Case Reports in Critical Care

Case Reports in Critical Care / 2015 / Article

Case Report | Open Access

Volume 2015 |Article ID 714902 | https://doi.org/10.1155/2015/714902

Konstantinos Raymondos, Jörg Ahrens, Ulrich Molitoris, "Combined Negative- and Positive-Pressure Ventilation for the Treatment of ARDS", Case Reports in Critical Care, vol. 2015, Article ID 714902, 5 pages, 2015. https://doi.org/10.1155/2015/714902

Combined Negative- and Positive-Pressure Ventilation for the Treatment of ARDS

Academic Editor: Nicolas Nin
Received01 May 2015
Accepted28 Jun 2015
Published28 Jul 2015

Abstract

Objective. Tracheal intubation and positive-pressure ventilation as the current standard of care for the adult respiratory distress syndrome (ARDS) seem to have reached their limit in terms of a further relevant reduction of the still very high mortality. Case Presentation. A 75-year-old male patient developed ARDS after abscess drainage with deteriorating oxygenation, despite positive end-expiratory pressure (PEEP) values above 15 cm H2O. We applied external negative-pressure ventilation with a chamber respirator using −33 cm H2O at inspiration and −15 cm H2O at expiration, combined with conventional pressure support using a PEEP of about 8 cm H2O and a pressure support of 4–12 cm H2O. Alveolar infiltrates disappeared rapidly and PaO2/FiO2 values surpassed 300 mmHg after the first application and 500 mmHg after the second. Negative-pressure ventilation was used for 6–18 hours/day over five days. Now, 13 years later, the patient is still alive and has a good quality of life. Conclusion. Using this or similar concepts, not only in intubated patients but also as a noninvasive approach in patients with ARDS, offers new options that may genuinely differ from the present therapeutic approaches and may, therefore, have the potential to decrease the present high mortality from ARDS.

1. Introduction

Continuous positive-pressure ventilation (CPPV) still represents the standard method of treating the adult respiratory distress syndrome (ARDS), despite the fact that it aggravates both lung injury and multisystem organ failure [1], with mortality from ARDS still as high as 50% [2, 3]. However, there are alternatives for the symptomatic treatment of ARDS. Decades ago, modified Emerson tank respirators were successfully used to treat ARDS with continuous negative pressure [46]. These patients had pneumonia and were neither intubated nor ventilated but breathed spontaneously surrounded by negative pressure [46]. According to observations of lung injury, it is not only spontaneous breathing under negative pressure that differs substantially from CPPV: this is certainly also the case for ventilation with negative pressure. Continuous external negative-pressure ventilation (CENPV) improves oxygenation under more physiological conditions with lower transpulmonary, airway, and intra-abdominal pressures than with CPPV [7, 8].

Apart from these physiological studies, there are no reports on clinical experience with CENPV in ARDS or the combined use of negative- and positive-pressure ventilation.

2. Clinical Case

A 75-year-old male patient suffered from a peritonsillar abscess, which extended down to the hypopharynx. After anesthesia induction, the patient was intubated without any problems, and tonsillectomy and abscess drainage were performed. Following extubation, the peripheral oxygen saturation in the anesthesia recovery room decreased to 85% despite oxygen administration. Coarse bubbling and moist rales were auscultated over both lungs. Administration of intravenous furosemide administrations had no effect, and the initial chest X-ray revealed patchy bilateral infiltrates but without enlarged heart (Figure 1). A cardiac etiology for the pulmonary edema was ruled out, also clinically, as a physical examination failed to reveal heart murmurs, jugular venous distension, or peripheral edema, and there was no sign of hemodynamic instability. The patient was ventilated noninvasively via a facemask with positive end-expiratory pressure (PEEP) of at least 5 cm H2O and, from the second day, with a FiO2 of 0.5. On the third day, respiratory insufficiency deteriorated and the patient was intubated. Two days later the patient was tracheostomized; CT scans of the lungs were performed at a PEEP level of 15 cm H2O and showed bilateral patchy infiltrates and dorsal consolidation extending from cranial to caudal lung regions (Figure 1).

During the following day, the PaO2/FiO2 ratio again decreased below 200 mmHg, despite high PEEP values of not less than 15 cm H2O (Figure 2) that were not sufficient to maintain lung volumes; even recruitment maneuvers using airway pressures up to 85 cm H2O were unable to substantially improve oxygenation. In this situation, six days after the development of ARDS and three days after invasive CPPV, we decided to apply CENPV with the chamber respirator (Figure 3).

This device was constructed drawing on our clinical experience with a tank respirator that was built in our hospital in the early 1980s [7]. Gull-wing doors at both sides and one at the head enabled rapid access to the intubated patient who was placed completely inside the chamber (Figure 3). Three air-sealing outlets at each side and two at the top enabled simple and rapid introduction of medical support devices; moreover, during their introduction (or when the doors were opened/closed), there was no need to disconnect any lines or connections.

After receiving permission from the patient’s next of kin we started CENPV, applying chamber pressures of −33 cm H2O at inspiration and −15 cm H2O at expiration. We combined CENPV with conventional PEEP of about 8 cm H2O and pressure support of 4–12 cm H2O (Figure 2), applying tidal volumes of 6–8 mL/kg predicted bodyweight. For pressure support, we used the BIPAP assist mode of a conventional intensive care respirator (Evita 4, Dräger, Lübeck, Germany).

During the first application of the chamber ventilator (that lasted for 7 hours), the PaO2/FiO2 value increased from 236 to more than 300 mmHg (Figure 2), and alveolar infiltrates showed an impressive decrease. However, it was only during the second application time (after eight hours of CENPV) that the PaO2/FiO2 value increased to more than 500 mmHg (Figure 2), indicating significant recruitment of lung volume without the use of any recruitment maneuvers. Before opening the chamber respirator again, the PEEP level was elevated by at least 8 cm H2O to compensate for the discontinuation of the end-expiratory negative chamber pressure (Figure 2).

During these first two applications of the chamber respirator, the patient was deeply sedated and CENPV was applied with a fixed setting without triggering the negative-pressure pump. During subsequent applications of CENPV, the patient’s spontaneous breathing efforts triggered the external negative-pressure pump unit (Coppa, Biella, Italy) of the chamber ventilator via a thermistor that was fixed at the tracheal cannula. The resulting breaths triggered the pressure support function of the conventional respirator.

After applying CENPV for 5 days for 6–18 h/day, we decided to wean the tracheostomized patient from the ventilator and increased the PEEP to 19 cm H2O before opening the chamber ventilator. Following cessation of CENPV, the patient breathed spontaneously at this high PEEP level with pressure support of only 4–8 cm H2O (Figure 3). Most remarkably, he breathed slowly and very effectively, making almost sole use of his diaphragm and only very marginal use of his accessory respiratory muscles. Subsequently, higher levels of pressure support became necessary and oxygenation deteriorated again, with PaO2/FiO2 values mainly between 200 and 300 mmHg (Figure 2). Three weeks after CENPV, the patient was successfully extubated and discharged to the normal ward.

Now, 13 years later, the patient is still alive and has a good quality of life, travelling extensively with his wife and enjoying his grandchildren, and one of his favorite and frequent activities is cycling.

3. Discussion

This patient probably developed ARDS due to the focus of infection that spread following abscess drainage; however, the definitive reason for the immediate postoperative development of lung injury remains unknown. Despite high pressure values, oxygenation could not be maintained using PEEP, and recruitment maneuvers proved unable to recruit lung volume. This not only reflects the severity of lung injury but also, in particular, indicates the limitations of conventional ventilator therapy in which only positive pressure is used.

In this situation, CENPV using the chamber respirator in combination with PEEP and pressure support was able to recruit and maintain lung volume, as indicated by persistently improved oxygenation over five days with PaO2/FiO2 values above 300 mmHg, associated with an impressive reduction of alveolar infiltrates. These effects may be caused by the different way in which ventilator pressures are applied, resulting in a much more effective means of distending the lungs and maintaining lung volumes, as the negative pressure acts across a broad surface of both the chest wall and abdomen. Therefore, in both surfactant-depleted rabbits and patients with ARDS, at matched end-expiratory and inspiratory lung volumes, applying lower transpulmonary pressures, CENPV presumably also resulted in better oxygenation as compared to CPPV [7, 8].

