Detection of reverse triggering in a 55-year-old man under deep sedation and controlled mechanical ventilation
Case Report

Detection of reverse triggering in a 55-year-old man under deep sedation and controlled mechanical ventilation

Xuan He, Xu-Ying Luo, Guang-Qiang Chen, Jian-Xin Zhou

Department of Critical Care Medicine, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China

Correspondence to: Jian-Xin Zhou, MD. Department of Critical Care Medicine, Beijing Tiantan Hospital, Capital Medical University, No. 6, Tiantan Xili, Dongcheng District, Beijing 100050, China. Email: zhoujx.cn@icloud.com.

Submitted Feb 07, 2018. Accepted for publication Jul 22, 2018.

doi: 10.21037/jtd.2018.08.09


Introduction

Reverse triggering is a frequently unrecognized form of patient-ventilator asynchrony (1). Previous studies have reported that patient-ventilator asynchrony is associated with adverse outcomes including prolonged duration of ventilation and length of stay in the intensive care unit and increased mortality (2-4). Reverse triggering may also generate higher plateau pressure, large tidal volume, and transpulmonary pressure swings (1,5). Monitoring of esophageal pressure or the electrical activity of the diaphragm can help diagnose reverse triggering (6,7). During assist-control ventilation, patient-ventilator asynchrony can occur under deep sedation, and reverse triggering should be suspected. The pathophysiological mechanisms of reverse triggering remain unclear. Previous research showed that, compared to the increase in sedation, switching the ventilator mode to pressure support ventilation significantly reduced breath stacking asynchrony (8). However, pressure support ventilation may not be tolerable by some patients, such as those with unstable chest wall injuries. Reverse triggering treatment strategies in these patients need to be further investigated.


Case presentation

A 55-year-old man suffering from chest trauma with multiple rib fractures was admitted to the intensive care unit. After admission, the patient became agitated due to pain and hypoxia. As his pulse oxygen saturation was less than 85%, endotracheal intubation was immediately performed and mechanical ventilation was initiated in pressure support ventilation using an AVEA ventilator (CareFusion Co., San Diego, CA, USA). The patient exhibited signs of paradoxical respiration and tachypnea. Midazolam and sufentanil were continuously infused to titrate the sedation depth on the Richmond Agitation Sedation Scale to −4 to −5, that is, no response to voice but any movement to physical stimulation (9). Due to the chest trauma with multiple rib fractures and sign of paradoxical respiration of the patients, the ventilator mode was switched to pressure assist-control ventilation set at an inspiratory pressure of 15 cmH2O, a respiratory rate of 20 breaths/min, an inspiratory time of 1 s, a positive end-expiratory pressure of 8 cmH2O, and a fraction of inspired oxygen of 0.4. A more sensitive flow trigger (sensitivity of 1 L/min with base flow of 2 L/min) was set to avoid deeper inspiration efforts. The ventilator monitor showed a respiratory rate of 20 breaths/min and an expiratory tidal volume of 430 to 460 mL. Hemodynamic monitoring showed a heart rate of 87 beats/min and a noninvasive blood pressure of 132/77 mmHg without vasoactive drugs. The pulse oxygen saturation was 97%. An arterial blood gas analysis was performed and the results were pH of 7.39, a partial oxygen pressure of 95 mmHg, a partial carbon dioxide pressure of 33 mmHg, and a base excess of −4.4 mmol/L.

Patient-ventilator asynchrony was suspected based on a mismatch between the flow and the airway pressure waveforms on the ventilator screen. Esophageal pressure monitoring was performed using a SmartCath-G catheter (LOT 7003300, CareFusion Co., San Diego, CA, USA) that can also be used for enteral feeding. Mechanical ventilation and esophageal pressure data were bedside displayed and collected by a dedicated acquisition system (VOXP Research Data Collector 3.2, Applied Biosignals GmbH, Weener, Germany) at 100 Hz. Figure 1 shows the flow, airway pressure, and esophageal pressure tracings at a ventilator machine rate of 20 breaths/min. Red dash lines indicated the onset of the patient’s inspiratory efforts. Reverse triggering with a stable 1:1 patient-ventilator entrainment pattern was diagnosed, indicating that one neural respiratory cycle was associated with one machine cycle (1).

