Driving Pressure Optimization, RV-PA Coupling, and AKI in Mechanically Ventilated Critically Ill Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNardin Aymn Boshra

About this trial

This study evaluates the effect of driving pressure optimization on right ventricular-pulmonary artery (RV-PA) coupling, assessed by TAPSE/PASP ratio, and its association with acute kidney injury (AKI) progression in mechanically ventilated critically ill patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years.

ICU admission.

Invasive mechanical ventilation expected to continue for ≥48 hours.

Adequate transthoracic echocardiographic acoustic window for assessment of TAPSE/PASP.

Disqualifiers

Pre-existing end-stage renal disease on chronic dialysis.

Severe pulmonic or tricuspid valve disease precluding reliable TAPSE/PASP assessment.

Pre-existing RV dysfunction of a non-pulmonary cause.

Pregnancy.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Driving Pressure-Guided Ventilator Optimization

    Other intervention

    A ventilator management strategy in which tidal volume and/or PEEP are titrated to minimize driving pressure (plateau pressure - PEEP) to a pre-specified target, aiming to improve RV-PA coupling and reduce AKI progression.

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: Driving Pressure-Optimized Ventilation GroupExperimental treatment 1 intervention
Group B: Standard Ventilation GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

TAPSE/PASP ratio (RV-PA coupling)

Baseline transthoracic echocardiography will be performed before initiation of the intervention whenever feasible, recording: TAPSE, PASP (estimated from tricuspid regurgitant jet velocity and estimated right atrial pressure), MAPSE (LV longitudinal function parameter), Inferior vena cava (IVC) collapsibility index. Repeat echocardiography will be performed approximately 48-72 hours after initiation of the intervention, using the same measurements.

Time frame
On admission and 48-72 hours after

Secondary outcomes

1

Acute kidney injury progression

Serum creatinine and urine output will be recorded at baseline and daily for the first 7 days of mechanical ventilation, or until ICU discharge/death if earlier. AKI will be staged according to KDIGO criteria with primary renal endpoint: AKI progression, defined as an increase in KDIGO stage during the 7-day observation period. New AKI and worsening of established AKI may also be described separately.

Time frame
1 week

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Nardin Aymn Boshra

Lead sponsor

Assiut University

Sponsor institution

Assiut University

Collaborator

This trial is not recruiting at the moment. You can still explore other options: