Background and Methods: Active duty US Army and Air Force military personnel undergo mandatory biennial HIV antibody screening. We compared pre- and post-HIV seroconversion health status by conducting a case-control study, which evaluated all medical encounters and sociodemographic factors among incident HIV seroconverters and HIV-negative controls from June 2000 through February 2004.
Results: A total of 274 HIV seroconverters and 6205 HIV-negative personnel were included. In multivariate analysis restricted to male personnel (cases = 261, controls = 5801), single marital status (adjusted odds ratio [AOR] = 14.37), clinical indicators or symptoms within four years of HIV diagnosis (AOR = 6.22), black race (AOR = 5.88), nonindicator clinical syndromes within 2 years of HIV diagnosis (AOR = 3.31), any mental disorder within 4 years of HIV diagnosis (AOR = 3.04), increasing service-connected time (AOR = 1.69), and older age (AOR = 1.12) were associated with HIV diagnosis among males. A prior history of a sexually transmitted infection (STI) was associated with post-HIV seroconversion STI (ORM-H = 4.10). Similarly, a prior history of mental disorder was associated with post-HIV seroconversion mental disorder (ORM-H = 4.98). Forty-seven (18%) male cases were hospitalized at least once after HIV diagnosis; infectious diseases, and mental disorders made up 53% of initial admissions.
Conclusions: HIV seroconversion was associated with increased health care-seeking behavior, STIs, and mental disorders, some of which may be amenable to screening. The higher STI rate after HIV diagnosis may partially be a consequence of monitoring, but secondary transmission of STI and possibly HIV require further definition and subsequent tailored preventive interventions.
From the *Department of Epidemiology and Threat Assessment, United States Military HIV Research Program, Henry M. Jackson Foundation for the Advancement of Military Medicine, Rockville, MD; †U.S. Military Tropical Medicine, Navy Medicine Manpower, Personnel, Training & Education Command, Bethesda, MD; ‡Department of Preventive Medicine and Biometrics, Uniformed Services University of the Health Sciences, Bethesda, MD; §Division of Retrovirology, Walter Reed Army Institute of Research, Rockville, MD; ‖The Department of Defense Global Emerging Infections Surveillance and Response System (DoD-GEIS), Armed Forces Health Surveillance Center, Silver Spring, MD; and ¶Infectious Disease Clinical Research Program, Uniformed Services University, Bethesda, MD.
Received for publication October 21, 2010; accepted December 8, 2010.
This work was supported by funds from the Military Infectious Disease Research Program (Proposal 1A0001_06_WR_OC) and approved by the Walter Reed Army Institute of Research Institutional Review Board (#1109).
The views expressed are those of the authors and should not be construed to represent the positions of the US Department of Defense, the US Government, or any of its agencies.
Correspondence to: Dr. Shilpa Hakre, Epidemiology and Threat Assessment, US Military HIV Research Program, 1 Taft Ct. Suite 250, Rockville, MD 20850 (e-mail: firstname.lastname@example.org).
