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Fluid Responsiveness Tested by the Effective Pulmonary Blood Flow During a Positive End-expiratory Trial

The Reliability of Noninvasive Effective Pulmonary Blood Flow to Detect Fluid Responsiveness During a Positive End-expirator Trial in Ventilated Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03693365
Enrollment
30
Registered
2018-10-03
Start date
2018-09-05
Completion date
2022-04-12
Last updated
2022-08-26

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

Conditions

Cardiovascular Diseases

Keywords

Carbon dioxide, Pulmonary blood flow, Ventilation

Brief summary

Fluid responsiveness is difficult to assess at the bedside. The accuracy of published techniques to detect preload-dependent patients have many pitfalls and limitations. The present study test the role of noninvasive effective pulmonary blood flow measured by expired carbon dioxide to detect fluid responsivess in mechanically ventilated patients.

Detailed description

This is a prospective and observational study designed to test the accuracy of the non-invasive effective pulmonary blood flow measured by the capnodynamic methodology for detect preload-dependent patients. Fourty patients undergoing mechanical ventilation during surgery will be studied. Preload-depency (fluid responsiveness) will be tested during an increase in end-expiratory pressure (PEEP) from 5 to 10 cmH2O during one minute. Pulse pressure variation will be use as the reference method to detect preload-dependency. The effective pulmonary blood flow will be continuously recorded during the PEEP maneuver. Receiver Operator Curves will be used to detect fluid responsiveness taking a pulse pressure variation higher than 13%.The corresponding cut off value for the effective pulmonary blood flow signal will be determined..

Interventions

PROCEDUREPEEP trial

Positive end-expiratory pressure (PEEP) is increased from 5 to 10 cmH2O during one minute.

Sponsors

Hospital Privado de Comunidad de Mar del Plata
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

* Written informed consent * Programmed cardiac and noncardiac surgeries * Need of invasive arterial blood pressure monitoring.

Exclusion criteria

* Emergency surgeries. * Acute pulmonary diseases * Arrhytmias * Congestive cardiac failure

Design outcomes

Primary

MeasureTime frameDescription
Fluid responsivess assessment with the effective pulmonary blood flow10 monthsComparison between standard method (pulse pressure variation) with a new method of fluid responsiveness (Effective pulmonary blood flow).

Countries

Argentina

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026