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Coule, M.D.O =7:#Chemical and Biological Terrorism$$0oPhillip L. Coule, M.D. Medical College of Georgia Assist. Professor of Emergency Medicine Director, EMS and ECC$p YJ5  ObjectivesReview history and define Nuclear, Chemical and Biological Terrorism Review previous ChemBio events Overview of CDC Class A bioterrorism agents Overview of chemical agents and toxins Types of nuclear terrorist events Specific information on agents,W o  Definitions`Nuclear, Biological or Chemical agents to terrorize attack or terrorize a population NBC  nuclear, biological, chemical  Biochem  Chembio WMD  Weapons of Mass Destruction 6U[U[,z% Other TermsNBC  nuclear, biological, chemical  Biochem  Chembio WMD  Weapons of Mass Destruction,%$P:Biological terrorismkDispersal of microbes or their toxins to produce illness, death and terror Microbes Bacteria Viruses Toxins&TTIs this something new?14th Century  Kaffa City on Crimean Peninsula Strategic to Silk trade routes between China and Europe Rival trade groups captured city Multiple unsuccessful attempts to retake city Hurled plague infested corpses over walls of city to infest it<ZZ?Z?Is this something new?18th Century French and Indian War British Officers gave blankets from smallpox victims to indians aligned with French Caused an epidemic in tribes Effective means of incapacitating group8$ \YBioterroism- the 20th Century$  i1943 US Biological Warfare program 1953 Defensive program established 1969 Offensive program disbandedt  NBC Events since 1970 >1972-  Order of the Rising Sun Possession of 30-40 kg of Typhoid Cultures Were going to poison water supplies of Chicago, St Louis, and other large Midwestern cities Thwarted by FBI:1984  Bhagwan Shree RajneeshThe Dalles, Oregon fall 1984 Sprayed Salmonella on salad bars at 10 restaurants Attempt to sway local election by decreasing turnout of voters 751 Ill 45 Hospitalized 0 fatalitiesZ41990 s Aum Shinrinkyo CultAttempted release of Anthrax on at least 8 occasions- no illness Sarin Subway Attack 1995- 5,510 affected Dead 8 Critical 17 Severe 37 Moderate 984 Outpatient 4,073 Unknown 391 .jZIZjIAlIdeal Biological WeaponEasy to manufacture/obtain Lethality / Incapacitation Easy to store Easy to deliver to target in large quantities large population  particle size Highly infective / contagious Incubation period Fear factor - untreatable  Q<CDC Threat ClassificationCategory A Agents that pose a threat to National Security Easily disseminated or transmitted from person to person Cause high mortality  public health impact Public panic / Social disruption Require special action for PH preparedness&::T>CDC Threat ClassificationCategory B Moderately easy to disseminate Moderate morbidity and low mortality Require specific enhancement of CDC and PH surveillanceU?CDC Threat ClassificationEmerging pathogens that could be engineered for mass dessemination Availability Ease of production and dissemination Potential for high morbidity and mortality and major health impact 5v hCDC Critical Biological Agents  Category A - Viruses55 R;jCDC Critical Biological Agents  Category A - Bacteria66 S=hCDC Critical Biological Agents  Category A - Toxins55V@LCDC Threat Classification  