R01HD106996
Project Grant
Overview
Grant Description
Optimizing Tracheal Intubation Outcomes and Neonatal Safety (OPTION SAFE) - Project Summary
Tracheal intubation (TI) is a common life-saving intervention for the resuscitation of critically ill infants in neonatal intensive care units (NICUs). Through our NICHD-funded NICU multicenter registry (National Emergency Airway Registry for Neonates: NEAR4NEOS), we have identified that adverse TI-associated events (TIAEs) occur in 22% of TIs, severe TIAEs occur in 4% of TIs, and multiple attempts occur in 23% of TIs. Additionally, oxygen desaturations (captured separately from TIAEs) are frequent and pronounced, with a mean 28% decline in SpO2 during neonatal TI. Furthermore, neonates who experienced adverse TIAEs were at a higher risk of extubation failure and NICU mortality.
We have identified key factors strongly associated with adverse TIAEs: 1) patient risk, 2) provider skill, 3) premedication with paralysis, and 4) video laryngoscopy. We have developed, refined, and tested a personalized intubation safety (PINS) bundle aimed at addressing these factors and prompting a prospective plan for TI management. The prototype safety bundle resulted in a sustained 66% reduction in severe TI adverse events in our pilot single-center study.
In this proposal, we will perform a pragmatic stepped-wedge cluster randomized trial across 8 NEAR4NEOS NICUs to assess the impact of the personalized intubation bundle on TI safety events. The timing of introducing the bundle intervention will be randomized at the NICU site level. Our primary outcome is adverse TIAEs; secondary outcomes are severe TIAEs, multiple (>2) attempts, and magnitude of oxygen desaturation. We will test whether there is a significant variability in the treatment effect of the PINS bundle based on the airway provider skill. This will provide important information about the impact of the bundle intervention and its components for novice vs. experienced providers, which will help NICUs to contextualize study findings.
Finally, we will explore the impact of the PINS bundle intervention on relevant NICU patient outcomes, including extubation failure, duration of mechanical ventilation, intraventricular hemorrhage, and NICU mortality. Upon successful completion of this project, we will establish the effectiveness of a prospective personalized intubation safety bundle to reduce adverse events, multiple attempts, and oxygen desaturation during neonatal TI. These results will generate a paradigm shift to improve neonatal intubation procedural safety.
Tracheal intubation (TI) is a common life-saving intervention for the resuscitation of critically ill infants in neonatal intensive care units (NICUs). Through our NICHD-funded NICU multicenter registry (National Emergency Airway Registry for Neonates: NEAR4NEOS), we have identified that adverse TI-associated events (TIAEs) occur in 22% of TIs, severe TIAEs occur in 4% of TIs, and multiple attempts occur in 23% of TIs. Additionally, oxygen desaturations (captured separately from TIAEs) are frequent and pronounced, with a mean 28% decline in SpO2 during neonatal TI. Furthermore, neonates who experienced adverse TIAEs were at a higher risk of extubation failure and NICU mortality.
We have identified key factors strongly associated with adverse TIAEs: 1) patient risk, 2) provider skill, 3) premedication with paralysis, and 4) video laryngoscopy. We have developed, refined, and tested a personalized intubation safety (PINS) bundle aimed at addressing these factors and prompting a prospective plan for TI management. The prototype safety bundle resulted in a sustained 66% reduction in severe TI adverse events in our pilot single-center study.
In this proposal, we will perform a pragmatic stepped-wedge cluster randomized trial across 8 NEAR4NEOS NICUs to assess the impact of the personalized intubation bundle on TI safety events. The timing of introducing the bundle intervention will be randomized at the NICU site level. Our primary outcome is adverse TIAEs; secondary outcomes are severe TIAEs, multiple (>2) attempts, and magnitude of oxygen desaturation. We will test whether there is a significant variability in the treatment effect of the PINS bundle based on the airway provider skill. This will provide important information about the impact of the bundle intervention and its components for novice vs. experienced providers, which will help NICUs to contextualize study findings.
Finally, we will explore the impact of the PINS bundle intervention on relevant NICU patient outcomes, including extubation failure, duration of mechanical ventilation, intraventricular hemorrhage, and NICU mortality. Upon successful completion of this project, we will establish the effectiveness of a prospective personalized intubation safety bundle to reduce adverse events, multiple attempts, and oxygen desaturation during neonatal TI. These results will generate a paradigm shift to improve neonatal intubation procedural safety.
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Philadelphia,
Pennsylvania
191044318
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 395% from $728,980 to $3,606,509.
The Children's Hospital Of Philadelphia was awarded
Neonatal Intubation Safety Study (NISS)
Project Grant R01HD106996
worth $3,606,509
from the National Institute of Child Health and Human Development in September 2022 with work to be completed primarily in Philadelphia Pennsylvania United States.
The grant
has a duration of 4 years 9 months and
was awarded through assistance program 93.865 Child Health and Human Development Extramural Research.
The Project Grant was awarded through grant opportunity Research Project Grant (Parent R01 Clinical Trial Required).
Status
(Ongoing)
Last Modified 6/22/26
Period of Performance
9/1/22
Start Date
6/30/27
End Date
Funding Split
$3.6M
Federal Obligation
$0.0
Non-Federal Obligation
$3.6M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01HD106996
Transaction History
Modifications to R01HD106996
Additional Detail
Award ID FAIN
R01HD106996
SAI Number
R01HD106996-3845897874
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Nonprofit With 501(c)(3) IRS Status (Other Than An Institution Of Higher Education)
Awarding Office
75NT00 NIH Eunice Kennedy Shriver National Institute of Child Health & Human Development
Funding Office
75NT00 NIH Eunice Kennedy Shriver National Institute of Child Health & Human Development
Awardee UEI
G7MQPLSUX1L4
Awardee CAGE
0GXU0
Performance District
PA-03
Senators
Robert Casey
John Fetterman
John Fetterman
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Institute of Child Health and Human Development, National Institutes of Health, Health and Human Services (075-0844) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,457,830 | 100% |
Modified: 6/22/26