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{{Anthrax}}
{{Anthrax}}
{{CMG}}; {{AE}} {{JS}}
{{CMG}}; {{AE}} {{JS}}
==Overview==
==Overview==
Well-timed and effective postexposure [[prophylaxis]] can potentially save thousands of lives. Postexposure [[prophylaxis]] of [[asymptomatic]] persons should ideally start as soon as possible after exposure because its effectiveness decreases with delay in implementation. After exposure to anthrax, it is recommended 60 days of [[antibiotic]] drug [[prophylaxis]] for immediate protection and a 3-dose series of Anthrax Vaccine Adsorbed (AVA) for long-term protection.<ref name="pmid20651644">{{cite journal| author=Wright JG, Quinn CP, Shadomy S, Messonnier N, Centers for Disease Control and Prevention (CDC)| title=Use of anthrax vaccine in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2009. | journal=MMWR Recomm Rep | year= 2010 | volume= 59 | issue= RR-6 | pages= 1-30 | pmid=20651644 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20651644  }} </ref> To ensure adequate and continued protection, everyone exposed to aerosolized [[Bacillus anthracis]] [[spores]] should receive a full 60 days of postexposure prophylaxis antibiotic drugs, whether they are unvaccinated, partially [[vaccinated]], or fully vaccinated.<ref name=CDC>{{cite web | title = Centers for Disease Control and Prevention Expert Panel Meetings on Prevention and Treatment of Anthrax in Adults | url = http://wwwnc.cdc.gov/eid/article/20/2/13-0687_article }}</ref>
[[Prevention]] of anthrax infection can be achieved with post-exposure [[prophylaxis]] [[antibiotic]]s and [[vaccination]]. The US Advisory Committee on Immunization Practices recommended 60 days of [[antibiotic]] drug [[prophylaxis]] for immediate protection and a 3-dose series of Anthrax Vaccine Adsorbed (AVA) for long-term protection.  Postexposure [[prophylaxis]] of [[asymptomatic]] persons should start as soon as possible after exposure because its effectiveness decreases with delay in implementation.  Everyone exposed to aerosolized [[B. anthracis]] spores should receive a full 60 days of post-exposure prophylaxis antimicrobial drugs, whether they are unvaccinated, partially vaccinated, or fully vaccinated.  Protective measures should also be implemented to prevent the [[transmission]] of the disease.<ref name="pmid20651644">{{cite journal| author=Wright JG, Quinn CP, Shadomy S, Messonnier N, Centers for Disease Control and Prevention (CDC)| title=Use of anthrax vaccine in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2009. | journal=MMWR Recomm Rep | year= 2010 | volume= 59 | issue= RR-6 | pages= 1-30 | pmid=20651644 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20651644  }} </ref>


==Primary Prevention==
==Primary Prevention==
Well-timed and effective postexposure [[prophylaxis]] can potentially save thousands of lives. Postexposure [[prophylaxis]] of [[asymptomatic]] persons should start as soon as possible after exposure because its effectiveness decreases with delay in implementation. Initial [[symptoms]] may resemble a common [[cold]], including [[sore throat]], mild [[fever]], [[myalgia]], and [[malaise]]. After a few days, the [[symptoms]] may progress to severe breathing problems [[shock]], and ultimately death.<ref name=CDC>{{cite web | title = Centers for Disease Control and Prevention Expert Panel Meetings on Prevention and Treatment of Anthrax in Adults | url = http://wwwnc.cdc.gov/eid/article/20/2/13-0687_article }}</ref>  After exposure to [[anthrax]], it is recommended 60 days of [[antibiotic]] drug [[prophylaxis]] for immediate protection and a 3-dose series of Anthrax Vaccine Adsorbed (AVA) for long-term protection.<ref name="pmid20651644">{{cite journal| author=Wright JG, Quinn CP, Shadomy S, Messonnier N, Centers for Disease Control and Prevention (CDC)| title=Use of anthrax vaccine in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2009. | journal=MMWR Recomm Rep | year= 2010 | volume= 59 | issue= RR-6 | pages= 1-30 | pmid=20651644 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20651644  }} </ref>


===Antibiotic Drugs===
===Antibiotic Drugs===
To ensure adequate and continued protection, everyone exposed to aerosolized [[Bacillus anthracis]] [[spores]] should receive a full 60 days of postexposure prophylaxis antibiotic drugs, whether they are unvaccinated, partially [[vaccinated]], or fully vaccinated.<ref name=CDC>{{cite web | title = Centers for Disease Control and Prevention Expert Panel Meetings on Prevention and Treatment of Anthrax in Adults | url = http://wwwnc.cdc.gov/eid/article/20/2/13-0687_article }}</ref>
[[Ciprofloxacin]], [[levofloxacin]], and [[doxycycline]] are [[FDA]]-approved for the [[antibiotic]] drug portion of postexposure [[prophylaxis]] for inhalation anthrax in adults ≥18 years of age.  
[[Ciprofloxacin]], [[levofloxacin]], and [[doxycycline]] are [[FDA]]-approved for the [[antibiotic]] drug portion of postexposure [[prophylaxis]] for inhalation anthrax in adults ≥18 years of age.  


