- Research Note
- Open access
- Published:
HIV and hepatitis C Virus in internally displaced people with and without injection drug use experience in the region of Shida Kartli, Georgia
BMC Research Notes volume 17, Article number: 315 (2024)
Abstract
Objective
Internally displaced persons (IDPs) can have limited access to HIV and hepatitis C Virus (HCV) treatment and prevention. IDPs comprise > 7% of Georgian population but prevalence and levels of HIV and HCV knowledge in this population remain unknown. We tested 100 IDPs in Georgia for HIV and HCV, many of whom had drug injecting experience, and interviewed them about their migration experience, sexual and drug injecting practices, and HIV/HCV transmission knowledge.
Results
The average age of participants was 37.5 years (range 18–63); 31% were women. Almost half (N = 48) of participants reported ever injecting drugs; 17% of those (N = 8) started injecting drugs within the last year. Anti-HCV and HIV prevalence was 11% and 0%, respectively. Fewer people without drug use experience compared to people who inject drugs correctly answered all questions on the HIV knowledge test (13% vs. 35%, p = 0.015) or knew where to get tested for HIV (67% vs 98%, p < 0.001). There was no difference in HCV knowledge between the two groups. HIV and HCV prevalence remains low among Georgian IDPs, but levels of HIV knowledge were much lower than levels of HCV knowledge.
Introduction
Internally displaced persons (IDPs) compose approximately 60% of forced migrants worldwide. Forced displacement impacts the distribution and spread of infectious diseases, including blood borne chronic diseases like HIV and hepatitis C Virus (HCV) [1]. Countries experiencing internal displacement often have limited resources, making infectious disease surveillance in IDPs challenging [2].
Since 1991 Georgia, an Eastern European country of 3.7 million, has experienced significant internal displacement; 286,000 people (7.7% of the total population) were IDPs in 2022 as a result of the occupation of Abkhazia since the early 1990s and South Ossetia since 2008 [Fig. 1] [3]. Displacement-associated stressors can cause depression/anxiety, and IDPs can resort to using drugs/alcohol to cope [4,5,6,7], which might put them at higher risk for HIV or HCV [8].
Georgia has been heavily affected by HCV since the 1990s [6]. In 2015, 7.7% of the adult population were estimated to be anti-HCV positive and 5.4%—HCV RNA/cAg positive [9]. In 2015, in response to high HCV prevalence, Georgia adopted a national HCV elimination program, aiming to reduce prevalence of HCV infection by 90% by 2020, which resulted in > 80% of those diagnosed (approximately 72,000 patients) being cured between 2015 – 2020 [10, 11]. In 2021, 6.8% of the adult population was estimated to be anti-HCV positive and 1.8% HCV RNA/cAg positive, indicating a 67% reduction in chronic HCV since 2015 [12]. As of 2020, HIV prevalence remains low (0.4%) in the general population in Georgia [13].
People who inject drugs (PWID) are often at higher risk for HIV and HCV; indeed, anti-HCV prevalence among PWID in Georgia was 58.1% in 2022 and 51.1% in 2015 (8, [14]. However, Georgia has lower HIV prevalence among PWID than many Eastern European/Central Asian countries (2.3% vs. 21.9% in Ukraine, 25.1% in Belarus, 18.5% in Latvia, 8.5% in Azerbaijan, and 48.3% in Estonia) [15]. Multiple interventions in PWID also resulted in high levels of HIV knowledge in PWID who are clients of the Georgian Harm Reduction Network (GHRN)(16).
Data regarding infectious diseases among IDPs is scarce and outdated if available; a 2004 study showed that prevalence and incidence of infectious and parasitic diseases among IDPs on average is 3 times higher than in the general population in Georgia[17, 18]. In 2006, IDPs represented a disproportionately high number of people living with HIV (PLWH); IDPs made up 5.5% of the Georgian population and 8.9% of PLWH [19]. To our knowledge, there is no previous data about HCV prevalence among Georgian IDPs. This study is the first to provide some data on HIV/HCV knowledge and awareness of testing and treatment, and current HIV/HCV prevalence among IDPs in Georgia.
