Skip to main content
Brazilian Journal of Anesthesiology logoLink to Brazilian Journal of Anesthesiology
. 2018 Jan 9;68(3):225–230. doi: 10.1016/j.bjane.2017.11.003

Behavior of stroke volume variation in hemodynamic stable patients during thoracic surgery with one-lung ventilation periods

Comportamento da variação do volume sistólico em pacientes hemodinamicamente estáveis durante cirurgia torácica com períodos de ventilação monopulmonar

María Lema Tome 1,, Francisco Andrés De la Gala 1, Patricia Piñeiro 1, Luis Olmedilla 1, Ignacio Garutti 1
PMCID: PMC9391809  PMID: 29477233

Abstract

Introduction

In last few years, emphasis was placed in goal-directed therapy in order to optimize patient's hemodynamic status and improve their prognosis. Parameters based on the interaction between heart and lungs have been questioned in situations like low tidal volume and open chest surgery. The goal of the study was to analyze the changes that one-lung ventilation can produce over stroke volume variation and to assess the possible impact of airway pressures and lung compliance over stroke volume variation.

Methods

Prospective observational study, 112 patients undergoing lung resection surgery with one-lung ventilation periods were included. Intravenous fluid therapy with crystalloids was set at 2 mL.g−1. Hypotension episodes were treated with vasoconstrictive drugs. Two-lung Ventilation was implemented with a TV of 8 mL.g−1 and one-lung ventilation was managed with a TV of 6 mL.g−1. Invasive blood pressure was monitored. We recorded the following cardiorespiratory values: heart rate, mean arterial pressure, cardiac index, stroke volume index, airway peak pressure, airway plateau pressure and static lung compliance at 3 different times during surgery: immediately after lung collapse, 30 min after initiating one-lung ventilation and after restoration of two-lung ventilation.

Results

Stroke volume variation values were influenced by lung collapse (before lung collapse 14.6 (DS) vs. OLV 9.9% (DS), p < 0.0001); or after restoring two-lung ventilation (11.01 (DS), p < 0.0001). During two-lung Ventilation there was a significant correlation between airway pressures and stroke volume variation, however this correlation lacks during one-lung ventilation.

Conclusion

The decrease of stroke volume variation values during one-lung ventilation with protective ventilatory strategies advices not to use the same threshold values to determine fluid responsiveness.

Keywords: Thoracic surgery, One-lung ventilation, Stroke volume variation, Goal-directed therapy, Heart-lung interaction

Introduction

During the last few years, emphasis was placed in goal-directed therapy (GDT) in order to optimize patient's hemodynamic status and thus improve their prognosis. These appear to be based on the dynamic parameters used to predict the volume response: stroke volume variation (SVV), pulse pressure variation (VPP) and pulse delta variation. Some authors have recently shown that these hemodynamic parameters may be useful to guide fluid therapy in thoracic surgery.1, 2, 3, 4, 5, 6

However, other researches have questioned their usefulness in different situations such as the use of a tidal volume (TV) under 8 mL.kg−1, under open-chest surgery or during one-lung ventilation (OLV) because of the greater shunt that takes place.7, 8, 9 These circumstances coincide in the regularly handling during protective ventilation in thoracic surgery during OLV.

During OLV, even with protective ventilation, the airflow cut to the prone lung, is associated with a decrease of lung compliance and the increase of airway pressures (Paw). There are different lines of investigation that experimentally have shown that in patients with Acute Respiratory Stress Syndrome (ARDS) the decrease in lung compliance or Paw can disturb SVV values even though a constant blood volume is maintained. However, to our knowledge, this line of research has not been carried out in thoracic surgery. In this type of surgery, the interaction between heart and lung during OLV have fail to consider the influence of lung compliance or airway pressure when it comes to evaluating the outcomes.

We hypothesized that modifications in ventilatory parameters during open-chest surgery periods may induce changes in hemodynamic parameters based on the interaction between heart and lung.

