- Open Access
Heart–lung interactions during neurally adjusted ventilatory assist
Critical Care volume 18, Article number: 499 (2014)
Assist in unison to the patient’s inspiratory neural effort and feedback-controlled limitation of lung distension with neurally adjusted ventilatory assist (NAVA) may reduce the negative effects of mechanical ventilation on right ventricular function.
Heart–lung interaction was evaluated in 10 intubated patients with impaired cardiac function using esophageal balloons, pulmonary artery catheters and echocardiography. Adequate NAVA level identified by a titration procedure to breathing pattern (NAVAal), 50% NAVAal, and 200% NAVAal and adequate pressure support (PSVal, defined clinically), 50% PSVal, and 150% PSVal were implemented at constant positive end-expiratory pressure for 20 minutes each.
NAVAal was 3.1 ± 1.1cmH2O/μV and PSVal was 17 ± 2 cmH20. For all NAVA levels negative esophageal pressure deflections were observed during inspiration whereas this pattern was reversed during PSVal and PSVhigh. As compared to expiration, inspiratory right ventricular outflow tract velocity time integral (surrogating stroke volume) was 103 ± 4%, 109 ± 5%, and 100 ± 4% for NAVAlow, NAVAal, and NAVAhigh and 101 ± 3%, 89 ± 6%, and 83 ± 9% for PSVlow, PSVal, and PSVhigh, respectively (p < 0.001 level-mode interaction, ANOVA). Right ventricular systolic isovolumetric pressure increased from 11.0 ± 4.6 mmHg at PSVlow to 14.0 ± 4.6 mmHg at PSVhigh but remained unchanged (11.5 ± 4.7 mmHg (NAVAlow) and 10.8 ± 4.2 mmHg (NAVAhigh), level-mode interaction p = 0.005). Both indicate progressive right ventricular outflow impedance with increasing pressure support ventilation (PSV), but no change with increasing NAVA level.
Right ventricular performance is less impaired during NAVA compared to PSV as used in this study. Proposed mechanisms are preservation of cyclic intrathoracic pressure changes characteristic of spontaneous breathing and limitation of right-ventricular outflow impedance during inspiration, regardless of the NAVA level.
Clinicaltrials.gov Identifier: NCT00647361, registered 19 March 2008
Cyclic increases in intrathoracic pressure during positive pressure ventilation may reduce venous return and increase the afterload of the right ventricle ,. Neurally adjusted ventilatory assist (NAVA) delivers inspiratory support in synchrony and in linear proportion to the neural inspiratory effort by using the electrical activity of the diaphragm (EAdi) to drive the ventilator . The inspiratory muscle activity, that is synchronous and proportional to assist delivery during NAVA, is likely to attenuate the increases in pleural pressure associated with conventional positive pressure ventilation. This attenuation should reduce negative effects of positive pressure ventilation on cardiovascular function. Data on cardiovascular function during NAVA are very limited. The cardiovascular effects of NAVA depend on the pleural pressure changes and the consequent transmural vascular and cardiac pressures, but these have not so far been studied.
We hypothesized that the synchronous inspiratory muscle activity during NAVA and the feedback controlled limitation of lung volumes during increasing NAVA support avoid the adverse effects of conventional pressure support ventilation (PSV) on right ventricular afterload and venous return. We therefore compared the short-term hemodynamic effects of three NAVA and three PSV levels using simultaneous analysis of intravascular, intracardiac, esophageal pressure (Pes), airway pressure, breathing pattern, and echocardiography in patients with impaired cardiac function, chronic obstructive pulmonary disease, or both.
Materials and methods
The Ethics Committee of Canton Bern, Switzerland approved the protocol (KEK Nr 217–06). Recruitment lasted from March to November 2010. Written informed consent from the patient’s family and deferred consent after recovery were obtained. A detailed description of the methods is provided in Additional file 1.
The main inclusion criteria were invasive mechanical ventilation, pneumatic triggering, pulmonary artery catheter monitoring for clinical reasons, and at least one of the following: left ventricular ejection fraction ≤40%; inotropic drugs (dobutamine ≥2 μg/kg/minute or adrenaline ≥0.03 μg/kg/minute); pulmonary artery occlusion pressure ≥18 mmHg; or history of chronic obstructive pulmonary disease.
