Objective To summarise the extent and quality of evidence on the association between prison cell spatial density (a measure of crowding) and infectious and communicable diseases transmission among prisoners.
Design Systematic review.
Data sources Embase, PubMed, Medline, Scopus, Web of Science, PsycINFO, PsycExtra, ProQuest Databases, ProQuest Dissertations and Theses Global, Index to Legal Periodicals, InformitOnline, Cochrane Library, Criminal Justice Abstracts and ICONDA were searched to 31 December 2018.
Eligibility criteria Studies that reported on the association between prison cell spatial density (measured in square feet or square metres of cell floor area per person) and infectious and communicable diseases in juvenile and adult populations incarcerated in a correctional facility.
Data extraction and synthesis A review protocol was developed in consultation with an advisory panel. Two reviewers independently extracted data and used the Australian National Health and Medical Research Council’s (NHMRC) checklist to critically appraise individual studies. An assessment of the overall body of the evidence was conducted using the NHMRC’s Evidence Scale and Statement Form.
Results A total of 5126 articles were initially identified with seven included in the review from Pakistan (2003), Chile (2016), Nigeria (2012, 2013) and the USA (1980s). Infectious and communicable disease outcomes included pneumococcal disease/acute pneumonia, Mycobacterium tuberculosis, latent tuberculosis infection, infectious skin conditions and contagious disease reporting to the prison clinic. Five articles reported statistically significant positive associations but were countered by associations possibly being explained by chance, bias or confounding factors. Heterogeneity prevented meta-analysis.
Conclusion Overall, the body of evidence provides some support for an association between prison cell special density and infectious and communicable diseases, but care should be taken in the interpretation and transferability of the findings. Future research and policy responses should adequately consider prospective mediating factors implicated in associations between cell spatial density and health effects.
- communicable diseases
- public health
- spatial density
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Strengths and limitations of this study
This is the first systematic review of the association between prison cell spatial density (a measure of crowding) and infectious and communicable diseases.
We used an expert advisory panel to guide review protocols and the Australian National Health and Research Council frameworks to evaluate the strength and quality of the evidence.
Most included studies had incomplete reporting of methodology and findings.
This review was limited by the small number of studies in this area and the heterogeneity of study design.
Globally, the number of prisoners is increasing. Two per cent above world population growth,1 since the year 2000, the world’s prisoner population has grown by approximately 20%, imposing a significant financial burden on society and having profound social and health consequences.2 More than 11 million people are held in penal institutions globally, either as remand (pretrial detainees) or convicted prisoners. Currently, 17 countries in the world have an incarceration rate of more than 400 per 100 000 population in prison. USA is the largest incarcerator, accounting for approximately 20% of the world’s prisoners with an incarceration rate of 655 per 100 000 population.3
A rising prison population without a corresponding expansion of infrastructure has raised health concerns in many countries over prison crowding,3 making prison cell size a key public health issue. For example, in the Australian state of New South Wales (NSW), prison cell size as a public health issue emerged in recent times with the publication of the Inspector of Custodial Services report Full House: the growth of the inmate population in NSW,4 the increase in the prisoner population, and the issue that a significant number of prison cells did not meet public health regulations on the minimum floor area requirements per prisoner. Historically, Corrective Services NSW had been exempted from such regulation provided a range of conditions imposed by the NSW Ministry of Health were met. In 2012, the Ministry required the NSW Department of Justice, Corrective Services to engage an independent (from Corrective Services) group to review the international literature on prison cell crowding and adverse health effects, a review of the international cell size guidelines, and a review of health surveillance data to advise the Ministers for Health and Justice.
