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Surveillance and Reporting Guidelines for
Lassa Fever
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back to
Lassa Fever index page |
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Disease
Reporting |
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In Washington |
Endemic to equatorial Africa, Lassa fever has never occurred in
Washington State. One or more cases may indicate an act of
terrorism and constitute a public health emergency. |
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Purpose of Reporting and
Surveillance |
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To identify rare diseases
associated with travel.
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To identify potentially exposed
laboratory personnel and to provide counseling.
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To raise the index of suspicion of
a possible bioterrorism event if no natural exposure source is
identified.
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Reporting Requirements |
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Health care providers:
immediately notifiable to Local Health Jurisdiction
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Hospitals: immediately
notifiable to Local Health Jurisdiction
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Laboratories: immediately
notifiable to Local Health Jurisdiction, specimen
submission required
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Local health jurisdictions:
suspected or confirmed cases are immediately notifiable to DOH
Communicable Disease Epidemiology: 1-877-539-4344
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Case Definition for Surveillance |
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Clinical Criteria for Diagnosis:
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Clinical
criteria for diagnosis
A severe illness with temperature ≥101oF (38.3oC) of <3
weeks duration, no predisposing factors for hemorrhage, no
established alternative diagnosis with at least two of the
following:
Bleeding from other sites. |
Laboratory Criteria for Diagnosis
(to be completed by Level D laboratories only) |
Identification of Lassa virus from a clinical specimen. |
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Case Definition |
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Probable: A case that meets the
clinical case definition, is not laboratory confirmed, and
is not epidemiologically linked to a confirmed case, but has
appropriate exposure history.
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Confirmed: A case that is
laboratory confirmed, or a case that meets the clinical case
definition and is not laboratory confirmed, but is
epidemiologically linked to a confirmed case.
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A. Description |
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1. Identification |
An acute viral illness of 1-4 weeks duration. Onset is gradual,
with malaise, fever, headache, sore throat, cough, nausea,
vomiting, diarrhea, myalgia and chest and abdominal pain; fever
is persistent or spikes intermittently. Inflammation and
exudation of the pharynx and conjunctivae are commonly observed.
About 80% of human infections are mild or asymptomatic; the
remaining cases have a severe multisystem disease. In severe
cases, hypotension or shock, pleural effusion, hemorrhage,
seizures, encephalopathy and edema of the face and neck are
frequent. Albuminuria and hemoconcentration are common. Early
lymphopenia may be followed by late neutrophilia. Platelet
counts are only moderately depressed, but platelet function is
abnormal. Disease is more severe in pregnancy, and fetal loss
occurs in more than 80% of cases. Transient alopecia and ataxia
may occur in convalescence, and 8th cranial nerve deafness
occurs in 25% of patients; only half recover some function after
1-3 months. Though only about 1% of infected persons die, the
case-fatality rate is about 15% among hospitalized cases; higher
rates may be observed in epidemics. Women in the third trimester
of pregnancy and fetuses fare poorly. AST levels more than 150
and high viremia indicate poor prognosis. Inapparent infections,
diagnosed serologically, are common in endemic areas.
Diagnosis is made by IgM antibody capture and antigen detection
by ELISA or by PCR; by isolation of virus from blood, urine or
throat washings; and immunoglobulin G (IgG) seroconversion by
ELISA or IFA. Laboratory specimens may be biohazardous and must
be handled with extreme care that includes BSL-4 containment, if
available. Heating serum at 60°C (140°F) for 1 hour will largely
inactivate the virus, and the serum can then be used to measure
heat stable substances such as electrolytes, BUN or creatinine. |
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2. Infectious Agent |
Lassa virus, an arenavirus, serologically related to lymphocytic
choriomeningitis, Machupo, Junin, Guanarito and Sabia viruses. |
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3. Worldwide Occurrence |
Endemic in Sierra Leone, Liberia, Guinea and regions of Nigeria.
Cases have also been reported from the Central African Republic.
