Considerations for the management of pediatrics with suspected or confirmed COVID‑19

COVID‑19 INFORMATION & RESOURCES

Last Updated: 24 January 2022, 3:44PM (NZDT)

This information resource has been compiled to assist healthcare professionals with the management of neonates, infants, and children with suspected or confirmed COVID-19. This information is not intended to replace the recommendations or requirements of your local hospital policies.  


This resource refers to the World Health Organization (WHO) guidelines.1 Please use the link within this resource to ensure you are accessing the WHO’s most up-to-date advice.

In most pediatric cases, there is no evidence to suggest therapy decisions should be changed. Care should be driven by the patient’s underlying physiological and clinical presentation in conjunction with current evidence-based respiratory-management strategies.
 

 
Jump to:
> Nasal High Flow
> CPAP
> Resuscitation
> Invasive ventilation
> Heated humidification
> Other useful resources and guidelines
> Further F&P Healthcare product resources

Respiratory management of pediatrics in the context of COVID-19


Patients requiring respiratory support due to COVID-19 illness will have a high viral load, and they pose a potential infection risk to healthcare professionals and other patients. All patients with confirmed or suspected COVID-19 illness must be managed with appropriate isolation and personal protective equipment (PPE) precautions. Refer to your hospital policy or the WHO guidelines.

Nasal high flow (NHF)

The WHO guidelines suggest commencing oxygen therapy with nasal cannula or prongs is the preferred oxygen therapy-delivery method for young children as they may be better tolerated, and NHF may be considered in select patients with hypoxemic respiratory failure. All patients treated with NHF should be closely monitored for clinical deterioration.1

For data on aerosol dispersion, please visit Nasal High Flow Therapy COVID-19 Information.


Fisher & Paykel (F&P) Healthcare Nasal High Flow pediatric products#

  • Optiflow™ Junior, Optiflow Junior 2, and Optiflow Junior 2+ nasal high flow interfaces, F&P high flow circuits, and associated accessories are intended for single-patient use only.

CPAP

The WHO guidelines note that in situations where mechanical ventilation might not be available, bubble nasal CPAP may be used for patients with severe hypoxemia and may be more readily available.1

For institutions where bubble CPAP is the current standard of care for newborn infants requiring respiratory support (for non-COVID-19 reasons), there are currently no recommendations to change clinical practice for the majority of neonatal patients.

With any bubble CPAP delivery system there are two main places where gases and potential aerosols are likely to leak: between the patient and the mask/prongs (patient leak), and where the air exits from the bubble CPAP generator (intentional leak).

  • Bubble CPAP therapy should be treated as an aerosol-generating therapy and appropriate PPE should be employed.  
  • A well-sized and fitted mask/prong should be used to reduce patient leak.
  • Attempts to filter the expiratory gas should consider the effects of that filtration on the therapy efficacy.2


F&P Healthcare Infant CPAP products#

  • The F&P Bubble CPAP generator, F&P FlexiTrunk™ nasal interface, F&P Infant CPAP circuits, and all associated accessories are intended for single-patient use only.
  • Addition of an anti-viral solution to bubble CPAP generators has been documented previously.3 F&P Healthcare has not tested the efficacy of such solutions in terms of their ability to reduce aerosolization of a virus from the bubble CPAP system effectively. However, use of a 0.1% acetic acid solution (vinegar) will have no adverse effects on the material of the bubble CPAP generator. The F&P Bubble CPAP generator should always be mounted below the level of the patient.    
  • The placement of a filter anywhere in the expiratory gas path of the bubble CPAP system is not advised. F&P Healthcare recommends extreme caution when using filters in unapproved or improvised ways. Resistance to flow, filtration efficiency in different conditions, instrumental dead space, flow dynamics through the system and the potential for gas-trapping are just some of the important safety factors healthcare professionals should consider. If placing a filter on the bubble CPAP system where it vents to the atmosphere, be aware that the bubble CPAP generator is not designed to be sealed, and therefore not all exiting expiratory gas will be filtered.
  • For placement of a filter on ventilator-driven CPAP circuits, please consult the ventilator manufacturer. For questions related to the use of filters with F&P ventilator circuits, please visit Viral & Bacterial Filtration of F&P Healthcare Filters and F&P Evaqua™ 2 Circuits.

Resuscitation


F&P Healthcare Infant Resuscitation products#

  • The F&P Neopuff™ is intended for multiple-patient use. Neopuff is a positive-pressure device which provides unidirectional gas flow. Gas exits the system through the positive end expiratory pressure (PEEP) valve. This prevents any of the patient’s exposed fluids re-entering the device, which reduces the risk of contamination between patients. Please refer to the product technical manual for instructions for cleaning Neopuff between use on patients.
  • F&P Infant Resuscitation circuits and masks are intended for single-patient use only.
  • The placement of a filter between the T-piece and resuscitation mask is not advised. F&P Healthcare recommends extreme caution when using filters in unapproved or improvised ways. Resistance to flow, filtration efficiency in different conditions, instrumental dead space, flow dynamics through the system and the potential for gas-trapping are just some of the important safety factors healthcare professionals should consider.  

Invasive ventilation


When invasive ventilation is needed, delivering heated and humidified gas is widely recommended and practiced during invasive respiratory support.1


F&P Healthcare Infant Invasive Ventilation humidified circuits#

  • F&P Infant Invasive circuits are intended for single-patient use only.
     
  • For pediatric/neonatal ventilators that do not have an inherent expiratory filter and vent to the atmosphere, a disposable filter may be used.
    • Ensure that the filter has 15mm connections to facilitate secure connections, minimize dead space and optimize ventilator performance.
    • Use only regulatory agency-approved filters. They have been tested in accordance with internationally recognized standards for filtration efficiency against bacteria and viruses.
    • Be aware that the filtration efficiency of filters changes with operation. Check ventilator settings periodically, and replace filters as per the manufacturer’s specification.
       
  • F&P Filters (RT016, RT019, RT020) are not intended for use with F&P neonatal invasive ventilation circuits. For further information on the use of inspiratory/expiratory filters with invasive ventilation circuits, please visit Viral & Bacterial Filtration of F&P Healthcare Filters and F&P Evaqua™ 2 Circuits.
     

Heated humidification


COVID‑19 patients, who are critically ill with severe respiratory disease, need high levels of humidity to assist with secretion management and mucus plugging.5 Heated humidification promotes efficient ventilation and gas exchange,6 and preserves optimal mucociliary function.7

For information about heated humidification for healthcare professionals managing COVID-19 patients, please visit Heated Humidification for Healthcare Professionals Managing COVID-19 Patients.

Other useful resources and guidelines

 

Further F&P Healthcare product resources


For further information on our pediatric product range, including specification sheets, instructions for use, and instructional videos, please visit our Infant Respiratory Care support page. 

For further information on our F&P heated humidifiers and flow generators, please visit: 


# Always refer to the user instructions supplied with the product for full setup instructions, warnings, cautions and contraindications. If a device setup is off-label, the user recognizes that it is not the approved setup of the device and that the responsibility for doing so is their own. 

 
 

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