The Effect of Chest Compression and Ventilation Coordination During Cardiopulmonary Resuscitation.

April 1, 2015 updated by: National Taiwan University Hospital

The Effect of Chest Compression and Ventilation Coordination During Cardiopulmonary Resuscitation

Airway management and maintaining adequate ventilation during cardiopulmonary resuscitation (CPR) are important. The rule of 30:2 compression-to-ventilation ratios before endotracheal intubation and keeping 1 breath every 6-8 seconds with advanced airway are generally accepted according to 2010 Advanced Cardiac Life Support (ACLS) guideline. This recommendation emphasizes on the timing and frequency of ventilation during CPR. However, poor clinical evidence had been established concerning adequate volume, airway flow and pressure in each cycle.

There are increasing evidence that hyperventilation during resuscitation reduces pulmonary venous return and, therefore, compromises cardiac output and circulation. Another research reported that using high flow oxygen mask alone during basic life support (BLS) results in better survival rate and overall outcome compared with conventional positive pressure ventilation.

Our study applies flowmeter to measure ventilation parameters as frequency, duration, exhaled volume and airway pressure on intubated patients who received artificial ventilation during CPR. The parameters will correlate with information from accelerometry and capnometry simultaneously during resuscitation. . Investigators also focus on the influence of chest compression, which increases intra-thoracic pressure considerably. This effect may act against positive pressure ventilation and probably minimize the efficiency in each ventilation or circulation..

Details about how to ventilate one patient during CPR include right timing, duration, adequate volume and coordination are in debate. Unfortunately, current practice based on clinical guidelines emphasizes little on this issue. Investigators are committed to refine contemporary practices and hopefully improve qualities of resuscitation.

Investigators proposed the hypothesis that coordinate chest compression and ventilation may minimize the increasement of airway pressure and improve the effect of circulation

Study Overview

Study Type

Observational

Enrollment (Anticipated)

50

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

      • Taipei, Taiwan, 10002
        • Recruiting
        • National Taiwan University Hospital
        • Contact:

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

20 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Cardiac arrest patient received CPR in Emergency Department Age > 20 years old

Description

Inclusion Criteria:

  • age > 20 years old, < 100 years old

Exclusion Criteria:

  • Trauma related out of hospital cardiac arrest

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

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Out of hospital cardiac arrest
Out of hospital cardiac arrest of non-traumatic cause
Unexpected in-hospital cardiac arrest
Unexpected cardiac arrest during emergency department stay

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
rate of 2- hour recover of spontaneous circulation
Time Frame: 2 hours
Recover of spontaneous circulation lasting for 2 hours describe as successful recover of spontaneous circulation, otherwise failure.
2 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
End tidal carbon-dioxide level
Time Frame: Measured during and end of resuscitation
End tidal carbon-dioxide level correlates with successful recovery of spontaneous circulation event
Measured during and end of resuscitation
Arterial blood gas data
Time Frame: measured during and end of resuscitaiton
Oxygen and carbon-dioxide tension changes in different ventilation strategy in cardiopulmonary resuscitation
measured during and end of resuscitaiton
30-day survival rate
Time Frame: 30 days
30 days
90-day neurologic outcome
Time Frame: 90 days
90 days
Survive to discharge
Time Frame: 90 days
Duration of hospital stay, usually will be recorded in 90 days, occasionally will more than 90 days
90 days
Timing of first shockable rhythm
Time Frame: measured during resuscitaion
measured during resuscitaion

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Hui-Chih Wang, Emergency department, National Taiwan University Hospital

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

October 1, 2013

Primary Completion (Actual)

February 1, 2015

Study Completion (Anticipated)

July 1, 2015

Study Registration Dates

First Submitted

January 21, 2014

First Submitted That Met QC Criteria

February 4, 2014

First Posted (Estimate)

February 6, 2014

Study Record Updates

Last Update Posted (Estimate)

April 3, 2015

Last Update Submitted That Met QC Criteria

April 1, 2015

Last Verified

April 1, 2015

More Information

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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