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Ventilation - Overview of Ventilation in PICU
Ventilation - Overview of Ventilation in PICU
Ventilation - overview of
ventilation in PICU
Date last published: 09 October 2019
A significant number of patients in ICU undergo ventilation for other than respiratory
failure. Optimal ventilation in these patients can be achieved using a variety of ventilatory
strategies and the main aim is to use a ventilatory mode that the patient tolerates
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A significant number of patients in ICU undergo ventilation for other than respiratory failure. Optimal ventilation in these
patients can be achieved using a variety of ventilatory strategies and the main aim is to use a ventilatory mode that the patient
tolerates, while at the same time avoiding ventilation induced lung injury.
The standard mode of ventilation in children has historically been some form of pressure control ventilation which compensates
for a variable leak and protects against excess airway pressures. A small amount of PEEP is added to replace physiologic PEEP
and to prevent atelectasis. Tidal volumes were not routinely measured and rates were set to match what the patient wanted to
breathe at. Adults were ventilated in a volume control mode.
Modern ventilation practices for children are more volume control based and with ventilators having much better sensing and
triggering there is the ability for more forms of triggered assisted ventilation. This has had the advantages of allowing less
sedation/paralysis to be used and maintaining patient respiratory muscle use. There is however scant evidence that any of
these new modes have a great impact on outcome.
This same technology has been applied to noninvasive ventilation allowing the use of this in even very small children which
prevents the adverse effects of tracheal intubation.
Other noninvasive techniques based on the application of CPAP and/or high flows are increasingly used as they are well
tolerated and highly effective when used appropriately.
Equipment
Ventilators
The advent of new ventilation modes has made classification difficult. Traditionally ventilators were classified according to type
of flow generation and how they were cycled and this is perhaps the easiest way of understanding the machines although each
ventilator can operate in a number of modes.
Drager V500
Replacement for the Drager XL.
Capable of ventilating all weights/ages.
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Usual modes that we use are SIMV Volume or Pressure Control + Pressure Support.
Need the neonatal flow sensor for patients less than 5kg
Drager Evita XL
Advantages are active exhalation valve, ATC, variable flow triggering, MMV, autoflow, non-invasive ventilation, APRV
Biggest mistakes are not checking default settings and not confirming changes when selecting settings.
Transport Ventilators
Incubator setups -Crossvent 2+ (neonates and small infants) < 5-6kg (limited by maximum flow rate and incubator size. Can
be used to supply CPAP with constant flow up to 29lpm).
Stretcher setups - Elisse 300. Can be used for mask ventilation as well as invasive ventilation but NOT for high flow.
Endotracheal Tubes
Traditionally in infants and children noncuffed ETTs have been used to avoid damage to the subglottis. This is not
necessary as long as care is taken to avoid excess cuff pressures when using cuffed tubes (cuff pressure should be less
than 20mmHg) or allowing a small leak at inspiratory pressures of 20cm H20.The advantage of the uncuffed tube is that a
larger internal lumen can be achieved.
Nasal tubes are easier to secure in small children and are preferable for those under 5 years unless contraindicated.
Older children use oral ETTs.
Some longer term patients will have tracheostomies.
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Modes
The machine will give the set number of breaths of a set type regardless of patient effort. These may be synchronised to
patient effort (SIMV). If the patient takes additional breaths these may be supported (PS) or be solely patient effort
related.
2. Assist/Control
The machine will give at a minimum the set number of breaths. Patient effort results in a machine breath being delivered.
If the patients breath rate is > machine set rate then the set rate is a back-up rate only
Pressure Control
Routine paediatric mode on Servo and mode to use for those difficult to ventilate.
Can have either SIMV or Assist/Control settings. If using Termination Sensitivity the ventilator may cycle prior to the set
inspiratory time.
Volume Control
Some ventilators will give a decelerating flow wave which may improve oxygenation.
