VPDC

Diseases

What is Diphtheria?Updated 4-14-26
  • Diphtheria is an infection caused by bacteria called Corynebacterium diphtheriae. The bacteria make a toxin that can harm the body.
  • It usually affects the respiratory tract (nose and throat). It can also affect the skin, eyes, ears and genitals.
  • Symptoms usually start 2 to 5 days after being infected. Symptoms depend on which part of the body is affected.
  • It can be treated with medications. However, even with treatment, diphtheria can be especially dangerous for children.
  • Diphtheria is very rare in the United States because most people are vaccinated.
Diphtheria: Symptoms and Complications

There are two main types of diphtheria:

Respiratory (nose and throat) diphtheria
Symptoms may include:

  • Weakness
  • Sore throat
  • Nasal discharge
  • Mild fever
  • Trouble breathing or fast breathing
  • Swollen glands (enlarged lymph nodes) in the neck

The bacteria produce a toxin that destroys healthy tissues in the respiratory system. Within two to three days, a thick gray coating may form in the nose or throat. This coating can cover tissues in the nose, tonsils, voice box, or throat and make it very hard to breathe and swallow.

If the toxin spreads through the blood, it can damage the heart, nerves, and kidneys. Severe illness can lead to breathing problems, heart failure, paralysis, or death.


Skin diphtheria
Diphtheria can also infect the skin. Symptoms may include:

  • Redness and swelling
  • Open sores or ulcers

Skin infections caused by diphtheria rarely cause severe disease.

How Does Diphtheria Spread?
  • Diphtheria usually spreads from person to person through droplets in the air (coughing, sneezing and spitting). People can also get sick from touching open sores or ulcers from an infected person.
  • A person can spread diphtheria even if they have mild symptoms or no symptoms at all.
  • People who are not vaccinated have a higher risk of getting sick.

People may also have a higher risk if they:

  • Have a weakened immune system
  • Live with or have close contact with an infected person
  • Touch an open sore on an infected person
  • Are experiencing unstable housing
  • Recently used illicit substances
  • Travel to areas where diphtheria is more common, including Africa, Haiti, the Dominican Republic; Asia, the South Pacific, Eastern Europe, and the Middle East

If You Are Exposed to Diphtheria
The American Academy of Family Physicians (AAFP) recommends that people who are exposed to diphtheria receive antibiotics to prevent illness.

In addition to antibiotics, people who are exposed should:

  • Monitor for symptoms for 7 to 10 days after their last exposure
  • Be tested for diphtheria using samples from the blood, urine, sputum, spinal fluid, nose, throat, or an open sore/ulcer
  • Get a diphtheria booster vaccine if they are not up to date with their vaccines
Information for the Public
Vaccine Information

Getting vaccinated is the best way to protect yourself from diphtheria. The diphtheria vaccines protect about 97 out of 100 people and protection usually lasts about 10 years.

There are three vaccines available in the United States to help protect against diphtheria. All of these vaccines also provide protection against other diseases:

  • DTaP vaccine: protects against diphtheria, tetanus, and pertussis
  • Tdap vaccine: protects against tetanus, diphtheria, and pertussis
  • Td vaccine: protects against tetanus and diphtheria
Vaccine Recommendations

The American Academy of Pediatrics (AAP) and American Academy of Family Physicians (AAFP) recommend vaccination for infants, children, teenagers, and adults.

Who SHOULD get the vaccine:

  • Babies and children younger than 7 years should get the DTaP vaccine.
  • Older children, teenagers, and adults should get the Tdap or Td vaccine.
  • Babies need 3 shots of DTaP to build a high level of protection. Then, children need 2 booster shots to maintain protection through early childhood.
  • It is recommended that children get 5 doses of DTaP at these ages:
    • 2 months
    • 4 months
    • 6 months
    • 15-18 months
    • 4-6 years – before entering kindergarten
  • DTaP can be given alone or as part of a combination vaccine. It can also be given at the same time as other vaccines.
    • A combination vaccine combines more than one vaccine together into one shot.
  • It is recommended that preteens receive a Tdap booster at 11-12 years old. After that, they should get a Tdap or Td booster every 10 years.
  • A Tdap booster is also recommended during the 3rd trimester of pregnancy.

Who should NOT get the vaccine:

  • Anyone with a severe, life-threatening allergy or who has had an allergic reaction to any part of the DTaP, Tdap, or Td vaccine
  • Anyone who has had a coma or seizures within a week of a previous dose of DTaP

Who should talk to their doctor before getting the vaccine:

  • Anyone who has ever had Guillain-Barré syndrome (also called “GBS”) less than 6 weeks after getting the DTaP, Tdap, or Td vaccine
  • Anyone who has had severe pain or swelling after a previous shot of DTaP, Tdap, or Td (this is sometimes called an Arthus reaction)

Talk to your doctor if you have any of these health conditions or other precautions for vaccination.

