International Journal of
Environmental Research
and Public Health
Review
Vaccination Coverage among Prisoners:
A Systematic Review
Nancy Vicente-Alcalde 1 , Esther Ruescas-Escolano 2 , Zitta Barrella Harboe 3,4
and José Tuells 4,5, *
1
2
3
4
5
*
Penitentiary Center Alicante II, Carretera N-330, Km. 66, 03400 Villena, Spain;
[email protected]
Servicio de Urgencias, Hospital Universitario del Vinalopó-Elche, Calle Tonico Sansano Mora,
03293 Elche, Spain;
[email protected]
Department of Pulmonary and Infectious Diseases, University Hospital of Copenhagen,
North Zealand Dyrehavevej 29, 3400 Hillerød, Denmark;
[email protected]
European Society of Clinical Microbiology and Infectious Diseases, Vaccine Study Group—EVASG,
4010 Basel, Switzerland
Department of Community Nursing, Preventive Medicine and Public Health and History of Science,
University of Alicante, San Vicente del Raspeig, 03690 Alicante, Spain
Correspondence:
[email protected]
Received: 30 August 2020; Accepted: 14 October 2020; Published: 19 October 2020
Abstract:
Prison inmates are highly susceptible for several infectious diseases,
including vaccine-preventable diseases. We conducted a systematic international literature
review on vaccination coverage against hepatitis B virus (HBV), hepatitis A virus (HAV),
combined HAV/HBV, tetanus-diphtheria, influenza, pneumococcal, and combined measles, mumps,
and rubella (MMR) in prison inmates, according to the PRISMA guidelines. The electronic databases
were used Web of Science, MEDLINE, Scopus, and Cinhal. No language or time limit were
applied to the search. We defined vaccination coverage as the proportion of vaccinated prisoners.
There were no limitations in the search strategy regarding time period or language. Of 1079
identified studies, 28 studies were included in the review. In total, 21 reported on HBV vaccine
coverage (range between 16–82%); three on HAV (range between 91–96%); two studies on combined
HAV/HBV (77% in the second dose and 58% in the third); three studies on influenza vaccine
(range between 36–46%), one of pneumococcal vaccine coverage (12%), and one on MMR coverage
(74%). We found that data on vaccination coverage in prison inmates are scarce, heterogeneous,
and do not include all relevant vaccines for this group. Current published literature indicate that
prison inmates are under-immunized, particularly against HBV, influenza, MMR, and pneumococci.
Strengthen immunization programs specifically for this population at risk and improvement of data
record systems may contribute to better health care in prisoners.
Keywords: prisoners; inmates; vaccination coverage; immunization programs
1. Introduction
Today, there are more than 11 million prison inmates around the world [1]. Prison inmates
are at higher risk of acquiring communicable diseases compared to the background population [2].
This increased risk is not only related to factors such as overcrowding and high turnover rates of
prisoners, but also to factors inherent to the inmates, such as higher proportions of individuals with
high-risk behaviors including injecting drug use, sexual risk, and higher prevalence of communicable
diseases among others [3,4].
Many prevalent communicable diseases in prisons can be prevented by vaccination. Even though
several of these vaccines should be administered as a part of routine national immunization programs
Int. J. Environ. Res. Public Health 2020, 17, 7589; doi:10.3390/ijerph17207589
www.mdpi.com/journal/ijerph
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during early childhood, factors such as social marginalization, migration, and coming from areas with
poor access to health care may contribute to a lower immunization rates, with a higher number of
individuals susceptible to vaccine-preventable diseases in prisons around the world [3].
The higher prevalence of communicable diseases among prison inmates may contribute as well to
the risk of infectious diseases in the general population since prisoners are often released after short
periods of incarceration back into society [5–7]. On the other hand, prison inmates belong often to what
are considered hard-to-reach populations (e.g., injecting drug users (IDUs), illegal migrants, and sex
workers), who may often be reluctant to participate in public health programs [8,9]. Thus, the period
of imprisonment can be considered as an opportunity for relevant public health interventions that is
often underutilized [10].
Several international health authorities and organizations including the World Health
Organization [11], the European Centers for Disease Control [12], and the Centers for Disease
Control and Prevention [13] provide a framework with recommendations for the vaccination of prison
inmates. A recent review in prisons settings evaluates the acceptance and cost-effectiveness of vaccines,
although it is limited in European countries [14].
However, local implementation of these recommendations largely varies across countries;
while high-income countries might have specific vaccination guidelines for this group [15–18], these may
be absent or precarious in less industrialized countries. Furthermore, general recommendations may
not be very applicable to the reality of prisons in resource-limited settings [4].
Estimates of vaccine coverage are one of the main tools that can be used to indirectly estimate
the level of immunity against diseases in any given population. Vaccine coverage estimates also
reflect the level of adherence to recommendations for immunization and allow us to tailor preventive
interventions according to the specific immunization gaps in the population. In this systematic review,
we aimed to identify studies on vaccination coverage against several vaccine-preventable diseases in
prison inmates and thus identify areas for possible public health interventions.
2. Materials and Methods
A systematic review of the international literature was carried out following the PRISMA
methodology to compile the existing evidence on vaccination coverage in prisons at international level.
The literature search by two reviewers was performed on 20 February 2020 in the
electronic databases Web of Science, MEDLINE, Scopus, and Cinhal. The search keywords
that were used were: vaccines, vaccination coverage, immunization programs, prisons,
prisoners, and inmates in jail.
In the search string, the operators “OR” and “AND”
were used when relevant, obtaining the following search string: ((((((((“Vaccines”[Mesh])
OR “Vaccines”[Title/Abstract])) OR ((vaccination Coverage[MeSH Terms]) OR vaccination
Coverage[Title/Abstract])) OR ((Immunization Programs[MeSH Terms]) OR Immunization
Programs[Title/Abstract]))) AND ((((((“Prisons”[Title/Abstract]) OR Prisons[MeSH Terms])) OR
((prisoners[MeSH Terms]) OR prisoners[Title/Abstract])) OR “inmate”[Title/Abstract]) OR
“jail”[Title/Abstract])) AND Humans[Mesh]). No language or time limit were applied to the search.
The following steps were carried out in the bibliographic search: analysis of the documents
with extraction of the most relevant information; synthesis of the information that was ordered,
combined and evaluated in a comparative way; finally, the end of the search, where we obtained the
selected articles included in the review (Figure 1).
The articles were selected through the screening of titles, abstracts and by reading the full text
articles, based on predefined inclusion and exclusion criteria based on the PICO (patient, intervention,
comparison, outcome) model. Prisoners were defined as any person admitted to prisons.
Correctional facilities were defined as jails or prisons and custodial settings that function as
prisons, excluding immigrant centers and police detection rooms. The intervention included
any strategy that provided data on HIV status and vaccination against communicable diseases
upon entry and during prison stay (including outbreak situations). The researchers considered
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studies with data from community settings, those comparing the inmate population and community
settings, those that compared inmates with each other, and those that compared between different
risk groups. The following items were considered: people reached by a certain intervention,
people who have completed the vaccination, people with serological status, and vaccination coverage.
Vaccination coverage was defined as the proportion of prisoners who receive the vaccines recommended
by the prison health authorities of their country.
Figure 1. Flowchart selection process (PRISMA).
The selected articles had to provide the vaccination coverage of the prisoners regardless of the
vaccine studied. Systematic reviews, articles that did not study vaccines, those that did not provide
data on vaccination coverage, and those carried out outside the prison setting were excluded.
All search and selection steps were performed was made by three independent researchers
(NVA, ERE, ZBH) and the results were compared and discussed between the three. All selected
registries (including articles that raised doubts) were verified by an investigator with experience in the
field of vaccine research (JT). The outline of the review can be seen in Figure 1.
Data from selected studies were extracted into tables designed by one investigator and reviewed
by a second investigator. The tables contained information on the characteristics of the study: author,
year of publication, country (ISO 3166-2), type of study, vaccine studied, methodology for obtaining
results (serology, questionnaire, database), type of vaccination carried out (systematic, update of the
vaccination program, vaccination of risk groups, or upon admission to prison), vaccination regimen
used during the study, study sample, and vaccination coverage.
3. Results
Of a total of 1079 results obtained in the four databases consulted, 475 articles were excluded
because of duplicates. Subsequently, the remaining 604 articles were reviewed, 576 of which were
excluded when applying the inclusion and exclusion criteria, resulting in a final sample of 28 articles
(Table 1).
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Table 1. Characteristics of included studies.
Author
Year
Country
Design
Vaccine
Metodology
Target Group
Vaccination Schedule
Sample
Coverage
Costumbrado J. et al. [19]
2012
US
Cross-sectional
Hepatitis A+B
N
S
0, 7, 21–30 days,
12 months booster
1633 inmates
(M)
Dose 2: 77%
Dose 3: 58%
Booster dose: 11%
Getaz L. et al. [20]
2016
CH
Cross-sectional
Hepatitis A
SA
A-RG
single dose
116 inmates
(NR)
96%
Bayas J.M. et al. [21]
1993
ES
Cross-sectional
