Respiratory Syncytial Virus (RSV) Hospitalizations of US Preterm Infants Born at 29–35 Weeks Gestational Age: Proportions by Chronologic Age and Birth Month. (4th October 2017)
- Record Type:
- Journal Article
- Title:
- Respiratory Syncytial Virus (RSV) Hospitalizations of US Preterm Infants Born at 29–35 Weeks Gestational Age: Proportions by Chronologic Age and Birth Month. (4th October 2017)
- Main Title:
- Respiratory Syncytial Virus (RSV) Hospitalizations of US Preterm Infants Born at 29–35 Weeks Gestational Age: Proportions by Chronologic Age and Birth Month
- Authors:
- Anderson, Evan J
Simões, Eric A
Forbes, Michael L
Checchia, Paul A
Domachowske, Joseph B
Krilov, Leonard R
Halasa, Natasha B
Devincenzo, John P
Rizzo, Christopher
McLaurin, Kimmie K
Ambrose, Christopher S - Abstract:
- Abstract: Background: Respiratory syncytial virus hospitalizations (RSVH) in preterm infants 29–35 weeks gestational age (wGA) are often severe, frequently resulting in intensive care unit admission and the need for invasive mechanical ventilation. Assessing both chronologic age and birth month (a marker of RSV-seasonal exposure) may provide a practical approach to stratifying RSVH risk in otherwise healthy preterm infants 29–35 wGA. The objective of this study was to evaluate the comparative distributions of community-acquired RSVH by chronologic age and birth month among infants 29–35 wGA not receiving immunoprophylaxis. Methods: The SENTINEL1 study (NCT02273882) was conducted at 46 US sites over 2 RSV seasons (1 Oct–30 Apr) in 2014–2015 and 2015–2016. At each site, all infants 29–35 wGA with community-acquired, laboratory-confirmed RSV were included if aged <12 mo, hospitalized for ≥24 hours with RSV, and had not received RSV immunoprophylaxis. Information on RSVH by chronologic age, gestational age, and birth month was systematically collected on all eligible infants. Results: 1378 infants 29–35 wGA were identified over 2 RSV seasons. Case distribution by chronologic age and gestational age is presented in Figure 1, and distribution by birth month and gestational age is presented in Figure 2. Among infants 29–32 wGA, 55% of RSVH occurred among those <4 mo chronologic age. Among infants 33–34 wGA and 35 wGA, 55% of RSVH occurred among those <3 mo chronologic age. AmongAbstract: Background: Respiratory syncytial virus hospitalizations (RSVH) in preterm infants 29–35 weeks gestational age (wGA) are often severe, frequently resulting in intensive care unit admission and the need for invasive mechanical ventilation. Assessing both chronologic age and birth month (a marker of RSV-seasonal exposure) may provide a practical approach to stratifying RSVH risk in otherwise healthy preterm infants 29–35 wGA. The objective of this study was to evaluate the comparative distributions of community-acquired RSVH by chronologic age and birth month among infants 29–35 wGA not receiving immunoprophylaxis. Methods: The SENTINEL1 study (NCT02273882) was conducted at 46 US sites over 2 RSV seasons (1 Oct–30 Apr) in 2014–2015 and 2015–2016. At each site, all infants 29–35 wGA with community-acquired, laboratory-confirmed RSV were included if aged <12 mo, hospitalized for ≥24 hours with RSV, and had not received RSV immunoprophylaxis. Information on RSVH by chronologic age, gestational age, and birth month was systematically collected on all eligible infants. Results: 1378 infants 29–35 wGA were identified over 2 RSV seasons. Case distribution by chronologic age and gestational age is presented in Figure 1, and distribution by birth month and gestational age is presented in Figure 2. Among infants 29–32 wGA, 55% of RSVH occurred among those <4 mo chronologic age. Among infants 33–34 wGA and 35 wGA, 55% of RSVH occurred among those <3 mo chronologic age. Among infants 29–32 wGA, 67% of RSVH occurred among infants born Aug-January Among infants 33–34 wGA and 35 wGA, 66% and 65% of RSVH, respectively, occurred in infants born Sep-January Conclusion: RSVH remains an important problem among preterm infants 29–35 wGA. Incorporating chronologic age and birth month can enhance risk stratification around prevention and improve anticipatory guidance to families of preterm infants. Study supported by AstraZeneca. Disclosures: E. J. Anderson, AbbVie: Consultant, Consulting fee; NovaVax: Research Contractor, Research support; Regeneron: Research Contractor, Research grant; MedImmune: Research Contractor, Research grant and Research support; E. A. Simões, AstraZeneca/MedImmune: Investigator, Research support; M. L. Forbes, AstraZeneca/MedImmune: Investigator and Speaker's Bureau, Research support and Speaker honorarium; P. A. Checchia, AstraZeneca/MedImmune: Investigator, Research support; J. B. Domachowske II, AstraZeneca/MedImmune: Investigator, Research support; L. R. Krilov, AstraZeneca/MedImmune: Consultant, Research grant and Research support; N. B. Halasa, sanofi pasteur: Research Contractor, Research support; Astra Zeneca: Research Contractor, Grant recipient; J. P. Devincenzo, AstraZeneca/MedImmune: Investigator, Research support; C. Rizzo, AstraZeneca: Employee, Salary; K. K. McLaurin, AstraZeneca: Employee, Salary; C. S. Ambrose, AstraZeneca: Employee, Salary … (more)
- Is Part Of:
- Open forum infectious diseases. Volume 4(2017)Supplement 1
- Journal:
- Open forum infectious diseases
- Issue:
- Volume 4(2017)Supplement 1
- Issue Display:
- Volume 4, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 4
- Issue:
- 1
- Issue Sort Value:
- 2017-0004-0001-0000
- Page Start:
- S567
- Page End:
- S568
- Publication Date:
- 2017-10-04
- Subjects:
- Communicable diseases -- Periodicals
Medical microbiology -- Periodicals
Infection -- Periodicals
616.9 - Journal URLs:
- http://ofid.oxfordjournals.org/ ↗
http://www.oxfordjournals.org/en/ ↗ - DOI:
- 10.1093/ofid/ofx163.1483 ↗
- Languages:
- English
- ISSNs:
- 2328-8957
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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