Where to Get the Vaccine

If you have insurance:

  • Talk to your doctor or check with your local pharmacy to see what vaccines they offer.
  • Most health insurance plans cover the cost of recommended vaccines for children and adults.

If you are uninsured or underinsured:

  • Programs are available to help cover the cost of vaccines.
  • Children 18 years or younger may receive vaccines at no cost through the Vaccines for Children (VFC) Program if they are:
    • Eligible for or are enrolled in Medi-Cal
    • American Indian or Alaskan Native
    • Uninsured (do not have health insurance)
    • Underinsured (private health insurance does not cover the full cost of vaccines)
  • Adults who are uninsured or underinsured may be able to get free or low-cost vaccines at clinics enrolled in the Vaccines for Adults (VFA) program. For more information on who is eligible, read VFA Eligibility Based on Insurance Status.

Locating Vaccine Clinics:

  • A list of free and low-cost clinics in Los Angeles County.
  • Interactive county map to locate free and low-cost vaccine clinics.
  • Call 1-833-540-0473 (Public Health InfoLine) for a list of free or low-cost vaccine clinics. This includes Vaccines for Children (VFC) provider locations that serve Medi-Cal eligible children and uninsured or underinsured adults.
Keeping Track of Your Immunization Records

If you are unsure of your diphtheria vaccination status, you can request a copy of your records.

To request your record:

If your vaccines are not listed, ask your doctor, pharmacist, or vaccine provider for a copy of your vaccine records. You can also ask them to add your vaccines to the California Immunization Registry (CAIR).

Other tips to find your records:

Information for Providers
Clinical Presentation

Infection with C. diphtheriae can present with respiratory or cutaneous disease, but can disseminate to affect the heart, the nervous system, and the kidneys.

Respiratory diphtheria

  • Respiratory diphtheria can present with a grayish-white membrane (pseudomembrane), a key diagnostic feature of diphtheria, along with sore throat, low-grade fever, neck swelling due to cervical lymphadenopathy (bull neck), and difficulty swallowing.
  • The membrane can involve all parts of the respiratory tract from the nasal passages to trachea.
  • Most complications of respiratory diphtheria, including death, are attributable to effects of the diphtheria toxin. The most common complications of respiratory diphtheria include myocarditis and neuritis. Other complications include otitis media and respiratory insufficiency due to airway obstruction, especially in infants.
  • The risk of developing myocarditis and other toxicities is proportional to the severity of local infection and can range from 10-25% of all patients.
  • The overall case-fatality rate for diphtheria is 5%–10%, with higher death rates (up to 20%) among persons younger than 5 or older than 40 years.

Cutaneous diphtheria

  • Cutaneous diphtheria causes a scaling rash or non-healing skin ulcers that have clearly demarcated edges and an overlying membrane. Cutaneous diphtheria infections rarely cause system disease.
Disease Reporting

Do not wait for laboratory confirmation - report immediately by telephone for both confirmed and suspected cases upon clinical suspicion of diphtheria per Title 17, California Code of Regulations, Section 2500.

Public Health will guide you through the collection of specimens for testing and management of the patient under investigation. Consultation is required before sending specimens to the Public Health Laboratory.

  • Weekdays 8:30 am - 5:00 pm: Call 213-351-7800 - Epidemiologist on Duty
  • Non-Business Hours, Holidays & Weekends: Call 213-974-1234, option 8 - Administrative Officer on Duty

After the initial report, please send the patient’s medical records and any available immunization records and/or laboratory results via secure email to vpdc@ph.lacounty.gov or fax to 213-351-2782.

Diagnostic Testing

A presumptive diagnosis of respiratory diphtheria is usually made on the basis of clinical presentation and epidemiological risk factors (e.g. travel to endemic areas with low immunization coverage) since it is imperative to begin therapy for presumptive diphtheria quickly. However, a definitive diagnosis for diphtheria infection is made by isolating C. diphtheriae and testing the isolate for toxin production by the Elek test.

Collect specimens in consultation with Vaccine Preventable Disease Control (VPDC) before starting the patient on antibiotic treatment.

