eMedicine Specialties > Pediatrics: General Medicine > Infectious Disease
Plague: Follow-up
Updated: Nov 24, 2008
Follow-up
Further Inpatient Care
- Admit patients with plague for antibiotic therapy and isolation.
Further Outpatient Care
- Patient may be discharged on oral tetracycline or doxycycline after 48 hours if hemodynamically stable and symptoms are resolving.
- Follow up closely for potential relapse.
Inpatient & Outpatient Medications
- Antibiotics include streptomycin, tetracycline, doxycycline, and chloramphenicol. Y pestis is often susceptible in vitro to ampicillin, but this antibiotic is rarely effective in vivo. Gentamicin is equally as effective as streptomycin. Antipyretics are useful for patient comfort.
Transfer
- Transfer may be required for further hemodynamic and respiratory monitoring and isolation.
Deterrence/Prevention
- Identifying the source of infection is vital in preventing outbreaks. If an urban area is involved, rodent control should be undertaken. In rural plague-endemic areas, the public must be instructed to avoid handling sick or dead animals and to avoid places where wild animals live. Pets should be kept free of fleas.
- Contacts of pneumonic plague victims should receive antibiotic prophylaxis. Ciprofloxacin or doxycycline is typically used. Trimethoprim-sulfamethoxazole has also been effective for prophylaxis. Contacts of those with bubonic or septicemic plague have no need for prophylaxis.
- Plague vaccine is no longer available in the United States.
Complications
- Polyarthritis
- Lung abscesses
- Suppuration or superinfection of buboes
- Meningitis
- Death
Prognosis
- Mortality rate for untreated plague is 40-70%.
- Untreated pneumonic plague is nearly 100% fatal.
- From 1947-1996, reported mortality rate in the United States was 15%.
- Because plague is often a difficult disease to consider in the differential diagnosis, many patients who succumb to it have previously sought medical care.
Miscellaneous
Medicolegal Pitfalls
- Failure to consider plague in the differential diagnosis
- Failure to take adequate precautions in patients with pneumonic plague against transmission to others
- Failure to differentiate septicemic plague from gram-negative bacterial sepsis
Special Concerns
- Disease reporting
- By law, cases of suspected plague must be reported to the state or local health department. The health department then alerts the Centers for Disease Control and Prevention (CDC). Both organizations investigate all suspected cases.
- Confirmed cases are reported to the WHO.
- Bioterrorism
- Y pestis has been used as a bioweapon, notably by the Japanese during World War II. In addition, in the midst of the Cold War, the former Soviet Union weaponized the plague bacillus. Today, the use of plague as a biological weapon has clear advantages for terrorists.
- Plague is endemic in many parts of the world and is easily found in nature. Only a small inoculum of fewer than 500 organisms needs to be inhaled to result in pneumonic plague, which is then very contagious to individuals within a 2-m radius. Mortality is high if patients are not treated rapidly. The 3-4 day incubation period, coupled with modern transportation systems, allows for swift widespread expansion of disease. Initial symptoms are clinically indistinguishable from various common illnesses, especially during the winter season.
- A high index of suspicion is required to discern plague from community-acquired pneumonia or numerous viral illnesses.
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References
Prentice MB, Rahalison L. Plague. Lancet. Apr 7 2007;369(9568):1196-207. [Medline].
Rocca P. The modern plague. Del Med J. May 2007;79(5):189-90. [Medline].
Thiagarajan B, Bai Y, Gage KL, Cully JF Jr. Prevalence of Yersinia pestis in rodents and fleas associated with black-tailed prairie dogs (Cynomys ludovicianus) at Thunder Basin National Grassland, Wyoming. J Wildl Dis. Jul 2008;44(3):731-6. [Medline].
Eisen RJ, Enscore RE, Biggerstaff BJ, et al. Human plague in the southwestern United States, 1957-2004: spatial models of elevated risk of human exposure to Yersinia pestis. J Med Entomol. May 2007;44(3):530-7. [Medline].
CDC. Human plague--four states, 2006. MMWR Morb Mortal Wkly Rep. Sep 1 2006;55(34):940-3. [Medline].
Ben Ari T, Gershunov A, Gage KL, et al. Human plague in the USA: the importance of regional and local climate. Biol Lett. Sep 2 2008;[Medline].