The goal of our study was to describe the existing changes in the dynamic parameters in patients managed with the same fluid therapy during surgery, and analyze the relationship between the respiratory mechanics (Paw and lung compliance) and SVV setting different TV (8 mL.kg−1 vs. 6 mL.kg−1) during open chest surgery (open vs. closed).

Methods

This was a prospective observational study approved by the Hospital Ethics Committee for Clinical Trials. Consecutive sampling was used and all patients gave written consent. One hundred seventy five consecutive patients undergoing elective lung resection with OLV period of at least one hour were studied. Exclusion criteria included pregnant or breastfeeding women, hypersensitivity to any of the anesthetics used, uncompensated cardiac disease or NYHA II patients, atrial fibrillation, or impossibility to achieve protective lung ventilation. Also patients who showed any episodes of hemodynamic instability (defined as a hypotension episodes, MAP < 60 mmHg) were treated with vasoactive drugs and/or fluid bolus were excluded.

After standard monitoring (pulse oxymetry, electrocardiogram and noninvasive blood pressure, urine output), general anesthesia was induced with propofol (2 mg.kg−1), fentanyl (3 mcgr.kg−1) and rocuronium (0.6–1 mg.kg−1). Propofol or sevoflurane (1–2.5%) were used for the maintenance of general anesthesia in order to obtain a BIS (biespectral index) between 40 and 60. A left double-lumen tube was introduced into the trachea (according to a formula based on the patient sex and height: 35–37 for women and 39–41 for men), checking the correct placement by fiberoptic bronchoscopy and auscultation. Patients were connected to mechanical ventilation (Primus Dräger Ventilator. Dräger Hispania SA, Madrid, Spain) and during two-lung ventilation (volume-controlled ventilation) the respiratory parameters set were to tidal volume of 8 mL.kg−1, PEEP of 3–5 cm H2O, and the appropriate respiratory rate to maintain the ETCO2 (end tidal CO2) between 30 and 35 mmHg, FiO2 used was 0.45. During the OLV period the tidal volume was 6 mL.kg−1, PEEP used was 5 cm H2O, permissive hypercapnia and FiO2 between 0.6 and 1 to maintain SpO2 > 90%. Hypoxemia episodes were treated with an increase of FiO2, CPAP in non-dependent lung and recruitment maneuvers. When the patient was positioned in lateral decubitus, a paravertebral catheter was inserted into the fifth-seven intercostal ipsilateral spaces to the surgical field through a 17 G Tuohy needle using Eason and Wyatt technique.

After general induction, invasive blood pressure using radial artery was monitored via connection to Flo-Trac system (Vigileo, Edwards Lifesciences, Irvine, CA, USA) to measure cardiac output (CO), cardiac index (CI), stroke volume variation (SVV), stroke volume (SV) and stroke volume index (SVI).

Intravenous fluid therapy with crystalloids was set at a rate of 2 mL.kg−1.h−1, maintaining urine output > 0.5 mL.kg−1 per hour.

We analyzed the hemodynamic and respiratory parameters at 3 different times during surgery: right before the lung collapse, 30 min after initiating OLV and after two-lung ventilation was restored. In addition to these hemodynamic measurements, blood gases and hemoglobin analysis were sampled.

Statistical analysis was conducted using SPSS (17.0). Pair test was used between basal and OLV and TLV situation, in order to analyze the different hemodynamic and respiratory parameters of the study. In addition, a bivariate correlation analysis was used to determine if the rising between the pressures at the beginning of OLV, the lung compliance decreasing and the SVV increasing. p-Values less than 0.05 were considered significant.

Results

A total of 175 consecutive patients undergoing lung resection surgery with OLV periods were included. Eight of them were excluded by atrial fibrillation. Also we excluded another 55 patients who needed fluid boluses or vasoactive drugs during OLV. Demographic characteristics are summarized in Table 1.

