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Introduction
Plague is a zoonotic infection caused by Yersinia pestis,
a Gram-negative bacillus. Naturally occurring infections
in humans are transmitted from rodents by fleas and are
characterized by the abrupt onset of high fever, painful
local lymphadenopathy draining at the exposure site,
and bacteremia. Three forms of plague are recognized:
- Bubonic plague - Characterized by the presence
of buboes, the inflammatory swelling of one or more
lymph nodes, usually in the groin;
- Septicemic plague - Plague sepsis which can ensue
from either untreated bubonic plague or de novo from
a flea bite;
- Pneumonic plague - Patients with bubonic plague
can develop secondary pneumonic infection, which
can then be spread from person-to-person without
the need for transmission through a flea vector.
Epidemiology
A total of 18,739 cases of plague in humans in 20
countries (in Africa, Asia, and the Americas) were
reported to the World Health Organization from 1980-1994.
Between 1970 and 1995, 341 cases of plague in the US
were reported to the Centers for Disease Control and
Prevention, with an average of 13 cases per year. Eighty
percent of these cases occurred in the southwestern
states of Arizona (14%), Colorado (10%) and New Mexico
(56%). An additional 9 percent of cases were reported
from California.
Clinical Manifestations of Bubonic Plague
I. Subjective Symptoms- all of the following are considered
presenting symptoms:
| Symptom |
Time
of onset |
| sudden
fever/chills, headache |
After
1-8 day incubation period |
| nausea/vomiting,
prostration/severe malaise, altered mentation,
cough, chest pain, abdominal pain |
A
few hours after appearance of fever, chills and/or
headache. |
II. Objective Symptoms:
| Organ/System |
Description |
Period
and Duration |
| Skin |
Appearance
of characteristic and intensely painful plague
bubo (femoral site most common, followed by inguinal,
axillary and cervical). |
Manifestation:
buboes appear after a 1-8 day incubation period
and 6-8 hours after the onset of the symptoms
described above. |
| Genitourinary |
bladder
distention oliguria and anuria |
Manifestation:
around the time that bubo appears. |
| Circulatory
cardiac blood |
Tachycardia
Hypotension Leukocytosis |
Manifestation:
around the time that bubo appears. |
| Respiratory |
5
to 15% of patients will develop secondary pneumonic
plague |
See
objective symptoms of pneumonic plague. |
| Immune |
pronounced
septicemia |
See
objective symptoms of septicemic plague. |
Clinical Manifestations of Septicemic Plague
I. Subjective Symptoms- all of the following are considered
presenting symptoms and are generally the same as those
for any other Gram-negative sepsis:
| Organ/System |
Description |
Period
and Duration |
| fever/chills |
usually
primary only |
Primary:
after 1-8 day incubation period
Secondary:
2-6 days after appearance of plague bubo
|
| nausea/vomiting |
primary
and secondary |
| diarrhea |
primary
and secondary |
II. Objective Symptoms: The only unique, objective
symptoms of primary or secondary septicemic plague
are purpuric lesions, disseminated intravascular coagulation
and acral cyanosis and necrosis. These are seen at
least 4-6 hours after the onset of symptoms.
Clinical Manifestations of Pneumonic Plague
Pneumonic plague occurs either primarily from aerosol
inhalation or secondarily from hematogenous dissemination
from bubonic plague. Subjective symptoms are the same
as for bubonic plague. The objective clinical presentation
of pneumonic plague is limited to a productive cough
with blood-tinged sputum occurring 24 hours after onset
of symptoms.
Antibiotic Treatment
Antibiotic treatment is essential for treating plague.
Without treatment, mortality is 60% for bubonic plague
and 100% for septicemic plague. Since time-to-death
is relatively short, the earlier the treatment is initiated,
the more favorable the outcome. Patients are not likely
to survive primary pneumonic plague if a course of
antibiotics is not initiated within the first 18 hours
of symptom onset. Plague buboes will subside in 10-14
days if treated with antibiotics.
Since 1948, streptomycin has been the preferred choice
for the treatment of bubonic, septicemic, and pneumonic
plague, although clinical isolates with plasmid-mediated
streptomycin resistance have been reported [Guiyoule
A et al. EID 2001; 7(1):43-8]. Streptomycin should
be administered intramuscularly. Although gentamycin
has been used less frequently, it can be used as an
alternative treatment to streptomycin. Alternate choices
in a contained casualty setting include intravenous
doxycycline, ciprofloxacin, or chloramphenicol. Treatment
should always continue for at least 10 days or for
3-4 days after clinical recovery.
Post-exposure prophylaxis
Any individuals who have been exposed to aerosols
should receive post-exposure prophylaxis for 7 days.
Current recommendations from the Working Group on Civilian
Biodefense are for doxycycline 100 mg twice daily for
adults, including pregnant women, and children >=45
kg. Children under 45 kg should receive 2.2 mg/kg orally
twice daily. For further details, consult the abstract
of the Working Group's paper1 available
from the CDC website at: http://www.bt.cdc.gov/agent/plague/index.asp
Immunization
No plague vaccine is currently available for use in
the United States, although a killed vaccine was previously
licensed. Animal and preliminary human studies have
indicated that a killed plague vaccine is not effective
for preventing pneumonic plague. A recombinant vaccine
candidate for the prevention of pneumonic plague after
inhalational challenge is currently being evaluated.
Reporting
All cases of plague must be reported to local public
health authorities in all 50 states. The local authorities
must notify the appropriate federal government officials
and the World Health Organization, as international
travelers suspected of plague infection may be quarantined
for up to six days under international law. The extremely
high level of contagion and high mortality and case-fatality
rates associated with pneumonic and septicemic plague
(the most likely outcomes in a biological attack) underscore
the importance of swift and accurate reporting.
Extensive Information
Please refer to the extensive information link for
more details regarding Plague.
_______________________________________
1 Inglesby TV, Dennis DT, Henderson DA,
et al. Plague as a biological weapon: Medical and public
health management. JAMA, May 3, 2000; vol. 283, no.
17: 2281-2290.
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