  • Culture – Nasal, oropharynx, and throat specimens can be collected on separate swabs (polyester, rayon, or nylon swab) and placed into separate Bacterial Culturettes or if available, a Diphtheria Culture Kit.
    • Collect a specimen from beneath the “adherent membrane” on the pharyngeal tonsillar area of the oral cavity for patients who are symptomatic. Store specimen in sterile saline (not formalin).
    • Specimens from an open sore or ulcer can also be obtained for culture to determine if the bacteria that causes diphtheria grows from the sample (again, use polyester, rayon, or nylon swabs).
    • Store swabs and pseudomembrane specimens in the refrigerator at 2-8°C.
    • Transport refrigerated on cold packs to the laboratory within 8 hours.
      • If specimen cannot be transported to Public Health Laboratory within 8 hours, store specimens refrigerated at 2-8°C (do not freeze) until lab transport the next day. Ship on cold packs. Specimens should be transported to/received by PHL within 24 hours of collection.
  • Virulence Testing - If C. diphtheriae is found on cultures of nose or throat, isolate should be sent to Public Health Lab for additional testing.
    • Store pure isolates from cultures on agar or transport medium that supports the growth of Corynebacterium species at room temperature between 15-25°C.
    • Transport refrigerated on cold packs to the laboratory.
Treatment

Patients who have suspect or confirmed respiratory diphtheria, according to the Council of State and Territorial Epidemiologists’ case definition, are eligible to receive Diphtheria Antitoxin (DAT) early in the course of disease. DAT may also be used in cases of respiratory diphtheria-like illness caused by laboratory-confirmed toxigenic C. ulcerans. A patient’s eligibility for treatment will be determined through discussion between the CDC diphtheria duty officer and the treating physician.

Physicians requesting DAT should contact the LA County Vaccine Preventable Disease Control Program (VPDCP) at 213-351-7800 during normal working hours to arrange for its release from the CDC Port Health Station at the Los Angeles International Airport. After working hours, contact the Administrative Officer of the Day through the County Operator at 213-974-1234, option 8.

Treatment of cutaneous diphtheria with antibiotics is usually sufficient, and antitoxin is typically not needed. Appropriate antibiotic therapy should be administered for at least 14 days to kill the organism and prevent further toxin production. Antibiotics recommended for the treatment of diphtheria include:

  • Erythromycin – 10 mg/kg/dose up to a maximum of 500 mg IV/po 4 times a day for 14 days.
  • Procaine Penicillin G – 300,000 units IM every 12 hours for patients <10kg, and 600,000 units IM every 12 hours for patients ≥10kg.
    • Switch to oral penicillin V (250 mg 4 times a day for 14 days) once the patient is able to tolerate oral intake.
Vaccine Recommendations
  • AAP recommends routine diphtheria vaccination across the lifespan. Children younger than 7 years of age should receive DTaP (diphtheria, tetanus, acellular pertussis), while older children and adults receive Tdap (tetanus, diphtheria, acellular pertussis) or Td (tetanus and diphtheria). See the table below for a list of diphtheria-containing vaccines and the recommended schedules.
  • Multiple combination vaccines containing diphtheria are available for use. Use of combination vaccines are also useful in reducing the number of injections in a single visit.
  • More than 97% of recipients develop protective antibody levels after 3 doses and booster (infants) or 3 doses (adults).
  • Diphtheria disease might not confer immunity. Unvaccinated or incompletely vaccinated persons recovering from diphtheria should begin or complete their immunization series with diphtheria toxoid during convalescence.

Adults

  • Administer a single dose of Tdap to adults who have never received Tdap regardless of when they last received Td. This should be followed by a Tdap booster every 10 years.

Catch-Up Guidance for Children 4 Months through 18 Years

  • Review the catch-up guidance for diphtheria, tetanus, and pertussis vaccination for children and adolescents whose vaccinations have been delayed.

Guidance for Td

  • TdVaxTM has been discontinued and is no longer available in the U.S.
  • A limited supply of TENIVAC® (Td) is still available, but due to constraints in vaccine supplies, vaccine providers should follow this guidance until the period of temporary ordering controls for Td vaccine ends:
    • Use Tdap vaccine in lieu of Td vaccine whenever possible while Td vaccine supplies are constrained.
    • Tdap vaccine is an acceptable alternative to Td vaccine, including when a tetanus booster is indicated for wound management.
    • Tdap vaccine isn't an acceptable alternative only when a person has a specific contraindication to pertussis-containing vaccines. Contraindications to DTaP and Tdap occur only very rarely, and in questioning about them, providers should probe whether a true contraindication actually exists. DTaP and Tdap contraindications are limited to only the following:
      • Severe allergic reaction (e.g., anaphylaxis) to a dose of DTaP or Tdap or to a vaccine component (Td) is a contraindication to DTaP, Tdap, or Td. Because of the importance of tetanus vaccination, people who experience anaphylactic reactions should be referred to an allergist to determine whether they have a specific allergy to tetanus toxoid and can be desensitized to tetanus toxoid.
      • Encephalopathy (e.g., coma, decreased level of consciousness, or prolonged seizures) not attributable to another identifiable cause within 7 days after administration of a previous dose of diphtheria and tetanus toxoids and pertussis vaccine (DTwP, DTaP, or Tdap) is a contraindication to the pertussis component.

