- Research article
- Open Access
- Open Peer Review
Retrospective analysis of demographic and clinical factors associated with etiology of febrile respiratory illness among US military basic trainees
BMC Infectious Diseasesvolume 14, Article number: 576 (2014)
Basic trainees in the US military have historically been vulnerable to respiratory infections. Adenovirus and influenza are the most common etiological agents responsible for febrile respiratory illness (FRI) among trainees and present with similar clinical signs and symptoms. Identifying demographic and clinical factors associated with the primary viral pathogens causing FRI epidemics among trainees will help improve differential diagnosis and allow for appropriate distribution of antiviral medications. The objective of this study was to determine what demographic and clinical factors are associated with influenza and adenovirus among military trainees.
Specimens were systematically collected from military trainees meeting FRI case definition (fever ≥38.0°C with either cough or sore throat; or provider-diagnosed pneumonia) at eight basic training centers in the USA. PCR and/or cell culture testing for respiratory pathogens were performed on specimens. Interviewer-administered questionnaires collected information on patient demographic and clinical factors. Polychotomous logistic regression was employed to assess the association between these factors and FRI outcome categories: laboratory-confirmed adenovirus, influenza, or other FRI. Sensitivity, specificity, positive and negative predictive value were calculated for individual predictors and clinical combinations of predictors.
Among 21,570 FRI cases sampled between 2004 and 2009, 63.6% were laboratory-confirmed adenovirus cases and 6.6% were laboratory-confirmed influenza cases. Subjects were predominantly young men (86.8% men; mean age 20.8 ± 3.8 years) from Fort Jackson (18.8%), Great Lakes (17.1%), Fort Leonard Wood (16.3%), Marine Corps Recruit Depot (MCRD) San Diego (19.0%), Fort Benning (13.3%), Lackland (7.5%), MCRD Parris Island (8.7%), and Cape May (3.2%). The best multivariate predictors of adenovirus were the combination of sore throat (odds ratio [OR], 2.94; 95% confidence interval [CI], 2.66-3.25), cough (OR, 2.33; 95% CI, 2.11-2.57), and fever (OR, 2.07; 95% CI, 1.90-2.26) with a PPV of 77% (p ≤.05). A combination of cough, fever, training week 0-2 and acute onset were most predictive of influenza (PPV =38%; p ≤ .05).
Specific demographic and clinical factors were associated with laboratory-confirmed influenza and adenovirus among military trainees. Findings from this study can guide clinicians in the diagnosis and treatment of military trainees presenting with FRI.
Historically, military basic trainees have been vulnerable to severe epidemics of febrile respiratory illness (FRI) ,. Several factors predispose military trainees to the spread respiratory infections, including crowded living conditions and stressful work environments. The epidemiology and pathogens causing FRI among military trainees is unique and differs from the civilian setting . Training populations are primarily prone to outbreaks caused by adenovirus and influenza, which often co-circulate and present with similar clinical signs and symptoms .
In the presence of an epidemic, it is generally acceptable to make a reasonable diagnosis based on clinical signs and symptoms until laboratory confirmation can be obtained. It is still debatable whether specific demographic and clinical symptoms can be used to distinguish among respiratory pathogens. A few studies have identified clinical predictors for influenza in civilian and military populations -. However, few studies have focused on other respiratory pathogens like adenovirus that have caused substantial morbidity among military trainees ,.
Adenovirus infections have caused significant morbidity among US military trainees since the virus was discovered in the1950s. With interrupted training schedules, high morbidity, and the occasional death, it has proved to be costly to the US Government ,. Live oral vaccines against types 4 and 7 adenovirus were developed in the late 1960s and were successful in reducing FRI rates and adenoviral morbidity after their introduction in 1971. However, the sole vaccine manufacturer stopped production in 1996, and adenovirus returned to US recruit training centers and commands (RTCs) at pre-vaccine levels after vaccine supplies were depleted in 1999. The clinical presentation of adenovirus-associated FRI has been described as more severe than non-adenovirus-associated FRI, particularly when it is a novel strain in which there is little to no immunity . Adenoviruses cases present with higher temperatures and have an increased number of cases with a cough and sore throat compared with non-adenovirus-associated FRI cases .