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Approximately, one-third of the US population with HIV infection is unaware of their serostatus.1 Undiagnosed HIV prevalence differs by racial makeup and behavioral risks.1 Early diagnosis of HIV provides opportunities for interrupting transmission of the virus and improving disease progression through earlier access to specialized medical care. Serum viral load levels are associated with HIV transmission especially during the early and late stages of HIV disease.2,3 In the era of antiretroviral therapy, treatment leads to reduced viral loads and transmission with improvement in health outcomes.3 In populations with access to health care, delayed HIV testing has been associated with late presentation and poor outcomes.4-6 Although recognition of acute HIV infection in presenting patients affords a public health opportunity for decreasing HIV transmission, attention to clinical indicators alone has not prompted targeted testing in clinical settings.7,8 Identification of additional factors such as recent sexually transmitted infection (STI) may aid in targeted testing.9
The US armed forces began mandatory periodic screening for HIV antibody in 1985.10 Screening was initiated for maintaining the health, well-being, and military readiness of personnel, ensuring a safe blood supply in combat situations of “buddy transfusions,” and preventing adverse events from live virus vaccinations among HIV-infected personnel.11 The interval in screening varied by Service from 1-5 years. Beginning in 2004, the screening interval was standardized across Services to 2 years as infected people rarely progressed to AIDS within 2 years.12 Although the US military's HIV incidence and prevalence average 0.02%, significantly lower than in the US civilian population,13 HIV incidence has been increasing among military personnel from 2000 to 2008.14,15 We conducted our study to identify factors which may promote earlier diagnosis of HIV, augmenting current screening strategies. We were interested in studying if medical conditions and visits before HIV seroconversion differed among HIV-infected compared with uninfected Soldiers and Airmen and to see if these associations persisted after HIV diagnosis. Additionally, we describe sociodemographic differences between HIV seroconverters and controls.
The data reported here were collected for a seroepidemiologic case-control study among active duty and reserve US Army and Air Force personnel, for which the methods have been described.16,17 Using HIV test dates for selection, the broader study randomly sampled 20 controls to a case and frequency matched by gender. The control to case ratio was driven by reported demographic differences among HIV-infected and HIV-uninfected military personnel, and to ensure that demographics of the controls were representative of the military population. Because females represent a small proportion of US military personnel and HIV seroconverters, frequency matching assisted similar proportions as cases.18,19
We restricted our study to active duty personnel. Active duty personnel can access care in the military health system throughout their service, whereas reservists have limited access when not activated. Cases were active duty US Army and Air Force personnel newly diagnosed with HIV from June 1, 2000, through February 29, 2004, with evidence of at least 1 medical encounter in the 4 years preceding diagnosis. Controls were active duty Army and Air Force personnel with a HIV-negative test in a 30-day interval of a case's first-positive HIV test with at least 1 medical encounter in the preceding 4 years. Index dates for cases were the date of blood draw of the first HIV confirmed positive serological test result and for controls the date of the HIV-negative serological test within the case date interval.
Longitudinal sociodemographic information, outpatient and inpatient medical encounters, duty assignment, and deployment histories were obtained from the Defense Medical Surveillance System.20 During the study period, active duty Soldiers were routinely screened for HIV every 2 years although Airmen were screened every 3-5 years.21 For HIV-infected military personnel with a last negative HIV test within 1 year of the first-positive HIV test result, the dates of last-negative HIV tests were obtained. Medical encounter records (up to 4 years preceding and after the index date) included visit dates and up to 8 (4 for outpatient, 8 for inpatient) International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) diagnostic codes. Duty assignment (up to 5 years before the index date) and deployment roster records (up to 4 years before and after the index date) provided start and end dates, and locations of assignments and military deployments.
Characteristics considered for analysis were disease groups, medical diagnoses, medical diagnosis clusters, medical encounter frequency, reasons for first postindex hospitalization, demographic characteristics at index date, frequencies of preindex permanent changes of station (PCS's) and deployments, deployment in the year before the index date, and period of observation in years before (follow-back) and after (follow-up) the index date. Follow-back time served as a surrogate for length of service connection. Medical visits were summarized before and after index dates, by visit type (inpatient or outpatient) and compared between cases and controls. Multiple records on the same day and health care setting were considered duplicate records and deleted for medical visit enumeration.
