Volume 23, Number 1—January 2017
Modeling Tool for Decision Support during Early Days of an Anthrax Event
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|EID||Rainisch G, Meltzer MI, Shadomy S, Bower WA, Hupert N. Modeling Tool for Decision Support during Early Days of an Anthrax Event. Emerg Infect Dis. 2017;23(1):46-55. https://dx.doi.org/10.3201/eid2301.151787|
|AMA||Rainisch G, Meltzer MI, Shadomy S, et al. Modeling Tool for Decision Support during Early Days of an Anthrax Event. Emerging Infectious Diseases. 2017;23(1):46-55. doi:10.3201/eid2301.151787.|
|APA||Rainisch, G., Meltzer, M. I., Shadomy, S., Bower, W. A., & Hupert, N. (2017). Modeling Tool for Decision Support during Early Days of an Anthrax Event. Emerging Infectious Diseases, 23(1), 46-55. https://dx.doi.org/10.3201/eid2301.151787.|
Health officials lack field-implementable tools for forecasting the effects that a large-scale release of Bacillus anthracis spores would have on public health and hospitals. We created a modeling tool (combining inhalational anthrax caseload projections based on initial case reports, effects of variable postexposure prophylaxis campaigns, and healthcare facility surge capacity requirements) to project hospitalizations and casualties from a newly detected inhalation anthrax event, and we examined the consequences of intervention choices. With only 3 days of case counts, the model can predict final attack sizes for simulated Sverdlovsk-like events (1979 USSR) with sufficient accuracy for decision making and confirms the value of early postexposure prophylaxis initiation. According to a baseline scenario, hospital treatment volume peaks 15 days after exposure, deaths peak earlier (day 5), and recovery peaks later (day 23). This tool gives public health, hospital, and emergency planners scenario-specific information for developing quantitative response plans for this threat.
Population exposure to aerosolized Bacillus anthracis spores is one of the most potentially catastrophic public health emergencies (1). The 2001 US anthrax attack, in which inhalation anthrax (IA) affected 11 persons and killed 5, led to multiple mass antimicrobial prophylaxis campaigns and considerable healthcare activity (2). Data in the first few days of such an event may be limited, leading to uncertainty regarding the scale of the event and difficulty making response decisions.
Public health officials lack widely available tools for rapidly estimating the number of cases, projecting medical surge, and evaluating response options during an anthrax event. Several efforts have evaluated response options in predefined scenarios, which are useful for planning but not during a response (3–6). Two other models have attempted to predict the number and timing of IA cases after exposure to aerosolized B. anthracis spores; 1 evaluated response options (7,8). However, neither model estimates the surge of patients in the healthcare system, and both models have constraints that limit their practical utility. Walden and Kaplan built a model that presumes equal probability of various event sizes and requires at least 5 days of case data before robust estimates of final attack sizes can be calculated (8). This timing may be insufficient given the US Cities Readiness Initiative (CRI) guideline that postexposure prophylaxis (PEP) dispensing be completed within 48 hours of event detection (9). The back-calculation techniques of Egan et al. permit estimation of the final outbreak size after a certain number of observed cases under different PEP assumptions (7,10). Although these models can be reconciled with the CRI timeline, they were not designed for direct use by public health practitioners (use requires the R coding language and understanding of maximum-likelihood functions), and the earlier work assumes 90% PEP uptake by the infected population, which is an overestimation (>25%) of the probable public response (11).
An alternative method for predicting the scale of IA events is plume modeling, which calculates the number of exposed persons by estimating the geographic spread of dispersed B. anthracis spores. Plume models require knowledge (or estimates) of the number of spores released, release timing and location, population densities, meteorologic data (e.g. wind speed and direction), and inhaled spore volume. It is unclear whether plume modeling is sufficiently timely and robust to guide local response decisions.