Close physical proximity in confined spaces such as in prisons has been reported to be associated with an increased risk of infectious and communicable disease transmission including, Mycobacterium tuberculosis (MTB), scabies, pneumococcus, Meningococcus and influenza.5–7 Rates of infectious diseases in prisons, particularly bloodborne viral infections (HIV and viral hepatitis) and airborne infections such as MTB, are typically higher than in the general community which exacerbates the risk of disease transmission.6 8 9 Additionally, it has been suggested that the close physical proximity in prisons may induce psychological stress or intensify the existing stressful conditions in a prison10 11 leading to alterations in immune and cardiovascular functions.12
The concept of crowding is understood in the academic literature and legislation as a mechanism that impacts adversely on the health and well-being of prisoners. Reports on prison conditions, prison standards and guidelines by international and regional agencies cite prison crowding as major health and human rights concerns impacting on this population.13–17 Left untreated in prison, the risk of disease transmission to family, friends, intimate partners and other community members is likely on leaving prison and returning to general society.18–22
Despite decades of research dedicated to prison conditions and its impact on health, there has been no systematic review to assess the quality of evidence of the association between prison crowding and infectious and communicable disease transmission. A lack of consensus exists on the best way to conceptualise and measure the essential element(s) of crowding with the debate centring on the need for objective versus subjective measurements of crowding.23 24 The latter focuses on the individual experience or perception of crowding using subjective ratings of conditions such as behavioural constraints, stimulus and cognitive overload, privacy, desire to augment space and loss of environmental control.12 25 26 The former, objective measures of prison crowding vary, but commonly revolve around metrics of prisoners per allocation of space to derive a measure of density (table 1).
Some of these measures have been criticised as being amenable to manipulation by prison authorities and thus regarded as invalid measures of prison crowding.24 27 Measures 4–10 (table 1) are regarded as objective measures of social and spatial density. Social density refers to the number of people in a defined area of the prison (eg, the whole facility, wing, dormitory or cell). Spatial density refers to the floor area of a defined area (eg, entire prison or cell) divided by the number of people in that space.11 Social and spatial densities are often dependent on one another, such as when the cell occupancy level increases, this causes a corresponding increase in both social density and spatial density. In this review, the area (measured in square feet or square metres) of the cell per person was selected as the cell crowding measure and is referred to as cell spatial density. This measure was adopted for two reasons. First, the lack of consensus in the academic literature on the conceptualisation and measurement of crowding impressed the need to define cell crowding as an objectively defined environmental factor. Second, an examination of international guidelines on prison conditions and standards over the last half a century has seen a shift towards standards based on cell spatial density (see Simpson, Simpson and Butler, 2016). Cell spatial density as a metric has also entered the legislative domain such as in the Australian Capital Territory’s Human Rights Act 2004 which recommends 8.9 m2 for single cells and 10.7 m2 for double cells.16
To determine the extent and quality of evidence on the association between prison cell crowding and health impacts, Kirby Institute researchers and authors (PLS, MS, AA and TB) were commissioned by the NSW Department of Justice, Correctives Services to conduct a systematic review of studies that analysed the association between prison cell spatial density and prisoner infectious and communicable diseases and mental health and well-being outcomes. In this paper, we present the results of our review of the association between cell spatial density and prisoner infectious and communicable disease effects, expressed in terms of the evidence of this association and the quality of the evidence.
Under the direction of the NSW Ministry of Health and the NSW Department of Justice, an expert advisory panel was formed to guide the review comprising infectious diseases experts, public health professionals, academic staff and custodial administrators. A review protocol was developed following consultations with the advisory panel covering search strategy and selection criteria and study eligibility and appraisal. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses guideline was adopted for the review.28
Search strategy and selection criteria
A search string was agreed to identify articles on the association between cell spatial density and infectious and communicable diseases and mental health outcomes (table 2). For the present paper, articles reporting on infectious and communicable disease outcomes were extracted from the final list of eligible studies. Reviews of the mental health outcome studies are reported elsewhere.29 Infectious and communicable diseases are defined ‘as an illness due to a specific infectious agent or its toxic products that arises through transmission of such agent or products from an infected person, animal or reservoir to a susceptible host, either directly or indirectly through an intermediate plant or animal host, vector or inanimate environment’.30
The scope of the search was limited to the availability of an English abstract and to human subjects. Publication date was not restricted. Studies were excluded if they did not specify cell size or a measurement of cell spatial density, examined only temporary accommodation within custodial settings such as segregation cells, police cells, lockups, prison transport/transfer units and prison clinic accommodation. Studies examining combined living and sleeping space preventing the differentiation of sleeping space were also excluded from the current review.
