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. Author manuscript; available in PMC: 2026 Apr 9.
Published in final edited form as: Int J Drug Policy. 2026 Feb 5;150:105062. doi: 10.1016/j.drugpo.2025.105062

The global epidemiology of injecting drug use, HIV, viral hepatitis and tuberculosis among people who are incarcerated: a multistage systematic review

Louisa Degenhardt a, Matthew Hickman a,b, Frederick L Altice c, Jason Grebely d, Sophia Taylor a, Michelle Lynch a, Aleksa Kamenjaš a, Jack Marsden a, Lucy T Tran a, Paige Webb a, Olivia Price a, Christel Macdonald a, Filipa Alves da Costa e, Justin Berk f, Anja Busse g, Evan Cunningham d, Colleen Daniels k, Behzad Hajarizadeh d, Linda Montanari h, Luis Royuela h, Keith Sabin a,i, Jack Stone b, Annette Verster j, Peter Vickerman b, Michael Farrell a, Thomas Santo Jr a,*
PMCID: PMC13058553  NIHMSID: NIHMS2157186  PMID: 41651703

Abstract

Background:

This global systematic review assesses the prevalence of injecting drug use (IDU) and key infectious diseases (HIV, hepatitis C virus [HCV], tuberculosis and hepatitis B virus [HBV]) among people who are incarcerated.

Methods:

We conducted a systematic search of peer-reviewed (Medline, Embase, PsycINFO), internet, and grey literature databases, from January 2000 through 2nd June 2025 and engaged international experts and relevant agencies liaising with key agencies focused on incarcerated populations (WHO, UNODC, UNAIDS and EUDA). Data on study methods, size of incarcerated populations and demographic characteristics, and prevalence of IDU, HIV, HCV, HBV and tuberculosis among incarcerated populations were extracted. Meta-analyses pooled data where multiple estimates were available for a country; regional and global estimates were calculated, weighted by incarcerated population size. We present overall country, regional and global prevalence estimates for each variable examined, stratified by sex. We then estimated the ratio of IDU, HIV, HCV, HBV and tuberculosis prevalence among incarcerated populations compared to the general population.

Results:

Of 75,755 screened documents, 2,968 were eligible for data extraction. There are approximately 11,322,000 people aged 15–64 years incarcerated globally with their incarceration rate being 221 per 100,000 (29 per 100,000 among females and 404 per 100,000 among males). Substantial variation in rates across countries and regions were observed with the highest regional rate being in North America. Globally, we estimate that 11·9% of people who are incarcerated have ever injected drugs (1,348,000; 95%CI 1,061,500–1,687,000), 51·4 times higher than the general population. We estimate that 3·7% (95%CI 2·5–5·4) of people who are incarcerated globally are living with HIV (25.1· times higher than the general population); 11·7% (95%CI 7·7–17·1) have current HCV infection (15·6 times higher); 4·4% (95%CI 2·4–7·7) have current HBV infection (2·2 times higher) and 2·5% (95%CI 1·5–3·8) have active tuberculosis (45·3 times higher than the general population). There is substantial variation geographically and among females and males.

Conclusion:

The substantial concentration of people with multiple risks and comorbidities requires improved strategies to screen, evaluate, treat and prevent these adverse consequences, which is crucial for global control efforts.

Funding:

Australian National Health and Medical Research Council.

Keywords: Incarceration, Criminal justice settings, Injecting drug use, HIV, Hepatitis, Tuberculosis, Epidemiology, Prevalence

Introduction

Incarcerated populations worldwide bear a disproportionately high risk for infectious diseases including HIV, tuberculosis and viral hepatitis (HCV and HBV) (Altice et al., 2016; Bosworth et al., 2022; Dolan et al., 2016). Moreover, people who inject drugs (PWID) are at increased risk of both being incarcerated having been infected with these infections and being at risk of exposure during incarceration (Altice et al., 2016; Bosworth et al., 2022; Dolan et al., 2016). In the absence of decarceration and decriminalisation efforts, “carceral environments” (defined here as jails, prisons, and correctional facilities, explicitly excluding immigration or compulsory detention centres) become pivotal venues for preventing, diagnosing, and treating globally prevalent infectious diseases.

There is a lack of robust evidence on population estimates of the health problems in people who are incarcerated, causing major barriers for national, regional, and global policymakers in evaluating progress towards UN Sustainable Development Goals (United Nations, 2025). A 2016 review examined HIV, HCV, HBV and tuberculosis in incarcerated populations (Dolan et al., 2016), with an update of this review among key populations published in 2018 (Wirtz et al., 2018), a 2018 review examined injecting drug use (Moazen et al., 2018), and reviews of tuberculosis prevalence among people who are incarcerated have been undertaken more recently (Martinez et al., 2023; Mera et al., 2023; Placeres et al., 2023). In every instance, the search scope was limited, often restricted to peer-reviewed literature, and failed to produce population size estimates, sex-disaggregated pooled estimates, or comparative risk assessments against the general population.

We undertook a multistage global systematic review of peer-reviewed and grey literature to estimate the prevalence and numbers of people with injecting drug use, HIV, and current HCV, HBV and tuberculosis infections among people who are incarcerated, including examining these among both females and males. We estimated prevalence and population sizes at country, regional and global levels and compared prevalence in people who are incarcerated to the general population.

Methods

Search strategy and selection criteria

We conducted a systematic review using methods consistent with previous global reviews (Degenhardt et al., 2017; Mathers et al., 2008; Nelson et al., 2011) and in accordance with PRISMA (Moher et al., 2009) and GATHER (Stevens et al., 2025) guidelines (Appendix 1). The review protocol was registered on PROSPERO (CRD42023425532). Searches were conducted in several stages with no limitations on languages. Searches and contacts with country experts and key agencies continued until December 2024.

We searched electronic peer-reviewed literature databases (Medline, EMBASE, PsycINFO, Web of Science, and CINAHL) using a comprehensive set of search terms developed in consultation with a specialist drug and alcohol librarian (Appendix 2). This included a set of terms for incarceration settings, injecting drug use, blood-borne viruses and tuberculosis, and harm reduction interventions for people who use drugs (Appendix 2). Searches were conducted March 7th-10th 2023, and were limited to those published from January 1st, 2000 onwards. An updated search was done on June 2nd 2025, and was limited to reports published between March 10th 2023 and June 2nd 2025 (Appendix 2). Systematic reviews were hand-searched for relevant original papers or reports within them.

Grey literature and online databases identified as sources of papers or reports on people who are incarcerated were systematically searched using their own search functions or Google Advanced Search (Appendix 2). These sources included websites of drug surveillance systems, regional harm-reduction networks, criminal justice-related websites, and country-specific ministries/departments of health, justice or interior. National and region-specific websites were searched in both English and the national language of the country, with translations facilitated by Google Translate (see Appendix 3 for sites; see also Ottaviano et al., 2023).

We searched key documents published by relevant international agencies, including UN Office on Drugs and Crime’s (UNODC) World Drug Reports (United Nations Office on Drugs & Crime, 2022), Harm Reduction International’s Global State of Harm Reduction reports (Harm Reduction International, 2022,2023), reports from the European Union Drug Agency (EUDA) (European Union Drug Agency, 2024a, 2024b), World Health Organization (WHO), UNAIDS and The Global Fund to Fight AIDS, Tuberculosis and Malaria. We contacted members of these organisations directly when additional information was required and liaised with those agencies until completion of the review.

Data were also requested from experts in November 2023, via an email distribution process and social media. This comprised initial emails sent to key experts and organisations, and posts on Twitter and Facebook, with requests to circulate to broader networks (Appendix 4). Searches and contacts with country experts and key agencies continued until December 2024.

Screening and data extraction

An EndNote 20 library was created to catalogue papers and reports, with duplicates removed. We had members proficient in reading English, French, Serbo-Croatian, Portuguese, and Spanish; other languages were read via Google Translate or the Microsoft Word 365 translate function. Initial screening of title and abstract was done by two independent reviewers (ST, LD, ML, SO, AK, PW, BY, BC, MB, JG, TS, RJ, OP, BH, EBC) with discrepancies resolved via consensus with at least one other reviewer. Papers were included at title and abstract or full-text stage if they met a defined set of criteria for inclusion in the review (Appendix 5). Full-text review was also independently undertaken by two reviewers (AK, ST, BY, JM, ML, LD, JW, NO, MB, TS, BC, EL, OP or CM). Papers and reports were excluded if they met any of the following: samples sizes fewer than 40; cohort studies without baseline data; case control studies; non-original works (e.g., reviews or editorials); papers with insufficient methodological details; or samples of subpopulations (e.g., only people with HIV) (Appendix 5). A classification system was used for grading studies included in the review according to the extent to which the study sample was representative of the entire country’s incarcerated population (Appendix 6).

Data from eligible studies were extracted into purpose-built databases using Microsoft Access and REDCap at city, sub-national, or country level and double-checked for accuracy. Countries and regional groupings were based upon those used by UNAIDS, WHO and UNODC (Colledge-Frisby et al., 2023; Degenhardt et al., 2017, 2023; Larney et al., 2017).

Data on the estimates of the size of incarcerated populations were obtained from the most recent data reported in the World Prison Brief (WPB) (https://www.prisonstudies.org/). Data were unavailable for some countries from the WPB, including incarcerated population estimates (Eritrea and Palestine) and ratios of females and males (Eritrea, Palestine, Cuba and Uzbekistan). Estimates of females and males for these countries were imputed from the population-weighted average female-to-male prisoner ratio in the relevant regions. We used data from the UN Population Division to obtain general population numbers aged 15–64 years, using country population data produced for 2023.

To estimate the potentially elevated rates of IDU and infectious diseases among incarcerated populations (people, females and males separately) compared to the general population, we used data on general population prevalence from the sources below: Injecting drug use prevalence (Degenhardt et al., 2023); prevalence of current HCV infection (RNA positive) (Grebely et al., 2018); UNAIDS data on HIV among the general population (van Schalkwyk et al., 2024); WHO data on active tuberculosis infection among the general population (World Health Organization, 2024b), and WHO data on current HBV infections (HBsAg detectable) among the general population (World Health Organization, 2024a).

Analysis of prevalence of IDU, blood-borne viruses, and tuberculosis

We used an approach consistent with the methods used in earlier reviews of people who inject drugs in the community (Degenhardt et al., 2017; Mathers et al., 2008; Nelson et al., 2011). Eligible data on the prevalence of injecting drug use, HIV antibody, HBsAg, HCV antibody, HCV RNA, and tuberculosis were extracted and, where multiple estimates were available, pooled for each country via random-effects meta-analyses in Stata (version 14 Stata Corporation, 2016, command: metaprop) (decision rules regarding selection of estimates are shown in the text box and Appendix 7). Metaprop allows meta-analyses of proportions for binomial data. The confidence intervals (CIs) were computed using an exact method (the Clopper-Pearson interval method) based on the binomial distribution (Clopper & Pearson, 1934; Puza & O’neill, 2006). In cases where CIs estimates fell outside the 0–100 % range, the double arcsine transformation method was used (command: ftt), because it is the preferred method for addressing the problem of variance instability in addition to the CI range problem. Current HCV infection was estimated using HCV RNA prevalence in countries where these data were available. If HCV RNA data were unavailable, HCV antibody prevalence data were used to estimate current HCV infection, assuming a 25 % clearance proportion as reported previously (Grebely et al., 2018). Tuberculosis infection was based on people whose sputum culture or GeneXpert was positive, or whose clinical presentation was consistent with TB and they responded to treatment.

Based on these extracted data, country-level prevalence estimates were calculated. The prevalence and estimated number of people with lifetime injecting drug use, and people living with HIV, HCV, tuberculosis and HBV were estimated by multiplying our prevalence or proportion estimates with the country, regional, and global population sizes of people who are incarcerated at country, regional and global levels.

Text box about here

Regional and global estimates

Regional and global estimates were produced using their respective country-level data. Countries where estimates for both females and males were not available had an imputed country-level prevalence estimate calculated using the methods stated in Appendix 8. Where data on females and males were located (which was often the case since most facilities are limited to females or males only), the overall country-level prevalence estimate was derived by aggregating relevant data for females and males. Following the collation of country-level estimates of incarceration and the prevalence of IDU and infectious diseases, regional and global estimates were derived. Region-specific, carceral population-weighted estimates were made using all the observed estimates and 95 % CIs of estimates in each country within that region, consistent with our previous reviews. Regional estimates were then used to estimate the global prevalence. Full details on methods of estimating regional and global numbers are in Appendix 8.

We estimated the prevalence and absolute numbers of incarcerated individuals with a history of injecting drug use, HIV, HCV, tuberculosis, and HBV by applying our prevalence rates to population sizes at the country, regional, and global levels.

Sensitivity analysis

A sensitivity analysis was undertaken to examine the potential effect of using only more recent data (and thereby providing some evidence about potential shifts over time in prevalence of injecting drug use and infectious disease among incarcerated people, if indeed data had been collected over an extended period within a country). In that analysis, only data from the most recent five years within a country for each indicator were included in the pooled estimates of regional and global prevalence of injecting drug use and infectious diseases. The results of that sensitivity analysis are presented in Appendix 10.

Risk of bias

We applied the Joanna Briggs Institute critical appraisal checklist for prevalence studies (Munn et al., 2020) to each included study. Each item was scored Yes (1), No (0), or Unclear (9) using the operational rules specified in Appendix 14 (Table 14.1). The results of this grading for each study included for each indicator are presented in Appendices 15-16.

Role of funding source

The funders had no role in the design, conduct, analysis or interpretation of findings.

Results

We screened 75,755 papers or reports published between 2000 and 2025, with 2,968 eligible for extraction (Fig. 1). The total number of eligible estimates extracted was 2468, including 362 for IDU, 708 for HIV, 671 for HCV antibody, 181 for HCV RNA, 335 for HBV, and 211 for tuberculosis prevalence. The number of estimates included in pooled analyses (after applying our decision rules) was 1,369: 267 for IDU, 401 for HIV, 359 for HCV, 169 for HBV and 173 for tuberculosis prevalence (Fig. 1). Fig. 1 displays further details on the record and estimate selection process. Appendix 11 provides details of every eligible study located in this review, including which pooled estimates each study contributed data to (Appendix 12 shows studies excluded at full text screening stage).

Fig. 1.

Fig. 1.

Flowchart.

Incarceration rates and population numbers

Overall, there are an estimated 11,322,000 people aged 15–64 years incarcerated globally (a rate of 221 per 100,000), with the weighted global incarceration rate being 29 per 100,000 among females and 404 per 100,000 among men (Fig. 2). Globally, the rate of incarceration varies considerably by region and between countries – with the highest rates for men and females in North America and the lowest rates in South Asia. At the country level, the highest number of people incarcerated was in the United States, which had the 21st highest rate of incarceration. The highest rates of incarceration were recorded in Turkmenistan, Tonga, American Samoa, Rwanda, Cuba and El Salvador (see Table 2 for incarceration rates by country).

Fig. 2.

Fig. 2.

Estimates of the rate and number of people who are incarcerated per 100,000 people aged 15-64 years.

Notes: Country level data that informed these regional and global estimates were sourced from the World Prison Brief, collated by the Institute for Crime and Justice Policy Research at Burbeck University. These contain the most recent available prison population estimates located by the WPB team. See: https://www.prisonstudies.org/world-prison-brief-data. Note that we used the country estimates to make rates for 15–64 years (not the total country population) so our rates differ from the World Prison Brief estimates.

Table 2.

Country estimates of the prevalence and number of people who are incarcerated who are living with HIV, have current HCV or HBV infection, have active tuberculosis and have injected drugs.

People who are incarcerated
People with lifetime injecting drug use
People living with HIV
People with current HCV
People with current HBV
People with active Tuberculosis
Country Estimated
number1
Rate per
100,000
% (CI) Estimated no. (CI) % (CI) Estimated no. (CI) % (CI) Estimated no. (CI) % (CI) Estimated no. (CI) % (CI) Estimated no. (CI)
Eastern Europe
Armenia 2469 132 ·· ·· 1·3 (0·5, 2·5) < 500 (<500,<500) 17·6 (14·5, 20·9) 500 (500,500) 3·6 (2·2, 5·4) < 500 (<500,<500) ·· ··
Azerbaijan 24698 345 32·0 (28·0, 36·1) 8000 (7000,9000) 3·6 (2·5, 5·1) 1000 (500,1500) 33·2 (22·7, 44·7) 8000 (5500,11000) 4·7 (3·2, 6·7) 1000 (1000,1500) ·· ··
Belarus 32556 498 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Bosnia & Herzegovina 2212 24 17·3 (14·5, 20·4) 500 (500,500) 0·0 (0·0, 0·3) < 500 (<500,<500) 9·8 (6·1, 14·3) < 500 (<500,500) 1·5 (0·7, 2·7) < 500 (<500,<500) ·· ··
Bulgaria 6378 146 28·5 (24·6, 32·6) 2000 (1500,2000) 0·7 (0·2, 1·4) < 500 (<500,<500) 21·4 (18·4, 24·6) 1500 (1000,1500) ·· ·· 0·3 (0·0, 1·0) < 500 (<500,<500)
Czechia 19649 294 ·· ·· ·· ·· ·· ·· 4·1 (1·7, 7·5) 1000 (500,1500) ·· ··
Estonia 1688 201 ·· ·· 15·6 (14·1, 17·1) 500 (<500,500) ·· ·· ·· ·· ·· ··
Georgia 10457 432 ·· ·· ·· ·· 20·9 (20·2, 21·5) 2000 (2000,2500) ·· ·· 6·0 (5·5, 6·5) 500 (500,500)
Hungary 18270 289 13·5 (11·8, 15·2) 2500 (2000,3000) 0·0 (0·0, 0·0) < 500 (<500,<500) 3·9 (2·9, 4·9) 500 (500,1000) 1·1 (0·6, 1·9) < 500 (<500,500) ·· ··
Latvia 3271 278 32·3 (29·1, 35·5) 1000 (1000,1000) ·· ·· ·· ·· ·· ·· ·· ··
Lithuania 4551 254 12·0 (3·5, 24·4) 500 (<500,1000) ·· ·· ·· ·· ·· ·· ·· ··
Republic of Moldova 5695 279 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Poland 70316 279 ·· ·· ·· ·· ·· ·· ·· ·· 1·6 (0·8, 2·8) 1000 (500,2000)
Romania 24534 195 ·· ·· 56·7 (46·7, 66·4) 14000 (11500,16500) 20·9 (3·5, 47·3) 5000 (1000,11500) 10·6 (6·0, 16·3) 2500 (1500,4000) 0·1 (0·0, 0·2) < 500 (<500,<500)
Russian Federation 433006 447 ·· ·· ·· ·· ·· ·· ·· ·· 5·4 (4·6, 6·4) 23500 (20000,27500)
Slovakia 8585 236 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Ukraine 44024 150 43·7 (38·9, 48·5) 19000 (17000,21500) 12·6 (10·8, 14·5) 5500 (4500,6500) 73·8 (50·5, 99·8) 32500 (22000,44000) 5·2 (3·2, 7·6) 2500 (1500,3500) ·· ··
Western Europe
Albania 4653 242 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Andorra 51 89 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Austria 9288 157 4·3 (0·5, 10·5) 500 (<500,1000) 0·0 (0·0, 2·6) < 500 (<500,<500) 1·5 (0·0, 6·4) < 500 (<500,500) ·· ·· ·· ··
Belgium 12575 169 20·4 (17·3, 23·6) 2500 (2000,3000) 1·1 (0·1, 3·3) < 500 (<500,500) 7·6 (3·7, 12·7) 1000 (500,1500) 0·8 (0·3, 1·5) < 500 (<500,<500) ·· ··
Croatia 4445 171 24·6 (22·9, 26·3) 1000 (1000,1000) 0·1 (0·0, 0·3) < 500 (<500,<500) 10·4 (9·3, 11·6) 500 (500,500) 1·1 (0·8, 1·6) < 500 (<500,<500) ·· ··
Denmark 4083 110 43·3 (37·9, 48·7) 2000 (1500,2000) 0·0 (0·0, 0·6) < 500 (<500,<500) 28·9 (24·1, 34·0) 1000 (1000,1500) 4·9 (2·7, 7·7) < 500 (<500,500) ·· ··
England and Wales 85867 223 23·7 (21·5, 26·1) 20500 (18500,22500) 0·2 (0·1, 0·4) < 500 (<500,500) 6·3 (3·5, 10·0) 5500 (3000,8500) 0·9 (0·0, 2·7) 500 (<500,2500) ·· ··
Finland 2912 85 54·5 (50·5, 58·5) 1500 (1500,1500) 0·9 (0·2, 1·9) < 500 (<500,<500) 32·3 (28·3, 36·4) 1000 (1000,1000) 0·3 (0·0, 1·5) < 500 (<500,<500) ·· ··
France 79631 201 19·0 (5·7, 37·3) 15000 (4500,29500) 2·7 (0·8, 5·6) 2000 (500,4500) 3·5 (1·2, 6·7) 3000 (1000,5500) 1·2 (0·1, 3·4) 1000 (<500,2500) ·· ··
Germany 57955 109 29·3 (21·5, 37·9) 17000 (12500,22000) 2·7 (0·7, 5·7) 1500 (500,3500) 5·5 (4·3, 6·9) 3000 (2500,4000) ·· ·· ·· ··
Greece 10242 155 37·1 (30·9, 43·6) 4000 (3000,4500) 0·0 (0·0, 2·3) < 500 (<500,<500) 11·2 (8·7, 14·0) 1000 (1000,1500) ·· ·· 13·3 (8·8, 18·4) 1500 (1000,2000)
Greenland 154 393 NK NK ·· ·· ·· ·· ·· ·· ·· ··
Iceland 140 57 ·· ·· ·· ·· 3·1 (0·1, 9·2) < 500 (<500,<500) ·· ·· ·· ··
Ireland 5074 156 30·4 (24·9, 36·1) 1500 (1500,2000) 1·2 (0·5, 2·1) < 500 (<500,<500) 10·8 (7·0, 15·4) 500 (500,1000) 0·3 (0·0, 0·8) < 500 (<500,<500) ·· ··
Italy 62110 166 27·7 (19·2, 38·0) 17000 (12000,23500) 3·1 (1·8, 4·9) 2000 (1000,3000) 11·1 (6·9, 16·2) 7000 (4500,10000) 3·0 (1·3, 5·3) 2000 (1000,3500) ·· ··
Liechtenstein 14 54 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Luxembourg 600 135 22·8 (17·1, 29·0) < 500 (<500,<500) ·· ·· ·· ·· ·· ·· ·· ··
Malta 671 187 ·· ·· 1·3 (0·4, 2·6) < 500 (<500,<500) 18·3 (15·0, 21·9) < 500 (<500,<500) ·· ·· 0·8 (0·1, 2·1) < 500 (<500,<500)
Monaco 31 165 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Montenegro 1046 254 16·4 (13·3, 19·8) < 500 (<500,<500) 0·0 (0·0, 0·7) < 500 (<500,<500) 16·0 (12·9, 19·3) < 500 (<500,<500) 1·5 (0·6, 2·9) < 500 (<500,<500) ·· ··
Netherlands 11537 102 8·6 (5·8, 12·0) 1000 (500,1500) 0·4 (0·0, 1·6) < 500 (<500,<500) 4·9 (2·4, 8·2) 500 (500,1000) 1·5 (0·2, 3·7) < 500 (<500,500) ·· ··
North Macedonia 2555 176 ·· ·· 0·0 (0·0, 0·9) < 500 (<500,<500) 15·0 (10·4, 20·3) 500 (500,500) ·· ·· ·· ··
Northern Ireland 1911 159 12·7 (8·9, 17·3) < 500 (<500,500) 0·0 (0·0, 0·3) < 500 (<500,<500) 0·8 (0·2, 1·6) < 500 (<500,<500) ·· ·· ·· ··
Norway 3052 87 51·6 (39·1, 64·0) 1500 (1000,2000) ·· ·· 24·2 (14·2, 35·7) 500 (500,1000) ·· ·· ·· ··
Portugal 12379 188 14·7 (12·2, 17·5) 2000 (1500,2000) 6·1 (4·5, 8·0) 1000 (500,1000) 9·6 (7·7, 11·9) 1000 (1000,1500) 2·7 (1·9, 4·0) 500 (<500,500) ·· ··
San Marino 1 4 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Scotland 8253 235 19·9 (13·1, 27·6) 1500 (1000,2500) 0·7 (0·0, 2·2) < 500 (<500,<500) 3·4 (2·5, 4·3) 500 (<500,500) ·· ·· ·· ··
Serbia 10787 227 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Slovenia 1798 133 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Spain 56698 181 25·4 (19·4, 32·0) 14500 (11000,18000) 5·4 (2·4, 9·5) 3000 (1500,5500) 12·0 (7·6, 18·3) 7000 (4500,10500) 2·0 (0·6, 4·2) 1000 (500,2500) 1·3 (0·1, 5·2) 1000 (<500,3000)
Sweden 10175 156 25·1 (17·5, 33·7) 2500 (2000,3500) 0·4 (0·0, 1·6) < 500 (<500,<500) 11·3 (8·0, 15·1) 1000 (1000,1500) 1·9 (0·8, 3·8) < 500 (<500,500) ·· ··
Switzerland 6881 120 4·5 (2·9, 6·5) 500 (<500,500) 2·2 (1·4, 3·1) < 500 (<500,<500) 3·7 (2·7, 4·8) 500 (<500,500) 2·0 (1·2, 2·9) < 500 (<500,<500) 1·7 (1·3, 2·2) < 500 (<500,<500)
East and South East Asia
Brunei Darussalam 636 199 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Cambodia 45122 417 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
China 1690000 13 ·· ·· ·· ·· ·· ·· ·· ·· 1·5 (0·9, 2·3) 26000 (15500,39000)
Hong Kong† 9079 178 ·· ·· ·· ·· ·· ·· ·· ·· 5·4 (4·0, 7·0) 500 (500,500)
Indonesia 274060 148 5·2 (4·2, 6·2) 14000 (11500,17000) 1·1 (0·3, 2·2) 3000 (1000,6000) 22·4 (6·3, 46·6) 61500 (17500,128000) 5·0 (2·8, 7·7) 13500 (8000,21000) 0·0 (0·0, 0·5) < 500 (<500,1500)
Japan 40881 56 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Lao People's Democratic Republic 11885 262 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Malaysia 87419 373 ·· ·· ·· ·· 16·2 (15·6, 16·7) 14000 (13500,14500) ·· ·· ·· ··
Mongolia 5700 270 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Myanmar 100324 274 ·· ·· 5·5 (4·9, 6·2) 5500 (5000,6000) ·· ·· ·· ·· ·· ··
Democratic People's Republic of Korea* 100000 552 NK NK ·· ·· ·· ·· ·· ·· ·· ··
Philippines 171247 235 ·· ·· 0·0 (0·0, 0·6) < 500 (<500,1000) ·· ·· 7·4 (5·2, 9·9) 12500 (9000,17000) ·· ··
Singapore 9536 217 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Republic of Korea 52940 143 ·· ·· 0·2 (0·1, 0·2) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Taiwan† 58889 346 42·3 (41·2, 43·3) 25000 (24500,25500) 0·0 (0·0, 2·4) < 500 (<500,1500) 20·3 (18·5, 22·1) 12000 (11000,13000) ·· ·· 0·2 (0·2, 0·2) < 500 (<500,<500)
Thailand 274277 550 6·8 (5·3, 8·4) 18500 (14500,23000) 4·0 (2·7, 5·5) 11000 (7500,15000) 3·7 (2·7, 4·9) 10000 (7500,13500) 6·5 (5·1, 8·2) 18000 (14000,22500) 1·7 (0·8, 2·9) 4500 (2000,8000)
Timor-Leste 763 97 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Viet Nam 133986 200 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
South Asia
Afghanistan 19000 87 1·9 (1·0, 3·2) 500 (<500,500) 0·8 (0·4, 1·4) < 500 (<500,500) 2·2 (1·2, 3·5) 500 (<500,500) ·· ·· ·· ··
Bangladesh 53831 47 ·· ·· ·· ·· ·· ·· ·· ·· 1·0 (0·9, 1·1) 500 (500,500)
Bhutan 1119 227 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
India 573220 60 3·0 (2·1, 4·1) 17500 (12000,23500) 0·9 (0·6, 1·3) 5000 (3000,7500) 8·9 (8·4, 9·6) 51000 (48000,55000) 7·9 (0·6, 22·0) 45500 (3500,126000) 3·5 (3·0, 4·0) 20000 (17500,23000)
Iran (Islamic Republic of) 189000 314 15·5 (13·2, 18·1) 29500 (25000,34000) 2·0 (1·2, 3·0) 4000 (2000,5500) 8·4 (4·3, 13·9) 16000 (8000,26500) 3·4 (2·6, 4·4) 6500 (5000,8500) 0·1 (0·1, 0·2) 500 (<500,500)
Maldives 1700 448 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Nepal 27550 142 10·8 (8·7, 13·1) 3000 (2500,3500) ·· ·· ·· ·· ·· ·· 1·8 (0·7, 3·2) 500 (<500,1000)
Pakistan 108643 80 19·5 (5·7, 38·7) 21000 (6000,42000) 1·9 (0·8, 3·5) 2000 (1000,4000) 8·3 (5·1, 12·1) 9000 (5500,13000) 2·7 (2·2, 3·4) 3000 (2500,3500) 0·5 (0·3, 0·7) 500 (500,1000)
Sri Lanka 29686 208 4·2 (2·4, 6·6) 1500 (500,2000) ·· ·· 0·6 (0·0, 1·9) < 500 (<500,500) 0·3 (0·0, 1·4) < 500 (<500,500) ·· ··
Central Asia
Kazakhstan 35228 294 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Kyrgyzstan 7728 194 48·2 (26·4, 70·3) 3500 (2000,5500) 8·4 (5·8, 11·5) 500 (500,1000) 31·8 (27·1, 36·6) 2500 (2000,3000) 6·3 (3·7, 9·5) 500 (500,500) ·· ··
Tajikistan 14000 238 4·1 (3·1, 5·2) 500 (500,500) 0·3 (0·2, 0·5) < 500 (<500,<500) ·· ·· ·· ·· 4·4 (3·4, 5·5) 500 (500,1000)
Turkmalesistan 35000 864 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Uzbekistan 29000 131 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Caribbean
Antigua & Barbuda 400 604 NK NK 2·9 (0·4, 7·1) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Bahamas 1912 653 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Barbados 692 367 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Bermuda 124 295 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Cuba 90000 1161 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Dominica 260 507 NK NK 2·6 (0·7, 5·4) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Dominican Republic 25987 357 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Grenada 385 468 NK NK 2·2 (0·3, 5·4) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Haiti 7523 104 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Jamaica 3559 174 ·· ·· 3·4 (2·3, 4·7) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Commonwealth of Puerto Rico 5798 278 31·6 (29·0, 34·3) 2000 (1500,2000) ·· ·· ·· ·· ·· ·· ·· ··
Saint Kitts & Nevis 160 476 NK NK 2·3 (0·5, 5·1) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Saint Lucia 572 438 NK NK 2·0 (0·7, 3·7) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Saint Vincent & the Grenadines 404 577 NK NK 4·0 (2·2, 6·3) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Trinidad & Tobago 3802 358 NK NK ·· ·· ·· ·· ·· ·· ·· ··
Latin America
Argentina 125041 426 ·· ·· 2·2 (1·4, 3·5) 2500 (1500,4500) 2·1 (1·3, 3·1) 2500 (1500,4000) 0·5 (0·3, 0·8) 500 (500,1000) ·· ··
Belize 1339 501 NK NK 4·1 (2·7, 5·8) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Bolivia (Plurinational State of) 31105 403 ·· ·· 0·2 (0·0, 0·6) < 500 (<500,<500) ·· ·· 0·5 (0·0, 1·6) < 500 (<500,500) ·· ··
Brazil 888791 593 7·0 (2·9, 12·6) 62000 (26000,112000) 3·2 (1·8, 5·1) 28500 (15500,45000) 4·9 (2·2, 8·6) 43500 (19500,76500) 1·1 (0·3, 2·6) 9500 (2500,23000) 3·8 (2·4, 5·8) 34000 (21000,51500)
Chile 59037 440 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Colombia 104346 291 0·7 (0·1, 1·7) 500 (<500,2000) 1·2 (0·3, 2·4) 1000 (500,2500) ·· ·· 0·4 (0·0, 1·3) 500 (<500,1500) 0·8 (0·5, 1·1) 1000 (500,1000)
Costa Rica 17829 502 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Ecuador 33669 286 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
El Salvador 109519 2625 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Guatemala 23361 213 4·9 (3·3, 6·8) 1000 (1000,1500) 0·8 (0·2, 1·7) < 500 (<500,500) ·· ·· ·· ·· ·· ··
Guyana 2300 439 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Honduras 19481 291 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Mexico 234514 277 6·5 (5·5, 7·5) 15000 (13000,17500) 0·6 (0·5, 0·8) 1500 (1000,2000) 2·3 (2·0, 2·7) 5500 (4500,6500) 0·1 (0·0, 0·2) < 500 (<500,500) ·· ··
Nicaragua 20918 496 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Panama 23798 841 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Paraguay 17712 408 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Peru 97605 443 ·· ·· 1·2 (0·5, 2·3) 1000 (500,2000) ·· ·· ·· ·· 24·1 (12·2, 39·9) 23500 (12000,39000)
Suriname 1000 270 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Uruguay 15767 707 ·· ·· 6·8 (4·1, 10·1) 1000 (500,1500) ·· ·· ·· ·· ·· ··
Venezuela (Bolivarian Republic of) 67200 375 5·2 (2·4, 8·8) 3500 (1500,6000) 0·6 (0·4, 0·8) 500 (500,500) 1·4 (0·2, 3·8) 1000 (<500,2500) 0·0 (0·0, 4·1) < 500 (<500,2500) ·· ··
North America
Canada 34986 139 29·7 (26·8, 32·7) 10500 (9500,11500) 1·7 (1·2, 2·3) 500 (500,1000) 13·6 (11·1, 16·4) 4500 (4000,5500) 0·0 (0·0, 2·5) < 500 (<500,1000) ·· ··
United States of America 1808100 522 13·1 (10·0, 16·4) 236000 (181000,297500) 1·6 (1·3, 2·0) 29500 (24000,35500) 15·1 (13·1, 17·2) 272500 (237000,310500) 2·9 (0·3, 9·2) 53000 (4500,166500) 0·0 (0·0, 0·0) 500 (500,500)
Pacific Island States & Terr·
American Samoa 301 1018 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Micronesia (Federated States of) 132 40 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Fiji 2276 377 ·· ·· 1·0 (0·0, 3·1) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
French Polynesia 575 275 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Guam 896 844 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Kiribati 129 179 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Marshall Islands 35 117 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Nauru 38 516 NK NK ·· ·· ·· ·· ·· ·· ·· ··
New Caledonia 609 317 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Northern Mariana Islands 170 501 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Palau 66 527 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Papua New Guinea 5373 87 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Samoa 358 296 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Solomon Islands 500 131 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Tonga 557 888 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Tuvalu 11 161 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Vanuatu 195 108 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Australasia
Australia‡§ 44051 261 51·0 (47·0, 54·9) 22500 (20500,24000) 0·8 (0·4, 1·7) 500 (<500,500) 8·0 (6·4, 9·9) 3500 (3000,4500) 0·5 (0·3, 1·1) < 500 (<500,500) ·· ··
New Zealand 9924 297 ·· ·· 0·0 (0·0, 0·1) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Sub Saharan Africa
Angola 24068 134 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Benin 19563 277 0·6 (0·1, 1·5) < 500 (<500,500) 1·4 (0·5, 2·7) 500 (<500,500) ·· ·· ·· ·· ·· ··
Botswana 3971 242 ·· ·· ·· ·· ·· ·· ·· ·· 2·0 (1·4, 2·7) < 500 (<500,<500)
Burkina Faso 8800 75 3·3 (2·4, 4·4) 500 (<500,500) 2·3 (1·6, 3·2) < 500 (<500,500) 5·7 (4·7, 6·8) 500 (500,500) 28·0 (22·9, 33·7) 2500 (2000,3000) 1·3 (0·3, 3·0) < 500 (<500,500)
Burundi 13824 215 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Cameroon 34419 231 2·8 (1·8, 3·9) 1000 (500,1500) 11·3 (9·5, 13·2) 4000 (3500,4500) ·· ·· 12·9 (10·8, 15·1) 4500 (3500,5000) 2·3 (0·6, 5·0) 1000 (<500,1500)
Cabo Verde 2700 676 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Central African Republic 2678 100 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Chad 9589 111 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Comoros 422 89 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Côte d'Ivoire 27149 177 ·· ·· 4·7 (4·0, 5·4) 1500 (1000,1500) ·· ·· ·· ·· 5·6 (4·4, 7·1) 1500 (1000,2000)
Democratic Republic of the Congo 44536 92 ·· ·· 6·1 (4·9, 7·4) 2500 (2000,3500) ·· ·· ·· ·· 22·7 (7·8, 42·5) 10000 (3500,19000)
Djibouti 750 105 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Equatorial Guinea 500 64 NK NK ·· ·· ·· ·· ·· ·· ·· ··
Eritrea** ·· ·· NK NK ·· ·· ·· ·· ·· ·· ·· ··
Eswatini 3405 468 ·· ·· 33·4 (28·9, 38·1) 1000 (1000,1500) ·· ·· ·· ·· ·· ··
Ethiopia 110000 166 5·6 (3·9, 7·6) 6000 (4500,8500) 3·1 (2·6, 3·5) 3500 (3000,4000) 1·8 (0·1, 5·0) 2000 (<500,5500) 7·3 (5·6, 9·1) 8000 (6000,10000) 2·3 (1·2, 3·9) 2500 (1500,4500)
Gabon 5501 394 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Gambia 543 38 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Ghana 14262 73 17·1 (16·2, 18·0) 2500 (2500,2500) 7·3 (5·0, 10·2) 1000 (500,1500) 14·4 (12·2, 16·9) 2000 (1500,2500) 16·9 (11·8, 22·7) 2500 (1500,3000) 0·5 (0·0, 1·7) < 500 (<500,<500)
Guinea 5549 75 2·5 (1·6, 3·5) < 500 (<500,<500)
Guinea-Bissau 596 58 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Kenya 60000 193 ·· ·· 9·6 (7·8, 11·6) 6000 (4500,7000) ·· ·· ·· ·· 10·2 (5·9, 15·5) 6000 (3500,9500)
Lesotho 2216 162 3·3 (0·7, 7·3) < 500 (<500,<500) ·· ·· ·· ·· ·· ·· ·· ··
Liberia 3000 104 33·0 (24·1, 42·6) 1000 (500,1500) 5·6 (3·9, 7·6) < 500 (<500,<500) 0·8 (0·2, 1·8) < 500 (<500,<500) 13·3 (6·3, 22·2) 500 (<500,500) ·· ··
Madagascar 30530 184 ·· ·· 0·2 (0·0, 0·7) < 500 (<500,<500) ·· ·· ·· ·· 11·4 (2·6, 24·5) 3500 (1000,7500)
Malawi 16536 154 ·· ·· 26·2 (17·6, 36·2) 4500 (3000,6000) 0·0 (0·0, 1·3) < 500 (<500,<500) 3·5 (1·0, 7·3) 500 (<500,1000) 1·0 (0·6, 1·6) < 500 (<500,500)
Mali 8670 79 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Mauritania 2826 112 NK NK ·· ·· ·· ·· ·· ·· ·· ··
Mauritius 2755 298 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Mozambique 22000 128 ·· ·· 12·0 (11·2, 12·9) 2500 (2500,3000) ·· ·· ·· ·· 3·3 (3·0, 3·7) 500 (500,1000)
Namibia 8900 589 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Niger 13005 106 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Nigeria 84011 73 0·0 (0·0, 0·6) < 500 (<500,500) 6·5 (3·1, 10·9) 5500 (2500,9000) 13·0 (9·7, 16·8) 11000 (8000,14000) 18·1 (15·1, 21·4) 15000 (12500,18000) 1·8 (0·2, 4·5) 1500 (<500,3500)
Congo 1388 45 2·1 (0·0, 6·2) < 500 (<500,<500) 8·3 (3·5, 14·8) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Rwanda 87621 1123 ·· ·· ·· ·· 5·5 (5·3, 5·7) 5000 (4500,5000) 4·3 (4·1, 4·5) 4000 (3500,4000) ·· ··
Sao Tome & Principe 300 239 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Senegal 13185 142 ·· ·· 1·8 (0·9, 2·9) < 500 (<500,500) 0·6 (0·0, 1·8) < 500 (<500,<500) 13·9 (10·4, 17·9) 2000 (1500,2500) ·· ··
Seychelles 474 646 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Sierra Leone 4453 92 ·· ·· 2·3 (1·0, 4·1) < 500 (<500,<500) ·· ·· ·· ·· ·· ··
Somalia 2799 33 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
South Africa 157056 405 1·4 (0·7, 2·2) 2000 (1000,3500) 16·3 (6·7, 30·1) 25500 (10500,47000) 3·2 (1·9, 4·7) 5000 (3000,7500) 3·2 (1·9, 4·8) 5000 (3000,7500) 0·6 (0·5, 0·8) 1000 (1000,1000)
United Republic of Tanzania 32671 96 ·· ·· 8·0 (5·6, 11·0) 2500 (2000,3500) 4·8 (2·9, 7·1) 1500 (1000,2500) 7·0 (4·7, 9·7) 2500 (1500,3000) 3·4 (1·4, 6·6) 1000 (500,2000)
Togo 4990 102 1·0 (0·5, 1·6) < 500 (<500,<500) 5·8 (3·9, 8·0) 500 (<500,500) 0·3 (0·0, 1·2) < 500 (<500,<500) 10·8 (7·8, 14·3) 500 (500,500) ·· ··
Uganda 78539 322 ·· ·· 10·9 (8·2, 13·9) 8500 (6500,11000) 0·8 (0·2, 1·6) 500 (<500,1500) ·· ·· 0·9 (0·3, 1·8) 500 (<500,1500)
Zambia 28225 264 ·· ·· 23·5 (21·7, 25·5) 6500 (6000,7000) 21·7 (18·2, 25·3) 6000 (5000,7000) ·· ·· 1·8 (1·3, 2·4) 500 (500,500)
Zimbabwe 20997 236 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Middle East & North Africa
Algeria 94749 340 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Bahrain 3485 310 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Cyprus 966 112 7·8 (3·9, 12·9) < 500 (<500,<500) ·· ·· ·· ·· ·· ·· ·· ··
Egypt 120000 177 ·· ·· 0·0 (0·0, 0·3) < 500 (<500,500) 12·2 (9·5, 15·2) 14500 (11500,18500) ·· ·· ·· ··
Iraq 73715 290 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Israel 19756 371 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Jordan 19140 270 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Kuwait 5300 168 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Lebanon 9254 264 12·3 (10·3, 14·6) 1000 (1000,1500) 0·2 (0·0, 0·7) < 500 (<500,<500) 1·9 (0·6, 3·8) < 500 (<500,500) 2·3 (0·8, 4·6) < 500 (<500,500) ·· ··
Libya 19103 428 ·· ·· 17·5 (16·6, 18·5) 3500 (3000,3500) 17·9 (17·3, 18·6) 3500 (3500,3500) 6·8 (6·2, 7·5) 1500 (1000,1500) ·· ··
Morocco 102653 421 ·· ·· 18·0 (3·8, 40·6) 18500 (4000,41500) ·· ·· ·· ·· ·· ··
Oman 1960 62 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Occupied Palestinian territories ·· ·· ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Qatar 2055 92 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Saudi Arabia 68056 280 ·· ·· 0·2 (0·1, 0·3) < 500 (<500,<500) 0·3 (0·0, 0·8) < 500 (<500,500) ·· ·· ·· ··
South Sudan 8400 149 NK NK ·· ·· ·· ·· ·· ·· ·· ··
Sudan 21000 93 ·· ·· 2·0 (0·4, 4·5) 500 (<500,1000) ·· ·· ·· ·· ·· ··
Syrian Arab Republic 10599 102 ·· ·· 0·0 (0·0, 0·4) < 500 (<500,<500) 1·3 (0·4, 2·6) < 500 (<500,500) 2·5 (1·2, 4·3) 500 (<500,500) ·· ··
Tunisia 23484 289 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Türkiye 371587 643 16·1 (14·3, 17·9) 59500 (53000,66500) 0·6 (0·1, 1·5) 2000 (500,5500) 3·8 (2·7, 5·4) 14000 (10000,20000) 3·3 (1·8, 5·2) 12500 (6500,19500) 0·1 (0·0, 0·2) 500 (<500,1000)
United Arab Emirates 9826 131 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··
Yemen 4268 23 ·· ·· ·· ·· ·· ·· ·· ·· ·· ··

Notes: References for studies included in pooled estimates are reported in Appendix 9. Study level data informing each pooled estimate are listed in Appendices 15.1-15.5. Data reporting on risk of bias for each study used in the pooled estimates are reported in Appendices 16.1-16.5. This table reports country-level estimates among total people incarcerated, country-level tables on females, males and combined (mixed estimates only) samples are reported in Appendices Table 9.3-9.8.

Lifetime injecting drug use among people in carceral settings

Data on the prevalence of lifetime IDU among people in carceral settings were available in 62 countries and territories, covering 54·4 % of the world’s incarcerated population. Globally, we estimate that 1,348,000 (95 %CI 1,061,500-1,687,000) people who are incarcerated aged 15–64 years have ever injected drugs, amounting to 11·9 % (95 % CI 9·4–14·9) of all people incarcerated, translating to a prevalence that is approximately 51 times higher than in the general community (Table 1). Regionally, the lifetime prevalence of IDU in incarcerated populations varied substantially, from 3·0 % (95 %CI 2·1–4·2) in Sub-Saharan Africa to 51·0 % (95 %CI 47·0–54·9) in Australasia (country-level prevalence varied even more; these estimates are presented in Appendix 9). The ratio of IDU prevalence among people in carceral settings compared to the general population varied from approximately 10-fold higher in North America to over 190-fold higher in Western Europe (Table 1; country-level estimates are provided in Table 2 and shown in Fig. 3; Appendix 9 reports country-level data and sources in detail, and Appendix 15-16 report study level characteristics and risk of bias for each study included in country estimates for each indicator). The proportion of incarcerated females with a history of IDU also varied substantially (Table 1), with Australasia having the highest prevalence: 68·5 % (95 %CI 63·1–73·8), and lowest levels in the Middle East & North Africa (1·7 % [95 %CI 1·5–1·9]) and Sub-Saharan Africa (0·3 % [95 %CI 0·2–0·4]). The regional variation in lifetime IDU prevalence was similar for incarcerated males, with Australasia (49·5 % [95 %CI 45·6–53·3]) being considerably higher than the next highest region of Eastern Europe (33·4 % [95 %CI 29·2–37·8]); both Latin America (6·1 % [95 % CI 3·1–10·3]) and Sub-Saharan Africa (3·1 % [95 %CI 2·2–4·3]) had relatively low prevalence (Table 1).

Table 1.

Regional and global estimates of the prevalence and number of people who are incarcerated who are living with HIV, have current HCV or HBV infection, have active tuberculosis and have injected drugs.

