Predictors of Intensive Care Admission in Hypoxemic Bronchiolitis Infants, Secondary Analysis of a Randomized Trial - 05/05/23
A Pediatric Acute Respiratory Intervention Study (PARIS) on behalf of PREDICT
Abstract |
Objectives |
To evaluate in a preplanned secondary analysis of our parent randomized controlled trial predictors of intensive care unit (ICU) admission in infants with bronchiolitis and analyze if these predictors are equally robust for children receiving high-flow or standard-oxygen.
Study design |
A secondary analysis of a multicenter, randomized trial of infants aged <12 months with bronchiolitis and an oxygen requirement was performed using admission and outcome data of all 1472 enrolled infants. The primary outcome was ICU admission. The predictors evaluated were baseline characteristics including physiological data and medical history.
Results |
Of the 1472 enrolled infants, 146 were admitted to intensive care. Multivariate predictors of ICU admission were age (weeks) (OR: 0.98 [95% CI: 0.96-0.99]), pre-enrolment heart rate >160/min (OR: 1.80 [95% CI: 1.23-2.63]), pre-enrolment SpO2 (transcutaneous oxygen saturation) (%) (OR: 0.91 [95% CI: 0.86-0.95]), previous ICU admission (OR: 2.16 [95% CI: 1.07-4.40]), and time of onset of illness to hospital presentation (OR: 0.78 [95% CI: 0.65-0.94]). The predictors were equally robust for infants on high-flow nasal cannula therapy or standard-oxygen therapy.
Conclusion |
Age <2 months, pre-enrolment heart rate >160/min, pre-enrolment SpO2 of <87%, previous ICU admission and time of onset of ≤2 days to presentation are predictive of an ICU admission during the current hospital admission of infants with bronchiolitis independent of oxygenation method used.
Trial registration |
ACTRN12613000388718.
Le texte complet de cet article est disponible en PDF.Keywords : intensive care admission, predictors in bronchiolitis
Abbreviations : HFNC, PICU, SpO2
Plan
The study is funded by a project grant from the National Health and Medical Research Council (NHMRC, GNT1081736 and GNT1058560), Canberra, Australia, and Queensland Emergency Medical Research Fund (QEMRF), Brisbane, Australia. The high-flow equipment and consumables for all study sites were provided free of charge by Fisher & Paykel Healthcare (Auckland, New Zealand). D.F., S.D., and A.S. report receiving travel support from Fisher and Paykel Healthcare, Auckland, New Zealand. The other authors declare no conflicts of interest. |
Vol 256
P. 92 - mai 2023 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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