POLICY STATEMENT |
| ABSTRACT |
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Key Words: chemical terrorism biological terrorism emergency preparedness
Abbreviations: AAPAmerican Academy of Pediatrics PPEpersonal protective equipment CDCCenters for Disease Control and Prevention SNSStrategic National Stockpile CHCcommunity health center DMATdisaster medical assistance team CISDcritical incident stress debriefing
| INTRODUCTION |
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Immediately after the September 11, 2001, terrorist attacks in the United States, which soon were followed by anthrax releases, the AAP, recognizing the need to address the impact of terrorism on children, initiated a series of unprecedented actions. These actions included (1) formation of the AAP Task Force on Terrorism, (2) creation of a comprehensive Web site on the AAP home page devoted to providing information on terrorism and its impact on children (www.aap.org/terrorism/index.html), (3) publication of the technical report "Radiation Disasters and Children,"2 (4) publication of a policy statement on smallpox immunization,3 (5) an addition to the Red Book of descriptions of biological weapons and management of the diseases they produce,4 (6) publication of a technical report5 and policy statement6 on the pediatrician and disaster preparedness, and (7) publication of the CD-ROM Feelings Need Checkups Too, designed to address mental health consequences of terrorism in children (www.aap.org/profed/childrencheckup.htm).
The continuing occurrence of chemical and biological terrorism makes clear the ongoing need to improve public health and health care system preparedness in all respects, including the detection of covert events, establishment of comprehensive response protocols for children, and implementation of plans for rapid resource mobilization. At the governmental level, these actions have been facilitated by the passage of key federal legislation (Table 1). 7 However, there remains a need for pediatricians to be knowledgeable about the chemical and biological weapons that could be used against a population that includes children. Moreover, many new principles in the care of children after chemical and biological terrorism have been developed. This policy statement replaces the 2000 policy statement, with an added focus on systems issues that are key in minimizing morbidity and mortality to children after their exposure to a chemical or biological weapon.
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| AGENTS OF CONCERN |
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Two recent acts of chemical terrorism involving children illustrate these new concepts. In 1999 in Fresno, California, patrons of a restaurant developed severe gastroenteritis. An investigation by public health authorities ultimately found that the carbamate insecticide methomyl had been maliciously added to the salt.8 More than 100 adults and children became ill with nausea, vomiting, and diarrhea; a perpetrator was never identified. In 2002 in Grand Rapids, Michigan, a disgruntled grocery worker placed a nicotine-containing insecticide into ground beef, making it available for purchase by unsuspecting customers. It was not until widespread illness (nausea, mouth burning, vomiting) was reported and there was a recall and analysis of the meat, revealing the presence of nicotine, that this was recognized as an act of terrorism.9 Ultimately, more than 100 people became ill, including more than 40 children, in what is now considered the largest act of chemical terrorism in US history.
The chemicals considered the most likely threat for use as chemical weapons are placed into 6 categories: nerve agents, vesicants, irritants/corrosives, choking agents, cyanogens, and incapacitators, including lacrimators (Table 2).
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In the 1995 sarin episode in Tokyo, the most unanticipated sequela was the degree of injury to health care professionals.10 Several hundred physicians, nurses, and other health care professionals became ill as a result of 2 factors: handling of sarin-contaminated victims without wearing personal protective equipment (PPE) and the entry of contaminated victims into health care facilities, leading to transmission of sarin vapor through the ventilation system.10,11 This event firmly demonstrated the importance of protecting health care professionals through the use of PPE and the importance of maintaining office or hospital safety by ensuring that victims are adequately decontaminated before entering the building.
Management of nerve-agent exposure includes supportive care and, when indicated, prompt administration of the antidotes atropine and pralidoxime.12 Both of these antidotes are available in autoinjector form, permitting rapid administration; autoinjectors are particularly important in mass-casualty incidents where there is a need to treat large numbers of victims as quickly and efficiently as possible. Until recently, the rapid administration of atropine and pralidoxime to children was complicated by the absence of pediatric autoinjectors; only the forms approved for adults, containing 2 mg of atropine and 600 mg of pralidoxime, were available. A pediatric atropine autoinjector was recently approved by the Food and Drug Administration for use in small children after nerve-agent exposure.13 However, the continued absence of a pediatric pralidoxime autoinjector, which is key in the successful treatment of central nervous system and muscular toxicity from nerve agents, leaves the use of standard, multidose vials as the only therapeutic option. To address this issue, consensus guidelines now recommend that children weighing 13 kg or more (23 years or older) receive a 600-mg dose of pralidoxime from an autoinjector, on the basis of the belief that this pralidoxime dose falls within the range of safety for the drug.5 Children weighing less than 13 kg should receive the customary weight-based (2050 mg/kg) dose, administered from a multidose vial; if unavailable, an autoinjector should be used.
