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Introduction: Monthly palivizumab prevents severe respiratory syncytial virus infection among high-risk children. Palivizumab is generally initiated early in an epidemic, but the best timing for initiation is unknown. Reducing the number of infected patients prior to palivizumab administration is a public health challenge.
Methods: Kanagawa Prefecture, Japan, has a regionally standardized protocol for the initiation of palivizumab based on epidemic prediction for the following season. We analyzed the efficacy of this prospective intervention during 2019-2022 using a questionnaire completed by regional hospitals.
Results: The survey response rate was 53.8 %. In 2019, 2021, and 2022, RSV epidemics began in July, May, and June; palivizumab was started in July, May, and April, respectively. In 2020, palivizumab was started in June, but there was no epidemic activity. The median number of palivizumab doses was eight per year. The number of hospitalized patients each year was 1381, 169, 1196, and 1028, with 28, 1, 11, and 13 patients having an indication for palivizumab, respectively. Among them, the number of hospitalized patients before or after the first dose of palivizumab was 16, 1, 10, and 4, respectively. Thirteen of 31 patients (41.9 %) infected before or after the first dose needed care in the pediatric intensive care unit and/or nasal high flow therapy; only three of 22 patients (13.6 %) received the second of more doses needed (p < 0.05).
Conclusions: A standardized regional protocol for palivizumab initiation could be effective in reducing the number of hospitalized and severely ill patients for whom palivizumab is indicated.
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http://dx.doi.org/10.1016/j.jiac.2025.102639 | DOI Listing |
Infect Drug Resist
August 2025
Department of Pediatric Cardiology, Taichung Veterans General Hospital, Taichung, Taiwan.
Background: Respiratory syncytial virus (RSV) is a significant cause of lower respiratory tract infections in adults, particularly the elderly, and can lead to severe outcomes, including respiratory failure. Current treatment options for RSV in immunocompetent adults are limited to supportive care.
Objective: This case series aims to describe the clinical course and outcomes of two immunocompetent adults with severe RSV infection treated with Palivizumab, a monoclonal antibody against RSV.
Lancet Infect Dis
August 2025
Department of Medical Biology, Faculty of Health Sciences, UiT The Arctic University of Tromsø, Tromsø 9027, Norway; Transplantation & Clinical Virology, Department of Biomedicine, University of Basel, Basel, Switzerland. Electronic address:
To update recommendations of the 4th European Conference on Infections in Leukaemia (ECIL-4) on community-acquired respiratory virus (CARV) infections published in 2013, we reviewed publications from between Jan 1, 2014, and June 30, 2024 on adenovirus, bocavirus, coronavirus, influenzavirus, metapneumovirus, parainfluenzavirus, respiratory syncytial virus (RSV), and rhinovirus in patients with haematological malignancies or undergoing haematopoietic cell transplantation (HCT), or both. In the current ECIL recommendations (ECIL-10), we outline a common approach to infection control, laboratory testing, and diagnosis for all CARVs (including SARS-CoV-2) and specific management and deferral strategies for CARVs other than SARS-CoV-2. For influenzavirus, seasonal inactivated-vaccines and early antivirals are recommended, whereas routine antiviral prophylaxis is discouraged for immunocompromised patients.
View Article and Find Full Text PDFHum Vaccin Immunother
December 2025
Department of Regulatory Science, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
The current standard-of-care prophylaxis for respiratory syncytial virus (RSV) is primarily administered to high-risk infant populations. We conducted a cost-effectiveness analysis to determine the economically justifiable price of nirsevimab compared with the standard of care in preventing medically attended RSV-associated lower respiratory tract infections from all infants and palivizumab-eligible children <2 years in South Korea. A month-age-specific static decision-tree model was used from a societal perspective, with a primary time horizon of one RSV season and an extended time horizon of three years.
View Article and Find Full Text PDFPediatr Pulmonol
August 2025
Pediatric Pulmonology Medical Residency program at UNICAMP State University of Campinas, Campinas, São Paulo, Brazil.
Introduction: Premature infants are at increased risk of developing chronic respiratory diseases, predisposing them to severe infections, such as those caused by respiratory syncytial virus (RSV). Palivizumab reduces the severity of RSV infections in high-risk children; however, its relationship with asthma development in premature infants remains unclear.
Objective: This systematic review with meta-analysis aimed to review the literature and assess whether prophylaxis with palivizumab protects premature infants without congenital heart disease from developing asthma.
Curr Opin Virol
August 2025
Center for Translational Antiviral Research, Georgia State University Institute for Biomedical Sciences, Atlanta, GA 30303, USA. Electronic address:
Respiratory syncytial virus (RSV) causes major morbidity and mortality in vulnerable populations. In infants, RSV infection is a leading cause of hospitalization and can result to severe respiratory complications marked by bronchiolitis and viral pneumonia. Currently, prophylaxis exists in the form of three licensed vaccines, all approved for adults aged >65 years or pregnant women, but no vaccination is available specifically for infants.
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