You are in: eMedicine Specialties > Emergency Medicine > WARFARE - CHEMICAL, BIOLOGICAL, RADIOLOGICAL, NUCLEAR AND EXPLOSIVES CBRNE - SmallpoxArticle Last Updated: Jul 16, 2008AUTHOR AND EDITOR INFORMATIONAuthor: Christopher J Hogan, MD, Assistant Professor, Department of Emergency Medicine, Medical College of Virginia/Virginia Commonwealth University Hospital Christopher J Hogan is a member of the following medical societies: American College of Emergency Physicians Coauthor(s): Fred Harchelroad, MD, FACMT, Chair, Department of Emergency Medicine, Director of Medical Toxicology, Department of Emergency Medicine, Associate Professor, Allegheny General Hospital Editors: Jerry L Mothershead, MD, Medical Readiness Consultant, Medical Readiness and Response Group, Battelle Memorial Institute; Advisor, Technical Advisory Committee, Emergency Management Strategic Healthcare Group, Veteran's Health Administration; Adjunct Associate Professor, Department of Military and Emergency Medicine, Uniformed Services University of the Health Sciences; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Rick Kulkarni, MD, Medical Director, Assistant Professor of Surgery, Section of Emergency Medicine, Yale-New Haven Hospital; John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center; Robert G Darling, MD, FACEP, Clinical Assistant Professor of Military and Emergency Medicine, Uniformed Services University of the Health Sciences, F Edward Hebert School of Medicine; Associate Director, Center for Disaster and Humanitarian Assistance Medicine Author and Editor Disclosure Synonyms and related keywords: smallpox, variola, variola major, variola minor, potential biological weapon, cowpox virus, orthopoxvirus genus, alastrim, hemorrhagic smallpox, flat smallpox, erythematous exanthem, smallpox vaccine, smallpox vaccination, smallpox immunization, Orthopoxvirus genus, INTRODUCTIONBackgroundSmallpox (variola) represents both the zenith and nadir of human achievement. It is the only disease that has been eradicated through a concerted and extensive effort that transcended political and ideologic boundaries. Because of these efforts, not one documented naturally occurring case of this infection, which once caused high mortality rates, has occurred since October 26, 1977. (The last naturally occurring case involved an unvaccinated hospital cook in For centuries, smallpox affected political and social agendas. Epidemics plagued Europe and In the Farr first accurately predicted variola infection rates in the 1830s. Once the disease and its method of spread were understood better, smallpox vaccination became mandatory in developed countries in the early 1900s. The development of the vaccinia virus and its subsequent vaccine enabled aggressive immunization by the WHO, which led to variola eradication in 1977. The variola virus no longer exists outside of a few laboratories around the world. The official virus repositories are at the Centers for Disease Control and Prevention (CDC) in Various sources from the former Variola, prior to eradication, carried a mortality rate of 30% in unvaccinated persons. Vaccination of the general population in the PathophysiologyVariola is a member of the Orthopoxvirus genus, of which cowpox, monkeypox, orf, and molluscum contagiosum are also members. Poxviruses are the largest animal viruses, larger than some bacteria. They have a large genome, composed of 200 kilobase (kb) double-stranded DNA enclosed in a double membrane layer. Poxviruses are the only viruses that can replicate in cell cytoplasm without the need of a nucleus. Although the variola virus was believed to infect only humans, infection has recently been elicited in cra-eating macaques when exposed to large amounts of injected and aerosolized virus, thus potentially providing an in vivo source of research that was previously unavailable. The virus is acquired from inhalation, although virus particles can remain viable on fomites (clothing, bedding, surfaces) for approximately 1 week. FrequencyUnited StatesNo recent case of systemic smallpox has been reported in the InternationalSince the last wild documented case in 1977, only 2 deaths from smallpox have been reported, one from a laboratory worker who infected her mother and the second from a photographer with an office next to the laboratory space where the accidental exposure to the virus occurred. Mortality/MorbidityVariola major, or smallpox, has an overall mortality rate of 30%. Variola minor, or alastrim, is a milder form of the virus, carrying a mortality rate of 1%. Four types of variola presentations exist: classic, hemorrhagic, malignant, and modified. Classic smallpox was believed to be the most communicable disease—approximately 30% of susceptible contacts became infected. The malignant and hemorrhagic forms of smallpox are not caused by unique variola strains but are thought to be due to host factors such as a deficient cellular immune response to the virus.