Other aspects of care to children who have been exposed to nerve agents are found in recent reviews.12,14
Vesicants
Vesicants include sulfur mustard and lewisite, an arsenic-based blistering agent. These chemicals, both of which are released as an aerosol, produce erythema, burning, vesiculation, and then desquamation of the skin. Victims of vesicant exposure typically develop skin tingling followed by burning; within 24 hours, skin sloughing begins to occur, with wounds having the appearance of partial-thickness burns. These agents are also immunosuppressive, further increasing the risk of severe infection. Treatment is largely supportive. Important principles of management include protection of health care professionals through the use of PPE and topical decontamination.15 Because vesicants are often oil based, a mild soap or shampoo should be used during decontamination.
Choking Agents
Choking agents are created to produce, usually in delayed fashion, pulmonary injury with resulting bronchospasm, pulmonary edema, and respiratory failure. Immediate symptoms include eye burning, tearing, and blepharospasm. The major agent of this group is phosgene; however, common industrial chemicals, including polytef (Teflon) and other chemical polymers, act as choking agents depending on their ambient concentration. Most choking agents are heavier than air, which could result in higher concentrations at the breathing level of the child. Treatment is supportive.
Cyanogens
The cyanogens are similar to cyanide in structure and/or function. Agents in this class include cyanide salts and sodium azide. The cyanogens interrupt cellular utilization of oxygen, producing respiratory distress, coma, and metabolic acidosis. Victims of cyanogen exposure must be recognized promptly to administer the life-saving antidotes sodium nitrite and sodium thiosulfate.
Incapacitating Agents
Incapacitating agents include several different chemical classes (eg, anticholinergic agents, hallucinogens, cannabinoids, and fentanyl derivatives). In the Russian theater hostage incident in 2002, what is thought to have been a fentanyl-based incapacitating agent was released during the rescue effort. The agent, although successful in overwhelming the hostage-takers, also killed 127 hostages.16
Many incapacitating agents are weapons of opportunity, being easily acquired pharmaceutical agents or substances of abuse that are surreptitiously added to common sources of food or drink.
Included among incapacitators are lacrimators. Often referred to collectively as Mace or "tear gas," lacrimators include the chemicals chloroacetophenone and chlorobenzylidene as well as capsaicin ("pepper spray"). Lacrimators are designed to produce incapacitation from irritation of the eye and other mucous membranes. Exposure to Mace results in eye burning, tearing, and blepharospasm; victims may become temporarily blind. Inhalation produces mouth pain, shortness of breath, and, in rare cases, laryngospasm. Because capsaicin is widely sold as a nonlethal weapon, episodes of capsaicin release into the ventilation system of schools and buildings are a relatively common prank, although such incidents meet the definition of terrorism (ie, an act designed to frighten, hurt, or kill).
Biological Agents
Most of the biological agents that could be used as weapons are now discussed in the Red Book,4 although some agents (eg, ricin) are not discussed in detail. Ricin is discussed in a subsequent section of this report.
The biological weapons of concern are listed in Table 3. These agents have been placed by the Centers for Disease Control and Prevention (CDC) into categories A, B, or C. Thirty-nine agents are included in these 3 categories.