Lifetime injecting drug use (IDU)
Incarc. per
100K people1
No.
estimates
% (CI) among
people
Estimated no. people who are
incarcerated who have injected
drugs (CI)
Ratio of IDU %
among
incarcerated
people relative
to gen. pop IDU
%
% (CI) among
females
Estimated no. females who are
incarcerated who have injected
drugs (CI)
% (CI) among
males
Estimated no. males who are
incarcerated who have injected
drugs (CI)
Eastern Europe 338 13 32·3 (28·2, 36·6) 230,000 (201,000, 260,500) 63·0 19·3 (16·9, 21·9) 10,500 (9,500, 12,000) 33·4 (29·2, 37·8) 219,500 (191,500, 248,500)
Western Europe 165 80 23·8 (17·0, 32·1) 111,500 (79,500, 150,000) 192·8 26·3 (19·5, 34·3) 6,000 (4,500, 8,000) 23·7 (16·9, 32·0) 105,500 (75,000, 142,000)
East and southeast Asia 192 10 9·5 (8·3, 10·8) 291,500 (255,000, 331,500) 54·5 8·6 (7·5, 9·7) 23,500 (20,500, 26,500) 9·6 (8·4, 10·9) 268,500 (234,500, 305,000)
South Asia 76 38 7·6 (4·9, 11·2) 77,000 (49,000, 112,500) 44·2 1·8 (1·1, 2·6) 500 (500, 1,000) 7·9 (5·0, 11·5) 76,000 (48,500, 111,500)
Central Asia 252 3 19·8 (11·4, 28·4) 24,000 (14,000, 34,500) 31·0 2·1 (1·2, 3·0) <500 (<500, <500) 20·9 (12·0, 29·9) 24,000 (13,500, 34,000)
Caribbean 499 1 12·7 (10·2, 15·7) 18,000 (14,500, 22,000) ·· 10·1 (8·0, 12·6) 500 (500, 500) 12·8 (10·2, 15·8) 17,500 (14,000, 21,500)
Latin America 459 28 6·2 (3·1, 10·5) 118,500 (59,000, 199,500) 44·8 8·7 (4·1, 15·0) 10,000 (4,500, 17,000) 6·1 (3·1, 10·3) 108,500 (54,500, 183,000)
North America 754 49 13·4 (10·3, 16·8) 246,500 (190,500, 308,500) 9·6 20·6 (15·9, 25·8) 33,500 (25,500, 41,500) 12·7 (9·8, 15·9) 213,500 (165,000, 267,000)
Pacific Islands & territories 146 0 ·· ·· ·· ·· ·· ·· ··
Australasia 267 23 51·0 (47·0, 54·9) 27,500 (25,500, 29,500) 84·9 68·5 (63·1, 73·8) 3,000 (2,500, 3,000) 49·5 (45·6, 53·3) 24,500 (22,500, 26,500)
Sub-Saharan Africa 165 16 3·0 (2·1, 4·2) 31,000 (22,000, 43,000) 39·6 0·3 (0·2, 0·4) <500 (<500, <500) 3·1 (2·2, 4·3) 30,500 (22,000, 42,500)
Middle East and North Africa 292 6 15·9 (14·2, 17·8) 158,000 (140,000, 176,500) 77·7 1·7 (1·5, 1·9) 500 (500, 500) 16·5 (14·6, 18·4) 157,000 (139,500, 176,000)
Global 221 267 11·9 (9·4, 14·9) 1,348,000 (1,061,500, 1,687,000) 51·4 10·5 (8·3, 13·1) 78,500 (62,000, 98,500) 12·0 (9·5, 15·0) 1,269,000 (999,500, 1,589,000)
HIV
Incarc. per
100K people1
No.
estimates
% (CI) among
people
Estimated no. people who are
incarcerated living with HIV (CI)
Ratio of HIV %
among
incarcerated
people relative
to
gen. pop HIV %
% (CI) among
females
Estimated no. females who are
incarcerated living with HIV (CI)
% (CI) among
males
Estimated no. males who are
incarcerated living with HIV (CI)
Eastern Europe 338 18 16·6 (13·7, 19·6) 118,500 (98,000, 140,000) 249·2 30·2 (24·9, 35·7) 17,000 (14,000, 20,000) 15·5 (12·8, 18·3) 102,000 (84,000, 120,000)
Western Europe 165 85 2·3 (0·9, 4·3) 10,500 (4,500, 20,500) 15·8 5·7 (2·3, 11·2) 1,500 (500, 2,500) 2·1 (0·9, 4·0) 9,500 (4,000, 17,500)
East and southeast Asia 192 14 2·1 (1·4, 3·2) 64,000 (43,500, 98,000) 3·1 6·5 (4·3, 10·4) 17,500 (12,000, 28,500) 1·7 (1·1, 2·5) 46,000 (31,500, 70,000)
South Asia 76 31 1·2 (0·7, 1·9) 12,500 (7,000, 19,500) 8·4 0·2 (0·1, 0·4) <500 (<500, <500) 1·3 (0·7, 2·0) 12,500 (7,000, 19,000)
Central Asia 252 2 3·2 (2·2, 4·4) 4,000 (2,500, 5,500) 11·0 0·3 (0·2, 0·5) <500 (<500, <500) 3·4 (2·3, 4·6) 4,000 (2,500, 5,500)
Caribbean 499 7 3·1 (1·7, 5·0) 4,500 (2,500, 7,000) 2·6 0·3 (0·2, 0·5) <500 (<500, <500) 3·2 (1·8, 5·1) 4,500 (2,500, 7,000)
Latin America 459 59 2·3 (1·3, 3·7) 44,000 (24,500, 70,000) 4·4 3·5 (1·9, 5·6) 4,000 (2,000, 6,500) 2·2 (1·2, 3·6) 40,000 (22,000, 63,500)
North America 754 88 1·6 (1·3, 2·0) 30,000 (24,500, 36,500) 4·4 2·6 (2·1, 3·1) 4,000 (3,500, 5,000) 1·5 (1·3, 1·9) 26,000 (21,000, 31,500)
Pacific Islands & territories 146 1 3·2 (2·0, 5·0) 500 (<500, 500) 3·5 6·1 (4·1, 9·0) <500 (<500, <500) 3·1 (1·9, 4·8) 500 (<500, 500)
Australasia 267 2 0·7 (0·3, 1·4) 500 (<500, 1,000) 6·6 0·6 (0·1, 3·8) <500 (<500, <500) 0·7 (0·3, 1·4) 500 (<500, 500)
Sub-Saharan Africa 165 83 9·6 (6·2, 14·1) 97,500 (63,500, 143,500) 2·8 16·1 (10·4, 23·6) 6,000 (4,000, 9,000) 9·3 (6·1, 13·7) 91,500 (59,500, 134,500)
Middle East and North Africa 292 11 3·4 (1·0, 7·2) 33,500 (10,500, 71,500) 57·5 0·3 (0·1, 0·6) <500 (<500, <500) 3·5 (1·1, 7·5) 33,500 (10,500, 71,500)
Global 221 401 3·7 (2·5, 5·4) 420,000 (281,000, 612,500) 25·1 7·0 (4·7, 10·3) 52,500 (35,500, 77,000) 3·5 (2·3, 5·1) 367,000 (245,500, 535,500)
Current HCV infection
Incarc. per
100K people1
No.
estimates
% (CI) among
people
Estimated no. people who are
incarcerated with current HCV
infection (CI)
Ratio of HCV %
among
incarcerated
people relative
to
gen. pop HCV
%
% (CI) among
females
Estimated no. females who are
incarcerated with current HCV
infection (CI)
% (CI) among
males
Estimated no. males who are
incarcerated with current HCV
infection (CI)
Eastern Europe 338 22 38·1 (24·8, 54·2) 271,500 (176,500, 386,000) 10·9 13·3 (8·6, 18·9) 7,500 (5,000, 10,500) 40·2 (26·2, 57·2) 264,500 (172,000, 375,500)
Western Europe 165 130 7·9 (5·0, 11·7) 37,000 (23,500, 54,500) 19·0 8·5 (5·3, 12·7) 2,000 (1,000, 3,000) 7·8 (5·0, 11·6) 35,000 (22,000, 51,500)
East and southeast Asia 192 7 14·0 (7·1, 24·3) 431,000 (217,500, 745,500) 25·5 1·5 (0·8, 2·5) 4,000 (2,000, 7,000) 15·3 (7·7, 26·4) 427,000 (215,500, 738,500)
South Asia 76 40 8·3 (6·7, 10·4) 83,500 (67,500, 104,500) 21·9 3·0 (2·3, 4·1) 1,000 (1,000, 1,500) 8·5 (6·9, 10·7) 82,000 (66,500, 103,000)
Central Asia* 252 1 13·0 (8·9, 18·3) 15,500 (11,000, 22,000) ·· 11·5 (7·6, 16·9) 1,000 (500, 1,000) 13·0 (9·0, 18·4) 15,000 (10,500, 21,000)
Caribbean 499 0 ·· ·· ·· ·· ·· ·· ··
Latin America 459 52 4·0 (2·0, 6·8) 76,000 (37,500, 128,500) 5·5 3·3 (1·6, 5·7) 3,500 (2,000, 6,500) 4·1 (2·0, 6·8) 72,000 (35,500, 122,000)
North America 754 63 15·1 (13·1, 17·2) 277,500 (241,000, 316,000) 17·7 21·1 (18·3, 24·0) 34,000 (29,500, 39,000) 14·5 (12·6, 16·5) 243,500 (211,500, 277,500)
Pacific Islands & territories 146 0 · · · · · · ·
Australasia 267 1 8·0 (6·4, 9·9) 4,500 (3,500, 5,500) 9·3 2·5 (0·9, 6·6) <500 (<500, 500) 8·2 (6·6, 10·2) 4,000 (3,500, 5,000)
Sub-Saharan Africa 165 30 5·3 (3·8, 7·3) 53,500 (39,000, 74,000) 6·6 4·1 (2·4, 6·8) 1,500 (1,000, 2,500) 5·3 (3·9, 7·3) 52,000 (38,000, 71,500)
Middle East and North Africa 292 13 5·5 (4·1, 7·2) 54,000 (41,000, 71,000) 6·0 22·9 (17·0, 30·5) 8,000 (6,000, 10,500) 4·9 (3·7, 6·4) 46,500 (35,000, 61,000)
Global 221 359 11·7 (7·7, 17·1) 1,321,500 (869,000, 1,934,000) 15·6 11·8 (7·8, 17·3) 88,500 (58,000, 129,500) 11·7 (7·7, 17·1) 1,233,000 (811,000, 1,804,500)
Current HBV infection
Incarc. per
100K people1
No.
estimates
% (CI) among
people
Estimated no. people who are
incarcerated with current HBV
infection (CI)
Ratio of HBV %
among
incarcerated
people relative
to
gen. pop HBV
%
% (CI) among
females
Estimated no. females who are
incarcerated with current HBV
infection (CI)
% (CI) among
males
Estimated no. males who are
incarcerated with current HBV
infection (CI)
Eastern Europe 338 11 5·3 (3·1, 8·1) 38,000 (22,000, 58,000) 3·8 2·9 (1·6, 4·5) 1,500 (1,000, 2,500) 5·5 (3·2, 8·4) 36,500 (21,000, 55,500)
Western Europe 165 41 1·7 (0·5, 3·6) 8,000 (2,500, 17,000) 2·0 4·8 (1·7, 10·4) 1,000 (500, 2,500) 1·5 (0·5, 3·3) 6,500 (2,000, 14,500)
East and southeast Asia 192 9 6·1 (4·3, 8·4) 188,000 (130,500, 257,000) 1·4 7·1 (4·9, 9·7) 19,500 (13,500, 26,500) 6·0 (4·2, 8·3) 169,000 (117,500, 231,000)
South Asia 76 24 6·1 (1·2, 15·4) 61,000 (12,000, 154,500) 2·6 1·3 (0·4, 2·8) 500 (<500, 1,000) 6·3 (1·2, 15·9) 60,500 (12,000, 153,500)
Central Asia 252 2 4·5 (2·4, 7·8) 5,500 (3,000, 9,500) 3·2 3·5 (1·8, 6·2) <500 (<500, 500) 4·5 (2·5, 7·9) 5,000 (3,000, 9,000)
Caribbean 499 0 ·· ·· ·· ·· ·· ·· ··
Latin America 459 30 0·8 (0·2, 2·0) 14,500 (4,000, 37,500) 0·6 0·6 (0·2, 1·6) 500 (<500, 2,000) 0·8 (0·2, 2·0) 13,500 (3,500, 36,000)
North America 754 9 2·9 (0·3, 9·1) 53,000 (4,500, 167,000) 8·2 0·6 (0·1, 1·9) 1,000 (<500, 3,000) 3·1 (0·3, 9·8) 52,000 (4,500, 164,000)
Pacific Islands & territories 146 0 ·· ·· ·· ·· ·· ·· ··
Australasia 267 1 0·5 (0·3, 1·1) 500 (<500, 500) 0·3 0·4 (0·2, 2·5) <500 (<500, <500) 0·5 (0·2, 1·1) 500 (<500, 500)
Sub-Saharan Africa 165 34 8·3 (6·4, 10·4) 84,500 (65,500, 106,000) 1·9 4·2 (3·0, 6·1) 1,500 (1,000, 2,500) 8·4 (6·6, 10·6) 83,000 (64,500, 104,000)
Middle East and North Africa 292 8 3·4 (2·0, 5·3) 34,000 (19,500, 52,500) 1·4 0·0 (0·0, 0·0) <500 (<500, <500) 3·5 (2·1, 5·5) 34,000 (19,500, 52,500)
Global 221 169 4·4 (2·4, 7·7) 492,500 (267,500, 872,000) 2·2 3·4 (1·8, 6·0) 25,500 (13,500, 45,000) 4·4 (2·4, 7·8) 467,500 (254,000, 826,500)
Active tuberculosis
Incarc. per
100K people1
No.
estimates
% (CI) among
people
Estimated no. people who are
incarcerated with active
tuberculosis (CI)
Ratio of TB %
among
incarcerated
people relative
to
gen. pop TB %
% (CI) among
females
Estimated no. females who are
incarcerated with active
tuberculosis (CI)
% (CI) among
males
Estimated no. males who are
incarcerated with active
tuberculosis (CI)
Eastern Europe 338 6 4·7 (3·8, 5·6) 33,000 (27,500, 39,500) 85·1 0·3 (0·3, 0·6) <500 (<500, 500) 5·0 (4·2, 6·0) 33,000 (27,500, 39,500)
Western Europe 165 5 3·0 (1·4, 6·7) 14,000 (6,500, 31,500) 502·4 5 (2·5, 10·4) 1,000 (500, 2,500) 2·9 (1·4, 6·5) 13,000 (6,000, 29,000)
East and southeast Asia 192 13 1·4 (0·8, 2·1) 41,500 (24,000, 65,500) 13·5 0·8 (0·5, 1·1) 2,000 (1,500, 3,000) 1·4 (0·8, 2·2) 39,500 (22,500, 62,500)
South Asia 76 21 2·3 (1·9, 2·7) 23,000 (19,500, 27,000) 8·6 0·6 (0·5, 0·7) <500 (<500, <500) 2·4 (2·0, 2·8) 23,000 (19,500, 27,000)
Central Asia 252 1 2·7 (1·7, 4·0) 3,000 (2,000, 5,000) 72·8 0·8 (0·5, 1·3) <500 (<500, <500) 2·8 (1·8, 4·2) 3,000 (2,000, 5,000)
Caribbean 499 0 ·· ·· ·· ·· ·· ·· ··
Latin America 459 42 5·4 (3·1, 8·4) 101,500 (58,500, 159,000) 112·6 0·1 (0·1, 0·2) <500 (<500, <500) 5·7 (3·3, 8·9) 101,500 (58,500, 159,000)
North America 754 6 0·0 (0·0, 0·0) 500 (500, 500) 5·3 0 (0, 0) <500 (<500, <500) 0·0 (0·0, 0·0) 500 (500, 500)
Pacific Islands & territories 146 0 ·· ·· ·· ·· ·· ·· ··
Australasia 267 0 ·· ·· ·· ·· ·· ·· ··
Sub-Saharan Africa 165 77 4·0 (1·8, 7·2) 41,000 (18,000, 73,500) 11·8 3·7 (1·9, 6·2) 1,500 (500, 2,500) 4·1 (1·8, 7·3) 40,000 (17,500, 71,500)
Middle East and North Africa 292 2 1·6 (0·9, 2·5) 15,500 (9,500, 24,500) 4·3 0·4 (0·3, 0·7) <500 (<500, <500) 1·6 (1·0, 2·5) 15,500 (9,000, 24,500)
Global 221 173 2·5 (1·5, 3·8) 278,500 (168,500, 434,500) 45·3 0·9 (0·5, 1·3) 6,500 (4,000, 10,000) 2·6 (1·6, 4·0) 272,500 (164,500, 424,500)

Notes: For country-level estimates of these characteristics and the sources for those estimates, please see Appendix 9. CI = confidence interval (see Appendix for details of estimation). IDU: injecting drug use; HIV: Human Immunodeficiency Virus; HCV: Hepatitis C; HBV: Hepatitis B; TB: tuberculosis; gen. pop. : general population; incarc.: incarcerated.

Indicates there were no data to inform a region’s estimate.

1

Country level data that informed these regional and global incarceration estimates were sourced from the World Prison Brief, collated by the Institute for Crime and Justice Policy Research at Burbeck University. See: https://www.prisonstudies.org/world-prison-brief-data. Note that we used the country estimates to make rates for 15-64 years (not the total country population) so our rates differ from the World Prison Brief estimates.

*

The ratio of HCV among people who are incarcerated relative to the general population for Central Asia could not be calculated as there was no HCV estimate for the general population in Kyrgyzstan (our only HCV estimate for Central Asia is from Kyrgyzstan).

Fig. 3.

Fig. 3

Fig. 3

a. Prevalence (%) of lifetime injecting drug use among people who are incarcerated by country.

Fig. 3b. Prevalence (%) of HIV among people who are incarcerated by country.

Fig. 3c. Prevalence (%) of current HCV infection among people who are incarcerated by country.

Fig. 3d. Prevalence (%) of HbsAg infection among people who are incarcerated by country.

Fig. 3e. Prevalence (%) of active tuberculosis among people who are incarcerated by country.

HIV, HCV, HBV and tuberculosis

Data from 92 countries, representing 65.6 % of the global incarcerated population, reveal that approximately 420,000 (95 %CI 281,000–612,500) incarcerated individuals, or 3·7 % (95 %CI 2·5–5·4), are people with HIV (the number of estimates informing our estimates by region are shown in the Table 2). This prevalence is 25·1 times higher than that in the general population. Notably, HIV prevalence globally (Table 1) is two-fold higher among females in carceral settings at 7·0 % (95 %CI 4·7–10·3) compared to males at 3·5 % (95 %CI 2·3–5·1). Regional variations show the lowest prevalence in Australasia at 0·7 % (95 %CI 0·3–1·4) and the highest in Eastern Europe at 16·6 % (95 %CI 13·7–19·6) and Sub-Saharan Africa at 9·6 % (95 %CI 6·2–14·1). Detailed country-level estimates are provided in Table 2 and Fig. 3 illustrates these findings (Appendix 9 reports country-level data and sources in detail, and Appendix 15-16 report study level characteristics and risk of bias for each study included in country estimates for each indicator). The disparity between HIV prevalence in incarcerated populations and the general population is most pronounced in Eastern Europe at 249 times higher, followed by the Middle East and North Africa at 59-fold higher, with the lowest ratios in Sub-Saharan Africa and the Caribbean at 2·9 and 2·6-fold higher, respectively.

