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Hough, Judith, Shearman, Andrew, Liley, Helen, Grant, Caroline, & Schi-bler, Andreas(2014)Lung recruitment and endotracheal suction in ventilated preterm infantsmeasured with electrical impedance tomography.Journal of Paediatrics and Child Health, 50(11), pp. 884-889.
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https://doi.org/10.1111/jpc.12661
1
Title: Lung recruitment and endotracheal suction in ventilated preterm
infants measured with Electrical Impedance Tomography
Hough JL1,2,3, Shearman AD1,4, Liley H1,4, Grant CA5, Schibler A3
Affiliations 1Critical Care of the Newborn Program, Mater Research, South Brisbane, QLD, Australia 2School of Physiotherapy, Australian Catholic University, Banyo, QLD, Australia 3Paediatric Critical Care Research Group, Paediatric Intensive Care Unit, Mater Children’s
Hospital, South Brisbane QLD, Australia 4Department of Neonatology, Mater Health Services, South Brisbane, QLD, Australia 5Institute of Health and Biomedical Innovation, Queensland University of Technology,
Brisbane, QLD, Australia
Address for correspondence
Dr Judy Hough
Department of Physiotherapy
Mater Children’s Hospital
South Brisbane 4101 QLD Australia
Phone: +61 (7) 3163 1143 Fax: +61 (7) 3163 1642
e-mail: [email protected]
Key Words: Electrical impedance tomography; Ventilation distribution; Suction; Infant,
newborn
Australia New Zealand Clinical Trials Registry: ACTRN12610000452099
2
What is already known on this topic:
1. Suctioning is a standard procedure in ventilated preterm infants and there are significant
associated risks.
2. Transient hypoxia and loss of lung volume are some of the documented associated
risks.
3. Electrical impedance tomography (EIT) is a non-invasive clinical tool which can be used
to measure end expiratory level (EEL) and ventilation distribution after suction in
neonates to enable assessment of lung volume loss with suction.
What this paper adds:
1. Despite significant derecruitment with ETT suction, there was rapid recovery resulting in
an increase in EEL immediately post suction. EEL remained increased for the next 2
hours, suggesting that the benefit of suction occurs much longer than many of the
previous studies have described.
2. There were regional differences in ventilation distribution suggesting heterogeneity in
the behaviour of the lung.
3. Retrospective analysis found that the mode of ventilation had little impact on changes in
EEL or ventilation distribution
3
ABSTRACT
Aims: Although suctioning is a standard airway maintenance procedure, there are significant
associated risks, such as loss of lung volume, due to high negative suction pressures. This
study aims to assess the extent and duration of change in end expiratory level (EEL) resulting
from endotracheal tube (ETT) suction and to examine the relationship between EEL and
regional lung ventilation in ventilated preterm infants with respiratory distress syndrome.
Methods: A prospective observational clinical study of the effect of ETT suction on twenty non-
muscle relaxed preterm infants with RDS on conventional mechanical ventilation in a Neonatal
Intensive Care Unit. Ventilation distribution was measured with regional impedance amplitudes
and EEL using electrical impedance tomography.
Results: ETT suction resulted in a significant increase in EEL post suction (p<0.01).
Regionally, anterior EEL decreased and posterior EEL increased post suction suggesting
heterogeneity. Tidal volume was significantly lower in volume guarantee compared with
pressure controlled ventilation (p=0.04).
Conclusions: ETT suction in non-muscle relaxed and ventilated preterm infants with RDS
results in significant lung volume increase which is maintained for at least 90 minutes.
Regional differences in distribution of ventilation with ETT suction suggest that the behaviour of
the lung is heterogeneous in nature.
Word count: 196
4
INTRODUCTION
Each year over 8000 infants born in Australia and New Zealand will require assistance with
their ventilation [1]. The presence of an endotracheal tube (ETT) stimulates increased mucus
production necessitating regular airway suction to remove secretions. Although suctioning is a
standard procedure used in airway maintenance, significant associated risks are well
documented. These risks include atelectasis and loss of lung volume due to high negative
suction pressures [2-5], hypoxaemia [6-8], cardiovascular instability and changes in
cerebrovascular volume [9, 10]
The physiological effect of suction is commonly monitored with pulse oximetry and blood gas
analysis. Both measurements are poor estimates of changes in ventilation distribution or lung
volume making it difficult to assess the degree of the suction induced lung collapse. Electrical
impedance tomography (EIT) has been used as a non-invasive clinical tool to measure end
expiratory level (EEL, as an equivalent to functional residual capacity) and ventilation
distribution after suction in neonates [11, 12].