Category BWA>CDC Classification  Category CXBChemical AgentsBlister / vesicants Cellular Respiration poisons Choking/ Pulmonary agents Incapacitating Agents Nerve Agents Riot Control / Tear Gases Emetic agentsYC5Comparison of Bioterrorism Toxins and Chemical Agents ZD7Comparison of Bioterrorism Toxins and Chemical Agents-2 [EChemical Terrorism Agents \F:Chemical Terrorism Agents  2O9Nuclear Terrorism  AnthraxH_Gram positive bacillus Spore Forming 1 micron spore size Spores are persistent in soil >100 yrs*`0 " dZ2`)#BotulismToxin produced by Clostridium botulinum Lethal dose is 1 ng/kg Neurotoxin Incubation 1-5 D (foodborne), blocks cholinergic synapses Diplopia, weakness, paralysis Death from respiratory failure Tx: ventilatory support, trivelant antitoxin* !   5  *$0Plague  Yersinia pestis  |Gram negative coccobacillus (rods) Two forms: Bubonic plague Pneumonic plague Can occur naturally, but usually as bubonic Sx s fever, cough with mucopurulent sputum, hemoptysis, chest painL. 3>. 3>P_   /&Plague - PathogenesisConsumed by macrophages transported to regional lymph nodes regional adenitis Bacteremia  spread Lungs Spleen Liver BrainT==F"1(2Pneumonic Plague Prevention of Secondary InfectionSecondary transmission is possible and likely Standard, contact, and aerosol Until sputum cultures are negative pneumonic plague is excluded PNA.A2)$Pneumonic Plague Signs and Symptoms2 to 3 day incubation High fever, myalgias, chills, HA, and cough and bloody sputum Pneumonia and sepsis develop acutely Dyspnea, stridor, cyanosis, circulatory collapse Patchy infiltrates or consolidation CXR Suspicion for lobar pneumonia out of season.UPXZTP,zv3+"Bubonic Plague Signs and Symptoms Erythema, fever, rigors Bubo formation in regional lymph nodes Bubo aspiration and gram stain is diagnostic Differentiate from Tularemia Cat-scratch fever Staph-strep lymphadenitis:l6l64*Acral Gangrene gAcral gangrene Late complication of pneumonic or septicemic plague Fingers Toes Earlobes Nose Penis. <Z4Z$Z4$$, ,5,Plague - TreatmentBCare is otherwise supportive Vaccine effective only for bubonic plague Prophylaxis - tetracycline or doxycycline Antibiotics must be started within 24 hours of symptoms to impact survival Streptomycin (30 mg/kg/day IM divided BID for 10 days) Doxycycline (100 mg IV BID for 10 days) Chloramphenicol for plague meningitis>rFK0FFC6-Smallpox - MicrobiologyVariola (Var--la) virus, an Orthopox virus, both minor and major forms of smallpox exist Structure is a large DNA virus Declared eradicated in 1980 and the U.S. stopped its civilian vaccination in 1981, U.S. military stopped in 1985H A0B1VHF PathogenesisFever, myalgias, prostration Shock, mucous membrane hemorrhage Conjunctival injection, petechial hemorrhage, and hypotension Abnormal renal and LFT - poor prognosis Mortality varies; 50 - 80% Ebola Zaire Disease severity and survival host factors target organ is the vascular bed.Dn/n/>>   C2 VHF TreatmentZ4Hemodynamic resuscitation and monitoring Invasive Swan Ganz catheter as feasible Careful fluid management use of colloid Vasopressors and cardiotonic drugs Cautious sedation and analgesia No anti-platelet drugs or IM injections Coagulation studies and replacement of clotting factors / platelet