No safety data are available for [[levofloxacin]] use beyond 30 days; thus, oral [[ciprofloxacin]] and [[doxycycline]] are recommended as first-line [[antibiotic]] drugs for postexposure [[prophylaxis]]. Alternative [[antibiotic]] drugs that might be used for postexposure [[prophylaxis]], if first-line agents are not tolerated or are unavailable, include:
No safety data are available for [[levofloxacin]] use beyond 30 days; thus, oral [[ciprofloxacin]] and [[doxycycline]] are recommended as first-line [[antibiotic]] drugs for postexposure [[prophylaxis]]. Alternative [[antibiotic]] drugs that might be used for postexposure [[prophylaxis]], if first-line agents are not tolerated or are unavailable, include:<ref name=CDC>{{cite web | title = Centers for Disease Control and Prevention Expert Panel Meetings on Prevention and Treatment of Anthrax in Adults | url = http://wwwnc.cdc.gov/eid/article/20/2/13-0687_article }}</ref>
* [[Levofloxacin]] and [[moxifloxacin]]
* [[Levofloxacin]] and [[moxifloxacin]]
* [[Amoxicillin]] and [[penicillin V Potassium]] if the isolate is [[penicillin]] susceptible
* [[Amoxicillin]] and [[penicillin V Potassium]] if the isolate is [[penicillin]] susceptible
* [[Clindamycin]].
* [[Clindamycin]]


===Vaccine===
===Vaccine===
There is evidence of [[seroconversion]] after 3 doses of AVA. The [[vaccine]] should be administered [[subcutaneous|subcutaneously]] at [[diagnosis]] and 2 and 4 weeks later.<ref name="pmid20651644">{{cite journal| author=Wright JG, Quinn CP, Shadomy S, Messonnier N, Centers for Disease Control and Prevention (CDC)| title=Use of anthrax vaccine in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2009. | journal=MMWR Recomm Rep | year= 2010 | volume= 59 | issue= RR-6 | pages= 1-30 | pmid=20651644 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20651644  }} </ref> AVA is not FDA-approved for postexposure [[prophylaxis]] and could be made available under an Investigational New Drug protocol or an Emergency Use Authorization in a declared emergency.
Despite the existence of a vaccine licensed to prevent anthrax, it is not typically available for the general public. It protects against cutaneous and inhalation anthrax. There is evidence of [[seroconversion]] after 3 doses of Anthrax Vaccine Adsorbed (AVA). The [[vaccine]] should be administered [[subcutaneous|subcutaneously]] at [[diagnosis]], and 2 and 4 weeks later.<ref name="pmid20651644">{{cite journal| author=Wright JG, Quinn CP, Shadomy S, Messonnier N, Centers for Disease Control and Prevention (CDC)| title=Use of anthrax vaccine in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2009. | journal=MMWR Recomm Rep | year= 2010 | volume= 59 | issue= RR-6 | pages= 1-30 | pmid=20651644 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20651644  }} </ref> AVA is not FDA-approved for postexposure [[prophylaxis]] and could be made available under an Investigational New Drug protocol or an Emergency Use Authorization in a declared emergency.
 
Anthrax [[vaccine]] is indicated  for the following risk groups of adults:<ref name=CDC2>{{cite web | title = Prevention | url = http://www.cdc.gov/anthrax/medicalcare/prevention/antibiotics.html }}</ref>
* Laboratory workers who work with anthrax
* People who handle animals or animal products
* Members of the United States military


==Prophylaxis Regimen==
==Prophylaxis Regimen==


<SMALL><font color="#FF4C4C">'''▸ Click on the following categories to expand treatment regimens.'''</font></SMALL><ref>{{Cite journal | doi = 10.3201/eid2002.130687 | issn = 1080-6059 | volume = 20 | issue = 2 | last = Hendricks | first = Katherine A. | coauthors = Mary E. Wright, Sean V. Shadomy, John S. Bradley, Meredith G. Morrow, Andy T. Pavia, Ethan Rubinstein, Jon-Erik C. Holty, Nancy E. Messonnier, Theresa L. Smith, Nicki Pesik, Tracee A. Treadwell, William A. Bower, Workgroup on Anthrax Clinical Guidelines | title = Centers for disease control and prevention expert panel meetings on prevention and treatment of anthrax in adults | journal = Emerging Infectious Diseases | date = 2014-02 | pmid = 24447897 | pmc = PMC3901462 }}</ref><ref>{{Cite journal | doi = 10.1542/peds.2014-0563 | issn = 1098-4275 | last = Bradley | first = John S. | coauthors = Georgina Peacock, Steven E. Krug, William A. Bower, Amanda C. Cohn, Dana Meaney-Delman, Andrew T. Pavia, AAP COMMITTEE ON INFECTIOUS DISEASES and DISASTER PREPAREDNESS ADVISORY COUNCIL | title = Pediatric Anthrax Clinical Management | journal = Pediatrics | date = 2014-04-28 | pmid = 24777226 }}</ref><ref>{{Cite journal | doi = 10.3201/eid2002.130611 | issn = 1080-6059 | volume = 20 | issue = 2 | last = Meaney-Delman | first = Dana | coauthors = Marianne E. Zotti, Andreea A. Creanga, Lara K. Misegades, Etobssie Wako, Tracee A. Treadwell, Nancy E. Messonnier, Denise J. Jamieson, Workgroup on Anthrax in Pregnant and Postpartum Women | title = Special considerations for prophylaxis for and treatment of anthrax in pregnant and postpartum women | journal = Emerging Infectious Diseases | date = 2014-02 | pmid = 24457117 | pmc = PMC3901460 }}</ref>
:* '''Bacillus anthracis, postexposure prophylaxis'''


{|
::* 1. '''For adults'''<ref name="pmid24447897">{{cite journal| author=Hendricks KA, Wright ME, Shadomy SV, Bradley JS, Morrow MG, Pavia AT et al.| title=Centers for disease control and prevention expert panel meetings on prevention and treatment of anthrax in adults. | journal=Emerg Infect Dis | year= 2014 | volume= 20 | issue= 2 | pages=  | pmid=24447897 | doi=10.3201/eid2002.130687 | pmc=PMC3901462 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24447897  }} </ref>
| valign=top |


<div style="border-radius: 5px 5px 0 0; border: solid 1px #20538D; border-bottom: 0px; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5); box-shadow: inset 0 1px 1px rgba(255, 255, 255, 0.5), 0 1px 1px rgba(0, 0, 0, 0.5); height: 30px; line-height: 30px; width: 350px; background: #A1BCDD; text-align: center;">
:::* 1.1 '''For all strains, regardless of penicillin susceptibility or if susceptibility is unknown'''
<font color="#FFF">
::::* Preferred regimen (1): [[Ciprofloxacin]] 500 mg IV q12h
'''PEP for Infection with B. anthracis'''
::::* Preferred regimen (2): [[Doxycycline]] 100 mg IV q12h
</font>
::::* Preferred regimen (3): [[Levofloxacin]] 750 mg IV q24h
</div>
::::* Preferred regimen (4): [[Moxifloxacin]] 400 mg IV q24h
::::* Preferred regimen (5): [[Clindamycin]] 600 mg IV q8h


<div class="mw-customtoggle-table01" style="cursor: pointer; border-radius: 0 0 0 0; border: solid 1px #20538D; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5); box-shadow: inset 0 1px 1px rgba(255, 255, 255, 0.5), 0 1px 1px rgba(0, 0, 0, 0.5); height: 30px; line-height: 30px; width: 350px; background: #4479BA;">
:::* 1.2 '''Alternatives for penicillin-susceptible strain'''
<font color="#FFF">
::::* Preferred regimen (1): [[Amoxicillin]] 1 g IV q8h
&nbsp;&nbsp;▸&nbsp;&nbsp;'''Adult Patients'''
::::* Preferred regimen (2): Penicillin VK 500 mg IV q6h
</font>
</div>


<div class="mw-customtoggle-table02" style="cursor: pointer; border-radius: 0 0 0 0; border: solid 1px #20538D; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5); box-shadow: inset 0 1px 1px rgba(255, 255, 255, 0.5), 0 1px 1px rgba(0, 0, 0, 0.5); height: 30px; line-height: 30px; width: 350px; background: #4479BA;">
::* 2. '''For children = 1 month'''<ref name="pmid24777226">{{cite journal| author=Bradley JS, Peacock G, Krug SE, Bower WA, Cohn AC, Meaney-Delman D et al.| title=Pediatric anthrax clinical management. | journal=Pediatrics | year= 2014 | volume= 133 | issue= 5 | pages= e1411-36 | pmid=24777226 | doi=10.1542/peds.2014-0563 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24777226  }} </ref>
<font color="#FFF">
&nbsp;&nbsp;▸&nbsp;&nbsp;'''Pediatric Patients'''
</font>
</div>


<div class="mw-customtoggle-table03" style="cursor: pointer; border-radius: 0 0 5px 5px; border: solid 1px #20538D; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5); box-shadow: inset 0 1px 1px rgba(255, 255, 255, 0.5), 0 1px 1px rgba(0, 0, 0, 0.5); height: 30px; line-height: 30px; width: 350px; background: #4479BA;">
:::* 2.1 '''For penicillin-resistant strains or prior to susceptibility testing'''
<font color="#FFF">
::::* Preferred regimen (1): [[Ciprofloxacin]] 30 mg/kg/day, PO, bid (not to exceed 500 mg/dose)
&nbsp;&nbsp;▸&nbsp;&nbsp;'''Pregnant Patients'''
::::* Preferred regimen (2):
</font>
:::::* If patients body weight < 45 kg: [[Doxycycline]] 4.4 mg/kg/day, PO, bid (not to exceed 100 mg/dose)
</div>
:::::* If patients body weight > 45 kg: [[Doxycycline]] 100 mg/dose, PO, bid
::::* Preferred regimen (3): [[Clindamycin]] 30 mg/kg/day, PO, tid (not to exceed 900 mg/dose)
::::* Preferred regimen (4):
:::::* If patients body weight < 50 kg: [[Levofloxacin]] 16 mg/kg/day, PO, bid (not to exceed 250 mg/dose)
:::::* If patients body weight > 50 kg: [[Levofloxacin]] 500 mg, PO, qd


<!--COLLECT ALL THE BOXES BELOW-->
:::* 2.2 '''For penicillin-susceptible strains'''
| valign=top |
::::* Preferred regimen (1): [[Amoxicillin]] 75 mg/kg/day, PO, tid (not to exceed 1 g/dose)
::::* Preferred regimen (2): [[Penicillin VK]] 50-75 mg/kg/day, PO, id or tid
::::* Note: '''Duration of Therapy is 60 days after exposure'''


{| class="mw-collapsible mw-collapsed" id="mw-customcollapsible-table01" style="background: #FFFFFF;"
::* 3. '''For children < 1 month'''
| valign=top |
:::* 3.1 '''For all strains, regardless of penicillin susceptibility or if susceptibility is unknown'''
{| style="float: left; cellpadding=0; cellspacing= 0; width: 450px;"
::::* 3.1.1 '''For 32–34 weeks gestational age'''
! style="height: 30px; line-height: 30px; background: #4479BA; border: 0px; font-size: 100%; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5);" align=center | {{fontcolor|#FFF|Postexposure Prophylaxis, Adult Patients}}
:::::* 3.1.1.1 '''For < 1 week of Age'''
|-
::::::* Preferred regimen (1): [[Ciprofloxacin]] 20 mg/kg/day, PO, bid
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Preferred Regimen
::::::* Preferred regimen (2): [[Clindamycin]] 10 mg/kg/day, PO, bid
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Ciprofloxacin]]  500 mg PO q12h'''''<BR> OR <BR> ▸ '''''[[Doxycycline]]  100 mg PO q12h'''''<br> OR <br> ▸ '''''[[Levofloxacin]]  750 mg PO q24h'''''<BR> OR <BR> ▸ '''''[[Moxifloxacin]] 400 mg PO q24h'''''<BR> OR <BR>  ▸ '''''[[Clindamycin]] 600 mg PO q8h'''''<br> OR <br>
|-
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Alternative Regimen
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Amoxicillin]] 1 g PO q8h'''''<BR> OR <BR>▸ '''''[[Penicillin VK]] 500 mg PO q6h'''''
|}
|}


{| class="mw-collapsible mw-collapsed" id="mw-customcollapsible-table02" style="background: #FFFFFF;"
:::::* 3.1.1.2 '''For 1–4 week of age '''
| valign=top |
::::::* Preferred regimen (1): [[Ciprofloxacin]] 20 mg/kg/day, PO,bid
{| style="float: left; cellpadding=0; cellspacing= 0; width: 450px;"
::::::* Preferred regimen (2): [[Clindamycin]] 15 mg/kg/day, PO, tid
! style="height: 30px; line-height: 30px; background: #4479BA; border: 0px; font-size: 100%; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5);" align=center | {{fontcolor|#FFF|Postexposure Prophylaxis, Pediatric Patients}}
|-
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Preferred Regimen
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Ciprofloxacin]] 30 mg/kg/day PO q12h, max: 500 mg/dose'''''<BR> OR <BR> ▸ '''''[[Doxycycline]]  4.4 mg/kg/day PO q12h, max: 100 mg/dose (<45 kg)''''' <BR> OR <BR>  ▸ '''''[[Doxycycline]]  100 mg/dose PO q12h (≥45 kg)'''''<BR> OR <BR> ▸ '''''[[Clindamycin]] 30 mg/kg/day PO q8h, max: 900 mg/dose''''' <BR> OR <BR> ▸ '''''[[Levofloxacin]]  16 mg/kg/day PO q12h, max: 250 mg/dose (<50 kg)'''''<BR> OR <BR> ▸ '''''[[Levofloxacin]]  500 mg PO q24h (≥50 kg)'''''
|-
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Alternative Regimen
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Amoxicillin]] 75 mg/kg/day PO q8h, max: 1 g/dose''''' <BR> OR <BR> ▸ '''''[[Penicillin VK]] 50–75 mg/kg/day PO q6–8h'''''
|}
|}


{| class="mw-collapsible mw-collapsed" id="mw-customcollapsible-table03" style="background: #FFFFFF;"
::::* 3.1.2 '''For 34–37 week gestational age'''
| valign=top |
:::::* 3.1.2.1 '''For < 1 week of age'''
{| style="float: left; cellpadding=0; cellspacing= 0; width: 450px;"
::::::* Preferred regimen (1): [[Ciprofloxacin]] 20 mg/kg/day, PO, bid
! style="height: 30px; line-height: 30px; background: #4479BA; border: 0px; font-size: 100%; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5);" align=center | {{fontcolor|#FFF|Postexposure Prophylaxis, Pregnant Patients}}
::::::* Preferred regimen (2): [[Clindamycin]] 15 mg/kg/day, PO, tid
|-
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Preferred Regimen
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Ciprofloxacin]] 500 mg PO q12h'''''
|}
|}


|}
:::::* 3.1.2.2 '''For 1–4 week of age''
::::::* Preferred regimen (1): [[Ciprofloxacin]] 20 mg/kg/day, PO, bid
::::::* Preferred regimen (2): [[Clindamycin]] 20 mg/kg/day, PO, id


::::* 3.1.3 '''Term newborn infant'''
:::::* 3.1.3.1 '''For < 1 week of age '''
::::::* Preferred regimen (1): [[Ciprofloxacin]] 30 mg/kg/day, PO, bid
::::::* Preferred regimen (2): [[Doxycycline]] 4.4 mg/kg/day, PO, bid (Loading dose 4.4 mg/kg)
::::::* Preferred regimen (3): [[Clindamycin]] 15 mg/kg/day, PO, tid


:::::* 3.1.3.2 '''For 1–4 week of Age'''
::::::* Preferred regimen (1): [[Ciprofloxacin]] 30 mg/kg/day, PO, bid
::::::* Preferred regimen (2): [[Doxycycline]] 4.4 mg/kg/day, PO, bid (Loading dose 4.4 mg/kg)
::::::* Preferred regimen (3): [[Clindamycin]] 20 mg/kg/day, PO, qid


==Precautions==
:::* 3.2 '''Alternatives for penicillin-susceptible strains'''
* If a person is suspected as having died from anthrax, every precaution should be taken to avoid skin contact with the potentially contaminated body and fluids exuded through natural body openings. The body should be put in strict quarantine and then cremated.  
::::* 3.2.1 '''For 32–34 weeks gestational age'''
:::::* 3.2.1.1 '''For < 1 week of age'''
::::::* Alternative regimen (1): [[Amoxicillin]] 50 mg/kg/day, PO, bid
::::::* Alternative regimen (2): Penicillin Vk  50 mg/kg/day, PO, bid


* Microscopic visualization of the encapsulated bacilli, usually in very large numbers, in a [[blood smear]] stained with polychrome methylene blue (McFadyean stain) is [[diagnostic]], although culture of the organism is still the gold standard for diagnosis.
:::::* 3.2.1.2 '''For 1–4 week of age'''
::::::* Alternative regimen (1): [[Amoxicillin]] 75 mg/kg/day, PO, tid
::::::* Alternative regimen (2): Penicillin Vk 75 mg/kg/day, PO, tid