FRI infections present with a wide range of clinical features. Identifying demographic and clinical factors associated with the primary viral pathogens causing FRI epidemics among military trainees will help improve differential diagnosis, allow for appropriate distribution of antiviral medications, and ultimately improve troop readiness. The objective of this study was to determine what demographic and clinical factors are associated with influenza and adenovirus among military trainees at RTCs in an effort to aid clinical diagnosis when laboratory confirmation is not available.
Since 1996, the Naval Health Research Center (NHRC) has conducted ongoing laboratory-based surveillance FRI at eight basic training centers across the United States: Fort Benning Army Training Center, Georgia; Fort Jackson Army Training Center, South Carolina; Fort Leonard Wood Army Training Center, Missouri; Lackland Air Force Base, Texas; Great Lakes Naval Training Command, Illinois; Marine Corps Recruit Depots (MCRDs) San Diego, California, and Parris Island, South Carolina; and Cape May Coast Guard Training Center, New Jersey. Length of basic training varies throughout branches of military service: 10 weeks for the Army, 7 weeks Navy, 8 weeks Air Force, 12 weeks Marine Corps, and 8 weeks Coast Guard. In support of surveillance, military basic trainees from these training sites meeting case definition for FRI (fever ≥38.0°C with either cough or sore throat; or provider-diagnosed pneumonia) were recruited for the study. All subjects provided informed consent. This study was approved by the Naval Health Research Center (NHRC) Institutional Review Board (protocol NHRC.1999.0002).
Specimen and data collection
Throat and nasal swabs and clinical data were systematically collected from consenting US military trainees meeting the case definition for FRI. Each training site except for Cape May had a trained research assistant dedicated to enrolling subjects in the study and collecting clinical specimens. Sampling of a maximum ranging from 10 to 20 recruits per site per week was performed. Subjects were systematically selected from trainees presenting to their local clinic meeting FRI case definition. Trainees were tracked throughout the entirety of their training, with the exception of MCRD San Diego where trainees left for Camp Pendleton for weeks 4 through 7 of training. Trainees awaiting the start of training were assigned to training week 0.
Questionnaires administered by research assistants (corpsmen at Cape May) collected information on patient demographic and clinical factors, including age, sex, number of days since symptoms began, number of visits to sick call during illness, diagnosis of pneumonia, history of asthma, smoking history (pack-years), history of influenza vaccination, week of training, and experience of any of the following symptoms during his or her current illness: sore throat, cough, shortness of breath, nasal congestion, headache, conjunctivitis, body aches, and nausea or vomiting. The patient's oral temperature was abstracted from the medical record or taken by the research assistant. Medical records were reviewed to abstract data needed for questionnaire.
Up to two throat and/or nasal swabs were collected by on-site personnel using Dacron respiratory swabs (MicroTest viral transport media (VTM), Remel, Inc., Lenexa, KS, USA). Swabs were immediately placed into the VTM and broken off so that the tip remained in the media. VTM were maintained on ice or refrigerated at 4°C (2-8°C) during processing and stored within 60 minutes at -70°C. Specimens were stored locally at -70°C until shipped on dry ice to NHRC for viral culture and molecular diagnostic processing. Shipping occurred on a weekly or biweekly basis (not to exceed 1 month) depending on season and FRI rates at respective training sites. The NHRC laboratory is accredited by the College of American Pathologists.
Upon arrival at NHRC, all specimens underwent molecular testing (polymerase chain reaction [PCR]) for a number of respiratory pathogens, including adenovirus and influenza A. Viral culture was performed on 20% of randomly selected specimens that were PCR positive for adenovirus and on all of the specimens that were PCR negative for adenovirus. Viral culture was performed using two different cell lines: primary monkey kidney cell line (either rhesus or cynomolgus) for influenza and an A549 cell line for adenovirus. Influenza-positive isolates were typed using hemagglutination inhibition, and adenovirus isolates were typed using microneutralization techniques ,. Viral culture was used to test for influenza A and B and other FRI pathogens (respiratory syncytial virus, and parainfluenza viruses 1 and 3).
