Hostname: page-component-7bb8b95d7b-nptnm Total loading time: 0 Render date: 2024-10-05T05:21:40.489Z Has data issue: false hasContentIssue false

A large outbreak of COVID-19 in a UK prison, October 2020 to April 2021

Published online by Cambridge University Press:  30 May 2022

James P. Adamson*
Affiliation:
Centre for Disease Surveillance and Control, Public Health Wales, Cardiff, Wales, UK UK Field Epidemiology Training Programme, UK Health Security Agency, London, UK
Christopher Smith
Affiliation:
Improvement Cymru, Public Health Wales, Cardiff, Wales, UK
Nicole Pacchiarini
Affiliation:
Pathogen Genomics Unit, Public Health Wales, Cardiff, Wales, UK
Thomas Richard Connor
Affiliation:
Pathogen Genomics Unit, Public Health Wales, Cardiff, Wales, UK Cardiff University School of Biosciences, Cardiff University, Cardiff, Wales, UK
Janet Wallsgrove
Affiliation:
Operations, ‘Prison A’, Wales, UK
Ian Coles
Affiliation:
Operations, ‘Prison A’, Wales, UK
Clare Frost
Affiliation:
Operations, ‘Prison A’, Wales, UK
Angharad Edwards
Affiliation:
Operations, ‘Prison A’, Wales, UK
Jaisi Sinha
Affiliation:
Microbiology, Public Health Wales, Cardiff, Wales, UK
Catherine Moore
Affiliation:
Microbiology, Public Health Wales, Cardiff, Wales, UK
Steph Perrett
Affiliation:
Health Protection Division, Public Health Wales, Cardiff, Wales, UK
Christie Craddock
Affiliation:
Health Protection Division, Public Health Wales, Cardiff, Wales, UK
Clare Sawyer
Affiliation:
Centre for Disease Surveillance and Control, Public Health Wales, Cardiff, Wales, UK UK Field Epidemiology Training Programme, UK Health Security Agency, London, UK
Alison Waldram
Affiliation:
UK Field Epidemiology Training Programme, UK Health Security Agency, London, UK
Alicia Barrasa
Affiliation:
UK Field Epidemiology Training Programme, UK Health Security Agency, London, UK
Daniel Rh. Thomas
Affiliation:
Centre for Disease Surveillance and Control, Public Health Wales, Cardiff, Wales, UK
Philip Daniels
Affiliation:
UK Health Security Agency, London, UK
Heather Lewis
Affiliation:
UK Health Security Agency, London, UK
*
Author for correspondence: James P. Adamson, E-mail: james.adamson2@wales.nhs.uk
Rights & Permissions [Opens in a new window]

Abstract

Prisons are susceptible to outbreaks. Control measures focusing on isolation and cohorting negatively affect wellbeing. We present an outbreak of coronavirus disease 2019 (COVID-19) in a large male prison in Wales, UK, October 2020 to April 2021, and discuss control measures.

We gathered case-information, including demographics, staff-residence postcode, resident cell number, work areas/dates, test results, staff interview dates/notes and resident prison-transfer dates. Epidemiological curves were mapped by prison location. Control measures included isolation (exclusion from work or cell-isolation), cohorting (new admissions and work-area groups), asymptomatic testing (case-finding), removal of communal dining and movement restrictions. Facemask use and enhanced hygiene were already in place. Whole-genome sequencing (WGS) and interviews determined the genetic relationship between cases plausibility of transmission.

Of 453 cases, 53% (n = 242) were staff, most aged 25–34 years (11.5% females, 27.15% males) and symptomatic (64%). Crude attack-rate was higher in staff (29%, 95% CI 26–64%) than in residents (12%, 95% CI 9–15%).

Whole-genome sequencing can help differentiate multiple introductions from person-to-person transmission in prisons. It should be introduced alongside asymptomatic testing as soon as possible to control prison outbreaks. Timely epidemiological investigation, including data visualisation, allowed dynamic risk assessment and proportionate control measures, minimising the reduction in resident welfare.