Data from 67 countries, representing 58.6 % of the world’s incarcerated population, estimate that 1,321,500 (95 %CI 869,000–1,934,000) incarcerated people have current HCV infection. This amounts to 11·7 % (95 %CI 7·7–17·1) of all people who are incarcerated aged 15–64 years, an estimated 15·6-fold increase relative to the general global population (Table 1). Global prevalence of current HCV infection was similar for incarcerated females 11·8 % (95 %CI 7·8–17·3) compared to males 11·7 % (95 %CI 7·7–17·1). The highest regional prevalence for current HCV infection in carceral settings was seen in Eastern Europe 38·1 % (95 %CI 24·8–54·2) and North America 15·1 % (95 %CI 13·1–17·2). Data gaps exist, however, with no data from the Caribbean or the Pacific Islands & Territories (Table 1). East and Southeast Asia had the highest ratio of current HCV infection in carceral settings compared to the general population (25·5-fold higher), followed by South Asia (21·9-fold higher; Table 1). Fig. 3 shows country level data and Table 2 reports country-level estimates; Appendix 9 reports country-level data and sources in detail, and Appendix 15-16 report study level characteristics and risk of bias for each study included in country estimates for each indicator).

Data from 54 countries, covering 56·4 % of the world’s incarcerated population, indicate that 492,500 people (95 %CI 267,500–872,000), or 4·4 % (95 %CI 2·4–7·7), of all incarcerated individuals aged 15–64 years have current HBV infection, which is 2·2-fold higher than the general population (Table 1). The global prevalence of current HBV infection was similar in incarcerated females (3·4 % [95 %CI 1·8–6·0]) to that in incarcerated males (4·4 % [95 %CI 2·4– 7·8]). The regional prevalence of HBV infection varied greatly: Australasia (0·5 % [95 % CI 0·3–1·1]) and Latin America (0·8 % [95 %CI 0·2–2·0]) had much lower estimates than East and South-East Asia (6·1 % [95 %CI 4·3–8·4]), South Asia (6·1 [95 %CI 1·2–15·4]) and Sub-Saharan Africa (8·3 % [95 %CI 6·4–10·4]); country level data are reported in Fig. 3 and Table 2 (Appendix 9 reports country-level data and sources in detail, and Appendix 15-16 report study level characteristics and risk of bias for each study included in country estimates for each indicator). The ratio of HBV infection in carceral settings compared to that of the general population was highest in North America (8·2-fold higher) and Eastern Europe (3·8-fold higher), with people incarcerated in Australasia and Latin America having a lower risk than the general population (at 0·3 and 0.6 times, respectively; Table 1; Appendix 9 shows regional and country level ratios).

Data from 42 countries, representing 69·4 % of the world’s incarcerated population, indicate that 278,500 people (95 %CI 168,500–434,500), or 2·5 % (95 %CI 1·5–3·8), of all incarcerated individuals aged 15–64 years have active tuberculosis. This prevalence is 45·3 times higher than that in the global general population (Table 1). The global prevalence of active tuberculosis was almost 3-fold higher in incarcerated males (2·6 % [95 %CI 1·6–4·0]) compared to females (0·9 % [95 %CI 0·5–1·3]). Latin America (5·4 % [95 %CI 3·1- 8·4]), Eastern Europe (4·7 % [95 %CI 3·8–5·6]) and Sub-Saharan Africa (4·0 [95 %CI 1·8–7·2]) were the regions with the highest active tuberculosis prevalence. The Middle East and North Africa (1·6 % [95 %CI 0·9–2·5]), East and South-East Asia (1·4 % [95 %CI 0·8–2·1]), and North America (less than 0.01 %) (0·0 % [95 %CI 0·0–0·0]) reported the lowest active tuberculosis prevalence among incarcerated people (country level data are reported in Fig. 3 and Table 2; Appendix 9 reports country-level data and sources in detail, and Appendix 15-16 report study level characteristics and risk of bias for each study included in country estimates for each indicator). The ratio of active tuberculosis in carceral settings compared to that of the general population was considerably higher in Western Europe (502·4 times the prevalence) and Latin America (112·6 times the prevalence) than other regions (Appendix 9 and Table 1 show regional and country level ratios).

Sensitivity analyses

We conducted sensitivity analyses examining the potential impact of restricting data to the most recent data for each country. In these analyses, we only included estimates from the most recent five years of data from within each country, for people, females and males. The regional estimates resulting from this approach are presented in Appendix 10. These estimates, although based on far fewer data points, were consistent with the estimates reported in the main analyses.

Risk of bias

As noted earlier, each study was graded according to a range of methodological characteristics that permitted assessment of risk of bias against the JBI Prevalence Risk of Bias appraisal tool (see Appendix 14). No study providing data for any indicator was rated nine (out of a score of nine, i.e. for every study, on at least one measure out of nine, there was some feature that reflected a methodological characteristic that increased potential risk of bias in the study findings). For each indicator (injecting drug use, HIV, HCV, HBV and tuberculosis), the modal risk of bias score was five, indicating that there were most commonly four areas where a risk of bias existed in studies. Fewer than ten studies received a score of 8 across any indicator.

Across all indicators, the most common characteristics introducing potential bias were a) the nature of the sampling of participants (which were almost never census or representative samples of the entire incarcerated population being studied); b) poor sample coverage (recruitment into the study not offered to every eligible person); c) inadequate description of the study settings and participants (defined as reporting timeframe of recruitment, setting, age of sample and sex of participants); and d) details and adequacy of response rate (response rate both stated and considered high uptake). Appendix Tables 16.1 to 16.5 show the grades for every included study reported by indicator and country.

Discussion

The incarceration epidemic involves an estimated 11.3 million people aged 15–64 incarcerated globally, with 30 to 70 million cycling through these settings annually, with the largest populations in East and South East Asia, Latin America and North America. There was clear variation in rates of incarceration, with the highest rate being in North America.

Overall, we estimate that one in nine people (11·9 %) who are incarcerated globally have injected drugs, which is over 50 times higher than in the general population. There was substantial variation across regions both in prevalence in incarcerated populations, from 3·0 % (Sub Saharan Africa) to 51·0 % (Australasia), and in IDU prevalence compared to the general population (Degenhardt et al., 2023). Crucial here is the magnitude of the elevated prevalence of infectious diseases in carceral settings relative to the general population, particularly for active tuberculosis (45·3-fold higher prevalence), HIV (25·1-fold higher) and HCV (15·6-fold higher). This review also estimated, for the first time, prevalence estimates for both females and males and compared prevalence within carceral settings to that of the general population.

Despite substantial geographic variation in the prevalence of all indicators examined, there remains a consistently elevated prevalence of infectious diseases and IDU in carceral settings across all regions compared to the general population, except for HBV. This trend was seen in both females and males, though regional differences exist in the relative prevalence between incarcerated females and males. For instance, Australasia and North America report a significantly higher prevalence of IDU among incarcerated females than males, whereas other regions generally exhibit lower prevalence rates among females.

This study provides the first systematic evidence across the globe showing the elevated prevalence of infectious disease in carceral populations, confirming that they are a critical target group in eliminating infectious disease. We estimated population sizes by country, region and globally, and also identified where incarcerated populations have a particularly elevated risk compared to the general population. This provides guidance at all levels on where and to what extent additional interventions within carceral settings are needed for countries to meet WHO targets to reduce morbidity and mortality due to tuberculosis, HIV, HCV and HBV as public health problems (World Health Organization, 2015, 2016, 2022, 2023). This can guide the extent to which the provision of prevention, harm reduction and treatment services are needed in carceral settings across countries, regions and the globe. We summarise the extent to which these services are currently being provided in carceral settings elsewhere (Santo et al., n.d.).

The scope of this review is far wider (incorporating peer-reviewed and grey literature and extensive interactions with key agencies focused on incarcerated populations) than previous reviews (Cords et al., 2021; Dolan et al., 2016). Our prevalence estimates are based on a much more rigorous and robust synthesis of the available evidence up until 2025. For example, the number of eligible data sources increased 10-fold compared to a previous global review (Dolan et al., 2016) (from 299 (Dolan et al., 2016) to 2968 in our review). We have generated the first estimates among females and males, and comparisons against the general population.

In this analysis we did not estimate the incidence of tuberculosis, as did a previous review (Cords et al., 2021), though we increased the number of studies of tuberculosis prevalence included in our review by 63 %. Our analysis revealed a global tuberculosis prevalence among incarcerated individuals of 2·5 %, which is more than double the previous estimate of 1·0 % (Cords et al., 2021). Moreover, the disparity in tuberculosis prevalence between incarcerated populations and the general population is 45-fold higher, far exceeding the earlier estimated of a 10-fold difference in tuberculosis incidence between prison and community (Cords et al., 2021).

Limitations

Despite the strengths of this review, several limitations should be acknowledged particularly of the evidence. First, data gaps in some countries, particularly the Pacific Island States and Territories, introduce some uncertainty in estimates. Although we imputed data for these regions to generate global estimates, regional-level imputed estimates were not presented.

Second, estimates of IDU may be conservative due to potential under-reporting, as some individuals may have been reluctant to disclose prior risk-taking, even in surveys conducted by researchers independent of carceral authorities. This may mean that the prevalence of injecting drug use among people who are incarcerated is even higher than the recorded estimates suggest.

Third, population estimates for incarcerated individuals were derived from the World Prison Brief (https://www.prisonstudies.org/), the most authoritative source available. This is the most comprehensive source of data and the sources of those estimates are reported. Country information is updated on a monthly basis, using data that are most commonly obtained from governmental sources, but we could not independently verify them. Nonetheless the clear reporting of these data with reference to the source, the nature of the data (often a census count reported by the national government or similar body) mean that these are the best resource of such global statistics that we have been able to locate.

Fourth, data on population-wide disease screening for HIV, HCV, tuberculosis and HBV were limited. Most prevalence estimates were based on studies from select (often a single) facilities rather than nationally representative surveys, with only six studies using a census-based sampling approach in a carceral setting, and only one study utilising a fully national census approach. As within-country prevalence estimates may vary (Bose, 2018; Spaulding et al., 2023; Varan et al., 2014), there is a need for more focus on national screening and reporting to inform policy and practice. Indeed, in highlighting the limited epidemiological data on prevalence, this review has made somewhat more explicit the likely more common approach of reliance upon data about infectious disease as obtained from targeted screening and notifications data. In that sense, notifications data that may be more commonly available in carceral settings are likely to reflect not just variations in epidemiology of disease prevalence, but also varied screening algorithms used in these settings. As a result, in many instances epidemiological understanding of prevalence will reflect under-notification in routine programmatic data, meaning that policy in carceral settings may be being based on a biased understanding of the extent of the public health challenges of these diseases in the carceral system and highlights the importance of routine screening for infectious diseases. Having said that, we note that in some settings, for pragmatic reasons countries may not conduct studies of some infectious diseases (example.g. in countries where hepatitis B vaccination is universally offered in carceral settings such as Scotland, HBsAg may no longer be routinely measured in prevalence surveys).

Fifth, variation in tuberculosis case definitions and screening methods (e.g., reliance on chest radiographs versus clinical diagnosis) may have led to inconsistencies in reported tuberculosis prevalence. Some studies may have excluded individuals with diagnosed tuberculosis who were quarantined, potentially leading to underestimation of cases, while differences in defining "probable" versus "confirmed" tuberculosis cases may have contributed to variability in reported rates. Furthermore, there may be a potential overestimation of tuberculosis prevalence due to inclusion of outbreak papers in prevalence calculations.

Sixth, the use of convenience samples, without clear sampling frames and where it was a decision of incarcerated individuals to participant, may have affected the prevalence estimates observed in those studies. These types of studies might underestimate injecting drug use and infectious diseases (as those who are at risk may not participate) or, by contrast, could potentially overestimate population-level injecting drug use and infectious diseases (as those who might not feel that they are at risk might not participate) estimates. These concerns are shared with many community-level studies of the same behaviours that use the same convenience sampling approach.

This is the first complete review of this topic that incorporates peer-reviewed and grey literature, involved extensive interactions with key agencies focused on incarcerated populations. We have sought to include all available studies, but may have missed some. To address this as much as possible, we liaised directly with WHO, EUDA, UNODC and UNAIDS staff, and with many researchers across our global networks. We encourage feedback at global.reviews@unsw.edu.au, including enquiries from those interested in collaboration.

Public health and policy implications

The extraordinary high burden of HIV, tuberculosis, and viral hepatitis in carceral settings identified here poses a significant challenge to global disease elimination efforts. The risk of within-prison disease transmission, compounded by poor access to screening and treatment, not only affects incarcerated individuals, but also drives infection rates in the broader population. Addressing this crisis requires an urgent public health response to expand evidence-based screening, prevention, and treatment interventions within prisons, and ensuring continuity of care both for transition into incarceration (e.g. ensuring that drug dependence or infectious disease treatment is continued following incarceration) and post-release.

The United Nations’ Mandela Rules mandate that individuals in prison should receive equivalent healthcare to that available in the community (United Nations Office on Drugs & Crime, 2015). Our review, alongside our companion paper on intervention coverage (Santo et al., n.d.) underscores the need to adopt and extend reach throughout countries for routine evidence-based screening, treatment and prevention for each condition. Routine HIV, HCV, HBV, and tuberculosis screening, alongside HBV vaccination and harm reduction programs, should be standard practice (World Health Organization, 2012). Interventions such as opioid agonist treatment (OAT) and needle and syringe programmes (NSPs) for people who inject drugs, which have been proven to reduce disease transmission (Degenhardt et al., 2019; Gowing et al., 2011; Platt et al., 2018) and improve continuity of care within prison and after release, must be implemented widely in correctional settings and maintained after release to reduce broader population transmission risks (Degenhardt et al., 2019; Macdonald et al., 2024).

