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RSV: Immunoprophylaxis and non-invasive respiratory support in ex-preterms: A northern UK perspective
Robert Tinnion1, Jill Spencer1, Samantha Moss2
1Department of Neonatal Medicine, Royal Victoria Infirmary, Newcastle upon Tyne Hospitals NHS Trust, Newcastle upon Tyne, United Kingdom.
Insights
Extending respiratory syncytial virus (RSV) immunoprophylaxis to moderate-to-late-preterm infants is unlikely to reduce hospitalizations. Noninvasive respiratory support (NIV) also showed no benefit for these infants with RSV bronchiolitis.
Area of Science:
- Pediatrics
- Infectious Diseases
- Neonatology
Background:
- Current guidance recommends extending monoclonal antibody immunoprophylaxis for respiratory syncytial virus (RSV) to moderate-to-late-preterm infants.
- Noninvasive respiratory support (NIV) is increasingly used for infant bronchiolitis despite limited evidence of efficacy.
Purpose of the Study:
- To evaluate the clinical and cost benefits of extending RSV immunoprophylaxis to moderate-to-late-preterm infants.
- To assess the efficacy of NIV in ex-preterm infants with RSV bronchiolitis.
Main Methods:
- Multicenter prospective audit and service evaluation.
- Analysis of infants with RSV positive bronchiolitis requiring respiratory support.
Main Results:
- The prevalence of RSV bronchiolitis requiring admission was 2.5%.
- Most ex-preterm infants requiring NIV for RSV bronchiolitis did not meet extended immunoprophylaxis criteria.
- NIV use (9% of admissions) did not reduce the need for subsequent formal ventilation in ex-preterms.
Conclusions:
- Extending RSV immunoprophylaxis is unlikely to significantly reduce hospitalizations in this population.
- NIV is not supported as a beneficial adjunct for ex-preterm infants with RSV bronchiolitis.
- Further randomized controlled trials are needed to evaluate NIV for bronchiolitis.
Abstract:
Recent guidance has suggested that immunoprophylaxis with monoclonal antibody against respiratory syncytial virus (RSV) should be extended to ex-preterm infants who are moderate-to-late-preterm and discharged home during the RSV season. Noninvasive respiratory support (NIV) for infants with bronchiolitis is becoming widespread with little supporting evidence for efficacy over nonpressure support methods. We used multicentre prospective audit and service evaluation to evaluate whether extension of current practice in line with the guidance would provide a clinical or cost benefit, and whether NIV provides any benefits in the ex-preterm population. The prevalence of bronchiolitic illness requiring admission in our population was similar to other studies (2.5%). We found that the majority of ex-preterm infants with RSV positive bronchiolitis who required NIV did not meet the extended criteria for immunisation. Our data suggest that extending RSV prophylaxis as recommended would be unlikely to reduce numbers of infants requiring respiratory support for RSV. NIV use has been widely adopted (9% of 'bronchiolitic' admissions) in our region but the data do not support it as a useful adjunct for ex-preterms with RSV positive illness requiring respiratory support: it does not appear to reduce the need for subsequent formal ventilation. Our study does not support a case for change to more widespread, protocol driven immunisation for RSV. Further research is needed in a randomised, controlled setting to examine the use of NIV in bronchiolitis in a wider context.
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