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FOR STAFF Staff working with children requiring acute usage of NIV
PATIENTS Patients from birth up to 18 years old, requiring the acute usage of NIV.
Contents Page
Introduction 2
Background
Mechanism
Advantages of NIV over invasive ventilation
Disadvantages of NIV compared to invasive ventilation
Think ‘ICEMAN’
Equipment 5
General equipment
Interfaces
Circuits
Ventilators
Modes 11
Next Steps 16
Patient improving
Patient deteriorating
V2 June 2022, review date June 2025 S. Coles, PICU Physiotherapist / C Stutchfield, PICU Consultant 1 of 33
Introduction
1.1 Background
Non-invasive ventilation (NIV) can be defined as ventilatory support using techniques that do not
require an endotracheal airway. These techniques are distinguished from those that bypass the
upper airway with a tracheal tube, laryngeal mask or tracheostomy and which are therefore
considered invasive.
1.2 Mechanism
To increase functional residual capacity
To decrease airway resistance and improve lung compliance, reducing work of breathing
and therefore reducing O2 consumption
To improve alveolar ventilation therefore reducing V/Q mismatch and improving gas
exchange
To decrease inspiratory muscle work and aid avoidance of respiratory muscle fatigue
Supports respiratory musculature
Beneficial effect on cardiac afterload and cardiac output
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THINK ’ICEMAN’
Contraindications: Cautions:
Need for airway protection Craniofacial trauma
Severe respiratory failure
Contraindication (Coma. GI bleed/vomiting)
C Severe ARDS Excessive secretions
Undrained
Pneumothorax
Recent GI surgery
Vomiting
A Clinical monitoring
Monitoring of complications
Analysis of failure
Failure troubleshooting
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Indications and contraindications
Respiratory insufficiency
Increased work of breathing and respiratory distress
Respiratory acidosis (pH ≤ 7.3)
Apnoeas with desaturations or bradycardia, particularly secondary to bronchiolitis
Upper airway obstruction
Neuromuscular illness (e.g. Guillain-Barre, SMA, muscular dystrophy)
Elective post extubation in difficult to wean or high risk patients
Rescue method to avoid re-intubation
For children normally on long term ventilation
2.2.1 Contraindications:
Need for airway protection
Coma
Active gastrointestinal bleed / severe vomiting
Severe PARDS: Acute respiratory failure with bilateral infiltrates and a PF ratio ≤100 or SF
ratio ≤150 (not explained by lung oedema).
Haemodynamic instability (particularly if not responsive to initial fluid resuscitation)
Fixed airway obstruction
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Equipment
3.1 General equipment for NIV
Hydrocolloid (Comfeel) dressings: we should aim to protect the patient’s skin prior to the
initial mask application to avoid pressure sores. Comfeel should be applied to the face
where the edges of the mask will sit.
o Oronasal masks are the most high risk, particularly over the bridge of the nose
o Full face masks have a wider distribution area of pressure, and therefore reduce the
risk of pressure areas. Comfeel is NOT required on those.
Straps and head gear will depend on the type of interface used. They can be interchanged
if required and there are spare sets kept separately on PICU or with the LTV team. Do not
overtighten straps. You should be able to fit two fingers between the mask and the patients
face.
Interfaces: Classification:
o Location: nasal, nasal prong, oro-nasal, full face mask, helmet
o Exhalation: vented (mask has a leak allowing for effective CO2 clearance) or non-
vented (they will need a CO2 exhalation port in the circuit or expiratory limb i.e dual
limb circuit).
o Safety: with or without an anti-asphyxia valve.
These masks contain valves which in the event of ventilator failure or power outage,
will open and allow you to breathe room air in, to prevent re-inhalation of CO 2 by the
patient.
They are essential for any patient that is not continuously cardiovascularly monitored,
on an NIV or home ventilator.
Please note: it is a safety feature, not a method of CO2 exhalation
In conventional ventilators, the valve can mistakenly drop and cause
asynchrony
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Of note:
Nasal masks are generally indicated for Type II chronic respiratory failure (CRF)
without acute deterioration. Can be a good option in patients who struggle to
tolerate oro-nasal or full face masks, and as option to cycle onto when devising a
weaning or progression plan. Also preferable in patients who normally use nasal
masks with LTV at home.