* Full isolation of the body is important to prevent possible contamination of others. Protective, impermeable clothing and equipment such as [[rubber glove]]s, rubber apron, and rubber boots with no perforations should be used when handling the body. No skin, especially if it has any wounds or scratches, should be exposed. Disposable personal protective equipment is preferable, but if not available, decontamination can be achieved by autoclaving. Disposable personal protective equipment and filters should be autoclaved, and/or burned and buried.
::::* 3.2.2 '''For 34–37 week gestational age'''
:::::* 3.2.2.1 '''For < 1 week of age'''
::::::* Alternative regimen (1): [[Amoxicillin]] 50 mg/kg/day, PO, bid
::::::* Alternative regimen (2): Penicillin Vk 50 mg/kg/day, PO, bid


* Anyone working with anthrax in a suspected or confirmed victim should wear respiratory equipment capable of filtering this size of particle or smaller.<ref>National Personal Protective Technology Laboratory [http://www.cdc.gov/niosh/npptl/default.html Respirators]. National Institute for Occupational Safety and Health. 30 April 2009.</ref>
:::::* 3.2.2.2 '''For 1–4 week of age'''
::::::* Alternative regimen (1): [[Amoxicillin]] 75 mg/kg/day, PO, tid
::::::* Alternative regimen (2): Penicillin Vk  75 mg/kg/day, PO, tid


* All possibly contaminated bedding or clothing should be isolated in double plastic bags and treated as possible biohazard waste. The victim should be sealed in an airtight body bag. Dead victims who are opened and not burned provide an ideal source of anthrax spores. Cremating victims is the preferred way of handling body disposal. No embalming or autopsy should be attempted without a fully equipped biohazard laboratory and trained, knowledgeable personnel.
::::* 3.2.3 '''Term newborn infant'''
:::::* 3.2.3.1 '''For < 1 week of age'''
::::::* Alternative regimen (1): [[Amoxicillin]] 75 mg/kg/day, PO, tid
::::::* Alternative regimen (2): Penicillin Vk 75 mg/kg/day, PO, tid


Delays of only a few days may make the disease untreatable, so treatment should be started even without symptoms if possible contamination or exposure is suspected.
:::::* 3.2.3.2 '''For 1–4 week of age'''
::::::* Alternative regimen (1): [[Amoxicillin]] 75 mg/kg/day, PO, tid
::::::* Alternative regimen (2): Penicillin Vk 75 mg/kg/day, PO, id or tid
::::::* Note: Duration of therapy is  60 days from exposure


* Initial symptoms may resemble a common cold—sore throat, mild fever, muscle aches, and malaise. After a few days, the symptoms may progress to severe breathing problems and shock, and ultimately death.
==Dealing with Victims==
 
In order to prevent [[infection]] and [[transmission]] of the [[Ebola|virus]], several measures should be implemented, particularly when handling victims of anthrax infection, including:
Early detection of sources of anthrax infection can allow preventive measures to be taken. In response to the anthrax attacks of October 2001, the [[United States Postal Service]] (USPS) installed biodetection systems (BDSs) in their large-scale mail cancellation facilities. BDS response plans were formulated by the USPS in conjunction with local responders including fire, police, hospitals and public health. Employees of these facilities have been educated about anthrax, response actions, and [[prophylaxis|prophylactic]] medication. Because of the time delay inherent in getting final verification that anthrax has been used, prophylactic antibiotic treatment of possibly exposed personnel must be started as soon as possible.
* All possibly contaminated bedding or clothing of [[infected]] patients should be isolated in double plastic bags and treated as possible biohazard waste.
* If a person is suspected of having died from [[anthrax]], every precaution should be taken to avoid [[skin]] contact with the potentially contaminated body. The body should be put in strict quarantine, sealed in an airtight body bag and then cremated. No embalming or autopsy should be attempted without a fully equipped biohazard laboratory and trained, knowledgeable personnel.
* Full isolation of the body is important to prevent possible contamination of others. Protective, impermeable clothing and equipment such as [[rubber glove]]s, rubber apron, and rubber boots with no perforations should be used when handling the body. No skin, especially if it has any wounds or scratches, should be exposed. Disposable personal protective equipment is preferable, but if not available, decontamination can be achieved by autoclaving. 
* Anyone working with anthrax in a suspected or confirmed victim should wear respiratory equipment capable of filtering this size of particle or smaller.<ref>National Personal Protective Technology Laboratory [http://www.cdc.gov/niosh/npptl/default.html Respirators]. National Institute for Occupational Safety and Health. 30 April 2009.</ref>


==References==
==References==
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: João André Alves Silva, M.D. [2]