We therefore developed a modeling tool, called Anthrax Assist, to provide public health officials with rapid projections of IA cases and response decision support during an aerosolized anthrax event. This tool can assist with responding to an anthrax event (or designing and conducting locally tailored training exercises) by providing critical information in the first few days of response.
We used Excel 2010 (Microsoft Corporation, Redmond, WA, USA) to construct Anthrax Assist (Technical Appendix 1). Anthrax Assist is composed of 3 linked models (Table 1). The Epidemic-Curve model combines daily case counts with incubation distributions to project the future number and timing of symptomatic IA cases in a nonvaccinated population. The PEP Impact model estimates the potential decrease in the projected trajectory of future cases (output from the Epidemic-Curve model) resulting from a PEP dispensing campaign. The Healthcare Impact model uses the projected unmitigated or PEP-mitigated incidence curves to project the size and timing of peak healthcare utilization and associated patient outcomes. Users can readily change a number of input values to reflect a desired attack scenario or response strategy (Table 2). To illustrate the models, we developed an attack scenario and used it to evaluate estimates resulting from various outbreak detection scenarios (using 1, 2, or 3 days of initial case count data) and PEP response strategies (Table 3).
We base our IA incubation distribution on the Wilkening model, which plots the probability of becoming symptomatic over a 60-day period for a given infectious dose of B. anthracis spores (Technical Appendix 2) (13). We combine this incubation probability distribution with the number of detected IA cases at a given time to calculate the total projected number of ill persons (final case count [FCC]) by using the following equation:
We assume a single, localized release that causes near-simultaneous population exposure. Because public health authorities will probably not know the average inhaled spore dose among affected persons, we designed the model to calculate a range of plausible outbreak sizes from a range of spores inhaled per person. To illustrate the model, we used a median value of 360 spores/person (range 1–8,000), resulting in a median incubation period of 6.9 days (range 10.3–5.0) (Table 2; Technical Appendix 2).
PEP Impact Model
The PEP Impact model uses median projected daily case counts (output from the Epidemic Curve model) to estimate the potential effects of a PEP campaign. This effect is calculated as the product of the number of persons who become symptomatic on any given day t; the effectiveness of PEP on day t (which is a product of antimicrobial efficacy and adherence); and the probability that an infected, asymptomatic person receives antimicrobial prophylaxis on or before day t. We calculate the probability that a person receives PEP on day t by multiplying the PEP uptake (proportion of persons seeking antimicrobial drugs) by the daily antimicrobial dispensing throughput and then dividing by the population targeted for PEP (Table 2). The FCC with a PEP campaign is the sum of detected cases and daily PEP-mitigated case count projections. We express PEP effect as both a difference measure (cases averted) and as a proportion (cases averted divided by the unmitigated FCC). We assume that symptomatic persons seeking PEP are referred for medical treatment and do not receive PEP (21). We further assume that all of the population suspected to be exposed would be targeted for PEP because there is no definitive PEP triage process for IA beyond exposure risk (Table 2).
In accordance with US CRI guidelines, we assume that PEP dispensing is completed in 2 (range 1–2) days after the decision to initiate PEP (9). Following SteelFisher et al., we also assume that of the population targeted to receive PEP, 65% (range 40%–90%) actually start taking PEP (11). Everyone starting PEP is assumed to fully adhere to the regimen on the first day. After that, adherence decreases linearly to 40% (range 25%–80%) at the conclusion of the event (Technical Appendix 2) (18). Last, we assumed 90% (range 10%–90%) antimicrobial drug efficacy and that this level of protection is achieved 1 day after initiation of the regimen (15,16) (Table 2).
Healthcare Impact Model
To calculate the demand for medical care, we used a compartmental model (based on one reported by Zaric et al.) and used the review of IA cases by Holty et al. to select the rates of patients’ transitions through illness stages (6,19) (Figure 1; Technical Appendix 2). This model is used to calculate daily patients initiating treatment, peak daily treatment caseload (i.e., census of hospitalized patients receiving treatment for IA), and the day of peak treatment caseload.