It has been shown that after endotracheal suction there is a transient hypoxia and a loss of
lung volume. These parameters recover within the first few minutes after reconnection of the
ETT and it has been speculated that maintaining spontaneous breathing is an important factor
in restoring EEL. Limited data are available on the effect of suction on respiratory mechanics,
EEL and regional ventilation distribution for the two hours post suction.
The purpose of this study was to assess the extent and duration of change in EEL resulting
from ETT suction and to examine the relationship between EEL and regional lung ventilation in
ventilated preterm infants with respiratory distress syndrome (RDS).
5
METHODS
Study design
This prospective, observational study investigated ETT suction in preterm infants on
mechanical ventilation to determine its effect on derecruitment of the lungs.
Subjects
Infants were recruited from the Neonatal Intensive Care Unit (NICU) at the Mater Mothers’
Hospital (MMH), South Brisbane, Australia. Inclusion criteria were infants’ ≤ 32 weeks
gestational age with a body weight of > 750 g who were less than 7 days of age at onset of
endotracheal ventilation and had an arterial sampling line (umbilical or extremity) in situ.
Exclusion criteria were cardiopulmonary instability, ETT leak >50%, lung anomaly affecting
regional ventilation, air leak syndrome, or poor skin integrity. The study protocol was approved
by the Human Research Ethics Committees of the Mater Health Services, South Brisbane,
Queensland. Informed written consent was obtained from the parents. All infants required
ventilation and surfactant therapy at birth for RDS. Ventilatory support was delivered in volume
guaranteed (VG) or the pressure controlled (PC) modes of synchronised intermittent positive
pressure ventilation (SIPPV) or synchronised mandatory ventilation (SIMV) (Babylog 8000+
ventilator, Dräger Medical AG Co, Lübeck, Germany) with a tidal volume (VT) determined by
the clinical team caring for the baby (usually 3-5mL/kg).
Suction procedure
ETT suction was performed via the Bodai Neo2-SAFEtm manifold within the RT235 ventilator
circuit (Fisher & Paykel Healthcare, Auckland, New Zealand). In all instances a size 6 FG
catheter was used for suction. The suction procedure commenced with the removal of the flow
sensor (ISO 15, Dräger Medical AG Co, Lübeck, Germany) from the circuit (RO sensor).
Following instillation of 0.2 – 0.3 ml saline, the catheter was inserted to just past the tip of the
ETT and suction was applied continuously at a pressure of 100mm Hg whilst the catheter was
6
withdrawn (S1). Suction took less than 10 seconds and was repeated (S2). After the
completion of suction the flow sensor was re-inserted into the circuit (IO sensor). The indication
for ETT suction was either routine 6 hourly suctioning or clinical signs of secretions in the
upper airways and/or ETT.
Measurements
A Göttingen GoeMF II EIT tomograph (VIASYS Healthcare, Netherlands) was used to measure
EEL, amplitudes and regional ventilation distribution. Sixteen conventional ECG electrodes
(Kendall, Kittycat 1050NPSM, Tyco Healthcare group, Mansfield, Massachusetts) were placed
circumferentially around the infants’ chest at nipple level. Prior to the commencement of the
suction procedure a one minute EIT measurement was performed with a frame rate of 44 Hz.
This period was used for referencing of all following measurements. A ten minute EIT
measurement was taken during the suction procedure and one minute EIT measurements
were repeated at 15 minute intervals for 120 minutes after completion of the suction procedure.
The infant was positioned supine throughout the study period. Data are reported during the
suction procedure and at 30, 60, 90 and 120 minutes. Software provided with the equipment
was used for data acquisition and reconstruction of functional relative EIT images [13]. Data
were further analysed off-line using Matlab 7.7 (R2008b, The MathWorks Inc, Natick, MA,
USA).
Data processing and analysis EIT data were band pass filtered to include the first and
second harmonic of the respiratory rate [14]. A cut-off mask of 20% of the peak impedance
signal was applied [15] to eliminate cardiac interference.[14] As the preterm infant often
displays a periodic respiratory pattern, noise-free, regular sections of data were selected for
analysis using predetermined criteria.[16]
Measurement of EEL. EEL, as measured by EIT, is the relative impedance measured at end
expiration and is analogous with functional residual capacity. Changes in EEL during and after
7
suction were compared to EEL immediately prior to suction for the global, the dependent
(posterior), and nondependent (anterior) lung.
