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Postural Recruitment Maneuver in Patients With Acute Respiratory Distress Syndrome Due to COVID-19 Infection

Feasibility and Physiological Effects of a Postural Recruitment Maneuver in Patients With Acute Respiratory Distress Syndrome Due to COVID-19 Infection

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04475068
Enrollment
15
Registered
2020-07-17
Start date
2020-07-17
Completion date
2020-10-31
Last updated
2021-08-25

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

Conditions

ARDS, Sars-CoV2

Brief summary

The purpose of this study is to evaluate if a postural recruitment maneuver (PRM) improves the aeration and distribution of lung ventilation in patients with Acute Respiratory Distress Syndrome (ARDS) caused by COVID-19 infection; without the need to reach high airway pressures as in the standard lung recruitment maneuver and / or place the patient in prone position. This strategy could be particularly useful in the context of a major health emergency in centers with limited resources.

Detailed description

The PRM is based on the known effect of gravity on transpulmonary pressure (PL). Two principles explain its mechanism of action: 1) the first indicates that atelectasis and poorly ventilated areas of the lung can improve their aeration by putting the lung in the highest position. Opposite lateral decubitus causes that upper lung to have a higher PL and allow a recruiting effect at moderate airway pressures. 2) The second principle is based on Laplace's Law and postulates that once the upper lung is recruited, it remains without lung collapse if a sufficient level of positive end-expiratory pressure (PEEP) is applied. Based on these two precepts, PRM consists of sequentially moving the patient from the supine to the left lateral decubitus to recover the aeration of the right lung. After that, the patient is placed in the right lateral position to recruit the left lung; keeping the right lung without collapse by continuous use of PEEP. Finally, the patient returns to the supine position looking for an improvement in the distribution of ventilation and global pulmonary aeration, with a subsequent improvement in gas exchange and pulmonary mechanics.

Interventions

PROCEDURELateral Position (left and right lateral decubitus)

Prior to initiating the protocol, patients will be sedated deeply with sedatives and opioids and paralyzed. Patients will be evaluated in 5 positions sequentially: 1) Supine 2) Left lateral 3) Supine 4) Right lateral 5) Supine. The side with the least ventilation evaluated by EIT will define which side will start the sequence. Each step will last 30 minutes. Aeration measured by Electric Impedance Tomography (EIT) and lung ultrasound, distribution of the lung ventilation and perfusion measured by EIT, ventilator and hemodynamic parameters, esophageal pressure, and blood gas analysis will be recorded at the end of each step. Continuous monitoring of blood pressure, heart rate and saturation of arterial blood (SpO2) will be carried out during all steps of the protocol to assess the tolerance to the procedure.

Sponsors

Universidad de Piura
CollaboratorUNKNOWN
Hospital Nacional Edgardo Rebagliati Martins
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patients \> 18 years of age * Patients with moderate-to-severe ARDS as per the Berlin definition * Infection due to COVID-19 * Body mass index (BMI) ≤ 35 kg /m\^2.

Exclusion criteria

* Contraindication for EIT monitoring 1. Unstable spine or pelvic fractures 2. Pacemaker, automatic implantable cardioverter defibrillator 3. Skin lesions between the 4th and 5th ribs where the EIT belt is worn * Pregnancy * Major hemodynamic instability:: 1. Mean arterial pressure lower than 60 mm Hg despite adequate fluid resuscitation and use of vasopressors. 2. FC\> 120 or \<60 per minute 3. Presence of uncontrolled arrhythmias. * More than 1 week of mechanical ventilation * Failure of more than 2 extrapulmonary organs.

Design outcomes

Primary

MeasureTime frameDescription
Effects of a postural recruitment maneuver in lung aerationThrough study completion (up to 24 hours)Lung aeration measured by ultrasound reaeration score, ranges from 0 (all regions are well aerated) to 36 (all regions are consolidated).
Effects of a postural recruitment maneuver in distribution of ventilationThrough study completion (up to 24 hours)Distribution of ventilation measured by EIT (distribution and changes in the impedance in AU, arbitray units)
Effects of a postural recruitment maneuver in gas exchangeThrough study completion (up to 24 hours)Gas exchange measured by blood gas analysis (PaO2, PaCO2, in mmHg) and capnography (end-tidal CO2, in mmHg)
Effects of a postural recruitment maneuver in respiratory mechanicsThrough study completion (up to 24 hours)Respiratory mechanics measured by esophageal balloon (esophageal pressure, transpulmonary pressure, in cmH2O)
Effects of a postural recruitment maneuver in hemodynamicThrough study completion (up to 24 hours)Hemodynamic data measured by invasive arterial monitoring (mean arterial pressure, in mmHg)

Secondary

MeasureTime frameDescription
Feasibility of a postural recruitment maneuverThrough study completion (up to 24 hours)Oxigenatory tolerance evaluated with pulse oximeter (arterial oxygen saturation, in percentage)

Countries

Peru

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026