In this model, medical intervention is required for recovery from symptomatic IA, and only patients with fulminant disease can die. We define treatment effectiveness as the percentage of patients who recover after receiving some type of medical intervention and pattern it after the 2001 US IA events. As such, treatment is 4 times more effective when started in the prodromal (80%), rather than fulminant (20%), stage of illness (Table 2). However, the probability that a patient in the fulminant stage seeks healthcare (95%) is roughly twice that for someone in the prodromal stage (40%) (22). In addition, we varied the likelihood that any patient seeks healthcare by the timing of public health messaging regarding screening and treatment recommendations. We assume that the proportion of persons in the prodromal stage who seek care would double as a result of widespread media attention (80% vs. 40%) (2) (Table 2). Last, we assume treatment effectiveness values based on full availability of medical countermeasures and resources at the time of treatment and no delay in access to care once sought (Table 2).
During the 2001 US IA event, treatment duration was highly associated with treatment outcomes (22). Thus, for those who recover, we assume a normal distribution with a mean of 18 (SD 3) treatment days from the date of transition to the fulminant stage of illness or from the sixth day of prodromal illness for patients whose illness does not progress to the fulminant stage. For patients who eventually recover from fulminant illness (in treated and yet-nontreated populations), we assume a 20% transition each day so that all have transitioned to the fulminant stage after 5 days in the prodromal stage. Among those who eventually die, half transition to the fulminant stage on the first day of symptoms and the other half on the next day. When treatment is not sought, we assume that death occurs on the same day as the transition to fulminant illness.
To illustrate use of the models, we created an attack case series scenario patterned after the 1979 Sverdlovsk, USSR, event, in which at least 70 people died of IA after accidental aerosol release of B. anthracis spores from a bioweapons facility (Table 2) (12). We created this Sverdlovsk-like case series by multiplying each day’s case count from the Sverdlovsk event by 10, resulting in a 40-day, 700-patient case series (Technical Appendix 2).
To illustrate the accuracy of the Anthrax Assist FCC projections under realistic conditions of limited reported case data in the first days of an event, we first ran the Epidemic-Curve portion of Anthrax Assist by using only the first 3 days of case data as input (20, 10, and 70 cases, respectively), then by using 2 days of case data, and then only the first day’s cases. To examine the effect of the number of days of case data on the accuracy of our FCC projection, we also incrementally added a day of case data, beyond the first 3 days, until the projection was within 10% of the true FCC.
Next, to evaluate prophylaxis response options, we developed 4 PEP scenarios by varying components of the PEP campaign implementation (logistics) and the public response to the campaign (utilization) (Table 3). Scenario 1 (no PEP) is an event without a PEP campaign. Scenario 2 (ideal) is an event wherein early detection of the event (e.g., through biosensors) and positive public perception results in a 1-day campaign starting 1 day after detection, 90% uptake, and 80% adherence at the event’s conclusion. Scenario 3 (practical) is an event in which PEP dispensing logistics follow current public health guidance and PEP utilization is based on data from the 2001 US IA event, resulting in a 2-day campaign starting 2 days after detection, 65% uptake, and 40% adherence at the event conclusion. Scenario 4 (constrained) is an event in which logistics hurdles (e.g. staffing shortages, traffic congestion [3,23]) and poor public perception impede rapid PEP coverage, resulting in a 4-day campaign starting 2 days after detection, 40% uptake, and 25% adherence at event conclusion. Hereafter, the baseline scenario comprises PEP scenario 3 and the Healthcare Impact model values in Table 2.
We conducted 2 sensitivity analyses. We first evaluated the influence of individual PEP-related parameters on outputs from the models as follows: prophylaxis campaign duration of 1–6 days at full throughput capacity, delay of 3–6 days until PEP campaign starts, a range of 15%–90% for PEP uptake, a range of 10%–90% for antimicrobial efficacy, and a range of 15%–90% for adherence to the regimen at the conclusion of the event. These ranges encompass reported values (3,4,11,18,24).