Methods
Data collection
In June 2022, we conducted a cross sectional study at mobile ambulances near IDP villages in Shida Kartli region of Georgia. Shida Kartli hosts approximately 17,000 IDPs across 75 settlements (Collective Centres (CCs) [5]. (Fig. 1). The local non-governmental organization (NGO) “Step to Future” (STF) that provides harm reduction services in the area conducted recruitment. The GHRN compiled a list of all locations visited by the mobile ambulances, then randomly selected one at a time for recruitment. Participants were recruited through convenience and snowball sampling, non-probability sampling techniques used among vulnerable populations [20, 21]. Inclusion criteria were: (1) IDPs (2) age 18 + (3) residence in a CC in Shida Kartli. Each primary respondent received three uniquely identified coupons, then distributed the coupons to others. Participants could participate by redeeming their coupon at STF’s mobile ambulances. Our sample size of 100 was selected/saturated by available resources given that this was a pilot study; additionally, our calculations showed this sample size would be sufficient to detect differences as 0.05 statistical level with 80% power if HCV prevalence among IDPs was at least 2 times higher than the estimated 7.7% anti-HCV prevalence in the general population [9, 18, 19]. Participants were surveyed about their migration/displacement experience, number of sexual partners and sexual practices within the past 6 months, whether they had ever injected drugs, drug injecting practices within the past 30 days, knowledge of HIV/HCV transmission routes, knowledge of HIV/HCV treatment and prevention programs, and medical history regarding HIV/HCV. (See Supplemental Tables 1 and 2, and Supplementary File 1 for more detail about survey questions). Survey questions were adapted from bio-behavioural surveys conducted by GHRN in Georgia since 2002 [22] and from our previous work with IDPs in Ukraine [23, 24]. After interviews, participants were tested for HIV and HCV (rapid tests), and offered to receive harm reduction services, case management if applicable, and legal services from STF. Participants with a positive rapid HCV test result were promptly assisted to obtain HCV confirmatory diagnostics, and if confirmed positive, supported in initiating direct-acting antiviral (DAA) treatment.
Measures
HIV and HCV transmission knowledge was measured by answering Correct/Incorrect to a set of questions (see Supplemental Table 1). As IDPs consistently report high levels of depression [25], the Patient Health Questionnaire depression scale (PHQ-9) (a tool with demonstrated high reliability (Cronbach’s α = 0.89)) was utilized [26].
Statistical analysis
Socio-demographic and behavioural characteristics of IDPs were summarized with descriptive statistics. Continuous variables were presented as mean and range; categorical variables were presented as proportions. To compare IDPs with and without injection drug use (IDU) experience, we used a chi-square (χ2) test for categorical variables and analysis of Variance (ANOVA) test for continuous variable. P-values < 0.05 were considered as statistically significant. Depression score was measured as a continuous variable.
Results
Socio-demographic data
Socio-demographic and behavioural characteristics of the participants (N = 100) are presented in Table 1. The average age of participants was 37.5 (range 18–63); 31% were women; 59% had partial or complete secondary education. Nearly all participants were displaced from Abkhazia (94%); most of those following the escalation of the conflict in 2008 (83%). Eighty percent of participants settled in IDP shelters immediately after displacement. No participants tested positive for HIV; 11 participants received a positive rapid anti-HCV test in the study; of those, 3 participants tested HCV RNA/cAg positive when linked to care to receive DAA treatment.
Forty-eight participants (48%) reported ever injecting drugs; and the average age at first injection was 22 years (range 14—35). Details of participants who reported IDU can be found in Table 2. The average duration of IDU experience was 6 years (range 1- 24); 8 participants (17%) started injecting drugs in the last 12 months. 52% with IDU experience (N = 25) had injected drugs in the last 30 days; the majority had never been in a Methadone/Buprenorphine + naloxone program (N = 43, 90%). Of those with recent IDU experience, 2% (N = 3) shared needles in the last 30 days.