The main outcome variables were laboratory-confirmed influenza or adenovirus, defined as having any specimen positive for influenza or adenovirus using PCR or culture. Adenovirus and influenza A results were determined by PCR or culture, and influenza B was determined by culture alone. The main outcome variable was categorized into a three-level variable based on FRI laboratory determination: adenovirus positive, influenza positive, or other FRI (negative for adenovirus and influenza). Categorical variables were constructed from continuous clinical variables based on clinical definitions. Acute onset was defined as ≤3 days since symptom onset. Fever was defined as temperature ≥38.0°C. Those who were afebrile were enrolled as provider-diagnosed pneumonia cases. Assuming influenza vaccine protection takes 14 days to develop, the influenza-vaccinated group was defined as those vaccinated longer than 14 days prior to testing. Data from the 2009 H1N1 pandemic were included in the analysis.
Statistical analysis was performed using SAS software, version 9.2 (SAS Institute Inc., Cary, NC, USA). Frequencies and descriptive statistics were performed. Mean and standard deviation were reported for normally distributed variables, and median and range were reported for non-normally distributed variables. A multivariate polychotomous logistic regression model was developed to model the probability of laboratory-confirmed adenovirus, laboratory-confirmed influenza, and other FRI against clinical and demographic predictors (age, sex, acute onset, fever, pneumonia diagnosis, sore throat, cough, shortness of breath, nasal congestion, headache, conjunctivitis, body aches, nausea/vomiting, asthma, smoking history, influenza vaccination status, training week, and enrollment site). Colinearity diagnostics were done to assess confounding between predictor variables. First clinic visit and cigarette pack-years were not incorporated in the model because of the possibility of collinearity with acute onset and smoking.
Manual stepwise model-building strategy was used to develop the model that included all variables significantly associated with the main outcome variables. Predictors were included in the model one at a time and removed if not significant at p <0.05. Asthma was the only predictor that fell out of the model. Parameter estimates and significance levels were reviewed during model building to assess the relative importance of each variable. Adjusted odds ratios (ORs) and confidence intervals (CIs) were reported for each multivariate logistic regression model. Variance inflation factor and tolerance values were evaluated to assess multicollinearity and model fitness. All variables were considered statistically significant at p <0.05.
Variables demonstrating associations with laboratory-confirmed adenovirus and influenza (ie, the predictors of influenza and adenovirus) in the reduced multivariate model were incorporated into various clinical combinations. Sensitivity, specificity, positive predictive value (PPV), and negative predictive value were calculated for individual predictors and various clinical combinations of predictors in an effort to model these as clinical diagnostic tests. Binomial proportions with 95% CIs were calculated.
Among 21,570 FRI cases sampled between November 2004 and October 2009, 63.6% were laboratory-confirmed adenovirus cases and 6.7% were laboratory-confirmed influenza cases. Trainees presented to the clinic 3 days after self-reported onset of symptoms (range 1-90). For 68.0% of trainees, it was their first illness-related clinic visit. Subjects were predominantly young men (86.8% men; mean years 20.8 ± 3.8) from Fort Jackson (18.8%), Great Lakes (17.1%), Fort Leonard Wood (16.3%), MCRD San Diego (19.0%), Fort Benning (13.3%), Lackland (7.5%), MCRD Parris Island (8.7%), and Cape May (3.2%). Most subjects were febrile (83.0%) and had a cough (89.2%) and/or sore throat (88.9%) because of study inclusion criteria. Adenovirus-confirmed cases had a higher percentage with a sore throat compared with influenza cases (adenovirus = 93%, influenza = 81.3%; P < .0001). Conversely, influenza-positive cases had a higher percentage with a cough compared with adenovirus-positive cases (influenza = 98.3%, adenovirus = 91.5%; P < .0001). Subject characteristics are reported in Table 1.
Regression modeling revealed associations with laboratory-confirmed adenovirus and clinical predictors (adjusted OR and 95% CI reported): sore throat (OR, 2.94; 95% CI, 2.66-3.25, cough (OR, 2.33; 95% CI, 2.11-2.57), fever (OR, 2.07; 95% CI, 1.90-2.26), nausea/vomiting (OR, 1.19; 95% CI, 1.11-1.27), and nasal congestion (OR, 1.12; 95% CI, 1.03-1.22). Regression modeling of laboratory-confirmed influenza showed significant associations with cough (OR, 13.85; 95% CI, 9.14-20.97), fever (OR, 1.99; 95% CI, 1.66-2.38), acute onset (OR, 1.46; 95% CI, 1.26-1.68), and body aches (OR, 1.31; 95% CI, 1.13-1.53). Sore throat, nasal congestion, and nausea/vomiting were associated with laboratory-confirmed adenovirus but not with influenza, while acute onset of illness (≤3 days) and body aches were associated with laboratory-confirmed influenza but not with adenovirus. Fever and cough were significantly associated with both adenovirus and influenza. Asthma fell out of the model all together.