transfusionsj)P)PPPP))>7>  D3(Prevention of Secondary VHF Transmission)Z)SNo vaccine is available at this time Single room w/ adjoining anteroom as only entrance handwashing facility with decontamination solution Negative air pressure if possible Strict barrier precautions gloves, gown, mask. shoe covers, protective eyeware/faceshield consider HEPA respirator for prominent hemorrhage, vomiting, diarrhea, coughrXZ3Z=ZZ$33=>W  NE4Isolation Precautions~Anthrax: Standard Plague: Respiratory (X 48 hrs) then droplet Smallpox: Respiratory Tularemia: Standard Brucellosis: Standard L7SummaryBioterrorism is not new, just more prevalent Diseases of greatest concern Anthrax Botulism Tularemia Plague Smallpox VHF s Disaster preparedness should focus on all threats Chemical Agents Nuclear Threats\JZ1Z2Z ZJ12  ]G/9;<=>?@FG H l ` 33ff̙` 3f3f` ___>?" dd@,?nKd@ u< t@ " d`  n?" dd@   @@``@n?" dd@  @@``PV    @ ` `p>> 0 &(6(   T   "r  B2? 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S   6 `P   \*  Z     6 `   ^*" Z  H   0޽h ? ̙33p @8(    0  P    d*  Z   0$     f*" Z   6 `P   d*  Z   6 `   f*" Z H  0޽h ? ̙33w9  l(  lr l S "   r l S #      l 0 OAn Overview of the Threat(20 l C AC:\Documents and Settings\pcloak\My Documents\My Pictures\newpic\slide1.jpgp l C AC:\Documents and Settings\pcloak\My Documents\My Pictures\newpic\slide1-a.jpg`  H l 0޽h ? 33ff̙  IA|(  | | Tlgֳgֳ ?"p I E Expert??? 8 Z2 0 | T0"gֳgֳ ?"@ W  PAfter September 11?  8 Z20 | C AC:\Documents and Settings\pcloak\My Documents\My Pictures\newpic\slide3.jpg H | 0޽h ? 33ff̙ 9 p$(  pr p S &"`   r p S ''  H p 0޽h ? 33ff̙  $(  r  S +"`0   r  S ,'  H  0޽h ? 33ff̙  $(  r  S 3"P   r  S <4'  H  0޽h ? 33ff̙  $(  r  S 9"P   r  S p:'  H  0޽h ? 33ff̙  t$(  tr t S >"P   r t S ?'  H t 0޽h ? 33ff̙  $(  r  S xF"P   r  S  G'  H  0޽h ? 33ff̙  $(  r  S hN"P   r  S $O'  H  0޽h ? 33ff̙  ?7 &,(   , C AC:\Documents and Settings\pcloak\My Documents\My Pictures\newpic\slide10.jpgfr  S ^"`0   p  Hd?0  p  Hd?0  p  HLd?0    Hgֳgֳ?d J 1972 Typhoid"  Z   N_ֳֳֳֳ1?. . fMarch 1995 Sarin     N d1?.  R12 Dead, 5500 Affected  pB  H8c?` UUP pB  H8c?`  pB  H8c?` P pB  H8c?`  pB  H8c?` @ pB  H8c?`   Nhֳֳֳֳ1?  \ November 1995 Radioactive Cesium ! !  Nlmֳֳֳֳ1?I s  ODecember 1995 Ricin    Npֳֳֳֳ1? p  MJune 1996 Uranium    N uֳֳֳֳ1? `   H 1992 Cyanide     NTxֳֳֳֳ1?   LMarch 1995 Ricin    N|ֳֳֳֳ1? Y   fApril 1995 Sarin     Nֳֳֳֳ1? P k/April-June 1995 Cyanide, Phosgene, Pepper Spray 0 0  Nԃ1? RFebruary 1997 Chlorine    Np1? U14 Injured, 500 Evacuated    Nֳֳֳֳ1?S.  eJune 1994 Sarin     N1?w. { O7 Dead, 200 Injured  pB  H8c?UU   N@ֳֳֳֳ1?\ KMay 1995 Plague    Nֳֳֳֳ1?- KApril 1997 U235   ! 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Questions? 8 Z20  C AC:\Documents and Settings\pcloak\My Documents\My Pictures\newpic\slide14.jpg'H  0޽h ? 33ff̙  `$(  r  S ϼ"P   r  S м'  H  0޽h ? 33ff̙  J B P  (  n  Z*xaxa?  818-20 15-18 7-12 4-6 (bronchioles) 1-5 (alveoli)  P Z  2   T/xaxa?p NInfection Severity 8 Z2  T9xaxa?A w-Particle Size (Micron, Mass Median Diameter)..8 Z2 W  T<xaxa?P   }The ideal aerosol contains a homogeneous population of 2 or 3 micron particulates that contain one or more viable organisms:~( 2u  T4Bxaxa? b9 ZMaximum human respiratory infection is a particle that falls within the 1 to 5 micron size[( 2[  TFxaxa?E ]!Less Severe More Severe " "   S BCDE,F4@? 