Ninety-five percent of participants reported sexual intercourse in the last 6 months; of those, 90% of women (N = 26) and 38% of men (N = 25) reported having 1 partner in that time period. No participants reported same-sex sexual partners. One woman reported sex work; 30% of men (N = 21) reported paying for sex. 37% of participants (N = 35) reported “always” using condoms when having sex in the last 6 months.
Differences in participants with and without IDU experience
PWID were overwhelmingly male (98%) compared to non-PWID (42%; p < 0.001) and older (mean age 40 vs 35, respectively; p = 0.024). More PWID compared to non-PWID knew where to access HIV testing (98% vs 67%, p < 0.001) and HCV testing (100% vs 90%, p = 0.027), had ever been tested for HIV (94% vs 46%, p < 0.001), and HCV (96% vs 69%, p < 0.001). Primary reasons reported by non-PWID for not getting tested for HIV were “never thinking about HIV testing” (79%) and “not knowing where to take a test” (61%). Primary reasons reported by non-PWID for not getting HCV tested were similar: “never thinking of HCV testing” (75%) and “not knowing where to take a test” (31%).
All participants who reported previously testing positive for HCV (N = 6) were PWID; all reported receiving treatment and clearing infection There were no reinfections in our sample. All participants (N = 11) who tested positive with HCV in this study had IDU experience, resulting in 23% anti-HCV prevalence in IDP who inject drugs (IDPWID).
More PWID compared to non-PWID answered all questions in the HIV knowledge test correctly (35% vs 13%, p = 0.015), but there was no difference in the HCV knowledge test (70% vs 67% correct, p = 0.7).
With regards to mental health, more PWID experienced moderately severe depression compared to non-PWID (23% vs 15%, p = 0.009) and felt that their behaviours became riskier after displacement (92% vs 15%, p < 0.001). In the last year, there were no differences between PWID and non-PWID in experiences of assault from family, neighbours, roommates, or colleagues, but more PWID (compared to non-PWID) reported being assaulted by police (10% vs 0%, p = 0.022) and by other IDPs (15% vs 2%, p = 0.022).
Discussion
Internal displacement is on the rise globally [2], making the monitoring of HIV and HCV transmission among IDPs an important task. In this exploratory work, we found evidence of a higher HCV prevalence in Georgian IDPs compared to previous reports from the general population, which can be explained by the fact that we have a high proportion of PWID in our sample. We did not find evidence of a higher HIV prevalence among IDPs with or without IDU experience compared to previously reported estimates in the general population.
While more participants in total tested anti-HCV positive (11%; all of whom had IDU experience) compared to an estimated 6.8% of the general population [11], this is likely explained by the high number of participants with IDU experience in our sample (48%). In the last general population survey conducted in 2015, an estimated 2.2% of adults reported IDU experience [27]. No reports exist on IDU prevalence among Georgian IDPs [8], but our sample likely had more PWID because recruitment was conducted by a local harm reduction NGO [8, 28]. When compared to non-displaced PWID, anti-HCV prevalence among IDPWID in this study (23%) was lower than the one reported among PWID in Gori (the regional capital of Shida Kartli) in the 2022 IBBS survey (66.7%); additionally, a simplified bio behavioural survey conducted among PWID in Gori in 2023 revealed anti-HCV prevalence of 57.7% [14]. Differences in HCV prevalence could be attributed to limited mixing between local PWID and IDPWID. Consistent with low estimates (2.3%) of HIV prevalence among PWID in Georgia, we found no HIV infections in our small sample of 48 IDPWID [12]. The Georgian HCV elimination campaign has been internationally recognized for its success; 41 specialized HCV treatment centres existed in the country as of 2018, and an estimated 72,000 people with HCV were cured between 2015 and 2020 [10, 11, 28].