Type
Original Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
Copyright © Public Health Wales, 2022. Published by Cambridge University Press

Introduction

Prisons are crowded communal settings. During the coronavirus disease 2019 (COVID-19) pandemic, prisons have been highly susceptible to outbreaks, resulting in higher levels of morbidity and mortality in residents and staff than the general population [13]. During the first wave, 7.6 confirmed COVID-19 cases were reported per 1000 prison residents in England and Wales compared with 4.9 in the general population [Reference Braithwaite4]. In the second wave, this rose to 75 cases per 1000 population in prisons, compared to 46 cases per 1000 overall, by the end of December 2020 [Reference Davies and Keeble5]. Control measures focusing on isolation and cohorting were initiated in prisons in Wales [6], reducing mixing and visits. These restrictive regimes can negatively affect physical and mental wellbeing through loss of control [Reference Weiss7Reference Dutheil, Bouillon-Minois and Clinchamps9], consequently reducing cooperation: COVID-19 caused prison unrest and rioting in Europe early in the pandemic [Reference Cingolani10]. This is concerning given prisoners have worse physical and mental health than the general population and are regularly exposed to many health risks including smoking, poor hygiene and weakened immunity [3]. Measures to limit the spread and impact of COVID-19 in Welsh prisons began several weeks before the first prison-cases were seen. On 11 February 2020, Public Health England circulated their first interim guidance for COVID-19 in prisons, which was adopted in Wales. Infection control processes were established in all Welsh prisons, continuing throughout the pandemic in line with further guidance.

In October 2020, Public Health Wales (PHW) was notified of a case of COVID-19 in a resident of a large male prison in South Wales, UK (‘Prison A’), which has approximately 1700 residents and 850 staff. This index case had a history of respiratory illness and was in the hospital at the time of notification. After a negative PCR result on hospital admission, they tested PCR positive during their stay, classifying them as a hospital-acquired case. Two weeks later, an incident management team (IMT) was convened to review 25 more cases (20 residents, 5 staff), epidemiologically linked to the index case. The IMT declared an outbreak and established an outbreak control team (OCT) which managed this outbreak through collaborative decisions, as defined in the outbreak plan for Wales [11].

Methods

The OCT met weekly to discuss case numbers, epidemiology, control measures and operational issues related to the outbreak. The roles and organisations of OCT members are given in Table 1. We describe the epidemiology and control measures implemented for this outbreak.

Table 1. Overview of roles of the OCT membership, October 2020–April 2021

UK FETP, UK Field epidemiology training programme; WGS, whole-genome sequencing; HMPPS, Her Majesty's Prisons and Probation Service.

A possible case was any staff or resident at Prison A on or after 14 October 2020 who had symptoms compatible with COVID-19 (cough and/or fever and/or loss of smell/taste), without a PCR test result. A probable case was a possible case with a positive PCR test result that had not been verified by PHW. A confirmed case was any probable case with a positive PCR test result, which had been verified by PHW. A discarded case was a possible case whose PCR test result was negative.

In accordance to then-current national guidance, symptomatic residents and staff were tested for the presence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA using PCR tests. Asymptomatic screening was introduced in the Admissions unit (A-Block) from December 2020 (see control measures).

We telephoned all staff cases to discuss their movements and contacts prior to testing positive; no resident interviewing was done due to concerns of breaking self-isolation to access a telephone. Instead, intelligence on resident cases was obtained from prison staff. Given the restrictions of movement in place during this outbreak, this information was deemed accurate and reliable by the OCT for contact tracing.

Case data were managed using an Excel line list containing demographic information (age, sex), staff residence postcode, resident cell number, work areas/dates, laboratory results (test dates, result status, laboratory IDs, whole-genome sequencing (WGS) links), interview dates/notes and resident prison-transfer dates. Line list management was performed by a single member of staff, in frequent contact with prison, ‘Test, Trace, Protect’ (TTP – contact tracing) and laboratory colleagues.

Epidemiological investigations

Cases were plotted on an epidemiological curve, then mapped by accommodation block and work location to show frequency and distribution over time (total and last 28 days). Prison A's accommodation is divided into 10 accommodation blocks (Box 1) and other functional areas including ‘Industries’ (where the residents of working age undertake assigned work-activities), laundry, canteen, gym and healthcare.