In our second sensitivity analysis, we altered the Epidemic-Curve model inputs used in the baseline attack scenario to illustrate potential data limitations and surveillance inaccuracies that might occur during an actual event. Doing so involved comparing estimates using the full complement of the initial 3 days of case data with a scenario in which 60% of cases are reported. This level of underreporting represents the plausible difficulties often encountered when initially collecting outbreak data.
For the scenario that uses the first 3 days of case data, no PEP campaign, and early public messaging, the tool projects a median 60-day FCC of 1,164 (66% higher than actual FCC, plausible range 675–1,612; Figure 2, panel A), 35% event mortality (408 deaths), and a peak hospital caseload of 692 patients on day 15 (Table 5). Running the same scenario with only 2 days of case data (i.e., 20 followed by 10 cases) yields a median FCC estimate of 1,441 (106% higher than actual FCC, range 963–1,464) (Figure 2, panel B), 35% event mortality (506 deaths), and a peak hospital caseload of 856 on day 14. Using only the first day of case data (20 cases) yields a median FCC estimate of 27,555 (3,800% greater than actual FCC, range 10,993–36,603), 35% event mortality (1,688 deaths), and a peak hospital caseload of 2,871 on day 14. In contrast, when 4 days of case data are used, the FCC projection (median 750, range 435–1,175) falls within 10% of actual FCC.
Irrespective of the number of days of case data available, the estimated effects of PEP ranged from ≈25% cases averted in scenario 4 (constrained) to 79% in scenario 2 (ideal) (54). These PEP effects are equally reflected in the percentage of averted deaths (Table 5). Even with rapid event detection, an aggressive PEP campaign, and unlimited treatment resources one-third of deaths expected under the unmitigated scenario will still occur (calculated as the ratio of deaths in PEP scenario 2 [ideal] to deaths in PEP scenario 1 [no PEP], using 3 days of case data) (Table 5).
In the baseline scenario, treatment initiation and deaths peak early in the event (days 4 and 5, respectively), and treatment load and recoveries peak later (days 15 and 23, respectively) (Figure 3). The treatment load curve exhibits a plateau-like shape because of the extended length of time required to treat and recover from IA.
Influence of Individual PEP Campaign Factors
The decision to take PEP (uptake) is the most influential PEP-related parameter (Figure 4). Projected cases averted differ as much as 59% when results using the lowest and highest plausible PEP uptake values (12% and 71%, respectively) are compared (Table 4). In contrast, adherence (at day 60) to the PEP regimen exhibits the least direct influence on averted cases and deaths. Averted cases differ by only 5% when the lowest and highest plausible adherence values are used (50% and 55%, respectively) in the baseline scenario. This small difference results from the fact that most infected persons become symptomatic well before declining adherence can affect PEP effectiveness (Technical Appendix 2).
Effects of Data Limitations
Because of the underlying model structure, case count inaccuracies are reflected in the final event size projections proportionately to the level of overreporting or underreporting. For example, when the first 3 days of detected cases are 40% underreported in the Sverdlovsk-like scenario (60 cases instead of 100: 12 cases with illness onset event day 1, 6 cases on day 2, and 42 cases on day 3), the median event size caseload was projected to be 698 (range 405–967), 40% less than the 1,164 cases projected in the original scenario.
Our modeling tool provides estimates of future IA caseloads over time and quantifies the effects of various prophylaxis and treatment response options. By integrating projections of the event scale with interventions reflecting healthcare utilization and patient outcomes, our tool permits evaluation of responses during the first days of a real or simulated event.
The accuracy of our FCC projections improves with the number of days of case data available and may provide estimates sufficient for response decisions when 3 days of data are available (Figure 2, panel B). FCC projections made before day 3 probably overestimate the eventual FCC, which may be informative for policymakers (Technical Appendix 2).
