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The effects of real-time waveform analysis software on patient ventilator synchronization during pressure support ventilation: a randomized crossover physiological study

BMC Pulmonary Medicine volume 24, Article number: 212 (2024) Cite this article

Abstract

Background

Patient-ventilator asynchrony commonly occurs during pressure support ventilation (PSV). IntelliSync + software (Hamilton Medical AG, Bonaduz, Switzerland) is a new ventilation technology that continuously analyzes ventilator waveforms to detect the beginning and end of patient inspiration in real time. This study aimed to evaluate the physiological effect of IntelliSync + software on inspiratory trigger delay time, delta airway (Paw) and esophageal (Pes) pressure drop during the trigger phase, airway occlusion pressure at 0.1 s (P0.1), and hemodynamic variables.

Methods

A randomized crossover physiologic study was conducted in 14 mechanically ventilated patients under PSV. Patients were randomly assigned to receive conventional flow trigger and cycling, inspiratory trigger synchronization (I-sync), cycle synchronization (C-sync), and inspiratory trigger and cycle synchronization (I/C-sync) for 15 min at each step. Other ventilator settings were kept constant. Paw, Pes, airflow, P0.1, respiratory rate, SpO2, and hemodynamic variables were recorded. The primary outcome was inspiratory trigger and cycle delay time between each intervention. Secondary outcomes were delta Paw and Pes drop during the trigger phase, P0.1, SpO2, and hemodynamic variables.

Results

The time to initiate the trigger was significantly shorter with I-sync compared to baseline (208.9±91.7 vs. 301.4±131.7 msec; P = 0.002) and I/C-sync compared to baseline (222.8±94.0 vs. 301.4±131.7 msec; P = 0.005). The I/C-sync group had significantly lower delta Paw and Pes drop during the trigger phase compared to C-sync group (-0.7±0.4 vs. -1.2±0.8 cmH2O; P = 0.028 and − 1.8±2.2 vs. -2.8±3.2 cmH2O; P = 0.011, respectively). No statistically significant differences were found in cycle delay time, P0.1 and other physiological variables between the groups.

Conclusions

IntelliSync + software reduced inspiratory trigger delay time compared to the conventional flow trigger system during PSV mode. However, no significant improvements in cycle delay time and other physiological variables were observed with IntelliSync + software.

Trial registration

This study was registered in the Thai Clinical Trial Registry (TCTR20200528003; date of registration 28/05/2020).

Peer Review reports

Background

Mechanical ventilation is an important life supporting treatment in patients with acute respiratory failure. After recovery from acute respiratory failure, pressure support ventilation (PSV) is the mode most commonly used during the weaning period [1,2,3]. PSV is patient-triggered, pressure-limited, and flow-cycled. During PSV, the ventilator is typically initiated by a traditional flow or pressure trigger system resulting from the inspiratory effort of the patient [4]. The ventilator then delivers the pressurization and is stopped when a predetermined flow cycle criterion is reached [5].

Patient ventilator asynchrony is defined as a mismatch in breathing delivery time between the mechanical ventilator and the patient [6]. Previous studies reported that patient ventilator asynchrony was significantly associated with poor clinical outcomes, including a longer duration of mechanical ventilation, a longer intensive care unit (ICU) and hospital length of stay, and increased mortality [7,8,9,10]. It commonly occurs during assisted ventilation, especially in PSV mode. Trigger and cycle asynchronies such as ineffective trigger, double trigger, premature cycling, and delay cycling, are commonly recognized in daily clinical practice [6, 11].

Identifying patient ventilator asynchrony using airway pressure (Paw) or airflow waveform is routinely used at the bedside; however, a previous study demonstrated that the sensitivity of these abnormal waveforms to recognize asynchrony were low [12]. Advanced monitoring tools such as esophageal pressure (Pes) or diaphragm electrical activity (EAdi) offer the benefit of detecting asynchrony; however, the use of these monitoring tools is limited due to invasiveness and its cost [6, 13]. Recent studies showed the feasibility of machine learning and computer algorithm to analyze Paw and airflow waveforms and to identify patient ventilator asynchrony [14,15,16]. IntelliSync + software (Hamilton Medical AG, Bonaduz, Switzerland) is a relatively new ventilation technology that continuously analyzes Paw and airflow waveforms by detecting the initiation and end of inspiration in real-time that can improve patient ventilator interaction; however, evidence of this software for improving patient ventilator synchronization is limited. The aim of this study was to evaluate the effect of IntelliSync + software on patient ventilator synchronization and breathing patterns in mechanically ventilated patients with PSV mode.