Table 1.

Demographic and surgery characteristics.

Sex (F/M) 41/71
ASA (I/II/III) 6/67/39
Age (years) 62 (12)
Weight (kg) 68 (11)
Height (cm) 165 (9)
Length OLV (min) 166 (67)
Length anesthesia (min) 285 (84)
FEV1 preop (%) 94 (23)
FVC preop (%) 105 (20)
Segmentectomy 59
Pneumonectomy 3
Lobectomy 58
Bilobectomy 2
Side surgery (L/R) 48/64

Data is presented as mean (SD) and the sample size (n).

F, female; M, male; OLV, one-lung ventilation; FEV1 preop, preoperatory forced expired volumen in the first second; FVC preop, preoperatory forced vital capacity; L, left; R, right.

During OLV an increase in airway pressures and decrease lung compliance were measured. After restoring TLV (two lung ventilation) these parameters returned to similar values than basal. Among the hemodynamic parameters evaluated, no changes were observed at the beginning of OLV, except by a decrease of SVV values (Table 2). Furthermore, SVV was the only hemodynamic parameter affected when changing to OLV from TLV with close-chest surgery. However, the reset of TLV did not generate those hemodynamic changes.

Table 2.

Hemodynamic and respiratory values during study.

Basal: before lung collapse 30 min after initiating
OLV
p-values
Basal vs. OLV
Two-lung ventilation restoration p-Values
OLV vs. TLV restoration
PaO2/FiO2 371 (138) 117 (50) 0.0001 322 (93) 0.0001
PaCO2 (mmHg) 43 (6) 49 (7) 0.0001 48 (7) 0.114
EtCO2 (mmHg) 33 (4) 35 (4) 0.0001 36 (6) 0.487
Peak pressure (cm H2O) 21 (3) 25 (4) 0.0001 21 (5) 0.0001
Plateau pressure (cm H2O) 19 (3) 21 (5) 0.0001 18 (5) 0.0001
Lung compliance (mL.cm H2O−1) 40 (11) 28 (9) 0.0001 42 (15) 0.0001
SVV (%) 14.6 (7) 9.9 (5) 0.0001 11.0 (5) 0.048
HR (Beat.min−1) 70 (14) 72 (15) 0.143 74 (14) 0.064
PAM (mmHg) 79 (15) 76 (15) 0.099 78 (15) 0.119
CI (mL.min−1.m−2) 2.91 (4) 3.05 (4) 0.177 3.04 (3) 0.942
SVI (mL.beat−1.m−2) 37 (13) 37 (11) 0.574 37 (10) 0.968

Data are presented as mean (SD).

CI, cardiac index; MAP, mean arterial pressure; Press, pressure; HR, hear rate, OLV, one-lung ventilation; TLV, two-lung ventilation; SVV, stroke volume variation; SVI, stroke volume index; EtCO2, end tidal of CO2; PaCO2, partial pressure of carbon dioxide; PaO2/FiO2, ratio of arterial oxygen partial pressure to fractional inspired oxygen.

A significant positive correlation was ground between SVV values and airway pressures (peak, plateau and media pressures) during TLV, right before and after OLV. During OLV no significant correlation between this parameters and airway pressures was noted. Similarly, no significant correlation was found between the rest of the hemodynamic parameters analyzed (MAP, HR, CI, SVI) and the ones provided by the ventilation unit (Fig. 1).

Figure 1.

Figure 1

Representation of SVV (stroke volumen variation) during the different times of surgery (BAS, basal; OLV30, 30 min after starting one lung ventilation; End, at the end of one lung ventilation) according to the airway pressures (peak and plateau) and lung compliance.

Discussion

The results of this study showed that in hemodynamically stable patients undergo thoracic surgery with OLV periods, SVV values were the unique hemodynamic parameter which suffer modifications during OLV and these changes reverted after TLV was restored.

