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Assessment of Fluid Responsiveness in Patients After Cardiac Surgery

Assessment of Fluid Responsiveness in Patients After Cardiac Surgery Comparison of Different Functional Hemodynamic Parameters and Tests

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02571465
Acronym
POP
Enrollment
40
Registered
2015-10-08
Start date
2015-04-30
Completion date
2015-12-31
Last updated
2016-11-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemodynamics, Patient Monitoring

Keywords

functional hemodynamic parameter, passive leg raising, stroke volume variation, pulse pressure variation

Brief summary

To overcome the limited accuracy of functional hemodynamic parameters such as stroke volume and pulse pressure variation (SVV and PPV) during spontaneous breathing, a Passive Leg Raising (PLR) manoeuvre has been suggested as a reliable predictor of fluid responsiveness. Aim of this study was to evaluate fluid responsiveness using SVV, PPV and PLR during the transition from controlled to spontaneous breathing in cardiac surgery patients

Detailed description

In patients after elective off-pump CABG are enrolled hemodynamic measurements are performed in the postoperative period upon arrival in the ICU using a PiCCO2 system (Pulsion Medical Systems, Munich, Germany). Controlled fluid challenges (500 ml) are done at 3 time-points: A) during controlled mechanical ventilation B) during pressure support ventilation with spontaneous breathing and C) after extubation. Stroke volume (SV), SVV and PPV as well as standard hemodynamic parameters (MAP = mean arterial pressure, HR = heart rate) are assessed. A PLR is performed before fluid administration at all 3 time points. A positive response is defined as an increase in SV\>15 %. Prediction of fluid responsiveness will be tested by AUC (area under the receiver operating characteristic - ROC - curve).

Interventions

Sponsors

Triemli Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* preserved left ventricular function * regular heart rhythm

Exclusion criteria

* emergency procedures * intra- and extra-cardial shunts * aortic and tricuspid valve insufficiencies * peripheral arterial occlusive disease

Design outcomes

Primary

MeasureTime frameDescription
Stroke volume increase > 15%20 minStroke volume increase defines fluid responsiveness

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026