DISEASE |
VACCINE |
CHEMOTHERAPY (Rx) |
CHEMOPRO-
PHYLAXIS (Px) |
COMMENTS |
Anthrax |
Bioport vaccine (licensed) 0.5 mL SC @ 0, 2, 4 wk, 6, 12, 18 mo
then annual boosters |
Ciprofloxacin 400 mg IV q 8-12 h
OR
Doxycycline 200 mg IV, then 100 mg IV q 8-12 h
|
Ciprofloxacin 500 mg PO bid x 4 wk If unvaccinated, begin initial
doses of vaccine |
Potential alternates for Rx: gentamicin, erythromycin, and chloramphenicol |
- |
- |
Penicillin 4 million units IV q 4 h
|
Doxycycline 100 mg PO bid x 4 wk plus vaccination |
PCN for sensitive organisms only |
Cholera |
Wyeth-Ayerst Vaccine 2 doses 0.5 mL IM or SC @ 0, 7-30 days, then
boosters Q 6 months |
Oral rehydration therapy during period of high fluid loss |
N/A |
Vaccine not recommended for routine protection in endemic areas
(50% efficacy, short term) |
- |
- |
Tetracycline 500 mg q 6 h x 3 d
|
- |
Alternates for Rx: erythromycin, trimethoprim and sulfamethoxazole,
and furazolidone |
- |
- |
Doxycycline 300 mg once, or 100 mg q 12 h x 3 d |
- |
Quinolones for tetra/doxy resistant strains |
- |
- |
Ciprofloxacin 500 mg q 12 h x 3 d |
- |
- |
- |
- |
Norfloxacin 400 mg q 12 h x 3 d |
- |
- |
Q Fever |
IND 610 - inactivated whole cell vaccine given as single 0.5 ml
s.c. injection |
Tetracycline 500 mg PO q 6 h x 5-7 d continued at least 2 d after
afebrite |
Tetracycline start 8-12 d post-exposure x 5 d |
Currently testing vaccine to determine the necessity of skin testing
prior to use. |
- |
- |
Doxycycline 100 mg PO q 12 h x 5-7 d continued at least 2 d after
afebrite |
Doxycycline start 8-12 d post-exposure x 5 d |
- |
Glanders |
No vaccine available |
Antibiotic regimens vary depending on localization and severity
of disease - refer to text |
Post-exposure prophylaxis may be tried with TMP-SMX |
No large therapeutic human trials have been conducted owing to
the rarity of naturally occurring disease. |
Plague |
Greer inactivated vaccine (FDA licensed) is no longer available |
Streptomycin 30 mg/kg/d IM in 2 divided doses x 10 - 14 d
OR
Gentamicin 5 mg/kg IM or IV once daily x 10 - 14 d
OR
Ciprofloxacin 400 mg IV q 12 h until clinically improved then
750 mg PO bid for total of 10 - 14 d
|
Doxycycline 100 mg PO bid x 7 d or duration of exposure
Ciprofloxacin 500 mg PO bid x 7 d |
Chloramphenicol for plague meningitis is required 25 mg/kg IV,
then 15 mg/kg qid x 14 d |
-
. |
. |
Doxycycline 200 mg IV then 100 mg IV bid, until clinically improved
then 100 mg PO bid for total of 10-14 d |
Tetracycline 500 mg PO qid x 7 d |
Alternate Rx: trimethoprim-
sulfamethoxazole |
Brucellosis |
No human vaccine available |
Doxycycline 200 mg mg/d PO plus rifampin 600 mg/d PO x 6 wk |
Doxycycline 200 mg mg/d PO plus rifampin 600 mg/d PO x 6 wk |
Trimethoprim-
sulfamethoxazole may be substituted for rifampin; however, relapse may reach 30% |
. |
. |
Ofloxacin 400/rifampin 600 mg/d PO x 6 wks |
. |
. |
Tularemia |
IND - Live attenuated vaccine: single 0.1ml dose by scarification |
Streptomycin 7.5 - 10 mg/kg IM bid x 10 - 14 d |
Doxycyline 100 mg PO bid x 14 d |
. |
. |
. |
Gentamicin 3 - 5 mg/kg/d IV x 10 - 14 d |
Tetracycline 500 mg PO qid x 14 d
Ciprofloxacin 500 mg PO q 12 h for 14 d
|
-
. |
. |
. |
Ciprofloxacin 400 mg IV q 12h until improved, then 500 mg PO q
12 h for total of 10 - 14 d |
. |
. |
. |
. |
Ciprofloxacin 750 mg PO q 12 h for 10 - 14 d |
. |
. |
Viral
Encephalitides |
VEE DOD TC-83 live attenuated vaccine (IND): 0.5 mL SC x 1 dose |
Supportive therapy: analgesics and anticonvulsants prn |
N/A |
TC-83 reactogenic in 20%
No seroconversion in 20%
Only effective against subtypes 1A, 1B, and 1C |
. |
VEE DOD TC-84 (formalin inactivated TC-83) (IND): 0.5 mL SC for
up to 3 doses |
. |
. |
. |
. |
EEE inactivated (IND): 0.5 mL SC at 0 & 28 d |
. |
. |
. |
. |
WEE inactivated (IND): 0.5 mL SC at 0, 7, & 28 d |
. |
. |
. |
Viral Hemorrhagic Fevers |
AHF Candid #1 vaccine (x-protection for BHF) (IND) |
Ribavirin (CCHF/Lassa) (IND)
30 mg/kg IV initial dose; then 16 mg/kg IV q 6 h x 4 d; then 8
mg/kg IV q 8 h x 6 d |
N/A |
Aggressive supportive care and management of hypotension very
important |
. |
RVF inactivated vaccine (IND) |
Passive antibody for AHF, BHF, Lassa fever, and CCHF |
. |
. |
Smallpox |
Wyeth calf lymph vaccinia vaccine (licensed): 1 dose by scarification |
No current Rx other than supportive; Cidofovir (effective in vitro);
animal studies ongoing |
Vaccinia immune globulin 0.6 mL/kg IM (within 3 d of exposure,
best within 24 h) |
Pre and post exposure vaccination recommended if > 3 years since
last vaccine |
Botulism |
DOD pentavalent toxoid for serotypes A - E (IND): 0.5 ml deep
SC @ 0, 2 & 12 wk, then yearly boosters |
DOD heptavalent equine despeciated antitoxin for serotypes A-G
(IND): 1 vial (10 mL) IV |
N/A |
Skin test for hypersensitivity before equine antitoxin administration |
. |
. |
CDC trivalent equine antitoxin for serotypes A, B, E (licensed) |
N/A |
. |
Staphylococcus Enterotoxin B |
No vaccine available |
Ventilatory support for inhalation exposure |
N/A |
. |
Ricin |
No vaccine available |
Inhalation: supportive therapy G-I : gastric lavage, superactivated
charcoal, cathartics |
N/A |
. |
T-2 Mycotoxins |
No vaccine available |
. |
Decontamination of clothing and skin |
. |