The results of our PEP and Healthcare Impact models are consistent with reports showing the benefits of initiating PEP as early as possible after exposure recognition (3,4,6,7,25). Zaric et al. (6) calculated 45.3% event mortality if a 65% effective PEP campaign was completed within 3 days after a 2-day detection delay; our comparable event mortality is 37.1% (by adjusting the associated parameter values in our baseline scenario). In highly effective PEP scenarios, Brookmeyer et al. (25) and Baccam et al. (3) separately calculated 16%–17% event mortality (we calculated 11% by adjusting our baseline PEP scenario to match theirs), if 100% effective drugs were used after a 2-day delay, 2-day dispensing campaign, 25% final adherence, and 90% inferred uptake (from 90% initial adherence used by Baccam et al., because uptake was not a parameter in either the Baccam or Brookmeyer model).
Unlike prior efforts to evaluate PEP strategies (3,4,6,7,25), our model includes a PEP uptake parameter in our evaluation of PEP strategies (Table 3; Figure 4). In our model, daily PEP uptake percentage by infected persons deteriorates as the number of unexposed persons requiring PEP increases and when the daily campaign throughput capacity cannot accommodate the increase (because uninfected persons dilute the infected population seeking PEP) (Technical Appendix 2).
The hospital occupancy estimates generated with our Healthcare Impact model are unique among published IA models (Figure 3). This output can support pre-event and intra-event collaboration between public health officials and healthcare system leaders. It also suggests that balancing efforts to allocate countermeasures between public health and healthcare delivery will be a dynamic process that would benefit from daily reassessments of caseloads and responder capabilities.
Our baseline scenario results in lower mortality than was reported for the 2001 US anthrax attacks (37% vs. 45%) (22), a result of our assumption of improved treatment effectiveness for persons initiating treatment during the fulminant stage of illness (20% vs. 0) (Table 2). In a large event, in which FCC exceeds treatment resources, treatment effectiveness would deteriorate. Anthrax Assist allows responders to alter effectiveness values (assume crisis standards of care) with regard to local treatment capacity.
Anthrax Assist has limitations. We do not account for gastrointestinal and cutaneous forms of B. anthracis infection (Technical Appendix 2). We assume a uniform exposure dosage and a consistent relationship between dose and incubation period across patient types, which may mask logistically relevant temporal variability of illness onset (earlier cases associated with higher inhaled spore counts and vice versa); furthermore, some evidence suggests that certain populations (e.g., children, pregnant women) may be more susceptible to infection or may progress through disease stages differently. Similarly, we do not fully address the consequences of a surge of worried-well patients or the routine demands for healthcare by new and existing patients. Last, although the Centers for Disease Control and Prevention (CDC) Advisory Committee on Immunization Practices recommends anthrax vaccine as part of the PEP regimen (26), we do not include vaccine in our PEP Impact model under the assumption that adherence to the full 60-day PEP regimen effectively protects against infection and to assess the effects of decreasing adherence.
Some limitations result from data uncertainties. For example, our Epidemic-Curve model does not pinpoint the timing and location of a release and cannot distinguish between prolonged, short, or multiple releases (Technical Appendix 2). This model is also sensitive to case surveillance uncertainty. To address this uncertainty, Anthrax Assist accepts simultaneous input of up to 3 case series variations. Thus, users can inflate or deflate counts on the basis of perceived underreporting or overreporting, can assign cases to different illness-onset dates, and can examine the influence on outputs. Last, in the absence of a compelling alternative, we rely on the Wilkening analyses of the Sverdlovsk outbreak for our incubation distribution (13,27), which is not without criticism (Technical Appendix 2). By definition, our Epidemic-Curve model FCC estimates demonstrated high accuracy when applied to the Sverdlovsk-like attack scenario (Figure 2). Use of a Sverdlovsk-like scenario should not be seen as a liability, however, because no evidence suggests that any future IA event would have a substantially different epidemiological profile and our tool permits users to specify other incubation distributions. Because its projections are relatively precise (differences between the highest and lowest FCC estimates are never larger than the estimate itself), Anthrax Assist enables responders to avoid having to consider response options based on event sizes, which differ on a log scale (as with other methods ).