Fourteen medical, social science and architectural databases were searched: EMBASE (1947–2018), PubMed (≈1800–2018), Medline (1946–2018), Scopus (1976–2018), PsycINFO (1806–2018), PsycExtra (1908–2018), Web of Science (1900–2018), ProQuest Databases (1763–2018), ProQuest Dissertations and Theses Global (1716–2018), Index to Legal Periodicals (1985–2018), Informit Online (1920–2018), Cochrane Library (≈1900–2018), Criminal Justice Abstracts (1910–2018) and ICONDA (1976–2018). Grey literature was also identified from these database searches; and a further search for grey literature was conducted using Google and selected websites including those of the United Nations, International Committee of the Red Cross, Amnesty International, International Centre for Prison Studies, WHO, Campbell Collaboration, the Criminal Justice Reference Service, the US National Library of Medicine and websites of the Australian Inspector of Custodial Services. A number of international experts in the prisoner health area were contacted to inquire as to whether they were aware of additional material of potential interest to the review.
To manage records identified, articles were exported from databases into EndNote V.X7.1. Grey literature from non-database sources were entered into Endnote manually. PDF versions of articles were located and attached to Endnote items.
All publications identified by the search were first screened by two independent teams of two reviewers (PLS, AA and MS, LG). To ensure consistency in the screening process and selection of eligible studies across the teams, titles and abstracts of the first 100 studies were independently reviewed by both teams and discussed as a group to ensure consistency. After achieving a consensus on eligibility for full-text review across both teams, the remaining articles were divided between the two teams of reviewers. Each person within the team independently reviewed their assigned literature, and on finishing, discussed the eligibility outcome with the other team member. In those instances where there was disagreement within a team, both teams met to resolve the issues and decide through consensus if the article was eligible for full-text review.
Articles were excluded from full-text review if the study design did not feature in the Australian National Health and Medical Research Council’s (NHMRC) Hierarchy of Evidence.31 This hierarchy includes systematic reviews of prospective cohort studies (level I evidence), prospective cohort study (level II evidence), ‘all or none’ study (ie, either all or none of the people with the risk factor(s) experienced the outcome of interest) (level III-1 evidence) retrospective cohort study (level III-2 evidence), case–control study (level III-3 evidence), or cross-sectional study or case series (level IV evidence).31 Articles were also excluded if they did not conduct an analysis that examined the relationship between the exposure variable of prison cells accommodating one or more persons with a specified cell spatial density or cell dimensions and an outcome variable of an infectious and/or communicable disease.
Critical appraisal of eligible studies
Critical appraisal of eligible studies involved three stages: (1) data extraction,32 (2) assessment of bias, chance and confounding33 and (3) an aggregated assessment of all studies using the NHMRC FORM Matrix and Evidence Statement to produce a final rating and evidence statement.31
An adapted version of the NHMRC’s standardised data summary table was used to extract data.32 Data extraction tables were prepared and cross-checked by two independent reviewers (PLS and MS). Extracted information included: general study details (citation, study design, length of follow-up, level of evidence and location and setting); study exposure and control descriptions; population characteristics; internal and external validity considerations; and study outcomes and results.
Assessment of bias, chance and confounding was guided by the NHMRC’s checklist to critically appraise aetiology or risk factor studies.33 Checklist items used to guide the assessment of studies included: exposure misclassification, outcome misclassification, selection bias, confounding and chance. Items were assessed on one of two 3-point scales: low (0), medium (1), high (2) risk; or poor (0), fair (1), good (2).
A systematic assessment of the overall body of the evidence was conducted using a modified (for study population relevance) NHMRC FORM Matrix and Evidence Statement covering34: (1) evidence base, (2) consistency of results, (3) population health impact and (4) generalisability. Each component was rated from excellent to poor (online supplementary appendx A) to allow a final overall rating and evidence statement to be derived ranging from ‘A’ to D’: ‘A’ indicating that the body of evidence can be trusted to ‘D’ indicating that the body of evidence is weak, and findings cannot be trusted (online supplementary appendx B).31 The final overall rating and evidence statement were undertaken by one reviewer (PLS) and cross-checked by another (MS).