Hepatitis B
SA
S
0 months, 15 days–3 months,
5–12 months
705 inmates
(M)
Dose 1: 31%
Dose 2: 81%
Dose 3: 43%
Clarke J. et al. [22]
2003
US
Cross-sectional
Hepatitis B
N
S
NR
236 inmates (F)
Dose 1: 67%
Dose 2: 48%
Dose 3: 27%
Christensen P.B. et al. [23]
2004
DK/EE
Open label
extension
Hepatitis B
SA
RG
schedule 1: 0, 1, 3 weeks
schedule 2: 0 months, 1 months,
6 months
72 DK
566 EE
(M/F)
DK:
schedule 1: 63%
schedule 2: 20%
EE: schedule 1:
Dose 1: 100%
Dose 2: 92%
Dose 3: 81%
Devine A. et al. [24]
2007
AU
Cross-sectional
Hepatitis B
SA
S-A
0 months, 1 months, 6 months
204 inmates
(F)
Dose 1: 83%
Dose 2: 40%
Dose 3: 16%
Jacomet C. et al. [25]
2015
FR
Cross-sectional
Hepatitis B
SA
S
NR
357 inmates
(M)
Dose 1: 23%
Dose 2: 73%
Dose 3: 40%
Rotily M. et al. [26]
1997
FR
Cross-sectional
Hepatitis B
SA-QS
S
0 months, 1 months, 2 months
391 inmates
(M/F)
Dose 1: 86%
Dose 2: 73%
Dose 3: 60%
Gilbert R.L. et al. [27]
2004
UK
Cross-sectional
Hepatitis B
D
S
>18 years 0, 7, 21 days,
12 months
<18 years 0, 1, 2 months,
12 months
42 prisons
(M/F)
Average rate 17%
Plugge E.H. et al. [28]
2007
UK
Cross-sectional
Hepatitis B
QS
S
NA
613 inmates
(F)
27.3%
Gilles M. et al. [29]
2008
AU
Cross-sectional
Hepatitis B
Influenza
Pneumococcal
D
S
NR
185 inmates
(M)
Hepatitis B 79%
Influenza 36%
Pneumococcal: 11%
Beck CR. et al. [30]
2012
UK
Retrospective
ecological
Hepatitis B
D
S
NR
9173 inmates
(M/F)
22%
Gidding HF. et al. [31]
2015
AU
Cross-sectional
Hepatitis B
QS-SA
S
0 months, 1 months, 2 months
12 months booster
531 inmates
(M/F)
Males: 24.1%
Females: 27.3%
Perrodeau F. et al. [32]
2016
FR
Cross-sectional
Hepatitis B
D
S
2 doses
231 inmates
(M/F)
63%
Taylor JEB. et al. [33]
2019
UK
Cross-sectional
Hepatitis B
QS
S
NR
346 inmates(M/F)
52.30%
Perrett S.E. et al. [34]
2019
UK
Cross-sectional
Hepatitis B
D
S
0 months, 1 months, 3 months
12 months booster
3560 inmates
(M)
2013 28.7%
2017 39.6%
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Table 1. Cont.
Author
Stasi C. et al. [35]
Year
2019
Country
Design
IT
Prospective
study
Vaccine
Hepatitis B
Metodology
SA
Target Group
S-A
Vaccination Schedule
Sample
Coverage
0, 7, 21 days, 12 months
1075 inmates
(M)
82.60%
Hepatitis B
IDUs 46.1%
nIDUs 37.8%
Hepatitis A
IDUs 57.1%
nIDUs 65.9%
Removille N. et al. [36]
2011
LU
Cross-sectional
Hepatitis A+B
QS-SA
S-RG
NR
368 inmates
(M)
Gilbert R.L. et al. [37]
2004
UK
Cross-sectional
Hepatitis A
QS
S-A
single dose
1363 inmates
(M)
91%
Nijhawan A.E. et al. [38]
2010
US
Cross-sectional
Hepatitis A+B
QS
S
NR
100 inmates
(F)
47%
Centre A
42% inmates
37% staff
Centre B
46% inmates
25% staff
Robinson S. et al. [39]
2012
US
Cross-sectional
Influenza
N
S
single dose
Centre A
802 inmates
(M)
184 staff
Centre B
193 inmates
(M)
51 staff
Seib K. et al. [40]
2013
US
Cross-sectional
Influenza
QS
S
single dose
25 correctional
(NR)
Seasonal 70%
H1N1 64%
Walkty A. et al. [41]
2011
CA
Cross-sectional
MMR
N
S
single dose
135 inmates
(M)
187 staff
inmates 74%
staff 36%
Awofeso N. et al. [42]
2001
AU
Cross-sectional
Hepatitis B
SA
RG
0 months, 1 months, 2 months
1037 inmates
(M)
1 cohort 85%
2 cohort 79%
Sutton A.J. et al. [43]
2006
UK
Model-based
Hepatitis B
N
A-RG
NR
NR
(M/F)
5% in 2002
10% in 2003
>50% in 2006
Hope V.D. et al. [44]
2007
UK
Prospective
survey
Hepatitis B
SA
RG
NR
11,393 inmates
(M/F)
1998: 27%
2004: 59%
Glasgow inmates
1993–1999 16–20%
2001–2004 52–59%
Scotland inmates
2008–2009 71%
2013–2014 77%
25%
Palmateer NE.et al. [45]
2018
UK
Cross-sectional
Hepatitis B
SA
RG
0 month, 1 month, 2 months 6
months booster
Glasgow prisoners,
Scotland prisoners
(M/F)
Winter R. et al. [46]
2016
AU
Cross-sectional
Hepatitis B
SA
A
NR
285 inmates
(M/F)
QS: Quest Survey, SA: Serological analysis, D: Database, N: Nothing, S: Systematic/program update, RG: Risk group (IDUs, HIV, HCV), A: Admission. Admission to prison, M: Male,
F: Female, NR: no report.
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The United Kingdom is the country from which most studies on vaccination coverage in prisoners
were retrieved (n = 9) [27,28,30,33,34,37,41,44,45], followed by the United States (n = 5) [19,22,38–40],
Australia (n = 5) [24,29,31,42,46] and France (n = 3) [25,26,32]. To a lesser extent, with one article
from each country, we found Spain [21], Italy [35], Luxembourg [36], Canada [41], Switzerland [20],
and Denmark [23].
We found the following vaccines and vaccine-preventable diseases studied: hepatitis B virus
(HBV), hepatitis A virus (HAV), combined HAV/HBV, influenza, pneumococcal, and combined measles,
mumps, and rubella (MMR) vaccines.
