Multicenter Quality Collaborative to Reduce Overuse of High-Flow Nasal Cannula in Bronchiolitis

Author:

Byrd Courtney1,Noelck Michelle2,Kerns Ellen3,Bryan Mersine4,Hamline Michelle5,Garber Matthew6,Ostrow Olivia7,Riss Valerie8,Shadman Kristin9,Shein Steven10,Willer Robert11,Ralston Shawn4

Affiliation:

1. aDepartment of Pediatrics, Emory University School of Medicine, Atlanta, Georgia

2. bDivision of Hospital Medicine, Department of Pediatrics, Oregon Health and Science University, Portland, Oregon

3. cDepartment of Pediatrics, University of Nebraska College of Medicine, Omaha, Nebraska

4. dDivision of Hospital Medicine and General Pediatrics, University of Washington College of Medicine, Seattle, Washington

5. eDivision of Clinical Pediatrics, University of California, Davis, Davis, California

6. fDivision of Hospital Pediatrics, Department of Pediatrics, University of Florida College of Medicine, Jacksonville, Florida

7. gDivision of Pediatric Emergency Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada

8. hDepartment of Pediatrics, University of Vermont College of Medicine, Burlington, Vermont

9. iDivision of Hospital Medicine and Complex Care, Department of Pediatrics, University of Wisconsin College of Medicine, Madison, Wisconsin

10. jDepartments of Pediatrics and Pediatric Critical Care, University Hospitals, Rainbow Babies and Children’s, Cleveland, Ohio

11. kDepartment of Pediatric Hospital Medicine, University of Utah College of Medicine, Salt Lake City, Utah

Abstract

BACKGROUND AND OBJECTIVES High-flow nasal cannula (HFNC) for bronchiolitis increased over the past decade without clear benefit. This quality improvement collaborative aimed to reduce HFNC initiation and treatment duration by 30% from baseline. METHODS Participating hospitals either reduced HFNC initiation (Pause) or treatment duration (Holiday) in patients aged <24 months admitted for bronchiolitis. Participants received either Pause or Holiday toolkits, including: intervention protocol, training/educational materials, electronic medical record queries for data acquisition, small-group coaching, webinars, and real-time access to run charts. Pause arm primary outcome was proportion of patients initiated on HFNC. Holiday arm primary outcome was geometric mean HFNC treatment duration. Length of stay (LOS) was balancing measure for both. Each arm served as contemporaneous controls for the other. Outcomes analyzed using interrupted time series (ITS) and linear mixed-effects regression. RESULTS Seventy-one hospitals participated, 30 in the Pause (5746 patients) and 41 in the Holiday (7903 patients). Pause arm unadjusted HFNC initiation decreased 32% without LOS change. ITS showed immediate 16% decrease in initiation (95% confidence interval [CI] −27% to −5%). Compared with contemporaneous controls, Pause hospitals reduced HFNC initiation by 23% (95% CI −35% to −10%). Holiday arm unadjusted HFNC duration decreased 28% without LOS change. ITS showed immediate 11.8 hour decrease in duration (95% CI −18.3 hours to −5.2 hours). Compared with contemporaneous controls, Holiday hospitals reduced duration by 11 hours (95% CI −20.7 hours to −1.3 hours). CONCLUSIONS This quality improvement collaborative reduced HFNC initiation and duration without LOS increase. Contemporaneous control analysis supports intervention effects rather than secular trends toward less use.

Publisher

American Academy of Pediatrics (AAP)

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