Box 1. Prison A accommodation description

There are approximately 1700 male residents, consisting of adult and young offenders aged 16 years and over. It has 850 staff, of whom approximately 375 are Prison Custody Officers with the balance made up of support, administration and teaching staff. Prisoners are made up of those on remand, short-term, long-term and life sentences. The residents’ accommodation is as follows:

  • A Block (Admissions): where the majority of new residents stay, known as ‘receptions’. There are four units housing around 95 prisoners each

  • B Block: four separate units housing around 95 prisoners each

  • C Block: learning needs and disability unit housing approximately 75 self-contained prisoners

  • D Block: (drug unit) housing around 95 self-contained prisoners

  • E & G Blocks: The young persons’ unit housing around 60 15–17 year olds, separated from other units with its own gym and education facilities. It has separate staff from other units. Prisoners from this unit do not mix with adult prison units

  • H Block: The safer custody unit housing around 10–20 people in a self-contained unit

  • T Block: comprises six separate units housing around 400 prisoners

  • X Block: separate from main prison with three self-contained wings housing around 350 prisoners. It has its own industries, education and gym facilities. Each unit has its own meal tables, kitchen area and association area

  • The vulnerable prisoners Unit: is comprised of X3 and T6, both separate from each other and other prison units

Epidemiological curves and case location mapping were updated weekly, providing dynamic visual aids for risk assessment. Where cases were present in multiple locations, the overlap was highlighted on the maps. Test date was used for asymptomatic cases and symptom onset date used for symptomatic cases. Crude attack rates were calculated by location using prison records for residents and staff (January 2021: 1693 residents and 832 staff). Variation in attack rates was measured using a two-proportion z test. Finally, case hospitalisation ratios for staff and residents were calculated.

Whole-genome sequencing was carried out by the PHW Pathogens Genomics Unit (PenGU) using the ARTIC protocol for ‘Illumina’ (standard turnaround) or Oxford ‘Nanopore’ (rapid turnaround) to assess the genetic relationship between cases, aid epidemiological investigation and determine control measures. Sequencing was performed only on samples meeting set quality criteria (including a diagnostic result with a cycle threshold value of less than 30). Samples were processed using the ncov2019 ARTIC Nextflow pipeline [Reference Anson12] and were analysed using the CLIMB COVID analysis platform [Reference Nicholls13] making use of the civet [Reference O'Toole14] and MircoReact [Reference Argimón15] tools for analysis and visualisation of the outbreak.

Outbreak control measures

Certain COVID-19 control measures were in place before this outbreak, mandated across the Welsh Prison estate start of the pandemic, and vaccination was introduced for residents during it. Residents were vaccinated by age-cohort by the prison healthcare team; the first vaccination was given in January 2021. Prison staff were offered vaccination in the community by age-cohort, commensurate with the public, which Prison A's management encouraged. The most severe control-measure restrictions (‘level four-regime’, including cell-isolation) could be lifted when positivity rates were low. To confirm this, asymptomatic testing (PCR) was used on a weekly basis, piloted in staff in the vulnerable prisoners unit (VPU) from December 2020 due to the high attack-rate. Testing was extended to staff in the YPU from January 2021 and offered to all staff and residents later that month. Lateral flow device (LFD) testing began in February 2021, becoming available to all staff and residents by the end of March 2021. Details of how and where control measures were applied are described in Table 2.

Table 2. Control measures used at Prison A, before and during outbreak

Results

Between October 2020 and April 2021 (189 days), Prison A reported 453 cases (staff n = 242, 53%; residents n = 211, 47%) (Table 3). Most were symptomatic (64%; staff n = 163, 67%; residents n = 126, 60%) (Table 3) with a mode of 25–34 years for both sexes (11.5% females, 27.15% males) (Fig. 1). Three staff were hospitalised due to their COVID-19 illness; case hospitalisation ratios were 0.36 for staff and 0.06 for residents. One death was linked to this outbreak; a resident with a positive PCR test result more than 28 days but fewer than 90 days before death. Telephone interviews were completed with 99% of staff cases.

Fig. 1. Distribution of cases by age and sex, Prison A, October 2020–April 2021 (N = 453).

Table 3. Overview of case types at Prison A, October 2020–April 2021 (N = 453)

The index case was resident in A-block prior to hospital admission; 12 staff cases worked hospital bed watch shifts for the index case during their infectious period and subsequently worked in A-block, T-block, young persons' unit (YPU) and safer custody unit (SCU). However, there were already staff cases in SCU prior to these staff working back in Prison A.