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Smallpox
The most widely discussed category A agent in recent years has been smallpox. In 2001, because of increasing concerns that smallpox was in the hands of terrorists and had the potential to produce widespread morbidity and mortality, the CDC recommended a "ring immunization" (surveillance and containment) strategy in the United States. This strategy of containment was reviewed and endorsed by the AAP Committee on Infectious Diseases in its 2002 policy statement "Smallpox Vaccine."3 Subsequently, the CDC recommended a 3-phase plan for smallpox immunization of health care professionals and other individuals.3 During the first phase, health care professionals in acute care facilities were to be immunized. In the second phase, there would be potential expansion to other health care professionals and first responders. In a possible third phase, voluntary immunization would be available to all those interested in being immunized. This campaign, to date, has struggled from several difficulties, including (1) the inability to quantitate the risk of a smallpox release, preventing individuals from making their own risk/benefit analysis, (2) an extensive list of contraindications to the vaccine, (3) general fears about the safety of the vaccine, (4) the appearance of unrecognized adverse effects from the vaccine (eg, fatal cardiac disease17,18), (5) lack of endorsement by several medical organizations,19 and (6) a high rate of vaccine refusal by health care professionals.20 Currently, the immunization campaign remains underway, still in phase I. Review and updating of the recommendations are ongoing.21,22
Ricin
Although it is a category B agent, ricin has become a major biological weapon of concern. A plant-derived, heat-stable toxin, ricin is an extract of the castor bean (Ricinus communis). Ricin acts by first entering cells through endocytosis; once in the cell, it is transported to the Golgi apparatus and endoplasmic reticulum. In the cytosol, ricin acts as a protease-resistant, enzymatically active structure that interacts with the sarcin-ricin domain of the large ribosome subunit RNA. This interaction can disturb translation by preventing the binding of elongation factors to the ribosome. Ricin is also capable of inactivating nonribosomal nucleic acid substrates.2326 With these effects, ricin produces severe morbidity and mortality. Rapidly dividing tissues, particularly the gastrointestinal epithelium, are most susceptible to ricin actions.
Ricin is a versatile agent that can be administered by ingestion, inhalation, or injection. When ingested, it can produce a syndrome of severe gastrointestinal upset, vomiting, hemorrhagic gastroenteritis, shock, and cardiovascular collapse. After inhalation, respiratory distress with a necrotizing pneumonitis may occur. Injection produces rapid shock and cardiovascular collapse. Treatment is supportive. A vaccine against ricin is currently under development.
Over the last 2 years, ricin has been associated with terrorist activity in the United States on multiple occasions. In October 2003, 2 ricin-containing letters were found in the US postal system.27 In a third incident, ricin was found in the mail sorter of a congressional post office in January 2004. There have also been multiple confiscations of ricin in the United States and abroad over the last 5 years.
| EXPOSURE VECTORS FOR CHEMICAL AND BIOLOGICAL WEAPONS |
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| SPECIFIC VULNERABILITIES IN CHILDREN |
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For each of the vectors of exposure to biological or chemical weapons (air, water, or food), children possess a significantly greater likelihood of exposure because of their intake patterns. Children inhale considerably more air on a per-weight basis than adults (400 vs 140 mL/kg per minute, respectively). Consequently, for any concentration of airborne toxin, a child will inhale more of the substance on a per-weight basis than an adult. Also, substances that are heavier than air have their highest concentration near the ground, closer to the breathing zone of the child. Because children have less-keratinized, more-permeable skin and/or a proportionately greater body-surface area, they have both greater exposure and a greater likelihood of systemic toxicity to agents that fall on their skin.30 Children have fluid and food intakes that differ significantly from adults. For example, children ingest approximately 100 mL/kg per day of water, compared with the 40 to 60 mL/kg per day that adults ingest. Children drink more milk than adults, placing them at risk of exposure to agents that can enter the milk supply through contamination of the grass on which cows feed; in the Chernobyl radiation disaster, cows grazed in contaminated pastures, resulting in excess radioactivity in their milk. Children drinking this milk sustained significant exposure to radioisotopes, including iodine and strontium. Finally, children not only eat more food on a per-kilogram basis but also have diets that are distinctly different from adults (eg, greater consumption of fruits).