Catheters were inserted for measurement of Pes (SmartCath; Viasys Healthcare, San Diego, CA, USA) and EAdi (Maquet, Solna, Sweden). Correct positioning of the Pes catheter was verified using an occlusion test ,. A schematic study protocol is depicted in Figure 1.
Adequate PSV (PSVal) was set by an independent intensivist blinded for the EAdi and Pes aiming to achieve optimal patient comfort, avoid unassisted wasted inspiratory efforts, and minimize negative inspiratory deflections in central venous and pulmonary artery pressures (indicating inspiratory effort). PSVlow was 50% PSVal, and PSVhigh was 150% PSVal. Positive end-expiratory pressure (PEEP) and other prescribed ventilator settings were kept constant throughout the protocol.
Adequate NAVA (NAVAal) was identified using a previously described titration procedure (Additional files 1 and 2-). NAVAlow was 50% NAVAal, and NAVAhigh was defined as the highest level sustaining a regular breathing pattern similar to that at NAVAal or 200% NAVAal, whichever occurred first.
The order of the ventilatory modes was randomized. The six ventilator settings were applied for at least 20 minutes each. All medications including sedation (Richmond agitation and sedation scale of −1 to −2 ) remained unchanged.
Intravascular pressures, airway pressure, Pes, EAdi (as the percentage of EAdi without assist at the beginning of NAVA titration), and airflow were recorded continuously (Neurovent Research Inc., Toronto, ON, Canada). Pulmonary artery occlusion pressure, right ventricular pressure, and blood gases were measured at the end of each experimental period.
All signals were analyzed off-line breath by breath, using a semi-automated detection of inspiration and expiration based on airflow reversal -. Two approaches were used to evaluate the hemodynamic responses. First, intravascular pressure and Pes during all breaths in each ventilator setting were averaged separately during inspiration and expiration. This was done in order to include the impact of variability in breathing pattern on hemodynamics. Transmural vascular pressures were obtained by subtraction of the time integral of Pes from the respective intravascular pressure. Changes of intravascular pressures from inspiration to expiration (cyclic pressure changes) were characterized by subtracting the mean expiratory pressure from the mean inspiratory pressure (Additional file 3). The mean inspiratory Pes deflection was calculated for the duration of inspiratory airflow and was referenced to the Pes immediately preceding the start of inspiratory airflow.
Second, representative single-breath cycles were manually selected for each experimental period. The selected breaths had mean inspiratory transpulmonary pressures equal to the mean of all breaths for the specific study period (the average breath). For each of these single breaths, the central venous pressure (CVP) was measured at the base of the c wave . The right ventricular isovolumetric pressure change was calculated as the difference between the base of the c wave of CVP and the pulmonary artery pressure (PAP) at valve opening , and the right ventricular total pressure generation was calculated as the pressure difference from the end-diastolic filling of the right ventricle (estimated as the base of the CVP c wave) to the systolic PAP. An example of this analysis is given in Additional file 4.
Pulsed wave Doppler profiles from both ventricular outflow tracts were recorded simultaneously with airway pressure during transthoracic echocardiography and were analyzed offline (Vivid 7, EchoPAC Dimension `06; GE Medical Systems, Glattbrugg, Switzerland). End-inspiratory and end-expiratory heart beats  from three ventilatory cycles were analyzed for each condition. To characterize the effects of lung inflation on the Doppler flow profiles, the values at end inspiration were expressed as a percentage of the values at end expiration measured during the same breathing cycle. A value >100% would thus reflect a higher value during inspiration compared with expiration, and vice versa.
Repeated-measures analysis of variance (within-subject factors: ventilation mode, support level) was used for analysis. Significant mode*support level interactions were analyzed post hoc within each mode between support levels using Sidak’s correction (IBM SPSS 20.0.0; IBM Corp, Armonk, NY, USA). Data are presented as mean ± standard deviation. P <0.05 was considered significant.
Ten patients (age 66 ± 10 years; five females; Simplified Acute Physiology Score II 41 ± 9) were studied (Table 1). Figure 2 illustrates the respiratory pattern and cyclic intravascular pressure changes for all experimental conditions in a single patient.
Five patients with reduced left ventricular ejection fraction and one patient with normal left ventricular ejection fraction (Patient 7) received inotropic drug support (dobutamine, mean dose 2.2 ± 1.9 μg/kg/minute), and four patients with reduced left ventricular ejection fraction did not receive inotropic medication. Biological valves were used for all valve surgery procedures.