Methods

Study design and population

A randomized crossover physiological study was conducted in the Respiratory Intensive Care Unit, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand, from September 2020 to February 2022. The study was approved by the Siriraj Institutional Review Board (certificate of approval No. Si632/2020; date of approval 22/07/2020) and was registered in the Thai Clinical Trial Registry (date of registration: 28/05/2020, the registration number: TCTR20200528003). Written informed consent to participate was obtained from each subject or their relatives. This research project was supported by the Faculty of Medicine Siriraj Hospital, Mahidol University (grant number [IO]R016331065(fund3)).

Mechanically ventilated patients with age ≥ 18 years who were ventilated in the PSV mode with the following criteria: pressure support level ≤ 16 cmH2O, positive end-expiratory pressure (PEEP) ≤ 10 cmH2O, and oxygen fraction (FiO2) ≤ 0.6 were enrolled. Patients were excluded if they met any of the following criteria under PSV: unstable hemodynamics (systolic blood pressure > 180 mmHg or < 90 mmHg, diastolic blood pressure > 100 mmHg or < 60 mmHg, heart rate > 140 beats/minute or < 60 beats/minute, or any sign of poor tissue perfusion), respiratory rate > 35 breaths/minute, oxygen saturation by pulse oximetry (SpO2) < 92%, severe acid-base disturbance (arterial pH < 7.30 or > 7.55), tracheostomized patient, contraindication for esophageal balloon catheter insertion, or pregnant woman.

Ventilator and equipment

The Hamilton S1 (Hamilton Medical AG, Bonaduz, Switzerland) with IntelliSync + software was used in this study. IntelliSync + software can be activated in the trigger phase (inspiratory trigger synchronization: I-sync), cycling phase (cycle synchronization: C-sync), or both phases (inspiratory trigger and cycle synchronization: I/C-sync). Airflow was measured with a pneumotachograph placed between the endotracheal tube and the Y-piece of the ventilator and connected to a differential pressure transducer (MP150, BIOPAC Systems, Gotela, California, USA). Paw was measured between the endotracheal tube and the pneumotachograph using a pressure transducer (MP150, BIOPAC Systems, Gotela, California, USA).

An esophageal balloon catheter (CooperSurgical, Trumbull, Connecticut, USA) was inserted through the nose and positioned in the lower third of the esophagus. The balloon was filled with 1 mL of air according to the manufacturer’s instructions and connected to a pressure transducer (BIOPAC Systems, Gotela, California, USA). The position of the esophageal balloon was checked by applying gentle pressure on the abdomen to verify the absence of fluctuating gastric pressure, then an occlusion test was performed to confirm the position [17, 18]. Pes was recorded with an MP150 Data Acquisition System (BIOPAC Systems, Gotela, California, USA).

The analog signals for airflow, Paw, and Pes were digitized at a sampling rate of 100 Hz and stored on a laptop for subsequent offline analysis using AcqKnowledge software (BIOPAC, Systems, Gotela, California, USA).

Study protocol

The patients were studied in a semi-recumbent position. At baseline, patients were ventilated with PSV mode using their clinical settings with conventional flow trigger and cycling for 10 min, then randomly assigned using a sealed opaque envelope to one of the following sequences: Sequence A – I-sync → C-sync → I/C sync, Sequence B – I/C-sync → I-sync → C-sync, or Sequence C – C-sync → I/C-sync → I-sync (Fig. 1). Each step was applied for 15 min (the first 10 min were devoted to ensure the full adaptation of the patient to the mode, and the signal acquisition was carried out during the last 5 min). Other ventilator settings were kept unchanged in all study sequences.