RaceNo racial predilection exists. SexWith the exception of pregnant women, males and females are infected in equal proportions. AgeNo age predilection exists, although mortality is higher in the extremes of age. In people who are unvaccinated, the distribution of illness mirrors that of the age distribution of the population. However, in India, prior to eradication, 70% of infections were in children younger than 14 years. CLINICALHistory
PhysicalCurrently, the clinical diagnosis of smallpox is based on several criteria.2 The major criteria are (1) a febrile prodrome 1-4 days before rash onset; (2) the classic smallpox lesions (ie, deep-seated, firm, round, well-circumscribed lesions); and (3) lesions that are at the same stage of development. The minor criteria include (1) a centrifugal distribution of lesions, with the first lesions on the oral mucosa or palate, face, or forearms; (2) a toxic or moribund appearance; (3) the slow evolution of lesions of 1-2 days per stage; and (4) lesions that appear on the palms and soles.
Causes
DIFFERENTIALSEczema vaccinatum Erythema Multiforme Molluscum Contagiosum Pediatrics, Chicken Pox or Varicella Scabies
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| Drug Name | Vaccinia virus vaccine (Dryvax) |
|---|---|
| Description | Vaccine contains live vaccinia virus but does not contain variola virus, which causes smallpox. Following inoculation, vaccine induces an immune reaction that serves to protect against smallpox. |
| Adult Dose | Using biohazard precautions, pick up a droplet of vaccine using bifurcated (eg, 2-pronged) needle (supplied with vaccine) and deposit on skin on upper arm; with same needle, prick skin percutaneously over droplet site 2-3 punctures for primary vaccination (15 punctures for revaccination) within a few seconds to allow vaccine to penetrate; wipe off any remaining vaccine from skin with sterile gauze and dispose in biohazard waste container; administration will create a sore and cause 1-2 droplets of blood to form |
| Pediatric Dose | Administer as in adults |
| Contraindications | Up to 50% of the US population would be excluded from a preemptive, voluntary vaccination program because they or close contacts have the following contraindications: documented hypersensitivity; eczema or atopic dermatitis and other acute, chronic, or exfoliative skin conditions; diseases, drugs, or conditions that cause immunodeficiency or immunosuppression; pregnancy and household contacts of pregnant women; infants <1 y; ACIP advises against nonemergent smallpox vaccination in children <18 y or in elderly persons; cardiovascular conditions (eg, history of myocardial infarction, angina, congestive heart failure, cardiomyopathy, stroke or transient ischemic attack, chest pain or shortness of breath with activity, any cardiac condition under the care of a physician) Note: No contraindications exist if patient was exposed to smallpox; contraindications exist only when vaccinating those without exposure. |
| Interactions | None reported |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Do not administer IM, IV, or SC; may cause rash (rare), fever, myalgias, or headache; soreness may occur at injection site; rare severe reactions include eczema vaccinatum, progressive vaccinia, or postvaccinal encephalitis; based on past experience, deaths due to severe reactions are estimated to occur in 1 person per million following primary vaccination and 1 person per 4 million for revaccination; vaccinia immune globulin IV is available from the CDC to treat extensive lesions following implantation, vaccinia necrosum, ocular exposure, eczema vaccinatum, and generalized vaccinia |
Immune globulins bind to the virus particle, stimulate an immune response, and offer transient protection while the host immune system develops antibodies. A new VIG is being developed. The IV route is anticipated to be the preferred method of administration, and new dosage recommendations (eg, lower dose than the current IM product) are expected. The new VIG contains low-aggregated protein levels, allowing IV or IM administration.
