|1

Dräger Ventilation Mini Manual

Brief explanation of ventilation modes and functions
 TABLE OF CONTENTS |3

Table of contents

PC-BIPAP vs. PC-AC 04 - 06

Pressure Control – Biphasic Positive Airway Pressure vs.
Pressure Control – Assist Control
PC-APRV (Pressure Control – Airway Pressure Release Ventilation) 07 - 08
VC-MMV + AutoFlow 09 - 10
Volume Control – Mandatory Minute Volume + AutoFlow
ATC – Automatic Tube Compensation 11 - 13
SPN-PPS (Proportional Pressure Support) 14 - 15
SmartCare® 16 - 22
P0.1 – Occlusion Pressure Measurement 23 - 24
Leak Compensation 25 - 27
NIV (Non-invasive Ventilation) 28 - 30
Variable PS (Variable Pressure Support) 31 - 33
PEEPi (Intrinsic PEEP / AutoPEEP) 34 - 36
Low Flow Manoeuvre 37 - 38
Ventilation Terms 39 - 40
Notes 41 - 42
4| PC-BIPAP VS. PC-AC

PC-BIPAP vs. PC-AC

Pressure Control – Biphasic Positive Airway
Pressure vs. Pressure Control – Assist Control

PC-BIPAP

PC-AC (BIPAP ASSIST)

–– machine- or patient-triggered, mechanical strokes with inspiratory
synchronisation
–– spontaneous breathing possible at any time
–– back-up frequency
 PC-BIPAP VS. PC-AC |5

With PC-BIPAP the patient can breathe spontaneously at any time, while
the number of mandatory strokes is pre-set. In this mode, the mandatory
strokes exhibit both an inspiratory as well as expiratory synchronisation
with the patient’s breathing efforts. If the mandatory stroke is reduced
due to expiratory synchronisation, the subsequent mandatory stroke is
extended. The inspiratory synchronisation shortens the expiration phase.
In this case, the subsequent expiration time is extended by the missing
time. This ensures that the set mandatory breathing frequency (f)
remains constant. Machine-triggered mechanical breaths are applied if
no spontaneous breathing is detected during the inspiration trigger
window. The patient may receive Pressure Support (PS) during
spontaneous breathing at the PEEP level.
D-7523-2014

Fig. 1 (PC-BIPAP with mandatory and spontaneous mechanical breaths)

 6| PC-BIPAP VS. PC-AC

With PC-AC, every attempt to breathe that is detected on the PEEP

level triggers a mandatory mechanical breath. This means that the patient
determines the time and the number of mandatory mechanical breaths.
To give the patient enough time for expiration, it is not possible to trigger
another mandatory breath directly after a mechanical breath. A mandatory
breath is applied (backup frequency), if no mechanical breath has been
triggered after the expiratory time has elapsed.
D-7529-2014

Fig. 2 (PC-AC with triggered and untriggered mechanical breaths)

 PC-APRV |7

PC-­APRV
(Pressure Control – Airway Pressure Release Ventilation)

–– pressure-controlled
–– time cycled
–– machine-triggered
–– spontaneous breathing under continuous positive breathing pressure
with brief pressure relief times (screenshot)

In PC-­APRV, the patient’s spontaneous breathing takes place at the

upper pressure level Phigh. This pressure level Phigh is maintained for the
duration of Thigh. To achieve active expiration, the pressure is reduced for
a brief period from Tlow to Plow. To support CO2 elimination, the pressure
is then reduced to Plow for the brief period Tlow. The alternation between
the two pressure levels is machine-­triggered and time-­cycled. The
breathing volume (VT) that expired during the relief times, results from
the pressure difference between Plow and Phigh and the lung mechanics.
If the resistance or compliance of the lungs changes during the
ventilation treatment, the supplied tidal volume (VT) and thus the minute
volume MV may also vary.

During the activation of AutoRelease, the duration of released pressure

is determined by the expiratory flow trace. The Exp. term. setting
determines the percentage by which the expiratory flow must fall short of
in relation to the peak flow for the ventilation to return to the high
pressure level.
D-7540-2014 8| PC-APRV

Fig. 1 (PC-APRV with AutoRelease on and measured Tlow in seconds)

D-7539-2014

Fig. 2 (PC-APRV with spontaneous breathing on Phigh level)

 VC-MMV + AUTOFLOW |9

VC-MMV + AutoFlow
Volume Control – Mandatory Minute Volume + AutoFlow

–– volume-controlled ventilation to backup a mandatory minute volume

–– the mechanical breaths are automatically and gradually reduced for
patients with increasing spontaneous breathing, which is possible at
any time
–– enables automatic weaning by reducing the mechanical breathing
frequency and
–– necessary ventilation pressure

VC-MMV behaves in a similar manner to VC-SIMV; however, the

mandatory breaths are only administered if the spontaneous breathing is
insufficient and falls below a set minute volume. If the spontaneous
breathing increases, fewer mandatory breaths are administered. This
allows VC-MMV to ensure that the patient always at least receives the set
minimum volume MV (MV=VT*f). The applied mechanically triggered,
timed breaths are synchronised with the patient’s inspiratory efforts. This
ensures that spontaneous breathing is always possible for the patient at
the PEEP level. If the patient’s spontaneous breathing is sufficient to
achieve the set MV, no further mandatory breaths are applied. This
means that the set breathing frequency (f) is the maximum number of
mandatory breaths. The patient may receive Pressure Support (PS)
during spontaneous breathing at the PEEP level. Every inspiratory effort
by the patient at the PEEP level, which meets the trigger criteria, triggers
a pressure-supported mechanical breath. The time, number and duration
of the pressure-supported mechanical breaths are determined by the
patient’s spontaneous breathing.
 10 | VC-MMV + AUTOFLOW

AutoFlow (AF) ensures that the set tidal volume (VT) is applied with the
minimum necessary pressure for all volume-controlled, mandatory
breaths. In the event of changing resistance (R) or compliance (C), the
pressure is gradually adjusted in order to administer the set VT. Both the
pressure and the flow are adapted automatically. The patient is able
to breath spontaneously during the entire breathing cycle, during
inspiration and expiration.

MV

Set MV
Mandatory MV
Spon. breathed MV
t
No Starting Sufficient
spontaneous spontaneous spontaneous
breathing breathing breathing
Fig. 1 (from 100% ventilation to 100% spontaneous breathing)
D-75-28-2014

Fig. 2 (VC-MMV + AF with mandatory breath and spontaneous breathing)

 ATC | 11

ATC
Automatic Tube Compensation

–– ensures that the set airway pressure is also obtained in the trachea
–– is calculated and displayed based on a mathematical tube model,
the set tube type and the tube’s internal diameter (tracheal pressure)
–– can be activated for any mode of ventilation

The tube as an artificial resistance in the airway is the main reason for
increased breathing effort by the patient. The automatic tube
compensation is a supplement for all ventilation modes and enables the
precise compensation of this increased work of breathing, with easy
setting options. The patient’s inspiratory effort should feel as if they are
not intubated. A gas flow through the tube leads to a pressure difference
(ΔP tube) between the start and end of the tube [Fig. 1]. This pressure
difference should stimulate the respiratory muscles in the form of
increased negative pressure in the lungs. However, the increased work
of breathing can be compensated by increasing the pressure in front of
the tube by precisely the amount of the pressure difference. This means
that the pressure in front of the tube also needs to be continuously
adapted to the relevant gas flow. The actual pressure difference is
calculated based on the gas flow measured by the ventilator. Automatic
tube compensation can be activated for any mode of ventilation. The tube
dimensions must first be set. The level of compensation (generally 100%)
can be used to fine-tune the settings for the relevant tube in order to
prevent overcompensation. The length of the tube does not have a
significant influence on the tube resistances, even for very short tubes,
and is not set.
 12 | ATC

The tube compensation is applied for both inspiration as well as

expiration. [see Fig. 3] If necessary for expiratory compensation, the
pressure in the tube system is reduced to no less than the ambient
pressure in order to facilitate the patient’s exhalation. The control
ensures that the tracheal pressure does not fall below the set CPAP
pressure.

without ATC with ATC

Paw
Paw

P trachea P tube P tube

P trachea

P mus
D-7480-2014

P mus

Fig. 1 Without ATC, the patient needs to apply the ΔP tube.

With ATC, the ventilator generates precisely this ΔP tube and provides relief for the
patient.
 ATC | 13

delta
P tube
25

Pressure difference between

the tube connector and the
20 tube tip for a 7.5 mm tube

15

10

PS undercompensation
5

PS overcompensation
PS pressure
D-7481-2014

10 20 30 40 50 60 70 80 Flow

Fig. 2 Set pressure support (PS) compared to pressure support required in principle (blue
line) for tube compensation.

Paw
Pressure at the Y-piece
Ptrach

Tracheal pressure

PEEP

t
Flow

Fig. 3 Pressure profile for tube compensation during inspiration and expiration.
14 | SPN-PPS

SPN-PPS
Spontaneous – Proportional Pressure Support

–– applies patient-triggered pressure support in proportion to the patient’s

inspiratory effort
–– the level of support can be set separately for restrictive or obstructive
work of breathing

For SPN-PPS, the pressure support should ideally be proportional to the

patient’s inspiratory effort. If the patient’s breathing is shallow, little
support is provided. More support is applied for a deep breath. The
absolute amount of support depends on both the Flow Assist and
Volume Assist parameter settings as well as the patient. The two types of
pressure support, pressure support proportional to volume (Volume
Assist) and pressure support proportional to flow (Flow Assist) [Fig. 1]
can be combined. If set correctly, only the illness-related higher work of
breathing is continuously adapted and compensated – the physiological
work of breathing continues to be provided by the patient alone. Flow
Assist helps overcome the resistance (R) and the pressure support is
proportional to the flow. In contrast, Volume Assist compensates the
elastic resistance (C) caused by reduced elasticity of the lungs. The
pressure support is proportional to the tidal volume. The relationship
between the inspiratory effort and the pressure support remains
constant for the same settings, while the pressure support varies for
every breath. If no spontaneous breathing is detected, the mechanical
support also ceases. Adequate apnoea and minute volume monitoring
must therefore be in place.
 SPN-PPS | 15

Flow Assist: pressure profile proportional Vol. Assist: inspiration pressure profile
to the flow proportional to the tidal volume VT

Flow Flow

VT VT

t t
Paw Paw
PEEP PEEP
t t
Inhalation Exhalation Inhalation Exhalation

Fig. 1 Rules for Flow and Volume Assist

D-7526-2014

Fig. 2 SPN-PPS, typical pressure and flow graph

16 | SMARTCARE®

SmartCare®

–– is an automatic clinical protocol

–– reduces the pressure support based on the averaged measured values
for the spontaneous respiratory rate, the tidal volume and the ETCO2
until the lowest possible level is reached
–– can reduce the overall ventilation period by up to 33% and the stay in
the intensive care unit by up to 20%1)

SmartCare®/PS is an automated clinical protocol, which was designed

to stabilise a patient’s spontaneous breathing in a “comfort zone” and
automatically reduce the respiratory support. The patient should be ready
for weaning, i.e. haemodynamically stable, and display adequate oxygen-
ation and spontaneous breathing. SmartCare/PS attempts to keep the
patient within the “normal ventilation” range and places the patient back
“on the right track” in the event of a contrasting diagnosis. The patient’s
ventilation status is classified into eight different diagnoses and defined
measures are taken in order to bring the patient back to the “normal
ventilation” range, also referred to as the “respiratory comfort zone”. The
three key criteria are the spontaneous respiratory rate
(RRspon), tidal volume (VT) and endtidal CO2 (ETCO2) [ventilator’s
measured values]. This protocol is active during all phases of
a SmartCare/PS session. In addition, the pressure support level is
gradually reduced during the “adapt” phase, while continuous checks
confirm whether the patient is able to tolerate the new level. If this is the
case, the pressure support is reduced further, if not, it is increased back
to a level that is appropriate for the patient. The optimal case involves the
gradual and direct reduction of the pressure support until the lowest
level is reached.
 SMARTCARE® | 17

1) Lellouche, F. et al.; a Multicenter Randomized Trial of Computer-driven Protocolized Weaning from Mechanical
Ventilation. am J Respir Crit Care Med Vol 174. pp 894 -900, 2006 – The results are based on a randomised
study in several European hospitals with 144 patients who displayed a stable ventilation situation, a stable hae-
modynamic and neurological status and no ARDS prior to their initial weaning.