Fig. 1
figure 1

Study protocol. C-sync – cycle synchronization, I-sync – inspiratory trigger synchronization, I/C-sync – inspiratory trigger and cycle synchronization, Paw – airway pressure, Pes – esophageal pressure, PSV – pressure support ventilation, P0.1 – airway occlusion pressure at 0.1 s

Full size image

Data collection

Baseline demographic and clinical data including age, sex, body mass index, and comorbidity were collected. Acute Physiologic and Chronic Health Evaluation (APACHE) II and Sequential Organ Failure (SOFA) scores were evaluated at admission. The Richmond Agitation-Sedation Scale (RASS) was assessed on the study date. During the study intervention period, blood pressure, respiratory rate, and heart rate were recorded every 5 min. SpO2 was continuously recorded throughout the study period. We continuously recorded Paw, airflow, and Pes waveforms for 5 min at the end of each step. The recorded waveforms were analyzed offline, with the investigator blinded to each intervention using the waveforms of the last 2 min of recording using a dedicated software program (AcqKnowledge Data Acquisition and Analysis Software, BIOPAC Systems, Gotela, California, USA). The airway occlusion pressure displayed by the ventilator at 0.1 s (P0.1) was also recorded for 5 consecutive breaths at the end of each intervention and the average value was reported. The ventilator automatically measured P0.1 breath-by-breath during pressure trigger system without airway occlusion by calculating the steepest slope of the pressure drop during an inspiratory effort and extrapolated the Paw drop at 100 msec below PEEP [19].

Inspiratory trigger delay time was defined as the time difference between the initial drop in the Paw and the beginning of the ventilator delivered pressurization (Fig. 2A). Delta Paw and Pes drops during trigger phase were calculated as the pressure difference in the initial drop in Paw and Pes and the beginning of ventilator delivered pressurization (Fig. 2A). The cycle delay time was calculated as the time difference between the end of patient inspiration (the point of Pes that elapsed 25% of time from its maximum Pes deflection to return to baseline [20,21,22]) and the opening of the expiratory valve (Fig. 2B).

Fig. 2
figure 2

Measurement of inspiratory trigger delay time, airway pressure drop (Paw) and esophageal pressure drop (Pes) during trigger phase, and cycling delay time

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The asynchrony index was calculated as the number of major asynchronous breaths (ineffective effort, double triggering, and auto triggering) divided by the total number of breaths [23]. We did not take into account the premature- and delayed cycling for the asynchrony index because the cycle delay time was our objective.

Outcomes

The primary outcome was inspiratory trigger and cycle delay time between each intervention. The secondary outcomes were delta Paw drop during the trigger phase, delta Pes drop during trigger phase, P0.1, respiratory rate, SpO2, mean arterial pressure and heart rate between each intervention.

Statistical analysis

The sample size was calculated based on the previous study by Mojoli and colleagues [24], IntelliSync + software significantly reduced cycle delay time compared to conventional PSV from 282 ± 315 msec to 54 ± 152 msec, using a significant level of 0.05 and a power of 80% to detect the difference between the two groups, a sample size of 14 subjects was calculated.

The Shapiro-Wilk test was used to assess the normality of the data. Continuous variables are presented as mean±standard deviation or median [interquartile range]. Categorical variables are presented as absolute numbers and percentages. For normally distributed data, we used an analysis of variance (ANOVA) with repeated measures followed by a post hoc pairwise comparison with Bonferroni correction. Nonnormally distributed data were compared using Friedman’s two-way ANOVA by ranks with a post hoc pairwise comparison. A P < 0.05 was considered statistically significant. Data were analyzed using PASW Statistics version 18 (SPSS, Inc., Chicago, Illinois, USA).

Results

Fourteen mechanically ventilated patients were enrolled and analyzed (Fig. 3). The mean age was 65±15 years, and 57.1% of enrolled subjects were men. The mean scores for APACHE II and SOFA scores were 15±9 and 6±4, respectively. Pneumonia was the most common cause of acute respiratory failure in this study (71.4%). Other clinical characteristics are shown in Table 1. All patients were ventilated in PSV mode at an average pressure support level of 11±3 cmH2O and PEEP of 6±2 cmH2O. Other baseline physiological variables are shown in Table 2.

Fig. 3
figure 3

CONSORT flow diagram. C-sync – cycle synchronization, I-sync – inspiratory trigger synchronization, I/C-sync – inspiratory trigger and cycle synchronization

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Table 1 Baseline demographic and clinical characteristics
Full size table
Table 2 Baseline ventilator settings and physiological variables
Full size table

The inspiratory trigger delay time was significantly shorter with I-sync and I/C-sync compared to baseline (208.9±91.7 vs. 301.4±131.7 msec; P = 0.002 and 222.8±94.0 vs. 301.4±131.7 msec; P = 0.005; respectively) (Fig. 4). The I-sync and I/C-sync groups had significantly shorter trigger delay time compared to C-sync group (208.9±91.7 vs. 308.4±153.0 msec; P = 0.008 and 222.8±94.0 vs. 308.4±153.0 msec; P = 0.015; respectively). Change in trigger delay time from baseline to each mode is shown in Supplementary Fig. 1 (Additional File 1).

Fig. 4
figure 4

Inspiratory trigger delay time between each intervention. C-sync – cycle synchronization, I-sync – inspiratory trigger synchronization, I/C-sync – inspiratory trigger and cycle synchronization

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There was a trend towards shorter cycle delay time between C-sync and I/C-sync compared to baseline; however, no statistically significant differences were observed (Table 3). Change in cycle delay time from baseline to each mode is shown in Supplementary Fig. 2 (Additional File 1). No significant differences in the modified asynchrony index, P0.1 and other physiological variables were found between the groups (Table 3).

Table 3 Waveform analysis and physiological variables between each intervention
Full size table

There was no significant difference in delta Paw drop and Pes drop during trigger phase between the baseline and the other three intervention groups; however, the I/C-sync group had significantly lower delta Paw and Pes drop during trigger phase compared to C-sync group (-0.7±0.4 vs. -1.2±0.8 cmH2O; P = 0.028 and − 1.8±2.2 vs. -2.8±3.2 cmH2O; P = 0.011, respectively). Changes in delta Paw and Pes drop from baseline to each mode are shown in Supplementary Figs. 3 and 4 (Additional File 1).

No adverse event was observed during the study period and all subjects tolerated both interventions until the end of the study.

Discussion

Our study demonstrated that IntelliSync + software significantly improved inspiratory trigger delay time compared to baseline ventilator settings. In addition, the drop in Paw and Pes during trigger phase was significantly better with I/C-sync compared to C-sync in mechanically ventilated patients receiving PSV mode. However, there was no significant difference in cycle delay time between IntelliSync + software and the conventional flow cycling system.

Patient ventilator asynchrony commonly occurs in mechanically ventilated patients, especially during PSV mode and it was associated with poor clinical outcomes [7,8,9]. Recently, many dedicated machine-learning software designed to continuously detect patient ventilator asynchrony have been developed. A systematic review demonstrated that these algorithms or software had high sensitivity and specificity to detect patient ventilator asynchrony compared to the reference standard using Pes or EAdi [25]. IntelliSync + software (Hamilton Medical AG, Bonaduz, Switzerland) is a new technology to detect the initiation and the end of inspiration by analyzing Paw and airflow waveforms. This waveform method has been evaluated in 16 mechanically ventilated patients and showed a precise assessment of the timing of patient spontaneous activity during PSV mode [23]. In addition, it was highly reproducible and reliable to detect both major and minor asynchronies. IntelliSync + software can be operated during the inspiratory and/or expiratory phases that can improve patient ventilator interaction; however, the data regarding the accuracy and feasibility of this software are scant. A study by Mojoli and colleagues in 15 mechanically ventilated patients with PSV mode demonstrated that IntelliSync + software significantly reduced cycling delay time and ineffective efforts compared to baseline PSV support [26]. In addition, increasing pressure support worsened patient ventilator interaction, but IntelliSync + software was superior to the setting by the expert in terms of patient ventilator synchronization.