We decided to apply negative- and positive-pressure ventilation simultaneously, as we have found this combination to be highly effective in ventilating patients with ARDS. During CENPV, regional pleural pressure gradients probably exhibit a substantially different development compared with those in CPPV [7, 8]. Furthermore, transpulmonary pressures (TPP = alveolar pressure minus esophageal pressure), involved in both ventilator modes, should be cumulative when CENPV is combined with CPPV. We speculate that the distribution of ventilation is much more effective with this combination, resulting in alveolar recruitment, reduction of alveolar edema, and stabilization of recruited lung volume, even in severe cases of ARDS; we believe that these effects contributed to the favorable outcome in the present patient.

We observed similar effects in most of our other five patients with severe ARDS who were treated in the chamber respirator in 2002 and also in six additional patients with ARDS who were treated in a tank respirator after completing physiological studies [8]. In these (albeit limited number of) patients, no relevant adverse effects were observed that could be directly related to the combined use of negative- and positive-pressure ventilation. However, especially in patients with severe capillary leakage, external edema increased and decreased again under ambient air. In these latter patients, we limited this therapy to only several hours per day. Particularly in hypovolemic patients, we administered intravenous fluid before starting CENPV to avoid a pronounced decrease in blood pressure associated with low intrathoracic pressures and redistribution of intravascular volume. Finally, of all these patients, 50% survived their stay in the intensive care unit.

In line with this current standard of care, the patient described here was intubated and ventilated with CPPV; we then commenced CENPV as a rescue therapy in late-stage ARDS. Because we did not wish to risk applying CENPV in this patient (or other patients) without a tracheal tube during an early stage of lung injury, CENPV was applied only in intubated patients with severe ARDS. Generally, securing the airway with a tracheal tube is still deemed necessary when a patient with lung injury depends on high ventilatory pressures in conjunction with a high FiO2 to maintain gas exchange. As in the presented case, noninvasive positive-pressure ventilation frequently fails in ARDS as a function of its severity and does not appear beneficial in severe ARDS [8]. We believe that CENPV has the potential to reduce this high failure rate, even in severe lung injury. Furthermore, after cessation of CENPV, our patient’s breathing pattern with a low breathing frequency and high tidal volumes (making almost sole use of his diaphragm) may also indicate the potential of CENPV to reduce weaning failure. However, due to the paucity of data on this topic, randomized trials comparing noninvasive positive- and negative-pressure ventilation in patients with ARDS are needed to further support this hypothesis.

Devices far less clumsy than our self-made tank respirator or chamber respirator are now available. These include a much more practical Goretex suit that is effectively used with a highly efficient negative-pressure ventilator (Pegaso Vent, Dima S.r.l., Bologna, Italy). This device can be synchronized with spontaneous breathing and can be coupled to a conventional ventilator to optimally synchronize CENPV with CPPV.

Tracheal intubation and CPPV as the current standard of care for ARDS seem to have reached their limit in terms of a further relevant reduction of the still very high mortality rate [2, 3]. This unacceptably high mortality rate calls for alternative techniques that substantially differ from the present methods. CENPV might be worth considering as an alternative, as it has proven less injurious and resulted in better oxygenation in experimental lung injury [7] and also improved gas exchange in a physiologic study on patients with ARDS [8].

The present report is the first to demonstrate how both techniques can be successfully combined in an intubated patient with severe late-stage ARDS. We believe that this therapy made a substantial contribution to the patient’s positive outcome and survival. The possibility of effectively applying this and similar concepts, not only in intubated but also in nonintubated patients with ARDS, offers new options that may genuinely differ from the present therapeutic approaches. Therefore, these options may have the potential to decrease the ongoing high mortality rate associated with ARDS.

Conflict of Interests

The authors declare that they have no competing interests.

Acknowledgments

The authors thank Dr. Ljiljana Verner, Professor Dr. Jörn Heine, and Professor Dr. Siegfried Piepenbrock for their support.

References

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Copyright © 2015 Konstantinos Raymondos et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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