Following the completion of the review by the team, an expert, independent of the reviewers and advisory panel, peer reviewed the methodology and findings.
Patient and public involvement
Patients and the public were not involved in the review.
After removing duplicate records and newspaper and magazine articles, a total of 5126 records were assessed for eligibility based on publication title and abstract content (figure 1). As a result of this screening, 41 records that reported on infectious and communicable diseases and/or mental health outcomes were identified for full-text review. For the present review, seven publications met the inclusion criteria for infectious and communicable disease outcomes; five articles were published in peer-reviewed journals35–39 and two were reports.27 40 Two articles related to the same research programme on prison crowding27 40; two articles derived from the same study on infectious skin conditions.37 38 Five articles examined the association between cell spatial density and pneumococcal disease or acute pneumonia,35 MTB,36 latent tuberculosis infection (LTBI)39 and infectious skin conditions,37 38 respectively, while two articles reported on communicable illness presentation to the prison clinic.27 39 Three studies were conducted in the USA,27 35 40 two in Nigeria,37 38 one in Chile39 and one in Pakistan (table 3).36 Meta-analysis was not possible due to heterogeneity and incomplete reporting of findings. Measures of effect reported in the six publications varied and included OR, risk ratio, and mean and group differences.
Six studies were cross-sectional in design (level IV aetiology evidence) and one included both a case–control and cohort study design reported in the same article (level III-3/III-2 aetiology evidence). Outcome measures for the pneumococcal disease35 and MTB36 studies were measured using a standardised and reliable approach (tuberculin sensitivity test using the Mantoux method, culture from blood, pleural or spinal fluid specimen and radiograph). LTBI was measured using interferon-gamma release assays (IGRAs) and those found to be IGRA positive underwent direct sputum smear microscopy and chest radiography to diagnose active TB or LTBI.39 Two articles measured infectious skin conditions37 38 ‘in part’ in a standardised and reliable way (clinical examination of the body by a consultant dermatologist and venereologist). The validity and reliability of the outcome measure for the two studies examining communicable illness presentations to a prison clinic27 40 were deemed poor. This is because presentations to a prison clinic may additionally capture other parameters of health service use besides and beyond health effects such as, dispositional characteristics of prisoners and the administration of medical care in the prison.40
Although the sampling framework was described well in most studies, the sampling method was absent in two articles37 38 and response rates were not reported in four articles.27 37 38 40 Self-report measures were used in six studies to determine potential confounders such as underlying medical conditions and demographic information, therefore, recall bias is a possibility. With the exception of the case–control and cohort studies (case–control: n=25 cases/75 controls; cohort: n=46),35 sample sizes were relatively similar across the five cross-sectional studies (n=289–428). Four studies considered or adjusted for confounding factors or effect modifiers in the analyses27 36 39 40; two studies did not,37 38 and it is unclear whether multivariate analysis was conducted in one study.35
Evidence of an association between cell spatial density and infectious and communicable diseases
While the review found mostly consistent evidence that cell spatial density is associated with clinically verifiable infectious and communicable diseases, with five articles reporting a statistically significant association between cell spatial density and infectious and communicable diseases (table 3), all but one of these associations could possibly be explained by chance, study bias or confounding.
In the study which investigated MTB infection in a random sample of 425 male prisoners in five Pakistan prisons, the association between cell spatial density and MTB was reported to be statistically significant (adjusted OR (aOR) 2.6; 95% CI 1.6 to 4.3) after adjusting for age, education, length of incarceration, tobacco use and other variables.36 However, caution is warranted when interpreting this result due to possible exposure and outcome misclassification. That is, the cell spatial density measure was a dichotomised average floor area per person (ie, >5.6 m2 per person and ≤5.6 m2 per person) and thus may be a crude measure. The study does not report on how this measure was determined. Additionally, the 100% response rate to the screening suggests possible coercion to participate in the study that may have affected the reliability of self-report data ta (eg, household income, occupation).
