Topics
Vaccination
Drivers of Vaccine Uptake for Aboriginal and Torres Strait Islander Children to Inform Tailored Strategies: A Qualitative Study Exploring Health Service Provider Perspective
Objectives To identify drivers of routine vaccination for Aboriginal and Torres Strait Islander children, from a health service provider perspective, to increase and maintain uptake.DesignThis qualitative study was designed, analysed and guided by Indigenous data sovereignty and governance principles. Data were analysed using inductive content analysis. Subcategories were refined using Miro (Miro Inc), an online collaboration platform. Aboriginal and Torres Strait Islander worldviews were privileged, with Aboriginal researchers leading data analysis in New South Wales (NSW) and contributing to analysis in the Northern Territory (NT).SettingThe study was conducted in NSW and the NT, Australia, with health service providers from urban, rural and remote settings.ParticipantsIndividual and group interviews were undertaken in person or online between 2 May and 28 August 2024, with 18 health service provider participants in the Hunter New England Local Health District in NSW and 17 health service provider participants in the NT.ResultsWe identified six key themes addressing drivers of vaccination for Aboriginal and Torres Strait Islander children for families (knowledge, attitudes and information sources; decision-making), health staff (workforce roles, responsibilities and relationships) and health services (improving access; health service operations; data for decision-making). Providers recommended strategies to improve uptake.ConclusionsHealth service providers in urban, rural and remote locations in Australia can provide valuable insights to inform tailored strategies to improve declining vaccine coverage for Aboriginal and Torres Strait Islander children, aligned with the priorities of the National Immunisation Strategy 2025–2030.
Bianca F. Middleton, Kristy Crooks, Kylie Taylor, Elizabeth Harwood, Katrina K. Clark, Caitlin Kent, Kelly McCrory, Marita Hefler, Jessica Kaufman, David N. Durrheim, Margie H. Danchin
Short-Term Safety and Adverse Event Risk Profiles for SARS-CoV-2 Booster Vaccine Doses in Australian Adults: A Survey Study
Objective This study quantifies the short-term risk profiles of seven severe acute respiratory syndrome coronavirus 2 virus (SARS-CoV-2) vaccines—Comirnaty Bivalent BA.1, Comirnaty Bivalent BA.4-5, Comirnaty XBB.1.5, Spikevax Bivalent BA.1, Spikevax Bivalent BA.4-5, Spikevax XBB.1.5 and Nuvaxovid—administered as booster doses in Australia. Design This is a survey study using data collected from online surveys sent via AusVaxSafety, the Australian active vaccine safety surveillance system, 3days post-vaccination, soliciting reports of adverse events following vaccination. Participants and Setting Individuals 18years and older who received a SARS-CoV-2 vaccine booster at an AusVaxSafety vaccine surveillance site between 1 January 2023 and 31 August 2024. Main Outcome Measures Bayesian logistic regression was used to estimate risk of reported adverse events, seeking medical advice and impact on daily activities. Results Of 197,476 respondents, 59,089 (29.9%) reported at least one adverse event, of which the most commonly reported symptoms were injection site reaction (23.8% [46,988/197,476]) and fatigue (19.4% [38,352/197,476]). Symptom resolution was reported by 69.9% (41,299/59,089) by day 3 and 5.6% (11,006/197,476) reported any time lost from daily activities. The unadjusted proportion of respondents who sought medical advice was higher in those who received Spikevax XBB.1.5 (1.2% [212/17,551]) than the other vaccines (0.5% [379/69,493] to 0.7% [147/20,271]), but the modelled, adjusted mean risk of medical advice was similar (<2.5%) across subgroups for vaccine brands, co-administered vaccines, medical conditions, age, sex and Indigenous status. The modelled risk of any adverse event at age 40years ranged from 35.2% (95% credible interval [CrI], 32.2%–38.5%) for men who had received Comirnaty XBB.1.5 to 75.5% (95% CrI, 71.9%–78.8%) for women who had received Spikevax XBB.1.5. At age 80years, this risk was lowest across all vaccines, ranging from 12.0% (95% CrI, 11.2%–13.0%) for men who had received Comirnaty BA4-5 to 36.7% (95% CrI, 34.6%–38.7%) for women who had received Spikevax XBB.1.5. Conclusions The results of this study confirm the short-term safety and low impact on daily living of SARS-CoV-2 booster vaccine administration to Australian adults.