The vast majority of participants knew where to get HCV tested, have been tested for HCV, and demonstrated knowledge of HCV transmission, showing evidence that previously evaluated successful HCV interventions like the 2015 country-wide HCV elimination campaign [29,30,31] had also resulted in higher levels of HCV knowledge among Georgians without IDU experience. At the same time, knowledge of HIV transmission and testing remains low, particularly among non-PWID. Programs aimed at increasing HIV knowledge among non-PWID can reduce stigma towards PLWH [32, 33].
In 2019, an estimated 10,500–12,000 people per month were being reached by GHRN’s harm reduction programs (about 20% of the estimated population of PWID in Georgia); PWID involved with these programs were less likely to have shared needles within 6 months and more likely to have been tested for HIV, compared to non-involved PWID [16, 34]. Despite these successes, 12% of recent PWID in our sample had shared needles and 90% had never been in a Methadone/Buprenorphine + naloxone program; furthermore, prevalence of condom use remained low. Alarmingly, a high proportion (17%) of IDPWID initiated IDU in the last 12 months despite being displaced in 2008 or earlier. High proportions of new PWID amongst IDPs create increased pools of individuals at increased risk for HIV/HCV [35] indicating a need for sustained harm reduction services. As the majority of IDPWID (92%) also reported that their behaviours became riskier after displacement, it is crucial to offer harm reduction services and conduct continuous surveillance of behaviour changes and prevalence of HIV/HCV (including testing) in internally and externally displaced PWID in Georgia, as these populations are expected to grow due to the Russian war against Ukraine [36].
While IDPs generally experience high levels of anxiety and depression [25], IDPWID participants had higher prevalence of depression than non-PWID. Correlations between substance use and depression are widely documented [37, 38]. The majority of IDPs were displaced in 2008, but the average duration of IDU experience was 6 years; thus, it seems unlikely that IDU was initiated as a coping mechanism immediately following displacement. Finally, IDPWID experience more assaults from police and other IDPs than non-PWID, likely due to widespread stigma against PWID in Georgia [34].
Intervention suggestions include developing targeted evidence-based interventions and policies using international best practices. Community-based workshops (including meetings with religious leaders) could address intracommunity stigma against IDPWID, and awareness campaigns could help dispel myths, spread factual information, and lessen stigma associated with IDU [7, 34]. Creating a stigma-free environment is a major responsibility of healthcare providers; training for healthcare practitioners about how to provide nonjudgmental, culturally competent care for PWID could help achieve this goal [39], as many PWID report experiences of stigma in medical settings as a barrier to receiving care, including HCV treatment [40, 41]. Lastly, Georgian laws against drug use are strict, and previous research points to a need for re-evaluation of national drug policy [42].
Limitations
Cross-sectional study design makes it impossible to assess HIV or HCV incidence in our IDP sample or make causal inference with respect to various behaviours or exposures [43]. Additionally, because IDPs are a hard-to-reach population, we used a non-probability sampling technique that makes our findings less generalizable [20]. As recruitment was conducted by a NGO that provides harm reduction services, the proportion of PWID was likely higher in our sample than in the general population of Georgian IDPs. Finally, this was a pilot study, and our sample size was determined and saturated by available resources.
Conclusions
The study revealed low HIV and HCV prevalence rates among Georgian IDPs. While IDPs have high levels of understanding of HCV, knowledge about HIV remains low. Nearly one in five IDPWID participants had initiated IDU within the past year, indicating opportunities for further research about IDU among IDPs in Georgia. As the number of displaced individuals in the region grows, preventive activities such as screenings and testing must be scaled up.
Availability of data and materials
Data available upon request from corresponding author.
References
Greenaway C, Castelli F. Infectious diseases at different stages of migration: an expert review. J Travel Med. 2019. https://doiorg.publicaciones.saludcastillayleon.es/10.1093/jtm/taz007.
