Effects of Invasive Mechanical Ventilation on the Right Ventricular Function

Sponsor
University of Giessen (Other)
Overall Status
Recruiting
CT.gov ID
NCT05710419
Collaborator
(none)
30
1
24
1.2

Study Details

Study Description

Brief Summary

The goal of this observational study is to learn about the influence of mechanical ventilation on the right ventricular (RV) function. The primary focus is on methods which are routinely used to improve gas exchange in ventilated patients (positive end expiratory pressure [PEEP], inhalation of NO, prone positioning). The main questions it aims to answer are:

  • Effects of prone positioning, PEEP and inhalation of NO on RV-function

  • Are there determinants (clinical, laboratory, demographic, echocardiographic) for the right ventricular response to the above?

RV-Function will be assessed with right ventricular pressure-volume loops recorded with a conductance catheter at

  • each PEEP-Level during titration of the best PEEP

  • before and every 5 minutes (for max. 45 minutes) after rotation to prone position

  • before and under continuous inhalation of NO (if required based on clinical grounds)

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Pressure-volume loop (PV-loop) analysis is the gold standard for the assessment of right ventricular properties and function in clinical research. PV-Loops can be generated in real-time by conductance catheterization, which allows a simultaneous acquisition of pressure and volume changes in high resolution. It is known that invasive mechanical ventilation, primarily through a change in intrathoracic pressure conditions, has a significant impact on the function of the right ventricle. However, the underlying mechanisms have not yet been investigated and understood in detail using the gold standard. Therefore, the aim of this observational study is to investigate the effects of invasive ventilation and ventilatory strategies to improve gas exchange (PEEP, prone position, inhaled NO) on the function of the right ventricle.

    The physiology of mechanical ventilation is fundamentally different than spontaneous breathing: While in spontaneous breathing the air fills the lungs driven by a negative intrathoracic pressure, in mechanical ventilation air has to be "pumped" into the lungs, resulting in a positive intrathoracic pressure. These unphysiological intrathoracic pressure conditions lead to complex interactions between the respiratory and cardiovascular system, can stress the right ventricle and cause hemodynamic instability. In addition to the stress of mechanical ventilation per se, there are changes in the pulmonary vasculature in caused by the pulmonary disease itself. A maximum expression of such changes is the acute respiratory failure syndrome (ARDS), which requires a complex ventilation strategy and is associated with a high mortality rate. ARDS is always associated with a dysfunction of the pulmonary vessels (hypoxic vasoconstriction, pulmonary microthrombosis, derecruitment of ventilated areas) leading to increased right ventricular afterload. In contrast to the left ventricle, the right ventricle has only a small contractile reserve and is therefore more sensible to a higher afterload. This is why the right ventricle can be seen as the weakest link of the circulatory system in patients with ARDS. This is also reflected in the fact that the high lethality of ARDS is more associated to circulatory failure and less to hypoxemia. A ventilation strategy that ensures adequate gas exchange and at the same time causes as little additional stress as possible on the right heart would be optimal.

    If the patient is eligible for the study according to the inclusion and exclusion criteria, an echocardiographic examination with 3D volumetric measurement of the right-sided heart cavities is performed. The conductance catheter will then be calibrated using this volumetric dataset. First, a conventional right heart catheterization is performed (conventional Swan-Ganz catheter), followed by the placement of the conductance catheter and the recording of a baseline. The "best PEEP" is then titrated by minimizing the "driving pressure" during volume-controlled ventilation as a descending sequence (from high PEEP to low PEEP). PV loops are recorded at each PEEP level. After determining the best PEEP level, the patient will be rotated to prone position. PV loops are recorded immediately after the rotation and within the following 45 minutes. The catheter is then removed. If the admixture of NO in the respiratory gas is indicated for medical reasons, the PV loops are recorded before and after the start of the admixture.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    30 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Effects of Invasive Mechanical Ventilation on the Right Ventricular Function
    Actual Study Start Date :
    Nov 4, 2022
    Anticipated Primary Completion Date :
    Nov 4, 2024
    Anticipated Study Completion Date :
    Nov 4, 2024

    Outcome Measures

    Primary Outcome Measures

    1. Changes in right ventricular pressure and volume and derived functional parameters caused by positive endexspiratory pressure [15 minutes at each PEEP-Level]

    2. Changes in right ventricular pressure and volume and derived functional parameters caused by prone positioning [1, 5, 10, 15, 20, 25, 35 and 45 minutes after rotation]

    3. Changes in right ventricular pressure and volume and derived functional parameters caused inhalation of NO [10 minutes after start of NO-Administration]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age > 18 years

    • Invasive mechanical ventilation and clinical indication for prone positioning (e.g. ARDS)

    • No contraindications for right heart catheterization or conductance catheterization

    • The written consent of the patient or his legal guardian

    Exclusion Criteria:
    • No written consent

    • contraindications for right heart catheterization or conductance catheterization

    • Pregnancy or breastfeeding

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Internal Medicine, Justus Liebig University Giessen, Universities of Giessen and Marburg Lung Center (UGMLC), German Center for Lung Research (DZL) Giessen Hesse Germany 35392

    Sponsors and Collaborators

    • University of Giessen

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Giessen
    ClinicalTrials.gov Identifier:
    NCT05710419
    Other Study ID Numbers:
    • 157/22
    First Posted:
    Feb 2, 2023
    Last Update Posted:
    Feb 2, 2023
    Last Verified:
    Jan 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 2, 2023