Variations in endotracheal tube cuff pressure: Is 8-hourly monitoring enough?
1 Department of Biomedical and Clinical Technology, Durban University of Technology, KwaZulu-Natal, South Africa
2 Department of Anaesthesiology and Critical Care, Nelson R Mandela School of Medicine, Durban, KwaZulu-Natal, South Africa
Background. Most patients admitted to an intensive care unit (ICU) for mechanical ventilation require endotracheal intubation. Cuffed endotracheal tubes (ETTs) are utilised as they provide a better seal to facilitate ventilation and minimise aspiration. Complications due to overinflation or underinflation of the cuff may occur. Neither the frequency of intermittent cuff pressure (Pcuff) measurement nor the advantage of continuous Pcuff monitoring has been clearly established.
Objective. To determine deviations in ETT Pcuff from the recommended range during the intervals between routine thrice-daily Pcuff measurements in adult ICU patients. Our key objective was to identify the extent and cause of ETT Pcuff changes during these intervals. In addition, we attempted to demonstrate the failure of routine thrice-daily Pcuff monitoring to detect the large variation in Pcuff of patients throughout the day.
Methods. This prospective, observational study was conducted in the King Edward VIII Hospital ICU, Durban, KwaZulu-Natal Province, South Africa. Ethical and institutional approval was obtained. Consent was obtained from patients’ next of kin. Intermittent Pcuff was recorded using mechanical manometers, and continuous measurements using pressure transducers.
Results. Thirty-five critically ill adult patients were enrolled. The mean study time was 11.1 h. The mean Pcuff was 25.6 (standard deviation 7.1) cmH2O for the intermittent group and 26.6 (8.7) cmH2O for the continuous group. The intermittent pressure measurements were in the low-pressure range (<20 cmH2O) 12% of the time compared with 83% in the target pressure range (20 - 30 cmH2O) and 5% in the high-pressure range (>30 cmH2O). For continuous pressures, 13% of the time was spent in the low-pressure range, 64% in the target pressure range, and 23% in the high-pressure range. For the entire study, 588 events causing Pcuff alterations were recorded.
Conclusion. Continuous monitoring of Pcuff indicated that the endotracheal Pcuff varied extensively during mechanical ventilation in critically ill patients, such variation being noted both between patients and within individual patients. Variations in individual patients occurred both during intrinsic patient activities and those of ICU personnel as part of routine patient maintenance. Intermittent monitoring may not detect these variations. Continuous monitoring of Pcuff during mechanical ventilation in ICUs is thus recommended for all patients.
Afr J Crit Care
Most patients admitted to an intensive care unit (ICU) for mechanical ventilation require endotracheal intubation. Endotracheal tubes (ETTs) with cuffs are utilised as they provide a better seal to facilitate ventilation and minimise aspiration.1 , 2 The cuff pressure (Pcuff) must be maintained within a target range that is adequate to ensure effective mechanical ventilation and prevent pulmonary aspiration, yet low enough to prevent compression of tracheal capillaries. 1 Several complications due to the Pcuff exerted on the tracheal mucosa have been identified. 3 Overinflation may cause partial or total obstruction of tracheal mucosal blood flow, resulting in tracheal necrosis leading to tracheal stenosis and granulomas, and rarely – but catastrophically – rupture of the trachea. 4-6 The close proximity of the oesophagus posteriorly, combined with the presence of, for example, a nasogastric tube, may lead to the formation of tracheo-oesophageal fistulas.7 Underinflation may cause air leakage, resulting in inadequate ventilation and an increased risk of aspiration. 8 , 9 In addition, ETT Pcuff may change radically owing to various factors that exert effects on the cuff. Such factors include patient airway suctioning, coughing, struggling, neck movements, modes of ventilation and temperature.10-12 Therefore, it is vitally important that Pcuff is diligently maintained within the recommended range.
The ideal range for Pcuff remains
contentious. Most studies recommend that Pcuffs be maintained
between 20 cmH2O and 30 cmH2O.13-15 However,
argue that monitoring Pcuff alone is insufficient
because tracheal damage may occur even in ideal ranges.13
Many researchers have also questioned the value of
intermittent monitoring as this often misses many episodes of
Pcuff changes.16-19 Continuous
monitoring has therefore been advocated as an alternative.
Sole et al.20
validated a method of continuous Pcuff measurement.
Subsequently, continuous Pcuff monitoring was shown to be
continuous monitoring itself may present potential problems,
e.g. there may be an increased cost and risk of infection. The
added attachments may hinder patient mobilisation and
increase the risk of tube disconnection and cuff deflation
The objective of this study was to
determine deviations in ETT Pcuff from the recommended range
during the intervals between routine thrice-daily Pcuff
measurements in adult ICU patients. A key objective was to identify
the extent and cause of ETT Pcuff changes during these
intervals. In addition, we attempted to demonstrate the
failure of routine thrice-daily Pcuff monitoring to detect the
large variation in Pcuff of patients throughout the day.