In conclusion, Anthrax Assist gives public health officials the ability to examine the future scale and consequences of alternative responses to a newly detected anthrax event. This modeling tool mirrors public health practice by using disease surveillance data and permits responders to update projections as new data arrive from the field. The results of our illustrative scenarios underscore the value of integrating epidemic curve projections with decision-based modeling of PEP use and healthcare resource planning. Furthermore, Anthrax Assist highlights the realistic benefit of public health countermeasures and the value of optimizing public perception of PEP.
Mr. Rainisch is an epidemiologist with the Health Economics Modeling Unit, Division for Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, CDC. His research interest is developing models used to plan for and respond to public health emergencies.
We thank the CDC Anthrax Management Team for their contributions to the development of the model; Jason Asher his for assistance with incubation distribution calculations; Julie Black, Mike Harryman, and Melissa Powell for testing the models and providing feedback; and John A. Muckstadt and Hee Kyun Yun for technical review of Excel calculations.
This investigation was supported in part by CDC through Interagency Professional Agreement 08IPAA895304 (N.H.).
- Inglesby TV, O’Toole T, Henderson DA, Bartlett JG, Ascher MS, Eitzen E, et al.; Working Group on Civilian Biodefense. Anthrax as a biological weapon, 2002: updated recommendations for management. JAMA. 2002;287:2236–52.http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=11980524&dopt=Abstract
- Jernigan JA, Stephens DS, Ashford DA, Omenaca C, Topiel MS, Galbraith M, et al.; Anthrax Bioterrorism Investigation Team. Bioterrorism-related inhalational anthrax: the first 10 cases reported in the United States. Emerg Infect Dis. 2001;7:933–44.
- Baccam P, Willauer D, Krometis J, Ma Y, Sen A, Boechler M. Mass prophylaxis dispensing concerns: traffic and public access to PODs. Biosecur Bioterror. 2011;9:139–51.
- Hupert N, Wattson D, Cuomo J, Hollingsworth E, Neukermans K, Xiong W. Predicting hospital surge after a large-scale anthrax attack: a model-based analysis of CDC’s cities readiness initiative prophylaxis recommendations. Med Decis Making. 2009;29:424–37.
- Wein LM, Craft DL; Anthrax Modeling working Group. Evaluation of public health interventions for Anthrax: a report to the secretary’s council on Public Health Preparedness. Biosecur Bioterror. 2005;3:348–56.
- Zaric GS, Bravata DM, Cleophas Holty JE, McDonald KM, Owens DK, Brandeau ML. Modeling the logistics of response to anthrax bioterrorism. Med Decis Making. 2008;28:332–50.
- Egan JR, Legrand J, Hall IM, Cauchemez S, Ferguson NM, Leach S. Re-assessment of mitigation strategies for deliberate releases of anthrax using a real-time outbreak characterization tool. Epidemics. 2010;2:189–94.
- Walden J, Kaplan EH. Estimating time and size of bioterror attack. Emerg Infect Dis. 2004;10:1202–5.
- Centers for Disease Control and Prevention. Strategic National Stockpile (SNS) [cited 2015 Apr 1]. http://www.cdc.gov/phpr/stockpile/stockpile.htm
- Egan JR, Hall IM. A review of back-calculation techniques and their potential to inform mitigation strategies with application to non-transmissible acute infectious diseases. J R Soc Interface. 2015;12:20150096.
- SteelFisher G, Blendon R, Ross LJ, Collins BC, Ben-Porath EN, Bekheit MM, et al. Public response to an anthrax attack: reactions to mass prophylaxis in a scenario involving inhalation anthrax from an unidentified source. Biosecur Bioterror. 2011;9:239–50.