Diphtheria Toxoid-Containing Vaccines and Brands*

Number of Doses
Recommended Age for All Doses
Dose & Route
Dose 1 Dose 2 Dose 3 Dose 4 Booster
DAPTACEL® (DTaP)
Sanofi Pasteur
5 6 wks-2 mos 4 mos 6 mos 15-20 mos 4-6 yrs 0.5mL
Intramuscular (IM)
INFANRIX (DTaP)
Sanofi Pasteur
5 6 wks-2 mos 4 mos 6 mos 15-20 mos 4-6 yrs 0.5mL
IM
PEDIARIX (DTaP-HepB-IPV)
GlaxoSmithKline (GSK)
3 6 wks-2 mos 4 mos 6 mos Not recommended** 0.5mL
IM
Pentacel® (DTaP-IPV/Hib)
Sanofi Pasteur
4 6 wks-2 mos 4 mos 6 mos N/A 15-18 mos 0.5mL
IM
VAXELIS® (DTaP-IPV-Hib-HepB)***
MSP Vaccine Company
3 6 wks-2 mos 4 mos 6 mos† N/A N/A 0.5mL
IM
KINRIX (DTaP-IPV) ††
GlaxoSmithKline (GSK)
1-2 N/A N/A  N/A 4-6 yrs†† 0.5mL
IM
Quadracel® (DTaP-IPV) †††
Sanofi Pasteur
1-2 N/A N/A  N/A 4 - 6 yrs††† 0.5mL
IM
Adacel® (Tdap) §
Sanofi Pasteur
Booster N/A N/A N/A N/A 7-64 yrs‡ 0.5mL
IM
Boostrix (Tdap) §
GlaxoSmithKline (GSK)
Booster N/A N/A N/A N/A 7-64 yrs‡ 0.5mL
IM
TENIVAC® (Td) ‡‡ 3 and/or Booster ≥7 yrs ≥7 yrs ≥7 yrs N/A ≥11 yrs‡‡‡ 0.5mL
IM

*Diphtheria-containing vaccines can be administered with other vaccines.
**Because the pertussis antigens contained in INFANRIX and KINRIX are the same as those in PEDIARIX, these children should receive INFANRIX as their fourth dose of DTaP and either INFANRIX or KINRIX as their fifth dose of DTaP. KINRIX or Quadracel® may be used to complete the 4-dose IPV series.
***Preferred for American Indian and Alaska Native infants based on the Haemophilus influenzae type b (Hib) component.
† The recommended minimum age for dose 3 of VAXELIS® is 24 weeks, the minimum age for completion of the hepatitis B vaccine series.
†† KINRIX is approved only for dose 5 of DTaP and dose 4 of IPV.
††† Quadracel® is approved only for dose 5 of DTaP and dose 4 or 5 of IPV.
§ Children 7-9 years old who have never been vaccinated against pertussis, tetanus, or diphtheria should receive a series of three tetanus and diphtheria toxoid-containing vaccines, which includes at least one dose of Tdap.
‡ Either Tdap vaccine administered to a person 65 years old or older is immunogenic and would provide protection; a dose of either vaccine would be considered valid.
‡‡ Primary immunization with TENIVAC® consists of 3 doses, with the first 2 doses administered 2 months apart. The third dose is administered 6-8 months after the second dose.
‡‡‡ TENIVAC® may be used as a booster beginning at 11-12 years of age, and every 10 years thereafter.

Vaccine Reporting, Storage, and Handling

Administration Data: California healthcare providers are required to report data on all valid immunizations that they administer to their patients into the California Immunization Registry (CAIR) within 2 weeks of administration per AB 1797.

Administration Errors: Healthcare providers are strongly recommended to report all vaccine administration errors to the Institute for Safe Medication Practices.

Adverse Events: Healthcare providers are required to report any adverse event on the reportable events list to the Vaccine Adverse Event Reporting System (VAERS) per HR 5546.

Storage and Handling: For general recommendations and guidance access the Vaccine Storage and Handling Job Aids.

Additional Resources


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