Figure 1 Flow, airway pressure and esophageal pressure tracings during pressure assist-control ventilation at machine respiratory rate of 20 breaths/min. Red dash lines indicate the onset of patient’s inspiratory efforts.

We decreased the machine’s respiratory rate to 18 breaths/min with no changes in the other ventilator settings. The patient-ventilator asynchrony pattern remained, but the percentage of reverse-triggered breaths fell to 30% (2). We further decreased the machine rate to 16 breaths/min, and entrainments were markedly reduced (Figure 2). During a 3-min observation period, 14% (7/50) of breaths were machine cycled, among which only two reverse-triggered breaths (4%) were found. Under this condition, the negative deflection in the esophageal pressure during the patient’s triggered breaths decreased from approximately 12 cmH2O at rate of 20 to 8 cmH2O at rate of 16. After the machine rate was set at 14 breaths/min, no reverse-triggered breath was identified during a 30-min period (3). The monitored respiratory rate stabilized at 14–16 breaths/min with the majority of breaths triggered by the patient. Without other changes in the ventilator settings, gradually decreasing the machine’s rate reduced reverse triggering, which was eventually eliminated until the machine’s rate was set below the patient’s spontaneous rate.

Figure 2 Flow, airway pressure and esophageal pressure tracings when machine respiratory rate was reduced to 16 breaths/min. Black arrow indicates the asynchronized breath.

The pressure-controlled ventilation was maintained for 7 days at a respiratory rate of 10–14 breaths/min, and no obvious reverse triggering was found. The patient was then switched to pressure support ventilation and was weaned on the ninth day.


Discussion

Patient-ventilator asynchrony is prevalent during mechanical ventilation and is associated with adverse outcomes, including prolonged duration of ventilation and length of stay in the intensive care unit as well as increased mortality (2-4). In 2013, Akoumianaki et al. (1) first reported reverse triggering as a new type of patient-ventilator asynchrony in eight patients with acute respiratory distress syndrome under deep sedation and assist-control ventilation. Asynchrony due to reverse triggering was reported in two brain-dead patients (5). To date, this type of asynchrony has been seldom reported and may frequently be unrecognized in mechanically ventilated patients.

Monitoring the esophageal pressure or electrical activity of the diaphragm can help diagnose reverse triggering (6,7). When a patient’s inspiratory effort occurs after the onset of time-initiated inspiration, indicating that the neural efforts have been apparently triggered by the ventilator, reverse triggering can be confirmed (1). Reverse triggering should be differentiated from double triggering characterized by the first breath also being triggered by the patient (4). Double triggering is characterized when the machine’s inspiration ceases while the patient’s inspiratory effort continues, usually during strong spontaneous efforts (2).

It has been reported that neural efforts could be entrained by the ventilator in different entrainment ratios, namely the patient’s effort induced by one (1:1), two (1:2), or three (1:3) time-initiated inspirations (1,5). In the present case, reverse triggering occurred periodically at a fixed 1:1 ratio during entrainment periods (Figure 1). After each 8–10 patient-triggered cycle, 8–10 entrained breaths emerged during time-initiated cycles. Thus, reverse-triggered breaths accounted for approximately 50% of total breaths. Some entrained neural efforts triggered the ventilator, demonstrating a kind of breath stacking (8,10) (#2, #4, #6, and #8 breaths in Figure 1), whereas other efforts did not trigger the ventilator (#1, #3, #5, and #7 breaths in Figure 1). It was difficult to recognize the asynchrony by observing the ventilator screen waveforms.

There are several clinical consequences of reverse triggering, including diaphragmatic muscle fiber damage, increase of work of breathing and oxygen consumption, enlarged tidal volume, and increased transpulmonary pressure (2). In our case, the esophageal pressure decreased profoundly during reverse-triggered breaths (the maximal negative esophageal pressure deflection reached 13 cmH2O) as well as patient-triggered breaths (6 to 10 cmH2O), indicating increased work of breathing and oxygen consumption.