The methods used to investigate the vaccination status of the inmates were: serological testing
(n = 10) [20,21,23–25,35,42,44–46], the use of questionnaires (n = 5) [28,33,37,38,40], the combination of
both (n = 3) [26,31,36], the screening of institutional databases (n = 5) [27,29,30,32,34], or directly by
conducting a survey (n = 5) [19,22,39,41,43].
The aim of the studies was to evaluate systematic vaccination or relevant update of the
adult vaccination program (n = 21) [19,21,22,24–41], to explore the coverage of risk groups
(n = 7) [20,23,36,42–45], including in some studies vaccination status at the time of admission to
prison (n = 6) [20,24,35,37,43,46]. The risk groups studied were IDUs and hepatitis C positive
(HCV) in the HBV studies [23,42–45], and men who have sex with men in a combined HAV/HBV
immunization study [19] and in another HAV immunization study [20]. In 11 studies (39.2%),
exclusively men were included [19,21,25,29,34–37,39,41,42], in 4 studies (14.2%) only women were
included [22,24,28,38], in 11 articles (39.2%) both sexes [23,26,27,30–33,43–46] and in 2 (7.1%) these data
were not recorded [20,40]. The most studied vaccination coverage was HBV (n = 21) [21–36,42–46]
followed by influenza (n = 3) [10,29,39], HAV (n = 3) [20,36,37], combined HAV/HBV vaccine
(n = 2) [19,38], pneumococcal (n = 1) [29] and MMR (n = 1) [41].
Among the 21 studies that focused on HBV vaccine, five studies detailed the reasons why prisoners
were not vaccinated [21–25]. As shown in Table 1, most of the studies sought to update HBV vaccination
programs to achieve improvements in vaccination coverage [21,22,25–34]. The vaccination schedules
used were different, most commonly at 0 (entry point), 1 month, 2 months, and a booster between
6–12 months. The vaccination coverage obtained ranged between 16% [24] and 82.6% [35].
The three studies that provided data on HAV vaccination coverage in prisons are
European [20,36,37]. One study was carried out in the United Kingdom as a result of a community
outbreak of HAV and included 1363 prisoners in a mass vaccination program and reached a vaccination
coverage of 91% [37]. In this study, a similar vaccine coverage (91%) was seen among IDUs [37].
Another study carried out in Luxembourg among 368 prisoners, showed a higher vaccination coverage
in non-IDUs (65.9%) than in IDUs (57.1%) [36]. The Swiss study in 2016 included 116 prisoners (52% of
African origin) who underwent serological testing that demonstrated immunity in 96% of them [20].
In this study, the authors only recommend HAV vaccination for risk-groups and not routinely for
all prisoners.
Two of the studies in our systematic reviewed explored the HAV/HBV combination vaccine [20,38].
The study from Costumbrado et al. [19] published in 2012 focused on a rapid vaccination program in
1633 prisoners (schedule at 0, 7, 21–30 days, and boosted at 12 months) with Twinrix® , in men who
have sex with men. The coverage achieved was 77% for the second dose, 58% for the third and 11% for
the fourth. In the same study, they offered HBV vaccination with the traditional schedule (at 0–1 month
and 4–6 months) to all prisoners, with a coverage of 59% for the second dose and 22% for the third
dose. The study from Nijhawan et al. [38] published in 2010, carried out on 100 female prisoners in the
US, indicated a vaccination coverage for HAV/HBV combined of 47% obtained through surveys.
Gilles and colleagues [29] assessed the coverage of public health interventions in 185 Australian
male and female prisoners by accessing local databases. They author found that even though 52% of
inmates had at least one chronic disease and an indication for immunization, vaccination coverage
for influenza was only 36%, pneumococcal vaccine coverage 12%, and HBV 79%. Robinson et al. [39]
studied influenza vaccination in the context of an influenza outbreak identified in two prisons, which led
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to a mass vaccination campaign of all prisoners. The campaign achieved a vaccination coverage of
42–46% in prisoners and 25–37% in staff. Seib et al. [40] carried out a study using a questionnaire
to evaluate vaccination strategies in 25 prisons; they provided data on the vaccination coverage of
seasonal influenza of 70% and H1N1 of 64%.
There is only one study reporting on mumps in prisoners in the context of an outbreak in Canada
in 2011, in which the MMR vaccine was offered to the entire inmate population. They campaign
achieved 83% of vaccination coverage in prisoners and 36% in staff [41].
4. Discussion
Vaccination coverage in prison inmates has been a subject of limited interest. Most studies
deal with HBV and its direct relationship with a risk group (IDUs or HCV positive inmates) [42–44].
In 2016, the World Health Assembly set as a goal eliminating viral hepatitis by 2030, including a 95%
reduction in new HBV infections through improved vaccine coverage [47]. The CDC recommends
HBV vaccination in prison inmates, considering this population as a high risk-group. The need to
achieve adequate HBV immunization levels in high risk populations (e.g., HCV and HIV positive
individuals, and IDUs) is widely recognized; however, of the 28 studies included, there were only data
from these groups in seven of them. Despite its efficacy and wide availability, HBV vaccine coverage
varies substantially by geographic region and prison category, even in high-income countries [30].