Disease groups were compared between cases and controls to identify those associated with HIV infection. Incident ICD-9-CM codes in any position on medical encounter records before the index date were categorized into 19 standard groups to include as follows: infectious and parasitic diseases; mental disorders; digestive system; blood and blood-forming organs; respiratory system; musculoskeletal and connective tissue system; endocrine, nutritional and metabolic diseases, and immunity disorders; genitourinary systems; complications of pregnancy, childbirth, and the puerperium; injury and poisoning; neoplasms; skin and subcutaneous tissue; symptoms, signs, and ill-defined conditions; circulatory system; and supplementary classification of factors influencing health status and contact with health services (V codes).22 Additionally, a literature search identified reported medical diagnoses and symptoms associated with primary HIV infection to include fever, fatigue, rash, headache, lymphadenopathy, arthralgias (myalgia, joint pain), pharyngitis (sore throat), nausea, vomiting, diarrhea, night sweats, neck stiffness, photophobia, weight loss (anorexia), loss of appetite, Bell's palsy, malaise, mucosal ulcers (oral or genital), leucopenia, thrombocytopenia, and elevated hepatic enzyme levels.23-33 Other reported risk conditions for HIV infection include STIs, infections (tuberculosis, candidiasis, Pneumocystis jirovecii pneumonia, varicella zoster virus), skin conditions (psoriasis, seborrheic dermatitis), and history of psychiatric hospitalization, alcohol dependence, homelessness, or cocaine use.
Incident ICD-9-CM codes among cases within statistically significant disease groups were selected for 2 periods, within 2 years and up to 4 years before HIV diagnosis, and subgrouped into reported HIV-associated medical diagnoses and other data-driven subgroups of interest: 9 STIs, 16 clinical indicators or symptoms for HIV infection, 4 mental disorders, and 5 potential clinical syndromes suggestive of primary HIV infection (see Appendix 1, Supplemental Digital Content 1, http://links.lww.com/QAI/A129). Medical diagnoses were collapsed into medical diagnosis clusters (MDC) and the effect of MDC on HIV status was evaluated for the 2 periods. For 10 HIV-infected cases with an inpatient or outpatient diagnosis of HIV (‘042’ ICD-9-CM or HIV disease) before the index HIV test date, the serological index date and analyses were adjusted to the earliest date of the ‘042’ medical encounter.
Incident ICD-9-CM codes, in any position on medical encounter records, after index dates were subgrouped into medical diagnoses evaluated preindex date and compared for male military personnel only and their controls. Additionally, postindex diagnoses were compared between cases and controls by stratifying for history of preindex MDC. The primary diagnosis for first hospitalizations after HIV diagnosis was compared among hospitalized and nonhospitalized cases. The ICD-9-CM code in the first position on an inpatient record was considered the primary diagnosis unless the code indicated HIV infection (042, V08, 647.8, 795.71, or 795.79) whereby the second or third position provided primary diagnosis.
Bivariate analysis using Pearson χ2, Student t test, and Wilcoxon rank sum test compared characteristics between cases and controls. The effect of a characteristic on HIV infection status was measured with an odds ratio. Two-sided confidence limits (CLs) for odds ratios and 2-sided P values for all analyses were assessed at a 95% significance level. MDC associations with HIV infection were assessed adjusting for age, race, and service-connected time with logistic regression. Multivariate logistic regression analysis identified characteristics most significantly associated with HIV infection using a stepwise method of selecting characteristics. All characteristics significantly associated with HIV infection at P < 0.25 in bivariate analysis were considered in multivariate models. In multivariate models, age, service-connected time, PCSs, deployments, deployment duration, and medical encounter frequency were evaluated as continuous variables, whereas branch of Service, race, marital status, and presence of medical diagnoses were evaluated as categorical variables. Race was collapsed into 2 categories (black and nonblack) based on contiguous levels having similar odds ratios. The Hosmer-Lemeshow test assessed the goodness of fit of the final model. All analysis was conducted using Statistical Analysis Software (SAS) version 9.1 (Cary, NC).