Analysis of demographic factors revealed interesting results. Female sex was a protective factor for adenovirus infection (OR, 0.72; 95% CI, 0.66-0.80) but was not associated with influenza. Being a smoker before training was protective for both adenovirus and influenza (OR, 0.92; 95% CI, 0.86-0.99) and OR, 0.77; 95% CI, 0.67-0.88, respectively). Adenovirus was seen year-round and associated with all training seasons, with a protective effect seen during the winter season. However, winter training was significantly associated with influenza, with a protective effect seen during other seasons. Distribution of study cases by seasons and years is illustrated in the Figure 1.
Furthermore, influenza was associated with the first 2 weeks of training (OR, 1.82, 95% CI, 1.50-2.21). Adenovirus was associated with weeks 3 and 4 of training (OR, 1.61; 95% CI, 1.47-1.76), these odds increased during training weeks 5 and 6 (OR, 1.91; 95% CI, 1.74-2.10), with no association seen with influenza during training weeks 3-6. Clinical and demographic factors associated with the development of laboratory-confirmed adenovirus and influenza, as determined by multivariate polychotomous logistic regression analysis, are shown in Figures 2 and 3.
Table 2 displays the performance of clinical diagnostic tests constructed from combinations of predictors for adenovirus. The highest specificity (92.4%) and PPV (81.7%) were noted for a combination of four criteria (sore throat, fever, training weeks 3-6, summer season), but the sensitivity was low (19.5%). The combination of three criteria (sore throat, cough, and fever) yielded both high sensitivity (74.4%) and PPV (71.2%) but had marginal specificity (47.3%). Table 3 displays the results of clinical diagnostic tests constructed from combinations of predictors for influenza. The combination of four criteria (cough, training week 0-2, winter season, and fever) had the highest specificity (97.0%) and PPV (39.4%) but had a sensitivity of 26.9%. The combination of two criteria (cough and fever) showed the highest sensitivity (84.3%), with a specificity of 27.1% and a PPV of 7.6%.
Adenovirus and influenza infections are the leading cause of FRI outbreaks among military trainees at RTCs. This study compared the predictive values of demographic and clinical factors for laboratory-confirmed adenovirus and laboratory-confirmed influenza from 2004 to 2009 among military trainees. The results of this study may help clinicians distinguish an influenza or adenovirus infection from an illness caused by other FRI, based on clinical symptoms and demographic factors. Distinguishing clinical and demographic factors may aid clinicians with differential diagnosis when laboratory confirmation is not available and allow for appropriate dissemination of antiviral medications for influenza.
Few studies have examined factors associated with specific viral pathogens causing FRI among military populations. A study by McNeill and colleagues investigated the clinical presentation of influenza, adenovirus, and other pathogens causing FRI among military members. They found that overall viral pathogens presented as clinically indistinguishable from one another . Conversely, this present study found several clinical symptoms to be independently associated with adenovirus (sore throat, nausea/vomiting, and nasal congestion) and influenza (acute onset and body aches). Cough and fever were associated with both adenovirus and influenza. However, although cough and fever were associated with both pathogens, recruits with a cough were significantly more likely to be positive for influenza (OR, 13.6; 95% CI, 9.03-20.48) than adenovirus (OR, 2.32; 95% CI, 2.07-2.59). This is consistent with other studies that have reported fever and cough as highly predictive of influenza infections, and with the Centers for Disease Control and Prevention definition for influenza-like illness ,,.
