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Research ArticleConference Proceedings

Monitoring Asynchrony During Invasive Mechanical Ventilation

José Aquino Esperanza, Leonardo Sarlabous, Candelaria de Haro, Rudys Magrans, Josefina Lopez-Aguilar and Lluis Blanch
Respiratory Care June 2020, 65 (6) 847-869; DOI: https://doi.org/10.4187/respcare.07404
José Aquino Esperanza
Critical Care Center, Hospital Universitari Parc Taulí, Institut d’ Investigació i Innovació Parc Taulí, Sabadell, Spain.
Centro de Investigaciones Biomedicas en Red Enfermedades Respiratorios, Instituto de Salúd Carlos III, Madrid, Spain.
Facultat de Medicina, Universitat de Barcelona, Barcelona, Spain.
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Leonardo Sarlabous
Critical Care Center, Hospital Universitari Parc Taulí, Institut d’ Investigació i Innovació Parc Taulí, Sabadell, Spain.
Centro de Investigaciones Biomedicas en Red Bioingenieria, Biomateriales y Nanotecnologia, Insituto de Salúd Carlos III, Madrid, Spain.
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Candelaria de Haro
Critical Care Center, Hospital Universitari Parc Taulí, Institut d’ Investigació i Innovació Parc Taulí, Sabadell, Spain.
Centro de Investigaciones Biomedicas en Red Enfermedades Respiratorios, Instituto de Salúd Carlos III, Madrid, Spain.
Universitat Autònoma de Barcelona, Bellaterra, Spain.
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Rudys Magrans
Bettercare SL, Sabadell, Spain.
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Josefina Lopez-Aguilar
Critical Care Center, Hospital Universitari Parc Taulí, Institut d’ Investigació i Innovació Parc Taulí, Sabadell, Spain.
Centro de Investigaciones Biomedicas en Red Enfermedades Respiratorios, Instituto de Salúd Carlos III, Madrid, Spain.
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Lluis Blanch
Critical Care Center, Hospital Universitari Parc Taulí, Institut d’ Investigació i Innovació Parc Taulí, Sabadell, Spain.
Centro de Investigaciones Biomedicas en Red Enfermedades Respiratorios, Instituto de Salúd Carlos III, Madrid, Spain.
Universitat Autònoma de Barcelona, Bellaterra, Spain.
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  • Fig. 1.
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    Fig. 1.

    Flow starvation seen on tracings of air flow, airway pressure (Paw), and tidal volume (VT) in a mechanically ventilated patient on volume-control continuous mandatory ventilation. Flow starvation (ie, inspiratory flow mismatching) occurs when the ventilator fails to meet the patient’s flow demand. In this case, ventilator air flow is set inappropriately low at 40 L/min. Inspiratory effort begins after a period of synchrony (line) during mechanical inflation manifested by a progressive decrease in Paw, along with shortening of the expiratory time and breath-stacking (arrow). Notice a progressive return to synchrony (line).

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    Fig. 2.

    Flow starvation with double-triggering seen on tracings of air flow, airway pressure (Paw), and tidal volume (VT) in a mechanically ventilated patient on volume-control continuous mandatory ventilation. Flow starvation (ie, inspiratory flow mismatching) occurs when the ventilator fails to meet the patient’s flow demand. Inspiratory effort continues during mechanical insufflation (green arrow in the Paw waveform) in each breath; sometimes it is strong enough to trigger a second mechanical insufflation (red arrow) without expiration (ie, double-triggering ) and consequent breath-staking (blue arrows). Notice that the VT in breath-stacking is almost double with the associated elevated Paw.

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    Fig. 3.

    Flow starvation seen on tracings of air flow, airway pressure (Paw), and tidal volume (VT) in a mechanically ventilated patient on volume-control continuous mandatory ventilation with decelerating flow. Flow starvation (ie, inspiratory flow mismatching) occurs when the ventilator fails to meet the patient’s flow demand. Inspiratory effort continues during mechanical insufflation in each breath. Notice a negative deflection in the Paw waveform (arrow) with a different magnitude in every breath.

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    Fig. 4.

    Short or premature cycling seen on tracings of air flow, airway pressure (Paw), and esophageal pressure (Pes) in a mechanically ventilated patient on pressure-control continuous mandatory ventilation. Every breath delivered is patient-triggered (ie, assist ventilation) with a decrease in flow, Paw, and Pes. Short or premature cycling develops when the neural inspiratory time is greater than the mechanical inspiration time. In this example, the inspiratory effort (solid line) continues after the mechanical insufflation ended (dashed line), with the negative deflection of the Pes persisting after the mechanical inflation terminates. This pattern develops in the 4 illustrative breaths. Image courtesy of Tai Pham and Laurent Brochard, Toronto, Canada.

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    Fig. 5.

    Relationship between tidal volume (VT) and peak inspiratory pressure (PIP) in a normal breath and in a double-tirggered breath, with or without reverse-triggering. Descriptive notched boxplots for VT (top) and PIP (bottom) in each ventilatory mode. (A, C) Breaths without double-triggering (DT) versus breaths with DT breaths. (B, D) Breaths with reverse-trigger–induced DT breaths (DT RT) versus patient-triggered DT breaths (DT PT). Dots represent means, and box plots indicate medians and 25th–75th percentiles. PCV = pressure-control continuous mandatory ventilation; VCV = volume-control continuous mandatory ventilation with constant flow; VCVDF = volume-control continuous mandatory ventilation with decelerated flow. Notice the higher VT, in both patient-triggered and reverse-triggered ventilation, delivered in double-triggered breaths without meaningful changes in PIP. From Reference 44, with permission.