Overview

Prevention of anthrax infection can be achieved with post-exposure prophylaxis antibiotics and vaccination. The US Advisory Committee on Immunization Practices recommended 60 days of antibiotic drug prophylaxis for immediate protection and a 3-dose series of Anthrax Vaccine Adsorbed (AVA) for long-term protection. Postexposure prophylaxis of asymptomatic persons should start as soon as possible after exposure because its effectiveness decreases with delay in implementation. Everyone exposed to aerosolized B. anthracis spores should receive a full 60 days of post-exposure prophylaxis antimicrobial drugs, whether they are unvaccinated, partially vaccinated, or fully vaccinated. Protective measures should also be implemented to prevent the transmission of the disease.[1]

Primary Prevention

Well-timed and effective postexposure prophylaxis can potentially save thousands of lives. Postexposure prophylaxis of asymptomatic persons should start as soon as possible after exposure because its effectiveness decreases with delay in implementation. Initial symptoms may resemble a common cold, including sore throat, mild fever, myalgia, and malaise. After a few days, the symptoms may progress to severe breathing problems shock, and ultimately death.[2] After exposure to anthrax, it is recommended 60 days of antibiotic drug prophylaxis for immediate protection and a 3-dose series of Anthrax Vaccine Adsorbed (AVA) for long-term protection.[1]

Antibiotic Drugs

To ensure adequate and continued protection, everyone exposed to aerosolized Bacillus anthracis spores should receive a full 60 days of postexposure prophylaxis antibiotic drugs, whether they are unvaccinated, partially vaccinated, or fully vaccinated.[2]

Ciprofloxacin, levofloxacin, and doxycycline are FDA-approved for the antibiotic drug portion of postexposure prophylaxis for inhalation anthrax in adults ≥18 years of age.

No safety data are available for levofloxacin use beyond 30 days; thus, oral ciprofloxacin and doxycycline are recommended as first-line antibiotic drugs for postexposure prophylaxis. Alternative antibiotic drugs that might be used for postexposure prophylaxis, if first-line agents are not tolerated or are unavailable, include:[2]

Vaccine

Despite the existence of a vaccine licensed to prevent anthrax, it is not typically available for the general public. It protects against cutaneous and inhalation anthrax. There is evidence of seroconversion after 3 doses of Anthrax Vaccine Adsorbed (AVA). The vaccine should be administered subcutaneously at diagnosis, and 2 and 4 weeks later.[1] AVA is not FDA-approved for postexposure prophylaxis and could be made available under an Investigational New Drug protocol or an Emergency Use Authorization in a declared emergency.

Anthrax vaccine is indicated for the following risk groups of adults:[3]

  • Laboratory workers who work with anthrax
  • People who handle animals or animal products
  • Members of the United States military