Helmets, Full face masks and oro-nasal masks are best suited for Type I and
Advanced Type II Acute Respiratory Failure (ARF), in which the patient cannot
breathe through the nose alone, especially for dyspnoeic patients that tend to
breathe through the mouth. These masks offer more support for patients. They
should be considered as a first option in patients who are likely to require a higher
level of support or present with an acute deterioration.
3.2. Interfaces
3.2.1 Non-Vented Masks (SE elbow- standard elbow – BLUE ELBOW).
To be used with Servo I/U and Hamilton
3.2.2 Non Vented masks with Anti-asphyxia Valve (EE elbow leak 1 – CLEAR ELBOW).
To be used with V60 or Trilogy
These masks contain valves which in the event of ventilator failure or power outage, will open and
allow you to breathe room air in, to prevent re-inhalation of CO 2 by the patient. They are a safety
feature, not a method of CO2 exhalation. If the valve opens, the patient will NOT BE VENTILATED.
V2 June 2022, review date June 2025 S. Coles, PICU Physiotherapist / C Stutchfield, PICU Consultant 6 of 33
Performax Full Face Mask
Available in sizes XXS, XS, S, L
Sizing guide available
Interface comes with cap (XXS, XS) or black head gear (S,L)
Elbows can be changed
Mask Fitting
Optimal management is for all patients that require 24/7 NIV use to have two
different masks to avoid pressure areas developing (full face and oronasal).
Remember the hats between the masks are interchangeable and you may need to
mix and match different sizes to achieve the best fit
Use the sizing guides when fitting the masks to avoid opening masks you don’t
use
To optimise fitting it should be a two person technique
Comfeel should be applied to pressure areas on the face when oronasal is used
You should always be able to fit two fingers between the mask and skin
The masks do not need to be overtightened, it is ok to have a leak as long as the
pressures and tidal volumes are being achieved.
The elbows are interchangeable so can keep the same mask if changing
ventilators
Remove mask at least 4 hourly and check pressure areas
Please refer to specific ventilator set ups guides (in Appendix) for mask fitting information
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3.2.4 CPAP for babies ≤4kg
For babies ≤ 4kg requiring CPAP only, Medin sets of nasal masks and nasal prongs are available.
They only fit on the neonatal ventilation circuit sets, but are compatible with both the Servo I and
Servo U ventilators. The pressure line is removed from the circuit when using the Medin sets. They
are for use in the Nasal CPAP NIV mode.
3.3 Circuits:
Single limb for specific NIV ventilators- V60, Resmed, NIPPY, Stella, Trilogy, Astral
o Home ventilator circuits do not have a leak, use vented masks
o V60 circuits are single limb but have a standard exhalation device within the circuit –
always use non-vented masks in that case
Dual limb for conventional ventilators- Servo I and Servo U
o Circuit doesn’t have an exhalation valve, exhalation occurs through the expiratory
limb - Use non-vented masks
3.4 Ventilators:
NIV specific ventilator equipped with an oxygen blender - V60, Trilogy 202
Conventional ventilator with a NIV option - Servo I and Servo U and Hamilton
NIV specific home ventilators without oxygen blender – Trilogy 100, Astral, Stella, Nippy
(add O2 through a port; allow an FiO2 of up to 0.6)
NIV specific ventilators will always be the optimum choice in bigger children, because they
compensate better for leaks, and the expiratory triggers are more sensitive than in
conventional ventilators.
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Maquet Servo I ventilator, NIV option
Dual limb circuit
Non vented mask
FiO2 up to 1.0
Use with SE elbow masks (blue)
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Trilogy 202 NIV specific ventilator
Single limb circuit
Vented mask
FiO2 up to 1.0
Licenced >5kg
Use with EE elbow masks (clear)
There is a home ventilation model (100)
without blender.
Resmed Stella
Single limb circuit
Vented mask
O2 delivered in litres, not able to titrate
percentage
FiO2 will be a mix from the air taken from
the air + the oxygen added
Use with home ventilation masks! Mask
will have to be vented.
Resmed Astral
Single limb circuit
Vented mask
O2 delivered in litres, machine will
calculate the percentage
Up to 30L/min O2 can be added
Use with home ventilation masks! Mask
will have to be vented.
MODE:
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When programming NIV we should take into account:
Age of the patient
o ≤3 months, likely asynchronous, consider CPAP as initial mode
o ≥ 3 months, more likely to synchronise, BLPAP can be used as first option.