The accuracy of a monitoring system used to guide fluid therapy may be critical if GDT is used in this type of surgery where it has been proven an important repercussion of fluid therapy over the acute lung injury or over the respiratory prognosis of these patients.10, 11

Nowadays the most frequently used parameters in protocols to guide fluid therapy are SVV and VPP, but it is known that they present some limitations which may difficult their use in certain intraoperative circumstances. One of the main limitations in thoracic surgery is the low tidal volume (VT) set during OLV period. VT effect over the absolute value of the dynamic index has been previously examined.2, 12, 13, 14, 15 Some authors have observed that SVV is only able to predict the volume response during OLV when a VT of 8 mL.kg−1 (ideal weight) or higher was set.16, 17, 18 However, Lee et al. have described that the VPP predictive power is possible to achieve during OLV with a VT of 6 mL.kg−1 while when a VT of 10 mL.kg−1 was set, VPP was not useful, contravening the physiological basis principles.19

The aim of our study was not to evaluate the predictive power of SVV to guide the intraoperatory fluid therapy. We only sought to assess the intraoperatory evolution of the hemodynamic parameters and analyze what the influence of other parameters over the SVV values, since the influence of lung compliance or airway pressures over the values of these indices appear to have been poorly analyzed in clinical practice.

Airway pressures and lung compliance

Considering that the dynamic indices used as a tool for evaluating fluid responsiveness are based on the concept that ventilation with positive pressure induces variations on stroke volume, it is reasonable to assume that these dynamic parameters are affected by the changes on intrathoracic and intrapulmonary pressures such as variation in airway pressures or lung compliance.20, 21

We observed that patients with higher airway pressures (peak as well as plateau pressure) tend to present higher SVV values. But this finding was only shown when we were ventilating both lungs with a VT of 8 mL.kg−1. During OLV with a low TV the interaction between the airway pressure and SVV was lost. We can explain this finding not only because of the use of low VT but also for the changes in pulmonary blood flow due to the effects of gravity and Hypoxic Pulmonary Vasoconstriction (HPV). Between 20% and 30% of the pulmonary blood flow during OLV will address to the non-ventilated lung, increasing the blood flow in the depended lung, being this lung the one that contributes to fill and unload the left ventricle during the ventilatory cycle. The blood remaining with the pulmonary shunt in the non-ventilated lung will remain unchanged and will not contribute to SVV generation.22 Besides, shunt magnitude will also influence the dynamic parameters calculus.18, 23

In addition, during OLV a drastic decrease of lung compliance will occur due to the inlet air in the declined and compressed lung by mediastinum structures, use of rollers to improve the surgical exposure of the hemithorax that goes under surgery, and also because of the pressured exerted by the abdominal content. Mesquida et al. demonstrated in an experimental model how the decreasing lung compliance, while maintaining a constant blood volume, was related to an increase of the dynamic parameters.24 Lung compliance is also recognized as a factor influencing the intrathoracic pressure.25 It is known that pulmonary stiffness may buffer the transmission of respiratory pressures to the cardiovascular system.26 Monnet et al. observed in patients suffering from ARDS that when the respiratory system compliance was less than 30 mL.cm−1 H2O, VPP lost its power to evaluate fluid responsiveness.27, 28 In our study, the increased SVV values during OLV could possibly be explained also by the decrease in lung compliance.

Open chest surgery

Open chest surgery has been another proposed limitation factor of the dynamic indices validity during OLV. Different studies show how under this condition the predictive power of SVV for fluid responsiveness decreases.29 Although there is some discrepancy in this findings because most of the research was conducted in cardiac surgery, where the ventilatory conditions take place with opened pleura. During OLV we maintain closed pleura in one lung while the one in the non-ventilated lung is open. In this situation, an amount of the pressure generated by the ventilator will be transmitted to the atmosphere instead of the intrathoracic vessels and heart, producing the effect that the ventilation over the volume load will be unpredictable.17, 30, 31, 32 In addition, if open chest surgery is combined with other conditions such as OLV and the modification in the pulmonary blood flow to he ventilated lung, the predictable response of fluid administration will be even more complex.

