Two Cycling Off Modes in Pressure Support: Study of Respiratory Mechanics, Breathing Comfort and Asynchrony Patterns

May 28, 2009 updated by: Hospital de Clinicas de Porto Alegre

VENTILAÇÃO MECÂNICA COM PRESSÃO SUPORTE: ESTUDO DA ASSINCRONIA EXPIRATÓRIA (in Portughese)

Objective: To compare termination criteria (TC) of pressure support ventilation (PSV).

Design: Randomized cross-over clinical trial.

Setting: Intensive Care Units.

Patients: Sixteen patients on PSV with ability to answer a visual analog scale (VAS).

Protocol and Measurements: Each patient was ventilated with two different TC ventilators, fixed and automatic, with measurements of ventilatory mechanic variables, breathing comfort and asynchrony patterns.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Two ventilators with different flow termination criteria (TC) were compared: Servo 300 (Siemens-Elema, Solna, Sweden) with fixed TC (5% of peak inspiratory flow) and Newport E500 (Newport Medical Instruments, Costa Mesa, CA) with automatic TC (varies between 5% to 55%). Each patient remained three hours in the protocol, one hour in each ventilator, after been randomized to one of two sequences of 3 steps: Fixed 5% / Automatic / Fixed 5% or Automatic / Fixed 5% / Automatic (Figure 1). The transition among the ventilators was realized through a three-way flow directional valve (Three-Way T-Shape TM, Hans Rudolph Incorporation, Kansas City, EUA).

The PS level was determined by clinical staff to partially unload the respiratory muscle without respiratory distress based on observation of the patient's breathing pattern. The PS, the positive end expiratory pressure (PEEP), the inspiratory oxygen fraction (FiO2) and the pressure trigger sensitivity levels were unchanged during the protocol.

Study variables: Patients' demographic, anthropometric and clinical data were obtained (Table 1).

The study variables were detected noninvasively using only airway pressure (Paw) and flow signals, obtained with a pressure differential pneumotachometer (CO2SMO Plus; Novametrix Medical Systems, Wallingford, CT) located at the distal end of the ventilator circuit . Three records of five minutes were realized in each study step: time = 0' (0-5 min), t = 30' (30-35 min) and t = 55' (55-60 min). Data were digitalized at 100 Hz and recorded on a personal computer for subsequent analysis (LabVIEW 7.1, National Instruments Corporation, Austin, TX). A total of nine record phases of five minutes from each patient were analyzed .The variables values were obtained by one hundred ventilatory cycles from each recorded phase

Measured variables:

The following variables were analyzed (detailed descriptions of each one were in the Electronic Supplementary Material - ESM):

  • Ventilatory parameters: PS (PSadjusted); measured PS (PSeffective) and PEEP (PEEPeffective); peak airway pressure; effective flow termination criterion (TC - V'ti/V'peak, %) .
  • Breathing pattern: tidal volume obtained by mathematical integration of the flow signal; respiratory rate; minute ventilation; inspiratory time; expiratory time; duty cycle (Ti/Ttot); time constant obtained by measuring the slope off the expiratory limb of the flow-volume plot .
  • Respiratory effort: pressure-time product required to ventilator trigger (PTPtrigger) ; inspiratory delivered assistance pressure-time products at 300 ms (PTPdelivered-assistance300) and 500 ms (PTPdelivered-assistance500) after the onset of inspiratory effort; over assistance pressure-time product (PTPover-assistance) (see Figure 2 for details); airway occlusion pressure at 0.1 second (P0.1) .
  • Breathing comfort: evaluated by a modified VAS, labeled 0 to 10 (0 = best comfort and 10 = worst comfort) .
  • Asynchrony patterns: ineffective efforts, both during inspiration and expiration, (IEinspiratory and IEexpiratory), double-triggering (D-T) and autotriggering (A-T) were detected by visual inspection of the flow and airway pressure signals recordings .

Statistical Analysis:

The statistical analysis was performed using the Statistical Package for Social Science (SPSS 15.0, Chicago, EUA) and the significance level was established as p < 0.05. Tests are detailed in the ESM.

Study Type

Interventional

Enrollment (Actual)

18

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • RS
      • Porto Alegre, RS, Brazil, 91900580
        • Hospital Mae de Deus

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patients under PSV for more than 24 hours,
  • Age > 18 years
  • Ability to answer to a symptom visual analog scale (VAS)

Exclusion Criteria:.

  • Hemodynamic instability (use of vasoactive drugs like dopamine, dobutamine or norepinephrine)
  • Bronchopleural fistula

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: VENTILATOR WEANING
Two ventilators with different flow termination criteria (TC) were compared: Servo 300 (Siemens-Elema, Sweden) with fixed TC (5% of peak inspiratory flow) and Newport E500 (Newport Medical Instruments, CA) with automatic TC (varies between 5% to 55%). Each patient remained three hours in the protocol, one hour in each ventilator, after been randomized to one of two sequences of 3 steps: Fixed 5% / Automatic / Fixed 5% or Automatic / Fixed 5% / Automatic . The PS, the positive end expiratory pressure (PEEP), the inspiratory oxygen fraction (FiO2) and the pressure trigger sensitivity levels were unchanged during the protocol.
The aim of the present study was to compare two different cycling off modes in PSV, a fixed and other automatic, about ventilatory mechanic variables, breathing comfort and patient-ventilator asynchrony patterns
Other Names:
  • pressure support

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
comfort
Time Frame: 30 minutes
30 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: josue a victorino, phd, Hospital de Clínicas de Porto Alegre

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

December 1, 2004

Primary Completion (Actual)

December 1, 2007

Study Completion (Actual)

June 1, 2008

Study Registration Dates

First Submitted

May 28, 2009

First Submitted That Met QC Criteria

May 28, 2009

First Posted (Estimate)

May 29, 2009

Study Record Updates

Last Update Posted (Estimate)

May 29, 2009

Last Update Submitted That Met QC Criteria

May 28, 2009

Last Verified

May 1, 2009

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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