Delivers set volume regardless of compliance but doesn't account for leaks.
Pressure Support
Breath is terminated when either flow has decreased to 5% of peak inspiratory flow or when 80% of the set breath cycle
time is reached (whichever comes first).
Volume Support
Ventilator is able to adjust the inspiratory pressure support within set limits to deliver desired tidal volumes.
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Assist/Control mode.
Adjusts pressure to achieve desired volume and delivers a set number of breaths if the patient is not breathing.
Limits peak pressure to 5cmH₂O below the upper pressure alarm limit.
Oscillation differs by having an active expiratory phase and it requires a special ventilator. The machine uses small tidal
volumes at very rapid rates (up to 900bpm).
Primarily used as a rescue ventilation therapy in hypoxic respiratory failure when conventional ventilation fails. Also used
for babies with congenital diaphragmatic hernia to limit VILI in those requiring high peak inspiratory pressures on
conventional ventilation.
CPAP
Provides a continuous positive expiratory pressure through out the respiratory cycle.
When used with spontaneous ventilation adequate flow is required to meet peak inspiratory flow and maintain level of
CPAP.
Not a specific mode as such but a ventilation strategy that can be used with any control mode by making the Inspiratory
Time greater than the Expiratory Time.
Works by Auto-PEEP and evenly distributing ventilation in lungs with variable time constants.
MMV
Allows for a preset minute ventilation to be set and the machine will give mandatory breaths depending on how much
spontaneous ventilation is occurring. With the Drager this mode uses autoflow which is a combination of PC and VC and
provides decelerating flow.
Pressure Control ventilation with Assist/Control for spontaneous breaths. The rate is a back up rate only.
Triggering
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To enable patient synchrony with the ventilator the trigger MUST ALWAYS be set to the maximum sensitivity. Both over and
undersensing are to be avoided.
ATC (AUTOMATIC TUBE Measures resistance continuously in the ventilator circuit and adjusts pressure
COMPENSATION) to maintain flow.
Theoretically superior to PS.
Weaning
The decision to wean the patient is based on an assessment of lung function (FiO₂, CXR, Ventilatory pressures, PEEP, Respiratory
rate), CVS function (Stability of BP, HR, Inotrope requirement), CNS function (Airway protection/maintenance, Cough, Muscle
strength, Co-operation) and disease progress.
Complicated predictors of successful extubation have been formulated but most are no better than clinician judgement.
The 3 things that prolong patient ventilation are excessive sedation, lack of attempt to extubate, and use of some weaning mode
rather than extubating the patient.
For the routine patient weaning is not involved. They merely need their prolonged "anaesthesia" terminated. Ie muscle
relaxation is ceased, sedation is decreased to allow for a patient who can protect their airway and have adequate respiratory
drive.
Once the patient begins making respiratory effort they are switched to a spontaneously breathing mode and when they are
breathing adequately on minimal support (e.g. PS 10cmH₂O) they can be extubated.
THIS IS NOT WEANING AND SHOULD NOT BE TREATED NOR DESCRIBED AS SUCH.
Remember that going from ventilated to spontaneous breathing changes intrathoracic pressures and may result in different
loading conditions for the heart and alterations in lung water.
Weaning of the more complex patient is not so straight forward. Patients who have been ventilated for some time or who have
muscle weakness may need a period of respiratory muscle retraining over a prolonged period. This may include a gradual
weaning of support levels and/or increasing lengths of time off the ventilator. It is important to not let patients perform excess
work during the weaning process as this will prolong weaning. It is also important to optimise their nutrition - provide adequate
calories but do not overfeed with CHO or water.
The management of ventilation for a serious respiratory illness has 3 components to it.
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Prolonged intubation in children tends to be well tolerated and the need for tracheostomy is very uncommon unless for airway
protection or very long term ventilation.
Once weaned from the ventilator extubation is usually not a problem but can be in cases of airway, CNS, or neuromuscular
abnormalities.