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B  Zgֳgֳo ?"@@ B  Tgֳgֳ1 ?"* @* H  0޽h ? 33ff̙  $(  r  S F"P   r  S L+'  H  0޽h ? 33ff̙  ,0(  r  S L"P   r 0p + #"*PPPpP@0p   ZTgֳgֳ ?" p _Vapor or aerosol delivery @`  Z\gֳgֳ ?"0  VAerosol delivery @`  Zdgֳgֳ ?" p p  S Many volatile @`  Zlgֳgֳ ?"0p  S None volatile @`   Ztgֳgֳ ?" pp  h"Large-scale, industrial production## @`   Z<|gֳgֳ ?"0 p  g!Difficult, small-scale production"" @`   Z0gֳgֳ ?" p  ZGenerally less toxic @`  Z$gֳgֳ ?"0  ZGenerally more toxic @`  Zgֳgֳ ?" `p NMan-made   @`  Zgֳgֳ ?"0`  TNatural origin @`   `gֳgֳ?" p` NChemical   @`   `gֳgֳ?"0 ` LToxins @`B   Zgֳgֳo ?"0pB   Tgֳgֳ1 ?"0`p`B  Tgֳgֳ1 ?"0pB  Tgֳgֳ1 ?"0 p B  Zgֳgֳo ?"0pB  Zgֳgֳo ?"00B  Tgֳgֳ1 ?"  B  Zgֳgֳo ?"ppB  Tgֳgֳ1 ?"0p pp B  Tgֳgֳ1 ?"0 p  , Tgֳgֳ ?"0 C H Source: AHLS 8 Z2 H  0޽h ? 33ff̙ 9 !(  r  S T"P   n 0`    #"&PPPpP0`   Zpgֳgֳ ?" p `  wPoor immunogens  @`!  Zgֳgֳ ?"0p  Many effective immunogens  @`  Zgֳgֳ ?" `p  _No legitimate medical use @`   Zgֳgֳ ?"0 p  ]Legitimate medical uses @`   Zgֳgֳ ?" `  oDermally active  @`   Z$gֳgֳ ?"0  |Not dermally active*  @`   Zgֳgֳ ?" `` _Noticeable order or taste @`   Zgֳgֳ ?"0`  ]Odorless and taste less @`   `gֳgֳ?" `` NChemical   @`   `pgֳgֳ?"0 ` LToxins @`B  Zgֳgֳo ?"0`B  Tgֳgֳ1 ?"0```B  Tgֳgֳ1 ?"0`B  Tgֳgֳ1 ?"0 ` B  Zgֳgֳo ?"0 ` B  Zgֳgֳo ?"00 B  Tgֳgֳ1 ?"  B  Zgֳgֳo ?"`` B  Tgֳgֳ1 ?"0p `p   Tgֳgֳ ?"0 f,* Exceptions, trichothecene (T-2) mycotoxins-0 Z2- ! 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P a TNuclear Weapon @`   Z(gֳgֳ ?"P   o)Disabling nuclear reactors cooling system** @`   Z$0gֳgֳ ?"P  ^Nuclear Reactor Sabotage @`   Z7gֳgֳ ?"P K ~8Spreading radioactive Material w/ conventional explosion99 @`   Z?gֳgֳ ?"KP  cRadiological Dispersal Device @`  Z@gֳgֳ ?"P K |6Dispersal of plutonium through bldg ventilation system77 @`  ZOgֳgֳ ?"P K `Simple Radiological Device @`  ZVgֳgֳ ?"P  MExample @`  ZXgֳgֳ ?"P  JName @`B   Zgֳgֳo ?"B  Tgֳgֳ1 ?"B  Tgֳgֳ1 ?"KKB  Tgֳgֳ1 ?"B  Zgֳgֳo ?"aaB  Zgֳgֳo ?"aB  Tgֳgֳ1 ?"P P aB  Zgֳgֳo ?"aB % Tgֳgֳ1 ?"   3 Tagֳgֳ ?"p E More likely 8 Z2  4 Thegֳgֳ ?" h E Less Likely 8 Z2 B 5  fgֳgֳD?"    9 TTigֳgֳ ?"0 C H Source: AHLS 8 Z2 H  0޽h ? 33ff̙ 9  P|(  |r | S o"    |  h0e0e ?'"  H | 0޽h ? 33ff̙  `$(  r  S tt"P   r  S 0u'  H  0޽h ? 33ff̙  p$(  r  S y"P   r  S Tz'F  H  0޽h ? 33ff̙  $(  r  S D"P   r  S Ԁ'  H  0޽h ? 3(  TL(    c ggggf ?"P     C xgֳgֳ ?'p  H  0޽h ? 3(  TL$(  $ $ c PgMgMf ?"    $ C x gֳgֳ ?'  H $ 0޽h ? 3(  4$(  4r 4 S "P   r 4 S x'  H 4 0޽h ? 3( 9 vn ,(  ,r  , S H""P   r  , S "'A     , C A C:\Documents and Settings\pcloak\My Documents\My Pictures\newpic\slide38.jpg H , 0޽h ? 3(  )! <(  < < c gMgMf ?"P    < C xx?gֳgֳ ?'y>   < Z Bxaxa?+  > 2  < TDgֳgֳ8c? r yCRespiratory isolation mandatory for the first 48 hours of treatmentD DH < 0޽h ? 3(  @D$(  Dr D S f"P   r D S Xg'  H D 0޽h ? 3( ME`X(  X X  fb1? JClose-up Smallpox rash 2 X  f$g1? ECDC/Public domain 2 X C A C:\Documents and Settings\pcloak\My Documents\My Pictures\newpic\slide41.jpg H X 0޽h ? f33  TL`\(  \ \ c ԃgMgMf ?"    \ C xgֳgֳ ?'@  H \ 0޽h ? 3(  9 TLd(  d d c gMgMf ?"    d C xLxaxa ?'pp  H d 0޽h ? 3(   TLl(  l l c gMgMf ?"