- Meselson M, Guillemin J, Hugh-Jones M, Langmuir A, Popova I, Shelokov A, et al. The Sverdlovsk anthrax outbreak of 1979. Science. 1994;266:1202–8.
- Wilkening DA. Sverdlovsk revisited: modeling human inhalation anthrax. Proc Natl Acad Sci U S A. 2006;103:7589–94.
- Toth DJ, Gundlapalli AV, Schell WA, Bulmahn K, Walton TE, Woods CW, et al. Quantitative models of the dose-response and time course of inhalational anthrax in humans. PLoS Pathog. 2013;9:e1003555.
- Kelly DJ, Chulay JD, Mikesell P, Friedlander AM. Serum concentrations of penicillin, doxycycline, and ciprofloxacin during prolonged therapy in rhesus monkeys. J Infect Dis. 1992;166:1184–7.
- Meyerhoff A, Albrecht R, Meyer JM, Dionne P, Higgins K, Murphy D. US Food and Drug Administration approval of ciprofloxacin hydrochloride for management of postexposure inhalational anthrax. Clin Infect Dis. 2004;39:303–8.
- Vietri NJ, Purcell BK, Lawler JV, Leffel EK, Rico P, Gamble CS, et al. Short-course postexposure antibiotic prophylaxis combined with vaccination protects against experimental inhalational anthrax. Proc Natl Acad Sci U S A. 2006;103:7813–6.
- Jefferds MD, Laserson K, Fry AM, Roy S, Hayslett J, Grummer-Strawn L, et al.; Centers for Disease Control and Prevention Anthrax Adherence Team. Adherence to antimicrobial inhalational anthrax prophylaxis among postal workers, Washington, D.C., 2001. Emerg Infect Dis. 2002;8:1138–44.
- Holty JE, Bravata DM, Liu H, Olshen RA, McDonald KM, Owens DK. Systematic review: a century of inhalational anthrax cases from 1900 to 2005. Ann Intern Med. 2006;144:270–80.
- Barakat LA, Quentzel HL, Jernigan JA, Kirschke DL, Griffith K, Spear SM, et al.; Anthrax Bioterrorism Investigation Team. Fatal inhalational anthrax in a 94-year-old Connecticut woman. JAMA. 2002;287:863–8.
- Hendricks KA, Wright ME, Shadomy SV, Bradley JS, Morrow MG, Pavia AT, et al.; Workgroup on Anthrax Clinical Guidelines. Centers for disease control and prevention expert panel meetings on prevention and treatment of anthrax in adults. Emerg Infect Dis. 2014;20:20.
- Jernigan DB, Raghunathan PL, Bell BP, Brechner R, Bresnitz EA, Butler JC, et al.; National Anthrax Epidemiologic Investigation Team. Investigation of bioterrorism-related anthrax, United States, 2001: epidemiologic findings. Emerg Infect Dis. 2002;8:1019–28.
- Walsh DM, Van Groningen C, Craig B. Logistics modelling: improving resource management and public information strategies in Florida. J Bus Contin Emer Plan. 2011;5:246–56.
- Shepard CW, Soriano-Gabarro M, Zell ER, Hayslett J, Lukacs S, Goldstein S, et al.; CDC Adverse Events Working Group. Antimicrobial postexposure prophylaxis for anthrax: adverse events and adherence. Emerg Infect Dis. 2002;8:1124–32.
- Brookmeyer R, Johnson E, Bollinger R. Modeling the optimum duration of antibiotic prophylaxis in an anthrax outbreak. Proc Natl Acad Sci U S A. 2003;100:10129–32.
- Wright JG, Quinn CP, Shadomy S, Messonnier N; Centers for Disease Control and Prevention (CDC). Use of anthrax vaccine in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2009. MMWR Recomm Rep. 2010;59(RR-6):1–30.
- Wilkening DA. Modeling the incubation period of inhalational anthrax. Med Decis Making. 2008;28:593–605.
Technical AppendicesCite This Article
1These senior authors contributed equally to this article.
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