Vasylyeva TI, Horyniak D, Bojorquez I, Pham MD. Left behind on the path to 90–90-90: understanding and responding to HIV among displaced people. J Int AIDS Soc. 2022;25(11): e26031.
Georgia MoIDPftOTotRo. Review of internally displaced persons in Georgia. 2019.
Makhashvili N, Chikovani I, McKee M, Bisson J, Patel V, Roberts B. Mental disorders and their association with disability among internally displaced persons and returnees in Georgia. J Trauma Stress. 2014;27(5):509–18.
Gogishvili D, Harris-Brandts S. The social and spatial insularity of internally displaced persons: “neighbourhood effects” in Georgia’s collective centres. Caucasus Surv. 2019;7(2):134–56.
Gvinjilia L, Nasrullah M, Sergeenko D, Tsertsvadze T, Kamkamidze G, Butsashvili M, et al. National progress toward hepatitis C elimination—Georgia, 2015–2016. MMWR Morb Mortal Wkly Rep. 2016;65(41):1132–5.
Elbaz J. Assessing the risk of HIV and hepatitis C among internally displaced persons in Georgia. Ann Glob Health. 2020;86(1):66.
Saxon L, Makhashvili N, Chikovani I, Seguin M, McKee M, Patel V, et al. Coping strategies and mental health outcomes of conflict-affected persons in the Republic of Georgia. Epidemiol Psychiatr Sci. 2017;26(3):276–86.
Hagan LM, Kasradze A, Salyer SJ, Gamkrelidze A, Alkhazashvili M, Chanturia G, et al. Hepatitis C prevalence and risk factors in Georgia, 2015: setting a baseline for elimination. BMC Public Health. 2019;19(Suppl 3):480.
Mitruka K, Tsertsvadze T, Butsashvili M, Gamkrelidze A, Sabelashvili P, Adamia E, et al. Launch of a nationwide hepatitis C elimination program-Georgia, April 2015. MMWR Morb Mortal Wkly Rep. 2015;64(28):753–7.
Hutin Y, Luhmann N, Easterbrook P. Evaluating the impact of Georgia’s hepatitis C elimination plan: lessons learned for the global initiative. Lancet Glob Health. 2020;8(2):e163–4.
Gamkrelidze A, Shadaker S, Tsereteli M, Alkhazashvili M, Chitadze N, Tskhomelidze I, et al. Nationwide hepatitis C serosurvey and progress towards hepatitis C virus elimination in the country of Georgia, 2021. J Infect Dis. 2023;228(6):684–93.
AIDS U. Global AIDS Monitoring 2020: Country progress report—Georgia. 2020.
Gogia M, Ruadze E, Kasrashvili T, Mathers B, Sabin K, Verster A, et al. Piloting a simplified bio-behavioural survey methodology, the BBS-Lite, among people who inject drugs in Georgia. Int J Drug Policy. 2024. https://doiorg.publicaciones.saludcastillayleon.es/10.1016/j.drugpo.2024.104326.
LaMonaca K, Dumchev K, Dvoriak S, Azbel L, Morozova O, Altice FL. HIV, drug injection, and harm reduction trends in Eastern Europe and Central Asia: implications for international and domestic policy. Curr Psychiatry Rep. 2019;21(7):47.
Gogia M, Lawlor C, Shengelia N, Stvilia K, Raymond HF. Hidden populations: discovering the differences between the known and the unknown drug using populations in the Republic of Georgia. Harm Reduct J. 2019;16(1):15.
DM ZA. IDP health profile review in Georgia. United Nations Development Programme in Georgia; 2004.
Zoidze Akaki MD. IDP Health profile review in Georgia. United Nations Development Programme in Georgia; 2004.
G T-M. Assessment of IDP Livelihoods in Georgia: Facts and Policies. UNHCR; 2009.