Eight studies from the United Kingdom on HBV vaccination coverage have been published,
and despite policy changes favoring vaccination in prisons in the 1990s, no major advances have
been observed in vaccine coverage [27]. In 2001, new actions were initiated that offered the vaccine
against HBV in a limited number of prisons, to all prisoners upon arrival through an accelerated
program (0, 1 and 3 weeks, with a booster at 12 months). Since the introduction of this intervention,
vaccine coverage has increased: in 2003, the mean HBV vaccine coverage in prisons in England and
Wales was 17% [27]; this increased to 22% in 2010 [30]. Perret et al. published data from 2013 where
they found coverage of 28.7% and 39.6% in 2017, documenting differences in trends by the type
of prison [34].
Regarding the type of interventions, accelerated HBV vaccination programs improved compliance
and may contribute to achieve higher immunization rates, particularly for the high proportion of
inmates serving short sentences [10,21,23,32,35]. In line with this finding, Palmateer et al. described an
association between a higher vaccination coverage in inmates who were imprisoned more than once [45].
The main reasons associated with non-vaccination when carrying out an intervention program
in prisons were the release before the administration of the vaccine, previous or current infection,
having previously received the vaccine, and refusal to vaccination [21–25,33]. In the Italian study
published by Stasi et al., being a foreigner was a risk factor associated with not being vaccinated [35],
and in the publication by Taylor et al., the most common reason for not being vaccinated was that
inmates never had been offered the vaccine or that they never came to complete the guidelines once
they started [33].
In this review, a limited number of studies on vaccination coverage of HVA, influenza,
pneumococcal, and MMR in prisoners were identified and none on diphtheria-tetanus or BCG
were included, similarly to what was published in the review by Madeddu et al. [14] in 2019, focused on
vaccination in prisoners of the European Union/European Economic Area.
Even though HAV vaccination of inmates is not routinely recommended by the CDC, vaccination of
certain risk groups including, among others, individuals with underling chronic liver diseases, HBV,
HCV, and HIV infected individuals, pregnancy, men who have sex with men, and homeless people,
all conditions that may be present among inmates [20,37]. HAV immunity in the study by Getaz et al.
was high (96%), but likely related to the development immunity during childhood in the regions of
origin of inmates. Targeted vaccination according to the area of origin and risk factors for complications
(such as chronic liver disease) would improve the immunity of this group and protect vulnerable
populations at risk of exposure in this precarious environment in cases of an outbreak of HAV [20].
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Few published studies on combined HAV/HBV vaccination were conducted in the US. In a
recent review by Madeddu et al. [14] in 2019, there were five studies on this vaccine that were also
including cost-effectiveness.
Regarding influenza, current guidelines recommend offering seasonal influenza vaccine to
high-risk groups in the general population, including the elderly and chronically ill, and do not
refer to incarcerated persons specifically [48]; except for the Australian study in 2008 [29], which is
a study focusing on influenza vaccination in the post-2009 H1N1 pandemic. In the publication by
Seib et al. [40] the importance of immunizations in prisons is highlighted given the greater rates
of transmission. Despite the experience from the 2009 H1N1 pandemic, influenza vaccines are not
routinely administered to prisoners with risk factors, but in contrast initiated in the context of outbreaks.
The only published study on MMR vaccine coverage summarizes the general conclusions of the
other studies included in the review: data on vaccine coverage in prisoners are scarce, state vaccination
registries are not usually available to verify the vaccination status of prisoners, and inmates are an
accessible risk-group [41]. To this should be added the lack of human resources to administer vaccines,
especially in emergencies or outbreaks [40].
The most common vaccination modality in a prison is the systematic approach, either as a primary
vaccination, as booster or as a post-exposure dose, although massive vaccination programs are also
used to control outbreaks. We must remember that, similarly to the general population, acceptance of
vaccination is voluntary.
Despite international guidelines and the publication of many evidence-based interventions that
demonstrate benefit, a huge gap remains in the introduction and expansion of vaccination programs
in prisons in both low- and high-income countries. Cooperation and coordination between the
penitentiary and public health systems is necessary to guarantee equity in access to prevention services
for the population during incarceration [7].
The extreme sociodemographic heterogeneity of the prisoners, influenced by migration, makes it
difficult to assume that the vaccination coverage of this specific population resembles to what otherwise
found in the general population at any given time. Carrying out an intervention in closed populations
with a large proportion of susceptible individuals exposed to a high risk of contagion, such as the
prison community, allows obtaining optimal vaccination coverage and better results compared to
vaccination carried out in the general population. This represents an opportunity to approach groups
that, under normal conditions, have little contact with the health system. Therefore, it is of special
interest to have data on vaccination coverage in prisons in order to prioritize interventions or reinforce
vaccination schedules according to the intrinsic risk of each prison; reach as many susceptible people
as possible by avoiding vaccinating people who have already been vaccinated or who have already
suffered from the disease.
The limitations of the study are mainly those derived from the heterogeneous methodology of
the selected studies, since vaccine coverage data are not the main objective of some of them and
interpretation of the data was made. This may at least in part explain some discrepancies in the
results, when compared to the review by Madeddu et al. [14] Likewise, the heterogeneity in vaccination
policies, when they exist, makes studies from different geographical locations not very comparable
due to the intrinsic characteristics of each area.