Specific Diseases
The aims of ventilation are to oxygenate the patient, stent the airway open, and allow time for exhalation.
Patients are often best breathing at slower rates with short inspiratory times and with variable amounts of PEEP/CPAP (NB avoid
auto-PEEP).
In the PICU setting this may entail sedating spontaneously breathing patients.
PaCO₂is seldom used as an indicator of the need for intubation. Clinical status is much more important. If the patient requires
ventilation do not try to ventilate to a normal PaCO₂.
The patient with airway collapse often requires a prolonged period of airway support, either via an ETT or with nasal or mask
CPAP. Airway collapse will be exacerbated by anything that causes increased respiratory effort.
These include any of the congenital myopathies. Certain very sick PICU patients may develop a critical illness polyneuropathy
which presents as diffuse weakness.
There are often 3 components to respiratory failure in these patients: respiratory pump weakness, inability to cough, and
inability to protect the airway.
Although many of these diseases are progressive and fatal short term respiratory support is indicated for some of these
patients.
If the problem has been respiratory pump failure these patients will need a rest on the ventilator before considering weaning.
Bronchopulmonary Dysplasia
Patients are often on home oxygen with a degree of respiratory distress/failure when "well" and can therefore deteriorate
rapidly with minor respiratory insults.
There is often a considerable obstructive component to their disease which may or may not be reversible.
It is important to minimise ventilatory pressures, avoid fluid overload, use antibiotics as indicated, and think of increasing
diuretics and adding steroids.
Pulmonary Oedema
If the pulmonary oedema is on the basis of myocardial dysfunction this needs treating (inotropes to improve contractility and
IPPV to unload the LV). The usual cause of this is severe sepsis with large volume infusion and a stiff heart.
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Do not disconnect the patient from PEEP to repeatedly suction as this will worsen the pulmonary oedema.
The commonest cause of this is infective pneumonia but this can be associated with other lung disease or systemic diseases.
These patients may be more hypoxic with ventilation.
Often there are large areas of collapsed/consolidated alveoli that can be recruited with PEEP and this is the initial treatment to
use.
If there is progressive disease diagnosis is important and in severe intraparenchymal disease from an unknown cause BAL and
lung biopsy may be needed to guide treatment.
Neonatal Ventilation
There are major differences in ventilation strategies between neonatologists and intensivists.
Neonatologists seldom paralyse or heavily sedate babies and aim to achieve patient-ventilator synchrony by ventilating at rapid
rates with short inspiratory times.
Intensivists tend to ventilate at slower rates with longer inspiratory times, use more sedation/paralysis, and accept higher
PaCO₂s.
Each believes that their ventilation strategy is the best and for the majority of patients there is little difference. It is becoming
more common to minimise ventilation in the hope of decreasing the incidence of BPD/VILI (see below) but how best to do this is
unclear.
Some neonatal conditions do require a high pH to maximise pulmonary vasodilatation and these in these patients higher rates
of ventilation may be required. It would be rare to ventilate at a rate above 40bpm using conventional ventilation.
Neonates who are failing conventional ventilation should be switched early to HFO and if appropriate discussed re ECMO.
Surfactant is used for RDS and should be given early then repeated if effect wears off.
1. Diagnostic accuracy.
2. Avoiding VILI.
5. Additional treatments.
1. Diagnostic Accuracy
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Tracheal Aspirate
Early BAL to diagnose infection
Radiology CXR.
? CT scan (High resolution).
2. Avoiding VILI
Avoid excessive volume/pressure (Small Vt, Pressure control, Long Tinsp, HFOV).
Avoid atelectasis (Alter patient position, Prone ventilation, Good suctioning technique, ???Chest physio).
3. Optimising O₂ delivery
Optimise PEEP.
Target Hb.
Maximise CO.
Maintain haemodynamics.
Optimise nutrition.