Evelyn Tay, Michael Dymock, Lucy Dawes, Lucy Deng, Thuy Nguyen, Alan Leeb, Julie A. Marsh, Nicholas Wood, Kristine Macartney, Thomas L. Snelling
Hospital-Admitted Injection-Related Infections Among Incarcerated People Who Inject Drugs in Australia: A Retrospective Cohort Study
Objectives To characterise the clinical, microbiological and economic burden of hospital-admitted, injection-related infections among incarcerated people who inject drugs. Study Type Retrospective observational cohort study. Setting Secure unit of the Princess Alexandra Hospital, Brisbane, Australia. Participants Adults incarcerated in Queensland prisons who were admitted to hospital with an injection-related infection between 1 July 2019 and 30 June 2023. Main Outcome Measures Types of injection-related infection, microbiological findings, requirement for surgical or radiological source control, hospital length of stay and inpatient healthcare costs. Results There were 321 hospital admissions for injection-related infection among 265 patients, accounting for 282 unique infections. Most patients were male (241; 90.9%), with a mean age of 33years (standard deviation [SD], 7.4years), and 76 (28.7%) identified as First Nations. The most frequent infections were soft tissue infections (77/282; 27.3%), acute hepatitis C (64/282; 22.7%) and cellulitis (43/282; 15.2%). Surgical or radiological source control was required in 95 infections (34.0%), and infectious diseases consultation occurred in 130 infections (46.1%). Among 39 true-positive blood cultures, Staphylococcus aureus was identified in 17 (43.6%), Burkholderia species in 10 (25.6%) and non-tuberculous Mycobacterium species in 3 (7.7%). Among the 218 non-acute hepatitis C infections, 50 (22.9%) were hepatitis C virus (HCV) RNA positive. Overall, HCV RNA was present in 114 of 282 infections (40.4%). The total inflation-adjusted inpatient cost was $8.39 million, with a median cost per infection of $11,602 (interquartile range, $7426–$34,544). Conclusion Injection-related infections among incarcerated people who inject drugs were associated with substantial morbidity and healthcare costs in this large hospital cohort. A wide clinical spectrum was observed, including atypical pathogens, and clinically overt acute hepatitis C requiring hospital admission. These findings describe a significant burden of preventable disease in custodial settings and support the introduction of established primary prevention and harm-reduction interventions in prisons.
Andrew Palmer, Matthew Carter, Jeremy Yeo, Cecilia Shim, Jason Connor, Jeremy Hayllar, Gerald Holtmann, Naomi Moy, Elliott G. Playford, Naomi Runnegar, Paul J. Clark
Impact of the 2025 New South Wales Respiratory Syncytial Virus Prevention Program on Infant Notifications and Hospitalisations: A Population-Based Analysis
The 2025 NSW RSV Prevention Program, which achieved an estimated coverage of 63% maternal vaccination and 18% for infant immunisation, led to more than 40% reduction in RSV notifications and hospitalisations among infants aged younger than 6months.
Janaki Amin, Sally L. Ellis, Christopher Lambeth, Jessica Gugusheff, Christine Selvey
Cervical Cancer Elimination in Australia and the Asia Pacific: Progress and Barriers
Australia has been at the forefront of innovation and implementation of cervical cancer control and is predicted to eliminate cervical cancer by 2035, the first country to achieve elimination using active measures. This is a result of Australia being an early adopter of universal human papillomavirus (HPV) vaccination and early transition to a primary HPV-based cervical screening program. However, to ensure timely and equitable elimination, disparities in coverage among underserved populations must be addressed, and recent declines in vaccination and screening uptake must be reversed. Improved routine data linkages are required to ensure gaps in participation in subpopulations can be identified. Primary health providers have an important role in checking vaccination and screening status and offering vaccination catch-up or screening as appropriate. A universal option of self-collection of an HPV sample for all screen-eligible people has increased acceptability overall, but further innovative and flexible models of service delivery are required to ensure equitable access for all. Australia has also played an important role in cervical cancer control globally and was a co-sponsor of the 2020 World Health Assembly resolution to accelerate the global elimination of cervical cancer as a public health problem. In the Indo-Pacific region, regional frameworks have been developed to advance strategic actions to progress implementation of the global strategy. The Elimination Partnership in the Indo-Pacific for Cervical Cancer (EPICC), a major initiative supported by the Australian Government and the Minderoo Foundation, provides tailored support to countries, considering local needs and priorities.