Type of respiratory failure we are supporting (although patients will usually have mixed
characteristics as the disease progresses):
o Type I acute respiratory failure (ARF): Characterized by V/Q mismatch without
alveolar hypoventilation. In paediatric patients it tends to occur with pneumonia, acute
pulmonary oedema, chest wall trauma, neonatal respiratory distress syndrome
(NRDS) and acute respiratory distress syndrome (ARDS).
o Type II ARF: Is characterized by alveolar hypoventilation. It tends to be associated
with conditions that affect the respiratory drive, as well as airway obstruction,
neuromuscular weakness, chest wall abnormalities and morbid obesity
Degree of hypoxaemia:
Titrate FiO2
for SpO2 92-
Figure 1. Algorithm for NIV failure analysis based on S/F ratio for a target SpO2 92-97%.
MV: Mechanical ventilation; BLPAP: Bilevel positive airway pressure; CPAP: Continuous positive airway pressure; APO: Acute pulmonary oedema;
ARDS: Acute respiratory distress syndrome, S/F: oxygen saturation/fraction of inspired oxygen; HR: Heart rate; RR: Respiratory rate.
From: Medina A, Pilar J, Humphry A, Christopherson M, Garcia Cusco M, editors. Handbook of paediatric and neonatal mechanical ventilation.
Oviedo (Spain): Tesela ediciones; 2018
General concepts
o CPAP provides one level of pressure (PEEP/EPAP)
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o It can be used in respiratory failure type I and apnoeas, particularly in asynchronous
patients (<3month age)
o The optimal PEEP for bronchiolitis is approximately 7cmH2O
General concepts
o Provides two levels of pressure: PEEP/EPAP and PIP/IPAP
o Requires synchrony for its optimal delivery
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breaths per minute you set as a back up- the V60 works out how many breaths
your patient should be taking. If the patient fails to trigger a breath within the
interval determined by the rate setting it will detect an apnoea and deliver a
mandatory breath. It is important to remember this when setting the back up
rate- if it is too high it will trigger unnecessarily It should be set as low as
possible to avoid this happening and to avoid asynchrony.
The rise time will determine how long it takes the patient to reach the target
pressure during inspiration. Altering this can improve patient comfort and
synchronisation. Aim for a starting point of 3.
Autotrack + is a feature to increase trigger sensitivity and expiratory cycle
sensitivity and can be used in younger patients, smaller patients and those that
find it harder to trigger i.e. patients with neuromuscular conditions.
Trigger sensitivity ranges from 1 being the least sensitive to 7 being the
most sensitive
The E-Cycle determines the expiratory cycle sensitivity. It determines the
threshold at which the ventilator will transition from inspiration to exhalation,
so lengthening or reducing the duration of inspiratory flow.
Ramp can be used to allow the patient to become accustomed to respiratory
ventilatory therapy over time. Ramp will allow the pressure to linearly increase
over a user-set period. It would be advised to no set it no longer than a
maximum of 10minutes
Please refer to specific ventilator set ups guides (in Appendix) for clear navigation to access
these additional settings
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ANALYSIS OF FAILURE / TROUBLESHOOTING:
5.1 Clinical Monitoring
Patients requiring NIV are critically ill and need monitoring, but we should aim to perform it as non-
invasively as possible, avoiding repeated blood gases.
Heart Rate
Respiratory Rate
SaO2 Hourly
FiO2
SatO2/FiO2
Chest X Ray- initially in hypoxemic patients (to rule out ARDS and pneumothorax) and if
clinical deterioration.
The P/F ratio is a measure of intrapulmonary shunting, and is obtained by comparing arterial to
inspired oxygen.
This value can be calculated by dividing the arterial oxygen tension (PO 2) by the fraction of inspired
oxygen (FiO2). S/F ratio is a correlation to P/F ratio and is calculated using the O 2 saturations
instead of the PO2. e.g.: SaO2 92/ FiO2 0.8 = 115
S/F ratios are a reasonable way of identifying early ALI and ARDS, e.g.:
o Acute lung injury S/F Ratio < 315
o Acute Respiratory Distress S/F Ratio < 23
SpO2/FiO2 (SF) ratio is a non-invasive, easily and continuously available figure that has been
shown to have a good correlation with the PaO2/FiO2 (PF ratio), that is a measure of shunt and a
predictor of mortality. According to this, a low SF ratio (below 150) would correspond to a severe
hypoxemic acute respiratory failure. SF ratio can only be calculated when SpO 2 is ≤97%. However,
as long as the oxygen saturation is kept between 93-97%, We can use FiO 2 required to estimate
the degree of respiratory failure.