Of 7027 active duty military personnel eligible for the study, 30 HIV-infected and 518 uninfected personnel were excluded. The 30 excluded individuals were in the Army, mostly male (97%), and older (mean, 43.6 years, P < 0.0001) than those included. HIV-infected cases and uninfected controls differed in demographic characteristics by Service (P < 0.05); Air Force cases were younger (mean years, 30.0; Army, 32.1), male (100%; Army, 93%), and single (72%; Army, 48%); Air Force controls were older (mean years, 28.6; Army, 27.5) and more frequently white (77%; Army, 66%) and less frequently single (61%; Army, 54%).
Of 274 HIV-infected cases in the study, most were male (95%). Among men, most were aged 25-34 years (45%), single (61%), of black race (57%), and had earned a high school diploma or less at time of HIV diagnosis (67%) (Table 1). Among male military personnel, age greater than 24 years (odds ratios [ORs] = 1.68-1.81), single marital status (OR = 2.37), black race (OR = 5.76), and senior enlisted pay grade (OR = 1.46 for pay grades E05 to E09) conferred higher odds of HIV infection (Table 1). Three or more PCS's had slightly greater odds of HIV infection compared with those with 2 or fewer PCS's (OR = 1.31, Table 2). Being deployed for 5 months or longer (OR = 0.57) was negatively associated with HIV infection compared with nondeployers (Table 2).
Only 13 (5%) cases in the study were female. At the time of HIV diagnosis all 13 were aged 21-42 years (mean, 28.9), in the Army and of enlisted pay grade, 7 were married, separated or divorced, 10 had a high school diploma or less, and 9 were of black racial origin. By comparison, 404 HIV-uninfected control females in the study were aged 18-49 years (mean, 27.1), 212 (52%) were in the Army, 339 (84%) were enlisted, 220 (54%) were married, separated, or divorced, 256 (63%) had a high school diploma or less, and 205 (51%) were of white race. Black race was associated with HIV infection (OR = 5.00, 95% CL = 1.33 to 18.77).
Before HIV Diagnosis
Overall, cases sought care more often (mean, 26.6 visits) than controls (mean, 21.3; P < 0.05). Males with 2.25 or more years of service connection had higher odds of HIV infection (ORs = 1.55-1.96) compared with those with less than 2 years (P ≤ 0.05, Table 2). Males with 8 or more total medical encounters had 2-fold to 3-fold greater odds of HIV infection compared with male military personnel with 7 or fewer encounters (ORs = 2.11-3.05, Table 2). Female cases than controls had longer service connection (mean years, 3.8 versus 3.5) and cases had more medical visits (mean, 49.5 versus 34.9; P > 0.05). In the 4 years preceding HIV diagnosis, female cases contributed only 382 codes (7%) to disease categories, of which none were associated with HIV infection (P ≥ 0.05, data not shown). Therefore, female military personnel were excluded from further evaluation in the study.
Overall, a higher proportion of cases than controls were diagnosed with incident conditions in 11 disease groups before HIV diagnosis: blood and blood-forming organs; circulatory system; endocrine, nutritional, metabolic, and immunity; digestive system; genitourinary system; infectious and parasitic diseases; mental disorders; respiratory system; skin and subcutaneous tissue; symptoms, signs, and ill-defined conditions; and V codes (ORs = 1.28-5.22, P < 0.05, data not shown). All MDC were associated significantly with recent HIV seroconversion in both the 2-year and 4-year periods before HIV diagnosis after adjustment for age, race and years of service connection (adjusted odds ratio [AOR] = 1.65-3.89, P < 0.05, Table 3).
In the final multivariate model including only male military personnel, 7 characteristics were associated the most with HIV infection (Table 4): single marital status (AOR = 14.37); having any clinical indicator or symptom within 4 years of HIV diagnosis (AOR = 6.22); black race (AOR = 5.88); having any other clinical syndrome within 2 years of HIV diagnosis (AOR = 3.31); any mental disorder within 4 years of HIV diagnosis (AOR = 3.04); longer service connection (AOR = 1.69); and increasing age (AOR = 1.12).
