Abstract
Purpose
Patients with acute respiratory distress syndrome (ARDS) requiring extracorporeal membrane oxygenation (ECMO) usually present very low respiratory system compliance (Cstrs) values (i.e., severe restrictive respiratory syndrome patients). As a consequence, they are at high risk of experiencing poor patient–ventilator interaction during assisted breathing. We hypothesized that monitoring of diaphragm electrical activity (EAdi) may enhance asynchrony assessment and that neurally adjusted ventilatory assist (NAVA) may reduce asynchrony, especially in more severely restricted patients.
Methods
We enrolled ten consecutive ARDS patients with very low Cstrs values undergoing ECMO after switching from controlled to pressure support ventilation (PSV). We randomly tested (30 min) while recording EAdi: (1) PSV30 (PSV with an expiratory trigger at 30 % of flow peak value); (2) PSV1 (PSV with expiratory trigger at 1 %); (3) NAVA. During each step, we measured the EAdi-based asynchrony index (AIEAdi) = flow-, pressure- and EAdi-based asynchrony events/EAdi-based respiratory rate × 100.
Results
AIEAdi was high during all ventilation modes, and the most represented asynchrony pattern was specific for this population (i.e., premature cycling). NAVA was associated with significantly decreased, although suboptimal, AIEAdi values in comparison to PSV30 and PSV1 (p < 0.01 for both). The PSV30–NAVA and PSV1–NAVA differences in AIEAdi values were inversely correlated with patients’ Cstrs (R 2 = 0.545, p = 0.01 and R 2 = 0.425, p < 0.05; respectively).
Conclusions
EAdi allows accurate analysis of asynchrony patterns and magnitude in ARDS patients with very low Cstrs undergoing ECMO. In these patients, NAVA is associated with reduced asynchrony.
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Introduction
Extracorporeal membrane oxygenation (ECMO) ensures viable blood gases while allowing protective mechanical ventilation (MV) in patients with severe acute respiratory distress syndrome (ARDS) [1, 2]. Recent studies showed that ECMO is safe and that an ECMO-based treatment strategy may improve survival without disability [3–6]. During the first days of ECMO, controlled MV is usually implemented with tidal volumes (V t) significantly lower than those adopted before ECMO [7]. The initial V t reduction allowed by ECMO may be particularly beneficial in severe ARDS patients with more serious lung injury and extremely low static respiratory system compliance (Cstrs) [8, 9]. After this phase, protective assisted MV may improve respiratory muscle function and gas exchange, decrease sedation and aid weaning from the ventilator [10–12]. However, Cereda et al. [13] showed that pressure support ventilation (PSV) may be difficult to implement in ARDS patients with low Cstrs, likely because peak inspiratory flow is reached rapidly and the flow-based expiratory phase of PSV starts while patient is still inspiring (premature expiratory cycling). Thus, ARDS patients with low Cstrs undergoing ECMO are at high risk of patient–ventilator asynchrony [14]. Asynchrony represents a serious threat, as higher asynchrony is associated with iatrogenic injury and delayed weaning from the ventilator [15–17].
Diaphragm electrical activity (EAdi) can be monitored during any assisted MV mode (e.g., during PSV) and represents a clinically reliable monitor of the respiratory center's neural activity [18]. EAdi monitoring increases accuracy in the assessment of patient–ventilator asynchrony [19], and neurally adjusted ventilatory assist (NAVA) is another assisted MV mode based on the EAdi and designed to improve synchrony [18, 20, 21]. To date, only a few pilot reports exist on the use of NAVA in severe ARDS patients undergoing ECMO, none of which systematically analyzed patient–ventilator interaction: (1) Bein et al. [22] reported the case of one severely injured soldier transported with pumpless ECMO and NAVA; (2) a study on six patients showed auto-regulation of EAdi and NAVA in the presence of reduced ECMO support [23]; (3) our group reported the successful application of NAVA in one severe ARDS patient undergoing ECMO, which generated the hypothesis of the present study [14].
In the present study, we monitored EAdi continuously while delivering NAVA and PSV, the latter at two different expiratory criteria (i.e., pre-set by the manufacturer and the one that allows the longest inspiratory time) in ARDS patients with extremely low Cstrs undergoing ECMO. We evaluated asynchronies during each ventilation mode and calculated an EAdi-based asynchrony index (AIEAdi). We hypothesized that: (1) EAdi monitoring would enhance asynchrony assessment; (2) NAVA would decrease patient–ventilator asynchrony; (3) the decrease in asynchrony during NAVA would be more evident in patients with lower Cstrs values.