Measurement of Regional Ventilation Distribution. Regional impedance amplitudes as a
measure of ventilation distribution were used to describe the magnitude of the regional tidal
volume change within an individual over time. Impedance amplitudes for the entire lung (global
impedance amplitudes), and the regional impedance amplitudes of the dependent (posterior)
and non-dependent (anterior) lung were calculated by averaging the impedance differences in
each pixel of the measurement period between the end expiratory and end inspiratory periods.
To account for the unequal number of pixels analysed in each region of interest (ROI), the
average amplitude for each ROI was reported.
Respiratory mechanics. Continuous flow and pressure measurement of the delivered
ventilator breaths were downloaded from the Babylog 8000/8000+ ventilator with v5.01
software (Dräger Medical AG & Co. KG, Lübeck, Germany). Tidal volumes (Vt), minute
volumes (MV), resistance (R), peak pressures (PIP) and PEEP were documented for each EIT
recording period. Due to the removal of the flow sensor during suction, these measurements
were unable to be taken during the suction period.
Physiological parameters. Invasive blood pressure (BP), inspired oxygen (FiO2), respiratory
rate (RR) and heart rate (HR) were monitored throughout the study. Oxygen saturations
(SpO2) were manually recorded at the time of each EIT recording using the Masimo Radical
pulse oximeter (software V.6.0.2) (Masimo, Irvine, CA, USA). Oxygen saturations of between
88 and 94% were targeted in the NICU by titrating the FiO2. As arterial blood gas sampling was
not undertaken due to concerns about excessive withdrawal of blood, the SpO2/FiO2 ratio was
calculated from the collected data as a surrogate measure for PaO2/FiO2.[17]
Mode of Ventilation. The delivered mode of ventilation was dependent on consultant
preference. Infants were ventilated using either the pressure controlled modes (PC) of
8
synchronised intermittent positive pressure ventilation (SIPPV) or synchronised intermittent
mandatory ventilation (SIMV), or the volume guaranteed mode (VG) of SIPPV and volume
guarantee (SIPPV+VG). With pressure controlled modes of ventilation, the maximum PIP was
limited and resulted in variable tidal volumes whereas in volume guarantee the tidal volume
was pre-set and the airway pressure changed in response to changes in lung compliance and
resistance. As there are differences in the way the different modes of ventilation deliver
ventilator inflations we performed a sub-analysis of our data to determine if the mode of
ventilation contributed to the differences found.
Statistical analysis. Results are described using mean and confidence intervals (CI), or
standard deviations (SD) for the biometric data. Mixed linear models (MLM) were used to
analyse the impact of ventilation mode (volume guarantee or pressure controlled, VG and PC
respectively) and time of measurement on impedance amplitude, EEL, physiological and
ventilator parameters. ANOVA with Bonferroni correction was then used to compare repeated
measures. A p-value of < 0.05 was considered significant. All statistical analyses were
performed using SPSS (v15.0, Lead Technologies, Inc., Chicago, IL, USA).
9
RESULTS
Patient characteristics. Twenty infants ventilated for RDS were included in the study. All
infants received surfactant therapy. The infants had a mean (±SD) gestational age of 26.6
(±1.8) weeks, study weight of 991.4 grams (± 234.1), and postnatal age of 1.9 days (±1.2).
Seven infants were ventilated using VG. There were no differences in demographics between
the infants ventilated with PC or VG (Table 1). At baseline VT was significantly lower in VG
mode (p=0.04) as was SpO2 (p=0.05). All other baseline characteristics were similar (Table 2)
Changes in EEL. No interaction between mode of ventilation and change in EEL could be
demonstrated (p=0.86). During suction the EEL dropped below the pre-suction level (p<0.01).
There was a distinct loss of lung volume after RO sensor with the greatest volume loss
occurring at S1. (Figure 1)
Post suction global EEL increased significantly (p < 0.01). Post hoc correction showed that the
improved EEL was maintained for 120 minutes (p<0.03) (Figure 2).
Similarly the anterior (non-dependent) and the posterior (dependent) lung showed an increase
in EEL irrespective of ventilation mode (Figure 2). EEL was higher for the first 90 minutes in
the anterior lung (p<0.10) and was back to baseline after 120 minutes (p=0.09). The posterior
lung showed an increased EEL even after 120 minute (p = 0.04).
