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Performance and safety of the PRICO closed-loop oxygen saturation targeting system in neonates: pragmatic multicentre cross-over study (TarOx Study)

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68407700%3A21460%2F24%3A00380971" target="_blank" >RIV/68407700:21460/24:00380971 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://doi.org/10.1136/bmjpo-2024-002583" target="_blank" >https://doi.org/10.1136/bmjpo-2024-002583</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1136/bmjpo-2024-002583" target="_blank" >10.1136/bmjpo-2024-002583</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Performance and safety of the PRICO closed-loop oxygen saturation targeting system in neonates: pragmatic multicentre cross-over study (TarOx Study)

  • Popis výsledku v původním jazyce

    Objective This study aims to evaluate the performance of the fabian-Predictive-Intelligent-Control-of-Oxygenation (PRICO) system for automated control of the fraction of inspired oxygen (FiO(2)). Design Multicentre randomised cross-over study. Setting Five neonatal intensive care units experienced with automated control of FiO(2) and the fabian ventilator. Patients 39 infants: median gestational age of 27 weeks (IQR: 26-30), postnatal age 7 days (IQR: 2-17), weight 1120 g (IQR: 915-1588), FiO(2) 0.32 (IQR: 0.22-0.43) receiving both non-invasive (27) and invasive (12) respiratory support. Intervention Randomised sequential 24-hour periods of automated and manual FiO(2) control. Main outcome measures Proportion (%) of time in normoxaemia (90%-95% with FiO(2)>0.21 and 90%-100% when FiO(2)=0.21) was the primary endpoint. Secondary endpoints were severe hypoxaemia (<80%) and severe hyperoxaemia (>98% with FiO(2)>0.21) and prevalence of episodes >= 60 s at these two SpO(2) extremes. Results During automated control, subjects spent more time in normoxaemia (74%+/- 22% vs 51%+/- 22%, p<0.001) with less time above and below (<90% (9%+/- 8% vs 12%+/- 11%, p<0.001) and >95% with FiO(2)>0.21 (16%+/- 19% vs 35%+/- 24%) p<0.001). They spent less time in severe hyperoxaemia (1% (0%-3.5%) vs 5% (1%-10%), p<0.001) but exposure to severe hypoxaemia was low in both arms and not different. The differences in prolonged episodes of SpO(2) were consistent with the times at extremes. Conclusions This study demonstrates the ability of the PRICO automated oxygen control algorithm to improve the maintenance of SpO(2) in normoxaemia and to avoid hyperoxaemia without increasing hypoxaemia.

  • Název v anglickém jazyce

    Performance and safety of the PRICO closed-loop oxygen saturation targeting system in neonates: pragmatic multicentre cross-over study (TarOx Study)

  • Popis výsledku anglicky

    Objective This study aims to evaluate the performance of the fabian-Predictive-Intelligent-Control-of-Oxygenation (PRICO) system for automated control of the fraction of inspired oxygen (FiO(2)). Design Multicentre randomised cross-over study. Setting Five neonatal intensive care units experienced with automated control of FiO(2) and the fabian ventilator. Patients 39 infants: median gestational age of 27 weeks (IQR: 26-30), postnatal age 7 days (IQR: 2-17), weight 1120 g (IQR: 915-1588), FiO(2) 0.32 (IQR: 0.22-0.43) receiving both non-invasive (27) and invasive (12) respiratory support. Intervention Randomised sequential 24-hour periods of automated and manual FiO(2) control. Main outcome measures Proportion (%) of time in normoxaemia (90%-95% with FiO(2)>0.21 and 90%-100% when FiO(2)=0.21) was the primary endpoint. Secondary endpoints were severe hypoxaemia (<80%) and severe hyperoxaemia (>98% with FiO(2)>0.21) and prevalence of episodes >= 60 s at these two SpO(2) extremes. Results During automated control, subjects spent more time in normoxaemia (74%+/- 22% vs 51%+/- 22%, p<0.001) with less time above and below (<90% (9%+/- 8% vs 12%+/- 11%, p<0.001) and >95% with FiO(2)>0.21 (16%+/- 19% vs 35%+/- 24%) p<0.001). They spent less time in severe hyperoxaemia (1% (0%-3.5%) vs 5% (1%-10%), p<0.001) but exposure to severe hypoxaemia was low in both arms and not different. The differences in prolonged episodes of SpO(2) were consistent with the times at extremes. Conclusions This study demonstrates the ability of the PRICO automated oxygen control algorithm to improve the maintenance of SpO(2) in normoxaemia and to avoid hyperoxaemia without increasing hypoxaemia.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    20601 - Medical engineering

Návaznosti výsledku

  • Projekt

  • Návaznosti

    S - Specificky vyzkum na vysokych skolach

Ostatní

  • Rok uplatnění

    2024

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    BMJ Paediatrics Open

  • ISSN

    2399-9772

  • e-ISSN

    2399-9772

  • Svazek periodika

    8

  • Číslo periodika v rámci svazku

    1

  • Stát vydavatele periodika

    GB - Spojené království Velké Británie a Severního Irska

  • Počet stran výsledku

    7

  • Strana od-do

  • Kód UT WoS článku

    001312956400001

  • EID výsledku v databázi Scopus

    2-s2.0-105001272340