NAVAal was identified at 3.1 ± 1.1 cmH2O/μV and PSVal at 17 ± 2 cmH2O, with a PEEP of 7 ± 2 cmH2O (Additional file 5). EAdi was lower with PSV than with NAVA. The tidal volume and transpulmonary pressure increased from NAVAlow to NAVAal and did not increase further at NAVAhigh, whereas both parameters increased with increasing PSV (Table 2 and Additional file 6). Table 2 presents data on the respiratory pattern and the systemic hemodynamic function.
There was no difference between the modes in intravascular or transmural CVP and PAP in expiration. The cyclic changes (inspiratory minus expiratory values) in transmural CVP were small with both NAVA and PSV, and decreased with increasing level of support more prominently with PSV (P = 0.03, level*mode interaction). The cyclic changes in transmural PAP were negative for all NAVA levels and PSVlow, and were positive for PSVal and PSVhigh (P = 0.026, level*mode interaction; Table 3). The inspiratory deflections in Pes became progressively positive with increasing PSV, while they remained negative with all NAVA levels (P < 0.001, level*mode interaction).
In the analysis of the representative single breath (Figure 3, Table 4), the cyclic changes in transmural CVP decreased with increasing support with both NAVA and PSV (level effect P = 0.015). The transmural CVP was higher in inspiration than in expiration at all NAVA levels, whereas increasing PSV resulted in higher CVP during expiration than during inspiration (mode effect P = 0.015).
Right ventricular ejection
The transmural inspiratory isovolumetric pressure change increased with increasing pressure support, whereas it remained unchanged with increasing NAVA levels (P = 0.005, level*mode interaction; Table 4). Accordingly, the cyclic alterations (inspiratory minus expiratory values) in the isovolumetric pressure change increased with increasing pressure support and remained unchanged with NAVA (P = 0.003, level*mode interaction; Figure 3). A similar pattern was observed for the cyclic changes in the total transmural pressure generation of the right ventricle from central venous end diastolic pressure to systolic pulmonary artery pressure (P = 0.033, level*mode interaction).
Both the ventilation mode and support level modified the right ventricular Doppler flow patterns (Table 5, Figure 4). During inspiration the flow period and the velocity time integral in the right ventricular outflow tract (RVOT VTI, a surrogate of stroke volume) both progressively decreased with increasing PSV level, whereas they remained unchanged with increasing NAVA levels (P = 0.028 for flow period and P = 0.025 for RVOT VTI, level*mode interaction).
RVOT VTI was equal or higher during inspiration compared with expiration for all NAVA levels. With PSV, RVOT VTI was equal during inspiration and expiration only with PSVlow but it was clearly lower during inspiration compared with expiration with PSVal and PSVhigh (P < 0.001, level*mode interaction). The highest RVOT VTI during inspiration compared with expiration was observed with NAVAal (109 ± 5%). The right ventricular stroke volume, as reflected by the RVOT VTI, during inspiration was thus preserved with all NAVA levels whereas it progressively decreased with increasing PSV level.
The left ventricular echocardiography results are summarized in Additional file 7. No relevant differences were observed between the modes.
The main finding of this study was that ventilation with NAVA in patients with impaired cardiac function but stable hemodynamics avoided an inspiratory increase in right ventricular outflow impedance by preserving the cyclic, negative deflections in intrathoracic pressure via feedback control of transpulmonary pressure and tidal volume. The hemodynamic pattern during NAVA closely resembled that of unassisted spontaneous breathing, regardless of the NAVA level used. In contrast, increased inspiratory assist with PSV progressively increased right ventricular outflow impedance, transpulmonary pressure, and tidal volume.
The pattern of decreasing right and increasing left ventricular stroke volume during inspiration is the characteristic pattern of heart–lung interactions during positive pressure ventilation -. The mechanisms of stroke volume variation during the breathing cycle include changes in venous return and consequent ventricular filling -, and changes in outflow impedance ,. Although these mechanisms have been known for decades, their implications and relevance during NAVA have not been addressed. Specifically, the actual pleural and transmural pressure profiles resulting from clinical application of NAVA will define the cardiac effects of NAVA. These have not been described before. In this respect, our study provides mechanistic insight into the heart–lung interactions of NAVA in a clinically relevant and realistic setting. We used RVOT VTI as a surrogate for right ventricular stroke volume assuming that the pulmonary valve annulus area does not vary with respiration . The progressive reduction in inspiratory RVOT VTI, flow period and maximum flow velocity, and inspiratory increases in right ventricular isovolumetric contraction pressure with increasing PSV indicate increased impedance to right ventricular outflow . In contrast, during all NAVA levels, right ventricular outflow impedance was lower during inspiration than during expiration, as indicated by increased inspiratory RVOT VTI, flow period and maximum flow velocity and reduced right ventricular isovolumetric contraction pressure. Reduced right ventricular afterload during inspiration with NAVA and increased inspiratory afterload with PSV is further supported by negative correlation between inspiratory changes in RVOT VTI and Pes (reflecting pleural pressure; Figure 4) and the decreased RVOT VTI with increased pressures in the pressure/flow diagrams (Additional file 8) .
Reduced right ventricular preload due to positive pressure ventilation-associated reduction in venous return ,, was also likely to contribute to changes in RVOT VTI. Since we did not measure pericardial pressure, we have no direct estimates of right ventricular end-diastolic wall tension. The transmural pressure at the base of the c wave of the CVP tracing, a surrogate of right ventricular end-diastolic wall tension, decreased slightly but significantly with increasing support both in inspiration and expiration without difference between modes. This result should be interpreted with caution, since pleural pressure may not adequately reflect pericardial pressure . Nevertheless, even if changes in preload were involved, the increased right ventricular isovolumetric contraction pressure in the presence of reduced RVOT VTI indicates increased impedance to right ventricular ejection  in inspiration with PSV, and the opposite changes indicate reduced impedance to ejection during inspiration with NAVA. The increase in the right ventricle afterload has been assumed to be relevant mainly at high lung volumes -. Our results clearly indicate the presence of this mechanism also at low tidal volumes, although it did not compromise cardiac performance in our patients with stable hemodynamics to a clinically relevant extent.
Mean inspiratory Pes deflection increased progressively with increasing PSV, whereas the initially slightly negative Pes deflection approached zero with increasing NAVA levels, but did not increase further. This may be related to a progressive downregulation of EAdi with increasing NAVA level, and might limit the effect of NAVA on right ventricular function. Such feedback mechanisms have been previously observed in healthy volunteers and mechanically ventilated patients with acute respiratory failure -,.
Several limitations must be addressed. The study was carried out to demonstrate the underlying physiology; due to safety concerns, patients with impaired cardiac function but stable hemodynamic and metabolic conditions were studied for short periods only. Hence, the relevance and consequences of treatment, if any, of these potentially beneficial effects of NAVA should be evaluated further in hemodynamically unstable patients with compromised right ventricular function and in patients with deranged metabolic conditions or with hypercapnia or hypoxemia – clinical conditions where substantial unloading of respiratory muscles with minimum compromise of right ventricular function may be considered.
Most of the patients were studied during the first day after cardiac surgery. Despite being clinically stable, some of these patients could have had relevant intravascular volume changes. In fact, hypovolemia is known to aggravate cyclic intravascular pressure swings -. Despite potential differences in preload status, the observed hemodynamic response seem consistent within and among individual patients.
There is no standard approach to titrate NAVA. We previously used the same NAVAal titration for several days in ICU patients with critical illness associated polyneuromyopathy (CIPM) without progression to respiratory distress, suggesting that NAVAal provides sufficient respiratory support .The average PSV adjusted by the clinicians in charge was based on clinical evaluation of patient comfort, and as a substitute for inspiratory effort, to minimize the cyclic changes in intrathoracic intravascular pressures. The resulting relatively high PSV can be criticized for augmenting the effects of PSV on right ventricular function. However, most patients were likely to have reduced chest wall compliance due to obesity and recent cardiac surgery. The average level of PSV also coincided with the reported average level associated with best patient comfort in difficult to wean patients . PEEP may influence respiratory drive and assist requirements , but PEEP was kept constant and should not have influenced the changes within patients. Finally, since PSV and NAVA result in different flow patterns and as flow reversal was used to identify the transition between inspiration and expiration, the investigators could not be blinded to the mode used when analyzing the data.