The LTBI study was conducted in 46 prisons in Chile and included 418 prisoner and non-prisoner contacts of 33 active TB cases recruited 12 months following the identification of active TB cases.39 The study found high TB incidence (123.9 per 100 000 prisoners) and high LTBI prevalence (29.4%) among contacts, with LTBI rates significantly higher in prisoners than in non-prisoners (33.2% vs 15.6%). Multivariate analyses showed a significant association between cell spatial density and LTBI (aOR 3.5; 95% CI 1.1 to 11.5) after adjusting for gender, age, illicit drug use, history of corticosteroid use and malnutrition, and length of incarceration. Assessing the extent of potential exposure misclassification was difficult as the spatial density measure used in analysis is not reported (unclear if continuous or categorical variable used). Cell type (ie, multiple-person cells, dormitories) across the different prisons was also not reported.
One US study investigating a pneumococcal disease outbreak35 examined the disease attack rate and its association with cell spatial density. Although more clarity and consistency in reporting of the analysis is needed to properly assess the findings, the results indicate that the attack rate was highest in four-person cells (2.9 m2 per person) compared with the two other cell types described (single cells at 4.2 m2 per person and open dormitories at 2.6 m2 per person). The study also reported that detainees housed in shared and single areas ≥7.4m2 per person (8% of the inmate population) had significantly fewer cases of pneumococcal disease than all other detainees (attack rate: 0 vs 4.7 per 1000 persons; p=0.03). This lower attack rate for detainees housed in shared areas ≥7.4 m2 per person may in part be explained by time spent outside cells as those housed in this area were engaged in work programmes and left their cells to undertake such work. Results were inconsistently reported across cell types with both univariate and aORs reported for the different cell types suggesting that some results were adjusted for and some not.
In the two studies conducted with mostly male (97%) prisoners in Nigeria, the prevalence of infectious and non-infectious skin conditions among prisoners living in single cells (0.9 m2 per person) and dormitories (2.4 m2 per person) was significantly different at 61.7% vs 43.2%37 and 82.9% vs 69.7%.37 38 However, the quality for these studies was assessed as ‘poor’ due to the absence of any multivariate analysis, no details of whether those conducting the physical examinations were blinded to the cell assignments of the prisoners, no response rates or sampling method described, and cell type details derived from self-report questionnaires.
Two other US articles reporting on the association between cell spatial density and illness reporting at the prison clinic were from a research programme spanning approximately 10 years reporting on data collected from 1400 prisoners from six federal prisons.27 40 Illness reporting rates were determined by dividing the number of days a participant was in a cell type (with a specific cell social or spatial density) by the number of visits to a clinic. Not all outcomes were measured at and/or reported for all prison sites, and prisoner population characteristics, sampling methods, response rates and analytical procedures are not consistently reported across and within publications. One article, the Danbury prison study, reported results on illness reporting by contagious status,27 covering: venereal disease; eye, ear, nose, throat infections; cough, cold, influenza; gastrointestinal, stomach problems; skin conditions; virus; chills and fever. However, the lack of detail on the statistical analysis means it is unclear if potential confounders and effect modifiers were adjusted for. Nonetheless, the findings reported a significant difference (although p values were not reported) in contagious illness reporting between those in single occupant cells of 4.5 and/or 5.6 m2 per person (0.03 reports per week) and those in dormitories with a spatial density of 4.6 and/or 5.5 m2 (0.06 reports per week) per person. As the reported cell spatial area range of these two cell types are nearly identical, this is likely to say more about the effect of social density (the number of individuals per cell) or cell type (dormitories vs singles) than it does on cell spatial density.
The second US study from this research examined cell spatial density in single occupancy cells alone in two federal prisons.40 Using multiple linear regression analysis, statistically significant effects were reported in only one of the prisons. However, for contagious illness, the cell spatial density variable was reported as not significant (p=0.88). However, the validity and reliability of the outcome measure used are questionable as the measure may capture other parameters of health service use besides health effects.
