Physiological effects of high-flow nasal cannula therapy in preterm infants

Arch Dis Child Fetal Neonatal Ed. 2020 Jan;105(1):87-93. doi: 10.1136/archdischild-2018-316773. Epub 2019 May 23.

Abstract

Objective: High-flow nasal cannula (HFNC) therapy is increasingly used in preterm infants despite a paucity of physiological studies. We aimed to investigate the effects of HFNC on respiratory physiology.

Study design: A prospective randomised crossover study was performed enrolling clinically stable preterm infants receiving either HFNC or nasal continuous positive airway pressure (nCPAP). Infants in three current weight groups were studied: <1000 g, 1000-1500 g and >1500 g. Infants were randomised to either first receive HFNC flows 8-2 L/min and then nCPAP 6 cm H2O or nCPAP first and then HFNC flows 8-2 L/min. Nasopharyngeal end-expiratory airway pressure (pEEP), tidal volume, dead space washout by nasopharyngeal end-expiratory CO2 (pEECO2), oxygen saturation and vital signs were measured.

Results: A total of 44 preterm infants, birth weights 500-1900 g, were studied. Increasing flows from 2 to 8 L/min significantly increased pEEP (mean 2.3-6.1 cm H2O) and reduced pEECO2 (mean 2.3%-0.9%). Tidal volume and transcutaneous CO2 were unchanged. Significant differences were seen between pEEP generated in open and closed mouth states across all HFNC flows (difference 0.6-2.3 cm H2O). Infants weighing <1000 g received higher pEEP at the same HFNC flow than infants weighing >1000 g. Variability of pEEP generated at HFNC flows of 6-8 L/min was greater than nCPAP (2.4-13.5 vs 3.5-9.9 cm H2O).

Conclusions: HFNC therapy produces clinically significant pEEP with large variability at higher flow rates. Highest pressures were observed in infants weighing <1000 g. Flow, weight and mouth position are all important determinants of pressures generated. Reductions in pEECO2 support HFNC's role in dead space washout.

Keywords: high flow nasal cannula oxygen; neonatology; physiology; respiratory.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Body Weight
  • Carbon Dioxide / blood
  • Continuous Positive Airway Pressure
  • Cross-Over Studies
  • Female
  • Humans
  • Infant, Newborn
  • Infant, Premature
  • Male
  • Oxygen / blood
  • Oxygen Inhalation Therapy / methods*
  • Positive-Pressure Respiration*
  • Prospective Studies
  • Respiratory Distress Syndrome, Newborn / therapy*
  • Tidal Volume
  • Vital Signs

Substances

  • Carbon Dioxide
  • Oxygen

Supplementary concepts

  • Respiratory Distress Syndrome In Premature Infants