Insufficient
Hypoventilation
ventilation
Severe tachypnoea

55 mmHg
Tachypnoe

Normal
Hyperventilation
ventilation
20 mmHg

Unexplained
hyperventilation
D-7482-2014

ETCO2
fspn
35 bpm 30 bpm 15 bpm

Fig. 1 Diagnostics diagram based on the key criteria

Initiate Adapt Monitor Maintain

No

Extubate?

Quickest path

Regression in case of permanent instabilities

D-7483-2014

Automatic protocol

User measures

Fig. 2 Functional principle – individual phases during SmartCare®

18 | SMARTCARE®

PREREQUISITES

It is important to choose the “right” patient. SmartCare/PS is ideal

for patients with primary restrictive problems and longer expected
weaning times. SmartCare/PS does not replace the clinician. The
advantage of SmartCare/PS is its ability to continuously monitor
the patient making appropriate changes to pressure support much
more often than this would be possible manually. Prior to starting
weaning with SmartCare/PS, the patient must be haemodynamically
stable, be ventilated with SPNCPAP/PS (optionally with ATC), and
the set PEEP must be ≤ 20 mbar.

QUICK START

1.PATIENT
a) Set the patient’s height; this
calculates the IBW and the
lower limit for the tidal volume
(Vt) can be derived from it.
b) Set the maximum permissible
PEEP value and the
inspiratory oxygen
concentration for the start of
the spontaneous breathing
test.

SmartCare/PS can be started with any PEEP setting between

0 and 20 mbar and with any selected FiO2 concentration. The
spontaneous breathing test starts once the target support pressure
(∆Psupp target, see 2.) has been reached and the PEEP and FiO2
values set by the user have been reached or undercut.
 SMARTCARE® | 19

2. A
 CCESS TO THE AIRWAY
These settings define the target
support pressure at which the
spontaneous breathing test
starts (provided that PEEP and
FiO2 are also below the set
values – see 1). The following
table shows the dependencies
of the different settings:

Access to the airway, ΔPsupp IBW

type of humidification target

Patient tracheostomised, active/no 5 mbar ≥ 36 kg

humidification, ATC OFF
Patient endotracheally intubated, active/no 7 mbar ≥ 36 kg
humidification, ATC OFF
Patient tracheostomised, HME filter, 9 mbar ≥ 36 kg
ATC OFF
Patient endotracheally intubated, HME filter, 10 mbar ≥ 36 kg
ATC OFF
Patient tracheostomised or endotracheally 0 mbar ≥ 36 kg
intubated, active humidification, ATC ON
Patient tracheostimised or endotracheally 5 mbar ≥ 36 kg
intubated, HME filter, ATC ON

If the therapists prefers to set target values for the pressure support
that differ from those that are shown in the table, he can enter
“wrong” specifications (e.g., tracheostomised rather than intubated)
to generate a different target value for the pressure support.
20 | SMARTCARE®

3. MEDICAL HISTORY
Selection of COPD and
neurological disorder for the
automatic adaptation of the
upper limit for etCO2 and the
respiratory rate (RR)

The COPD “Yes” setting means that the SmartCare/PS continues

to accept etCO2 values less than or equal to 64 mmHg (8.5Kpa) as
normal. This may also be helpful for patients with permissive
hypercapnia. The neurological disorder “Yes” setting means that the
SmartCare/PS continues to accept respiratory rates of up to 34/min
as normal. This may also be helpful for patients with higher
respiratory drive.

4. NIGHT’S REST
No active weaning takes place
during the selected period, i.e.,
SmartCare/PS maintains the
pressure support it had reached
prior to night rest commencing.
However, SmartCare/PS will
increase the pressure support if
the patients condition
deteriorates.
Night’s rest can also be set in order to give the patient a break
from weaning. It is also possible to set or switch off night’s rest
during an ongoing session.
 SMARTCARE® | 21

5. C HANGE THE GUIDELINE

Extended functionality for
customising the weaning
protocol.

This lets you define an individual respiratory comfort zone for the
patient. The set values of the medical history (see 3.) have no impact
if the guideline is changed.