Crude attack rate was higher in staff (29%, 95% CI 26–64%) than in residents (12%, 95% CI 9–15%). Accommodation-units' specific attack rates ranged from 0% to 26% in residents and 24% to 90% in staff (Table 4). Admissions (A-block), D-block, SCU and YPU experienced the highest overall attack rates (Table 4). An overview of staff cases in other work locations (Table 5) shows the highest attack rates in the testing and mentor teams.

Table 4. Overview of cases by accommodation units, Prison A, January 2021 (N = 332)

– Note: some staff worked in more than one location during this outbreak, so total is greater than 242.

Pop, population; Symp., symptomatic; Asymp., asymptomatic; AR, attack rate.

Table 5. Overview of staff cases by location or team, Prison A (N = 103), October 2020–April 2021

– Note: some staff worked in more than one location during this outbreak. (Some teams have been combined to maintain anonymity).

a Pop., population of staff location of team.

b AR, attack rate.

c Other contractors or short-term staff.

An epidemic curve (Fig. 2), highlighting dates of key control measures, shows that the first half of the outbreak (87 days) comprised 346 (76%) of the cases reported. Of these, 75 (22%) were asymptomatic. During the second half of the outbreak (86 days), 82 of the 106 cases (77%) were asymptomatic. Mapping cases by area of work or residence showed variation in attack rates by area and which cases were associated to more than one location (Fig. 3).

Fig. 2. Epidemiological curve of cases, by case type, Prison A, October 2020–April 2021 (N = 453).

Fig. 3. Mapping of cases, by case type and functional area, Prison A, October 2020–April 2021 (N = 453).

Sequencing of a sample from the index case and one prison staff member on bed watch for the index case revealed that the resident and staff member infections were of different lineages and not closely genetically related.

Subsequent WGS testing showed a third, different phylotype present in the prison; a cluster of seven X-block resident cases employed in the prison's print shop had identical phylotypes. One staff member's WGS result was this same phylotype; follow-up interviews revealed brief, informal contact between these cases whilst moving between locations. By the end of October 2020, 26 cases' test samples had been sequenced (15 residents, 11 staff), identifying 11 different phylotypes. Phylotypes are based upon the position of a sample on the global SARS-CoV-2 phylogenetic tree, and where two cases possess phylotypes that differ, it is possible to exclude those two cases from being a directly linked transmission. Where two cases possess the same phylotype, when combined with other epidemiological data, it is possible to conclude the cases are part of a transmission group. Taking these WGS results with the other epidemiological data, WGS demonstrated that there had been multiple introductions into the prison as well as subsequent person-to-person transmission.

WGS enabled a delineation of person-to-person spread, and helped demonstrate that this had occurred between residents and staff through identical phylotype results by time, place and person. Person-to-person spread was also found in the same way between staff working in the same location with no contact to residents (Fig. 4). Clusters by team, such as in Estates and Facilities Management, were examples of where keeping two metres apart was often difficult when completing essential duties.

Fig. 4. Distribution of staff and resident cases by phylotype address, resident accommodation and staff work location, Prison A, November 2020 (N = 26).

Discussion

We describe a large, long-running outbreak of COVID-19 affecting 211 prison residents and 242 staff. During the second peak in Wales in December 2020, there were 102 resident cases and 101 staff cases in this outbreak, representing a period-incidence of 60.4 cases per 1000 population (residents) and 118.8 cases per 1000 population (staff) respectively. This was higher for staff but lower for prisoners compared to the England and Wales prison average in the same period, highlighting the impact of community incidence on introductions to the prison. The proportion of cases hospitalised was six-times higher in staff than residents, highlighting potential differences in self-perception of disease severity or inequity of access to healthcare.

There were notable differences in infection patterns; YPU cases were mostly staff (38/40; 95%) and both resident infections were asymptomatic, consistent to community infections whereby young people generally experienced milder or no symptoms of COVID-19. Conversely, D-block cases were mostly residents (24/32; 75%) which may highlight difficulties in social-distancing for those with disabilities. The accommodation with the highest attack rates (SCU = 45.5%; YPU = 38.5%; D = 30.5%) were all self-contained units with fewer residents and staff; thus each new case contributed a higher weighting to attack rates than the larger accommodation units.

Where staff had greater exposure to others, attack rates were higher; exemplified by the Mentor and Testing Teams experiencing attack rates of 50%. These roles involved contact with many people and, for the Testing Team, an obvious and repeated risk of contact with infectious asymptomatic cases.

