Tidal volume challenge to predict fluid responsiveness in the operating room: An observational study

Eur J Anaesthesiol. 2019 Aug;36(8):583-591. doi: 10.1097/EJA.0000000000000998.

Abstract

Background: Pulse pressure variation (PPV) and stroke volume variation (SVV) do not predict fluid responsiveness when using a protective ventilation strategy: the use of functional haemodynamic tests can be useful to overcome this limitation.

Objectives: We tested the use of a tidal volume challenge (VTC), during 6 ml kg [predicted body weight (PBW)] ventilation, and the end-expiratory occlusion test (EEOT) for prediction of fluid responsiveness.

Design: An interventional prospective study.

Setting: Supine elective neurosurgical patients.

Interventions: The study protocol was, first, the initial EEOT test was performed during baseline 6 ml kg PBW ventilation; second, VTC was performed by increasing the VT up to 8 ml kg PBW and PPV and SVV changes were recorded after 1 min; third, a second EEOT was performed during 8 ml kg PBW ventilation; and VT was reduced back to 6 ml kg PBW and a third EEOT was performed. Finally, a 250 ml fluid challenge was administered over 10 min to identify fluid responders (increase in stroke volume index ≥10%).

Results: In the 40 patients analysed, PPV and SVV values at baseline and EEOT performed at 6 ml kg PBW did not predict fluid responsiveness. A 13.3% increase in PPV after VTC predicted fluid responsiveness with a sensitivity of 94.7% and a specificity of 76.1%, while a 12.1% increase in SVV after VTC predicted fluid responsiveness with a sensitivity of 78.9% and a specificity of 95.2%. After EEOT performed at 8 ml kg PBW, a 3.6% increase in cardiac index predicted fluid responsiveness with a sensitivity of 89.4% and a specificity of 85.7%, while a 4.7% increase in stroke volume index (SVI) with a sensitivity of 89.4% and a specificity of 85.7%.

Conclusion: The changes in PPV and SVV obtained after VTC are reliable and comparable to the changes in CI and SVI obtained after EEOT performed at 8 ml kg PBW in predicting fluid responsiveness in neurosurgical patients.

Trial registration: ACTRN12618000351213.

Publication types

  • Observational Study
  • Validation Study

MeSH terms

  • Aged
  • Blood Pressure / physiology
  • Elective Surgical Procedures / adverse effects*
  • Female
  • Fluid Therapy / adverse effects
  • Fluid Therapy / methods*
  • Humans
  • Hypovolemia / etiology
  • Hypovolemia / physiopathology
  • Hypovolemia / prevention & control*
  • Male
  • Middle Aged
  • Monitoring, Intraoperative / methods*
  • Neurosurgical Procedures / adverse effects*
  • Operating Rooms
  • Predictive Value of Tests
  • Prospective Studies
  • ROC Curve
  • Reproducibility of Results
  • Respiration, Artificial / adverse effects
  • Respiration, Artificial / methods
  • Stroke Volume / physiology
  • Tidal Volume / physiology
  • Treatment Outcome