Abstract
Background
Veterans face high risk for HIV and substance use, and thus could be disproportionately impacted by the HIV and substance use disorder (SUD) “syndemic.” HIV prevalence among veterans with SUD is unknown.
Objective
To project HIV prevalence and lifetime HIV screening history among US veterans with alcohol use disorder (AUD), opioid use disorder (OUD), or both.
Design
We conducted a retrospective cohort analysis using national Veterans Health Administration (VHA) data.
Participants
We selected three cohorts of veterans with SUD: (1) AUD, (2) OUD, and (3) AUD/OUD. Included veterans had ICD codes for AUD/OUD from 2016 to 2022 recorded in VHA electronic medical records, sourced from the VA Corporate Data Warehouse (CDW).
Main Measures
We estimated HIV prevalence by dividing the number of veterans who met two out of three criteria (codes for HIV diagnosis, antiretroviral therapy, or HIV screening/monitoring) by the total number of veterans in each cohort. We also estimated lifetime HIV screening history (as documented in VHA data) by cohort. We reported HIV prevalence and screening history by cohort and across demographic/clinical subgroups.
Key Results
Our sample included 669,595 veterans with AUD, 63,787 with OUD, and 57,015 with AUD/OUD. HIV prevalence was highest in the AUD/OUD cohort (3.9%), followed by the OUD (2.1%) and AUD (1.1%) cohorts. Veterans of Black race and Hispanic/Latinx ethnicity, with HCV diagnoses, and aged 50–64 had the highest HIV prevalence in all cohorts. Overall, 12.8%, 29.1%, and 33.1% of the AUD/OUD, OUD, and AUD cohorts did not have history of HIV screening, respectively.
Conclusions
HIV prevalence was high in all SUD cohorts, and was highest among veterans with AUD/OUD, with disparities by race/ethnicity and age. A substantial portion of veterans had not received HIV screening in the VHA. Findings highlight room for improvement in HIV prevention and screening services for veterans with SUD.
Supplementary Information
The online version contains supplementary material available at 10.1007/s11606-023-08452-5.
KEY WORDS: HIV infections (MeSH), substance-related disorders (MeSH), alcohol-related disorders (MeSH), opioid-related disorders (MeSH)
INTRODUCTION
In the United States (US), 2.7 million, 29.7 million, and 1.2 million people have opioid use disorder (OUD), alcohol use disorder (AUD), and HIV, respectively.1–3 People with HIV are more likely to have substance use disorders (SUD) than people without HIV, and people with SUD have higher HIV risk than those without SUD.4–8 Additionally, substance use exacerbates HIV morbidity, mortality, and transmission.4–6 In a large study of veterans, HIV prevalence was markedly higher than in the general US population.9 Other studies have found that veterans have higher SUD and problematic substance use rates, partly due to chronic pain and psychiatric co-morbidities.10–13 Thus, US veterans may be at particularly high risk for having HIV and SUD.9, 10
The intersection between SUD and HIV is a “syndemic” that compounds negative impacts for patients and can burden healthcare systems.14, 15 In a national survey, 24% of people with HIV reported needing alcohol/drug use treatment.16 The US Centers for Disease Control and Prevention (CDC) reports that people who inject drugs (PWID) are 22 times more likely to acquire HIV than people who do not, and recognizes opioid and alcohol use as risk factors for HIV acquisition.6, 17, 18 Evidence suggests that similar intersections exist among US veterans; Veterans Aging Cohort Study (VACS) analyses have found that veterans with HIV are more likely than those without HIV to have SUD.19, 20 Additionally, another study found that among veterans with AUD, those with HIV were more likely than those without HIV to have additional, non-alcohol SUD.21
While studies have described higher substance use among people with HIV and higher HIV risk among people with SUD, fewer studies describe HIV prevalence among people with SUD. Prior research suggests HIV prevalence may be elevated in people with SUD, but studies are limited to PWID or people with OUD.16, 22 Similarly, while evidence supports increased substance use among veterans with HIV, HIV prevalence among veterans with different SUDs remains unknown. Such research is critical given the high prevalence of adverse social determinants of health, co-occurring psychiatric disorders and medical complications, and mortality among veterans, as well as future downstream effects of the Iraq and Afghanistan conflicts (the longest war in US history).23–28
The United States Preventive Services Task Force (USPSTF), CDC, and Veterans Health Administration (VHA) recommend at least one universal HIV screening for all adults aged 18–65, and annual screening for those at high risk for HIV.29–32 The “high risk” category includes men who have sex with men, people with a sex partner with HIV, and PWID. While SUD may contribute to HIV risk, diagnosis with OUD and/or AUD alone is not an independent criterion for HIV screening. Consequently, physicians following USPSTF, CDC, or VHA guidelines may not annually screen veterans with SUD for HIV. The Substance Abuse and Mental Health Services Administration (SAMHSA) additionally suggests that providers offer ongoing HIV screening for people with SUD.4 Actual HIV screening rates in current VHA practices are uncertain; a 2009 study found that veterans with SUD have low HIV screening rates.33
Understanding HIV prevalence and screening history among veterans with SUD could provide insight into unmet need for increasing and streamlining access to HIV and SUD treatment and prevention, and could have implications for VHA system improvement.
