Impact of Inspiratory Muscle Pressure Curves on the Ability of Professionals to Identify Patient-ventilator Asynchronies

The presence of asynchrony was associated with increased mechanical ventilation time, morbidity, reduced hospital discharge rate and IMV free time in the survival analysis, when compared to synchronous patients with the ventilator. Therefore, its correct detection is necessary to optimize ventilatory adjustments and provide a better outcome for patients in the ICU. Recently, the use of software has been proposed with the advantage of being a real-time, automatic and continuous analysis. However these need further studies.

The patient-ventilator interaction is the result of two different pressure systems, the Pmus performed by the patient through the activation of the respiratory muscles and the pressure provided by the mechanical ventilator (Pvent). The tracings, provided by the mechanical ventilator, of pressure and flow are considered a graphical representation of the interaction between Pmus and Pvent, and can exemplify the control of the respiratory cycle by the patient under the influence of the ventilator. The use of these to identify asynchrony, despite being visual and suitable for a logical interpretation, in clinical practice, proved to be dependent on characteristics inherent to the observer, such as length of experience and the presence of previous training. The average sensitivity to correctly identify asynchrony using this interpretation technique was described as 28%, even considering only experienced professionals.

The FlexiMag Max ventilator (Magnamed, São Paulo, Brazil) provides in its interface non-invasively estimated Pmus waveforms through an artificial intelligence algorithm. The Pmus estimate, as it represents the effort performed by the patient both in time and in intensity, when viewed simultaneously with the other waveforms displayed by the ventilator, should provide a more representative graphic portrait of the patient-ventilator interaction. However, the impact of using Pmus estimation on the observer's ability to correctly identify asynchrony has not been studied so far.

Hypothesis The display of the estimated muscle pressure waveform performed by the patient, simultaneously with the pressure and airway flow waveforms over time, will help healthcare professionals in intensive care units to identify patient-ventilator asynchrony.

Methods

Sample For each participant, a sensitivity value defined as the relative frequency of correct answers for all studied asynchronies will be calculated. After that, the average sensitivity (or average hit percentage) as the average of all participants in each group will apply. The sample size was defined based on a previous study, which had a mean sensitivity (or mean percentage of correct answers) of 28.0% with a standard deviation of 15%. In order to have an increase in the mean sensitivity of participants from 28 to 38% in the correct detection of asynchrony, with a power of 90% and a two-tailed significance level of 0.05, it will be necessary to include 49 participants per group, totaling 98 participants. The sample calculation statistics site was used (http://calculoamostral.bauru.usp.br/calculoamostral/).

Study Protocol The study will consist of a preparatory phase, to level participants in defining the different types of asynchronies through preliminary training. In this, a class on the subject will be given, designed for the study in question, synchronously using the Zoom ® tool. The class will be held at 6 different times, with a maximum of 20 participants per session, to allow at the end of each session to clarify doubts with the experts present who will be made available.

Upon completion of this step, participants will be cluster-randomized to the conventional group or Pmus group. Randomization will be stratified by length of experience in intensive care (less or more than five years). In the conventional group, two tracings will be displayed (pressure and flow) while in the Pmus group, three tracings will be displayed (pressure, flow and muscle pressure estimated through artificial intelligence algorithm).

Both groups will be exposed to the same simulated asynchrony scenarios using an active mechanical ventilation simulator (ASL 5000, IngMar Medical, Pittsburgh, Pennsylvania). A total of 49 scenarios will include synchronous, ineffective effort, auto-triggering, double-triggering, reverse-triggering, premature cycling, and late cycling situations. Groups of a maximum of 10 simultaneous participants will view the simulation of 49 scenarios in real time projected on the screen of an auditorium. Each scenario will be visible for one minute. At the end of this period, each participant must choose an alternative among the 7 available options that best signal the situation observed.

The scenarios will be performed simulating the patient-ventilator interaction using the active servo lung 5000 (ASL 5000, IngMar Medical, Pittsburgh, Pennsylvania) connected to the FlexiMag Max mechanical ventilator (Magmamed, São Paulo, Brazil).

The ASL 5000 will play the role of the patient in the interaction, as this, through the digital control of a piston, allows the simulation of different levels of patient efforts under different mechanical conditions of the respiratory system. The 49 proposed scenarios will be elaborated through the combination of effortlessness, low and high effort under the condition of normal, restrictive and obstructive respiratory mechanics, defined by the combination of resistance and compliance of the respiratory system.

The role of the ventilator in the interaction will be played by the FlexiMag Max adjusted in the assist-controlled ventilation modes for volume and pressure and in the spontaneous pressure support mode.

The interaction will include synchronous and asynchronous tracings. Asynchronies will be simulated based on descriptions previously published in the literature, as shown in the table below.

Types of asynchronies Definition Ineffective effort. Presence of effort (Pmus) without ventilator triggering

Double triggering. Two ventilator cycles triggered by a single effort

Auto triggering. None patient effort (Pmus) with ventilator triggering

Reverse triggering. Pmus follows the controlled (or auto-triggered) cycle with a fixed frequency and delay. May or may not generate double cycle

Premature cycling. Inspiratory time too short compared to the patient, defined as cycling to the expiratory phase before peak Pmus.

Delayed cycling. Inspiratory time too long in relation to the patient: defined as cycling to the expiratory phase after the end of the effort (Pmus).

Statistical analysis

Usual descriptive analysis will be performed. Variables with normal distribution will be described using mean and standard deviation and compared between groups using the Student t test. Variables with non-normal distribution will be described as median and interquartile range and will be compared between groups using the Mann-Whitney test. Categorical variables will be described as absolute and relative frequency and compared using the chi-square test. Data normality will be verified by the Shapiro-Wilk test. For each participant, means of sensitivity, specificity, positive predictive value and negative predictive value of asynchrony detection will be calculated. The means of these variables will be compared between the participants of the conventional group and the Pmus group using the t test, or the Mann-Whitney test as indicated. It will be verified whether there is heterogeneity of effect regarding previous experience in intensive care.

The level of statistical significance will be set at 0.05 two-tailed. The R 3.3.2 software (www.r-project.org) will be used. The collected data will be stored in google forms - without identification.

Expected results If the hypothesis is confirmed, a superiority in the Pmus group compared to the conventional group is expected, with a difference of 10 percentage points in the mean sensitivity, in correctly identifying the different types of patient-ventilator asynchrony per participant.

Ethical aspects The study will be submitted to the Ethics Committee of the institution where it will be carried out. Participants will be included in the study after signing an informed consent form. The study will be entirely simulation-based and will not involve patient participation.