TY - JOUR
T1 - Uptake and predictors of newborn respiratory syncytial virus (RSV) immunisation with nirsevimab in Ireland’s national pilot programme
T2 - a cross-sectional study
AU - Masukume, Gwinyai
AU - McMorrow, Amy
AU - Dawood, Iyas
AU - Rafdhy, Khaulah
AU - O’Brien, Fiona
AU - Desmond, Carol
AU - O’Connell, Deirdre
AU - Murphy, Bernadette
AU - Ronan, Eileen
AU - Purtill, Helen
AU - Philip, Roy K.
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2026. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ Group. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: https://creativecommons.org/licenses/by-nc/4.0/.
PY - 2026/6
Y1 - 2026/6
N2 - Objectives: To assess uptake of nirsevimab, a long-acting monoclonal antibody for respiratory syncytial virus (RSV) prevention, during the first season of Ireland’s Pathfinder pilot universal newborn immunisation programme and to identify socio-demographic and perinatal predictors of uptake. Design: Cross-sectional analysis of routinely collected programme data. Setting: Ireland’s Mid-West region, served by University Maternity Hospital Limerick, the sole maternity and neonatal hospital for the region. Participants: Infants born 1 September 2024 to 28 February 2025. Outcome measure: Uptake of nirsevimab before hospital discharge. Results: Overall uptake was 89.4% (1600/1790) and did not vary by month (p=0.119); it was similar by sex (male 89.5%, female 89.2%; p=0.838). Preterm infants had higher uptake than term (96.9% vs 88.7%; p=0.001), and those admitted to the neonatal unit also had higher uptake (93.0% vs 88.4%; p=0.009). In adjusted analyses, maternal age (adjusted OR (aOR) 1.06 per year, 95% CI 1.03 to 1.09, p<0.001) and preterm birth (aOR 3.08 (95% CI 1.14 to 8.37), p=0.027) were associated with uptake. Uptake varied by maternal ethnicity: 91.5% in white Irish, 53.6% in Irish Traveller (aOR 0.13 (95% CI 0.08 to 0.23)), 79.7% in other white background (aOR 0.39 (95% CI 0.24 to 0.61)), 90.0% in black or black Irish, 98.3% in Asian or Asian Irish and 84.2% in other/mixed or prefer not to say. Although uptake among white Irish was high, they accounted for the largest absolute number of infants who did not receive nirsevimab, reflecting their predominance in the birth cohort. Conclusions: During the first season of Ireland’s Pathfinder RSV pilot programme in the Mid-West region, nearly 90% of newborns received nirsevimab before discharge. Uptake was consistently high across months, indicating effective implementation but lower among infants of Irish Traveller and other white background mothers, highlighting the need for targeted, culturally adaptable equity strategies within a high-uptake programme. These findings may inform national and international policies and offer practical lessons for universal RSV immunisation.
AB - Objectives: To assess uptake of nirsevimab, a long-acting monoclonal antibody for respiratory syncytial virus (RSV) prevention, during the first season of Ireland’s Pathfinder pilot universal newborn immunisation programme and to identify socio-demographic and perinatal predictors of uptake. Design: Cross-sectional analysis of routinely collected programme data. Setting: Ireland’s Mid-West region, served by University Maternity Hospital Limerick, the sole maternity and neonatal hospital for the region. Participants: Infants born 1 September 2024 to 28 February 2025. Outcome measure: Uptake of nirsevimab before hospital discharge. Results: Overall uptake was 89.4% (1600/1790) and did not vary by month (p=0.119); it was similar by sex (male 89.5%, female 89.2%; p=0.838). Preterm infants had higher uptake than term (96.9% vs 88.7%; p=0.001), and those admitted to the neonatal unit also had higher uptake (93.0% vs 88.4%; p=0.009). In adjusted analyses, maternal age (adjusted OR (aOR) 1.06 per year, 95% CI 1.03 to 1.09, p<0.001) and preterm birth (aOR 3.08 (95% CI 1.14 to 8.37), p=0.027) were associated with uptake. Uptake varied by maternal ethnicity: 91.5% in white Irish, 53.6% in Irish Traveller (aOR 0.13 (95% CI 0.08 to 0.23)), 79.7% in other white background (aOR 0.39 (95% CI 0.24 to 0.61)), 90.0% in black or black Irish, 98.3% in Asian or Asian Irish and 84.2% in other/mixed or prefer not to say. Although uptake among white Irish was high, they accounted for the largest absolute number of infants who did not receive nirsevimab, reflecting their predominance in the birth cohort. Conclusions: During the first season of Ireland’s Pathfinder RSV pilot programme in the Mid-West region, nearly 90% of newborns received nirsevimab before discharge. Uptake was consistently high across months, indicating effective implementation but lower among infants of Irish Traveller and other white background mothers, highlighting the need for targeted, culturally adaptable equity strategies within a high-uptake programme. These findings may inform national and international policies and offer practical lessons for universal RSV immunisation.
KW - Community child health
KW - Health Equity
KW - Immunisation Programmes
KW - Public health
UR - https://www.scopus.com/pages/publications/105042551260
U2 - 10.1136/bmjopen-2025-113533
DO - 10.1136/bmjopen-2025-113533
M3 - Article
C2 - 42331576
AN - SCOPUS:105042551260
SN - 2044-6055
VL - 16
JO - BMJ Open
JF - BMJ Open
IS - 6
M1 - e113533
ER -