Because some staff-teams were small and others worked in more than one area, attack rates should be interpreted with caution. What is clear is that the 242 staff cases in a stable population of 850 vs. 211 resident cases in a fluctuating population of over 1690 during this outbreak, means the attack rate was far higher in staff than residents (Overall AR = 29% in staff vs. 12% in residents). Attack rates could have been affected by testing policy; staff were able to access free testing in the community as frequently as they chose for the entirety of the outbreak (PCR and then LFD) whereas residents had to report symptoms and request a test. Residents might also have been reluctant to report symptoms knowing this would incur cell-isolation. The skew in male cases reflects the resident population and the majority of staff being male. The higher proportion of staff cases in this outbreak reached statistical significance. One explanation for this could be the long periods of resident cell-isolation and greatly reduced contact opportunities during socialisation times. Furthermore, staff mixed with others outside work, which might not have been detected by this investigation, despite interviewing. Contacts of cases in Wales were required to self-isolate from 1 June 2020. Testing was voluntary and results could be notified by phone or on the NHS COVID-19 app to aid contact tracing. Obviously, residents in Prison A could not use mobile phones so contact tracing relied on intelligence from staff and residents regarding people's movements. Testing of contacts of cases in the community was introduced in Wales on 10 March 2021, towards the end of this outbreak, by which time asymptomatic testing had already been rolled out in Prison A in line with other institutional settings.

Effective outbreak management requires preventative and reactive measures and a collaborative, multi-agency OCT that acts at all policy and operational levels, gathering accurate information and implementing appropriate and timely control measures. The principal control measures instigated by the OCT can be categorised as standard-unilateral measures and targeted-proportional measures. The latter expedited relaxation of other controls imposed based on evidence of reduced infection and transmission.

Cohorting and testing new-admissions reduced their ability to infect others. Asymptomatic screening identified cases who would otherwise have remained an infection risk and highlighted additional efforts required to end level four regime measures safely in specific areas. The timeline of the outbreak and key dates and control measures is shown in detail in Figure 5.

Fig. 5. Timeline of Prison A outbreak, October 2020–April 2021, from notification of first case to declaration of end of outbreak.

This OCT benefitted from dedicated and consistent epidemiological support, line listing management and case distribution mapping. The importance placed on an epidemiological investigation by the OCT chair improved its ability to determine and expedite control measures through a combination of case-location mapping and WGS results. Mapping revealed where further investigation and control measures were required and allowed phased relaxation of restrictions such as cell-isolation. WGS turnaround was two to seven (median = three) days and showed this outbreak was seeded by multiple introductions to the prison but also involved person-to-person transmission. In terms of the initial X-block cluster identified by WGS, the same phylotype was widely distributed in communities in Wales at this time in the pandemic and many staff were resident in these areas, giving rise to a plausible introduction-pathway.

Early or temporary release of prisoners was discussed widely early in the pandemic [Reference Simpson and Butler16], although little evidence suggests this happened at scale anywhere. Cohorting and reduced mixing worked well in this outbreak. However, residents undertake essential services (cooking, laundry, cleaning) resulting in mixing. Prisons have a continuous churn of residents; despite limiting transfers during the peak incidence of COVID-19 in the UK, they were not stopped, resulting in residual risk of infection. Mass screening is effective in identifying cases and limiting the spread of disease [Reference Wilburn17] and was employed here to minimise transmission between groups and identify cases who would have otherwise have remained an infection risk. Scaling-up testing capacity to all staff and residents demonstrated the majority of cases were asymptomatic in the second-half of this outbreak (106 cases in 86 days, 18 symptomatic). If other asymptomatic cases had been identified in this way at the start of this outbreak, its duration might have been reduced. It also highlights inequalities in testing practice and suggests the epidemic curve is not a true reflection of case rates by location, especially in the first-half of this outbreak. The collaborative OCT approach allowed them to discuss, consider, adapt and react within the changing guidance-landscape of the COVID-19 pandemic [Reference Clarke18].

Prisons, by design, control activities and movement but provide little personal space. Compared to the wider community, this complicated the control of COVID-19 spreading in a naïve population. As such, stringent social distancing measures were deemed necessary to control COVID-19 in Prison A. These measures were effective and likely reduced transmission to adjacent shared areas and within cultural groups, as reported in other prison outbreaks [Reference Ruggero19].

