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Nirsevimab immunisation of infants and respiratory syncytial virus (RSV)‐associated hospitalisations, Western Australia, 2024: a population‐based analysis

Lauren E Bloomfield, Nevada V Pingault, Rachel E Foong, Sarah French, Jo‐Anne Morgan, Ushma Wadia, Hannah C Moore, Christopher C Blyth, Peter C Richmond, Paul K Armstrong and Paul V Effler
Med J Aust || doi: 10.5694/mja2.52655
Published online: 26 May 2025

Respiratory syncytial virus (RSV) is a major cause of acute lower respiratory tract infections in young children; it is the leading cause in Australia of hospitalisations during the first year of life.1,2 Nirsevimab (trade name Beyfortus), a monoclonal antibody that binds RSV, provides protection against RSV‐associated lower respiratory tract disease.3,4 On 24 November 2023, nirsevimab was registered in Australia for preventing RSV lower respiratory tract disease in neonates and infants born during or entering their first RSV season, and children up to 24 months of age who remain vulnerable to severe RSV disease through their second RSV season.5

On 4 March 2024, the Western Australian government committed $11 million to the most age‐inclusive universal nirsevimab program in Australia.6 In most WA regions, RSV transmission is highly seasonal, typically starting in May and ending in October.7 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,6 as were Aboriginal children and children with conditions associated with severe RSV disease born during 1 October 2022 – 30 September 2023.6,8

We assessed the association between nirsevimab coverage of infants and the number of RSV‐associated hospitalisations in a population‐based cohort. We obtained the number of births in WA during 2022–2024 from the WA Registry of Births, Deaths and Marriages;9 we obtained the numbers of children under one year of age or aged 1–2 years who received nirsevimab during 2 April – 30 September 2024 from the Australian Immunisation Register10 on 6 January 2025. The catch‐up cohort included infants born before 1 May 2024; the newborn cohort included infants born on or after 1 May 2024.

Laboratory‐confirmed RSV infections and associated hospitalisations became notifiable in WA under the Public Health Act 2016 on 16 July 2021.11 We extracted data for all notified RSV infections in children under five years of age with dates of specimen collection during 2022–2024 from the WA Notifiable Infectious Disease Database (WANIDD) on 6 January 2025. Patient administration data systems are matched weekly with WANIDD using birthdate, surname, and first name initial. An admission was deemed an RSV‐associated hospitalisation if a positive RSV test result was recorded for a specimen collected between ten days before and seven days after an admission to hospital. We restricted the quantitative comparison of RSV‐associated hospitalisations by year to weeks 18–52 (May to December) to reduce bias caused by unusually high number of RSV infections in early 2022 following the easing of coronavirus disease 2019 pandemic control measures. The mean number of RSV‐associated hospitalisations in 2022 and 2023 was defined as the expected number for 2024.

The WA Chief Health Officer has approved the publication of aggregated notifiable disease surveillance data, and our analysis was determined to pose no risks requiring submission to a human research ethics committee, in accordance with the Public and Aboriginal Health Directorate Interim Policy on Non‐Research and Review and Approval of Lower Risk Research (unpublished WA Health document), on 26 August 2024.

The annual number of births in WA was stable during 2022–2024 (2022: 31 709; 2023: 32 282; 2024: 30 825). Of 30 920 eligible infants, 21 922 (71%) received nirsevimab during April–September 2024: 12 195 of 18 654 (65%) in the catch‐up cohort and 9727 of 12 266 (79%) in the newborn cohort. Of 30 657 children aged 1–2 years, 1221 (4%) received nirsevimab. The cumulative number of RSV‐associated hospitalisations of infants under one year of age was markedly lower in 2024 than in 2022 and 2023, but not that of children aged one to less than five years (Box 1).

The numbers of RSV‐associated hospitalisations by age group were similar during the winter RSV seasons of 2022 and 2023, and declined with age, as is usual. In 2024, the number of RSV‐associated hospitalisations of infants under one year of age was 505 lower than expected (57% lower); the numbers of hospitalisations in older age groups were similar to those in 2022 and 2023 (Box 2).

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. The number of hospitalisations of children aged one to less than five years was not affected, suggesting that the marked decline in hospitalisations of infants was not attributable to an aberrantly light RSV season in 2024. Further, a contemporary case–control study found that nirsevimab was 86.4% effective in averting RSV‐associated hospitalisations of infants in WA.12 As the cost of an infant RSV hospital admission is estimated to be $12 346 to $13 695,2,13 averting 505 admissions is likely to have saved $6.2–6.9 million in hospital costs.

Our assessment has limitations. First, our ecological evaluation cannot establish causality. Second, only two years of baseline data were available. Third, cost data based on one study only may not be robust. Finally, our case definition and matching process enabled timely identification of RSV‐associated hospitalisations, but may be imperfect. In a separate analysis, however, our process identified more than 96% of hospitalisations of infants ultimately assigned International Classification of Diseases, revision 10 (ICD‐10) codes for RSV bronchiolitis, pneumonia, or bronchitis in the final WA hospitalisation data collection for 2022 and 2023 (data not shown).

We examined the impact of a universal infant nirsevimab program on the tertiary health care system in WA. Immunising 71% of infants prior to and during the RSV season was associated with 57% fewer admissions with the leading cause of hospitalisation of infants in Australia.

Box 1 – Cumulative number of respiratory syncytial virus (RSV)‐associated hospitalisations of infants and children under five years of age, Western Australia, 2022–2024


 

Box 2 – Respiratory syncytial virus (RSV)‐associated hospitalisations of infants and children under five years of age, Western Australia, 2022–2024, by age group

 

 

 

 

 

Difference (2024 v 2022/2023 mean)


Age group (years)

2022

2023

Mean (2022/2023)

2024

Absolute

Proportion


0 to < 1

812

954

883

378

–505

–57%

1 to < 2

436

532

484

540

56

12%

2 to < 3

182

209

196

276

81

41%

3 to < 4

102

100

101

117

16

16%

4 to < 5

54

79

67

78

12

18%


 

Received 26 January 2025, accepted 27 March 2025

  • Lauren E Bloomfield1,2
  • Nevada V Pingault1
  • Rachel E Foong1
  • Sarah French1
  • Jo‐Anne Morgan1
  • Ushma Wadia3,4
  • Hannah C Moore4,5
  • Christopher C Blyth4,6
  • Peter C Richmond4
  • Paul K Armstrong1
  • Paul V Effler1,6

  • 1 Western Australia Department of Health, Perth, WA
  • 2 University of Notre Dame Australia, Fremantle, WA
  • 3 Perth Children's Hospital, Perth, WA
  • 4 Wesfarmers Centre of Vaccine and Infectious Diseases, the Kids Research Institute Australia, Perth, WA
  • 5 Curtin University, Perth, WA
  • 6 University of Western Australia, Perth, WA



Open access:

Open access publishing facilitated by the University of Notre Dame Australia, as part of the Wiley – the University of Notre Dame Australia agreement via the Council of Australian University Librarians.


Data Sharing:

De‐identified aggregate data can be made available on request pending approval of the relevant data custodians and stewards and in accordance with applicable laws.


Acknowledgements: 

Open access publishing facilitated by the University of Notre Dame Australia, as part of the Wiley – the University of Notre Dame Australia agreement via the Council of Australian University Librarians.

Competing interests:

No relevant disclosures.

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