Nevertheless, we do not believe that open chest surgery could influence the lack of relationship between ventilation and SVV because we observed that as the two-lung ventilation was restored (with open pleura) the relationship between the respiratory and cardiac parameters was reestablished. In our study we demonstrated that when we were ventilating two lungs with a VT of 8 mL.kg−1 both at the beginning of surgery (close chest surgery) and once again at the end of it (open chest surgery) the relationship between the respiratory parameters (airway pressures and lung compliance) and SVV was significant, but weak, reflecting that the increase of intrathoracic pressure due to mechanical ventilation led a greater variability in left ventricle filling. On the contrary, during OLV (in which we registered higher airway pressures and less lung compliance), setting a low VT (6 mL.kg−1) did not show any affect over SVV. It has to be emphasized another circumstance not always taken into account, being the VT chosen for the dependent lung would be higher than the one used during TLV (4 mL per lung).

Limitations

Likewise, those patients who needed volume administration or vasoconstrictive drugs in order to improve their hemodynamic status were not included in the analysis of the relationship between ventilatory and hemodynamic variables. However we believe that these patients withdrawal could make results more consistent because they could modify the values in presence of hypovolemia or hypotensive periods.

In conclusion, studies that evaluate the usefulness of SVV to detect patients who may benefit the administration of fluid boluses can not use the same threshold values during TLV or OLV. Relationship between cardiorespiratory values and SVV are lost during OLV with protective ventilation strategies.

Conflicts of interest

The authors declare no conflicts of interest.