Materials and methods
Study setting
The present study was performed in a ten-bed university hospital general intensive care unit (ICU), part of the Italian ECMOnet system [24], specialized in treatment of severe ARDS patients unresponsive to conventional therapy, including the use of ECMO [25].
Study population
Between June 2010 and February 2011, we enrolled ten consecutive ARDS patients [26] with low Cstrs values (as reported by the attending physician) undergoing ECMO (for patients’ clinical management see the online data supplement) within 48 h after switching from controlled ventilation to PSV. Exclusion criteria were: age <18 years, hemodynamic instability and contraindications to inserting a NAVA dedicated nasogastric tube (NGT) (e.g., nasal bleeding). Informed consent was obtained from each subject or next of kin before enrollment. The Institutional Review Board approved the study.
After enrollment, all patients were connected to a mechanical ventilator that could deliver both PSV and NAVA (SERVO-i®; MAQUET GmbH & Co. KG, Rastatt, Germany). EAdi was recorded during all study phases using a dedicated NGT with an array of electrodes placed at its distal end (EAdi catheter; MAQUET GmbH & Co. KG, Rastatt, Germany). Correct EAdi catheter positioning was checked using the appropriate built-in ventilator function and following the manufacturer’s instructions [18].
Data collection
Sex, age, predicted body weight, body mass index (BMI), Simplified Acute Physiology Score II (SAPS II) values [27], duration of mechanical ventilation and days on ECMO, total patient’s O2 consumption and the proportion granted by ECMO, and the Sepsis-related Organ Failure Assessment (SOFA) Score [28] and Lung Injury Score (LIS) [29] were recorded at enrollment. We also recorded in-hospital mortality.
Study protocol
We randomly applied the following assisted ventilation strategies for 30 min each: (1) PSV30: PSV with expiration cycling time set at 30 % of the flow peak value (i.e., pre-set on SERVO-i® ventilators by the manufacturer); (2) PSV1: PSV with expiration cycling time set at 1 % (i.e., the least allowed by SERVO-i® ventilators); (3) NAVA: NAVA with gain set between 0.5 and 2 cmH2O/μV to obtain, on average, the same V t as during pre-study clinically set PSV and with expiratory cycling pre-set by the manufacturer at 70 % of EAdi peak value (non-modifiable). All other PSV settings were left as clinically set, because they likely indicate a thoughtful selection of the “optimal” PSV level in each patient. Thus, during all phases, we left the following unchanged: (1) PSV level (i.e., set to obtain V t = 3–5 ml/kg with peak inspiratory pressure below 30 cmH2O and respiratory rate ≤35 breaths/min); (2) PSV and NAVA pressure- or flow-based inspiratory triggers (set at −2 cmH2O or at 2–5 l/min); (3) PSV inspiratory rise time (set at 0.15–0.25 s); (4) NAVA EAdi-based inspiratory trigger (set at 0.5–0.8 μV: NAVA starts inspiration on a first come-first serve criteria between flow- and EAdi-based inspiratory triggers); (5) PEEP and FiO2 levels; (6) ECMO blood and gas flows.
At the end of the study, patients were sedated, paralyzed and switched to volume assist/control ventilation in order to measure Cstrs value by means of end-expiratory and end-inspiratory holds.
Data acquisition and analysis
Each ventilator was connected through its serial port to a personal computer that recorded continuous waveforms of airway pressure, flow, volume and EAdi during all study phases. After the study was completed, by offline visual inspection of airway pressure, flow, volume and EAdi waveforms recorded during the last 5 min of each phase, we calculated AIEAdi as the number of flow-, pressure- and EAdi-based asynchrony events divided by patients’ EAdi-based respiratory rate:
We defined four different asynchrony patterns [30, 31]: (1) ineffective triggering: one positive EAdi deflection with or without airway pressure drop not followed by an assisted breath; (2) double triggering: two assisted breaths delivered during a single positive EAdi deflection; (3) auto-triggering: a mechanically delivered breath without an associated positive EAdi deflection and without airway pressure drop; (4) premature cycling: an assisted breath with expiration starting before the end of patient’s effort as assessed by EAdi (i.e., before EAdi peak or right after it) and/or with biphasic expiratory flow waveform (Figs. 1, 2).