The clinical presentation of adenovirus illness described in this paper is similar to other military studies ,. A study conducted by Brosch et al. looking at clinical predictors for adenovirus 14 showed that the majority of adenovirus cases had cough and fever . McNeill et al. found similar results ,. Several other studies have seen an association between adenovirus infection and either abdominal pain or nausea ,,, consistent with the present study. A recent study evaluating the clinical presentation of military personnel presenting with FRI found that influenza-positive cases were more likely to present with a runny nose, chills, and ocular symptoms than were other FRI cases, which were more likely to present with a sore throat and nausea/vomiting . Interestingly, our study found sore throat and nausea/vomiting to be solely associated with adenovirus.
In this study, demographic factors associated with adenoviral infections included male sex, smoking, training week (weeks 5 and 6) and training season (spring, summer, and fall months). The protective association seen between smoking and both adenovirus and influenza infections appears counterintuitive. Although the literature is conflicting, a protective effect has previously been seen with adenovirus infections . However, the majority of studies published have shown smoking is a risk factor for FRI ,,. That said, all military training facilities are smoke free and the protective effect seen among adenovirus-positive individuals may be a result of more frequent adenovirus infections seen among smokers in general, hence a natural immunity may have been present prior to military enlistment . Our results substantiate previous studies that reported adenovirus-associated illness in training weeks 3-6 and the protective effect of female sex ,,,. We found that influenza was more likely to occur within the first 2 weeks of training and during the winter season, whereas adenovirus was more likely to occur during weeks 3-6 of training and during the spring, summer, and fall seasons. Training week and seasons are potential tools that clinicians can use to aid in differential diagnosis of FRI among military trainees. Clinical predictors found in this study can aid with quarantine procedures during and FRI outbreak thus reducing the spread of disease and reducing costs to the US government.
After a 12-year absence, second-generation oral vaccines for adenovirus types 4 and 7 resumed distribution at RTCs in October 2011. Since that time, rates of FRI and adenoviral morbidity have decreased substantially. Although there is hope that the cross-protective effect of the vaccines will be seen among the non-vaccine-targeted adenovirus serotypes, it will be important to track the response of different serotypes to the vaccines. The body of literature could be enhanced by conducting further studies examining clinical and demographic characteristics of adenovirus subtypes causing FRI at RTCs, with a comparative analysis pre- and post-vaccine distribution.
Although our study included a robust sample size and laboratory-confirmed illness, it predominately consisted of young men in a military training environment. The epidemiology and pathogens causing respiratory illness among military recruits is often unique and different from that of the civilian setting. As a result, these finding may not be generalizable to the civilian population. Lastly, clinical predictors of influenza and adenovirus may differ among viral subtypes. Further studies are needed to explore the clinical presentation among sub-types of viral pathogens.
DSP participated in the design of the study, coordinated study activities, conducted data analysis, and drafted the manuscript. DF conceived of the study and participated in its design, supervised laboratory reference testing, and participated in manuscript revision. SB participated in the design of the study and manuscript revision. HL participated in the design of the study and assisted with data analysis. AH and SP assisted with data analysis, participated in the design, and assisted in manuscript revision. PB participated in manuscript revision. All authors read and approved the final manuscript.
Ms. Padin is a study coordinator and epidemiologist at the Naval Health Research Center (NHRC). Dr. Brodine is a researcher at NHRC, and a professor and Epidemiology Division Head at San Diego State University (SDSU) Graduate School of Public Health (GSPH). Dr. Lemus is an assistant professor at SDSU GSPH. Dr. Blair is department head for the NHRC Operational Infectious Diseases (OID) Department. Dr. Faix is assistant department head for NHRC OID. Mr. Hawksworth is the senior data manager and surveillance study coordinator for NHRC OID. Dr. Putnam is head of the Enteric Disease Surveillance Program for NHRC OID.
Hilleman MR: Epidemiology of adenovirus respiratory infections in military recruit populations. Ann N Y Acad Sci. 1957, 67 (8): 262-272. 10.1111/j.1749-6632.1957.tb46049.x.
Artenstein AW, Opal JM, Opal SM, Tramont EC, Peter G, Russell PK: History of U.S. military contributions to the study of vaccines against infectious diseases. Mil Med. 2005, 170 (4 Suppl): 3-11.
Gray GC, Callahan JD, Hawksworth AW, Fisher CA, Gaydos JC: Respiratory diseases among U.S. military personnel: countering emerging threats. Emerg Infect Dis. 1999, 5 (3): 379-385. 10.3201/eid0503.990308.