6. START PATIENT SESSION

Flow measurement, CO2
measurement and apnoea
ventilation must be switched on.

The following icon appears in the header bar once the SmartCare/
PS session has successfully started
22 | SMARTCARE®

TIPS AND TRICKS

– Alarm limits must generally be set above and below the Smart-
Care/PS limit values (see instructions for use).
– An apnoea alarm leads to the unwanted cancellation of the
SmartCare/PS session.
Therefore, possible disconnections should be shorter than the
set apnoea time.
– A functioning CO2 measurement is required for SmartCare/PS
(position the CO2 cuvette to prevent the accumulation of
moisture or secretion, e.g., between the Y-piece and the HME
filter or vertically, pointing upward).
– Configure a specific SmartCare/PS view with the required
specific information (SmartCare/PS values, status and trends).
– Use the O2/suction function to perform a suction manoeuvre.
This pauses the SmartCare/PS and gives the patient time to
recover.
– The SmartCare/PS is suitable for adult and paediatric patients.

More information: www.draeger.com/smartcare

 P0.1 – OCCLUSION PRESSURE MEASUREMENT | 23

P0.1 – Occlusion Pressure Measurement

–– occlusion pressure measurement at the start of inspiration

–– is a measure of the neuromuscular respiratory drive1)

During a P0.1 manoeuvre, the ventilator closes the inspiratory valve for a
brief period after expiration and measures the airway pressure generated
over 100 ms by the inspiratory effort [Fig. 1]. The pressure is not
influenced by physiological compensation reactions, e.g. reflective
respiratory arrest or increased drive, within 100 ms. This pressure also
fundamentally depends on the muscular strength of the diaphragm. As a
result, the negative mouth pressure P0.1 after 0.1 seconds is a measure
of the neuromuscular respiratory drive1). The ventilator displays the value
of the measured pressure difference [Fig. 2]. For patients with healthy
lungs and calm breathing, the P.01 value is between 3 and 4 mbar (3 to
4 cmH2O). A higher P0.1 value reflects a high respiratory drive, which can
only be maintained for a limited time. P0.1 values over 6 mbar
(6 cmH2O), e.g. for a COPD patient, reflect imminent fatigue (respiratory
muscle fatigue). As shown in figure 1, the 100 ms starts once negative
pressure of -0.5 mbar (–0.5 cmH2O) is measured during the inspiratory
effort under PEEP/CPAP. The second pressure value is determined
after the 100 ms have elapsed. The inspiratory valve is simultaneously
opened. The patient can then breathe normally once again. The pressure
difference value “P2 - P1” defines the occlusion pressure P0.1.
 24 | P0.1 – OCCLUSION PRESSURE MEASUREMENT

Normal value1):
P0.1 = 1 up to 4 mbar
P0.1 > 6 mbar, indication of imminent respiratory muscle fatigue,
high probability of weaning failure.
1) Oczenski W (ed). Atmen-Atemhilfen. 8. Auflage 2008
Tobin MJ (ed). Principles and Practice of Mechanical ventilation. Second Edition. McGraw-Hill, New York,
2006, Sasson CSH, et al. Airway Occlusion Pressure : An important Indicator for successful weaning in
patients with Chronic obstructive pulmonary disease. AM Respir Dis. 1987;135:107-113

Paw Inspiratory valve

closed
100m s Inspiratory valve open
PEEP
–0.5 mbar t
(–0.5cm H2O) P1
P0.1

P2

Fig. 1 Functional principle of the P0.1 measurement

D-7524-2014

Fig. 2 Screen layout during a P0.1 measurement

 LEAK COMPENSATION | 25

Leak Compensation

–– leaks are compensated for in volume- and pressure-controlled

ventilation
–– the inspiratory flow trigger threshold and the cancellation criteria for
pressure support are adapted automatically
–– leak compensation displays all the volume and flow measured values
with leak compensation

