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      COVID‐19 vaccination among people who inject drugs: Leaving no one behind

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          Abstract

          Timely rollout and widespread uptake of safe and effective vaccines will be necessary to reduce mortality, improve health outcomes, restore societal well‐being and inspire economic recovery from the coronavirus disease (COVID‐19) pandemic. Unprecedented efforts to accelerate vaccine development have resulted in the emergency or expedited approval of several COVID‐19 vaccines [1]. The Australian Government has secured access to both the Pfizer and the University of Oxford/AstraZeneca vaccines and plans to commence a national COVID‐19 vaccine rollout in early 2021. Phase 1a of the program will immunise priority populations, including frontline health‐care workers, quarantine and border staff and aged care and disability care residents and staff [2]. This will be followed by Phase 1b, delivering doses to people aged over 70 years, Aboriginal and Torres Strait Islander people aged over 55 years, younger adults with underlying medical conditions and critical and high‐risk workers [3]. These priority populations are similar to those identified in international vaccination efforts [4]. The Australian Technical Advisory Group on Immunisation (ATAGI) has specified those with an increased risk of developing severe disease or dying from COVID‐19, including people with pre‐existing select medical conditions, as priority populations for immunisation [5]. The ATAGI also noted that communities of low socioeconomic status and those belonging to culturally and linguistically diverse backgrounds are at increased risk of adverse health outcomes from COVID‐19 based on international data [5]. While the Commonwealth has provided in‐principle agreement to prioritise people living with human immunodeficiency virus (HIV) for vaccination during Phases 1a and 1b, the Australian Society for HIV Medicine, along with relevant peak bodies, is also advocating to ensure the strategy appropriately prioritises people living with all blood‐borne viral infections [6]. Although only one in four people infected with SARS Cov2, the virus that causes COVID‐19, have comorbidities, 60–90% of those hospitalised have physical health comorbidities [7]. People reporting problematic use of alcohol and other drugs may represent a high‐risk population in this respect, given their high prevalence of comorbid health conditions [8]. In particular, people who inject drugs (PWID) may be at elevated risk of adverse outcomes from COVID‐19 given their high prevalence of underlying medical conditions, including respiratory and pulmonary disease, chronic liver disease, cardiovascular disease, cerebrovascular disease, diabetes and compromised immunity [9, 10]. Importantly, such conditions may be underdiagnosed in this population [11, 12]. Early data also indicate that COVID‐19 has had a significant impact on patterns of injection drug use and service uptake. Interviews with 884 PWID recruited from Australian capital cities in mid‐2020 showed that 1 in 10 (12%) reported difficulties accessing sterile needles and syringes since COVID‐19 restrictions were introduced [13]. Among 1324 PWID attending Australian needle and syringe programs (NSP) surveyed in late 2020, the same proportion (12%) reported that they had found it more difficult to access NSP. Of those who last injected an opioid (n = 588), 5% reported starting depot buprenorphine, 15% had started or increased the number of takeaway opioid agonist treatment doses, and 26% had accessed take‐home naloxone since the start of the pandemic (Australian NSP Survey 2020, unpublished data). However, compared to the general population, PWID have low rates of vaccine uptake and completion, including for hepatitis B [14]. A recent survey of 872 Australian PWID found that only 24% reported being vaccinated for the 2020 influenza season (i.e. since March 2020) [15]—significantly lower than the 49% of the general population who reported vaccination between January and May 2020 [16]. In relation to hypothetical acceptability of a COVID‐19 vaccine, 57% of a sample of 100 PWID interviewed in Melbourne in December 2020 indicated that they would ‘definitely’ or ‘probably’ get vaccinated were a vaccine available [17]. However, 15% indicated that they would ‘definitely not’ get the vaccine and 20% were undecided. While the most frequently nominated concerns were related to vaccine safety, and anti‐vaccination beliefs were rare, COVID vaccine acceptability was lower than the 77% observed in a recent poll of the general population [18]. These data indicate the need for increased efforts to inform PWID about vaccine efficacy and safety to reduce hesitancy and uncertainty and increase acceptability. The logistics of reaching and vaccinating PWID are not insignificant. While the Australian government is responsible for selecting, purchasing and transporting vaccines and specifying priority populations, state and territory governments are responsible for providing the vaccine delivery workforce and identifying specific vaccination sites. Vaccination locations that have been identified include general practice (GP), GP respiratory clinics, dedicated vaccination clinics, workplace clinics, locations identified by the Aboriginal and Torres Strait Islander Community Controlled Health sector, pharmacies and in‐reach vaccination for aged care facilities and ‘other vulnerable people or targeted populations who cannot access another location’ [5]. It will be important to have a range of effective methods of