METHODS
Design, Population, and Data Collection
We conducted a retrospective cohort analysis using national VHA data. The VHA dataset includes diagnoses (International Classification of Disease [ICD] codes), patient encounters (Current Procedural Terminology [CPT] codes), medication fills (National Drug Codes [NDC]), and procedure codes (Healthcare Common Procedure Coding System [HCPC]) for all patients recorded in the VHA Corporate Data Warehouses (CDW), and the VA Informatics and Computing Infrastructure (VINCI). The cohort we created used data from 2016 to 2022 and included records predating this timeframe (e.g., prior diagnoses).34 The study was deemed exempt from VA Boston IRB and executed with approval from the Research & Development Committee, and meets Strengthening the Reporting of Observational Studies in Epidemiology guidelines for cross-sectional studies.35
We selected three SUD veteran cohorts for analysis: (1) AUD only (AUD cohort), (2) OUD only (OUD cohort), and (3) co-occurring AUD and OUD (AUD/OUD cohort). The cohorts included all veterans in the VHA with AUD and/or OUD, as indicated by having at least one inpatient or two outpatient encounters with an ICD-10 code for AUD or OUD in any healthcare encounters during the 2016–2022 study period (excluding remission codes, Supplemental Table 1).34
Study Variables
Demographic and Clinical Characteristics
SUD cohort demographic and clinical characteristics included age category (18–29, 30–39, 40–49, 50–64, 65 +), sex documented in medical records (male, female), race (white, American Indian/Alaska Native [AIAN], Asian, Black, multiple, Native Hawaiian or Pacific Islander [NHPI], unknown), ethnicity (Hispanic/Latinx, non-Hispanic/Latinx), and presence of hepatitis C virus (HCV) diagnosis (yes, no). Demographic characteristics were reported at earliest encounter during the study period; categories were based on documented categories in the medical record. HCV diagnosis presence was reported as “yes” if an individual had an ICD-10 code for HCV during the study period (Supplemental Table 1).
HIV Prevalence
HIV prevalence, defined as the number of veterans with HIV within AUD, OUD, and AUD/OUD cohorts divided by the total number of veterans in each cohort, was our primary outcome. Veterans were considered to have HIV if they met at least two out of three criteria at any point in their VHA medical history: (1) one or more ICD-9/ICD-10 diagnostic code for HIV, (2) one or more non-prophylaxis antiretroviral therapy HIV treatment, identified using NDC codes and drug names, or (3) one or more positive HIV screening test (i.e., antibody, antigen/antibody, or nucleic acid test) or one or more HIV monitoring test (e.g., viral load or CD4 test), identified by laboratory test names (Supplemental Table 1).36
HIV Screening History
We evaluated the proportion of veterans who ever had HIV screening (i.e., antibody, antigen/antibody, or nucleic acid test), defined as the number of veterans who had a record of receiving an HIV test at any point in their VHA medical history or who had HIV (as defined above), indicating a prior HIV screening, within the AUD, OUD, and AUD/OUD cohorts divided by the total number of veterans in each cohort.
Analyses
We described demographic and clinical characteristics within AUD, OUD, and AUD/OUD cohorts, and conducted chi-square tests to test for significant differences between cohorts. Overall HIV prevalence and screening history were calculated separately for the three SUD cohorts. Stratified subgroup analyses were similarly conducted to project HIV prevalence and screening history within each cohort by demographic and clinical characteristics. We tested for significant differences in HIV prevalence and screening history between the AUD, OUD, and AUD/OUD cohorts, deriving overall differences between SUD groups and within demographic and clinical characteristic subgroups, using linear probability models with robust standard errors. We applied Benjamini–Hochberg corrections to reduce false discovery rate across multiple subgroup analyses, and separately for pairwise post hoc comparisons.37 As a sensitivity check, we performed the same approach for age-adjusted HIV prevalence results.
All analyses were descriptive. Use of linear modeling with a binary outcome expresses coefficients as proportions in percent values, with mean comparisons reported herein relating to differences in the percent of veterans with HIV, and screened for HIV (separately), by SUD group and demographic or clinical characteristics. All analyses were conducted in R, version 4.1.2.
RESULTS
Demographic and Clinical Characteristics
We included 790,397 VHA patients, with 669,595 (84.7%) in the AUD cohort, 63,787 (8.1%) in the OUD cohort, and 57,015 (7.2%) in the AUD/OUD cohort. All cohorts were majority male (AUD: 93.7%, OUD: 91.0%, AUD/OUD: 93.7%), white (AUD: 66.1%, OUD: 78.5%, AUD/OUD: 69.8%), and non-Hispanic (AUD: 91.5%, OUD: 94.3%, AUD/OUD: 93.3%). The second largest racial/ethnic category was Black (AUD: 24.3%, OUD: 14.4%, AUD/OUD: 23.5%). A plurality was between ages 50 and 64 (AUD: 34.4%, OUD: 35.9%, AUD/OUD: 42.4%). The AUD/OUD cohort had the highest HCV diagnosis prevalence (28.1%, compared with 16.6% and 6.5% of the OUD and AUD cohorts, respectively) (Table 1; Supplemental Table 2).
Table 1.