Changes in regional ventilation distribution. There was no interaction between change in
global and regional amplitude and ventilation mode (p=0.68). There were no differences in
impedance amplitude during the suction procedure compared to pre-suction. The amplitude in
the anterior ROI was larger than during the pre-suction period (p<0.03), however no
differences remained post suction. The global amplitude increased 30 min post suction but the
change was not significant (Figure 3). The anterior amplitude decreased after suction and
remained lower, but the differences did not reach statistical significance. The posterior
amplitude increased after suction but not significantly.
10
Changes in Respiratory Mechanics and Physiological Parameters. There were no
significant differences pre and post suction for minute volume (p=0.60), PIP (p=0.91) or VT
(p=0.99). PEEP was maintained at 5 cm H2O for all patients. There was a significant difference
in resistance over time (p=0.03) with a reduction in resistance post suction compared to pre
suction.
There was a significant interaction between time point of measurement and SpO2 (p=0.02) with
SpO2 lower at 60 mins and 120 minutes post suction compared with pre-suction. There were
no differences pre, during and post suction for FiO2 (p=0.98), SpO2/FiO2 (p=0.46), RR
(p=0.39), HR (p=0.10) or mean BP (p=0.57).
11
DISCUSSION
Open ETT suction in non-muscle relaxed ventilated preterm infants with RDS results in a
significant increase in lung volume up to 120 minutes post suction.
Significant derecruitment and rapid recovery during open suction has previously been
described in the paediatric population during conventional ventilation [18, 19], during HFOV [5]
and in preterm infants on HFOV [11]. The consistency of findings over several studies
suggests that derecruitment caused by ETT suctioning is only transient and that a recruitment
manoeuver is not necessary. Whether closed or open suction was used did not impact on
outcome. Most studies only observed the first few minutes post suction and little is reported on
what happens over the longer time period post suction. Our study data shows that EEL
increased significantly after suction and remained increased for the next 2 hours, suggesting
that the benefit of suction occurs much longer than many of the previous studies have
described. As there was a concomitant reduction in resistance post suction, it would appear
that the clearance of secretions allowed gas exchange to occur in previously blocked airways.
This may be due to reopened alveolar spaces with little change in lung perfusion, but this
physiological phenomenon can only be speculated.
As some infants were in VG mode, it was hypothesised that the rapid reinstallation of the flow
sensor may have influenced the VG algorithm and delivered an increased PIP to counteract
suction induced derecruitment. On further retrospective analysis it was found that the mode of
ventilation had little impact on changes in EEL or ventilation distribution. This lack of difference
could be due in part to the small numbers in each ventilation mode. Additionally, there was no
difference in the delivered tidal volume or PIP between the two groups.
After ETT suction, there was a trend toward increased ventilation in the posterior (dependent)
lung compared to the non-dependent anterior lung illustrating that regional distribution of
ventilation in ventilated preterm infants with RDS is heterogeneous in nature. Heterogeneity in
12
regional ventilation distribution following ETT suction has been described previously [11, 12]
although no clear pattern has yet been established. Our findings are supported by those which
found that PEEP elevation induced a decrease in ventilation in the ventral lung regions with an
accompanying shift in ventilation towards the dependent dorsal regions [20]. However, in a
study performed on pigs, lung volume loss with disconnection and suctioning was more
pronounced in the dorsal lung regions and volume restitution was more rapid in the ventral
lung regions [12], and that during a decremental PEEP trial, derecruitment initially occurred in
dependent lung regions [21].
This finding of heterogeneity of regional ventilation distribution suggests that, despite
spontaneous recovery of global lung volume after suction, regional atelectasis and
overdistension might still be present. As it has been previously noted that regional ventilation
distribution is dependent on applied positive end expiratory pressure (PEEP) in ventilated
subjects [22], the use of a recruitment manoeuvre involving increasing PEEP may provide
some benefits in improving homogeneity of ventilation.
Previous studies have suggested that the magnitude of ETT occlusion and degree of applied
negative pressure are the most important factors in determining EEL and tidal volume change
during and after suction [23-25]. Although our study did not control for these factors, there was
no significant difference in ETT diameter between the PC and VG groups, in all instances a
size 6 Fg catheter was used for ETT suction, and a pressure of 100mm Hg was the standard
set suction pressure used.