vaccine rollout targeting PWID and other vulnerable groups, including incarcerated populations. Despite being at higher risk of a wide range of physical and mental health disorders [19], PWID are under‐served in relation to primary health care and are more likely to present late, increasing the risk of significant mortality and morbidity [20, 21]. PWID are also over‐represented among emergency department presentations [22, 23]. A study of 2395 Australian PWID found that emergency departments were the health provider most recently accessed by 14% of respondents [24]. A pilot project that placed a nurse‐led mobile immunisation service at locations accessed by vulnerable populations in Australia, including homeless shelters and an NSP, successfully increased the uptake of influenza vaccine [25]. Along with emergency departments, NSP, homeless shelters/temporary accommodation and prisons provide important access points to PWID; with an appropriately trained and qualified immunisation workforce and resources, including access to anaphylaxis management, these services could potentially be tasked to access and provide opportunistic vaccination to this population. With an estimated 1280 publicly funded alcohol and other drug (AOD) treatment services [26] and 2950 opioid agonist treatment (methadone and buprenorphine) dosing points [27] in Australia, AOD treatment services and dosing points also provide an important touchpoint for COVID‐19 immunisation rollout to vulnerable populations, ideally as sites for vaccination and, at minimum, as settings for education and referral. A recent study found that PWID who reported being vaccinated for influenza in the past year were more likely to be enrolled in opioid agonist treatment [15]. Contact with the health system through AOD treatment is also an important way to communicate health messages designed to increase vaccine confidence. AOD treatment providers, especially those with specialist peer workers, have the infrastructure and experience with low literacy health communications to work with clients to encourage cooperation with public health messages and recommendations, reduce misunderstanding and improve knowledge. Consideration of other evidence‐based strategies, such as conditional cash transfers or contingency management, may also be necessary to ensure that COVID‐19 vaccines reach PWID in a timely manner, especially because effective immunisation will require two doses within a specified time frame. Our randomised trial of per‐dose incentives for hepatitis B vaccine completion found that PWID randomised to the incentive condition were more than three times more likely to complete the series than those randomised to the control condition [28]. The use of incentives to encourage vaccine uptake and completion by PWID has also been adopted by the World Health Organization [29]. People with lived experience of injecting drug use have an essential role to play in informing and driving strategies to maximise vaccination uptake; community‐led networks must be key partners in developing and delivering vaccination systems and strategies [30]. While the strong engagement with scientific research and a commitment to best practice helps to ensure that Australia's services are well placed to interact with the drug‐using community, bolstering community infrastructure and resources to disseminate information and build trust and confidence will be crucial to this engagement. For many vulnerable communities, including PWID, COVID‐19 represents a pandemic on top of one or more epidemics [31], and the constant need for vigilance and risk reduction on multiple fronts is challenging and exhausting. In times of crisis, these communities face challenges such as being unable to access health services or receiving the same quality of health care as others due to high rates of social and economic disadvantage, homelessness and criminalisation, as well as low health literacy and stigma and discrimination from health‐care providers [10]. Consistent with the right to science, there is a need for public access to the knowledge and products of science in this pandemic [32]. Equity of access to interventions to prevent, diagnose and treat COVID‐19 means ensuring that vaccines are accessible and available free of charge to everyone everywhere, especially those who are under‐served and at increased risk of adverse health outcomes [33]. Given strong peer networks, high coverage of treatment and harm reduction interventions [34, 35], and the availability of other access points, which could serve as settings for COVID‐19 immunisation and/or points of contact for vaccine education and referral, Australia is well positioned to ensure PWID are not left behind. Funding AP is supported by a National Health and Medical Research Council Investigator Fellowship (#1174630) and LM is supported by a National Health and Medical Research Council Research Fellowship (#1154839). Conflict of Interest AP has received untied educational grants from Seqirus and Mundipharma for post‐marketing surveillance of opioid medications in Australia. Funding from these organisations has now ceased, funding was for work unrelated to this project, and the funding bodies had no role in study design, analysis and reporting. AD has received grants from Braeburn/Camurus AB to conduct clinical studies with buprenorphine products and travel support to Hunter New England Local Health District, which employs AD. AD is an honorary investigator on an Indivior‐funded study of buprenorphine products and has served as an honorary on an advisory board for Mundipharma. Other authors (JI, LM, OP, JB) have no conflicts.

