Employing End Tidal Capnography in Continuous Flow Ventricular Assist Device Patients



Status:Withdrawn
Conditions:Peripheral Vascular Disease, Cardiology, Cardiology
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:4/17/2018
Start Date:October 2016
End Date:February 2018

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The purpose of this study is to explore how the End Tidal Carbon Dioxide monitoring via nasal
cannula (ETCO2-NC) device may allow for earlier detection of respiratory complications. This
device will detect the amount of carbon dioxide exhaled with each breath and may better
predict high levels of this than traditional monitoring. This may reduce the number and
severity of respiratory issues. A convenience sample of 60 participants either scheduled for
continuous flow left ventricular assist device (CF-LVAD) implant or who have been readmitted
to an ICU with a CF-LVAD will be recruited and randomized to usual care or usual care plus
ETCO2-NC throughout their stay in the ICU.

The purpose of this proposal is to explore the relationships between End Tidal Carbon Dioxide
(ETCO2) via nasal cannula (ETCO2-NC) and routinely measured physiologic and participant
reported parameters in extubated participants who have received a continuous flow left
ventricular assist device (CF-LVAD), and to determine if the addition of ETCO2-NC monitoring
to usual care is associated with decreased incidence and severity of respiratory issues.

A convenience sample of 60 participants either scheduled for mechanical circulatory support
device (MCSD) implant or who have been readmitted to an intensive care unit (ICU) with a
CF-LVAD will be recruited and randomized to usual care or usual care plus ETCO2-NC throughout
their stay in the ICU.

Investigators seek to examine the relationship between ETCO2-NC with traditional physiologic
measures, clinical assessments, and participant reported symptoms in persons with a CF-LVAD.
Additionally, this study intends to compare the respiratory outcomes of extubated persons
with a CF-LVAD randomized to usual care to those receiving usual care plus ETCO2- NC.

Inclusion Criteria:

- Scheduled for mechanical circulatory support device (MCSD) implant or have been
readmitted to an intensive care unit (ICU) with a continuous flow left ventricular
assist device (CF-LVAD)

- New York Heart Association (NYHA) functional class III to IV

- Ability to read, write, and speak English

Exclusion Criteria:

- Requiring mechanical ventilation during the active phase of the trial
We found this trial at
1
site
1364 Clifton Rd NE
Atlanta, Georgia 30322
(404) 712-2000
Phone: 404-727-9658
Emory University Hospital As the largest health care system in Georgia and the only health...
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from
Atlanta, GA
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