Susan Yuill, Carol Naidu, Megan Smith, Deborah Bateson, Marion Saville, Boniface Damutalau, Karen Canfell
Effectiveness of COVID‐19 vaccine boosters for reducing COVID‐19 mortality among people aged 65 years or older, Australia, August 2023 – February 2024: a retrospective observational cohort study
Regular vaccine boosting saves lives, particularly of older Australians, who are at greatest risk of death from COVID-19
Bette Liu · Anish Scaria · Sandrine Stepien · Kristine Macartney
“No jab, no pay” pays off
The policy has been effective, albeit with modest closure of coverage gaps, and without substantial backlash
Terence M Nolan
New vaccines herald “era-defining advancements” in RSV prevention
A narrative review published in the Medical Journal of Australia examines the current landscape and future directions of respiratory syncytial virus (RSV) preventives in Australia. RSV is a major cause of acute lower respiratory tract infections, and disproportionally impacts children under the age of 4, who represent 50% of RSV hospitalisations. In November 2023, the long-acting monoclonal antibody nirsevimab was registered with the Therapeutic Goods Administration (TGA) for prevention of RSV-related infections in children under two years of age. Shortly after, in March 2024, a maternal RSV vaccine, Abrysvo, was registered with the TGA for prevention of RSV-related infections in infants under 6 months of age. The narrative review authors describe the availability of these vaccines as “an era defining advancement in RSV prevention.” “Both nirsevimab and Abrysvo have demonstrated substantial potential in reducing hospitalisation rates and mitigating long term health care costs associated with RSV infections in infants,” Sam Barnett of Monash University and co-authors wrote. Western Australia leading the charge at home Western Australia was the first Australian jurisdiction to announce a state-wide immunisation program, rolling out a government funded all-infant RSV immunisation program with nirsevimab in April 2024. A research letter published in the Medical Journal of Australia has examined the impact that the immunisation program had on the WA health care system. “From 2 April 2024, all WA infants born during 1 October 2023 – 30 September 2024 were eligible to receive nirsevimab in primary care services and birthing hospitals, as were Aboriginal children and children with conditions associated with severe RSV disease born during 1 October 2022 – 30 September 2023,” Dr Lauren Bloomfield and co-authors wrote. “With 71% of nirsevimab-eligible infants receiving RSV prophylaxis during April–September 2024, the number of RSV-associated hospitalisations in WA was 57% lower than expected during May–December 2024, equivalent to one hospitalisation averted per 43 infants immunised.” “Further, a contemporary case–control study found that nirsevimab was 86.4% effective in averting RSV-associated hospitalisations of infants in WA. As the cost of an infant RSV hospital admission is estimated to be $12 346 to $13 695, averting 505 admissions is likely to have saved $6.2–6.9 million in hospital costs.” The future of RSV prevention In 2025, Australia has a national RSV prevention program with free maternal vaccination with Abrysvo and targeted infant protection with nirsevimab. Analysing the data from this national program will be pivotal in evaluating and refining the national RSV prevention response going forward. “Program monitoring and evaluation, including cost-effectiveness modelling, from the 2025 RSV [Mother and Infant Protection Program] MIPPs will help guide future decisions regarding the optimal combination of maternal vaccination and nirsevimab,” Barnett and co-authors wrote in their narrative review. “These studies, which will incorporate Australian-specific data, will evaluate factors such as cost-effectiveness, timing, geographic variability and logistical considerations in relation to administration.” Successful implementation of RSV prevention programs will depend on maintaining cost effectiveness, addressing parental acceptance and uptake of the vaccines, and ensuring accessibility for groups at increased risk, such as First Nations children. “An evidence-based approach will be essential to ensure appropriate allocation of resources, tailoring programs to the specific needs of higher risk populations while maximising the economic and health benefits across Australia,” Barnett and co-authors wrote. Read the narrative review in the Medical Journal of Australia. Read the research letter in the Medical Journal of Australia.
Annika Howells