Kral AH, Malekinejad M, Vaudrey J, Martinez AN, Lorvick J, McFarland W, et al. Comparing respondent-driven sampling and targeted sampling methods of recruiting injection drug users in San Francisco. J Urban Health. 2010;87(5):839–50.
Gyarmathy VA, Johnston LG, Caplinskiene I, Caplinskas S, Latkin CA. A simulative comparison of respondent driven sampling with incentivized snowball sampling–the “strudel effect.” Drug Alcohol Depend. 2014;135:71–7.
Curatio International Foundation BPU. HIV risk and prevention behaviours among people who inject durgs in seven cities of Georgia, bio-behavioural surveillance survey report. Tbilisi: Curation International Foundation and Bemoni Public Union; 2015.
Kovalenko G, Yakovleva A, Smyrnov P, Redlinger M, Tymets O, Korobchuk A, et al. Phylodynamics and migration data help describe HIV transmission dynamics in internally displaced people who inject drugs in Ukraine. PNAS Nexus. 2023;2(3):pgad008.
Yakovleva A, Kovalenko G, Redlinger M, Smyrnov P, Tymets O, Korobchuk A, et al. Hepatitis C Virus in people with experience of injection drug use following their displacement to Southern Ukraine before 2020. BMC Infect Dis. 2023;23(1):446.
Morina N, Akhtar A, Barth J, Schnyder U. Psychiatric disorders in refugees and internally displaced persons after forced displacement: a systematic review. Front Psychiatry. 2018;9:433.
Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med. 2001;16(9):606–13.
Bemoni Public Union CIF. Population size estimation of people who inject drugs in Georgia, 2015. 2015.
Averhoff F, Shadaker S, Gamkrelidze A, Kuchuloria T, Gvinjilia L, Getia V, et al. Progress and challenges of a pioneering hepatitis C elimination program in the country of Georgia. J Hepatol. 2020;72(4):680–7.
Tsertsvadze T, Gamkrelidze A, Chkhartishvili N, Abutidze A, Sharvadze L, Kerashvili V, et al. Three years of progress toward achieving hepatitis C elimination in the country of Georgia, April 2015-march 2018. Clin Infect Dis. 2020;71(5):1263–8.
Walker JG, Tskhomelidze I, Shadaker S, Tsereteli M, Handanagic S, Armstrong PA, et al. Insights from a national survey in, and from modelling on progress towards hepatitis C virus elimination in the country of Georgia since 2015. Euro Surveill. 2021. https://doiorg.publicaciones.saludcastillayleon.es/10.2807/1560-7917.ES.2023.28.30.2200952.
Chikovani I, Ompad DC, Uchaneishvili M, Sulaberidze L, Sikharulidze K, Hagan H, et al. On the way to hepatitis C elimination in the Republic of Georgia-Barriers and facilitators for people who inject drugs for engaging in the treatment program: a formative qualitative study. PLoS ONE. 2019;14(4): e0216123.
Than PQT, Tran BX, Nguyen CT, Truong NT, Thai TPT, Latkin CA, et al. Stigma against patients with HIV/AIDS in the rapid expansion of antiretroviral treatment in large drug injection-driven HIV epidemics of Vietnam. Harm Reduct J. 2019;16(1):6.
Thapa S, Hannes K, Cargo M, Buve A, Peters S, Dauphin S, et al. Stigma reduction in relation to HIV test uptake in low- and middle-income countries: a realist review. BMC Public Health. 2018;18(1):1277.
Lawlor C, Gogia M, Kirtadze I, Stvilia K, Jikia G, Zurashvili T. Hidden populations: risk behaviours in drug-using populations in the Republic of Georgia through subsequent peer-driven interventions. Harm Reduct J. 2021;18(1):78.
Vasylyeva TI, Friedman SR, Lourenco J, Gupta S, Hatzakis A, Pybus OG, et al. Reducing HIV infection in people who inject drugs is impossible without targeting recently-infected subjects. AIDS. 2016;30(18):2885–90.