After HIV Diagnosis
Overall cases sought more care after diagnosis (mean visits, 48.9 versus 19.4) especially in the first year after diagnosis (P < 0.05). Higher overall health care seeking remained significant among cases after removing encounters where the primary diagnosis was HIV (mean, 35.7 visits, P < 0.05).
The odds of STI diagnosis was higher among male cases than controls (cases 88 of 261 [34%], controls 617 of 5801 [11%]; OR = 4.27, 95% CL = 3.26 to 5.60). After stratification for pre-HIV history of STI, the odds of a STI post-HIV diagnosis remained higher among cases; (ORs: 3.14-4.15, Table 5; odds ratio, Mantel Haenszel [ORM-H] = 4.10, 95% CL = 3.12 to 5.40). The earliest STI was diagnosed between 0 and 42 months after HIV diagnosis (median, 8.2, IQR, 3.4-21.9). The odds of a mental disorder after HIV diagnosis was higher among male cases than controls (cases, 98 of 261 [37%]; controls, 594 of 5801 (10%); OR = 5.27, 95% CL = 4.01 to 6.92). After stratification for pre-HIV history of mental disorder, the odds of a mental disorder post-HIV diagnosis remained higher among cases (ORs = 4.42-5.14, Table 5; ORM-H = 4.98, 95% CL = 3.77 to 6.58).
Forty-seven (18%) cases were hospitalized at least once after HIV diagnosis. Hospitalized cases had a higher number of visits before HIV diagnosis than non-hospitalized cases (mean, 34.5 versus 23.5; P = 0.001). More than 75% of primary diagnoses belonged to 4 disease groups: mental disorders, infectious diseases, digestive diseases, and respiratory diseases (see Appendix 2, Supplemental Digital Content 2, http://links.lww.com/QAI/A130). More than half of first hospitalizations (64%) occurred within the first year after diagnosis (mean 11.6 months, median 5.8 months). Eighty-one percent of infectious disease admissions and 71% of mental health hospitalizations occurred within the first year of diagnosis (mean months, 8.6 and 8.8, median months, 3.0 and 5.1, respectively). The top 3 diagnoses in the mental disorders category were due to depression.
Our primary goal was to compare medical diagnoses among HIV-infected and uninfected military personnel and to identify conditions that may aid in earlier diagnosis of HIV. Although all medical diagnosis clusters were associated significantly with recent HIV diagnosis, in multivariate analysis 3 clusters (clinical indicators or symptoms suggestive of an acute retroviral syndrome, mental disorders, and other non-indicator clinical syndromes up to 2 years before HIV diagnosis) and 4 nonclinical characteristics (single marital status, black race, higher age, and longer service connection) were associated with recent diagnosis. HIV-infected military personnel had 3-fold to 6-fold greater odds than uninfected personnel of having clinical indicators or symptoms, mental disorders, and other clinical syndromes preceding HIV diagnosis. This suggests that increased attention to clinical factors and mental disorders may aid current HIV screening efforts leading to earlier diagnosis. It may also provide a window of opportunity for targeted prevention messages. Furthermore, although the US military HIV prevalence is lower than the CDC guideline threshold of >0.1% for opt-out screening in health care settings, our data and reports of increasing HIV incidence among US Army military personnel since 2004 suggest that targeted HIV testing within the force testing interval may be indicated for males seeking care for clinical symptoms or mental health complaints, even in this highly HIV screened population.14,15,34
Earlier detection of HIV infection may curtail risk behaviors associated with HIV transmission through counseling. Some cohort studies have shown that an awareness of HIV infection decreased unprotected sex, other risk behaviors, and STIs compared with those with a negative HIV test or those not aware of their HIV infection.35 HIV-infected military personnel are counseled against unprotected consensual sex and are required to notify sexual partners of their infection status.21,36 However, HIV-infected Soldiers and Airmen in this study continued to have higher odds of STIs after HIV diagnosis than uninfected military personnel. Additionally, having a history of STI before HIV diagnosis was associated with STIs post-HIV diagnosis. Given the approximately 9-month median time frame to the earliest STI diagnosis after HIV infection it is likely these diagnoses were not due mainly to co-infections at time of HIV diagnosis. Although increased monitoring may have impacted this result, it suggests opportunities for antecedent prevention messages.