Prophylaxis Regimen

  • Bacillus anthracis, postexposure prophylaxis
  • 1. For adults[4]
  • 1.1 For all strains, regardless of penicillin susceptibility or if susceptibility is unknown
  • 1.2 Alternatives for penicillin-susceptible strain
  • Preferred regimen (1): Amoxicillin 1 g IV q8h
  • Preferred regimen (2): Penicillin VK 500 mg IV q6h
  • 2. For children = 1 month[5]
  • 2.1 For penicillin-resistant strains or prior to susceptibility testing
  • Preferred regimen (1): Ciprofloxacin 30 mg/kg/day, PO, bid (not to exceed 500 mg/dose)
  • Preferred regimen (2):
  • If patients body weight < 45 kg: Doxycycline 4.4 mg/kg/day, PO, bid (not to exceed 100 mg/dose)
  • If patients body weight > 45 kg: Doxycycline 100 mg/dose, PO, bid
  • Preferred regimen (3): Clindamycin 30 mg/kg/day, PO, tid (not to exceed 900 mg/dose)
  • Preferred regimen (4):
  • If patients body weight < 50 kg: Levofloxacin 16 mg/kg/day, PO, bid (not to exceed 250 mg/dose)
  • If patients body weight > 50 kg: Levofloxacin 500 mg, PO, qd
  • 2.2 For penicillin-susceptible strains
  • Preferred regimen (1): Amoxicillin 75 mg/kg/day, PO, tid (not to exceed 1 g/dose)
  • Preferred regimen (2): Penicillin VK 50-75 mg/kg/day, PO, id or tid
  • Note: Duration of Therapy is 60 days after exposure
  • 3. For children < 1 month
  • 3.1 For all strains, regardless of penicillin susceptibility or if susceptibility is unknown
  • 3.1.1 For 32–34 weeks gestational age
  • 3.1.1.1 For < 1 week of Age
  • 3.1.1.2 For 1–4 week of age
  • 3.1.2 For 34–37 week gestational age
  • 3.1.2.1 For < 1 week of age
  • 3.1.2.2 'For 1–4 week of age
  • 3.1.3 Term newborn infant
  • 3.1.3.1 For < 1 week of age
  • Preferred regimen (1): Ciprofloxacin 30 mg/kg/day, PO, bid
  • Preferred regimen (2): Doxycycline 4.4 mg/kg/day, PO, bid (Loading dose 4.4 mg/kg)
  • Preferred regimen (3): Clindamycin 15 mg/kg/day, PO, tid
  • 3.1.3.2 For 1–4 week of Age
  • Preferred regimen (1): Ciprofloxacin 30 mg/kg/day, PO, bid
  • Preferred regimen (2): Doxycycline 4.4 mg/kg/day, PO, bid (Loading dose 4.4 mg/kg)
  • Preferred regimen (3): Clindamycin 20 mg/kg/day, PO, qid
  • 3.2 Alternatives for penicillin-susceptible strains
  • 3.2.1 For 32–34 weeks gestational age
  • 3.2.1.1 For < 1 week of age
  • Alternative regimen (1): Amoxicillin 50 mg/kg/day, PO, bid
  • Alternative regimen (2): Penicillin Vk 50 mg/kg/day, PO, bid
  • 3.2.1.2 For 1–4 week of age
  • Alternative regimen (1): Amoxicillin 75 mg/kg/day, PO, tid
  • Alternative regimen (2): Penicillin Vk 75 mg/kg/day, PO, tid
  • 3.2.2 For 34–37 week gestational age
  • 3.2.2.1 For < 1 week of age
  • Alternative regimen (1): Amoxicillin 50 mg/kg/day, PO, bid
  • Alternative regimen (2): Penicillin Vk 50 mg/kg/day, PO, bid
  • 3.2.2.2 For 1–4 week of age
  • Alternative regimen (1): Amoxicillin 75 mg/kg/day, PO, tid
  • Alternative regimen (2): Penicillin Vk 75 mg/kg/day, PO, tid
  • 3.2.3 Term newborn infant
  • 3.2.3.1 For < 1 week of age
  • Alternative regimen (1): Amoxicillin 75 mg/kg/day, PO, tid
  • Alternative regimen (2): Penicillin Vk 75 mg/kg/day, PO, tid
  • 3.2.3.2 For 1–4 week of age
  • Alternative regimen (1): Amoxicillin 75 mg/kg/day, PO, tid
  • Alternative regimen (2): Penicillin Vk 75 mg/kg/day, PO, id or tid
  • Note: Duration of therapy is 60 days from exposure

Dealing with Victims

In order to prevent infection and transmission of the virus, several measures should be implemented, particularly when handling victims of anthrax infection, including:

  • All possibly contaminated bedding or clothing of infected patients should be isolated in double plastic bags and treated as possible biohazard waste.
  • If a person is suspected of having died from anthrax, every precaution should be taken to avoid skin contact with the potentially contaminated body. The body should be put in strict quarantine, sealed in an airtight body bag and then cremated. No embalming or autopsy should be attempted without a fully equipped biohazard laboratory and trained, knowledgeable personnel.
  • Full isolation of the body is important to prevent possible contamination of others. Protective, impermeable clothing and equipment such as rubber gloves, rubber apron, and rubber boots with no perforations should be used when handling the body. No skin, especially if it has any wounds or scratches, should be exposed. Disposable personal protective equipment is preferable, but if not available, decontamination can be achieved by autoclaving.
  • Anyone working with anthrax in a suspected or confirmed victim should wear respiratory equipment capable of filtering this size of particle or smaller.[6]

References

  1. 1.0 1.1 1.2 Wright JG, Quinn CP, Shadomy S, Messonnier N, Centers for Disease Control and Prevention (CDC) (2010). "Use of anthrax vaccine in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2009". MMWR Recomm Rep. 59 (RR-6): 1–30. PMID 20651644.
  2. 2.0 2.1 2.2 "Centers for Disease Control and Prevention Expert Panel Meetings on Prevention and Treatment of Anthrax in Adults".
  3. "Prevention".
  4. Hendricks KA, Wright ME, Shadomy SV, Bradley JS, Morrow MG, Pavia AT; et al. (2014). "Centers for disease control and prevention expert panel meetings on prevention and treatment of anthrax in adults". Emerg Infect Dis. 20 (2). doi:10.3201/eid2002.130687. PMC 3901462. PMID 24447897.
  5. Bradley JS, Peacock G, Krug SE, Bower WA, Cohn AC, Meaney-Delman D; et al. (2014). "Pediatric anthrax clinical management". Pediatrics. 133 (5): e1411–36. doi:10.1542/peds.2014-0563. PMID 24777226.
  6. National Personal Protective Technology Laboratory Respirators. National Institute for Occupational Safety and Health. 30 April 2009.

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