Journal article
Assessing Clinical Improvement of Infants Hospitalized for Respiratory Syncytial Virus-Related Critical Illness
The Journal of infectious diseases, Vol.232(6), pp.1283-1291
12/20/2025
DOI: 10.1093/infdis/jiaf018
PMCID: PMC12265475
PMID: 39812486
Abstract
Pediatric respiratory syncytial virus (RSV)-related acute lower respiratory tract infection (LRTI) commonly requires hospitalization. The Clinical Progression Scale Pediatrics (CPS-Ped) measures level of respiratory support and degree of hypoxia across a range of disease severity, but it has not been applied in infants hospitalized with severe RSV-LRTI.BACKGROUNDPediatric respiratory syncytial virus (RSV)-related acute lower respiratory tract infection (LRTI) commonly requires hospitalization. The Clinical Progression Scale Pediatrics (CPS-Ped) measures level of respiratory support and degree of hypoxia across a range of disease severity, but it has not been applied in infants hospitalized with severe RSV-LRTI.We analyzed data from a prospective surveillance registry of infants hospitalized for RSV-related complications across 39 U.S. PICUs from October through December 2022. We assigned CPS-Ped (0=discharged home at respiratory baseline to 8=death) at admission, days 2-7,10, and 14. We identified predictors of clinical improvement (CPS-Ped≤2 or 3-point decrease) by day 7 using multivariable log-binomial regression models and estimated the sample size (80% power) to detect 15% between-group clinical improvement with CPS-Ped versus hospital length of stay (LOS).METHODSWe analyzed data from a prospective surveillance registry of infants hospitalized for RSV-related complications across 39 U.S. PICUs from October through December 2022. We assigned CPS-Ped (0=discharged home at respiratory baseline to 8=death) at admission, days 2-7,10, and 14. We identified predictors of clinical improvement (CPS-Ped≤2 or 3-point decrease) by day 7 using multivariable log-binomial regression models and estimated the sample size (80% power) to detect 15% between-group clinical improvement with CPS-Ped versus hospital length of stay (LOS).Of 585 hospitalized infants, 138 (23.6%) received invasive mechanical ventilation (IMV). Of the 49 (8.4%) infants whose CPS-Ped score worsened by 2 points after admission, one died. Failure to clinically improve by day 7 occurred in 205 (35%) infants and was associated with age <3 months, prematurity, underlying respiratory condition, and IMV in the first 24 hours in the multivariable analysis. The estimated sample size per arm required for detecting a 15% clinical improvement in a potential study was 584 using CPS-Ped clinical improvement versus 2,031 for hospital LOS.RESULTSOf 585 hospitalized infants, 138 (23.6%) received invasive mechanical ventilation (IMV). Of the 49 (8.4%) infants whose CPS-Ped score worsened by 2 points after admission, one died. Failure to clinically improve by day 7 occurred in 205 (35%) infants and was associated with age <3 months, prematurity, underlying respiratory condition, and IMV in the first 24 hours in the multivariable analysis. The estimated sample size per arm required for detecting a 15% clinical improvement in a potential study was 584 using CPS-Ped clinical improvement versus 2,031 for hospital LOS.CPS-Ped can be used to capture a range of disease severity and track clinical improvement in infants who develop RSV-related critical illness and could be useful for evaluating therapeutic interventions for RSV.CONCLUSIONSCPS-Ped can be used to capture a range of disease severity and track clinical improvement in infants who develop RSV-related critical illness and could be useful for evaluating therapeutic interventions for RSV.
Details
- Title: Subtitle
- Assessing Clinical Improvement of Infants Hospitalized for Respiratory Syncytial Virus-Related Critical Illness
- Creators
- Shannon B Leland - Boston Children's HospitalLaura D Zambrano - Centers for Disease Control and PreventionSteven J Staffa - Boston Children's HospitalElizabeth R McNamara - Boston Children's HospitalMargaret M Newhams - Boston Children's HospitalNatasha Halasa - Vanderbilt University Medical CenterJustin Z Amarin - Vanderbilt University Medical CenterLaura S Stewart - Vanderbilt University Medical CenterSteven L Shein - Rainbow Babies & Children's HospitalChristopher L Carroll - Connecticut Children's Medical CenterJulie C Fitzgerald - Children's Hospital of PhiladelphiaMarian G Michaels - Children's Hospital of PittsburghKatherine Bline - Nationwide Children's HospitalMelissa L Cullimore - Children's Hospital & Medical CenterLaura Loftis - Baylor College of MedicineVicki L Montgomery - University of LouisvilleAsumthia S Jeyapalan - University of MiamiPia S Pannaraj - Rady Children's Hospital-San DiegoAdam J Schwarz - Children's Hospital of Orange CountyNatalie Z Cvijanovich - UCSF Benioff Children's HospitalMatt S Zinter - UCSF Benioff Children's HospitalAline B Maddux - Children's Hospital ColoradoMelania M Bembea - Johns Hopkins MedicineKatherine Irby - Arkansas Children's HospitalDanielle M Zerr - Seattle Children's HospitalJoseph D Kuebler - Golisano Children's HospitalChristopher J Babbitt - Miller Children's & Women's HospitalMary G Gaspers - Children's Medical CenterRyan A Nofziger - Akron Children's HospitalMichele Kong - University of Alabama at BirminghamBria M Coates - Northwestern UniversityJennifer E Schuster - Children's Mercy HospitalShira J Gertz - Saint Barnabas Medical CenterElizabeth H Mack - Medical University of South CarolinaBenjamin R White - University of UtahHelen Harvey - Rady Children's Hospital-San DiegoCharlotte V Hobbs - University of Mississippi Medical CenterHeda Dapul - New York UniversityAndrew D Butler - St. Christopher's Hospital for ChildrenTamara T Bradford - Louisiana State University Health Sciences Center New OrleansCourtney M Rowan - Riley Hospital for ChildrenKari Wellnitz - University of IowaMary Allen Staat - University of CincinnatiCassyanne L Aguiar - Children's Hospital of The King's DaughtersSaul R Hymes - Albany Medical Center HospitalAngela P Campbell - Centers for Disease Control and PreventionAdrienne G Randolph - Harvard UniversityRSV-PIC Investigators
- Resource Type
- Journal article
- Publication Details
- The Journal of infectious diseases, Vol.232(6), pp.1283-1291
- DOI
- 10.1093/infdis/jiaf018
- PMID
- 39812486
- PMCID
- PMC12265475
- NLM abbreviation
- J Infect Dis
- ISSN
- 1537-6613
- eISSN
- 1537-6613
- Publisher
- OXFORD UNIV PRESS INC
- Grant note
- Centers for Disease Control and Prevention: 75D30122C13330 National Heart, Lung, and Blood Institute of the National Institutes of Health: T32HL155020 National Heart, Lung, and Blood Institute of the National Institutes of HealthNational Heart, Lung, and Blood Institute of the National Institutes of Health
This research was supported by the Centers for Disease Control and Prevention (contract number 75D30122C13330). S. B. L. is supported by the National Heart, Lung, and Blood Institute of the National Institutes of Health (grant number T32HL155020).
- Language
- English
- Electronic publication date
- 01/15/2025
- Date published
- 12/20/2025
- Academic Unit
- Critical Care; Stead Family Department of Pediatrics
- Record Identifier
- 9984773425802771
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