5. Additional treatments
Surfactant.
Nitric oxide.
HFO.
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All these patients will be ventilated and most will require heavy sedation. Most will require paralysis. Some patients will
deteriorate with positive pressure ventilation due to increased V/Q mismatch, increased intrathoracic pressure, and/or
decreased RV function. These patients may oxygenate better if they are breathing spontaneously.
Current vogue in ARDS is the open lung strategy. This uses a prolonged high pressure inflation (eg 40cmH₂O for 40 sec) to open
recruitable lung units followed by high PEEP and small tidal volumes at low rates to maximise oxygenation while limiting injury.
A consequence of this approach is that there is permissive hypercarbia.
1. Supplemental oxygen
Toxic oxygen concentration in the diseased lung is unknown. Aim to get FiO₂ under 50% if possible.
2. PEEP
Aim for 'best PEEP' ie PEEP that maximises oxygen delivery. Start at 5cmH₂O and increase in 2.5cmH₂O increments
watching SpO₂, PIP, P - V curve, and haemodynamics. An alternative in lungs that are known to be very diseased is to start
with a prolonged high pressure inflation then use high PEEP e.g. 10 - 20cmH₂O and decrease it until saturations or PaO₂
drop, then return to level just above this.
Will need IV fluids +/- inotropes to maintain haemodynamics with high PEEP.
If needing >10cmH₂O PEEP do not disconnect to suction but use a Bodai connector and suction through this. If you do
need to disconnect the patient reinflate manually before reconnecting.
3. Tidal Volume
4. Pressure control
This can also be achieved using volume control with a decelerating flow.
Patients with severe respiratory disease on a ventilator often have inappropriate ADH secretion with retention of water.
This excess fluid tends to manifest itself as lung water.
Aim is for euvolemia as hypovolemia will cause haemodynamic instability and decreased oxygen delivery.
Start at an inspiratory time:expiratory time (I:E ) ratio of 1:2 and increase to 1:1.
If oxygenation is still inadequate increase the I:E beyond 1:1 to create inverse ratio ventilation. Few patients will tolerate
this unless paralysed.
This improves oxygenation primarily by causing increased PEEP due to inadequate time for complete expiration (this is
called autoPEEP).
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AutoPEEP needs to be monitored to ensure that it doesn't become excessive and interfere with haemodynamics and/or
ventilation. This is done by using expiratiory hold on the ventilator and seeing what the expiratory pressure is, or by
disconnecting the patient from the ventilator and watching how long expiration continues. Either of these manoeuvres
may result in much improved haemodynamics.
7. Recruitment Manoeuvres
Safest to perform using the ventilator with insp hold or very long I time and slow rate.
8. Permissive hypercapnia
Not in head injury or reactive pulmonary hypertension (may still allow a high PaCO₂ in pulmonary hypertension and
control pH with bicarbonate).
9. Prone Ventilation
Unstable patients will often deteriorate initially and take up to 20-30 mins to show improvement.
Consider cooling.
Variable responses.
Start at 20ppm and decrease as tolerated. Most responders need only 1-2ppm for effect.
Uses high mean airway pressures and small tidal volumes at very rapid rates.
Used early in infant lung disease this mode of ventilation does reduce long term lung injury.
3100A for < 30kg and 3100B for large children and adults.
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Bias flow 20L (40L on the B), power to wiggle, I time 33%, FiO₂=1
Check CXR to ensure adequate inflation - should show 9-10 ribs posteriorly
14. Surfactant
Effective in a number of conditions but prohibitively expensive for all but neonates and infants.
Augments tidal volume and PEEP, increases FiO₂, and washes out CO₂.
Small catheter placed beyond ETT tip and low flow oxygen is given.
16. ECMO
Limited availability.
17. Steroids
No place in acute management but can be beneficial in preventing excessive fibrosis during the resolution of ARDS.
The trick is getting the timing right and avoiding the complications.
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