Transmitted Home Oximetry and Duration of Home Oxygen in Premature Infants

Author:

Rhein Lawrence12,White Heather1,Simoneau Tregony3,Traeger Nadav4,Lahiri Thomas5,Kremer Ted2,Sheils Catherine6,Meyer Kathleen7,Rosenkrantz Ted8,Krishnan Sankaran4,Hartman Tyler9,Feldman Henry A.10,Abu Jawdeh Elie G.11

Affiliation:

1. Divisions of Neonatology and

2. Pediatric Pulmonology, University of Massachusetts Memorial Medical Center, Worcester, Massachusetts;

3. Division of Pediatric Pulmonology, School of Medicine, University of Connecticut and Connecticut Children’s Medical Center, Hartford, Connecticut;

4. Division of Pediatric Pulmonology, Maria Fareri Children’s Hospital, Valhalla, New York;

5. Division of Pediatric Pulmonology, Larner College of Medicine, The University of Vermont, Burlington, Vermont;

6. Department of Medicine, Harvard Medical School, Harvard University and Boston Children’s Hospital, Boston, Massachusetts;

7. Division of Neonatology, Baystate Health Center, Springfield, Massachusetts;

8. Division of Neonatology, Department of Pediatrics, University of Connecticut Health, Farmington, Connecticut;

9. Division of Neonatology, Geisel School of Medicine, Dartmouth College, Manchester, New Hampshire;

10. Institutional Centers for Clinical and Translational Research, Boston Children’s Hospital, Boston, Massachusetts; and

11. Division of Neonatology, Department of Pediatrics, College of Medicine, University of Kentucky, Lexington, Kentucky

Abstract

OBJECTIVES: To determine if a home oxygen therapy (HOT) management strategy that includes analysis of recorded home oximetry (RHO) data, compared with standard monthly clinic visit assessments, reduces duration of HOT without harm in premature infants. METHODS: The RHO trial was an unmasked randomized clinical trial conducted in 9 US medical centers from November 2013 to December 2017, with follow-up to February 2019. Preterm infants with birth gestation ≤37 + 0/7 weeks, discharged on HOT, and attending their first pulmonary visit were enrolled. The intervention was an analysis of transmitted RHO between clinic visits (n = 97); the standard-care group received monthly clinic visits with in-clinic weaning attempts (n = 99). The primary outcomes were the duration of HOT and parent-reported quality of life. There were 2 prespecified secondary safety outcomes: change in weight and adverse events within 6 months of HOT discontinuation. RESULTS: Among 196 randomly assigned infants (mean birth gestational age: 26.9 weeks; SD: 2.6 weeks; 37.8% female), 166 (84.7%) completed the trial. In the RHO group, the mean time to discontinue HOT was 78.1 days (SE: 6.4), compared with 100.1 days (SE: 8.0) in the standard-care group (P = .03). The quality-of-life scores improved from baseline to 3 months after discontinuation of HOT in both groups (P = .002), but the degree of improvement did not differ significantly between groups (P = .75). CONCLUSIONS: RHO was effective in reducing the duration of HOT in premature infants. Parent quality of life improved after discontinuation. RHO allows physicians to determine which infants can be weaned and which need prolonged oxygen therapy between monthly visits.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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