Positive EAdi deflections not related to patients’ breathing efforts (e.g., heart activity) were visually recognized by standardized criteria (e.g., very low amplitude and/or very different shape in comparison to preceding and subsequent EAdi deflections) and not included in the asynchrony analysis.
From the same time period, we also calculated: the time between the onset of ventilator inspiratory flow and the beginning of the expiratory one (ventilator inspiratory time, Ti); the mean time between the beginning of each positive EAdi deflection and the onset of ventilator inspiratory flow (inspiratory delay, ID); the mean time between EAdi peak and the beginning of the expiratory flow (cycle-off time, CT). CT values were negative (i.e., early cycle-off) if the expiratory flow of the ventilator started before the EAdi peak (Fig. 1).
Right after the end of each study phase and immediately prior to the next, we also collected: ventilator settings, arterial blood gas analysis, patient’s respiratory rate measured by mechanical ventilator, mean peak EAdi value (EAdipeak), the pressure generated by the patient during the first 0.1 s of a normal inspiratory act (p0.1, a measure of patient’s central respiratory drive obtained by end expiratory breath hold) [32] and hemodynamics.
Statistical analysis
Our study was powered to detect a 30 ± 30 % decrease in AI between PSV30 and NAVA [14], at a level of significance of 0.05 and power of 80 %. The sample size was similar to previous studies, too [33]. To detect possible carry-over effects, variables measured during different study phases were compared by two-way analysis of variance (ANOVA) for repeated measures with study phase as within-subject and randomization sequence as between-subject factors, or (for categorical variables) chi-square or Fisher’s exact test, as appropriate. If the ventilation strategy effect was statistically significant, a post hoc analysis was performed comparing the three treatments at each step (Tukey method). Association between two variables was assessed by linear regression. A level of p < 0.05 (two-tailed) was considered as statistically significant. Data are indicated as mean ± standard deviation, unless otherwise indicated. Statistical analyses were performed by SigmaPlot 11.0 (Systat Software Inc., San Jose, CA, USA) and IBM SPSS Statistics 19 (International Business Machines Corp., Armonk, NY, USA).
Results
Patient characteristics
Table 1 and Table E1 (online data supplement) report the main patient characteristics. The study was performed after 23 ± 17 days of MV but, at the time of the study, all patients still fulfilled ARDS criteria, LIS values were high, and Cstrs was very low (18 ± 8 mL/cmH2O). Only PaO2/FiO2 ratios were artificially high (245 ± 118 mmHg (Table 2) because of the increase in mixed venous oxygen content related to ECMO support. All ECMOs were veno-venous, except for one veno-arterial ECMO.
Effect of randomization sequence on studied parameters
Table E2 (online data supplement) reports the randomization sequence of different study phases for each patient. Statistical analysis did not disclose any significant interaction between randomization order and ventilation phase for any of the variables considered (p > 0.05 for all).
Effects of different assisted MV strategies on physiological parameters
During all study phases, patients’ global physiological parameters did not change significantly (Table 2): gas exchange and hemodynamics were not affected by the implementation of PSV30, PSV1 and NAVA.
Assessment of patient–ventilator synchrony
EAdi-based analysis of asynchrony showed that ineffective triggering was the least represented pattern during PSV, while premature cycling was the most frequent (Table 3; Fig. 2). During NAVA, incidence of premature cyclings decreased, and all patterns became more equally represented (Table 3). As a consequence, high PSV-related AIEAdi values significantly decreased during NAVA (p < 0.01, Fig. 3). Switching from PSV to NAVA, Ti was longer, ID significantly decreased, and CT improved (p < 0.01, p < 0.05 and p < 0.01; respectively, Table 3).
Determinants of asynchrony severity
AIEAdi was inversely correlated, during all study phases, with Ti (R 2 = 0.179, p < 0.05) and, more closely, with CT (R 2 = 0.548, p < 0.05). ID, instead, was not correlated with asynchrony severity. The decrease in AIEAdi values between PSV30 and NAVA and between PSV1 and NAVA were inversely correlated with patients’ Cstrs values (R 2 = 0.545, p = 0.01 and R 2 = 0.425, p < 0.05; respectively) (Fig. 4).
Effects of different assisted MV strategies on patients’ respiratory variables
V t did not change along different study phases, but P peak was lower during NAVA (p = 0.05, Table 4). RR displayed by ventilator significantly decreased during NAVA in comparison to PSV30 and PSV1 (p < 0.01), but patients’ EAdi-based neural RR didn’t change (Table 4).
Discussion
In the present study we described that in ARDS patients with very low Cstrs undergoing ECMO: (1) short inspiratory time and low Cstrs values lead to premature ventilator expiratory cycling and cause high patient–ventilator asynchrony; (2) EAdi monitoring allows specific and accurate assessment of patient–ventilator interaction; (3) NAVA is associated with improved, although still suboptimal, patient–ventilator interaction in comparison to PSV.
We assessed patient–ventilator interaction during PSV delivered by pre-set and prolonged cycle-off settings in ARDS patients with very low Cstrs undergoing ECMO. Previously, Cereda et al. [13] observed a 21 % incidence of failure of PSV in ARDS patients. PSV failure is often due to poor patient–ventilator interaction that can lead to patients’ discomfort, respiratory distress, barotrauma, prolonged intubation, muscular exhaustion and, possibly, increased mortality [15–17, 34]. The main reason for poor interaction during PSV is a mismatch between patient’s and ventilator’s inspiration and expiration, which is more likely to happen in patients with decreased Cstrs values (or with increased airway resistance) [13, 14]: in Cereda’s study, indeed, the presence of low Cstrs was associated with PSV failure. In the present study, patients’ Cstrs was extremely low, and implementation of both PSV modes yielded poor results. EAdi-based measure of asynchrony, indeed, was extremely high, with premature cycling being the most represented pattern. Premature cycling, which has already been described in two different patient populations undergoing volume-controlled and non-invasive ventilation [31, 35], was the asynchrony pattern that we expected to be predominant in our population because of the PSV flow-based early expiration trigger (see “Introduction”) [13]. Thus, EAdi monitoring during PSV might yield accurate and specific assessment of patient–ventilator interaction in ARDS patients with low Cstrs. Still, the fact that changing PSV expiratory trigger decreased asynchrony only to a limited extent may seem in contrast with previous findings by Chiumello et al. [36]. The discrepancy between our findings and previous results may be due to the clinical characteristics of our study population: in Chiumello’s paper patients’ mean Crsst was 61 ± 38 ml/cmH2O as compared to 18 ± 8 ml/cmH2O in ours (i.e., milder vs. severe restrictive ARDS patients) [36].
NAVA delivers ventilatory assist in proportion to EAdi [18]. This prompts ventilation that should more closely reflect patient’s central respiratory neural output and should be less influenced by the mechanical properties of patients’ respiratory system [37]. NAVA, in previous studies, reduced inspiratory and expiratory trigger mismatch, minimized wasted inspiratory efforts and reduced asynchrony in comparison to PSV [20, 21]. When we implemented NAVA in our patient population, asynchrony decreased and, as we hypothesized, the decrease was mainly due to a reduced presence of premature cyclings. In fact, NAVA’s longer Ti matched patient and ventilator breathing patterns more closely. These results were even more evident in patients with the lowest Cstrs and shortest Ti during PSV, who are at higher risks of developing elevated plateau pressure and ventilation injury during controlled MV and, therefore, might benefit more from switching to assisted ventilation [38]. However, asynchrony during NAVA decreased only to suboptimal values, and we tried to better analyze this finding. We observed that: (1) NAVA expiration cycling criteria in some patients are reached too early, causing premature ventilator cycling (as during PSV), but, at variance to PSV, the expiration trigger cannot be modified in NAVA mode; (2) auto-triggerings during NAVA are mainly due to unstable basal EAdi activity; (3) double triggering during NAVA happened in the presence of biphasic EAdi deflections, as already described by Piquilloud et al. [21]: the ventilator interprets the second rise as a new inspiratory effort and a new breath is delivered (Fig. 2). In conclusion, suboptimal asynchrony values obtained during NAVA are better than those obtained during PSV and might further improve with changes in ventilator pre-set algorithms.
Piquilloud et al. [21] compared the flow- and pressure-based asynchrony index during PSV and NAVA in intubated acute respiratory failure patients apparently not affected by ARDS and with Cstrs values in the normality range. Piquillod’s study showed that, in such patients, asynchrony significantly decreased during NAVA: thus, our data are in line with their result, albeit ours were obtained in a very peculiar and difficult to study patient population.
Our study presents a few major limitations: (1) it is a single-center crossover physiologic study, and we cannot draw definitive conclusions regarding clinical outcomes associated with asynchrony and/or NAVA use in severe ARDS patients undergoing ECMO (e.g., MV-free days). However, the analysis of patient–ventilator interaction during PSV and NAVA might give some indications on the potential clinical benefits of NAVA; (2) each study phase lasted only 30 min: this was the minimal time to obtain stable NAVA and PSV ventilation pattern based on previous data; (3) we studied PSV delivered only in two conditions, while other settings might have been changed (e.g., different inspiratory rise time or other expiratory trigger criteria). We chose PSV30 as it is the one pre-set by the manufacturer, thus likely being the one most widely adopted. PSV1, instead, was chosen to increase inspiratory time, likely to reduce asynchrony in sicker severe ARDS patients with lowest Cstrs values. The attending physician chose all other settings, thus implying an optimization process before the protocol start in each patient. Leaving these settings unchanged throughout the study allowed us to focus on the correlation among Ti, Cstrs and asynchrony, which was the object of this study. However, we must acknowledge that Ti could have also been modified by the application of different inspiratory rise times [36] and that the clinical choice of flow- versus pressure-based inspiratory triggers might yield, respectively, a higher incidence of auto- versus ineffective triggerings [39].
Conclusions
ARDS patients with very low Cstrs values undergoing ECMO experience high asynchrony during assisted MV. EAdi monitoring enhances recognition of asynchrony severity and of specific asynchrony patterns (i.e., premature cycling). In comparison to PSV, EAdi-based NAVA ventilation reduces patient–ventilator asynchrony to suboptimal levels. Reduced asynchrony during NAVA is more relevant in sicker patients, as defined by lower Cstrs values. Although preliminary, our findings seem to suggest that NAVA could be more appropriate than PSV when switching ARDS patients with very low compliance from controlled to assisted ventilation. However, adequately powered long-term studies are needed to confirm these hypotheses.
References
Hill JD, De Leval MR, Fallat RJ, Bramson ML, Eberhart RC, Schulte HD, Osborn JJ, Barber R, Gerbode F (1972) Acute respiratory insufficiency. Treatment with prolonged extracorporeal oxygenation. J Thorac Cardiovasc Surg 64:551–562
Gattinoni L, Kolobow T, Damia G, Agostoni A, Pesenti A (1979) Extracorporeal carbon dioxide removal (ECCO2R): a new form of respiratory assistance. Int J Artif Organs 2:183–185
Peek GJ, Mugford M, Tiruvoipati R, Wilson A, Allen E, Thalanany MM, Hibbert CL, Truesdale A, Clemens F, Cooper N, Firmin RK, Elbourne D, CESAR trial collaboration (2009) Efficacy and economic assessment of conventional ventilatory support versus extracorporeal membrane oxygenation for severe adult respiratory failure (CESAR): a multicentre randomised controlled trial. Lancet 374:1351–1363
Australia and New Zealand Extracorporeal Membrane Oxygenation (ANZ ECMO) Influenza Investigators, Davies A, Jones D, Bailey M, Beca J, Bellomo R, Blackwell N, Forrest P, Gattas D, Granger E, Herkes R, Jackson A, McGuinness S, Nair P, Pellegrino V, Pettilä V, Plunkett B, Pye R, Torzillo P, Webb S, Wilson M, Ziegenfuss M (2009) Extracorporeal membrane oxygenation for 2009 influenza A(H1N1) acute respiratory distress syndrome. JAMA 302:1888–1895
ANZIC Influenza Investigators, Webb SA, Pettilä V, Seppelt I, Bellomo R, Bailey M, Cooper DJ, Cretikos M, Davies AR, Finfer S, Harrigan PW, Hart GK, Howe B, Iredell JR, McArthur C, Mitchell I, Morrison S, Nichol AD, Paterson DL, Peake S, Richards B, Stephens D, Turner A, Yung M (2009) Critical care services and 2009 H1N1 influenza in Australia and New Zealand. N Engl J Med 361:1925–1934
Grasselli G, Bombino M, Patroniti N, Foti G, Benini A, Abbruzzese C, Fumagalli R, Pesenti A (2011) Management of acute respiratory complications from influenza A (H1N1) infection: experience of a tertiary-level Intensive Care Unit. Minerva Anestesiol 77:884–891
The Acute Respiratory Distress Syndrome Network (2000) Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. N Engl J Med 342:1301–1308
Mauri T, Foti G, Zanella A, Bombino M, Confalonieri A, Patroniti N, Bellani G, Pesenti A (2011) Long-term extracorporeal membrane oxygenation with minimal ventilatory support: a new paradigm for severe ARDS? Minerva Anestesiol 78:385–389
Grasselli G, Foti G, Patroniti N, Rona R, Perlangeli MV, Pesenti A (2008) Extracorporeal cardiopulmonary support for cardiogenic shock caused by pheochromocytoma: a case report and literature review. Anesthesiology 108:959–962
Carvalho AR, Spieth PM, Güldner A, Cuevas M, Carvalho NC, Beda A, Spieth S, Stroczynski C, Wiedemann B, Koch T, Pelosi P, de Abreu MG (2011) Distribution of regional lung aeration and perfusion during conventional and noisy pressure support ventilation in experimental lung injury. J Appl Physiol 110:1083–1092
Putensen C, Zech S, Wrigge H, Zinserling J, Stüber F, Von Spiegel T, Mutz N (2001) Long-term effects of spontaneous breathing during ventilatory support in patients with acute lung injury. Am J Respir Crit Care Med 164:43–49
Marini JJ (2011) Spontaneously regulated vs. controlled ventilation of acute lung injury/acute respiratory distress syndrome. Curr Opin Crit Care 17:24–29
Cereda M, Foti G, Marcora B, Gili M, Giacomini M, Sparacino ME, Pesenti A (2000) Pressure support ventilation in patients with acute lung injury. Crit Care Med 28:1269–1275
Mauri T, Bellani G, Foti G, Grasselli G, Pesenti A (2011) Successful use of neurally adjusted ventilatory assist in a patient with extremely low respiratory system compliance undergoing ECMO. Intensive Care Med 37:166–167
Sassoon CS, Foster GT (2001) Patient–ventilator asynchrony. Curr Opin Crit Care 7:28–33
Chao DC, Scheinhorn DJ, Stearn-Hassenpflug M (1997) Patient–ventilator trigger asynchrony in prolonged mechanical ventilation. Chest 112:1592–1599
de Wit M, Miller KB, Green DA, Ostman HE, Gennings C, Epstein SK (2009) Ineffective triggering predicts increased duration of mechanical ventilation. Crit Care Med 37:2740–2745
Sinderby C, Navalesi P, Beck J, Skrobik Y, Comtois N, Friberg S, Gottfried SB, Lindström L (1999) Neural control of mechanical ventilation in respiratory failure. Nat Med 5:1433–1436
Colombo D, Cammarota G, Alemani M, Carenzo L, Barra F, Vaschetto R, Slutsky AS, Della Corte F, Navalesi P (2011) Efficacy of ventilator waveforms observation in detecting patient–ventilator asynchrony. Crit Care Med 39:2452–2457
Richard JC, Lefebvre JC, Tassaux D, Brochard L (2011) Update in mechanical ventilation 2010. Am J Respir Crit Care Med 184:32–36
Piquilloud L, Vignaux L, Bialais E, Roeseler J, Sottiaux T, Laterre PF, Jolliet P, Tassaux D (2011) Neurally adjusted ventilatory assist improves patient–ventilator interaction. Intensive Care Med 37:263–271
Bein T, Osborn E, Hofmann HS, Zimmermann M, Philipp A, Schlitt HJ, Graf BM (2010) Successful treatment of a severely injured soldier from Afghanistan with pumpless extracorporeal lung assist and neurally adjusted ventilatory support. Int J Emerg Med 3:177–179
Karagiannidis C, Lubnow M, Philipp A, Riegger GA, Schmid C, Pfeifer M, Mueller T (2010) Autoregulation of ventilation with neurally adjusted ventilatory assist on extracorporeal lung support. Intensive Care Med 36:2038–2044