Serologic evidence of human infection has also been recognized
in the Congo, Mali and Senegal. Serologically related viruses of
lesser virulence for laboratory hosts from Mozambique and
Zimbabwe have not yet been associated with human infection or
disease. |
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4. Reservoir |
Wild rodents; in west Africa, the multimammate mouse of the
Mastomys species complex. |
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5. Modes of Transmission |
Primarily through aerosol or direct contact with excreta of
infected rodents deposited on surfaces such as floors and beds
or in food and water. Laboratory infections occur, especially in
the hospital environment, direct contact with blood through
inoculation with contaminated needles and pharyngeal secretions
or urine of a patient. Infection can also be spread from person
to person by sexual contact. |
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6. Incubation Period |
Commonly 6-21 days. |
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7. Period of Communicability |
Person to person spread may occur during the acute febrile phase
when virus is present in the throat. Virus may be excreted in
urine of patients for 3-9 weeks from onset of illness. |
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8. Susceptibility and Resistance |
All ages are susceptible; the duration of immunity following
infection is unknown. |
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B. Methods of Control |
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1. Preventive Measures |
Specific rodent control. |
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2. Control of Patient, Contacts
and the Immediate Environment |
- Report to local health authority.
- Isolation: Institute immediate strict barrier isolation in
a private hospital room away from traffic patterns. Entry of
nonessential staff and visitors should be restricted. Because
of the low incidence of nosocomial infections reported from
African hospitals, transfer to special isolation units is not
considered necessary; however, nosocomial transmission has
occurred, and strict procedures for isolation of body fluids
and excreta should be maintained. A negative pressure room and
respiratory protection is desirable. Male patients should
refrain from unprotected sexual activity until the semen has
been shown to be free of virus or for 3 months. To reduce
exposure to infectious materials, laboratory tests should be
kept to the minimum necessary for proper diagnosis and patient
care. Technicians should be alerted to the nature of the
specimens and supervised to ensure that appropriate specimen
inactivation/isolation procedures are followed. Dead bodies
should not be embalmed but rather sealed in leak proof
material and cremated or buried promptly in a sealed casket.
- Concurrent disinfection: Patient's excreta, sputum, blood
and all objects with which the patient has had contact,
including laboratory equipment used to carry out tests on
blood, should be disinfected with 0.5% sodium hypochlorite
solution or 0.5% phenol with detergent, and, as far as
possible, appropriate heating methods, such as autoclaving,
incineration or boiling. Laboratory tests should be carried
out in special high containment facilities; if there is no
such facility, tests should be kept to a minimum and specimens
handled by experienced technicians using all available
precautions such as gloves and biological safety cabinets.
When appropriate, serum may be heat inactivated at 60°C
(140°F) for 1 hour. Thorough terminal disinfection with 0.5%
sodium hypochlorite solution or a phenolic compound is
adequate; formaldehyde fumigation can be considered.
- Quarantine: Only surveillance is recommended for close
contacts (see B2f, below).
- Immunization of contacts: None.
- Investigation of contacts and source of infection:
Identify all close contacts (people living with, caring for,
testing laboratory specimens from or having noncasual contact
with the patient) in the 3 weeks after the onset of illness.
Establish close surveillance of contacts as follows: body
temperature checks at least 2 times daily for at least 3 weeks
after last exposure. In case of temperature greater than
38.3ºC (101ºF), hospitalize immediately in strict isolation
facilities. Determine patient's place of residence during 3
weeks prior to onset, and search for unreported or undiagnosed
cases.
- Specific treatment: Ribavirin (Virazole), most effective
within the first 6 days of illness, should be given IV, 30
mg/kg initially, followed by 15 mg/kg every 6 hours for 4 days
and 8 mg/kg every 8 hours for 6 additional days. See also:
Borio L, Inglesby TV, Peters, CJ, et al. Hemorrhagic fever
viruses as biological weapons: medical and public health
management. JAMA 2002; 287:2391-2405 (in Additional
Resources).
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3. Epidemic Measures |
Not determined. |
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4. International Measures |
Notification of source country and to receiving countries of
possible exposures by infected travelers. |
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