Integration of epidemiological techniques with WGS allowed the OCT to make balanced risk assessments with clarity about the direction and intensity of transmission events. As case-rates were reduced in a particular location, relaxation of control measures followed. The social distancing and enhanced hygiene campaigns in place for eight months before this outbreak clarified the impact of the OCT's control measures.

Vaccination is a key control measure strategy for many infectious diseases. There was much debate about vaccination prioritisation for prison residents and staff given the high propensity for transmission. This did not happen in prisons in England and Wales. Modelling has shown that vaccinating everyone living and working in prisons is the most effective strategy for reducing COVID-19 cases, transmission and outbreaks, with an 89% reduction in cases over three years [2] and would yield a similar impact to restrictive and intensive control measures [20]. The Joint Committee on Vaccination and Immunisation (JCVI) considered this twice but it did not support prioritising this population [20, 21]. The combination of high vaccine coverage with other non-pharmaceutical interventions was shown to reduce cumulative infections by up to 54% in another model [Reference Ryckman22]. Uptake figures for resident vaccination is affected by prison churn (amongst other things); COVID-19 vaccinations had been given to the majority of those requesting it in Prison A post outbreak (July and November 2021, Table 6).

Table 6. Resident COVID-19 vaccination status overview, Prison A (July and November 2021)

Our methods had several limitations. Different testing pathways for staff and residents limited the number of samples available for WGS, particularly early in this outbreak. Additional, early WGS intelligence might have identified other transmission routes, especially in terms of community introduction via staff and inter-prison introduction via A-block. However, there was huge pressure on WGS services due to the COVID-19 pandemic, and it wasn't until January 2021 that issues around accessing and sequencing Welsh Pillar 2 samples tested by Lighthouse Laboratories were largely resolved. We only considered activities and movements of staff and residents inside Prison A; it is likely that staff socialised outside Prison A, potentially in contact with asymptomatic cases. Telephone interviews with staff cases investigated plausible vehicles of transmission, such as household contacts, but asymptomatic spread in their communities was not investigated and would have been difficult to measure. Despite the agreement of the OCT members, not interviewing resident cases was an information bias and could have revealed additional information relevant to the investigation and control measures. Lack of ascertainment of resident denominators by accommodation area due to prison churn meant comparing staff and resident attack rates was not regularly possible.

We conclude that sufficient epidemiological capacity to thoroughly investigate outbreaks allows OCTs to assess changes and implement appropriate control measures. Traditional epidemiological investigations can be augmented with WGS to determine the phylogeny of infections and inform the epidemiological plausibility of community vs. prison transmission. Analysis of epidemiological investigation findings revealed that admissions-block was a persistent source of infections; particular attention should be given to admissions screening. Case-distribution location mapping tracked infection progression, visualising data and allowing easy interpretation to make timely control measure responses. Mapping was equally informative for deciding when to relax control measures safely to improve resident welfare.

Limiting staff movements to one area negatively affected prison operational capacity as more staff became absent due to infection, but helped reduce further transmission. Frequent communication of COVID-19 infection control measures to all staff and residents built an inclusive culture of behaviour applicable to all staff and residents.

COVID-19 is likely to be in circulation for several years. Given the vulnerability of prison residents to infectious diseases, the prioritisation of prisoners in COVID-19 vaccination campaigns should be considered.

Recommendations

  1. (1) Sufficient capacity for thorough epidemiological investigations is important for providing timely information for the OCT to determine actions

  2. (2) Data visualisation through case-distribution location mapping improves the speed of interpretation, aiding risk assessment to determine control measures

  3. (3) WGS is a powerful tool in assessing the plausibility of transmission chains and should be introduced as soon as possible in prison outbreak investigations where quick turnaround times are feasible

  4. (4) Cohorting, particularly in admissions blocks, is effective in limiting the transmission of COVID-19 in prisons

  5. (5) Asymptomatic testing is highly effective in identifying cases and can limit transmission events by having them isolate

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/S0950268822000991.

Acknowledgements

None.

Financial support

No additional funding was received to undertake the outbreak investigation; outbreaks represent part of the core duties of the Public Health Wales Health Protection Division. The sequencing of samples was funded by Welsh Government and as part of the COVID-19 Genomics UK Consortium (COG-UK). COG-UK is supported by funding from the Medical Research Council (MRC) part of UK Research & Innovation (UKRI), the National Institute of Health Research (NIHR) [grant code: MC_PC_19027], and Genome Research Limited, operating as the Wellcome Sanger Institute. Analysis of genome-sequenced samples was performed using the MRC CLIMB platform [grant reference MR/L015080/1].