`    l C xtxaxa ?'  H l 0޽h ? 3(  t<(  t~ t s *"P   ~ t s *t'  H t 0޽h ? f33  $(  r  S "`   r  S '  H  0޽h ? 33ff̙ ogp(    C AC:\Documents and Settings\pcloak\My Documents\My Pictures\newpic\slide47.jpg&  Tqgֳgֳ ?" u J Questions?$ 8 Z2 B  Txugֳgֳ ?" Q  o www.adls.info$8 Z2$H  0޽h ? 33ff̙& 0 2(    N1 ?    3 r b b ?    *PATHOGENESIS Following inhalation, the organism is phagocytosed by alveolar macrophages, and bacterial multiplication at 37 degrees C causes a variety of cytotoxins and virulence factors to be secreted into the local tissue area. Bacterial multiplication continues in the regional lymph nodes, followed by systemic infection. The photograph demonstrates a dilated blood vessel inside human lymphoid tissue. Note the plague bacilli in the endothelial cells and vessel lumen. After skin inoculation, the bacteria is consumed by dermal macrophages that transport the organism to regional lymph nodes and then into the blood to infect secondary organs, such as the lungs, spleen, liver, and brain. "    &&::MMx  TdRԟRԟ1?&z rNOTE: Yersinia pestis is the most invasive bacteria known to medical science. Its high biological decay rate is offset by the organism s high propensity to cause secondary infections.6      !!33CCH  0޽h ? a(( 0 bZ (      N1 ?   $  3 r b b ?    jPREVENTION OF SECONDARY INFECTION Pneumonic plague may be highly communicable under appropriate climate conditions. For patients with confirmed pneumonic plague, respiratory droplet isolation with precautions against airborne spread is required until sputum cultures are negative. Accidental exposures to health care workers are managed by giving post-exposure tetracycline or doxycycline therapy for a minimum of 7 days. Vaccine is ineffective against aerosol exposures to plague. 8 ! u  J  &&::MMH   0޽h ? a() 0 TL((  ( ( N1 ?    (3 r\ b b ?    \SIGNS AND SYMPTOMS Two to three days after inhaling the plague organism, the patient will develop high fever, myalgias, chills, headache, cough with bloody sputum, and signs of overwhelming infection (including pneumonia). Chest x-ray may show patchy infiltrates or consolidation, with pneumonia progressing rapidly, causing dyspnea, stridor, and cyanosis. Eventual respiratory failure, circulatory collapse, and laboratory evidence of disseminated intravascular coagulation (DIC) develop. The photo on left shows right middle and lower lobe consolidation in pneumonic plague. Post-mortem lung on right shows necrotic nodules with intense hyperemia and intervening compensatory emphysema in pulmonary parenchyma, hemorrhage in the lower lobe. "    &&::MMH ( 0޽h ? a(* 0 0(  0 0 N1 ?   O 03 rt2 b b ?    'PLAGUE - ACRAL GANGRENE Acral gangrene may be a late complication in survivors. The bacterial coagulase gene is temperature sensitive and becomes active at temperatures less than 37 C, (such as at the extremities). Blood supply to these areas becomes interrupted and tissue death ensues. "(    (&&::MMH 0 0޽h ? a(c + 0 #  8 (  8 8 N1 ?     83 r b b ?    p Classical bubonic plague occurs from the bite of an infected flea. There is initial erythema, fever, and rigors which typically progress to overt bubo formation in regional lymph nodes. Septicemia normally develops 2 to 10 days later. Buboes may be aspirated, but should not be surgically drained; a gram stain of aspiration fluid can differentiate bubonic plague from tularemia, cat-scratch fever, and staph or strep lymphadenitis.    &&::MMQ 8 TRԟRԟ1?& gNOTE: In the bubonic form of plague, symptoms will also develop acutely after an incubation period of 2 to 3 days with victims developing malaise, high fevers, and one or more buboes or pus-filled, swollen, or tender lymph nodes. In less than 25 percent of the cases, various skin lesions (pustules, vesicles, and papules) will occasionally develop along the distribution of the lymph nodes (usually in the lower legs). Bubonic plague may progress spontaneously to the septicemic form with organisms spreading to the central nervous system (CNS), lungs, and beyond, and may also cause vasculitis, purpura, thrombosis and gangrene. Bubonic plague is not usually transmitted directly from person to person unless there is contact with pus from suppurating buboes (infected, enlarged lymph nodes). For patients with bubonic plague, universal precautions are indicated.h h  h !!33CCH 8 0޽h ? a(/, 0 0@(  @ @ N1 ?    @3 rT b b ?    TREATMENT - PNEUMONIC, BUBONIC, or SEPTICEMIC PLAGUE Respiratory isolation and secretion precautions are mandatory for the first 48 hours of treatment of bubonic or pneumonic plague. Treatment must be started within 24 hours of the onset of symptoms to impact patient survival in the pneumonic form of the disease. Plague pneumonia is almost always susceptible to streptomycin (30mg/kg/day IM divided twice daily for 10 days) and doxycycline (200 mg IV initially, followed by 100 mg twice daily for 10 days). Chloramphenicol is used for plague meningitis (50 - 75 mg/kg/day in 6 hourly divided doses). Care is otherwise supportive. Incision and drainage (I and D) of the lymph nodes is not recommended. After antibiotic treatment is started, the swollen tissue typically resolves on its own. A vaccine is available which is effective in preventing bubonic plague, but not the pneumonic form. " 5 U  &&::MMH @ 0޽h ? a(o- 0 /'PH(  H H N1 ?    H3 rl| b b ?    0SMALLPOX - MICROBIOLOGY Smallpox is caused by the Variola virus, an Orthopox virus, which caused both a major and minor form of the disease. The smallpox virus only causes overt clinical disease in humans, and no animal reservoirs of the virus exist in nature. This was the major reason why the disease was selected for global eradication. Smallpox was declared eradicated in 1980 and It is the only disease to date that has earned this distinction. The U.S stopped its civilian vaccination program in 1981. Despite eradication, concerns over clandestine stockpiles of smallpox still remain. The issue for destruction of U.S. laboratory stocks of the virus is under review. 8    s  &&::MM H TrRԟRԟ1?& {NOTE: The smallpox virus has an extremely low natural biological decay rate and a high secondary infection rate. It can easily be manufactured in large quantities. These factors make smallpox an ideal biological warfare agent when used against a non-immune human population.    !!33CCH H 0޽h ? a(F1 0 p`(  ` ` N1 ?h    `3 rȕ b b ?'    