Once exposed to a chemical or biological agent, children have numerous physiologic vulnerabilities that could lead to a greater risk of harm.1 These vulnerabilities include undeveloped self-preservation skills that make them less able to flee danger; an immature immune system that makes them less able to contain infection (eg, plague)31; less fluid reserve, which can result in a greater risk of severe dehydration after exposure to agents that produce excess gastrointestinal fluid loss; and a greater risk of anxiety reactions and posttraumatic stress disorder after witnessing or being victim to a terrorist act.3234
| PUBLIC HEALTH PREPAREDNESS |
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Creation of all-hazards response systems has led to significant enhancements in public healthresponse capabilities. For example, the same protocol created to respond to the appearance of smallpox can be easily modified to contain an outbreak of severe acute respiratory syndrome (SARS). Similarly, an effective public healthresponse protocol for a sarin release would be equally effective for a hazardous-materials ("HAZMAT") release in the community.
Syndromic Surveillance
Overt acts of chemical and biological terrorism such as the sarin release in Tokyo present the challenge of rapidly identifying the agent and mobilizing the proper interventions. However, acts of chemical and biological terrorism may also be covert. Examples include the release of anthrax in 2001 and contamination of ground beef with nicotine in 2002. Covert incidents pose a significantly greater public health challenge and are more likely to induce widespread fear than overt events. Mechanisms for early recognition of a covert chemical or biological event, therefore, are necessary to contain the incident and minimize its impact.
Syndromic surveillance, a specialized type of outbreak detection, is a term used to describe mechanisms for monitoring health indices or events that reflect the early stages of an infection or disease of public health importance in an effort to minimize consequences.36,37 Syndromic surveillance is considered an important means of identifying public health emergencies in their initial stages. Syndromic surveillance techniques can be clinician based or automated. Many syndromic surveillance systems are emergency department based. In addition, most state and local health departments are pursuing automatic electronic laboratory disease reporting.
The traditional mechanism of syndromic surveillance has been the clinician who recognizes unusual patterns of disease and reports them to public health authorities. The "astute clinician" principle places all health care professionals (including physicians, nurses, emergency medical technicians, epidemiologists, and health educators) in the role of sentinels for the appearance of disease clusters or other clinical abnormalities. The pivotal role of physicians and other health care professionals in syndromic surveillance, particularly for acts of terrorism, has led the CDC and other agencies to educate clinicians about chemical and biological weapons release and the diseases they produce. Clinical cues, case definitions, and syndromes for chemical weapons exposure have been published (Table 4), along with numerous resources to expand clinicians ability to recognize covert terrorist incidents.37,38
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New Governmental Roles in Emergency Preparedness
Although emergency-preparedness legislation existed before 2001, passage of additional rules between 2002 and 2005 resulted in massive efforts by the federal government to improve public health readiness across the nation (Table 1). Over the last 4 years, appropriations from federal to state public health agencies have been substantial. The Department of Homeland Security was established as a new member of the federal cabinet. Several departments within the Department of Health and Human Services have undergone extensive change, such as the CDC, Food and Drug Administration, and National Institutes of Health, all of which have reorganized their practice, regulatory, and research priorities to include chemical and biological terrorism, along with other public health threats; in 2002, the CDC established the Office of Terrorism Preparedness and Emergency Response. At state and local levels, planning for chemical and biological terrorism is now coordinated by multiple agencies, including departments of health, emergency-management agencies, poison control centers,42 and law enforcement authorities.
The Strategic National Stockpile (SNS) has become one of the most important initiatives in mass-casualty disaster response.5 Designed to respond to disasters that overwhelm local resources, the SNS includes such capabilities as the delivery of medications and supplies to areas of need within 12 hours of the request. SNS supplies include a pediatric formulary and materials for compounding tablets and capsules into liquid formulations (www.bt.cdc.gov/stockpile/index.asp).
| SYSTEMS ISSUES IN PREPAREDNESS FOR CHEMICAL AND BIOLOGICAL TERRORISM |
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Ideally, every school should produce its own response protocols rather than following a one-size-fits-all disaster plan that fails to take into account the schools physical plant, student size and characteristics, the presence of children with special needs, school nurse availability, and proximity to certain areas such as industries, rail yards, or highways.40 All schools, in conjunction with local public health officials, should develop comprehensive evacuation and sheltering-in plans. Because local school bus fleets can typically evacuate only a fraction of children at one time, a means of mobilizing additional transport vehicles should be developed. General outlines for the development of a school emergency-response plan are found in Table 5.