Conflict of interest

None.

Ethical standards

Ethical oversight of the project was provided by the PHW Research and Development Division. As this work was carried out as part of the health protection response to a public health emergency in Wales, using routinely collected surveillance data, PHW Research and Development Division advised that NHS research ethics approval was not required. The use of named patient data in the investigation of communicable disease outbreaks and surveillance of notifiable disease is permitted under PHW's Establishment Order. Data were held and processed under PHW's information governance arrangements, in compliance with the Data Protection Act, Caldicott Principles and PHW guidance on the release of small numbers. No data identifying protected characteristics of an individual were released outside of the OCT.

Data availability statement

The data used in this investigation contain personal identifiable information of a vulnerable population. Anonymised information, including that contained in the supplementary information, required to reproduce these results is available from the corresponding author on reasonable request.

References

World Health Organization (2020) COVID-19 Dashboard. Geneva: World Health Organization. Published online. Available at https://covid19.who.int (Accessed 16 May 2021.Google Scholar
UK Government (2021) Scientific Advisory Group for Emergencies Transmission Group. COVID-19 Transmission in Prison Settings. London: UK Government. Published online March 2021. Available at https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/979807/S1166_EMG_transmission_in_prisons.pdf.Google Scholar
Braithwaite, I et al. (2021) High COVID-19 death rates in prisons in England and Wales, and the need for early vaccination. The Lancet Respiratory Medicine 9, 569570. Published online 16 March 2021. https://doi.org/10.1016/S2213-2600(21)00137-5.CrossRefGoogle ScholarPubMed
Davies, M and Keeble, E (2021) The Rising Tide of Covid-19 Infections in our Overcrowded Prisons. London: The Nuffield Trust. Published online 19 January 2021. Available at https://www.nuffieldtrust.org.uk/resource/chart-of-the-week-the-rising-tide-of-covid-19-infections-in-england-and-wales-s-overcrowded-prisons.Google Scholar
UK Government (2021) Guidance Preventing and Controlling Outbreaks of COVID-19 in Prisons and Places of Detention. London: UK Government. Published online 13 September 2021. Available at https://www.gov.uk/government/publications/covid-19-prisons-and-other-prescribed-places-of-detention-guidance/covid-19-prisons-and-other-prescribed-places-of-detention-guidance.Google Scholar
Weiss, JM (1970) Somatic effects of predictable and unpredictable shock. Journal of Psychosomatic Medicine 32, 397408.CrossRefGoogle ScholarPubMed
Liebrenz, M et al. (2020) Caring for persons in detention suffering with mental illness during the COVID-19 outbreak. Journal of Forensic Science International: Mind and Law 1, 100013. Published online 26 February 2020. doi: 10.1016/j.fsiml.2020.100013.Google ScholarPubMed
Dutheil, F, Bouillon-Minois, J-B and Clinchamps, M (2020) COVID-19: a prison-breaker? Canadian Journal of Public Health 111, 480481. Published online 29 June 2020. doi: https://doi.org/10.17269/s41997-020-00359-6.CrossRefGoogle ScholarPubMed
Cingolani, M et al. (2021) The COVID-19 epidemic and the prison system in Italy. Journal of Corrective Health Care 27, 37. Published online March 2021.CrossRefGoogle ScholarPubMed
Public Health Wales (2020) The Communicable Disease Outbreak Plan for Wales. Cardiff: Public Health Wales. Published online 10 July 2020. Available at https://phw.nhs.wales/topics/latest-information-on-novel-coronavirus-covid-19/the-communicable-disease-outbreak-plan-for-wales/ (Accessed 13 September 2021.Google Scholar
Anson, M et al. (2021) https://github.com/connor-lab/ncov2019-artic-nf (Accessed 13 September 2021.Google Scholar
Nicholls, SM et al. (2021) CLIMB-COVID: continuous integration supporting decentralised sequencing for SARS-CoV-2 genomic surveillance. Journal of Genome Biology 22, 121. Published online 1 July 2021. https://doi.org/10.1186/s13059-021-02395-y.Google ScholarPubMed
O'Toole, AN et al. (2021) Genomics-informed outbreak investigations of SARS-CoV-2 using civet. MedRXiv - Preprint. Published online 14 December 2021. https://www.medrxiv.org/content/10.1101/2021.12.13.21267267v1.Google Scholar
Argimón, S et al. (2016) Microreact: visualizing and sharing data for genomic epidemiology and phylogeography. Journal of Microbial Genomics 2, e000093. Published online 30 November 2016. https://doi.org/10.1099/mgen.0.000093.Google ScholarPubMed
Simpson, PL and Butler, TG (2020) COVID-19, prison crowding, and release policies. British Medical Journal 369, 1551. Published online 20 April 2020. doi: 10.1136/bmj.m1551.CrossRefGoogle ScholarPubMed
Wilburn, J et al. (2020) COVID-19 within a large UK prison with a high number of vulnerable adults, March to June 2020: an outbreak investigation and screening event. International Journal of Infectious Diseases 104, 349353. Published online 16 January 2021. doi: 10.1016/j.ijid.2021.01.027.CrossRefGoogle Scholar
Clarke, M et al. (2020) Establishing prison-led contact tracing to prevent outbreaks of COVID-19 in prisons in Ireland. Journal of Public Health 42, 519524. Published online 22 June 2020.CrossRefGoogle ScholarPubMed
Ruggero, G et al. (2021) COVID-19 outbreak investigation and response in a penitentiary setting: the experience of a prison in Italy, February to April 2020. Euro Surveillance 26, 2001385. Published online 8 February 2021. https://doi.org/10.2807/1560-7917.ES.2021.26.38.2001385.Google Scholar
UK Government (2021) Scientific Advisory Group for Emergencies: COVID-19 Response Meeting 84 Minutes. London: UK Government. Published online 9 April 2021. Available at https://www.gov.uk/government/publications/sage-84-minutes-coronavirus-covid-19-response-25-march-2021/sage-84-minutes-coronavirus-covid-19-response-25-march-2021.Google Scholar
UK Government (2021) Department of Health and Social Care. Letter from the JCVI to the Health and Social Care Secretary on Further Considerations on Phase 1 Advice. London: UK Government. Published online 1 March 2021. Available at www.gov.uk/government/publications/letter-from-the-health-and-social-caresecretary-on-covid-19-vaccination-phase-1-advice/letter-from-the-jcvi-to-the-healthand-social-care-secretary-on-further-considerations-on-phase-1-advice-1-march2021.Google Scholar
Ryckman, T et al. (2021) Outbreaks of COVID-19 variants in US prisons: a mathematical modelling analysis of vaccination and reopening policies. The Lancet Public Health 6, 760770. Published online 1 October 2021. https://doi.org/10.1016/S2468-2667(21)00162-6.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Overview of roles of the OCT membership, October 2020–April 2021