References

  • 1.Marik P.E., Monnet X., Teboul J.L. Hemodynamic parameters to guide fluid therapy. Ann Intensive Care. 2011;1:1. doi: 10.1186/2110-5820-1-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Reuter D.A., Bayerlein J., Goepfert M.S., et al. Influence of tidal volume on left ventricular stroke volume variation measured by pulse contour analysis in mechanically ventilated patients. Intensive Care Med. 2003;29:476–480. doi: 10.1007/s00134-003-1649-7. [DOI] [PubMed] [Google Scholar]
  • 3.Haas S., Eichhorn V., Hasbach T., et al. Goal-directed fluid therapy using stroke volume variation does not result in pulmonary fluid overload in thoracic surgery requiring one-lung ventilation. Crit Care Res Pract. 2012;2012:687018. doi: 10.1155/2012/687018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Magder S. Clinical usefulness of respiratory variations in arterial pressure. Am J Respir Crit Care Med. 2004;169:151–155. doi: 10.1164/rccm.200211-1360CC. [DOI] [PubMed] [Google Scholar]
  • 5.Preisman S., Kogan S., Berkenstadt H., et al. Predicting fluid responsiveness in patients undergoing cardiac surgery: functional haemodynamic parameters including the respiratory systolic variation test and static preload indicators. Br J Anaesth. 2005;95:746–755. doi: 10.1093/bja/aei262. [DOI] [PubMed] [Google Scholar]
  • 6.Zhang J., Chen C.Q., Lei X.Z., et al. Goal-directed fluid optimization based on stroke volume variation and cardiac index during one lung ventilation in patients undergoing thoracoscopy lobectomy operations: a pilot study. Clinics. 2013;68:1065–1070. doi: 10.6061/clinics/2013(07)27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Reuter D.A., Goephfert M.S.G., Goresch T., et al. Assessing fluid responsiveness during open chest conditions. Br J Anaesth. 2005;94:318–323. doi: 10.1093/bja/aei043. [DOI] [PubMed] [Google Scholar]
  • 8.Reuter D.A., Kirchner A., Felbinger T.W., et al. Usefulness of left ventricular stroke volume variations to assess fluid responsiveness in patients with reduced left ventricular function. Crit Care Med. 2003;31:1399–1404. doi: 10.1097/01.CCM.0000059442.37548.E1. [DOI] [PubMed] [Google Scholar]
  • 9.Monnet X., Rienzo M., Osman D., et al. Esophageal Doppler monitoring predicts fluid responsiveness in critically ill ventilated patients. Intensive Care Med. 2005;31:1195–1201. doi: 10.1007/s00134-005-2731-0. [DOI] [PubMed] [Google Scholar]
  • 10.Licker M., de Perrot M., Spiliopoulos A., et al. Risk factors for acute lung injury after thoracic surgery for lung cancer. Anesth Analg. 2003;97:1558–1565. doi: 10.1213/01.ANE.0000087799.85495.8A. [DOI] [PubMed] [Google Scholar]
  • 11.Wu C.Y., Lee T.S., Chan K.C., et al. Does targeted pre-load optimisation by stroke volume variation attenuate a reduction in cardiac output in the prone position. Anaesthesia. 2012;67:760–764. doi: 10.1111/j.1365-2044.2012.07116.x. [DOI] [PubMed] [Google Scholar]
  • 12.De Backer D., Heenen S., Piagnerelli M., et al. Pulse pressure variations to predict fluid responsiveness: influence of tidal volume. Intensive Care Med. 2005;31:517–523. doi: 10.1007/s00134-005-2586-4. [DOI] [PubMed] [Google Scholar]
  • 13.Charron C., Fessenmeyer C., Cosson C., et al. The influence of tidal volume on the dynamic variables of fluid responsiveness in critically ill patients. Anesth Analg. 2006;102:1511–1517. doi: 10.1213/01.ane.0000209015.21418.f4. [DOI] [PubMed] [Google Scholar]
  • 14.Kim H.K., Pinsky M. Effect of tidal volume, sampling duration, and cardiac contractility on pulse pressure and stroke volume variation during positive-pressure ventilation. Crit Care Med. 2008;36:2858–2862. doi: 10.1097/CCM.0b013e3181865aea. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.De Backer D., Taccone F.S., Holsten R., et al. Influence of respiratory rate on stroke volume variation in mechanically ventilated patients. Anesthesiology. 2009;110:1092–1097. doi: 10.1097/ALN.0b013e31819db2a1. [DOI] [PubMed] [Google Scholar]
  • 16.Suehiro K., Okutani R. Influence of tidal volume for stroke volume variation to predict fluid responsiveness in patients undergoing one-lung ventilation. J Anesth. 2011;25:777–780. doi: 10.1007/s00540-011-1200-x. [DOI] [PubMed] [Google Scholar]