The ventilator determines the difference between the dosed inspiratory

flow and the flow measured during expiration. This difference defines the
size of the leak and is displayed as the leak minute volume MVleak and
the relative leak % (MVleak to MV). The leak correction calculation takes
the pressures in the breathing circuit into account. The percentage
volume loss during inspiration is greater than the loss during expiration,
as the pressure is higher during inspiration. The leak minute volume MV-
leak also considers inspiratory leaks. During volume-controlled
ventilation, the ventilator provides additional volume to compensate for
the leak. The ventilator compensates volume losses up to 100% of the set
tidal volume Vt. Measured volume and flow values are displayed with leak
compensation. An exception is the measured expiratory minute volume
as well as measured values marked as inspiratory or expiratory, such as
VTi and VTe. The inspiratory flow trigger threshold and the cancellation
criterion are applied to the leak-corrected flow, while both settings are
continuously adapted with respect to the leak.
26 | LEAK COMPENSATION

Vt Tidal volume, leak-corrected

Vti Inspiratory tidal volume, without leak-correction
Vte Expiratory tidal volume, without leak-correction
Mv Minute volume
Mvi Inspiratory Minute volume, without leak-corrected
Mve Expiratory Minute volume, total, without leak-corrected
Mvleak Leak Minute volume
(based on the medium pressure Paverage)
D-7522-2014 LECKAGENKOMPENSATION | 27

Fig. 1 Screen example with VC-AC, large leak without leak compensation
D-7541-2014

Fig. 2 Screen example with VC-AC, large leak with leak compensation
 28 | NIV

NIV
Non-invasive ventilation

–– in all ventilation modes

–– with comprehensive monitoring
–– with alarm adaptation
–– with automatic leak compensation

When ventilating adults or children, non-invasive ventilation may help to

avoid intubation.1) In other cases, it supports the weaning process for
intubated patients. The additional availability of mask ventilation in the
weaning phase helps to improve workflows and can potentially reduce
the risk of intubation.1)
Irrelevant alarms, which are necessary during invasive ventilation, can be
suppressed during non-invasive ventilation. As a result, alarm settings
that are not required can be disabled. (E.g. MV low, Vti high and apnoea
monitoring).
Leak compensation is an important feature for non-invasive ventilation.
When leak compensation is activated, the patient always receives the
set Vt volume (i.e. leaks are taken into account for the tidal volume). The
flow trigger and the cancellation criteria are continuously adapted with
respect to the leaks. In addition, the set pressure is maintained if leaks
occur.

Prevention
D-7484-2014

Stabilisation

Fig. 1 Ventilation path

 NIV | 29

If the mask is removed, the Anti-Air Shower function (available with Evita
XL and Evita Infinity V500) detects this interruption and reduces the gas
flow provided by the ventilator to a minimum. This minimises the risk of
the possible contamination of the nursing staff and the ambient air.
1) Ferrer M; am J respir crit care Med vol 168. pp 1438–1444, 2003

Recovery Non-invasive ventilation

Weaning
Invasive ventilation
D-7532-2014 30 | NIV

Fig. 2 Example of a SPN/CPAP/PS setting window for activated NIV

D-7530-2014

Fig. 3 Example PC-AC screen for activated NIV

 VARIABLE PS | 31

Variable PS
Variable Pressure Support
(noisy ventilation/variable pressure support)

–– is an automatic variation of the pressure support (PS) in SPN-CPAP/PS

–– randomly changes the supporting pressure within a defined variation
range
–– supports the physiological variance of spontaneous breathing

The “variable pressure support” generates random pressure support

variations. This changes the tidal volume regardless of the patient’s
spontaneous breathing efforts, as different pressure support levels are
applied for each breath. The basic principle for pressure-supported
spontaneous breathing remains in place and is not modified.
A specific pressure support (ΔPsupp) is initially set. The amount of
variation is defined as a percentage of the set pressure support (PS) and
can vary from 0% to 100%. For example, a set pressure support of 10
mbar and a variance of 50% provides for a minimum pressure support of
5 mbar and a maximum pressure support of 15 mbar. Due to the variation
of the pressure support, different ventilation pressures and tidal volumes
are provided for every breath. The maximum pressure support, which can
be achieved by the variation, is limited by the maximum airway pressure
(Pmax) setting. The lower variation threshold is defined by the set CPAP
level.
The ventilation pressure amount is independent of the patient’s
inspiratory effort.
32 | VARIABLE PS