Prisons function as high-risk environments that amplify infectious disease transmission. Multiple mathematical models showing that the cumulative risk of exposure during incarceration is associated with much greater levels of infection risk (Altice et al., 2016; Liu et al., 2024; Stone et al., 2021, 2017). Conversely, effective case-finding and treatment in prison and linkage to care upon release are cost-effective (Shih et al., 2024; Ward et al., 2022) and can have disproportionate benefits in terms of reducing infectious disease transmission in the community. Expanding treatment access in prisons has the potential to reduce community transmission, helping countries meet WHO elimination targets for HIV, tuberculosis, and viral hepatitis (Girardin et al., 2019; Godin et al., 2021; Martin et al., 2020; Stone et al., 2023), and inform and improve progress in countries' SDG targets (Tavoschi et al., 2024; Winkelman et al., 2022; World Health Organization, 2023). Addressing the incarcerated population’s health needs is not just a prison health issue—it is a population-wide public health imperative.

One striking limitation that our review revealed is that insufficient data come from public health surveillance or programmatic sources. This highlights a lack of integration between carceral healthcare systems and national health systems. Although additional research can refine strategies, there is already sufficient data to justify immediate action. Instead of conducting further observational studies, resources should be directed toward evidence-informed intervention implementation and scaling up proven strategies in prisons to reduce transmission and improve health outcomes.

Given the elevated health risks and exposures in prison, there is a pressing need to re-evaluate criminal laws and sentencing policies, particularly for people who use/inject drugs, who are disproportionately incarcerated for minor, nonviolent offences. Incarceration-driven public health crises could be mitigated through decriminalisation strategies and alternatives to detention, such as evidence-based drug treatment and diversion programs that keep people out of prison and within community healthcare systems. Decarceration strategies have been shown to yield substantial cost savings, which could be reinvested into scaling up prevention and treatment interventions in both prison and community settings. Shifting resources away from punitive approaches toward evidence-based public health responses will reduce health inequities, limit disease spread and strengthen national progress toward Sustainable Development Goals (SDGs) (United Nations, 2025).

The incarcerated population is a critical but often neglected group in global disease elimination efforts. Without urgent action, the high burden of infectious diseases in prisons will continue to undermine public health progress worldwide. Governments and international organisations must prioritise: 1) Routine screening, prevention, and treatment of HIV, HCV, HBV, and tuberculosis in carceral settings; 2) Services to prevent drug-related harm and treat drug dependence, including OAT and NSPs; 3) Stronger linkage-to-care programs to ensure continuity of treatment post-release; 4) Reform of the criminal legal system to reduce unnecessary incarceration, particularly for people who use drugs; and 5) Integration of prison health with national health systems to ensure equivalent healthcare for all. These strategies will not only protect the health of incarcerated individuals but also yield broader community benefits, strengthening national and global efforts to end HIV, tuberculosis and viral hepatitis as public health threats.

Supplementary Material

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Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.drugpo.2025.105062.

Acknowledgements

This review was supported by the Australian National Health and Medical Research Council (NHMRC) ASCEND Program grant (1150078), a NHMRC Investigator Grant (2016825, 2034002) and NHMRC Senior Principal Research Fellowship (1135991) to LD, the US National Institute on Drug Abuse (NIDA) (1R01DA059822-01A1), the US National Institute of Allergy and Infectious Diseases (R01AI147490 RFA-AI-18-026) and the National Drug and Alcohol Research Centre (NDARC), UNSW Sydney. NDARC is funded by the Australian Government Department of Health. The views expressed in this publication do not necessarily represent the position of the Australian Government.

MH and PV acknowledge support from NIHR HPRU in in Behavioural Science and Evaluation and NIHR Programme Grant EPIToPe. FLA receives support from the U.S. National Institute of Health, including the National Institute on Drug Abuse (R01 DA029910, R01 DA025943, R21 DA041953, R01 DA054703, R01 DA054851), National Institute of Allergy and Infectious Diseases (R01 AI177082) and the Fogarty International Center (R01 TW012674, D43 TW011324, D43 TW012492). JG was supported by NHMRC Investigator Grants Award (1176131 and 2034002). PV and JS acknowledge support from the Wellcome Trust [WT 220866/Z/20/Z and 226619/Z/22/Z]. PW acknowledges support from an Australian Government Research Training Program (RTP) Scholarship as well as an NDARC Higher Degree Research scholarship. LT and OP acknowledge support from an NHMRC PhD scholarship as well as an NDARC Higher Degree Research scholarship. BH is supported by an NHMRC Investigator Grant (2026968). JB receives funding from the US National Institute on Drug Abuse (K23DA055695).

FAC worked as consultant for WHO Regional Office for Europe between 03/2020 and 12/2024 (or during the study period). The author alone is responsible for the views expressed in this publication, and these do not necessarily represent the decisions or the stated policy of the World Health Organization. She is affiliated with the WHO Regional Office for Europe and Research Institute for Medicines (iMED, University of Lisbon).

AB was a staff member of the United Nations (Office of Drugs and Crime) between 10/2005 and 01/2025. The author alone is responsible for the views expressed in this publication, and these do not necessarily represent the decisions or the stated policy of the United Nations.

Thanks to people who assisted with searches and extraction of data in this review: Marion Barault, Brodie Clark, Miranda Hendry, Eunice Ling, Christopher Manning, Noni O’Dea, Sophie Ottaviano, Jonathan Wu, Zachary Wilkinson, Benson Yiu (National Drug and Alcohol Research Centre, University of New South Wales, Sydney, NSW, Australia).

Assistance in sourcing and verifying data, circulation of our requests for data, and other feedback were provided by individuals from government, non-government, and research organisations, for which we are thankful. These individuals are listed in Appendix 13.

Declaration of competing interest

Past three years, JG is a consultant or advisor and has received research grants from Abbvie, Abbott, bioLytical, Cepheid, Gilead Sciences, Hologic, and Roche. EBC has received funding from the Canadian Network on Hepatitis C. These companies or organisations had no knowledge of or role in the design, conduct, interpretation, or publication of these findings. All other authors have no conflicts of interest to declare.

Footnotes

Given his/her/their role as International Journal of Drug Policy, Jason Grebely and Evan Cunningham had no involvement in the peer-review of this article and has no access to information regarding its peer-review. Full responsibility for the editorial process for this article was delegated to another journal editor.

CRediT authorship contribution statement

Louisa Degenhardt: Writing – review & editing, Writing – original draft, Supervision, Resources, Project administration, Methodology, Funding acquisition, Data curation, Conceptualization. Matthew Hickman: Writing – review & editing, Writing – original draft, Methodology, Conceptualization. Frederick L. Altice: Writing – review & editing, Conceptualization. Jason Grebely: Writing – review & editing, Methodology, Conceptualization. Sophia Taylor: Writing – review & editing, Formal analysis, Data curation. Michelle Lynch: Writing – review & editing, Formal analysis, Data curation. Aleksa Kamenjaš: Writing – review & editing, Data curation. Jack Marsden: Writing – review & editing, Formal analysis, Data curation. Lucy T. Tran: Writing – review & editing, Supervision, Methodology, Formal analysis, Data curation. Paige Webb: Writing – review & editing, Formal analysis, Data curation. Olivia Price: Writing – review & editing, Data curation. Christel Macdonald: Writing – review & editing, Data curation. Filipa Alves da Costa: Writing – review & editing, Data curation. Justin Berk: Writing – review & editing, Data curation. Anja Busse: Writing – review & editing, Data curation. Evan Cunningham: Writing – review & editing, Methodology. Colleen Daniels: Writing – review & editing, Data curation. Behzad Hajarizadeh: Writing – review & editing, Methodology. Linda Montanari: Writing – review & editing, Data curation. Luis Royuela: Writing – review & editing, Data curation. Keith Sabin: Writing – review & editing, Data curation. Jack Stone: Writing – review & editing, Methodology. Annette Verster: Writing – review & editing, Data curation. Peter Vickerman: Writing – review & editing, Methodology. Michael Farrell: Writing – review & editing, Funding acquisition, Conceptualization. Thomas Santo Jr.: Writing – review & editing, Writing – original draft, Supervision, Methodology, Conceptualization.