Our findings confirm that IntelliSync + software is beneficial in improving patient ventilator interaction by reducing the inspiratory trigger delay time with I-sync and I/C-sync compared to conventional PSV. In our study, we did not evaluate the effect of IntelliSync + software on inspiratory effort so the reduction of inspiratory trigger delay time with IntelliSync + software approximately 100 msec might not have the impact on clinical outcome. However, other clinical studies using a proportional mode of ventilation such as neurally adjust ventilatory assist or proportional assist ventilation demonstrated that these modes significantly improved inspiratory trigger delay time (varying from 100 to 150 msec) and reduced asynchrony index and inspiratory effort measured by pressure-time product compared to PSV [27,28,29,30,31]. In addition, IntelliSync + software reduced the drop in Paw and Pes during the trigger phase that may help alleviate the trigger work of breathing but the impact on clinical outcomes was beyond the scope of our study and it should be evaluated in the future. However, an improvement in cycle delay time was not observed in the present study, although there was a trend toward a shorter cycle delay time with C-sync. The setting of conventional flow cycling in our study was quite short at the baseline, which may explain why the reduction in cycle delay time was not observed. In addition, the small sample size in the present study may not be enough to detect the difference in the cycle delay time between C-sync and other interventions. Larger studies are needed to evaluate the effect of IntelliSync + software in terms of patient ventilator interaction and clinical outcomes.

Limitations

Our study has some limitations. First, this study had a small number of enrolled subjects. Second, the time spent on each intervention was relatively short. Third, our study was performed in the PSV mode, so our findings might not be generalizable to other modes of ventilation. Finally, this study was designed to evaluate the physiological effects of IntelliSync + software, but not on clinical outcomes. Future studies are needed to evaluate the longer effect of IntelliSync + software on patient-ventilator interaction and its impact on clinical outcomes.

Conclusions

IntelliSync + software improved inspiratory trigger delay time compared to conventional flow trigger system during PSV mode. However, no significant improvement in cycle delay time and other physiological variables was observed with IntelliSync + software.

Data availability

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

C-sync:

Cycle synchronization

FiO2 :

Oxygen fraction

ICU:

Intensive care unit

I-sync:

Inspiratory trigger synchronization

I/C-sync:

Inspiratory trigger and cycle synchronization

PaCO2 :

Arterial partial pressure of carbon dioxide

PaO2 :

Arterial partial pressure of oxygen

Paw :

Airway pressure

PEEP:

Positive end-expiratory pressure

Pes :

Esophageal pressure

PSV:

Pressure support ventilation

P0.1 :

Airway occlusion pressure at 0.1 s

SpO2 :

Oxygen saturation by pulse oximetry

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Acknowledgements

The authors greatefully acknowledge Miss Khemjira Karaketklang (Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University) for her assistance with sample size calculation and statistical analysis.

Funding

This research project was supported by the Faculty of Medicine Siriraj Hospital, Mahidol University (grant number [IO]R016331065(fund3)).

Open access funding provided by Mahidol University

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Authors and Affiliations

  1. Division of Respiratory Diseases and Tuberculosis, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand

    Barnpot Nakornnoi, Jamsak Tscheikuna & Nuttapol Rittayamai

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  1. Barnpot Nakornnoi
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Contributions

N.R., B.N., and J.T. conceived and designed the study. N.R. and B.N. collected the data. N.R., B.N., and J.T. analyzed and interpreted the data. N.R. and B.N. prepared the first draft of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Nuttapol Rittayamai.

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Ethics approval and consent to participate

The study was approved by the Siriraj Institutional Review Board (certificate of approval No. Si632/2020; date of approval 22/07/2020). Written informed consent to participate was obtained from each subject or their relatives.

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Not applicable.

Competing interests

The authors declare no competing interests.

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Nakornnoi, B., Tscheikuna, J. & Rittayamai, N. The effects of real-time waveform analysis software on patient ventilator synchronization during pressure support ventilation: a randomized crossover physiological study. BMC Pulm Med 24, 212 (2024). https://doi.org/10.1186/s12890-024-03039-0

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BMC Pulmonary Medicine

ISSN: 1471-2466

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