The pressure support variation provided by variable PS leads to an

increased variability of the tidal volume (VT) compared to conventional
pressure-supported ventilation, regardless of the patient’s inspiratory
effort. In addition, variable PS can improve oxygenation and result in the
redistribution of the pulmonary blood flow.1)
1) M. Gama de Abreu et al Noisy pressure support ventilation: A pilot study on a new assisted ventilation mode
in experimental lung injury. Crit Care Med 2008 vol. 36, no.3
D-7537-2014 VARIABLE PS | 33

Fig. 1 Screen for SPN-CPAP/PS with variable pressure support

D-52617-2012

Fig. 2 Setting window for the variable pressure support

34 | PEEPi

PEEPi
Intrinsic PEEP (intrinsic PEEP / AutoPEEP)

–– is the actual end-expiratory pressure in the lungs

–– is added to the PEEP set on the ventilator

There may be various reasons to explain why the total inhaled volume
cannot subsequently be exhaled. The unphysiological volume retained in
the lungs leads to an intrinsic PEEP. Overly short expiratory times,
obstructions, or slow lung compartments are likely to be the main reason
for this.

The measuring manoeuvre determines the volume that remains in the

lungs (Vtrap). The intrinsic PEEP measurement is performed in two
measurement phases. The ventilator keeps the inspiratory and the
expiratory valve closed for the duration of measurement phase 1. This
means that neither inhaled gas can enter the breathing circuit, nor other
gas can leave the breathing circuit. A pressure equalisation between the
lungs and the ventilation system takes place during this measurement
phase. The ventilator measures this pressure profile. The patient’s
breathing activity during the manoeuvre may distort the measured values.
Measurement phase 1 comes to an end:
–– when the pressure profile does not show any further changes.
The starting value is equal to the PEEP and the value at the end of the
measurement phase is the intrinsic PEEP.
At the end of measurement phase 1, the ventilator opens the expiratory
valve and measures the expiratory flow that is generated by the intrinsic
PEEP in measurement phase 2. The lungs are relieved to the PEEP.
 PEEPi | 35

Measurement phase 2 comes to an end:

–– when the expiratory flow has returned to 0. The measured flow
corresponds to the volume trapped in the lungs due to the intrinsic
PEEP (Vtrap).
Effective PEEP (PEEPtotal) = PEEP (PEEPset) + intrinsic PEEP

Paw Insp. and exp.

valves close Exp. valve opens

PEEPi
PEEP

Measurement phase 1 t
Measurement phase 2

Flow

t
Vtrap

Fig. 1 Functional principle of the intrinsic PEEP measurement

D-7525-2014 36 | PEEPi

Fig. 2 Screen example of the intrinsic PEEP measurement

 LOW FLOW MANOEUVRE | 37

Low Flow Manoeuvre

–– may record a virtually static inspiratory and expiratory PV loop

–– may provide information for the PEEP and Pinsp setting

Slowly filling the lungs with a low, constant flow (generally 4 to

10 L/min1)) determines the elastic properties of the PV loop. This virtually
static process displays a good correlation with the static Super Syringe
method, provided that the flow is low. The loop can only be recorded for
inspiration or for inspiration and expiration. Two cursors can be moved
over the PV loop in order to determine the lower inflection point (LIP) or
the upper inflection point (UIP) on the inspiratory limb and the critical
connection pressure (CCP) or the point of maximum curvature (PMC)
on the expiratory limb. This can also be used to calculate the static
compliance.

The user can define the gas flow, the maximum applied pressure and the
maximum applied volume for the manoeuvre. The user can also set a
starting pressure, which should normally be well below the set PEEP.

Valid data is only provided if the patient is not breathing spontaneously.

1) Blanc Q, sab JM, Philit F, Langevin B, Thouret JM, Noel P, Robert D, Guérin c. Inspiratory pressure-volume
curves obtained using automated low constant flow inflation and automated occlusion methods in arDs
patients with a new device. Intensive Care Med. 2002 Jul;28(7):990-4. epub 2002 Jun 12.
 38 | LOW FLOW MANOEUVRE

ml
Traditional interpretation:
Traditional interpretation: of little application of lung overdistension, remain
interest as it is difficult to obtain. below this point with Pinsp/Pplat!