Demographic and Clinical Characteristics in Veteran AUD, OUD, and AUD/OUD Cohorts
| Characteristic1 | n, %2, by cohort | P-value3 | ||||
|---|---|---|---|---|---|---|
| AUD n = 669,595 (84.7%) |
OUD n = 63,787 (8.1%) |
AUD/OUD n = 57,015 (7.2%) |
OUD vs. AUD | AUD/OUD vs. AUD | AUD/OUD vs. OUD | |
| Age category | ||||||
| 18–29 | 45,867 (6.8) | 2851 (4.5) | 5580 (9.8) | < 0.001 | < 0.001 | < 0.001 |
| 30–39 | 106,737 (15.9) | 9720 (15.2) | 12,265 (21.5) | |||
| 40–49 | 90,501 (13.5) | 6937 (10.9) | 7402 (13.0) | |||
| 50–64 | 230,227 (34.4) | 22,910 (35.9) | 24,172 (42.4) | |||
| 65 + | 196,258 (29.3) | 21,369 (33.5) | 7596 (13.3) | |||
| Sex in medical record | ||||||
| Male | 627,418 (93.7) | 58,062 (91.0) | 53,404 (93.7) | < 0.001 | 0.750 | < 0.001 |
| Female | 42,174 (6.3) | 5725 (9.0) | 3611 (6.3) | |||
| Race | ||||||
| White | 442,493 (66.1) | 50,092 (78.5) | 39,821 (69.8) | < 0.001 | < 0.001 | < 0.001 |
| AIAN | 7398 (1.1) | 589 (0.9) | 577 (1.0) | |||
| Asian | 4863 (0.7) | 207 (0.3) | 179 (0.3) | |||
| Black | 162,703 (24.3) | 9169 (14.4) | 13,360 (23.5) | |||
| Multiple | 7066 (1.1) | 682 (1.1) | 626 (1.1) | |||
| NHPI | 5960 (0.9) | 425 (0.7) | 336 (0.6) | |||
| Unknown | 39,109 (5.8) | 2623 (4.1) | 2116 (3.7) | |||
| Ethnicity | ||||||
| Hispanic or Latinx | 57,198 (8.5) | 3633 (5.7) | 3815 (6.7) | < 0.001 | < 0.001 | < 0.001 |
| Non-Hispanic or Latinx | 612,394 (91.5) | 60,154 (94.3) | 53,200 (93.3) | |||
| HCV in study period | ||||||
| No | 625,876 (93.5) | 53,209 (83.4) | 41,002 (71.9) | < 0.001 | < 0.001 | < 0.001 |
| Yes | 43,716 (6.5) | 10,578 (16.6) | 16,013 (28.1) | |||
HIV, human immunodeficiency virus; AUD, alcohol use disorder; OUD, opioid use disorder; AIAN, American Indian or Alaska Native; NHPI, Native Hawaiian or Pacific Islander; HCV, Hepatitis C Virus
1Age, sex in medical record, race, and ethnicity represent all categories reported at earliest encounter in the study period (2016–2022); HCV diagnosis reported based on ICD-9 or ICD-10 code for HCV during the study period (codes in Supplemental Table 1)
2Values may not add up to 100% due to rounding
3χ2 values are reported in Supplemental Table 2
HIV Prevalence
Overall, HIV prevalence was 1.1%, 2.1%, and 3.9% in the AUD, OUD, and AUD/OUD cohorts, respectively. HIV prevalence in the AUD/OUD cohort was significantly higher than in the other two cohorts, and HIV prevalence in the OUD cohort was significantly higher than in the AUD cohort (Table 2, Fig. 1; Supplemental Table 3). HIV prevalence was higher in the AUD/OUD cohort, followed by the OUD cohort and then the AUD cohort across all demographic and clinical characteristic subgroups. Differences between the three SUD cohorts were statistically significant in most subgroups (exceptions are AIAN, Asian, multiple race, and NHPI racial categories, likely due to small samples [Supplemental Table 3]).
Table 2.
Unadjusted HIV Prevalence in Veteran AUD, OUD, and AUD/OUD Cohorts Overall and by Demographic and Clinical Characteristics
| Unadjusted HIV prevalence1, n %2, by cohort | |||
|---|---|---|---|
| Characteristic | AUD3 n = 669,595 |
OUD3 n = 63,787 |
AUD/OUD3 n = 57,015 |
| Overall | 7219 (1.1) | 1315 (2.1) | 2232 (3.9) |
| Age category | |||
| 18–29 | 373 (0.8) | 41 (1.4) | 143 (2.7) |
| 30–39 | 989 (0.9) | 117 (1.2) | 359 (2.9) |
| 40–49 | 1069 (1.1) | 118 (1.7) | 265 (3.6) |
| 50–64 | 3643 (1.6) | 677 (3.0) | 1189 (4.9) |
| 65 + | 1145 (0.6) | 362 (1.7) | 276 (3.6) |
| Sex in medical record | |||
| Male | 6857 (1.1) | 1233 (2.1) | 2106 (3.9) |
| Female | 362 (0.9) | 82 (1.4) | 126 (3.5) |
| Race | |||
| White | 2882 (0.7) | 768 (1.5) | 1145 (2.9) |
| AIAN | 64 (0.9) | 8 (1.4) | 22 (3.8) |
| Asian | 28 (0.6) | 2 (1.0) | 7 (3.9) |
| Black | 3817 (2.3) | 485 (5.3) | 963 (7.2) |
| Multiple | 99 (1.4) | 10 (1.5) | 29 (4.6) |
| NHPI | 58 (1.0) | 5 (1.2) | 10 (2.9) |
| Unknown | 271 (0.7) | 37 (1.4) | 56 (2.6) |
| Ethnicity | |||
| Hispanic or Latinx | 665 (1.2) | 121 (3.3) | 194 (5.1) |
| Non-Hispanic or Latinx | 6554 (1.1) | 1194 (2.0) | 2038 (3.8) |
| HCV in study period | |||
| No | 5853 (0.9) | 759 (1.4) | 1128 (2.8) |
| Yes | 1366 (3.1) | 556 (5.3) | 1104 (6.9) |
HIV, human immunodeficiency virus; AUD, alcohol use disorder; OUD, opioid use disorder; AIAN, American Indian/Alaska Native; NHPI, Native Hawaiian or Pacific Islander; HCV, Hepatitis C Virus
1HIV defined based on meeting two out of three criteria for HIV; see “METHODS” and Supplemental Table 1
2Values may not add up to 100% due to rounding
3HIV prevalence was significantly different between the AUD and OUD cohorts, the OUD and AUD/OUD cohorts, and the AUD and AUD/OUD cohorts for the overall sample. Supplemental Table 3 shows P-values (adjusted using robust standard errors followed by Benjamini–Hochberg correction for multiple comparisons) for differences between the three cohorts overall and for each subgroup category. In omnibus tests, unadjusted HIV prevalence was statistically significantly different at the P < 0.05 level across AUD, OUD, and AUD/OUD cohorts overall and in all subgroups
Figure 1.
HIV prevalence and HIV screening history in veteran AUD, OUD, and AUD/OUD cohorts. Figure 1 shows HIV prevalence on the primary (left) vertical axis and the proportion of veterans with HIV screening history on the secondary (right) vertical axis. From left to right, values are shown separately with bars for the AUD, OUD, and AUD/OUD cohorts. HIV prevalence is shown with blue bars. HIV screening history is shown with yellow bars. Error bars represent 95% confidence intervals. Abbreviations: HIV, human immunodeficiency virus; AUD, alcohol use disorder; OUD, opioid use disorder.
