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Meningococcal Disease
For more
information about meningococcal disease, see our
meningococcal
disease fact sheet.
For more
information about meningococcal vaccine, see
http://www.cdc.gov/vaccines/vpd-vac/mening/default.htm.
Postexposure
Prophylaxis for Meningococcal Disease
EXCERPTED
FROM: Morbidity and Mortality Weekly Report, May 27, 2005 /
54(RR-7);16-17
(See
http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5407a1.htm for entire
statement, including references).
Prevention and
Control of Meningococcal Disease
ANTIMICROBIAL CHEMOPROPHYLAXIS
Antimicrobial
chemoprophylaxis of close contacts of sporadic cases of
meningococcal disease is the primary means for prevention of
meningococcal disease in the United States (see Table). Close
contacts include a) household members, b) day care center contacts,
and c) anyone directly exposed to the patient's oral secretions
(e.g., through kissing, mouth-to-mouth resuscitation, endotracheal
intubation, or endotracheal tube management). For travelers,
antimicrobial chemoprophylaxis should be considered for any
passenger who had direct contact with respiratory secretions from an
index-patient or for anyone seated directly next to an index-patient
on a prolonged flight (i.e., one lasting >8 hours). The attack rate
for household contacts exposed to patients who have sporadic
meningococcal disease has been estimated to be four cases per 1,000
persons exposed, which is 500-800 times greater than for the total
population . Because the rate of secondary disease for close
contacts is highest during the first few days after onset of disease
in the primary patient, antimicrobial chemoprophylaxis should be
administered as soon as possible (ideally within 24 hours after the
case is identified). Conversely, chemoprophylaxis administered
greater than 14 days after onset of illness in the index
case-patient is probably of limited or no value. Oropharyngeal or
nasopharyngeal cultures are not helpful in determining the need for
chemoprophylaxis and may unnecessarily delay institution of this
preventive measure.
Rifampin,
ciprofloxacin, and ceftriaxone are 90%--95% effective in reducing
nasopharyngeal carriage of N. meningitdis and are all
acceptable antimicrobial agents for chemoprophylaxis. See the table
below for recommended dosages and select comments about the
medications. Consult a drug handbook or pharmacist for a complete
list of contraindications and adverse effects.
Systemic
antimicrobial therapy of meningococcal disease with agents other
than ceftriaxone or other third-generation cephalosporins may not
reliably eradicate nasopharyngeal carriage of N. meningitidis.
If other agents have been used for treatment, the index patient
should receive chemoprophylactic antibiotics for eradication of
nasopharyngeal carriage before being discharged from the hospital.
TABLE. Schedule for
administering chemoprophylaxis against meningococcal disease
|
Drug |
Age
group |
Dosage |
Duration
and route of administration |
|
Rifampin* |
Children <1
month |
5 mg/kg
every 12 hrs
|
2 days,
oral |
|
Children ≥
1 months |
10 mg/kg
(max 600 mg) every 12 hrs
|
2 days,
oral |
|
Adults |
600 mg
every 12 hrs
|
2 days,
oral |
|
Ciprofloxacin§ |
Adults |
500 mg |
Single
dose, oral
|
|
Ceftriaxone |
Children
<15 years
|
125 mg |
Single
dose, intramuscular (IM) |
|
Adults
(including pregnant women) |
250 mg |
Single
dose, intramuscular |
* Rifampin is
not recommended for pregnant women, because it is teratogenic in
laboratory animals. Rifampin changes the color of urine to
reddish-orange and is excreted in tears and other body fluids; it
may cause permanent discoloration of soft contact lenses. Because
the reliability of oral contraceptives may be affected by rifampin
therapy, consideration should be given to using alternate
contraceptive measures while rifampin is being administered.
§
Ciprofloxacin is not generally recommended for persons less than 18
years of age or for pregnant and lactating women because the drug
causes cartilage damage in immature laboratory animals. However,
ciprofloxacin may be used for chemoprophylaxis of children when no
acceptable alternative therapy is available.
Table adapted from: Morbidity and Mortality Weekly Report, May 27,
2005 / 54(RR-7);16-17
(See
http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5407a1.htm for entire
statement, including references).
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