More current interpretation: of more More current interpretation:

interest, especially with regard to the PMC end of recruitment and/or lung
expiratory limb (as expiratory PEEP), overdistension possible in certain cases,
probably indicates the PEEP required to reduce Pplat.
maintain recruitment, influenced by the
volume history. UIP

Traditional interpretation:
lung fully recruited at this point, adapt
PEEP above this point.
LIP
More current interpretation:
0
use of alveoli recruitment with similar
D-7485-2014

0 10 20 30 40 50
starting 60 influenced
pressure, 70 by breast
Pressure wall.

Fig. 1 Information from the Low Flow manoeuvre

D-9096-2009

Fig. 2 Example evaluation menu screen following Low Flow measurement

 VENTILATION TERMS | 39

Ventilation in intensive care for adults

Volume-controlled ventilation modes

Previous IPPV/ IPPVassist/
nomenclature CMV CMVassist SIMV MMV
New VC-CMV VC-AC VC-SIMV VC-MMV
nomenclature

Pressure-controlled ventilation modes

Previous BIPAPassist/ BIPAP/
nomenclature PCV+assist PCV+ APRV
New PC-CMV PC-AC PC-SIMV PC-BIPAP PC-APRV PC-PSV
nomenclature

Supported spontaneous breathing modes

Previous CPAP/ASB/ PPS
nomenclature CPAP/PS
New
nomenclature SPN-CPAP/PS SPN-CPAP/VS SPN-PPS

Ventilation in intensive care for neonates

Pressure-controlled ventilation modes

Previous
nomenclature IPPV SIPPV SIMV PSV CPAP-HF
New
nomenclature PC-CMV PC-AC PC-SIMV PC-APRV PC-PSV PC-HFO PC-MMV

Supported spontaneous breathing modes

Previous
nomenclature CPAP
New
nomenclature SPN-CPAP/PS SPN-CPAP/VS SPN-PPS SPN-CPAP
40 | VENTILATION TERMS

Ventilation in anaesthesia

Volume-controlled ventilation modes

Previous IPPV SIMV
nomenclature
New Volume Control - CMV Volume Control - SIMV
nomenclature

Pressure-controlled ventilation modes

Previous PCV
nomenclature
New Pressure Control - CMV Pressure Control - BIPAP
nomenclature

Pressure-controlled ventilation modes

Previous Man. Spont.
nomenclature
New Pressure Support - CPAP Man./Spon
nomenclature

More information (e.g. product training material,

booklets and case studies) is available at
www.draeger.com under the Training heading in
the Hospital area.
 NOTES | 41

Notes
42 | NOTES
CORPORATE HEADQUARTERS REGION MIDDLE EAST, AFRICA
Drägerwerk AG & Co. KGaA Dräger Medical GmbH
Moislinger Allee 53–55 Branch Office
23558 Lübeck, Germany P.O. Box 505108
www.draeger.com Dubai, United Arab Emirates

90 69 812 | 15.03-1 | Communications & Sales Marketing | PR | LE | © 2015 Drägerwerk AG & Co. KGaA
Tel +971 4 4294 600
Fax +971 4 4294 699
As of August 2015:
contactuae@draeger.com
Dräger Medical GmbH changes
to Drägerwerk AG & Co. KGaA.
REGION ASIA / PACIFIC
Draeger Medical
REGION EUROPE CENTRAL South East Asia Pte Ltd.
AND EUROPE NORTH 25 International Business Park
Dräger Medical GmbH #04-27/29 German Centre
Moislinger Allee 53–55 Singapore 609916, Singapore
23558 Lübeck, Germany Tel +65 6572 4388
Tel +49 451 882 0 Fax +65 6572 4399
Fax +49 451 882 2080 asia.pacific@draeger.com
info@draeger.com
REGION CENTRAL
REGION EUROPE SOUTH AND SOUTH AMERICA
Dräger Médical S.A.S. Dräger Panama Comercial S. de R.L.
Parc de Haute Technologie d’Antony 2 Complejo Business Park,
25, rue Georges Besse V tower, 10th floor
92182 Antony Cedex, France Panama City
Tel +33 1 46 11 56 00 Tel +507 377 9100
Fax +33 1 40 96 97 20 Fax +507 377 9130
dlmfr-contact@draeger.com contactcsa@draeger.com