All studies were carried out in industrialized countries, leaving major gaps in the available
knowledge we have from prisons in developing countries.
5. Conclusions
Prisoners are often an ignored and neglected population regarding public health policies at the
international level. Harmonization of recommendations of vaccination strategies in prisons could be a
fundamental step to improve access to health care, and for minimizing economic, organizational and
disease burden in this setting.
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Vaccination strategies varied between countries and were often either targeting a specific
vaccine-preventable disease or being implemented as part of an outbreak response. However,
subsequent evaluations of the implemented interventions were not carried out systematically or are
simply missing. Thus, these approaches may seem arbitrary and we were not able to evaluate whether
specific interventions could have contributed to improve vaccination coverage and the overall health
conditions of prisoners.
Author Contributions: Conceptualization, J.T. and N.V.-A.; methodology, J.T. and N.V.-A.; software, N.V.-A.;
validation, N.V.-A., E.R.-E., and Z.B.H.; formal analysis, N.V.-A., E.R.-E.; investigation, N.V.-A., E.R.-E., and Z.B.H.;
data curation, N.V.-A., E.R.-E.; writing—original draft preparation, N.V.-A., E.R.-E. and J.T.; writing—review
and editing, N.V.-A., E.R.-E., Z.B.H., and J.T. All authors have read and agreed to the published version of
the manuscript.
Funding: This research received no external funding.
Conflicts of Interest: The authors declare no conflict of interest.
References
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
The World Prison Brief. Available online: https://www.prisonstudies.org (accessed on 1 July 2020).
European Centre for Disease Prevention and Control. Systematic Review on Hepatitis B and C Prevalence in the
EU/EEA; European Centre for Disease Prevention and Control: Stockholm, Sweden, 2016.
European Centre for Disease Prevention and Control; European Monitoring Centre for Drugs and Drug
Addiction. Public Health Guidance on Prevention and Control of Blood-Borne Viruses in Prison Settings;
ECDC: Stockholm, Sweden; EMCDDA: Stockholm, Sweden, 2018.
Bick, J.A. Infection Control in Jails and Prisons. Clin. Infect. Dis. 2007, 45, 1047–1055. [CrossRef]
Aebi, M.; Chopin, J.; Tiago, M.M.; Burkardt, C. SPACE I—C; Council of Europe: Strasbourg, France,
2018; Available online: http://wp.unil.ch/space/space-i/prison-stock-on-1st-january/2018-2/ (accessed on
13 May 2020).
World Health Organization.
Health in Prisons:
Fact Sheets for 38 European Countries.
Available online: https://www.euro.who.int/en/health-topics/health-determinants/prisons-and-health/
publications/2019/health-in-prisons-fact-sheets-for-38-european-countries-2019 (accessed on 26 May 2020).
Kamarulzaman, A.; Reid, S.E.; Schwitters, A.; Wiessing, L.; El-Bassel, N.; Dolan, K.A.; Moazen, B.; Wirtz, A.L.;
Verster, A.; Altice, F.L. Prevention of transmission of HIV, hepatitis B virus, hepatitis C virus, and tuberculosis
in prisoners. Lancet 2016, 388, 1115–1126. [CrossRef]
Dolan, K.; Wirtz, A.L.; Moazen, B.; Ndeffo-mbah, M.; Galvani, A.; Kinner, S.A.; Courtney, R.; McKee, M.;
Amon, J.J.; Maher, L.; et al. Global burden of HIV, viral hepatitis, and tuberculosis in prisoners and detainees.
Lancet 2016, 388, 1089–1102. [CrossRef]
Butler, T.; Simpson, M. National Prison Entrants’ Blood-Borne Virus Survey Report 2004, 2007, 2010, 2013,
and 2016; University of NSW: Sydney, Australia; The Kirby Institute: Sydney, Australia, 2017.
Li, H.; Cameron, B.; Douglas, D.; Stapleton, S.; Cheguelman, G.; Butler, T.; Luciani, F.; Lloyd, A.R. Incident
hepatitis B virus infection and immunisation uptake in Australian prison inmates. Vaccine 2020, 38, 3255–3260.
[CrossRef]
World Health Organization. Prisons and Health; World Health Organization: Geneva, Switzerland, 2014.
ECDC. Immunisation 2016. Available online: http://ecdc.europa.eu/en/healthtopics/immunisation/pages/
index.aspx (accessed on 28 May 2020).
Mast, E.E.; Weinbaum, C.M.; Fiore, A.E.; Alter, M.J.; Bell, B.P.; Finelli, L.; Rodewald, L.E.; Douglas, J.M.;
Janssen, R.S.; Ward, J.W. A comprehensive immunization strategy to eliminate transmission of hepatitis
B virus infection in the United States: Recommendations of the Advisory Committee on Immunization
Practices (ACIP) Part II: Immunization of adults. MMWR Morb Mortal Wkly. Rep. Recomm Rep. 2006, 55, 1–33.
Madeddu, G.; Vroling, H.; Oordt-Speets, A.; Babudieri, S.; O’Moore, É.; Noordegraaf, M.V.; Monarca, R.;
Lopalco, P.L.; Hedrich, D.; Tavoschi, L. Vaccinations in prison settings: A systematic review to assess the
situation in EU/EEA countries and in other high-income countries. Vaccine 2019, 37, 4906–4919. [CrossRef]
[PubMed]
Int. J. Environ. Res. Public Health 2020, 17, 7589
15.