Despite the attention that prison crowding receives, this review identified only seven articles examining cell spatial density and infectious and communicable diseases. While the methodological approach adopted in this review ensured that the largest number of peer-reviewed and grey literature publications were identified, some studies and outcomes may have been missed due to publication and outcome reporting bias. Some journals may be more likely to publish studies that report statistically significant results and overlook studies that are not consistent with previously published studies, present ‘negative data’ that disproves the investigators’ hypothesis, as well results that could be interpreted to be of little interest or relevance to their readership.41 Due to the difficulty in locating study protocols, assessment of selective reporting of outcomes was not conducted. Thus, outcome reporting bias may also be present.
The identified seven studies were conducted with mostly male prisoner populations in the USA, Pakistan, Chile and Nigeria. Infectious and communicable disease outcomes reported included pneumococcal disease, MTB, LTBI, skin conditions and prisoner reporting of communicable illness to the prison clinic. Six were cross-sectional studies and one was a combined case–control and cohort study.
Overall, the evidence concerning the association between prison cell spatial density and infectious and communicable disease effects was given a rating of ‘C’ on the NHMRC Evidence Rating Scale (ranging from ‘A’ to ‘D’) indicating that ‘the body of evidence provides some support for an association between cell spatial density and infectious and communicable diseases but care should be taken in the interpretation of the findings.’31 The review found that there was mostly consistent evidence that cell spatial density is associated with clinically verifiable infectious and communicable diseases. Although five of the seven studies reported a statistically significant positive association between cell spatial density and infectious and communicable disease effects (one additional study reporting a significant association regarding the effect of social density or cell type rather than cell spatial density), the quality of the studies was assessed as poor due to risk of exposure/outcome misclassification, bias, chance and/or confounding. However, the Pakistan study on MTB36 and the Chile Study on LTBI39 adjusted for potential confounders and chance.
The cross-sectional design of six of these studies means the ability to assess causality is limited in that they were carried out at one given point in time and provide no indication of the sequence of events. As such, it remains unclear whether cell spatial density exposure preceded or followed the onset of infectious or communicable diseases reported in these studies. However, one study provided some evidence that a number of infections occurred inside prisons following a repeat testing performed at 8 weeks after baseline, suggesting cell spatial density exposure contributed to these new infections.39 The associations and statistical precision observed in the articles suggest the possibility of a ‘slight’ health impact of cell spatial density on prisoners in regard to infectious diseases. However, it is possible that these associations are due to confounding, bias and/or chance. In addition, differences between the populations examined in these studies were apparent in terms of socio-cultural demographics, institutional settings and practices, and the background prevalence of infectious and communicable diseases outcomes in the respective countries (USA, Nigeria, Pakistan, Chile). Studies were also conducted in different decades. These apparent differences restrict the generalisability and transferability of the observed effects to correctional contexts outside the countries where the reviewed studies were conducted.
Implications for researchers and policy-makers
Further research is needed that addresses the confounding, bias and chance elements in studies examined by this review. We recommend that future studies include clinically verifiable health outcomes to ensure outcome misclassification is prevented or minimised and include adequate detail on how cell floor spatial density was determined to facilitate a clear assessment of exposure misclassification.
In most articles reviewed, inadequate attempts were made to adjust for personal characteristics of prisoners and/or prison-related factors as potential confounders. This statement acknowledges that cell spatial density, as an objective condition of crowding, is likely to be embedded in a complex interplay of psychological, social, cultural and institutional factors, and that variations of any health effects cannot be fully understood without their consideration. Thus, future research should seek to collect more extensive data on prospective confounding and mediating factors to examine how such factors interact with cell spatial density and health effects. To assist this, we reviewed the 12 eligible articles identified in this review (7) and the mental health and well-being review (5),29 in addition to key international reports on prisoner conditions, prison crowding and prisoner health to identify what factors might mediate the association between prison cell spatial density and adverse health effects.42 From this review, we recommend that future research on cell spatial density and health effects consider the following factors: (1) personal characteristics of prisoners such as age, education level, gender, ethnicity, underlying medical conditions and health risk behaviours (eg, current intravenous drug use); (2) physical environment measures such as air ventilation and privacy afforded to the prisoner and (3) social and policy environment of prison such as time confined in cell per day, cell allocation policy and practice, health service access, length of incarceration and custody and security classification of prisoner.42
Although the body of evidence assessed indicated cautious support for the association between prison cell spatial density and infectious and communicable diseases, we do not advocate increasing social and spatial density and there is likely to be reasonable grounds for policy responses to address prison crowding in the absence of scientific certainty. As one US Court of Appeals43 ruling stated:
Undoubtedly, certainty is the scientific ideal—to the extent that even science can be certain of its truth. But certainty in the complexities of environmental medicine may be achievable only after the fact, when scientists have the opportunity for leisurely and isolated scrutiny of an entire mechanism. Awaiting certainty will often allow for only reactive, not preventive regulation.
