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Ventilator Hyperinflation for intensive care patients: Influence of Pressure versus Volume controlled settings to optimise expiratory flow rate bias.

Ventilator Hyperinflation for intensive care patients: Influence of Pressure versus Volume controlled settings to optimise expiratory flow rate bias.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619001119189
Enrollment
48
Registered
2019-08-12
Start date
2019-09-06
Completion date
2020-06-30
Last updated
2019-08-26

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

Conditions

None listed

Brief summary

Ventilator hyperinflation (VHI) is used by physiotherapists in patients who are in intensive care and are receiving mechanical ventilation. VHI aims to move secretions out of the lungs towards the larger airways of the lung where they can be suctioned. This is achieved by giving a larger, slow breath via the ventilator and creating a fast expiration. Currently, little is reported on the actual ability to bias the flow inspiratory and expiratory flow rates during VHI. The primary aim of the study is to measure the characteristics of inspiratory and expiratory flows generated using different methods of VHI in patients receiving mechanical ventilation.

Interventions

Ventilator hyperinflation (VHI) is a technique used in Intensive Care Units by physiotherapists. VHI aims to assist in the removal of secretions from the lungs in patients who are intubated and receiving mechanical ventilation by adjusting the patient's mechanical ventilator settings to deliver breaths of a larger size in a slow controlled manner. While the use of VHI in Australia is increasing, different VHI protocols (i.e. ventilator setting adjustments) are utilised between hospitals. This

Ventilator hyperinflation (VHI) is a technique used in Intensive Care Units by physiotherapists. VHI aims to assist in the removal of secretions from the lungs in patients who are intubated and receiving mechanical ventilation by adjusting the patient's mechanical ventilator settings to deliver breaths of a larger size in a slow controlled manner. While the use of VHI in Australia is increasing, different VHI protocols (i.e. ventilator setting adjustments) are utilised between hospitals. This study will be conducted in the intensive care unit of a major tertiary hospital. A single Physiotherapist with >10 years experience will administer VHI to two groups of patients. Group 1: Low Positive End Expiratory Pressure (PEEP) 5-9 cmH2O Group 2: High PEEP 10-15 cmH2O Patients will be allocated to Group 1 or 2 according to the level of PEEP they are receiving as part of their clinical management (i.e. their ventilator settings including PEEP level prescribed by the medical staff as part of the management of their clinical presentation). The effect of VHI will be analysed within these groups. Each group will have three ventilator hyperinflation protocols applied. The protocols will vary the mode of ventilation and target pressures used. Group 1: Low PEEP 5-9 cmH2O VHI Protocols 1. Pressure support ventilation (PSV) with Pressure Support set so that PIP equals 35cmH2O 2. Synchronised Intermittent Mandatory Ventilation - Volume Control (SIMV-V) with maximum tidal volume to a peak inspiratory pressure (PIP) limit of 35cmH2O 3. SIMV-V with maximum tidal volume resulting in a driving pressure limit of 20cmH2O Group 2: High PEEP 10-15 cmH2O VHI Protocols 1. SIMV-V with maximum tidal volume resulting in a driving pressure limit of 20cmH2O 2. SIMV-V with maximum tidal volume to a PIP limit of 35cmH2O 3. BiLevel mode with High PEEP to low PEEP range equals 20cmH2O (driving pressure limit) The order that the VHI protocols are applied within each group will be randomised. Each protocol will be applied for 2 minutes. For each patient, when each VHI method is applied, the settings will be documented and reported to assess the fidelity to the described protocols. After the application of a VHI protocol, the patient’s ventilator settings will be returned to their baseline settings for a period of 10 minutes, before the next VHI protocol will be performed.

Sponsors

Peter Thomas
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Adult patients, aged > 18 years. Intubated and ventilated Stable on their current mechanical ventilation settings.

Exclusion criteria

Inspired oxygen (FiO2)greater than or equal to 0.7; Oxygen saturation (SpO2) less than 90%; PEEP greater than 15 cmH2O; Peak inspiratory pressure (PIP) greater than 35 cmH2O on baseline ventilator settings; Evidence of severe bronchospasm; Mean arterial blood pressure (MABP) less than or equal to 65mmHg Heart rate greater than 130 High dose vasopressors; The primary condition does not warrant hyperinflation techniques e.g. exacerbation of Chronic Obstructive Pulmonary Disease, acute pulmonary oedema.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026