| Drug Name | Immune globulin (IVIG; Gammagard, Sandoglobulin, Gamimune) |
|---|---|
| Description | Can be administered within 3 d of exposure but is best if given within 24 h; may be necessary to administer VIG in adverse reactions to vaccination; because production of VIG ceased in 1970s, its efficacy (because of its age) is under question; in possession of the CDC |
| Adult Dose | 0.6 mL/kg IM for exposed individuals |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; IgA deficiency; anti-IgE/IgG antibodies |
| Interactions | Increases toxicity of live-virus vaccine (MMR); do not administer within 3 mo of vaccine |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Check serum IgA before IVIG (use an IgA-depleted product, eg, Gammagard S/D); infusions may increase serum viscosity and thromboembolic events; infusions may increase risk of migraine attacks, aseptic meningitis (10%), urticaria, pruritus, or petechiae (2-30 d postinfusion) Increases risk of renal tubular necrosis in elderly patients and in patients with diabetes, volume depletion, and preexisting kidney disease; laboratory result changes associated with infusions include elevated antiviral or antibacterial antibody titers for 1 mo, 6-fold increase in ESR for 2-3 wk, and apparent hyponatremia |
Indicated for passive immunity. VIG is the only drug available for amelioration of some vaccinia-related complications. VIG is produced from pooled human sera taken from vaccinia-immunized individuals and is available only from the CDC. VIG has been effective when administered early in cases of vaccinia necrosum and eczema vaccinatum. VIG has not been effective in cases of encephalopathy. The use of VIG for generalized vaccinia reactions is usually not necessary. Recently, VIGIV has been FDA approved.
| Drug Name | Vaccinia immune globulin intravenous, human (VIGIV) |
|---|---|
| Description | Derived from human plasma and manufactured from pooled plasma donors who received booster immunizations with smallpox vaccine (Dryvax). Contains increased antibody levels against vaccinia virus. Indicated to treat rare adverse reactions and aberrant infections caused by vaccinia virus, including aberrant infections (eg, accidental implantation in eyes, mouth, other potentially hazardous areas), eczema vaccinatum, progressive vaccinia, severe generalized vaccinia, and vaccinia infections in immunocompromised individuals. |
| Adult Dose | 100 mg/kg (2 mL/kg) IV infusion; may repeat depending on severity of symptoms and response to initial dose; may consider higher dose (200-500 mg/kg) if response to initial dose is inadequate (see Precautions) Infusion rate: 1 mL/kg/h for first 30 min, then 2 mL/kg/h for next 30 min, then 3 mL/kg/h for remaining infusion |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity to this or other human IVIGs; vaccinia keratitis; selective IgA deficiency |
| Interactions | Antibodies present in immune globulin preparations may interfere with immune response to live-virus vaccines (eg, polio, MMR); defer vaccination with live-virus vaccines for 6 mo following VIGIV administration; may alter immune response of vaccines administered shortly before VIGIV |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Caution in renal failure; general precautions for all IVIGs include aseptic meningitis, hemolysis (due to blood group antibodies), transfusion-related lung injury (pulmonary edema), and infections (eg, CJD); acute renal failure, osmotic nephrosis, proximal tubular nephropathy, and death may occur because of high sucrose levels (typically associated with doses >400 mg/kg/dose); call manufacturer to identify appropriate lot with low IgA level if administering to individual with selective IgA deficiency |
In vitro studies demonstrated cidofovir to inhibit poxvirus replication and cell lysis.
| Drug Name | Cidofovir (Vistide) |
|---|---|
| Description | In vitro studies demonstrated cidofovir to inhibit poxvirus replication and cell lysis. New research demonstrates that chemical inhibitors of host-signaling pathways exploited by viral pathogens may represent potent antiviral therapies. This drug must be used under an FDA Investigational New Drug (IND) protocol because it is not licensed for use as a treatment of smallpox. Cidofovir is a nucleoside analog DNA polymerase inhibitor; if administered within 48 h of exposure, may attenuate or avoid infection; adefovir, cidofovir, and ribavirin are under investigation for use in smallpox. Ribavirin as an aerosol treatment for pediatric respiratory syncytial virus is under investigation. |
| Adult Dose | 5 mg/kg IV over 1 h |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; coadministration with other nephrotoxic agents; serum creatinine level >1.5 mg/dL; CrCl <55 mL/min; urine protein level >100 mg/dL |
| Interactions | Coadministration of aminoglycosides, amphotericin B, IV pentamidine, and foscarnet may increase nephrotoxicity |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Complications include renal toxicity, neutropenia, fever, anemia, headache, hair loss, uveitis and/or iritis, and abdominal pain; monitor neutrophil counts; IV prehydration with NS and coadministration of probenecid can minimize nephrotoxicity; monitor serum creatinine and urine protein levels 48 h prior to treatment (adjust dose accordingly) |
The authors and editors of eMedicine gratefully acknowledge the contributions of previous author, Thomas W McGovern, MD, to the development and writing of this article.