This study has several limitations that need to be addressed. First of all, EIT measures relative
changes in ventilation so it does not provide absolute lung volume changes in response to ETT
suction. In this study, where intra-subject variation with suction was considered, this does not
represent a problem. EIT measurements on small preterm infants are technically challenging
with electrode placement difficulties increasing recorded noise. Additionally, the back
13
projection algorithm which is used to produce the image is based on the mathematical premise
that the chest shape is constant, whereas it is in fact dependent on the population studied.
CONCLUSIONS
ETT suction in non-muscle relaxed and ventilated preterm infants with RDS results in
significant lung volume increase which is maintained for at least 90 minutes. Regional
differences in distribution of ventilation with ETT suction suggest that the behaviour of the lung
is heterogeneous in nature.
Word count: 2490
14
Acknowledgments
We are deeply thankful to all parents of preterm babies who volunteered to participate in the
study and Kristen Gibbons, Statistician, Mater Research for statistical advice.
We wish to acknowledge the financial support of the ANZ Trustees Children’s Medical
Research Establishment Grant and the provision of equipment by Masimo Australia Pty Ltd.
15
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19
Table 1 Demographic data of the study infants: Mean ± SD
Infants on PC
(n = 13) Infants on VG
(n = 7) p-value
Mean difference
Confidence intervals
Birth weight (g) 991.2 ± 273.1 1011.7 ± 206.6 p=0.86 -20.50 -228.6 – 269.6
Study weight (g) 974.2 ± 265.3 1018.6 ± 200.6 p=0.70 -44.40 -197.5 – 286.3
Gestational age (weeks) 26.7 ± 1.8 26.4 ± 1.9 p=0.77 0.26 -2.1 – 1.6
Postnatal age (days) 2.0 ± 1.4 1.7 ± 0.8 p=0.63 0.29 -1.5 – 0.9
Crib score 10.6 ± 3.0 10.1 ± 4.0 p=0.77 0.47 -3.8 – 2.6
Predicted Death Rate (%) 21.9 ± 20.6 21.6 ± 1.6 p=0.97 0.36 -20.3 – 19.6
Male: Female
ETT Size (mm)
Surfactant (doses)
6:7
2.6 ± 0.2
1.9 ± 0.3
5:2
2.7 ± 0.3
2.0 ± 0
p=0.30
p=0.61
p=0.49
0.06
0.08
-0.2 – 0.3
-0.2 – 0.3
PC pressure controlled ventilation
VG volume guarantee ventilation
20
Table 2 Baseline differences in respiratory mechanics and physiological characteristics of the study
infants: (Mean ± SE)
Infants on PC
(n = 13) Infants on VG
(n = 7) p-value
Confidence intervals
HR (beats per minute) 139.08 ± 2.93 147.53 ± 4.12 p=0.10 -1.6 – 18.5
RR (breaths per minute) 72.54 ± 3.82 82.92 ± 5.18 p=0.11 -2.6 – 23.3
DBP (mm Hg) 27.58 ± 0.58 27.27 ± 0.80 p=0.75 -2.3 – 1.6
Mean BP (mm Hg) 35.67 ± 1.57 37.60 ± 2.78 p=0.57 -4.5 – 8.4
SpO2 93.69 ± 0.49 92.00 ± 0.67 p=0.05* -3.0 – -0.03
PIP 15.58 ± 0.63 14.36 ± 0.89 p=0.27 -3.4 – 0.9
FiO2 0.23 ± 0.005 0.23 ± 0.006 p=0.80 -0.01 – 0.02
SpO2/FiO2 407.92 ± 7.97 397.60 ± 11.32 p=0.46 -37.8 – 17.2
Vt (ml/kg) 4.10 ± 0.18 3.43 ± 0.26 p=0.04* -1.3 – -0.04
MV 0.27 ± 0.02 0.27 ± 0.02 p=0.89 -0.05 – 0.06
R 109.56 ± 13.81 123.47 ± 26.43 p=0.14 -43.02 – 70.84
PC pressure controlled ventilation
VG volume guarantee ventilation
21
Figure Legends
Figure 1 The change in EEL expressed in amplitude units of the global lung (A. upper panel)
and posterior and anterior lung fields (B. lower panel) in the ventilated preterm infants during
ETT suction. Mean and CI displayed.
Figure 2 Change in EEL pre and post suction (mean and CI). # EEL change after 30, 60, 90
minutes were significantly different compared to pre suction for both global (upper) and
regional (lower) EEL but not at 120 minutes for anterior lung
Figure 3 Global (upper) and regional (lower) tidal impedance amplitudes pre and post suction.
Mean and CI are shown.