VHF - PATHOGENESIS Patients with VHF present initially with fever, myalgias, and prostration. Clinical evaluation may reveal conjunctival injection, petechial hemorrhages, and hypotension. Full-blown cases will evolve into shock and generalized mucous membrane hemorrhage with involvement of the respiratory, hematopoietic, and central nervous systems. Laboratory evaluation may reveal renal insufficiency, abnormal liver enzyme tests, and elevated bilirubin, all of which reflect a poor prognosis. There are differences between the numerous VHF strains; what is consistent among each of these viruses is that the target organ is the vascular bed, which causes widespread microvascular damage and changes in vascular permeability. The Marburg VHF has a 7 to 10 day incubation period, after which victims will experience the sudden onset of back and generalized muscle pain, headache, sore throat and nausea. A papular or macupapular skin rash will subsequently develop, followed by jaundice and the bleeding abnormalities characteristic of VHF. Pulmonary and gastrointestinal hemorrhage will progress to fatal severity, with encephalitis and fulminant hepatitis also likely.$0n   &&::MMH ` 0޽h ? a(2 0 hC(  h h N1 ?    h3 rPRԟRԟ ?    WVHF TREATMENT Treatment is largely supportive and typically requires intensive care monitoring to avoid fluid overload, while maintaining hemodynamic stability and providing appropriate comfort measures (sedation, pain medication). The acquired coagulopathy is typically difficult to counter. Based on animal models of the disease, full clotting factor assays should be performed and selective factor replacement and platelet transfusion may be considered. At this time there is no approved anti-viral medication for Marburg or Ebola virus infection and an effective vaccine awaits development. .X  I   X&&::MM h TRԟRԟ1?&n ^NOTE: Ribovirin is an antiviral medication that has shown effectiveness in treating other VHF disorders such as Congo Crimean Hemorrhagic Fever and Hemorrhagic Fever with Renal Syndrome (HFRS). Only Yellow Fever has an available effective vaccine.    !!33CCH h 0޽h ? a(p 3 0 0 ( p (  p p N1 ?     p3 r,RԟRԟ ?    8 VHF - PREVENTION OF SECONDARY TRANSMISSION Ebola and Marburg can be transmitted by body fluids, and aerosol transmission has been documented in animal models. The highest risk for secondary transmission is in the later stages of the disease when viral titers in the body are high and the patients may exhibit vomiting, bloody diarrhea, shock and hemorrhage. These diseases are known to spread in the hospital environment, so extreme care is necessary. Patients should be isolated in a single room with an adjoining anteroom that serves as the only entrance. The anteroom should be stocked with gloves, gowns, disposable aprons and masks for the staff. The patient s room should ideally have negative air pressure compared with the anteroom and outside hall and strict barrier-nursing techniques should be enforced. Transferring patients may increase the potential for secondary transmission. Ebola and Marburg Virus are inactivated with routine disinfectant solutions (MMWR Vol. 37, No. S-3, 2/26/88.) In previous outbreaks, simple barrier nursing was sufficient to reduce the health care provider infection rate to zero. 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