Figure 1

Table 2. Control measures used at Prison A, before and during outbreak

Figure 2

Fig. 1. Distribution of cases by age and sex, Prison A, October 2020–April 2021 (N = 453).

Figure 3

Table 3. Overview of case types at Prison A, October 2020–April 2021 (N = 453)

Figure 4

Table 4. Overview of cases by accommodation units, Prison A, January 2021 (N = 332)

Figure 5

Table 5. Overview of staff cases by location or team, Prison A (N = 103), October 2020–April 2021

Figure 6

Fig. 2. Epidemiological curve of cases, by case type, Prison A, October 2020–April 2021 (N = 453).

Figure 7

Fig. 3. Mapping of cases, by case type and functional area, Prison A, October 2020–April 2021 (N = 453).

Figure 8

Fig. 4. Distribution of staff and resident cases by phylotype address, resident accommodation and staff work location, Prison A, November 2020 (N = 26).

Figure 9

Fig. 5. Timeline of Prison A outbreak, October 2020–April 2021, from notification of first case to declaration of end of outbreak.

Figure 10

Table 6. Resident COVID-19 vaccination status overview, Prison A (July and November 2021)

Supplementary material: File

Adamson et al. supplementary material

Adamson et al. supplementary material 1

Download Adamson et al. supplementary material(File)
File 31 KB
Supplementary material: File

Adamson et al. supplementary material

Adamson et al. supplementary material 2
Download Adamson et al. supplementary material(File)
File 14.8 KB