dose given at 6 weeks of age, and at least 4 weeks between each of the first 3 doses. Even one dose of DTaP may offer some protection against fatal pertussis in young infants, so accelerating the first dose may be beneficial.
- Families should discuss accelerated dosing with their pediatrician to determine the most appropriate schedule based on age, vaccination history, and local outbreak activity.
- All pregnant persons should receive Tdap vaccine during every pregnancy regardless of pertussis vaccination history, preferably at the first opportunity between 27-36 weeks gestation to maximize the maternal antibody response and passive antibody transfer to the infant.
- All persons in contact with infants should be up to date for pertussis vaccine. Although only one dose of Tdap is recommended for nonpregnant adolescents and adults, persons may choose to be revaccinated if it has been several years since receipt of Tdap.
- Immunity to pertussis from vaccine or disease wanes over time and persons who have been vaccinated or had disease can become infected. Data on duration of protection from acellular vaccines suggest that waning occurs within several years of vaccination, particularly in persons who have never received whole-cell vaccine.
- For more information regarding vaccine schedules, see lacounty.gov/pertussis.
Box 3: Case Definition (CDC, 2020-Present)
Clinical Criteria
In the absence of a more likely diagnosis, a cough illness lasting ≥2 weeks with at least one of the following:
- Paroxysms of coughing; OR
- Inspiratory "whoop"; OR
- Post-tussive vomiting; OR
- Apnea (with or without cyanosis)
Laboratory Criteria
- Isolation of B. pertussis from a clinical specimen; OR
- Positive polymerase chain reaction (PCR) for B. pertussis
Epidemiologic Linkage
Contact with a laboratory-confirmed case of pertussis while case is infectious
Case Classification
Probable:
- In the absence of a more likely diagnosis, illness meeting the clinical criteria
OR - Illness with cough of any duration, with
- At least one of the following signs or symptoms:
- Paroxysms of coughing; OR
- Inspiratory whoop; OR
- Post-tussive vomiting; OR
- Apnea (with or without cyanosis)
- Contact with a laboratory confirmed case (epidemiologic linkage)
- At least one of the following signs or symptoms:
Confirmed:
Acute cough illness of any duration, with
- Isolation of B. pertussis from a clinical specimen OR
- PCR positive for B. pertussis
Table 1: Pertussis Infectious Period* by Age Group and Treatment
| Age Group |
Duration of Infectious Period | |
|---|---|---|
| No/Partial Treatment Given | Appropriate Antibiotic Treatment Given | |
| Persons < 1 year of age |
From catarrhal symptom onset until 6 weeks* (42 days) after onset |
From catarrhal symptom onset until after 5 days of treatment |
| Persons ≥ 1 year of age |
From catarrhal symptom onset until 3 weeks* (21 days) after onset |
|
*Note: These infectious periods are averages based on data on positive cultures for B. pertussis – they stay positive longer in infants under 1 year old who have not received treatment. Some people may stay infectious longer than these averages without appropriate antibiotic treatment.
Table 2: Recommended Treatment and Postexposure Prophylaxis, by Age Group‡
| Age Group |
Recommended Drugs | Alternative | ||
|---|---|---|---|---|
| Azithromycin | Erythromycin | Clarithromycin | TMP-SMX | |
| Infants younger than 1 month |
10 mg/kg per day as a single dose daily for 5 days§,** |
If azithromycin is unavailable, 40 mg/kg per day in 4 divided doses for 14 days** |
Not recommended |
Contraindicated |
| Infants 1 to 2 months old |
40 mg/kg per day in 4 divided doses for 14 days |
15 mg/kg (maximum 1 g) per day in 2 divided doses for 7 days |
||
| Infants 2 to 5 months old |
TMP, 8 mg/kg per day; SMX, 40 mg/kg per day in 2 divided doses for 14 days |
|||
| Infants 6 months or older and children |
10 mg/kg (maximum 500 mg) as a single dose on day 1, then 5 mg/kg (maximum 250 mg) per day as a single dose on days 2 through 5§,†† |
40 mg/kg (maximum 2 g) per day in 4 divided doses for 7-14 days |
||
| Adolescents and adults |
500 mg as a single dose on day 1, then 250 mg as a single dose on days 2 through 5§,†† |
2 g per day in 4 divided doses for 7-14 days |
1 g per day in 2 divided doses for 7 days |
TMP, 320 mg per day; SMX, 1600 mg per day in 2 divided doses for 14 days |
Adapted From: Red Book 2024-2027
SMX indicates sulfamethoxazole; TMP indicates trimethoprim.
‡ Centers for Disease Control and Prevention. Recommended antimicrobial agents for the treatment and postexposure prophylaxis of pertussis: 2005 CDC guidelines. MMWR Recomm Rep. 2005;54(RR-14):1–16
§ Azithromycin should be used with caution in people with prolonged QT interval and certain proarrhythmic conditions.
** Azithromycin is the preferred macrolide for infants under 1 month old because of risk of idiopathic hypertrophic pyloric stenosis (IHPS) associated with erythromycin. If infants under 1 month old are prescribed erythromycin, they should be monitored for IHPS.
†† A 3-day course of azithromycin for PEP or treatment has not been validated and is not recommended.
Resources
VPDC Pertussis Webpage: Information for Public & Providers
Pertussis Notification Letters and Flyers:
- Exposure Notification for Individuals Exposed to Pertussis: English | Spanish
- Exposure Notification for Legal Guardian of Individuals Exposed to Pertussis: English | Spanish
- Facility Notification of Pertussis Exposure: English | Spanish
- Pertussis End of Situation Letter: English | Spanish
- Unexposed Notification for Pertussis: English | Spanish
Pertussis Case Investigation Forms and Templates:
- Pertussis Case Report Form (CDPH 8258)
- CDPH Pertussis Quicksheet
- Pertussis Death Worksheet | Pertussis Death Worksheet Instructions
Pertussis Guidance and Protocols:
- Public Health Nursing Home Visit Protocol
- PROTOCOL: VPDCP Patient Referrals to Public Health Centers for Nasopharyngeal Pertussis PCR Testing
Pertussis Vaccination:

