key: cord-0887453-yrxy55ej
authors: Weaver, Liam; Das, Anup; Saffaran, Sina; Yehya, Nadir; Scott, Timothy E.; Chikhani, Marc; Laffey, John G.; Hardman, Jonathan G.; Camporota, Luigi; Bates, Declan G.
title: High risk of patient self-inflicted lung injury in COVID-19 with frequently encountered spontaneous breathing patterns: a computational modelling study
date: 2021-07-13
journal: Ann Intensive Care
DOI: 10.1186/s13613-021-00904-7
sha: 16a5d3cd1c8361ba2bf904c5cca33e15ed059658
doc_id: 887453
cord_uid: yrxy55ej

BACKGROUND: There is on-going controversy regarding the potential for increased respiratory effort to generate patient self-inflicted lung injury (P-SILI) in spontaneously breathing patients with COVID-19 acute hypoxaemic respiratory failure. However, direct clinical evidence linking increased inspiratory effort to lung injury is scarce. We adapted a computational simulator of cardiopulmonary pathophysiology to quantify the mechanical forces that could lead to P-SILI at different levels of respiratory effort. In accordance with recent data, the simulator parameters were manually adjusted to generate a population of 10 patients that recapitulate clinical features exhibited by certain COVID-19 patients, i.e., severe hypoxaemia combined with relatively well-preserved lung mechanics, being treated with supplemental oxygen. RESULTS: Simulations were conducted at tidal volumes (VT) and respiratory rates (RR) of 7 ml/kg and 14 breaths/min (representing normal respiratory effort) and at VT/RR of 7/20, 7/30, 10/14, 10/20 and 10/30 ml/kg / breaths/min. While oxygenation improved with higher respiratory efforts, significant increases in multiple indicators of the potential for lung injury were observed at all higher VT/RR combinations tested. Pleural pressure swing increased from 12.0 ± 0.3 cmH(2)O at baseline to 33.8 ± 0.4 cmH(2)O at VT/RR of 7 ml/kg/30 breaths/min and to 46.2 ± 0.5 cmH(2)O at 10 ml/kg/30 breaths/min. Transpulmonary pressure swing increased from 4.7 ± 0.1 cmH(2)O at baseline to 17.9 ± 0.3 cmH(2)O at VT/RR of 7 ml/kg/30 breaths/min and to 24.2 ± 0.3 cmH(2)O at 10 ml/kg/30 breaths/min. Total lung strain increased from 0.29 ± 0.006 at baseline to 0.65 ± 0.016 at 10 ml/kg/30 breaths/min. Mechanical power increased from 1.6 ± 0.1 J/min at baseline to 12.9 ± 0.2 J/min at VT/RR of 7 ml/kg/30 breaths/min, and to 24.9 ± 0.3 J/min at 10 ml/kg/30 breaths/min. Driving pressure increased from 7.7 ± 0.2 cmH(2)O at baseline to 19.6 ± 0.2 cmH(2)O at VT/RR of 7 ml/kg/30 breaths/min, and to 26.9 ± 0.3 cmH(2)O at 10 ml/kg/30 breaths/min. CONCLUSIONS: Our results suggest that the forces generated by increased inspiratory effort commonly seen in COVID-19 acute hypoxaemic respiratory failure are comparable with those that have been associated with ventilator-induced lung injury during mechanical ventilation. Respiratory efforts in these patients should be carefully monitored and controlled to minimise the risk of lung injury. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13613-021-00904-7.

On admission, some patients with COVID-19 acute hypoxaemic respiratory failure (AHRF) exhibit profound hypoxaemia, combined with relatively preserved lung compliance and lung gas volume on CT chest imaging, and substantial increases in respiratory effort-tidal volumes (VT) of 15-20 ml/kg [1] and respiratory rates (RR) of 34 breaths/min [2] have been reported. As noted in [3] , young, otherwise healthy adults can sustain tidal volumes of 20 ml/kg at a respiratory rate of 45 breaths/min almost indefinitely [4, 5] . There is significant debate regarding whether sustained high respiratory effort in these patients could risk causing further damage to the lungs through patient self-inflicted lung injury (P-SILI) [6] [7] [8] [9] [10] [11] .

Direct evidence for the existence of P-SILI in the context of purely spontaneous breathing is largely based on an animal study [12] , although two studies in asthmatic children suggested that increased breathing effort could promote negative pressure pulmonary oedema [13, 14] . A number of studies have also established the potential for injurious effects due to spontaneous breathing during mechanical ventilation in acute respiratory failure, see [15] and the review in [16] . In a recent study of inspiratory effort in non-invasive ventilation, reductions in the oesophageal pressure swings (pleural pressure) of 10 cm H 2 O or more after 2 h of treatment was strongly associated with avoidance of intubation and represented the most accurate predictor of treatment success-see [17] and discussion in [18, 19] . In the context of COVID-19, a recent study [20] , has asserted an association between increased respiratory effort and worsening of respiratory function during attempts to wean patients from mechanical ventilation, although without definitively establishing a delineation between cause and effect [10, 11] . Two recent case reports also noted the existence of spontaneous pneumothorax and pneumomediastinum in COVID-19 patients, suggesting the generation of injurious transpulmonary pressures [21, 22] .

To obtain some additional evidence, we hypothesised that a computational model of COVID-19 pathophysiology could be used to investigate the effects of increased respiratory effort on parameters that have been associated with lung injury, namely, tidal swings in pleural and transpulmonary pressure, and maximum values of mechanical power [23] , driving pressure and lung strain. The aim of the study was to quantify the levels of these indicators of lung injury that are generated in our model by breathing patterns that are frequently encountered in COVID-19 patients.

The core model used in this study is a multi-compartmental computational simulator that has been previously used to simulate mechanically ventilated patients with various pulmonary disease states [24] [25] [26] [27] [28] [29] [30] [31] , including COVID-19 ARDS [32] . The simulator offers several advantages, including the capability to define a large number of alveolar compartments (each with its own individual mechanical characteristics), with configurable alveolar collapse, alveolar stiffening, disruption of alveolar gas-exchange, pulmonary vasoconstriction and vasodilation, and airway obstruction. As a result, several defining clinical features of acute lung injury can be represented in the model, including varying degrees of ventilation perfusion mismatch, physiological shunt and deadspace, alveolar gas trapping with intrinsic positive end-expiratory pressure (PEEP), collapse-reopening of alveoli etc. A detailed description of the physiological principles and mathematical equations underlying the core computational model implemented in the simulator is provided in the Additional file 1. A list of key parameters in the model and their values are given in Additional file 1: Tables S1-S3.

The model was configured to represent a patient of 70 kg ideal body weight with COVID-19 acute hypoxaemic respiratory failure, as follows.

Based on recent data [1, [33] [34] [35] [36] [37] [38] suggesting that some COVID-19 patients have relatively well preserved lung gas volume and compliance, the model was set to have 8% of its alveolar compartments collapsed, i.e., non-aerated, by increasing the values of parameters representing alveolar extrinsic pressure and threshold opening pressure (see Additional file 1). To simulate the hyperperfusion of gasless tissue reported in [1, 39, 40] , we implemented vasodilation in the collapsed units by decreasing their vascular resistance by 80%. HPV is normally incorporated in our simulator via a mathematical function, to simulate the hypothesised disruption of HPV in COVID-19 we disabled this function in our model. We lung injury during mechanical ventilation. Respiratory efforts in these patients should be carefully monitored and controlled to minimise the risk of lung injury.

Keywords: COVID-19, Acute respiratory failure, Hypoxaemia, Patient self-inflicted lung injury, Computational modelling incorporated disruption of alveolar gas-exchange due to the effects of pneumonitis into the model by blocking alveolar-capillary gas equilibration in 20% of the alveolar compartments. As thrombotic complications have been reported to be a characteristic feature of COVID-19 [41, 42] , we also modeled the presence of microthrombi by increasing vascular resistance by a factor of 5 in 10% of the remaining compartments.

Implementing the above pathophysiological mechanisms in our model produced levels of shunt (49.5%) and deadspace (188.5 ml) leading to severe hypoxemia (SaO 2 84%, FiO 2 of 100%) consistent with recent clinical data on COVID-19 ARDS, while still maintaining relatively well preserved levels of respiratory system compliance (63 ml/ cm H 2 O)-see Additional file 1: Table S3 . To ensure that our results are not dependent on this particular model parameterization, we then created a "population" of 10 patients by varying the number of compartments affected by the various pathophysiological mechanisms around this nominal parameterisation, producing a range of hypoxemia/compliance levels that are still consistent with reported data; see Additional file 1: Table S3 .

For the current investigation, the core model was adapted to represent spontaneously breathing rather than mechanically ventilated patients. Spontaneous breathing is simulated by incorporating the variable P INSP , which represents the lumped effect of chest wall, muscle and pleura on the lung. During a single respiratory cycle, P INSP at time t k is calculated by adapting a model developed in [43, 44] based on breathing profiles of 12 patients:

The function consists of a parabolic profile during the inspiration phase of the respiratory cycle, representing the progressive increase in pressure exerted by the respiratory muscles. This is followed by an exponential profile during the expiration phase of the respiratory cycle, characterizing the passive relaxation of the muscles (a valid assumption up to a minute ventilation of 40 l/min, [45] ). P INSP decreases from zero to its minimum endinspiratory value ( P MIN ) (i.e., maximum effort) during inspiration and returns to zero at end of expiration. T is calculated from the set respiratory rate, RR, ( T = 60/ RR). T I and T E are the duration of inspiration and expiration, such that ( T = T I + T E ). T I is calculated from ( T I = T * DC) , where DC is the duty cycle, set to 0.33. τ

is the time constant of the expiratory profile and is set to T E / RR seconds.

Pressures inside the lung are calculated in the model in an iterative fashion, as follows:

Step 1. Calculate p i , the pressures inside each individual alveolar unit using the equation:

The parameter S i reflects the 'stiffness' of the compartment, P ext,i represents the effective net pressure acting on the alveolar compartments due to assorted localised mechanisms (e.g., oedema formation), and V c is defined as the volume at which the alveolar compartment is considered to be 'empty' , to avoid divide by 0 errors.

Step 2. Calculate P L using the values of alveolar pressures , p i , and airway resistances R Bi , as follows: assuming zero net flow between mouth and lungs, calculate the separate alveolar flows ( p i )/R Bi , add these together to get total flow, calculate total airway resistance, and divide total flow by total airway resistance to get global lung pressure. The values of R Bi are fixed and set to represent different pathophysiological mechanisms in the model.

Step 3. Calculate the respiratory system compliance C rs from where VT is the tidal volume, and P L is the difference between the minimum lung pressure and end expiratory lung pressure. Note that Eq. 1 gives us C rs , rather than C L , because we are applying P ext and P INSP to the alveoli directly (an anatomical modeling simplification but of no consequence mathematically).

Step 4. Calculate the dynamic lung compliance C L Since EL rs = EL L + EL cw , we have that

where C cw is the chest wall compliance (set to 144 mL/cmH 2 O based on data from COVID-19 patients in [46] ) and C rs has been found from Eq. 1.

Step 5. Calculate transpulmonary pressure P tp (equivalent to lung stress [47] ). Since C L = V P tp , then

if P tp = P tp − 0 , and V is the difference between the current lung volume and the unstressed volume of the lung (the residual volume, set to 1.2L).

Step 6. Calculate pleural pressure P pl from: P pl = P L − P tp

Step 7. Calculate the mechanical power applied to the lungs as the energy per breath (defined as the area of the triangle enclosed by the inspiratory limb of the P tp pressure-volume curve and the change in volume, i.e., 0.5 × VT × P tp , in Joules) multiplied by RR, as described in [23] .

Step 8. Calculate driving pressure P as P = VT × EL RS = P L (from Eq. 1).

Step 9. Calculate the total lung strain as the sum of dynamic and static strain [48] , where Dynamic strain = To observe the various pulmonary effects of interest, the following values were also computed and recorded: arterial oxygen partial pressure (PaO 2 ), arterial carbon dioxide partial pressure (PaCO 2 ), physiological shunt, calculated using the classical shunt equation, based on the calculated values of arterial, pulmonary end-capillary and mixed venous O 2 content. Physiological deadspace (and deadspace fraction; VD/VT) were calculated from PaCO 2, mixed expired CO 2 pressure ( PECO 2 ) and the exhaled tidal volume.

All model simulations were run for 30 min, with the reported data averaged over the final 1 min, and conducted using Matlab version R2019b.v9 (MathWorks Inc., Natick, MA, USA).

The simulated patient population replicates levels of hypoxaemia that have frequently been reported in spontaneously breathing COVID-19 patients. SaO 2 , PaO 2 and PaCO 2 on 100% oxygen at baseline were 83.8 ± 5.1%, 52.6 ± 7.1 mmHg, and 51.8 ± 1.5 mmHg, respectively ( Table 1) . Oxygenation improved at higher respiratory efforts (SaO 2 of 97.6 ± 0.8 at VT / RR of 10 ml/kg / 30 breath/min) and PaCO 2 decreased. Values of respiratory system compliance and end-expiratory lung volume (EELV) at baseline were 63 ± 1.4 ml/cmH 2 O and 1678.9 ± 35.3 ml, showing good agreement with the data for a cohort of COVID-19 patients reported in a recent study [38] . Compliance reduced significantly at higher respiratory rates (to 25 ± 0.3 ml/cmH 2 O at VT / RR of 7 ml/kg / 30 breath/min). Physiological shunt and deadspace were decreased and increased, respectively, at higher respiratory effort.

Inspiratory pressures required to generate the different increased breathing patterns (maximum P MIN of 35.4 ± 0.2 cmH 2 O at VT / RR of 10 ml/kg / 30 breath/ min) were well within the limits specified for a 70 kg Table 1 Oxygenation, lung mechanics, maximum pressure swings, and other injury indicators generated in our COVID-19 model for different levels of respiratory effort on 100% oxygen, data presents mean ± sd across the population of 10 patients adult male ( P MIN of 78.5 cmH 2 O at age 60, and 108.9 cmH 2 O at age 40, [49] ).

As shown in Table 1 and Fig. 1 , significant increases in multiple indicators of the potential for lung injury were observed at all higher VT / RR combinations tested. Pleural pressure swing increased from 12.0 ± 0.3 cmH 2 O at baseline to 33.8 ± 0.4 cmH 2 O at VT/RR of 7 ml/kg / 30 breaths/min and to 46.2 ± 0.5 cmH 2 O at 10 ml/kg / 30 breaths/min. Transpulmonary pressure swing increased from 4.7 ± 0.1 cmH 2 O at baseline to 17.9 ± 0.3 cmH 2 O at VT/RR of 7 ml/kg / 30 breaths/min and to 24.2 ± 0.3 cmH 2 O at 10 ml/kg / 30 breaths/min. Total lung strain increased from 0.29 ± 0.006 at baseline to 0.65 ± 0.016 at 10 ml/kg / 30 breaths/min. Mechanical power increased from 1.6 ± 0.1 J/min at baseline to 12.9 ± 0.2 J/min at VT/ RR of 7 ml/kg / 30 breaths/min, and to 24.9 ± 0.3 J/min at 10 ml/kg / 30 breaths/min. Driving pressure increased from 7.7 ± 0.2 cmH 2 O at baseline to 19.6 ± 0.2 at VT/RR of 7 ml/kg / 30 breaths/min, and 26.9 ± 0.3 cmH 2 O at 10 ml/kg / 30 breaths/min.

The effect of increased respiratory effort on the distribution of maximum compartmental volumes in the model is shown in Additional file 1: Figs. S4.1 and S4.2. As shown, at the higher values of tidal volume and respiratory rate, the proportion of model compartments experiencing larger maximum volumes is significantly increased.

During mechanical ventilation, the power required to inflate the lungs is provided by an external source of energy, whereas during spontaneous unassisted breathing it is provided by the respiratory muscles. However, as pointed out in [50] , lung injury (in the sense of mechanical lesions in the interstitial space due to microfractures of the extracellular matrix or the capillary walls) arises from the mechanical energy applied to the lungs, which generates the relevant pressures. There is, therefore, no reason to believe that the extent of injury will be significantly different whether excessive pressures are generated by respiratory muscles in spontaneous breathing or by a mechanical ventilator. Similarly to the case of VILI, there is also no reason to expect that, in the case of injured lungs, forces generated by respiratory muscles could not lead to injurious effects on a regional level due to lung heterogeneity. This may be a particular concern in the case of COVID-19 AHRF, since current understanding of the underlying pathophysiology points to a strongly heterogeneous lung profile incorporating alveolar collapse, oedema, and significant vascular derangement.

As well as increases in transpulmonary pressure swings, we also observed large increases in pleural pressure swings at higher respiratory effort, up to a maximum of 46.2 ± 0.5 cmH 2 O. As discussed in [16] , negative alveolar pressures created by large changes in pleural pressure and, therefore, positive changes in transvascular pressure, favour lung oedema, a mechanism that is amplified with increased vascular permeability, [51, 52] . Given that negative pressures from diaphragm contraction are not distributed uniformly, there is also the potential to cause pendelluft gas movement due to localised changes in pleural pressures in dependent regions, [53] . Finally, it is important to recognise that when dynamic systems (from aircraft engines to human lungs) are subjected to repeated cycles of excessive stresses and strains, their deterioration over time is often not linear; rather, damage can accumulate "silently" before eventually manifesting and spreading rapidly [54] .

In light of the above considerations, it is difficult to see how, for a respiratory effort that a patient (and their treating clinician) might consider tolerable, the levels of transpulmonary/pleural pressure swings, driving pressure and mechanical power produced in our model (Table 1 ) could be regarded as safe. Certainly, it is unlikely that any mechanical ventilation strategy that produced similar values would be considered "protective" according to current standard guidelines. Our results also highlight that improvements in PaO 2 /FiO 2 ratio associated with larger tidal volumes and respiratory rates should be interpreted in the context of the associated increased respiratory effort, and are not necessarily expressions of improved lung condition. Indeed, the improvement in PaO 2 /FiO 2 ratio we observed at higher respiratory effort was coupled with reduced lung compliance and the development of levels of mechanical power associated with worse short [55, 56] and long term [57] survival.

Our study has a number of limitations. The results are based on computational modelling of mechanisms that have been proposed to underlie COVID-19 pathophysiology, rather than on models matched to individual data from patients with COVID-19. Accordingly, many model parameters were manually adjusted to give overall outputs that are similar to reported data on COVID-19 patients, rather than being fit to data that explicitly defines the parameters. The model also neglects some physiological realities (namely, interdependence of alveoli, non-uniformity of diaphragm contraction, and gravitational effects); however, it seems reasonable to expect that inclusion of these effects would act to produce even higher localised values of the reported lung injury indices in certain lung regions. Due to a lack of data we have also not modelled the potential effects of variations in the ratio of inspiratory/expiratory time at higher respiratory rates.

Our results are limited to the case of purely spontaneous breathing with oxygen support-consideration of the effects of high respiratory effort during positive pressure non-invasive ventilation (CPAP, BIPAP, etc.) is an important open question, but requires further development of the model and will be the subject of future studies.

Investigating the issues raised here in clinical trials is likely to prove challenging both from an ethical and practical point of view, and suitable animal models of COVID-19 pathophysiology with which to study these questions are yet to emerge [58] . In these circumstances, we hope that insights from detailed computational models that recapitulate patient breathing patterns and lung mechanics can provide useful evidence with which to inform current and future debates [59] .

Our results indicate that transpulmonary and pleural pressure swings, and levels of driving pressure, lung strain and mechanical power that have been associated with VILI during mechanical ventilation can develop in spontaneously breathing patients with COVID-19 acute respiratory failure, at levels of respiratory effort that are being frequently encountered by clinicians. Respiratory efforts in these patients should be carefully monitored and controlled to minimise the risk of lung injury.

The online version contains supplementary material available at https:// doi. org/ 10. 1186/ s13613-021-00904-7.

Additional file 1. Full description of computational simulator, additional results and figures.

COVID-19 pneumonia: different respiratory treatments for different phenotypes?

Effectiveness of prone position in spontaneously breathing patients with COVID-19: a prospective cohort study

Using applied lung physiology to understand COVID-19 patterns

Ventilatory failure. Can you sustain what you need?

Sustained maximum voluntary ventilation

Spontaneous breathing, transpulmonary pressure and mathematical trickery

P-SILI is not justification for intubation of COVID-19 patients

P-SILI as justification for intubation in COVID-19: readers as arbiters

A physiological approach to understand the role of respiratory effort in the progression of lung injury in SARS-CoV-2 infection

The respiratory drive: an overlooked tile of COVID-19 pathophysiology

Respiratory drive measurements do not signify conjectural patient self-inflicted lung injury

Acute respiratory failure following pharmacologically induced hyperventilation: an experimental animal study

The pathology of asthma, with special reference to changes in the bronchial mucosa

Mechanical forces producing pulmonary edema in acute asthma

The comparison of spontaneous breathing and muscle paralysis in two different severities of experimental lung injury