Refugees UNHCf. Europe | Global focus 2024 https://reporting.unhcr.org/operational/regions/europe#:~:text=Europe's%20forcibly%20displaced%20and%20stateless,displaced%20inside%20Ukraine%20in%202024.
Esmaeelzadeh S, Moraros J, Thorpe L, Bird Y. Examining the association and directionality between mental health disorders and substance use among adolescents and young adults in the us and canada-a systematic review and meta-analysis. J Clin Med. 2018;7(12):543.
Colledge S, Larney S, Peacock A, Leung J, Hickman M, Grebely J, et al. Depression, post-traumatic stress disorder, suicidality and self-harm among people who inject drugs: a systematic review and meta-analysis. Drug Alcohol Depend. 2020;207: 107793.
Stringer KL, Mukherjee T, McCrimmon T, Terlikbayeva A, Primbetovac S, Darisheva M, et al. Attitudes towards people living with HIV and people who inject drugs: a mixed method study of stigmas within harm reduction programs in Kazakhstan. Int J Drug Policy. 2019;68:27–36.
Muncan B, Walters SM, Ezell J, Ompad DC. “They look at us like junkies”: influences of drug use stigma on the healthcare engagement of people who inject drugs in New York city. Harm Reduct J. 2020;17(1):53.
Goodyear T, Brown H, Browne AJ, Hoong P, Ti L, Knight R. “Stigma is where the harm comes from”: exploring expectations and lived experiences of hepatitis C virus post-treatment trajectories among people who inject drugs. Int J Drug Policy. 2021;96: 103238.
Otiashvili D, Tabatadze M, Balanchivadze N, Kirtadze I. Policing, massive street drug testing and poly-substance use chaos in Georgia—a policy case study. Subst Abuse Treat Prev Policy. 2016;11:4.
Wang X, Cheng Z. Cross-sectional studies: strengths, weaknesses, and recommendations. Chest. 2020;158(1S):S65–71.
Acknowledgements
We thank social workers from the non-governmental organization “Step to Future” in collection of epidemiological and behavioural data. We also express our sincere gratitude towards study participants.
Funding
Funding Declaration: TIV is supported by the Branco Weiss Society in Science Fellowship. AY acknowledges support from Somerville College MTST Development Award and Catherine Hughes Fund. GK is supported by grants from the Wellcome Trust (Refs: 207498/Z/17/Z and 206298/B/17/Z). BS is supported by an NIH-NIDA K01 (DA049665).
Author information
Authors and Affiliations
Contributions
AT; primary author. TIV; editor. AA; TK; GK; AY; BS; MG. TIV wrote the first draft; AT revised and conducted additional analysis. TIV and MG designed the study. AA, TK, GK, AY, and BS edited the manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
The interviews were conducted after respondents received information about the project and gave their written informed consent. Ethical approval for the study was received from the IRB of the University of California San Diego (Protocol Number 802892), the ethics committee of the Infectious Diseases, AIDS, and Clinical Immunology Research Center in Tbilisi (Protocol Number 22-002) and the Georgian Harm Reduction Network (Protocol Number 22-002).
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
13104_2024_6891_MOESM1_ESM.docx
Supplementary file 1: Table S1: (uploaded separately) HCV and HIV knowledge questions asked to participants. Supplemental Table S2: (uploaded separately) Question blocks with descriptions of the categories of questions and summaries of questions asked to participants. Table S3: (uploaded separately) Full questionnaire of questions asked to participants.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Trovato, A., Gogia, M., Aslanikashvili, A. et al. HIV and hepatitis C Virus in internally displaced people with and without injection drug use experience in the region of Shida Kartli, Georgia. BMC Res Notes 17, 315 (2024). https://doiorg.publicaciones.saludcastillayleon.es/10.1186/s13104-024-06891-9
Received:
Accepted:
Published:
DOI: https://doiorg.publicaciones.saludcastillayleon.es/10.1186/s13104-024-06891-9