Plague

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Biological Agent Patient Medical ManagementMedical Management of Biological Agent Patients

The following information contains adaptations and excerpts from the US Army Center for Health Promotion and Preventive Medicine (USACHPPM) Tech Guide 244, The Medical NBC Battlebook.

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bubonic plagueCharacteristics. Plague is a zoonotic disease caused by Yersinia pestis. Under natural conditions, humans become infected as a result of contact with rodents and their fleas. Transmission of this gram-negative coccobacillus is by the bite of an infected flea. Under natural conditions. three syndromes are recognized: bubonic, primary septicemic, or pneumonic plague. In a biological attack scenario, the plague bacillus could be delivered via contaminated vectors (fleas) causing the bubonic type or, more likely, via aerosol causing the pneumonic type. In bubonic plague, the incubation period ranges from 2 to 10 days.

bubonic plagueClinical Features. The onset is acute and often fuliminant with malaise, high fever, and one or more tender lymph nodes. Inguinal lymphadenitis (bubo) predominates, but cervical and axillary lymph nodes can also be involved. The involved nodes are tender, fluctuant, and necrotic. bubonic plagueBubonic plague may progress spontaneously to the septicemic form with organisms spreading to the central nervous system, lungs (producing pneumonic disease), and elsewhere. Mortality is 50 percent in untreated patients with the terminal event being circulatory collapse, hemorrhage, and peripheral thrombosis. In primary pneumonic plague, the incubation period is 2 to 3 days. The onset is acute and fulminant with malaise, high fever, chills, headache, myalgia, cough with production of a bloody sputum, and toxemia. The pneumonia progresses rapidly, resulting in dyspnea, stridor, and cyanosis. In untreated patients, the morality is 100 percent with the terminal event being respiratory failure, circulatory collapse, and a bleeding diatheses.

Vaccine. A formalin-inactivated (licensed). Y. pestis vaccine is produced in the United States and has been extensively used. Live-attenuated vaccines are available elsewhere, but are highly reactogenic and without proven efficacy against aerosol challenge. The current plague vaccine does not reliably protect laboratory animals from aerosol challenge and would not be an effective biological attack countermeasures versus aerosol attack. Chemoprophylaxis is recommended for contacts of pneumonic plague patients. Post-exposure prophylaxis with either doxycycline or tetracycline has been recommended in known exposures. The addition of ceftraxone is recommended for plague meningitis.

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