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          Most cited references32

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          Pathophysiology, Transmission, Diagnosis, and Treatment of Coronavirus Disease 2019 (COVID-19): A Review

          The coronavirus disease 2019 (COVID-19) pandemic, due to the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has caused a worldwide sudden and substantial increase in hospitalizations for pneumonia with multiorgan disease. This review discusses current evidence regarding the pathophysiology, transmission, diagnosis, and management of COVID-19.
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            Contemporary Epidemiology of Chronic Liver Disease and Cirrhosis

            Accurate estimates for the contemporary burden of chronic liver disease (CLD) are vital for setting clinical, research, and policy priorities. We aimed to review the incidence, prevalence, and mortality of CLD and its resulting complications, including cirrhosis and hepatocellular carcinoma (HCC).
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              Is Open Access

              Morbidity and mortality in homeless individuals, prisoners, sex workers, and individuals with substance use disorders in high-income countries: a systematic review and meta-analysis

              Summary Background Inclusion health focuses on people in extremely poor health due to poverty, marginalisation, and multimorbidity. We aimed to review morbidity and mortality data on four overlapping populations who experience considerable social exclusion: homeless populations, individuals with substance use disorders, sex workers, and imprisoned individuals. Methods For this systematic review and meta-analysis, we searched MEDLINE, Embase, and the Cochrane Library for studies published between Jan 1, 2005, and Oct 1, 2015. We included only systematic reviews, meta-analyses, interventional studies, and observational studies that had morbidity and mortality outcomes, were published in English, from high-income countries, and were done in populations with a history of homelessness, imprisonment, sex work, or substance use disorder (excluding cannabis and alcohol use). Studies with only perinatal outcomes and studies of individuals with a specific health condition or those recruited from intensive care or high dependency hospital units were excluded. We screened studies using systematic review software and extracted data from published reports. Primary outcomes were measures of morbidity (prevalence or incidence) and mortality (standardised mortality ratios [SMRs] and mortality rates). Summary estimates were calculated using a random effects model. Findings Our search identified 7946 articles, of which 337 studies were included for analysis. All-cause standardised mortality ratios were significantly increased in 91 (99%) of 92 extracted datapoints and were 11·86 (95% CI 10·42–13·30; I 2=94·1%) in female individuals and 7·88 (7·03–8·74; I 2=99·1%) in men. Summary SMR estimates for the International Classification of Diseases disease categories with two or more included datapoints were highest for deaths due to injury, poisoning, and other external causes, in both men (7·89; 95% CI 6·40–9·37; I 2=98·1%) and women (18·72; 13·73–23·71; I 2=91·5%). Disease prevalence was consistently raised across the following categories: infections (eg, highest reported was 90% for hepatitis C, 67 [65%] of 103 individuals for hepatitis B, and 133 [51%] of 263 individuals for latent tuberculosis infection), mental health (eg, highest reported was 9 [4%] of 227 individuals for schizophrenia), cardiovascular conditions (eg, highest reported was 32 [13%] of 247 individuals for coronary heart disease), and respiratory conditions (eg, highest reported was 9 [26%] of 35 individuals for asthma). Interpretation Our study shows that homeless populations, individuals with substance use disorders, sex workers, and imprisoned individuals experience extreme health inequities across a wide range of health conditions, with the relative effect of exclusion being greater in female individuals than male individuals. The high heterogeneity between studies should be explored further using improved data collection in population subgroups. The extreme health inequity identified demands intensive cross-sectoral policy and service action to prevent exclusion and improve health outcomes in individuals who are already marginalised. Funding Wellcome Trust, National Institute for Health Research, NHS England, NHS Research Scotland Scottish Senior Clinical Fellowship, Medical Research Council, Chief Scientist Office, and the Central and North West London NHS Trust.
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                Author and article information

                Contributors
                lmaher@kirby.unsw.edu.au
                Journal
                Drug Alcohol Rev
                Drug Alcohol Rev
                10.1111/(ISSN)1465-3362
                DAR
                Drug and Alcohol Review
                John Wiley & Sons Australia, Ltd (Melbourne )
                0959-5236
                1465-3362
                01 March 2021
                : 10.1111/dar.13273
                Affiliations
                [ 1 ] Kirby Institute for Infection and Immunity Faculty of Medicine, UNSW Sydney Sydney Australia
                [ 2 ] National Drug and Alcohol Research Centre Faculty of Medicine, UNSW Sydney Sydney Australia
                [ 3 ] Australian Injecting and Illicit Drug Users League Canberra Australia
                [ 4 ] Drug and Alcohol Clinical Services Hunter New England Local Health District Newcastle Australia
                [ 5 ] Faculty of Health University of Newcastle Newcastle Australia
                [ 6 ] Burnet Institute Melbourne Australia
                Author notes
                Author information
                https://orcid.org/0000-0002-0062-7300
                https://orcid.org/0000-0002-5705-2026
                https://orcid.org/0000-0003-2394-5966
                https://orcid.org/0000-0001-6020-6519
                Article
                DAR13273
                10.1111/dar.13273
                8013693
                33650174
                d6cd9553-0164-4dbf-b4ac-e7fce1304754
                © 2021 Australasian Professional Society on Alcohol and other Drugs

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 11 February 2021
                : 11 February 2021
                Page count
                Figures: 0, Tables: 0, Pages: 4, Words: 3081
                Funding
                Funded by: National Health and Medical Research Council Investigator Fellowship
                Award ID: 1174630
                Funded by: National Health and Medical Research Council Research Fellowship
                Award ID: 1154839
                Categories
                Editorial
                Editorials
                Custom metadata
                2.0
                corrected-proof
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.1 mode:remove_FC converted:01.04.2021

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