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To be fully prepared for chemical or biological terrorism, pediatric and general hospitals must also have an evacuation plan should the hospital environment become uninhabitable. Although protocols for "vertical evacuation" (ie, the removal of patients to other floors within the same building) are well established in hospital-based disaster response, comprehensive plans for complete building evacuation are less well developed. Pediatric hospitals requiring full evacuation may have the additional challenge of transporting pediatric patients to health care facilities with relatively few pediatric resources. Nonetheless, memoranda of agreement with nearby or affiliated institutions are a key part of a comprehensive pediatric hospital disaster plan.
After exposure to a chemical or biological weapon, children may become covered by toxic material that can produce skin injury or be absorbed, producing systemic toxicity. In the case of infectious material, the contamination of skin could be sufficient to represent a threat to health care professionals as well as the victim. When children are covered with unknown but potentially dangerous chemical or infectious material, immediate decontamination is required.43 Topical decontamination has 2 distinct components: disrobing and showering. To minimize exposure to health care professionals and patients within the health care facility, the child should be disrobed outdoors, before entering the ambulance or building. Disrobing alone accounts for more than 85% of topical decontamination and is an extremely effective means of ending exposure. When possible, the victim should disrobe himself or herself to minimize exposure to others. Health care professionals should not assist in disrobing unless they are wearing appropriate PPE.
Showering complements disrobing by further removing chemicals, microbes, and debris. As with disrobing, showering must occur outdoors; protocols should include strategies for preventing hypothermia in children. Principles of showering include the establishment of 3 management zones in the decontamination staging area (so-called hot, warm, and cold in reference to the sites degree of contamination), use of water that has been warmed to a temperature of 100°F, a water pressure of 60 psi, and, if possible, containment of the wastewater. If the toxic material is oily or firmly adherent to the childs skin, soap or a mild shampoo should be used; solutions such as mild bleach should not be used on children because of the risk of skin injury.5 If an outdoor shower is not available, the child can be simply disrobed before being brought into the health care facility for care. Decontamination can be a frightening procedure for children, exacerbated by the identity-concealing PPE that clinicians are wearing. Efforts should be made to keep parents nearby; when possible, parents should be used to assist with their childs decontamination.
All health care professionals who assist in decontamination must protect themselves by wearing appropriate PPE. Currently, there are 4 levels of PPE, ranging from level A, which is the highest level of protection, to level D, which consists of simple gown, gloves, and surgical mask. For hospital personnel, level C PPE (a chemical-resistant suit and gloves, with an air-purifying respirator) is considered adequate for hospital-based management of most contaminated victims. Health care facilities should develop plans for rapid access to such equipment. Staff should be appropriately trained. Other principles of decontamination and PPE are outlined in Table 6 and have been published recently.44,45
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Office Preparedness
The pediatrician should have an important role in the community response to any disaster involving children. First, the pediatricians office may be the preferred site of care for many victims who are transporting themselves for treatment. Both chemically contaminated children and children with suspected illness from a biological weapon might go directly to the pediatricians office. Consequently, pediatricians should consider the development of office protocols for disasters, including (1) management of a child who requires decontamination, (2) management of a child with a potentially transmissible infection, and (3) management of a sudden influx of pediatric patients after a large-scale incident.5 The AAP textbook Childhood Emergencies in the Office, Hospital, and Community46 is a useful resource to assist in office planning for such emergencies. Pediatricians should also consult their state and local health departments, because most have electronic health alert networks.
Surge Capacity
An effective response to large-scale chemical or biological terrorism (ie, an incident with more casualties than routine operations can accommodate) requires the creation of surge-capacity protocols. Federal, state, and local public health authorities are essential in assisting health facilities during crises of large magnitude. Nonetheless, both pediatric and nonpediatric hospitals should consider how a large-scale event would affect their facility. Plans for such an event might include (1) the creation of additional bed spaces through cohorting, (2) mechanisms for the rapid discharge of inpatients to increase capacity, (3) an inventory of all sites in the hospital where critical care can be provided, (4) establishment of a site, ideally out of the hospital, for patient triage, (5) identification of care sites for those whose injuries are minor, (6) mechanisms for labeling and tracking patients, particularly children who arrive without personal identification, and (7) plans for maintaining hospital security by preventing the entry of contaminated victims and other unauthorized individuals. For nonpediatric hospitals, surge-capacity plans for a mass-casualty chemical or biological incident involving children should also include mechanisms for mobilizing health care professionals with pediatric expertise. Surge-capacity principles are summarized in Table 7. Disaster medical assistance teams (DMATs), supported by the US Public Health Service, have been created by the National Disaster Medical System to provide assistance to regions after a large-scale disaster. However, among the 27 DMATs in the United States, only 2 are dedicated pediatric DMATs, significantly limiting the federal response capability to a pediatric mass-casualty incident. The Metropolitan Medical Response System, another federal effort designed to create regional "medical strike teams," has no clearly established pediatric capability or standards.
