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Updated: Aug 11, 2026

An In vitro Model to Study Immune Responses of Human Peripheral Blood Mononuclear Cells to Human Respiratory Syncytial Virus Infection
Published on: December 11, 2013
Lower respiratory tract illness and RSV prophylaxis in very premature infants
T Lacaze-Masmonteil1, P Truffert, D Pinquier
1Service de Réanimation et Pédiatrie Néonatales, Hôpital Antoine-Béclère, Assistance Publique-Hôpitaux de Paris, Clamart, France. tlacaze@club-internet.fr
Insights
Nearly one in four very premature infants without bronchopulmonary dysplasia were readmitted, with respiratory infections being a major cause. Respiratory syncytial virus (RSV) infections significantly contributed to these readmissions in infants not receiving RSV prophylaxis.
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Infectious Diseases
Background:
- Very premature infants face significant respiratory morbidity post-discharge.
- Lower respiratory tract illness (LRTI) is a common cause of readmission in this vulnerable population.
- Respiratory syncytial virus (RSV) is a primary pathogen responsible for severe LRTI in neonates.
Purpose of the Study:
- To determine the incidence and risk factors for readmission due to any LRTI and RSV-documented LRTI.
- To evaluate the impact of RSV prophylaxis on readmission rates in very premature infants.
- To identify specific risk factors associated with readmission for respiratory illnesses.
Main Methods:
- A multicenter prospective longitudinal cohort study involving 2813 infants born before 33 weeks of gestational age.
- Infants were followed through the respiratory epidemic season.
- Data collected included gestational age, bronchopulmonary dysplasia status, intrauterine growth restriction, and RSV prophylaxis use.
Main Results:
- Among infants without bronchopulmonary dysplasia and not receiving prophylaxis, 15.1% were readmitted for LRTI and 7.2% for RSV-related LRTI.
- Infants born before 31 weeks' gestation, with intrauterine growth restriction, or from single-mother families had higher readmission risks.
- For infants receiving prophylaxis, 6.1% were readmitted for RSV-related LRTI.
Conclusions:
- A significant proportion of very premature infants without bronchopulmonary dysplasia are readmitted, with LRTI and RSV infections being key contributors.
- Gestational age, intrauterine growth restriction, and family structure are associated with increased readmission risk.
- Further research is needed to understand the role of other respiratory pathogens in post-discharge morbidity.
Aims:
To determine the frequency of and the risk factors for readmissions for any lower respiratory tract illness (LRTI) and for respiratory syncytial virus (RSV) documented LRTI in children born very prematurely who had or had not received RSV prophylaxis.
Methods:
Multicentre prospective longitudinal cohort study of 2813 infants, born between April 2000 and December 2000 at less than 33 weeks of gestational age, and followed until the end of the epidemic season.
Results:
Among the 2256 children who had no bronchopulmonary dysplasia at 36 weeks of postmenstrual age and were not submitted to RSV prophylaxis, 27.4% were readmitted at least once for any reason during the epidemic season; 15.1% and 7.2% were readmitted at least once for any LRTI and RSV related LRTI, respectively. Children born at less than 31 weeks' gestation, having an intrauterine growth restriction, or living in a single mother family were at a significantly higher risk of readmission for LRTI in general as well as for RSV related LRTI. Of the 376 children submitted to prophylaxis, 28.2% were readmitted at least once for any LRTI and 6.1% for RSV related LRTI.
Conclusion:
One out of four children who had received no prophylaxis, was born very prematurely, and was without bronchopulmonary dysplasia at 36 weeks of postmenstrual age, was readmitted at least once for any reason. Roughly 50% and 20% of these readmissions were related to a LRTI and an RSV infection, respectively. Further epidemiological studies are warranted to assess the aetiology and impact of other respiratory pathogens on post-discharge readmission and respiratory morbidity in this population.
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