  • 17.Suehiro K., Okutani R. Stroke volume variation as a predictor of fluid responsiveness in patients undergoing one-lung ventilation. J Cardiothorac Vasc Anesth. 2010;24:772–775. doi: 10.1053/j.jvca.2010.03.014. [DOI] [PubMed] [Google Scholar]
  • 18.Fu Q., Zhao F., Mi W., et al. Stroke volume variation fail to predict fluid responsiveness in patients undergoing pulmonary lobectomy with one-lung ventilation using thoracotomy. BioScience Trends. 2014;8:59–63. doi: 10.5582/bst.8.59. [DOI] [PubMed] [Google Scholar]
  • 19.Lee J.H., Jeon Y., Bahk J.H., et al. Pulse pressure variation as a predictor of fluid responsiveness during one-lung ventilation for lung surgery using thoracotomy: randomised controlled study. Eur J Anaesthesiol. 2011;28:39–44. doi: 10.1097/EJA.0b013e32834089cf. [DOI] [PubMed] [Google Scholar]
  • 20.Novak R.A., Matuschak G.M., Pinsky M.R. Effect of ventilatory frequency on regional pleural pressure. J Appl Physiol. 1988;65:1314–1323. doi: 10.1152/jappl.1988.65.3.1314. [DOI] [PubMed] [Google Scholar]
  • 21.Monnet X., Teboul J.L. Assessment of volumen responsiveness during mechanical ventilation: recent advances. Crit Care. 2013;17:217. doi: 10.1186/cc12526. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Slinger P.D., Campos J.H. In: Miller's anesthesia. 7th ed. Miller R.D., editor. Elsevier Churchill Livingstone; Philadelphia, USA: 2009. Anesthesia for thoracic surgery; pp. 1819–1887. [Google Scholar]
  • 23.Trepte C., Hass S., Nitzschke R., et al. Prediction of volume-responsiveness during one-lung ventilation: a comparison of static, volumetric, and dynamic parameters of cardiac preload. J Cardiothorac Vasc Anesth. 2013;27:1094–1100. doi: 10.1053/j.jvca.2013.05.003. [DOI] [PubMed] [Google Scholar]
  • 24.Mesquida J., Kim H.K., Pinsky M.R. Effect of tidal volume, intrathoracic pressure and cardiac contractility on variations in pulse pressure, stroke volume and intrathoracic blood volume. Intensive Care Med. 2011;37:1672–1679. doi: 10.1007/s00134-011-2304-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Romand J.A., Shi W., Pinsky M.R. Cardiopulmonary effects of positive pressure ventilation during acute lung injury. Chest. 1995;108:1041–1048. doi: 10.1378/chest.108.4.1041. [DOI] [PubMed] [Google Scholar]
  • 26.Jardin F., Genevray B., Brun-Ney D., et al. Influence of lung and chest wall compliances on transmission of airway pressure to the pleural space in critically ill patients. Chest. 1985;88:653–658. doi: 10.1378/chest.88.5.653. [DOI] [PubMed] [Google Scholar]
  • 27.Monnet X., Rienzo M., Osman D., et al. Passive leg raising predicts fluid responsiveness in the critically ill. Crit Care Med. 2006;34:1402–1407. doi: 10.1097/01.CCM.0000215453.11735.06. [DOI] [PubMed] [Google Scholar]
  • 28.Monnet X., Bleibtreu A., Ferré A., et al. Passive leg-raising and end-expiratory occlusion tests perform better than pulse pressure variation in patients with low respiratory system compliance. Crit Care Med. 2012;40:152–157. doi: 10.1097/CCM.0b013e31822f08d7. [DOI] [PubMed] [Google Scholar]
  • 29.Kubitz J.C., Annecke T., Kemming G.I., et al. The influence of positive end-expiratory pressure on stroke volume variation and central blood volume during open and closed chest conditions. Eur J Cardiothorac Surg. 2006;30:90–95. doi: 10.1016/j.ejcts.2006.04.008. [DOI] [PubMed] [Google Scholar]
  • 30.De Waal E.E., Rex S., Kruitwagen C.L., et al. Dynamic preload indicators fail to predict fluid responsiveness in open-chest conditions. Crit Care Med. 2009;37:510–515. doi: 10.1097/CCM.0b013e3181958bf7. [DOI] [PubMed] [Google Scholar]
  • 31.Whyffels P., Sergeant P., Wouters P. The value of pulse pressure and stroke volume variation as predictors of fluid responsiveness during open chest surgery. Anaesthesia. 2010;65:704–709. doi: 10.1111/j.1365-2044.2010.06371.x. [DOI] [PubMed] [Google Scholar]
  • 32.Trepte C., Haas S., Meyer N., et al. Effects of one-lung ventilation on thermodilution-derived assessment of cardiac output. Br J Anaesth. 2012;108:922–928. doi: 10.1093/bja/aes032. [DOI] [PubMed] [Google Scholar]

Articles from Brazilian Journal of Anesthesiology are provided here courtesy of Elsevier

RESOURCES