key: cord-0000883-wwjbzj1g
authors: Charron, Cyril; Repesse, Xavier; Bouferrache, Koceïla; Bodson, Laurent; Castro, Samuel; Page, Bernard; Jardin, François; Vieillard-Baron, Antoine
title: PaCO(2 )and alveolar dead space are more relevant than PaO(2)/FiO(2 )ratio in monitoring the respiratory response to prone position in ARDS patients: a physiological study
date: 2011-07-25
journal: Crit Care
DOI: 10.1186/cc10324
sha: 06cfa5d8ed55752e73d2cc570c6da1770e2cb2eb
doc_id: 883
cord_uid: wwjbzj1g

INTRODUCTION: Our aims in this study were to report changes in the ratio of alveolar dead space to tidal volume (VD(alv)/V(T)) in the prone position (PP) and to test whether changes in partial pressure of arterial CO(2 )(PaCO(2)) may be more relevant than changes in the ratio of partial pressure of arterial O(2 )to fraction of inspired O(2 )(PaO(2)/FiO(2)) in defining the respiratory response to PP. We also aimed to validate a recently proposed method of estimation of the physiological dead space (VD(physiol)/V(T)) without measurement of expired CO(2). METHODS: Thirteen patients with a PaO(2)/FiO(2 )ratio < 100 mmHg were included in the study. Plateau pressure (Pplat), positive end-expiratory pressure (PEEP), blood gas analysis and expiratory CO(2 )were recorded with patients in the supine position and after 3, 6, 9, 12 and 15 hours in the PP. Responders to PP were defined after 15 hours of PP either by an increase in PaO(2)/FiO(2 )ratio > 20 mmHg or by a decrease in PaCO(2 )> 2 mmHg. Estimated and measured VD(physiol)/V(T )ratios were compared. RESULTS: PP induced a decrease in Pplat, PaCO(2 )and VD(alv)/V(T )ratio and increases in PaO(2)/FiO(2 )ratios and compliance of the respiratory system (Crs). Maximal changes were observed after six to nine hours. Changes in VD(alv)/V(T )were correlated with changes in Crs, but not with changes in PaO(2)/FiO(2 )ratios. When the response was defined by PaO(2)/FiO(2 )ratio, no significant differences in Pplat, PaCO(2 )or VD(alv)/V(T )alterations between responders (n = 7) and nonresponders (n = 6) were observed. When the response was defined by PaCO(2), four patients were differently classified, and responders (n = 7) had a greater decrease in VD(alv)/V(T )ratio and in Pplat and a greater increase in PaO(2)/FiO(2 )ratio and in Crs than nonresponders (n = 6). Estimated VD(physiol)/V(T )ratios significantly underestimated measured VD(physiol)/V(T )ratios (concordance correlation coefficient 0.19 (interquartile ranges 0.091 to 0.28)), whereas changes during PP were more reliable (concordance correlation coefficient 0.51 (0.32 to 0.66)). CONCLUSIONS: PP induced a decrease in VD(alv)/V(T )ratio and an improvement in respiratory mechanics. The respiratory response to PP appeared more relevant when PaCO(2 )rather than the PaO(2)/FiO(2 )ratio was used. Estimated VD(physiol)/V(T )ratios systematically underestimated measured VD(physiol)/V(T )ratios.

Since its first description in 1967 [1] , it has been accepted that acute respiratory distress syndrome (ARDS) includes a number of lung injuries of various origins whose consequences are decreased lung capacity available for ventilation, leading to the concept of "baby lung" [2] . Considerable progress has been made over the past decade in the ventilatory management of patients with ARDS. In particular, a strict limitation of tidal volume (V T ) and plateau pressure (Pplat) below 30 cmH 2 O reduces mortality [3] . The application of positive end-expiratory pressure (PEEP) is recognized to recruit the lung and to restore functional residual capacity [4] , but its optimum level is still widely debated [5] .

The prone position (PP) may also be part of the ventilatory strategy. This method was proposed more than 30 years ago, initially in pathophysiological studies [6, 7] . Recently, Sud et al. [8] suggested, on the basis of pooled data from randomized, controlled trials, that PP may improve survival in the subgroup of patients with the most severe ARDS, that is, those with a ratio of partial pressure of arterial O 2 to fraction of inspired O 2 (PaO 2 / FiO 2 ) < 100 mmHg. Many questions remain unresolved. In particular, response to PP is usually defined according to changes in PaO 2 , with responders being those in whom the PaO 2 /FiO 2 ratio increases > 20 mmHg after one to six hours in the PP [9] [10] [11] . However, we have previously reported that PP allows recruitment of a slow compartment previously excluded from ventilation [12] . This was associated with a decrease in partial pressure of arterial CO 2 (PaCO 2 ), an indirect reflection of the reduction of the alveolar dead space (VD alv ) [12] . Gattinoni et al. [10] also reported that the prognosis is improved in patients in whom PaCO 2 declines after an initial PP session. Finally, VD alv appears to be an independent risk factor for mortality in patients with ARDS [13] . In a recent study, Siddiki et al. [14] proposed evaluating the physiological dead space fraction (VD physiol / V T ) by using a rearranged alveolar gas equation for PaCO 2 without any expired CO 2 measurement.

In this context, we conducted a prospective physiological study to evaluate the impact of PP on ventilatory mechanics, gas exchange and VD alv . Our main objective was to validate our hypothesis that changes in PaCO 2 and VD alv might be more relevant than changes in PaO 2 in defining the respiratory response to PP. Our second objective was to validate the method of evaluation of the VD physiol /V T proposed by Siddiki et al. [14] .

In our unit, patients with a PaO 2 /FiO 2 ratio < 100 mmHg after 24 to 48 hours of mechanical ventilation are systematically turned to PP when hemodynamically stable [15] . Our study was approved by the Ethics Committee of the "Société de Réanimation de Langue Française" (SRLF-CE 07-213). After obtaining informed consent from the patients' relatives, 15 patients were included in the study between January 2008 and March 2010. Inclusion criteria were (1) the presence of ARDS according to the definition of the Acute Respiratory Distress Syndrome Network [3] ; (2) persistence of severe hypoxemia after 48 hours of mechanical ventilation, defined as a PaO 2 /FiO 2 ratio < 100 mmHg; and (3) hemodynamic stability, defined as systolic blood pressure > 90 mmHg with norepinephrine infusion at a rate < 0.5 μg/kg/minute. Patients with chronic obstructive pulmonary disease were excluded.

All patients were ventilated in volume-controlled mode (Servo-i; Maquet SA, Ardon, France), sedated and paralyzed by infusion of atracurium. The heat and moisture exchanger was routinely removed and replaced by a heated humidifier to reduce instrumental dead space as previously reported [16] . The ventilator settings included a "moderately restricted" V T of 6 to 8 mL/kg measured body weight, a respiratory rate allowing us to limit hypercapnia without generating intrinsic PEEP and an inspiration/expiration ratio of 1:2 with an end inspiratory pause of 0.5 seconds. Pplat was strictly limited < 30 cmH 2 O, and the PEEP selected was that which corrected the intrinsic PEEP, if any [17] . Ventilator settings were kept constant throughout the study. A recruitment maneuver was never used, and suction was not systematically performed. All patients were continuously monitored in terms of blood pressure with an arterial catheter, heart rate and O 2 saturation by pulse oximetry.

The study was conducted during the first session of PP. Our sessions routinely last 15 to 18 hours per day. Blood gas analysis, Pplat, total PEEP, end-tidal CO 2 (P etCO2 ) and mixed expired CO 2 (P ECO2 ) were recorded with the patient in the supine position, just before turning the patient to the PP, and every 3 hours in the PP until 15 hours had elapsed. Expired CO 2 was measured by a sensor positioned between the proximal end of the endotracheal tube and the Y piece of the ventilator circuit (COSMO; Novametrix, Wallingford, CT, USA). The ratio of VD/V T was calculated using the simplified Bohr equation [18] as follows: (1) VD alv /V T = 1 -P etCO2 / PaCO 2 and (2) VD physiol /V T = 1 -P ECO2 /PaCO 2 .

The estimated VD physiol /V T ratio was calculated as 1 -[(0.86 × VCO 2est )/(VE × PaCO 2 )], where VCO 2est is the estimated CO 2 production calculated using the Harris-Benedict equation [19] and VE is the expired minute ventilation.

Intrinsic PEEP was measured during a four-second end-expiratory occlusion period. Pplat was measured during a 0.5-second end-inspiratory pause. Respiratory system compliance (Crs) was calculated as Crs = V T / (Pplat -PEEP total ). Responders to PP were defined in two different ways: (1) an increase in PaO 2 /FiO 2 ratio > 20 mmHg after 15 hours of PP or (2) a decrease in PaCO 2 > 2 mmHg after 15 hours of PP.

Statistical analysis was performed using StatView 5 software (SAS Institute Inc., Cary, NC, USA). The continuous variables were expressed as medians (1st to 3rd interquartile range). Analysis of variance for repeated measurements was used for each parameter, and P < 0.05 was considered statistically significant. Measured VD physiol /V T and estimated VD physiol /V T were compared according to Bland-Altman analysis, together with the concordance correlation coefficient in 78 paired data. The same method was used to compare variations of measured and estimated VD physiol /V T every three hours while the patient was in PP.

Two patients were excluded from the study because of a history of severe chronic obstructive pulmonary disease, which left a study population of 13 patients. The patients' median age was 53 years (1st to 3rd interquartile range, 48 to 59 years), their median Simplified Acute Physiology Score II score was 62 (1st to 3rd interquartile range, 35 to 71) and their median Sequential Organ Failure Assessment score was 11 (1st to 3rd interquartile range, [8] [9] [10] [11] [12] [13] . All patients except one had ARDS of pulmonary origin. Eight patients had pneumonia, with six cases related to streptococcus pneumonia and two due to influenza (H1N1 virus). Two patients had aspiration, one had toxic shock syndrome and two had ARDS due to miscellaneous causes. No patient had abdominal hypertension or traumatic lung injury. Eleven patients required norepinephrine infusion. Respiratory parameters and blood gas analysis at the time of inclusion are reported in Table 1 .

A significant increase in PaO 2 /FiO 2 ratio occurred after 15 hours of PP, from 70 mmHg (51 to 77) in the supine position to 99 mmHg in the prone (83 to 139) (P < 0.0001) ( Table 2) . A significant decrease in PaCO 2 was also observed, from 58 mmHg (52 to 60) to 52 mmHg (47 to 56) (P = 0.04) ( Table 2) , with the lowest value occurring after nine hours of PP. As noted in Table 2 , Pplat was significantly reduced (P = 0.0004) and Crs improved (from 16 mL/cmH 2 O (13 to 30) to 18 mL/ cmH 2 O (15 to 30); P = 0.02). Finally, the VD alv /V T ratio was significantly reduced from 0.42 (0.35 to 0.47) to 0.40 (0.26 to 0.45), with the lowest value occurring after three hours in PP (hour 3) (0.31) ( Table 2) .

Seven patients were classified as "PaO 2 responders" and six were classified as "PaO 2 nonresponders" according to PaO 2 /FiO 2 ratio changes. No differences in VD alv /V T ratios or PaCO 2 or Pplat alterations during PP were observed between groups (Table 3 and Figure 1 ), whereas Crs increased more in the responders (Table 3) . Seven patients were also classified as "PaCO 2 responders" and six as "PaCO 2 nonresponders" according to the PaCO 2 changes. However, when compared with the PaO 2 /FiO 2 classification, four patients were classified differently. As shown in Table 4 and Figure 2 , VD alv /V T , PaO 2 /FiO 2 , PaCO 2 , Pplat and Crs were significantly more altered in responders than in nonresponders. As shown in Figure 3 , we found no correlation between changes in VD alv /V T and changes in PaO 2 /FiO 2 (P = 0.95), whereas we found a negative correlation between changes in VD alv /V T and changes in Crs (r = 0.29, P = 0.03).

As shown in Figure 4 , estimated VD physiol /V T systematically underestimated measured VD physiol /V T , with a poor concordance correlation coefficient of 0.19 (95% confidence interval (95% CI) 0.091 to 0.28), a bias of 0.16 and an agreement between -0.05 and 0.37. Concerning changes in VD physiol /V T during PP, estimated VD physiol /V T had a concordance correlation coefficient of 0.51 (95% CI 0.32 to 0.66) (Figure 4 ).

One of the objectives of our study was to describe alterations in VD alv induced by PP. ARDS is characterized by a heterogeneous lung with the existence of a slow compartment [18, 20] , defined as areas available for, but partially or totally excluded from, ventilation due in part to a bronchiolar collapse [12, 21] . In a previous study, we reported that PP may induce recruitment of this slow compartment, as suggested by its ability to counteract intrinsic PEEP and to decrease the expiratory time constant [12] . In the same study, we also reported that PP leads to a decrease in PaCO 2 , suggesting diminution of VD alv (alveolar dead space) [12] . Our present study demonstrates that PP may induce a decrease in VD alv . It occurred from the third hour and was maintained throughout the PP session. VD alv may be the consequence of nonperfused or poorly perfused lung areas in ventilated anterior areas, but also of a slow compartment partially excluded from ventilation. Our results suggest that PP induces functional lung recruitment, especially since decreases in VD alv related to PP were associated with a decrease in Pplat and strongly correlated with improvement in compliance. did not report a decrease in Pplat in PP, as we found, but after returning patients to the supine position [22] . This could be explained by the fact that they used roll under the upper part of the chest wall, leading to a significant impairment in chest wall compliance [22] , whereas we did not. The most beneficial reported effect of PP is oxygenation improvement [24, 25] . However, this better oxygenation can be due to (1) lung recruitment related to restoration of functional residual capacity [7] and improvement of the diaphragmatic movement in the posterior part [26] [27] [28] or (2) simply to an improvement in the ventilation/perfusion ratio due to a decreased hydrostatic gradient between the anterior and posterior parts of the lung [26, 29] . Whereas the first mechanism is crucial, one can say that the second mechanism is less important. This is why the second objective of our study was to test whether the response to PP in terms of PaCO 2 was physiologically more relevant than in terms of PaO 2 /FiO 2 ratio. Gattinoni et al. [10] reported that an increase in PaO 2 /FiO 2 ratio > 20 mmHg after six hours of PP is not predictive of the patient's prognosis, whereas a decline in PaCO 2 ≥1 mmHg is. In our present study, 7 of 13 patients were PaO 2 responders (increased PaO 2 /FiO 2 ratio > 20 mmHg after 15 hours of PP). However, changes in Pplat, PaCO 2 and VD alv did not differ between PaO 2 responders and PaO 2 nonresponders. On the other hand, 7 of 13 patients were PaCO 2 responders (decreased PaCO 2 > 2 mmHg after 15 hours of PP). PaCO 2 responders had a significant decrease in Pplat and VD alv , as well as a significant increase in oxygenation and compliance, compared with nonresponders. Our results are in accordance with a recent study of 32 ARDS patients [23] , in which the investigators reported that PaCO 2 variation induced by PP, and not PaO 2 /FiO 2 variation, is associated with lung recruitability. Interestingly, in our study, changes in VD alv were not correlated with changes in oxygenation but were strongly correlated with changes in compliance of the respiratory system.

An unexpected result of our work concerns the change over time of respiratory mechanics, blood gas analysis and VD alv . For many years, our PP protocol has been to turn patients to PP for up to 15 to 18 hours per day for 3 days [15] . In the study by Mancebo et al. [30] , which concluded that PP may reduce mortality in patients with severe ARDS, PP sessions lasted 20 hours/ day. In a recent study, we demonstrated that PP sessions that lasted 18 hours/day were independently associated with survival [31] . In the present study, the maximum effect of PP for VD alv , PaCO 2 and Pplat occurred six to nine hours after turning patients to PP. Later the effect seemed to be a decline. How this affects the effect of PP on patient prognosis remains to be elucidated.

The second objective of our study was to validate a recently proposed method to evaluate the VD physiol /V T ratio [14] . The method is based on CO 2 production calculated from the Harris-Benedict equation [19] and on the expired minute ventilation. Siddiki et al. [14] reported that it was associated with mortality in acute lung injury patients in a dose-response manner and proposed its routine use to estimate VD physiol /V T . However, they did not report any comparison with measured VD physiol /V T . In the present study, we have demonstrated that this method significantly underestimates VD physiol /V T , rendering it not accurate enough to assess the degree of lung injury. Interestingly, changes in estimated VD physiol /V T during PP appeared better correlated with changes in measured VD physiol /V T and could be proposed in the future in this field. Siddiki et al. [14] proposed the method in the context of a much larger series than ours and in patients with less severe ARDS, rendering it difficult to draw any definitive conclusions. Our work is limited by the small number of patients included. This is a consequence of our routine protocol, which strictly restricts PP to patients with the most severe ARDS, that is, those with a PaO 2 /FiO 2 ratio < 100 mmHg after 48 hours of ventilation. This also explains why it is not possible to link our results to outcomes. However, despite this limitation, we consider our results relevant from a physiological point of view.

In conclusion, our study demonstrates that PP induces a decrease in PaCO 2 and VD alv . This is related to an improvement in respiratory mechanics, with a decrease in Pplat and an increase in compliance. Testing the response to PP appeared to be physiologically more relevant using PaCO 2 changes than PaO 2 /FiO 2 changes. How this may affect management at the bedside remains to be studied. Estimated VD physiol /V T ratios systematically underestimated measured VD physiol /V T ratios.

• PP induced a decrease in VD alv /V T , which was correlated with an improvement in respiratory mechanics.

• Defining the respiratory response to PP appeared more relevant when using PaCO 2 changes rather than PaO 2 /FiO 2 changes. • Estimated VD physiol /V T using the Harris-Benedict equation systematically underestimated measured VD physiol /V T .

Abbreviations ARDS: acute respiratory distress syndrome; P ECO2 : mixed expired PCO 2 ; PEEP: positive end-expiratory pressure; P etCO2 : end-tidal PCO 2 ; PP: prone position; Pplat: plateau pressure; VD alv : alveolar dead space; VD physiol : physiological dead space.

Acute respiratory distress in adults

The concept of "baby lung

Altman representation (left) and a linear correlation (right). (A) and (B) Comparison for each paired data set (n = 78) in the supine position and after 3, 6, 9, 12 and 15 hours in the prone position. (C) and (D) Comparison of changes in VD physiol /V T assessed according to the two methods between each time of measurement and the previous one

The Acute Respiratory Distress Syndrome Network: Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome

Regional distribution of gas and tissue in acute respiratory distress syndrome. III. Consequences for the effects of positive end-expiratory pressure. CT Scan ARDS Study Group. Adult Respiratory Distress Syndrome

Tidal recruitment and overinflation in acute respiratory distress syndrome: yin and yang

Comments of a devil's advocate

Improved oxygenation in patients with acute respiratory failure: the prone position

Prone ventilation reduces mortality in patients with acute respiratory failure and severe hypoxemia: systematic review and meta-analysis

Prone position in mechanically ventilated patients with severe acute respiratory failure

Decrease in PaCO 2 with prone position is predictive of improved outcome in acute respiratory distress syndrome

Effects of the prone position on gas exchange and hemodynamics in severe acute respiratory distress syndrome

Prone position improves mechanics and alveolar ventilation in acute respiratory distress syndrome

Pulmonary dead-space fraction as a risk factor for death in the acute respiratory distress syndrome

Bedside quantification of dead-space fraction using routine clinical data in patients with acute lung injury: secondary analysis of two prospective trials

Low stretch ventilation strategy in acute respiratory distress syndrome: eight years of clinical experience in a single center

Ability and safety of a heated humidifier to control hypercapnic acidosis in severe ARDS

Pressure-volume curves in acute respiratory distress syndrome: clinical demonstration of the influence of expiratory flow limitation on the initial slope

Respiratory dead space and distribution of the inspired gas

The Harris Benedict equation reevaluated: resting energy requirements and the body cell mass

Respiratory mechanics in mechanically ventilated patients with respiratory failure

Expiratory flow limitation and intrinsic positive end-expiratory pressure at zero positive end-expiratory pressure in patients with adult respiratory distress syndrome

Effects of the prone position on respiratory mechanics and gas exchange during acute lung injury

Relationship between gas exchange response to prone position and lung recruitability during acute respiratory failure

The prone position improves arterial oxygenation and reduces shunt in oleic-acidinduced acute lung injury

Mechanism by which the prone position improves oxygenation in acute lung injury

Short-term effects of prone position in critically ill patients with acute respiratory distress syndrome

Effects of prone position on alveolar recruitment and oxygenation in acute lung injury

Position and motion of the human diaphragm during anesthesia-paralysis

Effect of prone position on regional shunt, aeration, and perfusion in experimental acute lung injury

A multicenter trial of prolonged prone ventilation in severe acute respiratory distress syndrome

Routine prone position in patients with severe ARDS: feasibility and impacts on prognosis

An expanded definition of the adult respiratory distress syndrome

PaCO 2 and alveolar dead space are ARDS patients: a physiological study

We thank Maquet SA (Ardon, France) for covering the cost of publication. Maquet SA did not participate in the design or conduct of the study or in the interpretation of the data. 

Authors' contributions CC contributed to the acquisition of data, performed the data analysis, participated in the design of the study and the interpretation of the data, and wrote the manuscript. XR contributed to the acquisition of data, performed the data analysis and participated in the design of the study and the interpretation of the data. KB, SC, VC and BP contributed to the acquisition of data. AVB performed the data analysis, participated in the design of the study and the interpretation of the data, and wrote the manuscript. FJ participated in the design of the study and the interpretation of the data. All authors read and approved the final manuscript.

The authors declare that they have no competing interests, except that of receiving funds from Maquet SA (Ardon, France) to support the cost of publication.