Russell KL: Respiratory Infections in Military Recruits. Textbooks of Military Medicine: Recruit Medicine. Edited by: DeKoning BI. 2006, Bordon Institute, Washington, DC, 227-253.
Puzelli S, Valdarchi C, Ciotti M, Dorrucci M, Farchi F, Babakir-Mina M, Perno CF, Donatelli I, Rezza G: Viral causes of influenza-like illness: insight from a study during the winters 2004-2007. J Med Virol. 2009, 81 (12): 2066-2071. 10.1002/jmv.21610.
Boivin G, Hardy I, Tellier G, Maziade J: Predicting influenza infections during epidemics with use of a clinical case definition. Clin Infect Dis. 2000, 31 (5): 1166-1169. 10.1086/317425.
Peltola V, Reunanen T, Ziegler T, Silvennoinen H, Heikkinen T: Accuracy of clinical diagnosis of influenza in outpatient children. Clin Infect Dis. 2005, 41 (8): 1198-1200. 10.1086/444508.
Lee VJ, Yap J, Cook AR, Tan CH, Loh JP, Koh WH, Lim EA, Liaw JC, Chew JS, Hossain I, Chan KW, Ting PJ, Ng SH, Gao Q, Kelly PM, Chen MI, Tambyah PA, Tan BH: A clinical diagnostic model for predicting influenza among young adult military personnel with febrile respiratory illness in Singapore. PLoS One. 2011, 6 (3): e17468-10.1371/journal.pone.0017468.
Kasper MR, Wierzba TF, Sovann L, Blair PJ, Putnam SD: Evaluation of an influenza-like illness case definition in the diagnosis of influenza among patients with acute febrile illness in Cambodia. BMC Infect Dis. 2010, 10: 320-10.1186/1471-2334-10-320.
Gray GC, McCarthy T, Lebeck MG, Schnurr DP, Russell KL, Kajon AE, Landry ML, Leland DS, Storch GA, Ginocchio CC, Robinson CC, Demmler GJ, Saubolle MA, Kehl SC, Selvarangan R, Miller MB, Chappell JD, Zerr DM, Kiska DL, Halstead DC, Capuano AW, Setterquist SF, Chorazy ML, Dawson JD, Erdman DD: Genotype prevalence and risk factors for severe clinical adenovirus infection, United States 2004-2006. Clin Infect Dis. 2007, 45 (9): 1120-1131. 10.1086/522188.
Faix DJ, Houng HS, Gaydos JC, Liu SK, Connors JT, Brown X, Asher LV, Vaughn DW, Binn LN: Evaluation of a rapid quantitative diagnostic test for adenovirus type 4. Clin Infect Dis. 2004, 38 (3): 391-397. 10.1086/380972.
Russell KL, Hawksworth AW, Ryan MA, Strickler J, Irvine M, Hansen CJ, Gray GC, Gaydos JC: Vaccine-preventable adenoviral respiratory illness in US military recruits, 1999-2004. Vaccine. 2006, 24 (15): 2835-2842. 10.1016/j.vaccine.2005.12.062.
Sivan AV, Lee T, Binn LN, Gaydos JC: Adenovirus-associated acute respiratory disease in healthy adolescents and adults: a literature review. Mil Med. 2007, 172 (11): 1198-1203.
Grayston JT, Woolridge RL, Loosli CG, Gundelfinger BF, Johnston PB, Pierce WE: Adenovirus infections in naval recruits. J Infect Dis. 1959, 104 (1): 61-70. 10.1093/infdis/104.1.61.
van Elden LJ, Nijhuis M, Schipper P, Schuurman R, van Loon AM: Simultaneous detection of influenza viruses A and B using real-time quantitative PCR. J Clin Microbiol. 2001, 39 (1): 196-200. 10.1128/JCM.39.1.196-200.2001.
Schmidt-Schläpfer G, Liese JG, Porter F, Stojanov S, Just M, Belohradsky BH: Polymerase chain reaction (PCR) compared with conventional identification in culture for detection of Bordetella pertussis in 7153 children. Clin Microbiol Infect. 1997, 3 (4): 462-467. 10.1111/j.1469-0691.1997.tb00283.x.
