Smallpox Vaccine Adverse Events Among Civilians --- United States, March 4--10, 2003
During the civilian smallpox vaccination program, CDC, the Food and Drug Administration, and state health departments are conducting surveillance for vaccine-associated adverse events. In the first stage of the program, active surveillance is being conducted for potentially life-threatening, moderate-to-severe, and other serious adverse events and for vaccinia transmission to contacts of vaccinees (1) (Table). Nonserious events are reported through passive surveillance and are expected to be underreported. This report summarizes smallpox vaccine adverse events reported among civilians vaccinated as of March 7, 2003, and among contacts of vaccinees, received by CDC from the Vaccine Adverse Event Reporting System (VAERS) as of March 10.
Potentially life-threatening and moderate-to-severe events are classified on the basis of evidence in support of the reported diagnoses. For probable cases, possible alternative etiologies are investigated, and supportive information is available. Events are classified as suspected if they have clinical features compatible with the diagnosis but either further investigation is required or additional investigation of the case did not provide supporting evidence for the diagnosis and did not identify an alternative diagnosis. CDC and state and local health departments also receive reports of other events that are associated temporally with smallpox vaccination. Reported adverse events are not necessarily associated with vaccination, and some or all of these events might be coincidental.
During January 24--March 7, smallpox vaccine was administered to 16,919 civilian health-care and public health workers in 50 jurisdictions. No potentially life-threatening adverse events of a type known previously to be caused by smallpox vaccination have been reported as of March 10.
During March 4--10, three moderate-to-severe adverse events were reported (Table). All were cases of inadvertent inoculation and were traced to contact with military personnel who received smallpox vaccine.
On February 15, a man aged 23 years with no history of smallpox vaccination wrestled with a military recruit who had recently received smallpox vaccine and who had no covering in place over his inoculation site. On February 17, the patient noted a small pimple on his chest. A few days later, he noted a pustular lesion on his right shoulder. On March 3, the patient was assessed by local health authorities, who observed a 1.5 cm lesion on the patient's chest, with a well-defined scab and indurated center. A second 1.0 cm lesion was noted on the patient's face just below the nose and above his lip. The patient reported mild malaise but was otherwise well. Right axillary lymphadenopathy was noted on physical examination. On March 4, a swab specimen obtained from a pustular lesion tested positive for vaccinia DNA by real-time polymerase chain reaction (RT-PCR); confirmatory testing at CDC is pending.
On March 4, a woman aged 18 years with no history of smallpox vaccination reported to a local health department with a 0.5 cm pustular lesion on her right forearm, surrounded by a nearly 6.0 cm area of erythema. The lesion had developed during the previous 4 days after close physical contact with her partner, a military vaccinee who was vaccinated on February 10. The vaccinee had maintained a small adhesive bandage over the lesion at all times, and the patient reported no sharing of towels or clothing; however, considerable oozing through the bandage was reported, which might have contaminated shared sheets and bedding. On March 6, a swab specimen from the pustular lesion tested positive for vaccinia DNA by RT-PCR.
On March 5, a woman aged 25 years with no history of smallpox vaccination was seen in an emergency department with three vesicular lesions on the proximal lateral aspect of her right arm. The patient was otherwise well. She reported close physical contact with a military vaccinee during February 14--17, 2003. Swab specimens were obtained from the vesicular lesions for viral culture and direct flourescent antibody testing for vaccinia, herpes zoster, and herpes simplex virus; results are pending.
Four other serious adverse events were reported during March 4--10 (Table). None of these events was of a type known to be associated causally with vaccination.
On February 16, a woman aged 43 years was hospitalized 4 days after vaccination with chest pain and dyspnea. Cardiac catheterization revealed a pre-existing coronary artery anomaly. Angina considered to be related to this condition was diagnosed, and she was discharged the following day.
On February 26, a woman aged 53 years was hospitalized 8 days after vaccination with vomiting and diarrhea. Her symptoms improved after treatment with intravenous fluids and an antibiotic, and she was discharged the following day.
On February 28, a woman aged 57 years with a history of chronic obstructive pulmonary disease (COPD) was hospitalized 6 days after vaccination with an exacerbation of COPD, diarrhea, and dehydration. She was treated with intravenous fluids and was discharged the following day.
On February 28, a woman aged 45 years with a history of smallpox vaccination had sharp left shoulder pain and chest pain 2 days after vaccination. Her symptoms resolved after treatment with a nonsteroidal anti-inflammatory medication. Approximately 2 weeks before vaccination, she had onset of influenza-like illness (ILI) with fever, chill, myalgias, malaise, and cough, which were resolving at the time of vaccination after 1 week away from work. On March 3, she complained again of exertional chest pain and was hospitalized the following day with dyspnea and exertional chest pain that radiated to her neck. An echocardiogram on March 5 demonstrated a small pericardial effusion, left ventricular wall motion abnormality, and a mild decrease in left ventricular function. Cardiac catheterization found no evidence of coronary artery narrowing. Viral myocarditis judged to be associated with the antecedent ILI was diagnosed. On March 6, the patient was discharged after 2 days of hospitalization.
Among the 76 vaccinees with reported other nonserious adverse events during January 24--March 10 (Table), the most common signs and symptoms were rash (n = 20), fever (n = 18), pruritus (n = 17), and pain (n = 12). All of these commonly reported events are consistent with mild expected reactions following receipt of smallpox vaccine. Some vaccinees reported multiple signs and symptoms.
Surveillance for adverse events during the civilian smallpox vaccination program is ongoing; regular surveillance reports will be published in MMWR.
Disclaimer All MMWR HTML versions of articles are electronic conversions from ASCII text into HTML. This conversion may have resulted in character translation or format errors in the HTML version. Users should not rely on this HTML document, but are referred to the electronic PDF version and/or the original MMWR paper copy for the official text, figures, and tables. An original paper copy of this issue can be obtained from the Superintendent of Documents, U.S. Government Printing Office (GPO), Washington, DC 20402-9371; telephone: (202) 512-1800. Contact GPO for current prices.
**Questions or messages regarding errors in formatting should be addressed to firstname.lastname@example.org.
Page converted: 3/13/2003
This page last reviewed 3/13/2003