This was a prospective, observational study conducted in the King Edward VIII Hospital ICU, Durban, KwaZulu-Natal Province, South Africa. Ethical and institutional approval was obtained. All patients admitted to the ICU were screened for eligibility to be enrolled in the study. Patients were included if they were between 18 and 60 years old, intubated with high-volume, low-pressure cuff tubes, and expected to be mechanically ventilated for more than 24 h. Patients who had anatomical laryngeotracheal abnormalities or who were expected to have a short duration of mechanical ventilation were excluded. Consent was obtained from the patients’ next of kin.
The Posey cufflator manometer (Posey Company, USA) was used to record Pcuff at three times during the day. In addition, Pcuffs were continuously monitored using a Deltran IV disposable pressure transducer (Utah Medical Products Inc, USA). This was transduced onto an independent Nihon Kohden bedside monitor (Nihon Kohden Corp., Japan). A Physiotrac laser level (Edwards Life Sciences, USA) was used to ensure that the transducer was placed in line with cervical spine/cricoid cartilage at C6.
Patients were positioned with the head end of the bed elevated to 30°. ETT position was confirmed by auscultation and radiology as per the unit protocol. A three-way stopcock was connected to the ETT cuff to allow for an interchange between intermittent and continuous recordings.
Each patient was monitored for a period of 12 h. Intermittent Pcuff was recorded in cmH2O at three intervals using the Posey cufflator. The three readings were taken at the beginning (T0), middle (T6) and end (T12) of the study period (Table 1). Continuous Pcuff was displayed on the monitor screen and recorded on the monitor at 1-min intervals. The maximum, minimum and mean pressures were recorded. These data were later manually extracted and recorded at 5-min intervals. Continuous Pcuff was measured in mmHg and converted to cmH2O. The continuous Pcuff measurements were assessed as being in one of three groups: low-pressure range (<20 cmH2O), target pressure range (20 - 30 cmH2O) and high-pressure range (>30 cmH2O) (Table 2).
ICU staff were blinded to both the intermittent and continuous readings measured by the principal investigator. ICU staff were allowed to check and adjust Pcuff if necessary as per the unit protocol, which dictated an 8-hourly measurement using the mechanical manometer.
The principal investigator also recorded any events that were likely to alter Pcuff, noting the time at which these occurred, including adjustment of Pcuff by staff, suctioning, patient coughing or struggling, movement of head only and/or whole body, and changes in position for procedures.
The Pcuff readings collected were analysed using a signed-rank
test for paired analysis to compare values for the same patient.
The test was also used to determine whether the continuous
readings identified significant adverse events. Variation in
endotracheal Pcuff was expressed as interquartile ranges and
shown graphically for both methods over time. Pearson’s
correlation was also used to compare the intermittent and
continuous readings at the same time.
Thirty-five critically ill adult patients were enrolled, of whom 19 (54.3%) were male. Mean age was 34 (range 18 - 60) years. A total of 29 of the subjects were studied for the entire study period. The mean time of study of the group was 667 (135 - 720) min. Monitoring was discontinued early in 6 patients: 3 patients were taken to theatre, 1 patient died, 1 patient was extubated and 1 was restless and ICU staff felt the patient should be removed from the study as it was affecting patient care.
Table 1 reflects the data from the
intermittent readings from all patients. Only
maximum readings were recorded. The mean (standard
deviation (SD)) Pcuff of all patients for T0 was
25.3 (6.9) cmH2O; for T6 25.9
and for T12
24.8 (3.8) cmH2O. The overall mean (SD)
for all readings was 25.6 (7.1) cmH2O.
Overall, 12% of the time was spent in the low-pressure
range (<20 cmH2O), 83%
in the target pressure range (20 - 30 cmH2O) and
5% in the high-pressure range (>30 cmH2O) (Fig.
Fig. 1. Continuous v. intermittent readings in the different ranges. (Pcuff = cuff pressure.)
Table 2 reflects the data from the continuous
readings of all patients. The maximum, minimum and mean
pressures were recorded and analysed. The mean (SD) maximum
Pcuff was 27.4 (9.3) cmH2O, minimum 22.1 (8.7) cmH2O, and mean
26.6 (8.7) cmH2O. The median values for each
of the three sets of data were 26, 21 and 25 cmH2O,
respectively. The group mean (SD) Pcuff was 26.6 (8.7) cmH2O (median 25
continuous readings. Overall, 13% of the time was spent in the
low-pressure range, 64% in the target pressure range, and 23% in
the high-pressure range (Fig. 1).
A total of 588 events causing alterations in
Pcuffs was recorded for the entire patient group over the whole
observation period. The average number of events per hour per
patient monitored was 1.5 (range 0.7 - 3.0). An increase in
pressure resulted from 85% of the events and a drop in pressure
from 15%. Table 3 reflects the distribution of the
events that occurred. The most frequently encountered events
that caused pressure changes were body movement, coughing, head
movement and suctioning.
