Septicemic plague - Chem-Bio-Rad Suspicion
Primary septicemic plague results from direct inoculation of the bacteria into the bloodstream, typically via the bite of an infected animal or flea or direct contact with infected tissues. Secondary septicemic plague occurs when there is progression of disease and dissemination of bacteria following bubonic presentation.
Septicemic plague has sudden onset and rapid progression (with an incubation period of 1-6 days) causing fever, chills, weakness, abdominal pain, shock, and bleeding underneath the skin or other organs and may result in disseminated intravascular coagulation (DIC), necrosis of small vessels, and purpura. Acral regions such as the fingers, toes, and nose may become gangrenous, hence the term "black death." Alone, septicemic plague is rarely transmissible human to human but may become transmissible if the disease reaches the pneumonic stage or is associated with buboes.
It is important to recognize that the initial symptomatology is nonspecific and commonly seen in many types of severe bacterial sepsis, so the clinician must have a high index of suspicion based on endemic locations, recent travel, and close contact with rodents or domestic animals that have recently become sick. Indeed, early diagnosis in the Emergency Department for an incident may be difficult. Unless the link to exposure is readily apparent, most cases will be diagnosed after admission based on culture data (sputum or blood), but if the outbreak is intentional and patients with plague have been identified in the community, all patients presenting with sepsis should be considered to have plague unless an alternate diagnosis is found. Human-to-human transmission is possible in secondary septicemia due to pneumonic plague, so if septicemic plague is suspected, appropriate infection control practices must be rapidly implemented. Control measures and personal protective equipment for health care workers should be geared toward droplet / contact transmission at a minimum. Consult your infection control experts to determine whether additional protection is warranted.
Concern for bioterrorism should also be triggered if multiple patients arrive with similar symptoms, especially when urban-dwelling persons without any identified exposure become ill. Rapid patient isolation, use of personal protective equipment for health care workers, antibiotic delivery, and notification of public health professionals are essential preliminary steps when the disease is suspected. The clinician should have a low threshold to activate the hospital incident command system and notify public health authorities.
Plague is endemic to the southwestern United States (Colorado, New Mexico, Arizona, California) as well as Vietnam, India, the former Soviet Union, and parts of Africa. Hikers, campers, veterinarians, and owners of infected cats, especially those living in or visiting endemic areas, are at greater risk for contracting plague.
Other risk factors include a rural or nonurban environment, especially in known endemic areas; contact with sick or dead animals, especially small rodents or other possible hosts; wilderness activities; known flea bite; occupation as veterinarian; and recent plague in the community.
Plague is classified as a Category A bioterrorism agent because of its ease of dissemination, contagiousness, and high mortality rate. The most likely method of dispersal would be as an aerosol, but simply having an infected individual walk around infecting others is another possible mode of dissemination, albeit less efficient at making many persons ill.
A20.7 – Septicemic plague
9012003 – Septicemic plague
Differential Diagnosis & Pitfalls