In the absence of scientific certainty, international standards and recommendations provide guidance by way of mitigating prison and prison cell crowding and any potential infectious and communicable disease effects this may bring. The International Red Cross Association (ICPA) handbook on Water, Sanitation, Hygiene and Habitat in Prisons recognises that any technical focus on prisons to address potential adverse health effects, such as cell spatial density, cannot be separated from addressing other factors that mediate prisoner health and well-being.17 Some ICPA guidelines and recommendations are feasible in terms of implementation in the short term to address immediate need (eg, access to healthcare and sanitary facilities and extending time ‘out-of-cell’ to participate in meaningful activities). A public health approach to addressing any adverse health effects associated with prison cell crowding should include prevention strategies ranging from the micro to the macrolevel. The United Nations’ Office of Drugs and Crime Handbook on Strategies to Reduce Overcrowding in Prisons13 acknowledges that to address the health effects associated with crowding, ‘decarceration’ strategies to prevent prison crowding occurring in the first instance is required. Decarceration strategies involve processes that remove people from prisons and prevent them from (re)entering prison. This is likely to be a longer term strategy that will require extensive work involving multiple agencies from different sectors, and changes in political and societal attitudes to incarceration.
We would like to acknowledge advisory panel members Wayne Smith and Benjamin Scalley of the New South Wales Ministry of Health; Garry Forrest and Denise Monkley of the Justice Health and Forensic Mental Health Network; and Janaya Ho of Corrective Services New South Wales. We would also like to acknowledge the independent peer review undertaken by Jeffrey Post and Lorraine Yap and Marina Talevski with respect to their contributions to this review.
Contributors PLS is the guarantor. PLS, MS, AA and TB drafted the manuscript. All authors contributed to the development of the selection criteria. PLS, MS and TB contributed to the risk of bias assessment strategy, data extraction templates and developed the search strategies. All authors read, provided feedback and approved the final manuscript.
Funding Under the direction of the New South Wales Ministry of Health, the New South Wales Department of Justice funded this review. To ensure appropriate management of perceived or potential conflicts of interest, the expert advisory panel that was formed to guide the review comprised diverse stakeholders, including medical practitioners, infectious diseases experts, public health professionals, a custodial administrator and academic staff. Author and custodial administrator LG, who although contributed to the scope of the search criteria and provided feedback and approval of the final manuscript, did not contribute to data extraction, confounder, bias and chance assessment, aggregated evidence appraisal and ratings and the interpretation of findings.
Competing interests There was grant support from the New South Wales Department of Justice during the conduct of the study. There are no financial relationships with any other organisations that might have an interest in the submitted work in the previous 3 years. Author LG is a custodial administrator and could give the appearance of potentially influencing findings. Although LG contributed to the scope of the search criteria and provided feedback and approval of the final manuscript, he did not contribute to data extraction, confounder, bias and chance assessment, aggregated evidence appraisal and ratings and the interpretation of findings. At the time of the review, MS was employed as a research associate of the Kirby Institute, University of New South Wales, Sydney.
Ethics approval Ethics approval was not required. Please see ‘Ethical approval for literature reviews and meta-analyses’ on the UNSW Sydney Research Ethics & Compliance Support Frequently Asked Questions (FAQs) page (https://research.unsw.edu.au/frequently-asked-questions-faqs).
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement No additional data are available.
Patient consent for publication Not required.
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