Fig. 2 illustrates the variability of the data from the
continuously monitored readings expressed as the interquartile
range using the maximum Pcuffs recorded.
The variability in the high-pressure range (>30
cmH2O) was notably greater.
Pearson’s correlation (Fig. 3) showed good correlation
between the intermittent and continuous readings taken at the
same time (r=0.87).
Fig. 2. Interquartile range of maximum Pcuffs for continuous measurement readings.
(Pcuff = cuff pressure.)
Fig. 3. Correlation between intermittent and continuous readings at the same time (r=0.87).
(Pcuff = cuff pressure.)
Fig. 1 represents the percentage of time in each of the three pressure ranges for the intermittent and continuous readings.
Continuous monitoring of Pcuff indicated
that endotracheal Pcuff varies extensively during
mechanical ventilation in critically ill patients, both
between patients and in individual patients. However, the
intermittent measurements showed minimal
variation. The study monitored Pcuffs continuously for 12 h in
35 patients. Several studies have reported important
variations in endotracheal Pcuff in ICU patients.19
However, these studies differ in that they only recorded Pcuffs
intermittently, ranging from every 3 to 8 h.
Pcuff was monitored continuously for a period of 12 h. The Pcuffs for 64% of the study time for all patients were within the target recommended range (20 - 30 cmH2O) for the entire data collection time. Table 4 compares our study with previous studies and shows the results to be consistent.
A total of 23% of the Pcuff measurements was <20 cmH2O, similar to the 30% reported by Sole et al.21 (Table 4). Nseir et al.11 demonstrated that underinflation of Pcuff increases with time. This concurs with the present study, as nine patients had gradually decreasing pressures throughout the study. Other studies have also noted a decrease in Pcuff over time. 21 , 24 , 25 This decrease may be due to air escaping from the ETT cuff or an increasing airway pressure. Episodes of low pressure may increase the risk for aspiration and ventilator-associated pneumonia.9 , 14 , 26
In the present study, 13% of Pcuff readings were >30
This is similar to the findings by other
researchers, as reflected in Table 4. The exception was Duguet
who showed a higher rate of time spent above 30 cmH2O. Most
increases in Pcuff were associated with patient coughing,
suctioning and head movement; however, these spikes in
pressure did not last for more than 5 min, with the pressure
usually returning to baseline or a slightly higher level (~2
Other increases in pressure were due to weaning from sedation
and mechanical ventilation. In these cases, the changes lasted
for longer periods. Positioning of patients for procedures and
changing of neck position by the patient seemed
to increase Pcuff for longer periods. This is supported by
findings from other studies.3
10 We did not
specifically look for the numerous complications of cuff
overinflation in our patients.
Intermittent Pcuff measurement results
reflected a minor variation in Pcuff. Pcuffs in our study were
within the accepted range for 83% of the study time. This
would suggest a high concordance with the recommended range.
As these were merely intermittent measurements, no conclusions
could be drawn about pressure variations between the
measurements. To do this, we looked at the continuous
measurements between the intermittent readings to highlight
the variations in Pcuff.
Intermittent v. continuous m easurements
Considering intermittent measurements only, 24 of 35 patients had their Pcuff within the range for the entire study. This was not the case when compared with continuous readings, where variations in Pcuff were demonstrated below the recommended range in 37% of patients and above the range in 77% of patients. This showed that many pressure variations were missed during intermittent recording, which may have lead to underinflation or overinflation not being detected.
In an attempt to compare intermittent and continuous
measurements taken at the same time, a good correlation (r=0.87) between the two
measurements was demonstrated (Fig. 3). This
implies that the measurement techniques for the two were
consistent. Differences were therefore not due to the
Pcuff was monitored continuously for 12 h, recorded on the monitor at 1-min intervals, with only the 5-min readings being analysed. Computer software for more frequent analysis was not available. Five-minute readings were therefore manually extracted. Smaller time intervals may have indicated more variations.
Pcuff was not adjusted to a fixed absolute baseline pressure.
Any reading between 20 cmH2O and 30 cmH2O was
accepted. Confounders such as sedation, neuromuscular blocking
drugs, changes in ventilator parameters and age-related pressure
changes were not considered.
Continuous monitoring of Pcuff indicated that endotracheal Pcuff varies extensively during mechanical ventilation in critically ill patients, such variation being noted both between patients and in individual patients. Variations in an individual patient occur both during intrinsic patient activities and during activities of ICU personnel as part of routine patient maintenance. Intermittent monitoring may not detect these variations.
Continuous monitoring of Pcuff during mechanical ventilation in ICUs is therefore recommended for all patients. Where this is not possible, intermittent monitoring should be performed more frequently than thrice daily. Rechecking the Pcuff after any event that may interfere with the ETT should further complement this. Pcuff should be clearly documented as part of the patient monitoring chart. Where pressures are deemed to be too high or too low, these should be appropriately adjusted and documented as such. It is recommended that a pressure range of 20 - 30 cmH2O still be used as the target range. The role of self-adjusting pressure devices, although needing further exploration, holds much promise.
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