In descriptive subgroup analysis of demographic and clinical characteristics (Table 2), HIV prevalence was highest among veterans age 50–64 compared with the other ages. HIV prevalence was higher in males than in females, and in Black veterans compared with veterans of other races. Veterans of Hispanic/Latinx ethnicity had higher HIV prevalence than non-Hispanic/Latinx veterans. Last, veterans with an HCV diagnosis in the study period had higher HIV prevalence than those without an HCV diagnosis. Age-adjusted HIV prevalence values were similar to unadjusted values (Supplemental Table 4).
HIV Screening History
Veterans in the AUD/OUD cohort (87.2%) were significantly more likely to have a VHA history of HIV screening compared with those in the OUD (70.9%) and AUD cohorts (66.9%), and veterans in the OUD cohort were more likely to have HIV screening history than those in the AUD cohort (Table 3).
Table 3.
HIV Screening History in Veteran AUD, OUD, and AUD/OUD Cohorts Overall and by Demographic and Clinical Characteristics
| HIV screening history1, n %2, by cohort | |||
|---|---|---|---|
| Characteristic | AUD3 n = 669,595 |
OUD3 n = 63,787 |
AUD/OUD3 n = 57,015 |
| Overall | 447,863 (66.9) | 45,245 (70.9) | 49,719 (87.2) |
| Age category | |||
| 18–29 | 30,806 (67.2) | 2070 (72.6) | 4875 (87.4) |
| 30–39 | 74,287 (69.6) | 7266 (74.8) | 10,732 (87.5) |
| 40–49 | 62,725 (69.3) | 5089 (73.4) | 6427 (86.8) |
| 50–64 | 166,391 (72.3) | 17,294 (75.5) | 21,516 (89.0) |
| 65 + | 113,653 (57.9) | 13,526 (63.3) | 6169 (81.2) |
| Sex in medical record | |||
| Male | 415,741 (66.3) | 40,924 (70.5) | 46,459 (87.0) |
| Female | 32,112 (76.2) | 4321 (75.5) | 3260 (90.3) |
| Race | |||
| White | 275,776 (62.3) | 34,422 (68.7) | 33,998 (85.4) |
| AIAN | 4908 (66.3) | 404 (68.6) | 506 (87.7) |
| Asian | 3345 (68.8) | 158 (76.3) | 161 (89.9) |
| Black | 131,726 (81.0) | 7810 (85.2) | 12,489 (93.5) |
| Multiple | 5056 (71.6) | 500 (73.3) | 574 (91.7) |
| NHPI | 3829 (64.3) | 282 (66.4) | 284 (84.5) |
| Unknown | 23,223 (59.4) | 1669 (63.6) | 1707 (80.7) |
| Ethnicity | |||
| Hispanic or Latinx | 42,311 (74.0) | 2865 (78.9) | 3451 (90.5) |
| Non-Hisp. or Latinx | 405,552 (66.2) | 42,380 (70.5) | 46,268 (87.0) |
| HCV in study period | |||
| No | 408,620 (65.3) | 35,643 (67.0) | 34,301 (83.7) |
| Yes | 39,243 (90.0) | 9602 (90.8) | 15,418 (96.3) |
HIV, human immunodeficiency virus; AUD, alcohol use disorder; OUD, opioid use disorder; AIAN, American Indian/Alaska Native; NHPI, Native Hawaiian or Pacific Islander; HCV, Hepatitis C Virus
1HIV screening history defined as record of at least one HIV diagnostic test in a patient’s lifetime VHA medical record, HIV diagnostic tests identified based on laboratory names (see Supplemental Table 1)
2Values may not add up to 100% due to rounding
3HIV screening history was significantly different between the AUD and OUD cohorts, the OUD and AUD/OUD cohorts, and the AUD and AUD/OUD cohorts for the overall sample. Supplemental Table 5 shows P-values (adjusted using robust standard errors followed by Benjamini–Hochberg correction for multiple comparisons) for differences between the three cohorts overall and for each subgroup category. In omnibus tests, unadjusted HIV screening history was statistically significantly different at the P < 0.05 level across AUD, OUD, and AUD/OUD cohorts overall and in all subgroups
In subgroup analyses, groups with the highest HIV prevalence were also more likely to have a history of HIV screening. For example, veterans aged 50–64 years, of Black race, of Hispanic/Latinx ethnicity, and with an HCV diagnosis in the study period were more likely to have HIV screening history than their counterparts in respective categories. An exception to this was the sex subgroup; women had lower HIV prevalence than men, but were more likely to have been screened. The subgroup most likely to have HIV screening history was veterans with an HCV diagnosis; over 90% of veterans in all three SUD cohorts who had an HCV diagnosis had been screened for HIV in their VHA history (Table 3; Supplemental Table 5).
DISCUSSION
We found HIV prevalence ranged from 1.1 to 3.9% in veterans with AUD, OUD, and both. In all SUD cohorts, HIV prevalence was higher than published estimates for the US population (∼0.3%) and VHA veterans (∼0.5%).2, 9 While HIV prevalence was high overall, there was a significant rank-order effect wherein the AUD/OUD cohort had the highest HIV prevalence, then the OUD cohort, and finally the AUD cohort. Additionally, we found that nearly a third of veterans with AUD or OUD did not have a HIV screening history in the VHA system data, while most (∼90%) of veterans with both AUD/OUD had HIV screening history in VHA care. While this unscreened prevalence is low compared with older estimates (e.g., a 2009 study reported 80% of veterans with SUD were not screened),33 proportions are still high given that the VHA, CDC, and USPSTF recommend at least one HIV screening for all adults aged 18–65 and annual screening for high-risk populations.29, 30, 32 Our findings highlight room for improvement in HIV prevention and screening among veterans with SUD.