In patients with impaired cardiac function, right ventricular performance is less impaired during NAVA titrated to the breathing pattern compared with PSV selected based on clinical criteria. Proposed mechanisms are preservation of cyclic intrathoracic pressure changes characteristic of spontaneous breathing and limitation of right-ventricular outflow impedance during inspiration, regardless of the NAVA level. Thus, NAVA not only prevents lung overdistension and potentially diaphragm disuse, but also the characteristic side effects of positive pressure ventilation on right ventricular function.
During NAVA, a ventilatory mode that delivers assist in proportion to the neural inspiratory effort, the right-ventricular hemodynamic pattern resembles that of unassisted spontaneous breathing, regardless of the NAVA level used.
The proposed mechanism includes a lack of increase in right ventricular outflow impedance and a lack of decrease in venous return during lung inflation.
During NAVA, lung inflation and tidal volume are restricted by neural feedback, while near-zero negative deflections in intrathoracic pressure are preserved.
DB and SB share the position of first author.
central venous pressure
electrical activity of the diaphragm
neurally adjusted ventilator assist
adequate neurally adjusted ventilator assist level identified by a titration procedure
200% of the adequate neurally adjusted ventilator assist level
50% of the adequate neurally adjusted ventilator assist level
pulmonary artery pressure
positive end-expiratory pressure
pressure support ventilation
adequate level of pressure support ventilation identified on clinical grounds
150% of adequate pressure support level
50% of adequate pressure support level
- RVOT VTI:
velocity time integral in right ventricular outflow tract
Scharf SM, Caldini P, Ingram RH: Cardiovascular effects of increasing airway pressure in the dog. Am J Physiol. 1977, 232: H35-H43.
Vieillard-Baron A, Loubieres Y, Schmitt JM, Page B, Dubourg O, Jardin F: Cyclic changes in right ventricular output impedance during mechanical ventilation. J Appl Physiol (1985). 1999, 87: 1644-1650.
Sinderby C, Navalesi P, Beck J, Skrobik Y, Comtois N, Friberg S, Gottfried SB, Lindstrom L: Neural control of mechanical ventilation in respiratory failure. Nat Med. 1999, 5: 1433-1436. 10.1038/71012.
Baydur A, Cha EJ, Sassoon CS: Validation of esophageal balloon technique at different lung volumes and postures. J Appl Physiol Respir Environ Exerc Physiol. 1987, 62: 315-321.
Baydur A, Behrakis PK, Zin WA, Jaeger M, Milic-Emili J: A simple method for assessing the validity of the esophageal balloon technique. Am Rev Respir Dis. 1982, 126: 788-791.
Brander L, Leong-Poi H, Beck J, Brunet F, Hutchison SJ, Slutsky AS, Sinderby C: Titration and implementation of neurally adjusted ventilatory assist in critically ill patients. Chest. 2009, 135: 695-703. 10.1378/chest.08-1747.
Passath C, Takala J, Tuchscherer D, Jakob SM, Sinderby C, Brander L: Physiologic response to changing positive end-expiratory pressure during neurally adjusted ventilatory assist in sedated, critically ill adults. Chest. 2010, 138: 578-587. 10.1378/chest.10-0286.
Tuchscherer D, Z’Graggen WJ, Passath C, Takala J, Sinderby C, Brander L: Neurally adjusted ventilatory assist in patients with critical illness-associated polyneuromyopathy. Intensive Care Med. 2011, 37: 1951-1961. 10.1007/s00134-011-2376-0.
Ververidis D, Van Gils M, Passath C, Takala J, Brander L: Identification of adequate neurally adjusted ventilatory assist (NAVA) during systematic increases in the NAVA level. IEEE Trans Biomed Eng. 2011, 58: 2598-2606. 10.1109/TBME.2011.2159790.
Sessler CN, Gosnell MS, Grap MJ, Brophy GM, O'Neal PV, Keane KA, Tesoro EP, Elswick RK: The Richmond Agitation–Sedation Scale: validity and reliability in adult intensive care unit patients. Am J Respir Crit Care Med. 2002, 166: 1338-1344. 10.1164/rccm.2107138.
Magder S: Central venous pressure: a useful but not so simple measurement. Crit Care Med. 2006, 34: 2224-2227. 10.1097/01.CCM.0000227646.98423.98.
Jardin F, Brun-Ney D, Cazaux P, Dubourg O, Hardy A, Bourdarias JP: Relation between transpulmonary pressure and right ventricular isovolumetric pressure change during respiratory support. Catheter Cardiovasc Diagn. 1989, 16: 215-220. 10.1002/ccd.1810160402.
Vieillard-Baron A, Chergui K, Augarde R, Prin S, Page B, Beauchet A, Jardin F: Cyclic changes in arterial pulse during respiratory support revisited by Doppler echocardiography. Am J Respir Crit Care Med. 2003, 168: 671-676. 10.1164/rccm.200301-135OC.
Pinsky MR: Heart lung interactions during mechanical ventilation. Curr Opin Crit Care. 2012, 18: 256-260. 10.1097/MCC.0b013e3283532b73.
Pinsky MR: Hemodynamic effects of ventilation and ventilatory maneuvers. Respiratory–Circulatory Interactions in Health and Disease. Edited by: Scharf S. 2001, Marcel Dekker, New York, 183-208.
Jardin F, Farcot JC, Gueret P, Prost JF, Ozier Y, Bourdarias JP: Cyclic changes in arterial pulse during respiratory support. Circulation. 1983, 68: 266-274. 10.1161/01.CIR.68.2.266.
Magder S: Clinical usefulness of respiratory variations in arterial pressure. Am J Respir Crit Care Med. 2004, 169: 151-155. 10.1164/rccm.200211-1360CC.
Robotham JL, Lixfeld W, Holland L, MacGregor D, Bryan AC, Rabson J: Effects of respiration on cardiac performance. J Appl Physiol Respir Environ Exerc Physiol. 1978, 44: 703-709.
Fessler HE, Brower RG, Wise RA, Permutt S: Effects of positive end-expiratory pressure on the canine venous return curve. Am Rev Respir Dis. 1992, 146: 4-10. 10.1164/ajrccm/146.1.4.
Naeije R: Pulmonary vascular resistance. A meaningless variable?. Intensive Care Med. 2003, 29: 526-529.
Magder S, Scharf SM: Venous return. Respiratory–Circulatory Interactions in Health and Disease. Edited by: Scharf S. 2001, Marcel Dekker, New York, 93-110.
Lansdorp B, Hofhuizen C, van Lavieren M, van Swieten H, Lemson J, van Putten MJ, van der Hoeven JG, Pickkers P: Mechanical ventilation-induced intrathoracic pressure distribution and heart–lung interactions. Crit Care Med. 2014, 42: 1983-9023. 10.1097/CCM.0000000000000345.
Permutt S, Bromberger-Barnea B, Bane HN: Alveolar pressure, pulmonary venous pressure, and the vascular waterfall. Med Thorac. 1962, 19: 239-260.
De Backer D, Heenen S, Piagnerelli M, Koch M, Vincent JL: Pulse pressure variations to predict fluid responsiveness: influence of tidal volume. Intensive Care Med. 2005, 31: 517-523. 10.1007/s00134-005-2586-4.
Vieillard-Baron A, Prin S, Chergui K, Dubourg O, Jardin F: Echo-Doppler demonstration of acute cor pulmonale at the bedside in the medical intensive care unit. Am J Respir Crit Care Med. 2002, 166: 1310-1319. 10.1164/rccm.200202-146CC.
Sinderby C, Beck J, Spahija J, de Marchie M, Lacroix J, Navalesi P, Slutsky AS: Inspiratory muscle unloading by neurally adjusted ventilatory assist during maximal inspiratory efforts in healthy subjects. Chest. 2007, 131: 711-717. 10.1378/chest.06-1909.
Michard F, Teboul JL: Using heart–lung interactions to assess fluid responsiveness during mechanical ventilation. Crit Care. 2000, 4: 282-289. 10.1186/cc710.
Michard F, Boussat S, Chemla D, Anguel N, Mercat A, Lecarpentier Y, Richard C, Pinsky MR, Teboul JL: Relation between respiratory changes in arterial pulse pressure and fluid responsiveness in septic patients with acute circulatory failure. Am J Respir Crit Care Med. 2000, 162: 134-138. 10.1164/ajrccm.162.1.9903035.
Perel A, Pizov R, Cotev S: Systolic blood pressure variation is a sensitive indicator of hypovolemia in ventilated dogs subjected to graded hemorrhage. Anesthesiology. 1987, 67: 498-502. 10.1097/00000542-198710000-00009.
Vitacca M, Bianchi L, Zanotti E, Vianello A, Barbano L, Porta R, Clini E: Assessment of physiologic variables and subjective comfort under different levels of pressure support ventilation. CHEST J. 2004, 126: 851-859. 10.1378/chest.126.3.851.
Kahn JM, Andersson L, Karir V, Polissar NL, Neff MJ, Rubenfeld GD: Low tidal volume ventilation does not increase sedation use in patients with acute lung injury. Crit Care Med. 2005, 33: 766-771. 10.1097/01.CCM.0000157786.41506.24.
Teboul JL, Andrivet P, Ansquer M, Besbes M, Rekik N, Lemaire F, Brun-Buisson C: Bedside evaluation of the resistance of large and medium pulmonary veins in various lung diseases. J Appl Physiol (1985). 1992, 72: 998-1003.
Pinsky MR: Pulmonary artery occlusion pressure. Intensive Care Med. 2003, 29: 19-22. 10.1007/s00134-003-1971-0.
The authors are indebted to the study patients for their participation, to Norman Comtois for his excellent technical assistance, to Jennifer Beck for the expert review of the manuscript, and to the study nurses from our institution, especially Michael Lensch, for their assistance with the experimental setup. The authors thank the physicians and the nursing staff of the Department of Intensive Care Medicine, Bern University Hospital (Inselspital) for their valuable cooperation. The study was supported by a grant from the Swiss National Science Foundation (SNF) 3200B0-113478/1 and from the Stiftung für die Forschung in Anästhesiologie und Intensivmedizin (Foundation for Research in Anesthesiology and Intensive Care), Bern (18/2006) awarded to LB.
The Department of Intensive Care Medicine of University Hospital Bern has a research and development collaboration contract with Maquet Critical Care AB. None of the authors from this department received any personal financial gain from this collaboration. LB and JT were invited speakers at symposiums sponsored by Maquet Critical Care AB but did not receive any personal financial gain. DB and SB do not have any nonfinancial competing interests.
CS has patented inventions related to neural control of mechanical ventilation. The license for these patents belongs to Maquet Critical Care AB. Commercial use of this technology provides financial benefit to CS through royalties. CS owns 50% of Neurovent Research Inc., a research and development company for research studies. Neurovent Research Inc. has a consulting agreement with Maquet Critical Care AB.
DB was involved in the development of the study protocol, conducted the study, analyzed respiratory and hemodynamic data, and made the first draft of the manuscript. SB was involved in the development of the protocol, conducted the study, performed and analyzed all echocardiography studies, and contributed to the manuscript. JT was involved in the development of the protocol, in data interpretation, and in writing the manuscript. CS was involved in the development of the study protocol, in data interpretation, and in writing the manuscript. LB designed the study and wrote the final version of the study protocol, established the experimental equipment, and was involved in data acquisition and interpretation and in writing the manuscript. LB is the guarantor of the manuscript’s content. All authors read and approved the final version of the manuscript.
Electronic supplementary material
Additional file 1: Materials and Methodssection.(PDF 128 KB)
Additional file 2: -. The NAVA level was reduced to a minimum of 0 cmH2O/μl resulting in delivery of 2 cmH2O (default assist level) when the inspiratory effort exceeded the pneumatic trigger threshold. When sufficient electrical activity of the diaphragm (EAdi, green tracing; middle plot) was detectable, the NAVA level (white tracing; uppermost plot) was manually increased by 0.1 cmH2O/μV every 20 seconds. By observing the airway pressure (Paw, yellow tracing; uppermost plot) and tidal volume (Vt, blue tracing; lowermost plot) on the trend screen of the ventilator monitor, NAVAal was determined as the NAVA level early after the transition from an initial steep increase in Paw and Vt (first response) to a less steep increase or even plateau in Paw and Vt (second response). NAVAlow was arbitrarily defined as 50% of NAVAal. NAVAhigh was defined as the highest level resulting in a breathing pattern similar to that observed at NAVAal (that is, before the breathing pattern became unstable and airway pressure started to increase further)  or at 200% of NAVAal, whatever occurred first. (PPTX 561 KB)
Additional file 3: Is a schematic representation of changes in intravascular pressures over the respiratory cycle. The sample is recorded during ventilation with pressure support (PSV). In order to assess the cyclic change in pressures, the mean expiratory values (represented by the green bar) for central venous, pulmonary artery and systemic arterial pressures were subtracted from their respective mean inspiratory values (represented by the red bar). Thus, a positive result (that is, positive cyclic pressure change) indicates that the pressure was higher during inspiration compared to expiration. (PPTX 206 KB)
Additional file 4: shows the single-breath analysis. A single breath (Patient 1, PSVal) was manually selected, based on the mean inspiratory transpulmonary pressure retrieved from the semi-automated analysis. The image thus represents the average breath of this patient in this experimental period. CVP at the base of the c wave (red circles), the opening pressure of the pulmonary valve (blue circles) and the systolic pulmonary artery pressure (green circle) were measured together with their corresponding esophageal pressure (grey circle). The measurements were taken in the cardiac beats closest to end inspiration and end expiration. (PPTX 456 KB)
Additional file 5: FiO2, fraction of inspired oxygen; PEEP, positive end-expiratory pressure; PSV, pressure support ventilation; EAdi, electrical activity of the diaphragm; NAVA, neurally adjusted ventilatory assist; Insp rise, inspiratory rise time. (PDF 52 KB)
Additional file 6: Left: Respiratory cycle and tidal volume for each experimental condition. PBW, predicted body weight . While remaining constant under NAVA, the tidal volume increased (P < 0.001 for level*mode interaction) and the duty cycle (the inspiratory proportion total cycle time) and respiratory rate decreased (P < 0.005 and P < 0.001 respectively, level*mode interaction) with increasing the PSV level. NAVA, neurally adjusted ventilatory assist; PSV, pressure support ventilation; respective support levels, low, al (adequate level), and high. Values presented as mean ± standard deviation. Right: Transpulmonary pressure (Ptp) isobars (dotted ascending lines). Transpulmonary pressure increased from NAVAlow to NAVAal but remained stable when further increasing the assist to NAVAhigh. With PSV the transpulmonary pressure steadily increased from PSVlow to PSVhigh. Mean inspiratory airway pressure (including PEEP) and Ptp were lower during NAVA compared with the corresponding PSV levels (P < 0.05 for all, level*mode interaction). Mean inspiratory esophageal pressure deflection was negative for all NAVA levels, whereas it was negative only for PSVlow and positive for PSVal and PSVhigh (P < 0.001 for all comparisons). (PPTX 272 KB)
Is a table presenting Doppler flow profiles in the left ventricular outflow tract could be obtained from seven patients.
Additional file 7: Absolute values at end expiration did not differ between NAVA and PSV. To describe cyclic changes, the inspiratory values are given as a percentage of the corresponding expiratory value. Values are mean ± standard deviation. *P values from repeated-measures analysis of variance (ANOVA; within-subject factors: ventilation mode, support level). (PDF 16 KB)
Additional file 8: To support the concept of increasing inspiratory impedance to flow during PSV, we have constructed figures plotting the cyclic changes (inspiratory minus expiratory values) for absolute mean pulmonary artery pressure (referenced to atmosphere (A)) and for transmural mean pulmonary artery pressure (referenced to esophageal pressure (B)) against cyclic changes (inspiratory minus expiratory value) in RVOT VTI, assuming that the RVOT VTI is an adequate surrogate of right ventricular (RV) stroke volume . The common starting point in the center represents the expiration, the movement along the vector the change in inspiration. The simultaneous increase in stroke volume and reduction of transmural pulmonary artery pressure during inspiration and increase in RV stroke volume (lower right quadrant) is consistent with reduced RV afterload, whereas increasing PSV leads to reduction of stroke volume and unchanged or increased pulmonary artery pressure during inspiration, which is consistent with increased RV afterload . This analysis assumes similar changes in left atrial pressure from inspiration to expiration ,. Values are means. (PPTX 75 KB)
About this article
Cite this article
Berger, D., Bloechlinger, S., Takala, J. et al. Heart–lung interactions during neurally adjusted ventilatory assist. Crit Care 18, 499 (2014). https://doi.org/10.1186/s13054-014-0499-8
- Pressure Support Ventilation
- Pulmonary Artery Occlusion Pressure
- Transpulmonary Pressure
- Pleural Pressure
- Intravascular Pressure