Pulse-wave transit time with ventilator-induced variation for the prediction of fluid responsiveness
- PMID: 32002187
- PMCID: PMC6985177
- DOI: 10.1002/ams2.484
Pulse-wave transit time with ventilator-induced variation for the prediction of fluid responsiveness
Abstract
Aim: Although pulse pressure variation is a good predictor of fluid responsiveness, its measurement is invasive. Therefore, a technically simple, non-invasive method is needed for evaluating circulatory status to prevent fluid loading and optimize hemodynamic status. We focused in the pulse-wave transit time (PWTT) defined as the time interval between electrocardiogram R wave to plethysmograph upstroke, which has been recently introduced to non-invasively assess cardiovascular response. In the present study, we evaluated the efficacy of pulse-wave transit time (PWTT) with ventilator-induced variation (PWTTV) in predicting fluid responsiveness.
Methods: We evaluated six domestic pigs weighing 46.0 ± 3.5 kg. After anesthesia induction, electrocardiogram, femoral arterial blood pressure, plethysmograph on the tail, and carotid artery blood flow were monitored and hemorrhage was induced by withdrawing 20 mL/kg blood over 20 min; 5 mL/kg blood volume was then autotransfused over 10 min. Then PWTTV and pulse pressure variation were measured at tidal volumes of 6 and 12 mL/kg.
Results: Area under the receiver operating curve values for the prediction of a >10% change in carotid artery blood flow were 0.979 for pulse pressure variation and 0.993 for PWTTV at a tidal volume of 6 mL/kg and 0.979 and 0.979, respectively, at a tidal volume of 12 mL/kg (all P < 0.0001).
Conclusions: Measured non-invasively, PWTTV showed similar utility to pulse pressure variation in predicting >10% changes in carotid artery blood flow induced by autotransfusion.
Keywords: Autotransfusion; blood volume; hemodynamic; non‐invasive; pulse pressure.
© 2020 The Authors. Acute Medicine & Surgery published by John Wiley & Sons Australia, Ltd on behalf of Japanese Association for Acute Medicine.
Conflict of interest statement
Approval of the research protocol: The present study was carried out at the Kochi Medical School (Kochi, Japan) and was approved by the Institutional Animal Research Ethics Committee (H‐00094). Informed consent: N/A. Registry and the registration no. of the study/trial: N/A. Animal studies: All animal experiments were undertaken following the national guidelines and the relevant national laws on the protection of animals. Conflict of interest: None.
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