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5.4 Failure Troubleshooting
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NEXT STEPS
(for medics and NIV trained physiotherapists and nurses)
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If no improvement after optimisation
Of note:
Ensure stomach is vented with NGT (or PEG) on free drainage or regularly aspirated
Always think about your patient position, particularly their airway
The humidifier should always be set to the ‘non-invasive’ setting regardless of the circuit
If you are cycling off NIV and turning the humidifier off, on turning it back on it will always
restart on the ‘invasive setting’
Dummies can be used only after being risk assessed by NIV specialist (
RELATED Continuous Positive Airways Pressure (CPAP) For Infants in Paediatric Critical Care
DOCUMENTS (Paediatric HDU/ICU)
Bubble CPAP Competency Document
Neurally adjusted ventilatory assist NAVA
SAFETY Wrong connection of equipment can lead to inability to ventilate or instability of the
patient. Please double check that correct equipment is used.
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APPENDIX 1
AVOID USING V60 IF AT ALL POSSIBLE
MHRA/NPSA ALERT (March 2022) – potential unexpected shutdown
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Set –up
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3. Ensure temperature wires in place and circuit connected
Temperatur
e wires
Temperatur
Note: the circuit is a single limb circuit, with a CO2 exhalation port that MUST NOT BE
COVERED e probe
attached to
the
connector
below
CO2 the
elbow piece
exhalation
onport
the
mask
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4. Turn V60 on, button located at the front of the machine
5. Check the right mode is selected i.e. CPAP or Batch S/T (BLPAP)
6. Check the alarm settings are appropriate for the patient and reset as required
Note… Alarms can be silenced, paused and reset using the touch screen options along the
top of the screen
7. Program in type of mask used by leak number- leak number can be found on elbow of the
mask, this allows the ventilator to compensate for the anticipated leak and tidal volumes for
the specific mask. Go to MENU, MASK/PORT, press arrows to get required LEAK
NUMBER then press ACCEPT
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Once you input the mask and press accept it will also ask you for the type of CO2 clearance device.
Always select ‘DEP’ (disposable expiration port) unless you are not using our standard circuit and
set up
8. Doctors; physios or nurses who have successfully completed the ventilation weaning
course can program the appropriate ventilation settings for the patient
9. Once the V60 is on and the settings are correct then fit the mask to the patient (Note: the
mask should not be fitted until the V60 is set up and on)
MASK FITTING
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Oxygen delivery
Oxygen percentage is set using the touch screen function and is accessed from the main screen
To go into standby…
Only Doctors, nurses and physios who have successfully completed the ventilation
management course are able to alter the V60 ventilator settings
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V60 modes: AVOID USING V60 IF AT ALL POSSIBLE
MHRA/NPSA ALERT (March 2022) –potential unexpected shutdown
CPAP mode
S/T mode
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1. Trigger settings
2. Monitor Tidal volume and the trend and ensure it is within acceptable range for your patient (6-
12mls/kg). e.g. 10kg patient would have an estimated TV of between 60-120mls
3. Observe Patient trigger in conjunction with respiratory pattern for feedback on respiratory effort
and synchronisation
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patient comfort and synchronisation.
5. Ramp can be used to allow the patient to become accustomed to respiratory ventilatory therapy
over time. Ramp will allow the pressure to linearly increase over a user-set period. It would be
advised to no set it no longer than a maximum of 10minutes.
1. Press and release the ON/Shutdown key. The Shutdown window opens.
2. Select Ventilator Shutdown.
Screen Lock
Deactivates all buttons and tabs on the touchscreen except Alarm Silence, Alarm Reset, the
Alarm/Message button, and Help.
Tabs are greyed out.
This message bar is displayed at the top of the screen: To unlock the screen, press the
Accept button in the centre of the navigation ring.
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APPENDIX 2
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Nasal CPAP interface
Required:
o Neonatal circuit and additional NIV connector
o A bonnet
o An interface → Medin nasal prongs or mask
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Bonnets
Ensure the MEDIN fixation label is on the outside to ensure the 2 ventilation limbs sit
securely within it
Set up:
1. Connect your circuit to the ventilator
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2. Connect humidifier and fill- set to NON INVASIVE SETTING
Servo I
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6. Ensure appropriate interface selected
BLPAP Interfaces
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2. Oro-nasal masks (SE elbow)
Require:
o Paediatric or adult circuit
o Mask appropriately sized
o Can be used on the Servo I/U
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