Consistent with prior research documenting disparities, HIV prevalence varied across subgroups. Notably, HIV prevalence was higher in veterans with an HCV diagnosis during the study period compared with those without HCV. While injection drug use is not consistently recorded in VHA medical records, HCV is commonly acquired through sharing injection drug equipment.9 These results are consistent with evidence of increased HIV risk for PWID.17 Similarly, HIV screening history varied between subgroups. Within all cohorts and subgroups (except sex), categories with the highest HIV prevalence also were most likely to have received an HIV screening. This may reflect higher actual or perceived differences in HIV prevalence or high-risk patient demographics. Alternatively, higher testing rates could be driving higher HIV prevalence estimates, for example, higher-risk populations (e.g., AUD/OUD cohort) may have more interaction with health systems and opportunities for testing. Sex category was an exception to this pattern; women had lower HIV prevalence but higher probability of HIV screening than men (possibly due to reproductive-age screening).
Despite variation within subgroups, HIV prevalence and screening trends between AUD, OUD, and AUD/OUD cohorts were consistent for all subgroups, with the AUD/OUD cohort having the highest HIV prevalence and screening, followed by the OUD and then AUD cohorts. Higher HIV prevalence in veterans with AUD/OUD could be partly driven by compounding HIV risk factors among veterans with more than one SUD21 (e.g., injection-drug-related and sexual risk behaviors).6 People with two SUDs may also be more likely to experience adverse social determinants of health associated with both SUD and HIV risk, such as trauma, racism, or homelessness.38, 39 Ongoing efforts have characterized syndemic conditions among marginalized groups such as women experiencing physical/sexual violence,40, 41 but more research is needed to understand how polysubstance use and HIV risk intersect among veterans.
Our finding that veterans with AUD, OUD, and AUD/OUD have higher HIV prevalence than the general population has implications for improving veteran health services. Prior work has documented high SUD prevalence among people with HIV,4 and we now document elevated HIV prevalence among veterans with SUD, emphasizing the extent of the SUD and HIV syndemic. An important health service factor to examine further is to what extent these co-occurring concerns are being addressed within and across clinics, as opposed to being addressed separately (or at all) across siloed clinics treating one at the expense (or under-acknowledgement) of the other. From the patient perspective, siloed/fragmented care can be inconvenient or costly and can increase disengagement from services.42, 43 From the health system perspective, it can result in inefficiencies and decrease service quality.44 Thus, preventing care fragmentation through integrative care coordination between substance use, behavioral health, and HIV services could address gaps in HIV prevention and detection within VHA systems.
The 2022–2025 HIV/AIDS strategy emphasizes the need for integration of HIV and substance use services as a strategy to end the US HIV epidemic.45 In a systematic review, Haldane et al. identified three models for integrated HIV/SUD systems: (1) SUD services integrated at HIV treatment facilities, (2) HIV services integrated at SUD treatment facilities, and (3) SUD and HIV services integrated simultaneously into alternative care settings (e.g., drop-in or street-based settings).44 These models may streamline services and increase numbers of people diagnosed, treated, and retained in care for both HIV and SUD.42 For example, SUD services (or other services provided to people with SUD, such as mental health services) could be designed to implement universal HIV screenings, coordinate with infectious disease clinics, and connect patients to preventive healthcare such as pre-exposure prophylaxis.46, 47 Such models may be useful for veteran populations with SUD who have high HIV prevalence and/or low HIV screening rates.48
Reviews and studies of VHA care have noted the importance of integrated SUD, HIV, and mental health care. In a resource for providers, the Department of Veterans Affairs describes a model of integrated care that could include co-located services, diverse teams of providers, stigma-reducing cultures, availability of comprehensive services, and effective communication strategies.49 A RAND corporation report suggests that all treatment facilities serving post-9/11 veterans should screen for co-occurring disorders; however, the report does not describe current implementation of integrated HIV/SUD screening and care.46 One study found that HIV testing can successfully be incorporated into some VHA clinics, but other sites faced barriers such as lack of laboratory support and nursing resistance.50 Another study found that an integrated alcohol treatment intervention increased treatment uptake among veterans with HIV, but noted that such integrated approaches are rare.51 In the US generally, barriers to system integration include policy- and system-level factors such as SUD treatment waiver requirements, prior authorization rules, and gaps in workforce training/development.52 More research is needed to understand which models of integrated HIV/SUD systems are effective in VHA settings, and how optimal models can be adapted to local contexts and successfully scaled.50, 53 This work should include policy and implementation studies investigating facilitators and barriers to successful integrated VHA SUD/HIV services.
Strengths of our study include the large sample size from the VHA CDW, a database that includes medical record history for included patients, which is important for identifying HIV (a lifelong disease). Additionally, this is the first study to our knowledge to document HIV prevalence among veterans with different SUD types, including co-occurring AUD/OUD. Our study also has limitations. The VHA CDW includes medical encounter data which may contain inaccuracies in encounter codes. However, we used a multi-criteria method that was previously validated using VHA data to identify veterans with HIV.36 Also, VHA CDW data does not capture all encounters outside of the VHA system, so while we restricted the analysis to veterans with at least one inpatient or two outpatient visits with an SUD diagnosis within the VHA system, we may have missed veterans who received screening or SUD diagnoses outside of VHA. Last, our study is descriptive and does not establish causal relationships between SUD and HIV.
In conclusion, we find that VHA patients with AUD, OUD, and both AUD and OUD have high HIV prevalence. Veterans with both AUD and OUD have the highest HIV prevalence, followed by veterans with OUD and then veterans with AUD. Additionally, a substantial proportion of veterans with SUD do not have a history of HIV screening in their lifetime VHA data, despite USPTF recommendations that everyone age 18–65 should have at least one HIV screening, and that people at high risk for HIV should have annual screening. Our findings call attention to gaps in HIV prevention and screening services for veterans, and may be useful to veterans’ health service program managers and implementation researchers interested in improving integrated care, including screening, prevention, and treatment options, for the substance use and HIV syndemic.
Supplementary Information
Below is the link to the electronic supplementary material.
Funding
This work was funded by the National Institute for Drug Abuse (McCann and Stein: 1T32DA041898-01A1) and the Patient Centered Outcomes Research Institute (Davenport, Mandavia, Stein, and Livingston: COVID2020C2-11081).