16.
17.
18.
19.
20.
21.
22.
23.
24.
25.
26.
27.
28.
29.
30.
31.
32.
33.
34.
10 of 11
National Institute for Health and Care Excellence. Physical Health of People in Prison; National Institute for
Health and Care Excellence: London, UK, 2016.
Health Protection Agency and Department of Health—Offender Health. Prevention of Communicable Disease
and Infection Control in Prisons and Places of Detention. A Manual for Healthcare Workers and Other Staff ;
Health Protection Agency: London, UK, 2011.
Società italiana di Malattie Infettive e Tropicali. Linee Guida Italiane sull’utilizzo dei farmaci antiretrovirali e sulla
gestione diagnostico-clinica delle persone con infezione da HIV-1; Società Italiana di Malattie Infettive e Tropicali:
Prato, Italy, 2016.
Grupo de Trabajo Vacunación en Población Adulta y Grupos de Riesgo de la Ponencia de Programa y
Registro de Vacunaciones. Vacunación en Grupos de Riesgo de Todas las Edades y en Determinadas Situaciones;
Comisión de Salud Pública del Consejo Interterritorial del Sistema Nacional de Salud; Ministerio de Sanidad,
Consumo y Bienestar Social: Madrid, Spain, 2018.
Costumbrado, J.; Stirland, A.; Cox, G.; El-Amin, A.N.; Miranda, A.; Carter, A.; Malek, M. Implementation of
a hepatitis A/B vaccination program using an accelerated schedule among high-risk inmates, Los Angeles
County Jail, 2007–2010. Vaccine 2012, 30, 6878–6882. [CrossRef] [PubMed]
Getaz, L.; Casillas, A.; Motamed, S.; Gaspoz, J.M.; Chappuis, F.; Wolff, H. Hepatitis A immunity and
region-of-origin in a Swiss prison. Int. J. Prison. Health 2016, 12, 98–105. [CrossRef]
Bayas, J.M.; Bruguera, M.; Martin, V.; Vidal, J.; Rodes, J.; Salleras, L.Y. Hepatitis B vaccination in prisons:
The Catalonian experience. Vaccine 1993, 11, 1441–1444. [CrossRef]
Clarke, J.; Schwartzapfel, B.; Pomposelli, J.; Allen, S.; Spaulding, A.; Rich, J.D. Hepatitis B vaccination of
incarcerated women: A pilot program. J. Health Care Poor Underserved 2003, 14, 318–323. [CrossRef]
Christensen, P.B.; Fisker, N.; Krarup, H.B.; Liebert, E.; Jaroslavtsev, N.; Christensen, K.; Georgsen, J. Hepatitis
B vaccination in prison with a 3-week schedule is more efficient than the standard 6-month schedule. Vaccine
2004, 22, 3897–3901. [CrossRef] [PubMed]
Devine, A.; Karvelas, M.; Sundararajan, V. Evaluation of a prison-based hepatitis B immunisation pilot
project. Aust. N. Z. J. Public Health 2007, 31, 127–130. [CrossRef] [PubMed]
Jacomet, C.; Guyot-Lénat, A.; Bonny, C.; Henquell, C.; Rude, M.; Dydymski, S.; Lesturgeon, J.A.; Lambert, C.;
Pereira, B.; Schmidt, J. Addressing the challenges of chronic viral infections and addiction in prisons:
The PRODEPIST study. Eur. J. Public Health 2016, 26, 122–128. [CrossRef] [PubMed]
Rotily, M.; Vernay-Vaisse, C.; Bourlière, M.; Galinier-Pujol, A.; Rousseau, S.; Obadia, Y. HBV and HIV
screening, and hepatitis B immunization programme in the prison of Marseille, France. Int. J. STD AIDS
1997, 8, 753–759. [CrossRef]
Gilbert, R.L.; Costella, A.; Piper, M.; Gill, O.N. Increasing hepatitis B vaccine coverage in prisons in England
and Wales. Commun. Dis. Public Health 2004, 7, 306–311.
Plugge, E.H.; Yudkin, P.L.; Douglas, N. Predictors of hepatitis B vaccination in women prisoners in two
prisons in England. J. Public Health 2007, 29, 429–433. [CrossRef]
Gilles, M.; Swingler, E.; Craven, C.; Larson, A. Prison health and public health responses at a regional prison
in Western Australia. Aust. N. Z. J. Public Health 2008, 32, 549–553. [CrossRef]
Beck, C.R.; Cloke, R.; O’Moore, É.; Puleston, R. Hepatitis B vaccination coverage and uptake in prisons across
England and Wales 2003–2010: A retrospective ecological study. Vaccine 2012, 30, 1965–1971. [CrossRef]
Gidding, H.F.; Mahajan, D.; Reekie, J.; Lloyd, A.R.; Dwyer, D.E.; Butler, T. Hepatitis B immunity in Australia:
A comparison of national and prisoner population serosurveys. Epidemiol. Infect. 2015, 143, 2813–2821.