Patroniti N, Zangrillo A, Pappalardo F, Peris A, Cianchi G, Braschi A, Iotti GA, Arcadipane A, Panarello G, Ranieri VM, Terragni P, Antonelli M, Gattinoni L, Oleari F, Pesenti A (2011) The Italian ECMO network experience during the 2009 influenza A(H1N1) pandemic: preparation for severe respiratory emergency outbreaks. Intensive Care Med 37:1447–1457
Grasselli G, Foti G, Patroniti N, Giuffrida A, Cortinovis B, Zanella A, Pagni F, Mergoni M, Pesci A, Pesenti A (2009) A case of ARDS associated with influenza A—H1N1 infection treated with extracorporeal respiratory support. Minerva Anestesiol 75:741–745
Bernard GR, Artigas A, Brigham KL, Carlet J, Falke K, Hudson L, Lamy M, Legall JR, Morris A, Spragg R (1994) The American–European Consensus Conference on ARDS: definitions, mechanism, relevant outcomes, and clinical trial coordination. Am J Respir Crit Care Med 149:818–824
Le Gall JR, Lemeshow S, Saulnier F (1993) A new Simplified Acute Physiology Score (SAPS II) based on a European/North American multicenter study. JAMA 270:2957–2963
Vincent JL, Moreno R, Takala J, Willatts S, De Mendonça A, Bruining H, Reinhart CK, Suter PM, Thijs LG (1996) The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med 22:707–710
Murray JF, Matthay MA, Luce JM, Flick MR (1988) An expanded definition of the adult respiratory distress syndrome. Am Rev Respir Dis 138:720–723
Thille AW, Rodriguez P, Cabello B, Lellouche F, Brochard L (2006) Patient–ventilator asynchrony during assisted mechanical ventilation. Intensive Care Med 32:1515–1522
Vignaux L, Vargas F, Roeseler J, Tassaux D, Thille AW, Kossowsky MP, Brochard L, Jolliet P (2009) Patient–ventilator asynchrony during non-invasive ventilation for acute respiratory failure: a multicenter study. Intensive Care Med 35:840–846
Alberti A, Gallo F, Fongaro A, Valenti S, Rossi A (1995) P0.1 is a useful parameter in setting the level of pressure support ventilation. Intensive Care Med 21:547–553
Patroniti N, Bellani G, Saccavino E, Zanella A, Grasselli G, Isgrò S, Milan M, Foti G, Pesenti A (2011) Respiratory pattern during neurally adjusted ventilatory assist in acute respiratory failure patients. Intensive Care Med 38:230–239
Mauri T, Pivi S, Bigatello LM (2008) Prolonged mechanical ventilation after critical illness. Minerva Anestesiol 74:297–301
Kallet RH, Campbell AR, Dicker RA, Katz JA, Mackersie RC (2006) Effects of tidal volume on work of breathing during lung-protective ventilation in patients with acute lung injury and acute respiratory distress syndrome. Crit Care Med 34:8–14
Chiumello D, Pelosi P, Taccone P, Slutsky A, Gattinoni L (2003) Effect of different inspiratory rise time and cycling off criteria during pressure support ventilation in patients recovering from acute lung injury. Crit Care Med 31:2604–2610
Spahija J, de Marchie M, Albert M, Bellemare P, Delisle S, Beck J, Sinderby C (2010) Patient–ventilator interaction during pressure support ventilation and neurally adjusted ventilatory assist. Crit Care Med 38(2):518–526
Spieth PM, Carvalho AR, Güldner A, Kasper M, Schubert R, Carvalho NC, Beda A, Dassow C, Uhlig S, Koch T, Pelosi P, Gama de Abreu M (2011) Pressure support improves oxygenation and lung protection compared to pressure-controlled ventilation and is further improved by random variation of pressure support. Crit Care Med 39:746–755
Sassoon CSh (2011) Triggering of the ventilator in patient–ventilator interactions. Respir Care 56:39–51
Acknowledgments
We thank all the patients who participated in this study and their families. We thank all the staff members of the general ICU of the San Gerardo Hospital, Monza, Italy, for their work and support.
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Mauri, T., Bellani, G., Grasselli, G. et al. Patient–ventilator interaction in ARDS patients with extremely low compliance undergoing ECMO: a novel approach based on diaphragm electrical activity. Intensive Care Med 39, 282–291 (2013). https://doi.org/10.1007/s00134-012-2755-1
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DOI: https://doi.org/10.1007/s00134-012-2755-1