References

  1. Altice FL, Azbel L, Stone J, Brooks-Pollock E, Smyrnov P, Dvoriak S, Taxman FS, El-Bassel N, Martin NK, & Booth R (2016). The perfect storm: incarceration and the high-risk environment perpetuating transmission of HIV, hepatitis C virus, and tuberculosis in Eastern Europe and Central Asia. The Lancet, 388(10050), 1228–1248. https://www.sciencedirect.com/science/article/pii/S014067361630856X?via%3Dihub. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bose S. (2018). Demographic and spatial disparity in HIV prevalence among incarcerated population in the US: A state-level analysis. International Journal of STD & AIDS, 29(3), 278–286. 10.1177/0956462417724586 [DOI] [PubMed] [Google Scholar]
  3. Bosworth RJ, Borschmann R, Altice FL, Kinner SA, Dolan K, & Farrell M (2022). HIV/AIDS, hepatitis and tuberculosis-related mortality among incarcerated people: A global scoping review. International Journal of Prisoner Health, 18(1), 66–82. https://www.emerald.com/ijoph/article-abstract/18/1/66/389695/HIV-AIDS-hepatitis-and-tuberculosis-related?redirectedFrom=fulltext. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Clopper CJ, & Pearson ES (1934). The use of confidence or fiducial limits illustrated in the case of the binomial. Biometrika, 26(4), 404–413. 10.1093/biomet/26.4.404 [DOI] [Google Scholar]
  5. Colledge-Frisby S, Ottaviano S, Webb P, Grebely J, Wheeler A, & Cunningham E (2023). Global coverage of interventions to prevent and manage drug-related harms among people who inject drugs: A systematic review. The Lancet Global Health. https://www.sciencedirect.com/science/article/pii/S2214109X2300058X?via%3Dihub. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cords O, Martinez L, Warren JL, O'Marr JM, Walter KS, Cohen T, Zheng J, Ko AI, Croda J, & Andrews JR (2021). Incidence and prevalence of tuberculosis in incarcerated populations: A systematic review and meta-analysis. The Lancet Public Health, 6(5), e300–e308. 10.1016/S2468-2667(21)00025-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Degenhardt L, Grebely J, Stone J, Hickman M, Vickerman P, Marshall BDL, Bruneau J, Altice FL, Henderson G, Rahimi-Movaghar A, & Larney S (2019). Global patterns of opioid use and dependence: Harms to populations, interventions, and future action. The Lancet, 394(10208), 1560–1579. 10.1016/s0140-6736(19)32229-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Degenhardt L, Peacock A, Colledge S, Leung J, Grebely J, Vickerman P, Stone J, Cunningham EB, Trickey A, Dumchev K, Lynskey M, Griffiths P, Mattick RP, Hickman M, & Larney S (2017). Global prevalence of injecting drug use and sociodemographic characteristics and prevalence of HIV, HBV, and HCV in people who inject drugs: A multistage systematic review. The Lancet Global Health, 5 (12), e1192–e1207. 10.1016/s2214-109x(17)30375-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Degenhardt L, Webb P, Colledge-Frisby S, Ireland J, Wheeler A, Ottaviano S, Willing A, Kairouz A, Cunningham EB, Hajarizadeh B, Leung J, Tran LT, Price O, Peacock A, Vickerman P, Farrell M, Dore GJ, Hickman M, & Grebely J (2023). Epidemiology of injecting drug use, prevalence of injecting-related harm, and exposure to behavioural and environmental risks among people who inject drugs: A systematic review. The Lancet Global Health, 11(5), e659–e672. 10.1016/s2214-109x(23)00057-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dolan K, Wirtz AL, Moazen B, Ndeffo-Mbah M, Galvani A, Kinner SA, Courtney R, McKee M, Amon JJ, Maher L, Hellard M, Beyrer C, & Altice FL (2016). Global burden of HIV, viral hepatitis, and tuberculosis in prisoners and detainees. The Lancet. 10.1016/s0140-6736(16)30466-4 [DOI] [PubMed] [Google Scholar]
  11. European Union Drugs Agency. (2024a). Interventions in prisons (Section of “Harm reduction - the current situation in Europe”, European Drug Report 2024; ) https://www.euda.europa.eu/publications/european-drug-report/2024/harm-reduction_en#level-5-section5. [Google Scholar]
  12. European Union Drug Agency. (2024b). Statistical Bulletin 2024 – Drug use and prison. Lisbon: European Union Drugs Agency. https://www.euda.europa.eu/data/stats2024/dup_en. [Google Scholar]
  13. Girardin F, Hearmon N, Castro E, Negro F, Eddowes L, Gétaz L, & Wolff H (2019). Modelling the impact and cost-effectiveness of extended hepatitis c virus screening and treatment with direct-acting antivirals in a Swiss custodial setting [Article]. Clinical Infectious Diseases, 69(11), 1980–1986. 10.1093/cid/ciz088 [DOI] [PubMed] [Google Scholar]
  14. Godin A, Kronfli N, Cox J, Alary M, & Maheu-Giroux M (2021). The role of prison-based interventions for hepatitis C virus (HCV) micro-elimination among people who inject drugs in Montréal, Canada. International Journal of Drug Policy, 88, Article 102738. 10.1016/j.drugpo.2020.102738 [DOI] [PubMed] [Google Scholar]
  15. Gowing L, Farrell MF, Bornemann R, Sullivan LE, & Ali R (2011). Oral substitution treatment of injecting opioid users for prevention of HIV infection. The Cochrane Database of Systematic Reviews, (8), Article Cd004145. 10.1002/14651858.CD004145.pub4 [DOI] [PubMed] [Google Scholar]
  16. Grebely J, Larney S, Peacock A, Colledge S, Leung J, Hickman M, Vickerman P, Blach S, Cunningham E, Dumchev K, Lynskey M, Stone J, Trickey A, Razavi H, Mattick RP, Farrell M, Dore GJ, & Degenhardt L (2018). Global, regional, and country-level estimates of hepatitis C infection among people who have recently injected drugs. Addiction. 10.1111/add.14393 [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Harm Reduction International (2022). Global State of Harm Reduction 2022. London: Harm Reduction International. https://hri.global/wp-content/uploads/2022/11/HRI_GSHR-2022_Full-Report_Final.pdf. [Google Scholar]
  18. Harm Reduction International (2023). The Global State of Harm Reduction: 2023 Update to Key Data. London: Harm Reduction International. https://hri.global/publications/global-state-of-harm-reduction-2023-update-to-key-data/. [Google Scholar]
  19. Larney S, Peacock A, Leung J, Colledge S, Hickman M, Vickerman P, Grebely J, Dumchev KV, Griffiths P, & Hines L (2017). Global, regional, and country-level coverage of interventions to prevent and manage HIV and hepatitis C among people who inject drugs: A systematic review. The Lancet Global Health. 10.1016/s2214-109x(17)30373-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Liu YE, Mabene Y, Camelo S, Rueda ZV, Pelissari DM, Dockhorn Costa Johansen F, Huaman MA, Avalos-Cruz T, Alarcón VA, Ladutke LM, Bergman M, Cohen T, Goldhaber-Fiebert JD, Croda J, & Andrews JR (2024). Mass incarceration as a driver of the tuberculosis epidemic in Latin America and projected effects of policy alternatives: A mathematical modelling study. The Lancet Public Health, 9(11), e841–e851. 10.1016/s2468-2667(24)00192-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Macdonald C, Macpherson G, Leppan O, Tran LT, Cunningham EB, Hajarizadeh B, Grebely J, Farrell M, Altice FL, & Degenhardt L (2024). Interventions to reduce harms related to drug use among people who experience incarceration: Systematic review and meta-analysis. The Lancet Public health, 9(9), e684–e699. 10.1016/s2468-2667(24)00160-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Martin NK, Hickman M, Spaulding AC, & Vickerman P (2020). Prisons can also improve drug user health in the community [Note]. Addiction, 115(5), 914–915. 10.1111/add.14971 [DOI] [PubMed] [Google Scholar]
  23. Martinez L, Warren JL, Harries AD, Croda J, Espinal MA, Olarte RAL, Avedillo P, Lienhardt C, Bhatia V, Liu Q, Chakaya J, Denholm JT, Lin Y, Kawatsu L, Zhu L, Horsburgh CR, Cohen T, & Andrews JR (2023). Global, regional, and national estimates of tuberculosis incidence and case detection among incarcerated individuals from 2000 to 2019: A systematic analysis. The Lancet Public health, 8(7), e511–e519. 10.1016/s2468-2667(23)00097-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Mathers BM, Degenhardt L, Phillips B, Wiessing L, Hickman M, Strathdee SA, Wodak A, Panda S, Tyndall M, Toufik A, Mattick RP, & Reference Grp UNHIVI. (2008). Global epidemiology of injecting drug use and HIV among people who inject drugs: A systematic review. The Lancet, 372(9651), 1733–1745. 10.1016/s0140-6736(08)61311-2 [DOI] [PubMed] [Google Scholar]
  25. Mera HB, Wagnew F, Akelew Y, Hibstu Z, Berihun S, Tamir W, Alemu S, Lamore Y, Mesganaw B, Adugna A, & Tsegaye TB (2023). Prevalence and predictors of pulmonary tuberculosis among prison inmates in sub-Saharan Africa: A systematic review and meta-analysis. Tuberculosis Research and Treatment, 2023, Article 6226200. 10.1155/2023/6226200 [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Moazen B, Saeedi Moghaddam S, Silbernagl MA, Lotfizadeh M, Bosworth RJ, Alammehrjerdi Z, Kinner SA, Wirtz AL, Bärnighausen TW, Stöver HJ, & Dolan KA (2018). Prevalence of drug injection, sexual activity, tattooing, and piercing among prison inmates. Epidemiologic Reviews, 40(1), 58–69. 10.1093/epirev/mxy002 [DOI] [PubMed] [Google Scholar]
  27. Moher D, Liberati A, Tetzlaff J, & Altman DG (2009). Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement. Annals of Internal Medicine, 151(4), 264–269. https://renhyd.org/index.php/renhyd/article/download/114/99. [DOI] [PubMed] [Google Scholar]
  28. Munn Z, Moola S, Lisy K, Riitano D, & Tufanaru C (2020). Chapter 5: Systematic reviews of prevalence and incidence. In Aromataris E, & Munn Z (Eds.), JBI manual for evidence synthesis. JBI. 10.46658/JBIRM-17-05. [DOI] [Google Scholar]
  29. Nelson PK, Mathers BM, Cowie B, Hagan H, Des Jarlais D, Horyniak D, & Degenhardt L (2011). Global epidemiology of hepatitis B and hepatitis C in people who inject drugs: Results of systematic reviews. The Lancet, 378(9791), 571–583. 10.1016/S0140-6736(11)61097-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Ottaviano S, Degenhardt L, & Santo T Jr (2023). Searching the grey literature to access research on illicit drug use, blood borne virus, and coverage of interventions among people who are incarcerated. In https://www.unsw.edu.au/content/dam/images/medicine-health/ndarc/research/2024-02-ndarc/Prison%20data%20sources-NDARC%20technical%20report.pdf. [Google Scholar]
  31. Placeres AF, de Almeida Soares D, Delpino FM, Moura HSD, Scholze AR, dos Santos MS, Arcêncio RA, & Fronteira I (2023). Epidemiology of TB in prisoners: A metanalysis of the prevalence of active and latent TB. BMC Infectious Diseases, 23(1), 20. 10.1186/s12879-022-07961-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Platt L, Minozzi S, Reed J, Vickerman P, Hagan H, French C, Jordan A, Degenhardt L, Hope V, Hutchinson S, Maher L, Palmateer N, Taylor A, Bruneau J, & Hickman M (2018). Needle and syringe programmes and opioid substitution therapy for preventing HCV transmission among people who inject drugs: Findings from a Cochrane Review and meta-analysis. Addiction, 113(3), 545–563. 10.1111/add.14012 [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Puza B, & O'neill T (2006). Generalised Clopper–Pearson confidence intervals for the binomial proportion. Journal of Statistical Computation and Simulation, 76(6), 489–508. https://www.tandfonline.com/doi/full/10.1080/10629360500107527. [Google Scholar]
  34. Shih STF, Stone J, Martin NK, Hajarizadeh B, Cunningham EB, Kwon JA, McGrath C, Grant L, Grebely J, Dore GJ, Lloyd AR, Vickerman P, & Chambers GM (2024). Scale-up of direct-acting antiviral treatment in prisons is both cost-effective and key to hepatitis C virus elimination. Open Forum Infectious Diseases, 11(2), ofad637. 10.1093/ofid/ofad637 [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Spaulding AC, Kennedy SS, Osei J, Sidibeh E, Batina IV, Chhatwal J, Akiyama MJ, & Strick LB (2023). Estimates of hepatitis C seroprevalence and viremia in state prison populations in the United States. The Journal of Infectious Diseases, 228(Supplement_3), S160–S167. https://academic.oup.com/jid/article/228/Supplement_3/S160/7273008?login=false. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. StataCorp. (2015). Stata Statistical Software: Release 14. College Station, TX: StataCorp LP. https://www.stata.com/stata14/. [Google Scholar]
  37. Santo T Jr, et al. (n.d.). Global coverage of interventions for infectious disease and injecting drug use in prisons and other carceral settings. doi: 10.1016/j.drugpo.2025.105069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Stevens G, Alkema L, Black R, Boerma J, Collins GG, & McAllister MC, Ezzati M, Grove J, Hogan D, Hogan M, Horton R, Lawn J, Marusic A, Mathers C, Murray C, Rudan I, Salomon J, Simplson P, Vos T, & Welch V (in press). Guidelines for accurate and transparent health estimates reporting: The GATHER statement. [DOI] [PubMed] [Google Scholar]
  39. Stone J, Fraser H, Young AM, Havens JR, & Vickerman P (2021). Modeling the role of incarceration in HCV transmission and prevention amongst people who inject drugs in rural Kentucky [Article]. International Journal of Drug Policy, 88. 10.1016/j.drugpo.2020.102707. Article 102707. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Stone J, Lim AG, Dore GJ, Borquez A, Geddes L, Gray R, Grebely J, Hajarizadeh B, Iversen J, & Maher L (2023). Prison-based interventions are key to achieving HCV elimination among people who inject drugs in New South Wales, Australia: A modelling study. Liver International, 43(3), 569–579. https://pmc.ncbi.nlm.nih.gov/articles/PMC10308445/pdf/LIV-43-569.pdf. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Stone J, Martin NK, Hickman M, Hutchinson SJ, Aspinall E, Taylor A, Munro A, Dunleavy K, Peters E, & Bramley P (2017). Modelling the impact of incarceration and prison-based hepatitis C virus (HCV) treatment on HCV transmission among people who inject drugs in Scotland. Addiction, 112(7), 1302–1314. https://pmc.ncbi.nlm.nih.gov/articles/PMC5461206/pdf/ADD-112-1302.pdf. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Tavoschi L, Cocco N, Alves Da Costa F, Lloyd AR, & Kinner SA (2024). People living in prison must be included in country monitoring systems to accurately assess HCV elimination progress. The Lancet Gastroenterology & Hepatology, 9(6), 500–501. 10.1016/s2468-1253(24)00075-x [DOI] [PubMed] [Google Scholar]
  43. United Nations. (2025). Sustainable development goals. https://unstats.un.org/sdgs/report/2025.
  44. United Nations Office on Drugs and Crime. (2015). The United Nations standard minimum rules for the treatment of prisoners (Nelson Mandela Rules). https://www.unodc.org/documents/justice-and-prison-reform/Nelson_Mandela_Rules-E-ebook.pdf.
  45. United Nations Office on Drugs and Crime. (2022). World drug report 2022. https://www.unodc.org/unodc/en/data-and-analysis/world-drug-report-2022.html.
  46. van Schalkwyk C, Mahy M, Johnson LF, & Imai-Eaton JW (2024). Updated data and methods for the 2023 UNAIDS HIV estimates. JAIDS Journal of Acquired Immune Deficiency Syndromes, 95(1S), e1–e4. https://pmc.ncbi.nlm.nih.gov/articles/PMC10769173/pdf/qai-95-e1.pdf. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Varan AK, Mercer DW, Stein MS, & Spaulding AC (2014). Hepatitis C seroprevalence among prison inmates since 2001: Still high but declining. Public Health Reports, 129(2), 187–195. https://journals.sagepub.com/doi/10.1177/003335491412900213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Ward Z, Stone J, Bishop C, Ivakin V, Eritsyan K, Deryabina A, Low A, Cepeda J, Kelly SL, Heimer R, Cook R, Altice FL, Litz T, Terlikbayeva A, El-Bassel N, Havarkov D, Fisenka A, Boshnakova A, Klepikov A, … Vickerman P (2022). Costs and impact on HIV transmission of a switch from a criminalisation to a public health approach to injecting drug use in eastern Europe and central Asia: A modelling analysis. The Lancet HIV, 9(1), e42–e53. 10.1016/s2352-3018(21)00274-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Winkelman TNA, Dasrath KC, Young JT, & Kinner SA (2022). Universal health coverage and incarceration. The Lancet Public Health, 7(6), e569–e572. 10.1016/s2468-2667(22)00113-x [DOI] [PubMed] [Google Scholar]
  50. Wirtz AL, Yeh PT, Flath NL, Beyrer C, & Dolan K (2018). HIV and viral hepatitis among imprisoned key populations. Epidemiologic Reviews, 40(1), 12–26. 10.1093/epirev/mxy003 [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. World Health Organization. (2012). WHO, UNODC, UNAIDS technical guide for countries to set targets for universal access to HIV prevention, treatment and care for injecting drug users –2012 revision, https://www.who.int/publications/i/item/978924150437.
  52. World Health Organization. (2015). The end TB strategy, https://www.who.int/publications/i/item/WHO-HTM-TB-2015.19.
  53. World Health Organization. (2016). Combating hepatitis B and C to reach elimination by 2030: advocacy brief, https://www.who.int/publications/i/item/combating-hepatitis-b-and-c-to-reach-elimination-by-2030.
  54. World Health Organization. (2022). Global health sector strategies on, respectively, HIV, viral hepatitis and sexually transmitted infections for the period 2022-2030. World Health Organization. https://www.who.int/publications/i/item/9789240053779. [Google Scholar]
  55. World Health Organization. (2023). Prisons and other places of detention in pandemic preparedness plans across the WHO European Region in the context of the COVID-19 pandemic. Prisons and other places of detention in pandemic preparedness plans across the who european region in the context of the COVID-19 pandemic. https://www.who.int/europe/publications/i/item/WHOEURO-2023-8031-47799-70574. [Google Scholar]
  56. World Health Organization. (2024a). Global hepatitis report 2024: Action for access in low- and middle-income countries. World Health Organization. https://www.who.int/publications/i/item/9789240091672. [Google Scholar]
  57. World Health Organization. (2024b). Global tuberculosis report 2024. World Health Organization. https://www.who.int/publications/i/item/9789240101531. [Google Scholar]
  58. World Health Organization. (2023). Recommended package of interventions for HIV, viral hepatitis and STI prevention, diagnosis, treatment and care for people in prisons and other closed settings (Policy brief), https://www.who.int/publications/i/item/9789240075597.

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