McNeill KM, Vaughn BL, Brundage MB, Yuanzhang L, Poropatich RK, Gaydos JC: Clinical presentations for influenza and influenza-like illness in young, immunized soldiers. Mil Med. 2005, 170 (1): 94-97.
Monto A, Gravenstein S, Elliot M, Colopy M, Schweinle J: Clinical signs and symptoms predicting influenza infection. Arch Intern Med. 2000, 160: 3243-3247. 10.1001/archinte.160.21.3243.
Crum-Cianflone NF, Blair PJ, Faix D, Arnold J, Echols S, Sherman SS, Tueller JE, Warkentien T, Sanguineti G, Bavaro M, Hale BR: Clinical and epidemiologic characteristics of an outbreak of novel H1N1 (swine origin) influenza A virus among United States military beneficiaries. Clin Infect Dis. 2009, 49 (12): 1801-1810. 10.1086/648508.
Brosch L, Tchandja J, Marconi V, Rasnake M, Prakash V, McKnight T, Bunning M: Adenovirus serotype 14 pneumonia at a basic military training site in the United States, spring 2007: a case series. Mil Med. 2009, 174 (12): 1295-1299. 10.7205/MILMED-D-03-0208.
Update: swine influenza A (H1N1) infections-California and Texas, April 2009. MMWR Morb Mortal Wkly Rep. 2009, 58 (16): 435-437.
Ryan MAK, Gray GC, Smith B, McKeehan JA, Hawksworth AW, Malasig MD: Large epidemic of respiratory illness due to adenovirus types 7 and 3 in healthy young adults. Clin Infect Dis. 2002, 34 (5): 577-582. 10.1086/338471.
Sanchez JL, Binn LN, Innis BL, Reynolds RD, Lee T, Mitchell-Raymundo F, Craig SC, Marquez JP, Shepherd GA, Polyak CS, Conolly J, Kohlhase KF: Epidemic of adenovirus-induced respiratory illness among US military recruits: epidemiologic and immunologic risk factors in healthy, young adults. J Med Virol. 2001, 65 (4): 710-718. 10.1002/jmv.2095.
Blake GH, Abell TD, Stanley WG: Cigarette smoking and upper respiratory infection among recruits in basic combat training. Ann Intern Med. 1988, 109 (3): 198-202. 10.7326/0003-4819-109-3-198.
Tate JE, Bunning ML, Lott L, Lu X, Su J, Metzgar D, Brosch L, Panozzo CA, Marconi VC, Faix DJ, Prill M, Johnson B, Erdman DD, Fonseca V, Anderson LJ, Widdowson MA: Outbreak of severe respiratory disease associated with emergent human adenovirus serotype 14 at a US Air Force training facility in 2007. J Infect Dis. 2009, 199 (10): 1419-1426. 10.1086/598520.
Kolavic-Gray SA, Binn LN, Sanchez JL, Cersovsky SB, Polyak CS, Mitchell-Raymundo F, Asher LV, Vaughn DW, Feighner BH, Innis BL: Large epidemic of adenovirus type 4 infection among military trainees: epidemiological, clinical, and laboratory studies. Clin Infect Dis. 2002, 35 (7): 808-818. 10.1086/342573.
Rosenbaum MJ, Edwards EA, Frank PF, Pierce WE, Crawford YE, Miller LF: Epidemiology and prevention of acute respiratory disease in naval recruits. I. Ten years' experience with microbial agents isolated from naval recruits with acute respiratory disease. Am J Public Health Nations Health. 1965, 55: 38-46. 10.2105/AJPH.55.1.38.
We are grateful to research assistants at the recruit training centers and laboratory staff at the Naval Health Research Center who performed all subject enrollments and testing, without whose support such studies could not be conducted.
This work was supported by the Armed Forces Health Surveillance Center, Global Emerging Infections Surveillance and Response System (GEIS) operations, under work unit number 60501. The funding organization was not involved in study design, data collection, analysis, interpretation of results, or manuscript writing. The views expressed in this article are those of the authors and do not reflect the official policy or position of the Department of the Navy, Department of Defense, or the US Government. Approved for public release; distribution is unlimited. This research has been conducted in compliance with all applicable federal regulations governing the protection of human subjects in research (protocol NHRC.1999.0002).
The authors declare that they have no competing interests.