Plague
(Redirected from Plague (Yersinia pestis))
Background
- The plague is a severe, acute infection caused by Gram Negative bacillus, Yersinia pestis.
- Y. pestis is transmitted by fleas (vector) and occurs naturally in a variety of animals, including rodents (reservoir) [1]
- Two main forms are bubonic and pulmonic forms
- Considered a Class A bioterrorism agent
Clinical Features
Bubonic plague
- Eschar often forms at site of vector bite (usually flea bite)
- Buboes (inflamed, necrotic or hemorrhagic lymph nodes) are pathognomonic
- Usually in axilla or groin
- Typically non-fluctuant, but can suppurate (rare)
- Liver and splenic involvement
- Septicemia
- The disease disseminates in about 50% of patients
- Leads to necrosis of tissues, especially digits and nose
- Can either be first manifestation of the disease or develop from untreated bubonic plague
- Death if untreated in 2-10 days
Pulmonic plague
- Very contagious
- Can be hematogenous or aerosolized (weapon form)
- Hemoptysis
- Mulilobar hemorrhagic pneumonia
- Sepsis
- Death if untreated in 48 hours
- Mortality rate nearly 100% without treatment [2]
Differential Diagnosis
Lower Respiratory Zoonotic Infections
- Psittacosis
- Anthrax (Bacillus anthracis)
- Brucellosis (Brucella species)
- Q fever (C. burnetti)
- Pasteurellosis (Pasteurella multocida)
- Melioidosis (Burkholderia pseudomallei)
- Rocky Mountain Spotted Fever (R. rickettsii)
- Pulmonic Plague (Yersinia pestis)
- Influenza A
- Hantavirus
Bioterrorism Agents[3]
Category A
Category B
- Ricin
- Brucellosis
- Epsilon toxin
- Psittacosis
- Q Fever
- Staph enterotoxin B
- Typhus
- Glanders
- Melioidosis
- Food safety threats
- Water safety threats
- Viral encephalitis
Category C
- Influenza
- Yellow fever
- Tickborne hemorrhagic fever
- Tickborne encephalitis
Lymphadenopathy
- Cat-scratch disease
- Tularemia
- Staphylococcal and streptococcal infections
Evaluation
Should be considered in any patient with clinical signs of plague and a recent history of travel to the western United States or any other plague endemic area.
Possible diagnostic samples:
- Lymph node aspirate
- Affected bubo should contain numerous organisms that can be evaluated microscopically and by culture.
- Blood cultures
- Organisms may be seen in blood smears if the patient is septicemic.
- Blood smears taken from suspected bubonic plague patients early in the course of illness are usually negative for bacteria by microscopic examination but may be positive by culture.
- Sputum
- Culture is possible from sputum of very ill pneumonic patients
- However, blood is usually culture-positive at this time as well.
- Bronchial/tracheal washing
- May be taken from suspected pneumonic plague patients
- Not ideal for isolation of plague, since they often contain many other bacteria that can mask the presence of plague.
Gram, Wright, Giemsa, or Wayson's stained smears of peripheral blood, sputum, or lymph node specimen. Visualization of bipolar-staining, ovoid, Gram-negative organisms with a "safety pin" appearance permits a rapid presumptive diagnosis of plague.
- If cultures yield negative results, and plague is still suspected, serologic testing is possible to confirm the diagnosis.
- One serum specimen should be taken as early in the illness as possible, followed by a convalescent sample 4-6 weeks or more after disease onset.
Management
Droplet precautions if pneumonic form suspected
- Plague is a reportable disease to the CDC
- If bioterrorism suspected, health authorities must be contacted immediately
- Consult ID
- Do not perform an I&D as the buboes are responsive to antibiotics; performing an I&D risks disseminating the bacterium to health-care providers [4]
Antibiotics
Should be given within 24 hours for effective outcomes and continued for at least 10 days [5]
Postexposure Prophylaxis
- Doxycycline 100mg (2.2mg/kg) PO q12hrs daily OR
- Ciprofloxacin 500mg (20mg/kg) PO q12hrs daily OR
- Chloramphenicol 1mg (25mg/kg) PO q6hrs
- only if age > 2
Active Disease
- Gentamicin 5mg/kg IV/IM once daily x 10 days OR
- Ciprofloxacin 500mg (20mg/kg) PO q12hrs x 10 days OR
- Doxycycline 200mg (2.2mg/kg) PO/IV daily
Disposition
- Admit
- Droplet precautions if pneumonic form suspected for at least 4 days after initiation of antibiotics [6]
See Also
External Links
References
- ↑ Schultz, C., & Koenig, K. Weapons of Mass Destruction. In Rosen's Emergency Medicine: Concepts and Clinical Practice (9th ed.). Philadephia, PA: Elsevier/Saunders.
- ↑ Schultz, C., & Koenig, K. Weapons of Mass Destruction. In Rosen's Emergency Medicine: Concepts and Clinical Practice (9th ed.). Philadephia, PA: Elsevier/Saunders.
- ↑ https://www.niaid.nih.gov/topics/biodefenserelated/biodefense/pages/cata.aspx Accessed 02/26/16
- ↑ Schultz, C., & Koenig, K. Weapons of Mass Destruction. In Rosen's Emergency Medicine: Concepts and Clinical Practice (9th ed.). Philadephia, PA: Elsevier/Saunders.
- ↑ Schultz, C., & Koenig, K. Weapons of Mass Destruction. In Rosen's Emergency Medicine: Concepts and Clinical Practice (9th ed.). Philadephia, PA: Elsevier/Saunders.
- ↑ Schultz, C., & Koenig, K. Weapons of Mass Destruction. In Rosen's Emergency Medicine: Concepts and Clinical Practice (9th ed.). Philadephia, PA: Elsevier/Saunders.