Centers for Disease Control and Prevention. Fatal human plague--Arizona and Colorado, 1996. MMWR; Can Commun Dis Rep. 1997;46:617-620. [Medline].
Cleri DJ, Vernaleo JR, Lombardi LJ, et al. Plague pneumonia disease caused by Yersinia pestis. Semin Respir Infect. Mar 1997;12(1):12-23. [Medline].
World Health Organization. Human plague in 2002 and 2003. Wkly Epidemiol Rec. Aug 13 2004;79(33):301-6. [Medline].
Gupta ML, Sharma A. Pneumonic plague, northern India, 2002. Emerg Infect Dis. Apr 2007;13(4):664-6. [Medline].
Josko D. Yersinia pestis: still a plague in the 21st century. Clin Lab Sci. Winter 2004;17(1):25-9. [Medline].
Cornelius C, Quenee L, Anderson D, Schneewind O. Protective immunity against plague. Adv Exp Med Biol. 2007;603:415-24. [Medline].
Crook LD, Tempest B. Plague. A clinical review of 27 cases. Arch Intern Med. Jun 1992;152(6):1253-6. [Medline].
Dattwyler RJ. Community-acquired pneumonia in the age of bio-terrorism. Allergy Asthma Proc. May-Jun 2005;26(3):191-4. [Medline].
Dennis DT, Chow CC. Plague. Pediatr Infect Dis J. Jan 2004;23(1):69-71. [Medline].
Dutt AK, Akhtar R, McVeigh M. Surat plague of 1994 re-examined. Southeast Asian J Trop Med Public Health. Jul 2006;37(4):755-60. [Medline].
Galimand M, Guiyoule A, Gerbaud G, et al. Multidrug resistance in Yersinia pestis mediated by a transferable plasmid. N Engl J Med. Sep 4 1997;337(10):677-80. [Medline].
Hoyle JD Jr, White LJ. Treatment of pediatric and adolescent mental health emergencies in the United States: current practices, models, barriers, and potential solutions. Prehosp Emerg Care. Jan-Mar 2003;7(1):66-73. [Medline].
Laudisoit A, Leirs H, Makundi RH, Van Dongen S, Davis S, Neerinckx S, et al. Plague and the human flea, Tanzania. Emerg Infect Dis. May 2007;13(5):687-93. [Medline].
Ligon BL. Plague: a review of its history and potential as a biological weapon. Semin Pediatr Infect Dis. Jul 2006;17(3):161-70. [Medline].
Mittal V, Bhattacharya D, Rana UV, Rai A, Pasha ST, Kumar A, et al. Prompt laboratory diagnosis in timely containment of a plague outbreak in India. J Commun Dis. Dec 2006;38(4):317-24. [Medline].
Perry RD, Fetherston JD. Yersinia pestis--etiologic agent of plague. Clin Microbiol Rev. Jan 1997;10(1):35-66. [Medline].
Russell P, Nelson M, Whittington D, et al. Laboratory diagnosis of plague. Br J Biomed Sci. Dec 1997;54(4):231-6. [Medline].
Smego RA, Frean J, Koornhof HJ. Yersiniosis I: microbiological and clinicoepidemiological aspects of plague and non-plague Yersinia infections. Eur J Clin Microbiol Infect Dis. Jan 1999;18(1):1-15. [Medline].
Solomon T. Hong Kong, 1894: the role of James A Lowson in the controversial discovery of the plague bacillus. Lancet. Jul 5 1997;350(9070):59-62. [Medline].
Titball RW, Leary SE. Plague. Br Med Bull. 1998;54(3):625-33. [Medline].
Tomaso H, Jacob D, Eickhoff M, et al. Preliminary validation of real-time PCR assays for the identification of Yersinia pestis. Clin Chem Lab Med. 2008;46(9):1239-44. [Medline].
Weir E. Plague: a continuing threat. CMAJ. Jun 7 2005;172(12):1555. [Medline].
Further Reading
Keywords
plague, black death, black plague, bubonic plague, septicemic plague, pneumonic plague, ambulant plague, Yersinia pestis, bioterrorist agent, bioterrorism, bacteremia, pneumonia, septicemia, meningitis, polyarthritis, lung abscess, pharyngitis
Follow-up: Plague