Mechanical ventilation to minimize progression of lung injury in acute respiratory failure

Early inspiratory effort assessment by esophageal manometry predicts noninvasive ventilation outcome in de novo respiratory failure. A pilot study

The dark side of spontaneous breathing during noninvasive ventilation. From hypothesis to theory

Continued vigorous inspiratory effort as a predictor of noninvasive ventilation failure

High respiratory drive and excessive respiratory efforts predict relapse of respiratory failure in critically Ill patients with COVID-19

COVID-19 with spontaneous pneumothorax, pneumomediastinum, and subcutaneous emphysema in the intensive care unit: Two case reports

Spontaneous pneumothorax and pneumomediastinum as a rare complication of COVID-19 pneumonia: Report of 6 cases

Mechanical power and development of ventilatorinduced lung injury

Validation and application of a high-fidelity, computational model of acute respiratory distress syndrome to the examination of the indices of oxygenation at constant lung-state

Evaluation of lung recruitment maneuvers in acute respiratory distress syndrome using computer simulation

High PEEP in acute respiratory distress syndrome: quantitative evaluation between improved arterial oxygenation and decreased oxygen delivery

Hemodynamic effects of lung recruitment maneuvers in acute respiratory distress syndrome

What links ventilator driving pressure with survival in the acute respiratory distress syndrome? A computational study

High-fidelity computational simulation to refine strategies for lung-protective ventilation in paediatric acute respiratory distress syndrome

Utility of driving pressure and mechanical power to guide protective ventilator settings in two cohorts of adult and pediatric patients with acute respiratory distress syndrome: a computational investigation

Efficacy of continuous positive airway pressure in casualties suffering from primary blast lung injury: a modeling study

In silico modeling of coronavirus disease 2019 acute respiratory distress syndrome: pathophysiologic insights and potential management implications

COVID-19 does not lead to a "Typical" acute respiratory distress syndrome

Management of COVID-19 respiratory distress

Advanced respiratory monitoring in COVID-19 patients: use less PEEP! Crit Care

PEEP levels in COVID-19 pneumonia

Effect of PEEP decremental on respiratory mechanics, gasses exchanges, pulmonary regional ventilation, and hemodynamics in patients with SARS-Cov-2-associated acute respiratory distress syndrome

Physiological and quantitative CT-scan characterization of COVID-19 and typical ARDS: a matched cohort study

Hypoxaemia related to COVID-19: vascular and perfusion abnormalities on dualenergy CT

2019-novel Coronavirus severe adult respiratory distress syndrome in two cases in Italy: an uncommon radiological presentation

High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study

Postmortem examination of COVID-19 patients reveals diffuse alveolar damage with severe capillary congestion and variegated findings in lungs and other organs suggesting vascular dysfunction

Ventilatory assistance and respiratory muscle activity. 2: Simulation with an adaptive active ("aa" or "a-squared") model lung

An integrated mathematical model of the human cardiopulmonary system

Chicago: Year Book Medical Publishers

Respiratory mechanics of COVID-19-versus non-COVID-19-associated acute respiratory distress syndrome

Therapeutic range of spontaneous breathing during mechanical ventilation

Which is the most important strain in the pathogenesis of ventilator-induced lung injury

Determinants of maximal inspiratory pressure. The Baltimore longitudinal study of aging

Ventilation-induced lung injury exists in spontaneously breathing patients with acute respiratory failure: we are not sure. Intensive Care Med

Patient self-inflicted lung injury: implications for acute hypoxemic respiratory failure and ARDS patients on non-invasive support

Paying attention to patient self-inflicted lung injury

Spontaneous effort during mechanical ventilation: maximal injury with less positive end-expiratory pressure

Metal fatigue and basic theoretical models: a review. Alloy steel-properties and use

Mechanical power of ventilation is associated with mortality in critically ill patients: an analysis of patients in two observational cohorts

Mechanical power normalized to predicted body weight as a predictor of mortality in patients with acute respiratory distress syndrome

Epidemiology, mechanical power, and 3-year outcomes in acute respiratory distress syndrome patients using standardized screening

Evidence of a wide gap between COVID-19 in humans and animal models: a systematic review

Spontaneous breathing and evolving phenotypes of lung damage in patients with COVID-19: review of current evidence and forecast of a new scenario

Not applicable.