[CrossRef]
Perrodeau, F.; Pillot-Debelleix, M.; Vergniol, J.; Lemonnier, F.; Receveur, M.C.; Trimoulet, P.; Raymond, I.;
Le Port, G.; Gromb-Monnoyeur, S. Optimizing hepatitis B vaccination in prison. Med. Mal. Infect. 2016,
46, 96–99. [CrossRef]
Taylor, J.; Surey, J.; MacLellan, J.; Francis, M.; Abubakar, I.; Stagg, H.R. Hepatitis B vaccination uptake in
hard-to-reach populations in London: A cross-sectional study. BMC Infect. Dis. 2019, 19, 372. [CrossRef]
[PubMed]
Perrett, S.E.; Cottrell, S.; Shankar, A.G. Hepatitis B vaccine coverage in short and long stay prisons in Wales,
UK 2013–2017 and the impact of the global vaccine shortage. Vaccine 2019, 37, 4872–4876. [CrossRef]
Int. J. Environ. Res. Public Health 2020, 17, 7589
35.
36.
37.
38.
39.
40.
41.
42.
43.
44.
45.
46.
47.
48.
11 of 11
Stasi, C.; Monnini, M.; Cellesi, V.; Salvadori, M.; Marri, D.; Ameglio, M.; Gabbuti, A.; Di Fiandra, T.; Voller, F.;
Silvestri, C. Screening for hepatitis B virus and accelerated vaccination schedule in prison: A pilot multicenter
study. Vaccine 2019, 37, 1412–1417. [CrossRef] [PubMed]
Removille, N.; Origer, A.; Couffignal, S.; Vaillant, M.; Schmit, J.C.; Lair, M.L. A hepatitis A, B, C and HIV
prevalence and risk factor study in ever injecting and non-injecting drug users in Luxembourg associated
with HAV and HBV immunisations. BMC Public Health 2011, 11, 351. [CrossRef] [PubMed]
Gilbert, R.L.; O’Connor, T.; Mathew, S.; Allen, K.; Piper, M.; Gill, O.N. Hepatitis A vaccination–a prison-based
solution for a community-based outbreak? Commun. Dis. Public Health 2004, 7, 289–293.
Nijhawan, A.E.; Salloway, R.; Nunn, A.S.; Poshkus, M.; Clarke, J.G. Preventive healthcare for underserved
women: Results of a prison survey. J. Women’s Health 2010, 19, 17–22. [CrossRef] [PubMed]
Robinson, H.F.; Centers for Disease Control and Prevention (CDC). Influenza outbreaks at two correctional
facilities—Maine, March 2011. MMWR. Morb. Mort. Wkly. Rep. 2012, 61, 229–232.
Seib, K.; Gleason, C.; Richards, J.L.; Chamberlain, A.; Andrews, T.; Watson, L.; Whitney, E.; Hinman, A.R.;
Omer, S.B. Partners in immunization: 2010 survey examining differences among H1N1 vaccine providers in
Washington state. Public Health Rep. 2013, 128, 198–211. [CrossRef]
Walkty, A.; Van Caeseele, P.; Hilderman, T.; Buchan, S.; Weiss, E.; Sloane, M.; Fatoye, B. Mumps in prison:
Description of an outbreak in Manitoba, Canada. Can. J. Public Health 2011, 102, 341–344. [CrossRef]
Awofeso, N.; Levy, M.; Harper, S.; Jones, M.; Hayes, M.; Douglas, J.; Fisher, M.; Folpp, D. Response to HBV
vaccine in relation to vaccine dose and anti-HCV positivity: A New South Wales correctional facilities’ study.
Vaccine 2001, 19, 4245–4248. [CrossRef]
Sutton, A.J.; Gay, N.J.; Edmunds, W.J. Modelling the impact of prison vaccination on hepatitis B transmission
within the injecting drug user population of England and Wales. Vaccine 2006, 24, 2377–2386. [CrossRef]
[PubMed]
Hope, V.D.; Ncube, F.; Hickman, M.; Judd, A.; Parry, J.V. Hepatitis B vaccine uptake among injecting
drug users in England 1998 to 2004: Is the prison vaccination programme driving recent improvements?
J. Viral Hepat. 2007, 14, 653–660. [CrossRef]
Palmateer, N.E.; Goldberg, D.J.; Munro, A.; Taylor, A.; Yeung, A.; Wallace, A.; Mitchell, A.; Shepherd, S.J.;
Gunson, R.N.; Aitken, C.; et al. Association between universal hepatitis B prison vaccination, vaccine uptake
and hepatitis B infection among people who inject drugs. Addiction 2017, 113, 80–90. [CrossRef] [PubMed]
Winter, R.J.; White, B.; Kinner, S.A.; Stoové, M.; Guy, R.; Hellard, M.E. A nurse-led intervention improved
blood-borne virus testing and vaccination in Victorian prisons. Aust. N. Z. J. Public Health 2016, 40, 592–594.
[CrossRef] [PubMed]
World Health Organisation. Global Health Sector Strategy on Viral Hepatitis 2016–2021. 2016.
Available online: https://www.who.int/hepatitis/strategy2016-2021/ghss-hep/en/ (accessed on 3 March 2020).
Who Fact Sheet. Seasonal Influenza. Available online: http://www.who.int/mediacentre/factsheets/fs211/en/
(accessed on 14 July 2020).
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