Data Availability
The United States Department of Veterans Affairs (VA) places legal restrictions on access to veteran’s health care data, which includes both identifying data and sensitive patient information. The analytic data sets used for this study are not permitted to leave the VA firewall without a Data Use Agreement. This limitation is consistent with other studies based on VA data. However, VA data are made freely available to researchers behind the VA firewall with an approved VA study protocol. For more information, please visit https://www.virec.research.va.gov or contact the VA Information Resource Center (VIReC) at vog.av@CeRIV.
Declarations
Conflict of Interest
The authors have no conflicts of interest to declare.
Footnotes
Publisher's Note
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Contributor Information
Nicole C. McCann, Email: ncmccann@bu.edu.
Nicholas A. Livingston, Email: Nicholas.livingston@va.gov.
References
- 1.National Institute on Drug Abuse. Medications to Treat Opioid Use Disorder Research Report: Overview. National Institutes of Health. Published December 2021. https://nida.nih.gov/publications/research-reports/medications-to-treat-opioid-addiction/overview#:~:text=Disorder%20Research%20Report-,Overview,a%20prescription%20opioid%20use%20disorder. Accessed 20 July 2023.
- 2.HIV.gov. U.S. Statistics. Published October 27, 2022. https://www.hiv.gov/hiv-basics/overview/data-and-trends/statistics. Accessed 31 January 2023.
- 3.National Institute on Alcohol Abuse and Alcoholism. Alcohol Facts and Statistics. Published 2023. https://www.niaaa.nih.gov/alcohols-effects-health/alcohol-topics/alcohol-facts-and-statistics/alcohol-use-disorder-aud-united-states-age-groups-and-demographic-characteristics. Accessed 31 January 2023.
- 4.Substance Abuse and Mental Health. Treating Substance Use Disorders Among People with HIV. SAMHSA Advisory. https://store.samhsa.gov/sites/default/files/pep20-06-04-007.pdf. Accessed 22 February 2022.
- 5.Cernasev A, Veve MP, Cory TJ, et al. Opioid Use Disorders in People Living with HIV/AIDS: a Review of Implications for Patient Outcomes, Drug Interactions, and Neurocognitive Disorders. Pharm Basel Switz. 2020;8(3):168. doi: 10.3390/pharmacy8030168. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.U.S. Centers for Disease Control and Prevention. HIV and Substance Use. Accessed January 26, 2023. https://www.cdc.gov/hiv/basics/hiv-transmission/substanceuse.html#:~:text=However%2C%20drinking%20alcohol%20and%20ingesting,to%20get%20and%20transmit%20HIV.
- 7.Duko B, Ayalew M, Ayano G. The Prevalence of Alcohol Use Disorders Among People Living with HIV/AIDS: a Systematic Review and Meta-analysis. Subst Abuse Treat Prev Policy. 2019;14(1):52. doi: 10.1186/s13011-019-0240-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Tsui JI, Akosile MA, Lapham GT, et al. Prevalence and Medication Treatment of Opioid Use Disorder Among Primary Care Patients with Hepatitis C and HIV. J Gen Intern Med. 2021;36(4):930–937. doi: 10.1007/s11606-020-06389-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Noska AJ, Belperio PS, Loomis TP, O’Toole TP, Backus LI. Prevalence of Human Immunodeficiency Virus, Hepatitis C Virus, and Hepatitis B Virus Among Homeless and Nonhomeless United States Veterans. Clin Infect Dis Off Publ Infect Dis Soc Am. 2017;65(2):252–258. doi: 10.1093/cid/cix295. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.National Institute on Drug Abuse. Substance Use and Military Life DrugFacts. nida.nih.gov. Published October 2019. https://nida.nih.gov/download/4539/substance-use-military-life-drugfacts.pdf?v=3c3fef9abe44dfc6f720af9c882ac8d9. Accessed 14 August 2023.
- 11.Seal KH, Cohen G, Waldrop A, Cohen BE, Maguen S, Ren L. Substance Use Disorders in Iraq and Afghanistan Veterans in VA Healthcare, 2001–2010: Implications for Screening. Diagnosis and Treatment. Drug Alcohol Depend. 2011;116(1–3):93–101. doi: 10.1016/j.drugalcdep.2010.11.027. [DOI] [PubMed] [Google Scholar]
- 12.Teeters JB, Lancaster CL, Brown DG, Back SE. Substance Use Disorders in Military Veterans: Prevalence and Treatment Challenges. Subst Abuse Rehabil. 2017;8:69–77. doi: 10.2147/SAR.S116720. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Hoggatt KJ, Chawla N, Washington DL, Yano EM. Trends in Substance Use Disorder Diagnoses Among Veterans, 2009–2019. Am J Addict. 2023;32(4):393–401. doi: 10.1111/ajad.13413. [DOI] [PubMed] [Google Scholar]
- 14.Garner BR. Elucidating the substance use disorder-HIV health syndemic. Researchoutreach.org. https://researchoutreach.org/wp-content/uploads/2022/02/Bryan-R.-Garner.pdf. Accessed 1 March 2023
- 15.Eller AJ, DiDomizio EE, Madden LM, Oliva JD, Altice FL, Johnson KA. Strengthening Systems of Care for People with or at Risk for HIV, HCV and Opioid Use Disorder: a Call for Enhanced Data Collection. Ann Med. 2022;54(1):1714–1724. doi: 10.1080/07853890.2022.2084154. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.National Survey on Drug Use and Health. The NSDUH Report: HIV/AIDS and Substance Use. SAMHSA. Published 2010. https://www.samhsa.gov/sites/default/files/hiv-aids-and-substance-use.pdf. Accessed 1 March 2023