| Media file 1: Characteristic skin lesion of variola on the arms and legs of an adolescent. Photo used with permission from the World Health Organization (WHO). | |
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| Media file 2: Small child with pustular lesions of variola. Photo used with permission of the World Health Organization (WHO). | |
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| Media file 3: Infant with advanced lesions of variola. Photo used with permission of the World Health Organization (WHO). | |
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| Media file 4: Unvaccinated infant with centrifugally distributed umbilicated pustules on day 3 of ordinary form of variola major strains of smallpox. Reprinted with permission from Fenner F, Henderson DA, Arita I, et al: Smallpox and its eradication. Geneva, Switzerland: World Health Organization; 1988: 10-14, 35-36; photographs by Arita. | |
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| Media file 5: Unvaccinated infant with centrifugally distributed umbilicated pustules on day 5 of ordinary form of variola major strains of smallpox. Reprinted with permission from Fenner F, Henderson DA, Arita I, et al: Smallpox and its eradication. Geneva, Switzerland: World Health Organization; 1988: 10-14, 35-36; photographs by Arita. | |
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| Media file 6: Unvaccinated infant with centrifugally distributed umbilicated pustules on day 7 of ordinary form of variola major strains of smallpox. Reprinted with permission from Fenner F, Henderson DA, Arita I, et al: Smallpox and its eradication. Geneva, Switzerland: World Health Organization; 1988: 10-14, 35-36; photographs by Arita. | |
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| Media file 7: Ordinary form of variola minor strain of smallpox (alastrim) in an unvaccinated woman 12 days after onset of skin lesions. The facial lesions are sparser and evolved more rapidly than the extremity lesions. Reprinted with permission from Fenner F, Henderson DA, Arita I, et al: Smallpox and its eradication. Geneva, Switzerland: World Health Organization; 1988: 10-14, 35-36; photographs by Arita. | |
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| Media file 8: Ordinary form of variola minor strain of smallpox (alastrim) in an unvaccinated woman 12 days after onset of skin lesions. The facial lesions are sparser and evolved more rapidly than the extremity lesions. Reprinted with permission from Fenner F, Henderson DA, Arita I, et al: Smallpox and its eradication. Geneva, Switzerland: World Health Organization; 1988: 10-14, 35-36; photographs by Arita. | |
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| Media file 9: Ordinary form of variola minor strain of smallpox (alastrim) in an unvaccinated woman 12 days after onset of skin lesions. The facial lesions are sparser and evolved more rapidly than the extremity lesions. Reprinted with permission from Fenner F, Henderson DA, Arita I, et al: Smallpox and its eradication. Geneva, Switzerland: World Health Organization; 1988: 10-14, 35-36; photographs by Arita. | |
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| Media file 10: Adult with variola major with hundreds of pustular lesions distributed centrifugally. Fitzsimmons Army Medical Center slide file. | |
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| Media file 11: Hemorrhagic-type variola major lesions. Death usually ensued before typical pustules developed. Reprinted with permission from Herrlich A, Mayr A, Munz E, et al: Die pocken; Erreger, Epidemiologic und klinisches Bild. 2nd ed. Stuttgart, Germany: Thieme; 1967. In: Fenner F, Henderson DA, Arita I, et al: Smallpox and its eradication. Geneva, Switzerland: World Health Organization; 1988: 10-14, 35-36. | |
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| Media file 12: Boy with monkeypox in Democratic Republic of the Congo in 1996. Note the centrifugal distribution as was typical of smallpox. Courtesy of William Clemm. | |
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| Media file 13: Boy with monkeypox in Democratic Republic of the Congo in 1996. Note synchronicity of lesions as was typical of smallpox. Courtesy of William Clemm. | |
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| Media file 14: Bioterrorist Agents. Signs and symptoms. Chart courtesy of North Carolina Statewide Program for Infection Control and Epidemiology (SPICE), copyright University of North Carolina at Chapel Hill, www.unc.edu/depts/spice/bioterrorism.html. | |
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Article Last Updated: Jul 16, 2008