Driving uptake of missed routine vaccines in adolescent and adult migrants: a prospective observational mixed-methods pilot study of catch-up vaccination in UK general practice

medrxiv(2023)

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Background Migrants in Europe may be vulnerable to vaccine preventable diseases (VPDs) because of missed routine vaccines in childhood in their country of origin and marginalisation from health and vaccine systems. To align with European schedules, migrants should be offered catch-up vaccinations, considering MMR, Td/IPV, and age-appropriate MenACWY and HPV. However, awareness and implementation of catch-up guidelines by primary care staff in the UK is considered to be poor, and there is a lack of research on effective approaches to strengthen the primary-care pathway. Methods We conducted a prospective observational mixed-methods pilot study ‘Vacc on Track’ (May 2021-September 2022) to better understand and define new care pathways to increase catch-up vaccination for adolescent and adult migrants presenting to primary care (≥16 years, born outside Western Europe, North America, Australia, or New Zealand) in two London boroughs. We designed a standardised data collection tool to assess rates of under-vaccination in migrant populations and previous VPDs, which then prompted a referral to practice nurses to deliver catch-up vaccination for those with uncertain or incomplete immunisation status, following UK guidelines. We explored views of practice staff on delivering catch-up vaccination to migrant populations through focus group discussions and engaged migrants in in-depth interviews around approaches to catch-up vaccination. Data were analysed in STATA12 and Microsoft Excel. Results We recruited 57 migrant participants (mean age 41 [SD 7.2] years; 62% female; mean 11.3 [SD 9.1] years in UK) from 18 countries, with minimum 6 months’ follow-up. We did 3 focus groups with 30 practice staff and 39 qualitative in-depth interviews with migrants. Nearly all migrant participants required catch-up vaccination for MMR (86%) and Td/IPV (88%) and most reported not having been previously engaged in UK primary care around catch-up vaccination. 12 (55%) of 22 participants in Site 1 reported a past VPD, including measles and rubella. 53 (93%) of participants were referred for catch-up vaccination. However, although 43 (81%) had at least one dose (at follow-up) of a required vaccine, only 6 (12%) referred for Td/IPV and 33 (64%) of those referred for MMR had completed their required course and vaccination pathway at follow-up, suggesting there were a range of personal and environmental obstacles to migrants accessing vaccinations and all multiple doses of vaccines that need to be better considered. Staff identified seven barriers to delivering catch-up vaccines to migrants, including limited time for appointments and follow-up, language and literacy barriers when taking histories and to encourage vaccination, lack of staff knowledge of current guidelines, inadequate engagement routes, and the absence of primary care targets or incentives. Conclusions Our findings suggest adolescent and adult migrants are an under-vaccinated group and would benefit from being offered catch-up vaccination on arrival to the UK. Primary care is an important setting to deliver catch-up vaccination, but effective pathways are currently lacking, and improving vaccine coverage for key routine vaccines across a broader range of migrant groups will require designated staff champions, training, awareness-raising and financial incentives. Novel ways to deliver vaccinations in community settings should be explored, along with co-designing community-based interventions to raise awareness among these populations of the benefits of life-course immunisation. ### Competing Interest Statement FW is a member of the Vulnerable Migrants Wellbeing Project Advisory Board, led by the University of Birmingham and Doctors of the World and funded by the Nuffield Foundation. All other authors declare no conflicts of interests. The views expressed are those of the author(s) and not necessarily those of the NHS, Department of Health and Social Care, or the NIHR. ### Clinical Trial ISRCTN39246519 ### Funding Statement This study was funded by the National Institute for Health Research (NIHR300072). AFC, LPG and SH are funded by the NIHR (NIHR300072); AFC, FS, and SH are funded by the Academy of Medical Sciences (SBF005\1111), SH acknowledges funding from the Medical Research Council (MRC), La Caixa, Research England, WHO, and Research England. AD, SHE and KL are supported by MRC PhD Studentships (MR/N013638/1, MR/W006677/1). JC is funded by an NIHR-In practice clinical fellowship (NIHR300290). AM is supported by the NIHR Applied Research Collaboration NW London. The funders did not have any direct role in the writing or decision to submit this manuscript for publication. The views expressed in the paper are those of the authors and not necessarily those of the NIHR or Department of Health and Social Care. ### Author Declarations I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained. Yes The details of the IRB/oversight body that provided approval or exemption for the research described are given below: The NHS Health Research Authority Yorkshire and Humber - South Yorkshire Research Ethics Committee gave ethical approval for this work. The St George's University of London Research Ethics Committee gave ethical approval for this work. I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals. Yes I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance). Yes I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable. Yes All data produced in the present study are available upon reasonable request to the authors
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routine vaccines,vaccination,adult migrants,mixed-methods
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