Height Measurement Procedures Influence the Risk of Ventilator-induced Lung Injury in ARDS

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire, Amiens

About this trial

Acute respiratory distress syndrome is characterized by heterogeneous lung injury, with dependent regions often collapsed and non-dependent regions relatively well-aerated, forming the so called "baby lung." Mechanical ventilation, while essential, can induce additional lung injury (VILI) via overdistension (baro/volutrauma) or repetitive alveolar collapse (atelectrauma). Protective ventilation strategies with low tidal volumes (VT 6-8 mL/kg predicted body weight, PBW) reduce mortality, but their efficacy relies on accurate PBW estimation, which is derived from patient height. In critical care, height measurement is often challenging, and common methods such as visual estimation or tape measurement can be inaccurate, leading to inappropriate VT settings and increased risk of lung stress and VILI. Alternative methods, including heel-to-knee distance and laser measurement, may offer more precise PBW estimation, yet their impact on lung mechanics in ARDS remains unexplored. This study addresses the knowledge gap by evaluating whether differences in height measurement methods significantly affect lung stress, tidal volume distribution, and ventilatory mechanics in ARDS patients.

Patients' heights will be measured using five methods (stadiometer, visual, tape, laser, heel-to knee). Corresponding PBW and tidal volumes (VT = 6 mL/kg PBW) will be calculated and applied in randomized order, each for 30 minutes. Lung stress, ventilatory mechanics, gas exchange, and regional ventilation distribution will be assessed for each VT setting, preceded by a short alveolar recruitment maneuver. During the study, continuous monitoring of hemodynamics and oxygenation will be performed.

Ventilatory parameters including plateau pressure, driving pressure, and transpulmonary pressures will be recorded. Electrical impedance tomography will assess regional tidal volume distribution. Each patient's participation is limited to approximately two hours with no further follow-up.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patient

Mechanical ventilation on volumetric mode

Sedated and curarized patient

Diagnosis of ARDS according to the Berlin criteria

Disqualifiers

Patient opposing the use of his/her data for research purposes.

Contraindication to placement of an esophageal balloon catheter (e.g., esophageal fistula, esophageal varices).

Contraindication to strict supine positioning for height measurement (e.g., proven or suspected intracranial hypertension with intracranial pressure >18 mmHg).

Impossibility of measuring height with the reference method (stadiometer) due to deformity or amputation of both lower limbs.

Trial design

Design model

Single group

Treatments tested in this trial

  • height measured

    Other intervention

    Patients with ARDS will have their height measured using five different methods: stadiometer (reference), visual estimation, measuring tape, infrared laser, and heel-to-knee distance. For each height, the predicted body weight (PBW) and corresponding tidal volume (VT = 6 mL/kg PBW) will be calculated and applied in a randomized order, each for 30 minutes. During each VT period, lung stress (end-inspiratory transpulmonary pressure), ventilatory mechanics, gas exchange, and regional ventilation distribution (assessed using electrical impedance tomography) will be assessed. Prior to each VT application, a short alveolar recruitment maneuver will be performed to standardize lung volume.

Treatment groups

39 Participants
are divided into 1 treatment group
Group A: ards patientsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Pulmonary stress

Pulmonary stress assessed by measuring end-inspiration transpulmonary pressure using a balloon esophageal probe.

Time frame
one day

Secondary outcomes

1

measured height variation

Agreement of measured height across the different height-measurement methods.

Time frame
one day
2

predicted body weight variation

Agreement of predicted body weight across the different height-measurement methods.

Time frame
one day
3

tidal volume variation

Agreement of tidal volume across the different height-measurement methods.

Time frame
one day
4

Transpulmonary pressures at end-expiratory

Time frame
one day

Other outcomes

Sponsors and contacts

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