- 17.Handanagic S, Finlayson T, Burnett JC, Broz D, Wejnert C, National HIV Behavioral Surveillance Study Group HIV Infection and HIV-Associated Behaviors Among Persons Who Inject Drugs - 23 Metropolitan Statistical Areas, United States, 2018. MMWR Morb Mortal Wkly Rep. 2021;70(42):1459–1465. doi: 10.15585/mmwr.mm7042a1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Montain J, Ti L, Hayashi K, Nguyen P, Wood E, Kerr T. Impact of Length of Injecting Career on HIV Incidence Among People Who Inject Drugs. Addict Behav. 2016;58:90–94. doi: 10.1016/j.addbeh.2016.02.020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Green TC, Kershaw T, Lin H, et al. Patterns of Drug Use and Abuse Among Aging Adults with and Without HIV: a Latent Class Analysis of a US Veteran Cohort. Drug Alcohol Depend. 2010;110(3):208–220. doi: 10.1016/j.drugalcdep.2010.02.020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Kraemer KL, McGinnis KA, Fiellin DA, et al. Low Levels of Initiation, Engagement, and Retention in Substance Use Disorder Treatment Including Pharmacotherapy Among HIV-Infected and Uninfected Veterans. J Subst Abuse Treat. 2019;103:23–32. doi: 10.1016/j.jsat.2019.05.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Davy-Mendez T, Sarovar V, Levine-Hall T, et al. Treatment for Alcohol Use Disorder Among Persons with and Without HIV in a Clinical Care Setting in the United States. Drug Alcohol Depend. 2021;229:109110. doi: 10.1016/j.drugalcdep.2021.109110. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Peltier MR, Sofuoglu M, Petrakis IL, Stefanovics E, Rosenheck RA. Sex Differences in Opioid Use Disorder Prevalence and Multimorbidity Nationally in the Veterans Health Administration. J Dual Diagn. 2021;17(2):124–134. doi: 10.1080/15504263.2021.1904162. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Shipherd JC, Lynch K, Gatsby E, Hinds Z, DuVall SL, Livingston NA. Estimating Prevalence of PTSD Among Veterans with Minoritized Sexual Orientations Using Electronic Health Record Data. J Consult Clin Psychol. 2021;89(10):856–868. doi: 10.1037/ccp0000691. [DOI] [PubMed] [Google Scholar]
- 24.El-Serag HB, Kunik M, Richardson P, Rabeneck L. Psychiatric Disorders Among Veterans with Hepatitis C Infection. Gastroenterology. 2002;123(2):476–482. doi: 10.1053/gast.2002.34750. [DOI] [PubMed] [Google Scholar]
- 25.Livingston NA, Farmer SL, Mahoney CT, Marx BP, Keane TM. Longitudinal Course of Mental Health Symptoms Among Veterans with and Without Cannabis Use Disorder. Psychol Addict Behav J Soc Psychol Addict Behav. 2022;36(2):131–143. doi: 10.1037/adb0000736. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Betancourt JA, Granados PS, Pacheco GJ, et al. Exploring Health Outcomes for U.S. Veterans Compared to Non-veterans from 2003 to 2019. Healthc Basel Switz. 2021;9(5):604. doi: 10.3390/healthcare9050604. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Livingston NA, Gatsby E, Shipherd JC, Lynch KE. Causes of Alcohol-Attributable Death and Associated Years of Potential Life Lost Among LGB and Non-LGB Veteran Men and Women in Veterans Health Administration. Addict Behav. 2023;139:107587. doi: 10.1016/j.addbeh.2022.107587. [DOI] [PubMed] [Google Scholar]
- 28.Lynch KE, Livingston NA, Gatsby E, Shipherd JC, DuVall SL, Williams EC. Alcohol-Attributable Deaths and Years of Potential Life Lost due to Alcohol Among Veterans: Overall and Between Persons with Minoritized and Non-minoritized Sexual Orientations. Drug Alcohol Depend. 2022;237:109534. doi: 10.1016/j.drugalcdep.2022.109534. [DOI] [PubMed] [Google Scholar]
- 29.U.S. Preventive Services Tast Force. Human Immunodeficiency Virus (HIV) Infection: Screening. Published June 11, 2019. https://www.uspreventiveservicestaskforce.org/uspstf/recommendation/human-immunodeficiency-virus-hiv-infection-screening. Accessed 23 Jan 2023
- 30.Department of Veterans Affairs, Veterans Health Administration. National Human Immunodeficiency Virus Program: VHA Directive 1304. U.S. Department of Veterans Affairs. Published August 15, 2019. https://www.hiv.va.gov/provider/policy/index.asp#S1X. Accessed 5 September 2023
- 31.Goulet JL, Martinello RA, Bathulapalli H, et al. STI Diagnosis and HIV Testing Among OEF/OIF/OND Veterans. Med Care. 2014;52(12):1064–1067. doi: 10.1097/MLR.0000000000000253. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Centers for Disease Control and Prevention. HIV Testing. https://www.cdc.gov/hiv/testing/index.html. Accessed 5 September 2023
- 33.Dookeran NM, Burgess JF, Bowman CC, Goetz MB, Asch SM, Gifford AL. HIV Screening Among Substance-Abusing Veterans in Care. J Subst Abuse Treat. 2009;37(3):286–291. doi: 10.1016/j.jsat.2009.03.003. [DOI] [PubMed] [Google Scholar]
- 34.Livingston NA, Davenport M, Head M, et al. The Impact of COVID-19 and Rapid Policy Exemptions Expanding on Access to Medication for Opioid Use Disorder (MOUD): a Nationwide Veterans Health Administration Cohort Study. Drug Alcohol Depend. 2022;241:109678. doi: 10.1016/j.drugalcdep.2022.109678. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.STROBE Statement- Checklist of items that should be included in reports of cross-sectional studies. https://www.equator-network.org/wp-content/uploads/2015/10/STROBE_checklist_v4_cross-sectional.pdf. Accessed 29 July 2022
- 36.Kramer JR, Hartman C, White DL, et al. Validation of HIV-Infected Cohort Identification Using Automated Clinical Data in the Department of Veterans Affairs. HIV Med. 2019;20(8):567–570. doi: 10.1111/hiv.12757. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Benjamini Y, Hochberg Y. Controlling the False Discovery Rate: a Practical and Powerful Approach to Multiple Testing. J R Stat Soc Ser B Methodol. 1995;57(1):289–300. doi: 10.1111/j.2517-6161.1995.tb02031.x. [DOI] [Google Scholar]