Eighteen percent of male HIV-infected military personnel had at least 1 hospitalization. This is lower than other studies in the US that evaluated hospitalizations in the post-highly active antiretroviral therapy (HAART) era. Utilization of inpatient services in these studies varied from 21% to 34%.37-39 Although the racial makeup of hospitalized cases in our study was similar to these studies, our cases were younger (mean, 29.6 years) which may explain our lower rate. Older age was associated with higher number of hospitalizations in one study which followed a US military cohort of HIV-infected individuals.39 Additionally, interval HIV-screening promotes earlier diagnosis as evidenced by high CD4 cell counts at diagnosis.40
Similar to studies in both civilian and military populations, infectious diseases and mental disorders were the primary reasons for hospitalization. In these studies, hospitalization occurred due to a variety of AIDS-defining illness and infections such as pneumonia or methicillin-resistant Staphylococcus aureus, gastrointestinal diseases such as pancreatitis and mental disorders, and primarily major depressive disorder or substance use-related diagnoses.37,39 HIV viral load, CD4 cell counts, and use of HAART were associated with the type of hospitalization and rate of hospitalization. The infectious diseases that made up the primary reasons for hospitalization in our study were non-AIDS-related and suggest that HIV-infected Soldiers and Airmen were not late presenters for HIV medical care. Outpatient medical utilization for ICD9 primary diagnoses other than HIV was significantly greater postdiagnosis. A similar finding was apparent in a recent case-control study of mild asthma among Navy recruits.41 Implications for resourcing treatment facilities and costs merit further investigation.
We found single marital status, black race, male gender, older age, and longer service connection were associated with HIV seroconversion. These findings are consistent with trends of the HIV epidemic in the US Army since the mid-1980s.42,43 Although we did not evaluate the effect of length of active duty service history on HIV acquisition, time in service may be associated with HIV seroconversion. Infected military personnel had longer service connection in our study and higher HIV seroconversions have been reported among those with 3 or more years of service.19
There are limitations to our study. We were unable to reliably assess women cases, Hispanic race, or ethnicity as our population has very few women cases, and race or ethnicity were aggregated for fewer population numbers. We evaluated archived records of medical encounters with commonly used nosology. The ICD-9-CM codes were not validated with medical chart reviews and therefore may not reflect actual diagnoses or capture encounters in locations where diagnostic coding does not occur. The association between both indicator and nonindicator MDC and HIV infection is limited by the absence of laboratory confirmation and potential lack of specificity of these diagnoses as representing clinically apparent acute retroviral illnesses. However, this limitation is mitigated by laboratory-confirmed HIV infection that followed these events. It is possible that providers might have selectively coded HIV-related visits using non-specific diagnostic coding to maintain patient confidentiality with respect to HIV infection status. This possibility, and any potential impact, could not be evaluated.
In conclusion, HIV-infected Soldiers and Airmen frequently sought health care for symptoms suggestive of acute or early stage HIV infection and mental disorders in the 2-4 years preceding HIV diagnosis. Although validation of these findings is necessary in site-specific prospective studies which incorporate behavioral risk factors and cost-benefit analysis of point-of-care HIV testing, increased attention by health care providers to the mental health and care-seeking patterns in their military patients may increase earlier detection of HIV infection, reduce ongoing HIV transmission, and facilitate earlier access to antiretroviral therapy. STI rates increased after HIV diagnosis, which implies increased risk behavior or increased susceptibility. Further study is needed in this population to determine the impact of HIV infection on subsequent STI risk.
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medical encounters HIV Army Air Force; ;
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