The pathophysiological mechanisms of reverse triggering remain unclear. The Hering-Breuer reflexes, vagal nervous fibers, and cortical and subcortical influences seem to be responsible for neural inspiratory efforts entrained by the ventilator (5). In our patient, all reverse-triggered breaths were induced by the time-initiated cycles, while no entrainment occurred during the patient-triggered cycles. In other words, we did not find double triggering during the entire observation period (4). Although he was under deep sedation, our patient preserved spontaneous breathing. In patient-triggered cycles, the patient’s inspiratory effort was well matched by mechanical inspiration. But in time-initiated cycles, the ventilator delivered insufflation-induced inspiratory muscle contractility. The pattern of our reported reverse triggering raises questions for the investigation into the underlying mechanisms.

In conclusion, patient-ventilator asynchrony can occur under deep sedation. During assist-control ventilation, reverse triggering should be suspected. Monitoring of the esophageal pressure or the electrical activity of the diaphragm can confirm the diagnosis of reverse triggering. Reverse triggering may be eliminated by adjusting the machine rate or tidal volume, but these treatment strategies need to be further investigated.


Acknowledgements

Funding: This work is supported by the Beijing Municipal Science and Technology Commission (No. Z161100000116081).


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.

Informed Consent: Written informed consent was obtained from the patient for publication of this case report and any accompanying images.


References

  1. Akoumianaki E, Lyazidi A, Rey N, et al. Mechanical ventilation-induced reverse-triggered breaths: a frequently unrecognized form of neuromechanical coupling. Chest 2013;143:927-38. [Crossref] [PubMed]
  2. Blanch L, Villagra A, Sales B, et al. Asynchronies during mechanical ventilation are associated with mortality. Intensive Care Med 2015;41:633-41. [Crossref] [PubMed]
  3. Thille AW, Rodriguez P, Cabello B, et al. Patient-ventilator asynchrony during assisted mechanical ventilation. Intensive Care Med 2006;32:1515-22. [Crossref] [PubMed]
  4. Mellott KG, Grap MJ, Munro CL, et al. Patient ventilator asynchrony in critically ill adults: frequency and types. Heart Lung 2014;43:231-43. [Crossref] [PubMed]
  5. Delisle S, Charbonney E, Albert M, et al. Patient-Ventilator Asynchrony due to Reverse Triggering Occurring in Brain-Dead Patients: Clinical Implications and Physiological Meaning. Am J Respir Crit Care Med 2016;194:1166-8. [Crossref] [PubMed]
  6. Dres M, Rittayamai N, Brochard L. Monitoring patient-ventilator asynchrony. Curr Opin Crit Care 2016;22:246-53. [Crossref] [PubMed]
  7. Murias G, de Haro C, Blanch L. Does this ventilated patient have asynchronies? Recognizing reverse triggering and entrainment at the bedside. Intensive Care Med 2016;42:1058-61. [Crossref] [PubMed]
  8. Chanques G, Kress JP, Pohlman A, et al. Impact of ventilator adjustment and sedation-analgesia practices on severe asynchrony in patients ventilated in assist-control mode. Crit Care Med 2013;41:2177-87. [Crossref] [PubMed]
  9. Ely EW, Truman B, Shintani A, et al. Monitoring sedation status over time in ICU patients: reliability and validity of the Richmond Agitation-Sedation Scale (RASS). Jama 2003;289:2983-91. [Crossref] [PubMed]
  10. Beitler JR, Sands SA, Loring SH, et al. Quantifying unintended exposure to high tidal volumes from breath stacking dyssynchrony in ARDS: the BREATHE criteria. Intensive Care Med 2016;42:1427-36. [Crossref] [PubMed]
Cite this article as: He X, Luo XY, Chen GQ, Zhou JX. Detection of reverse triggering in a 55-year-old man under deep sedation and controlled mechanical ventilation. J Thorac Dis 2018;10(9):E682-E685. doi: 10.21037/jtd.2018.08.09