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    Fig. 6.

    Relationship between comfort and level of assistance. Patient comfort was assessed with 2 different methods: (A) Borg scale; (B) visual analog scale. Notice that the extreme levels of assistance during pressure support ventilation generated the least comfort. From Reference 51, with permission.

  • Fig. 7.
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    Fig. 7.

    Flow, airway pressure (Paw), and inspiratory and expiratory muscle activity in a patient with COPD who received pressure support ventilation with delayed or prolonged cycling. The electromyograms in the lower portion of the figure show inspiratory muscle activity in the patient’s diaphragm and expiratory muscle activity in the transversus abdominis. The patient’s increased inspiratory effort caused Paw to fall below the set trigger threshold, and inadequate delivery of flow by the ventilator resulted in a scooped contour on the Paw curve during inspiration. Although the ventilator was still pumping gas into the patient, his/her expiratory muscles were recruited, causing a bump in the Paw curve. Notice that neural inspiratory time is not coupled with machine inspiratory time; after the neural inspiration finished, the ventilator still provided air flow while the patient’s expiration begins. The dotted line shows Paw in another patient who generated just enough effort to trigger the ventilator and in whom there was adequate delivery of gas by the ventilator. From Reference 3, with permission.

  • Fig. 8.
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    Fig. 8.

    Reverse-triggering and elimination of reverse-triggered breaths during an end-expiratory hold: airway pressure (Paw), flow, esophageal pressure (Pes), and transpulmonary pressure during 6 breaths and an expiratory hold. The first 4 breaths show signs of respiratory entrainment; there seems to be a 2:1 pattern of mandatory breaths to reverse-triggered breaths that start as a passive insufflation but are rapidly followed by patient effort, as can be concluded from the drop in Pes (ie, the mandatory insufflations elicit a neural response that leads to patient effort). Larger drops in Pes than in Paw trigger the ventilator before exhalation of the previous breath, leading to breath-stacking with high tidal volumes. These breaths with patient effort are likely reverse-triggered. An expiratory hold was administered at the first asterisk and continued until the next asterisk, which abolished respiratory muscle activity for > 12 s. The arrow on the transpulmonary pressure (PL) curve marks the moment that inspiratory effort was expected if patient effort was generated spontaneously. After the expiratory hold, another mandatory insufflation was administered by the ventilator; patient effort immediately follows. This is suggestive of reverse-triggering because the patient effort seems to depend on the external stimulus provided by mandatory ventilator insufflation. From Reference 71, with permission.

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    Fig. 9.

    Distribution of asynchronies during mechanical ventilation. The asynchrony index, noted as percentage (%) per hour, was recorded continuously over several days in 4 representative patients. Recordings show that periods of very low asynchrony alternated with periods of high levels of asynchrony. From Reference 4, with permission.

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    Fig. 10.

    Relationship between asynchrony and dose of sedatives (left) and opioids (right). On opioids-only days (white circles in B, D, F), the opioid dose was inversely associated with AI, IEE, and DC. On sedatives + opioids days (black circles in A, C, E), opioid dose was still inversely associated with AI, IEE, and DT. Sedative + opioid dose was directly associated with AI and IEE (black circles in A, C), but not with DT (black circles in E). On sedatives-only days (white cirlces in A, C, E), the sedative dose was only inversely related to DT. AI = asychrony index; IEE = ineffective expiratory effort; DT = double-triggering. From Reference 113, with permission.

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    Fig. 11.

    Analysis of the mixed effects of SOFA score and asynchrony index in ICU survival at ICU using a Bayesian joint model of bivariate longitudinal and competing risks data. SOFA score is strongly related with survival status at ICU discharge. The distributions do not overlap, indicating strong association of the SOFA score with respect to vital status. In contrast, asynchrony index at time t does not seem to be associated with vital status as clearly when overall severity is taken into account. For the event “Survived,” the asynchrony index has a positive support, indicating that patient–ventilator interactions could be a sign of good prognosis. For the event “Died,” the asynchrony index parameter indicates that patient–ventilator interactions at time t do not provide a more accurate indication of death prognosis than the SOFA score alone. From Reference 123, with permission.

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Respiratory Care: 65 (6)
Respiratory Care
Vol. 65, Issue 6
1 Jun 2020
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Monitoring Asynchrony During Invasive Mechanical Ventilation
José Aquino Esperanza, Leonardo Sarlabous, Candelaria de Haro, Rudys Magrans, Josefina Lopez-Aguilar, Lluis Blanch
Respiratory Care Jun 2020, 65 (6) 847-869; DOI: 10.4187/respcare.07404

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Monitoring Asynchrony During Invasive Mechanical Ventilation
José Aquino Esperanza, Leonardo Sarlabous, Candelaria de Haro, Rudys Magrans, Josefina Lopez-Aguilar, Lluis Blanch
Respiratory Care Jun 2020, 65 (6) 847-869; DOI: 10.4187/respcare.07404
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  • Article
    • Abstract
    • Introduction
    • Insufficient Assistance: Patients With High Respiratory Drive
    • Overassistance: Patients With Low Respiratory Drive
    • Reverse-Triggering: Entrainment Phenomenon
    • Assessment of Asynchronies
    • Asynchronies and Sleep in Critically Ill Patients
    • Management
    • Outcomes
    • Future Directions
    • Discussion
    • Acknowledgments
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Keywords

  • asynchrony
  • mechanical ventilation
  • patient–ventilator interactions
  • respiratory monitoring
  • respiratory physiology

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