- 38.Neale J, Parkin S, Hermann L, et al. Substance Use and Homelessness: a Longitudinal Interview Study Conducted During COVID-19 with Implications for Policy and Practice. Int J Drug Policy. 2022;108:103818. doi: 10.1016/j.drugpo.2022.103818. [DOI] [PubMed] [Google Scholar]
- 39.Hien DN, Bauer AG, Franklin L, Lalwani T, Pean K. Conceptualizing the COVID-19, Opioid Use, and Racism Syndemic and Its Associations With Traumatic Stress. Psychiatr Serv Wash DC. 2022;73(3):353–356. doi: 10.1176/appi.ps.202100070. [DOI] [PubMed] [Google Scholar]
- 40.Meyer JP, Springer SA, Altice FL. Substance Abuse, Violence, and HIV in Women: a Literature Review of the Syndemic. J Womens Health 2002. 2011;20(7):991–1006. doi: 10.1089/jwh.2010.2328. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Johnson KA, Hunt T, Puglisi L, et al. HIV/STI/HCV Risk Clusters and Hierarchies Experienced by Women Recently Released from Incarceration. Healthcare. 2023;11(8):1066. doi: 10.3390/healthcare11081066. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Oldfield BJ, Muñoz N, McGovern MP, et al. Integration of Care for HIV and Opioid Use Disorder. AIDS Lond Engl. 2019;33(5):873–884. doi: 10.1097/QAD.0000000000002125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Drainoni ML, Farrell C, Sorensen-Alawad A, Palmisano JN, Chaisson C, Walley AY. Patient Perspectives of an Integrated Program of Medical Care and Substance Use Treatment. AIDS Patient Care STDs. 2014;28(2):71–81. doi: 10.1089/apc.2013.0179. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Haldane V, Cervero-Liceras F, Chuah FL, et al. Integrating HIV and Substance Use Services: a Systematic Review. J Int AIDS Soc. 2017;20(1):21585. doi: 10.7448/IAS.20.1.21585. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Das S, Muhetaer K, ALvarado HA. Changes in integrated HIV care in substance use treatment facilities (2015-2020). SAMHSA. Published May 2022. https://www.samhsa.gov/data/report/changes-integrated-hiv-su-facilities. Accessed 23 March 2023.
- 46.Pedersen ER, Bouskill KE, Holliday SB, et al. Improving Substance Use Care: Addressing Barriers to Expanding Integrated Treatment Options to Post-9–11 Veterans. RAND Corporation. Published 2020. https://www.rand.org/content/dam/rand/pubs/research_reports/RR4300/RR4354/RAND_RR4354.pdf. Accessed 14 August 2023.
- 47.Ho SB, Bräu N, Cheung R, et al. Integrated Care Increases Treatment and Improves Outcomes of Patients With Chronic Hepatitis C Virus Infection and Psychiatric Illness or Substance Abuse. Clin Gastroenterol Hepatol. 2015;13(11):2005–2014.e3. doi: 10.1016/j.cgh.2015.02.022. [DOI] [PubMed] [Google Scholar]
- 48.Caniglia EC, Khan M, Ban K, Braithwaite RS. Integrating Screening and Treatment of Unhealthy Alcohol Use and Depression with Screening and Treatment of Anxiety, Pain, and Other Substance Use Among People with HIV and Other High-Risk Persons. AIDS Behav. 2021;25(Suppl 3):339–346. doi: 10.1007/s10461-021-03245-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Department of Veterans Affairs. Integrated Mental Health Care. https://www.hiv.va.gov/mobile/index.asp?page=/provider/integrated-mental-health&m=y. Accessed 14 August 2023.
- 50.Conners EE, Hagedorn HJ, Butler JN, et al. Evaluating the Implementation of Nurse-Initiated HIV Rapid Testing in Three Veterans Health Administration Substance Use Disorder Clinics. Int J STD AIDS. 2012;23(11):799–805. doi: 10.1258/ijsa.2012.012050. [DOI] [PubMed] [Google Scholar]
- 51.Edelman EJ, Maisto SA, Hansen NB, et al. Integrated Stepped Alcohol Treatment for Patients with HIV and Alcohol Use Disorder: a Randomised Controlled Trial. Lancet HIV. 2019;6(8):e509–e517. doi: 10.1016/S2352-3018(19)30076-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.National Academies of Sciences, Engineering, and Medicine; Health and Medicine Division; Board on Population Health and Public Health Practice; Committee on the Examination of the Integration of Opioid and Infectious Disease Prevention Efforts in Select Programs. Opportunities to Improve Opioid Use Disorder and Infectious Disease Services: Integrating Responses to a Dual Epidemic. National Academies Press (US); 2020. https://www.ncbi.nlm.nih.gov/books/NBK555809/?term=Opportunities%20to%20Improve%20Opioid%20Use%20Disorder%20and%20Infectious%20Disease%20Services%3A%20Integrating%20Responses%20to%20a%20Dual%20Epidemic. Accessed 14 August 2023. [PubMed]
- 53.Bokhour BG, Saifu H, Goetz MB, et al. The Role of Evidence and Context for Implementing a Multimodal Intervention to Increase HIV Testing. Implement Sci. 2015;10(1):22. doi: 10.1186/s13012-015-0214-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The United States Department of Veterans Affairs (VA) places legal restrictions on access to veteran’s health care data, which includes both identifying data and sensitive patient information. The analytic data sets used for this study are not permitted to leave the VA firewall without a Data Use Agreement. This limitation is consistent with other studies based on VA data. However, VA data are made freely available to researchers behind the VA firewall with an approved VA study protocol. For more information, please visit https://www.virec.research.va.gov or contact the VA Information Resource Center (VIReC) at vog.av@CeRIV.