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Parents may similarly become psychological casualties after chemical or biological terrorism. Visual replay of events on television may contribute to the development of long-term behavioral disturbances. As with children, the parent may have overt or subtle signs of distress. Adults typically display loss of appetite, insomnia, depression, hopelessness, and acute anxiety.
Finally, health care professionals who care for victims of chemical or biological terrorism can develop mental health consequences. There is an extensive body of literature indicating that health care professionals can become extremely depressed, developing posttraumatic stress disorder after caring for victims. To reduce the risk of this occupational hazard, the concept of critical incident stress debriefing (CISD) was created many years ago. In principle, a prompt debriefing session can be therapeutic by permitting staff to verbalize their feelings and anxieties about what they have experienced. CISD has become a common part of postevent disaster management. Recently, however, questions about the efficacy of CISD in reducing mental health sequelae among health care professionals have been raised.49 There are increasing concerns that the process of debriefing forces health care professionals to relive events, undoing internal resolution that is already underway. In addition, the process of group debriefing may carry the risk of having health care professionals hear about disturbing events that they themselves did not witness, creating anxiety and depression that was not present initially. Although this issue remains controversial, there is consensus that efforts should be made to identify health care professionals who are suffering psychological sequelae from their involvement in responding to an act of chemical or biological terrorism.
Individual/Family Preparedness
Large-scale disasters, whether they are natural (eg, hurricanes or floods), unintentional (eg, hazardous-materials release), or intentional (ie, terrorist), can occur at any time. All families, particularly families with children, should have a disaster plan. Such plans should include communication in the event of cellular phone failure, a reunification plan if disaster occurs when family members are not together, and emergency provisions in the home. Multiple resources are available to assist families in home disaster planning (www.ready.gov/index.html and www.fema.gov/plan/index.shtm).
| RECOMMENDATIONS TO PEDIATRICIANS |
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| RECOMMENDATIONS TO GOVERNMENT |
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| Committee on Environmental Health, 20052006 |
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Dana Best, MD, MPH
Helen J. Binns, MD, MPH
Joel A. Forman, MD
Christine L. Johnson, MD
Catherine J. Karr, MD, PhD
Janice J. Kim, MD, PhD, MPH
Lynnette J. Mazur, MD, MPH
James R. Roberts, MD, MPH
| Liaisons |
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US Environmental Protection Agency
Robert H. Johnson, MD
Centers for Disease Control and Prevention/Agency for Toxic Substances and Disease Registry
Martha Linet, MD
National Cancer Institute
Walter Rogan, MD
National Institute of Environmental Health Sciences
| Staff |
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| Committee on Infectious Diseases, 20042005 |
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H. Cody Meissner, MD, Vice Chairperson
Carol J. Baker, MD
Robert S. Baltimore, MD
Joseph A. Bocchini, Jr, MD
Penelope H. Dennehy, MD
Robert W. Frenck, Jr, MD
Caroline B. Hall, MD
Sarah S. Long, MD
Julia A. McMillan, MD*
Keith R. Powell, MD
Lorry G. Rubin, MD
Thomas N. Saari, MD
| Liaisons |
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American Academy of Family Physicians
Steven Cochi, MD
Centers for Disease Control and Prevention
Joanne Embree, MD
Canadian Paediatric Society
Marc Fischer, MD
Centers for Disease Control and Prevention
Bruce Gellin, MD, MPH
National Vaccine Program Office
Mamodikoe Makhene, MD
National Institutes of Health
Douglas Pratt, MD
Food and Drug Administration
Jeffrey R. Starke, MD
American Thoracic Society
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Red Book Editor
| Consultant |
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| STAFF |
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