Hemodynamic Survey Cardiac Surgical Scenarios

Sponsor
University of Iowa (Other)
Overall Status
Completed
CT.gov ID
NCT02529033
Collaborator
(none)
64
9

Study Details

Study Description

Brief Summary

The purpose of this study is to find out the Lidco Rapid ( monitoring tool gives cardiac output) is as equivalent in determining the hemodynamic assessment in cardiac surgical scenarios as the most often used pulmonary artery catheter, which is much more invasive than the Lidco Rapid. This will be accomplished through online surveys which have different cardiac surgery scenarios and will be distributed to cardiac fellowship trained anesthesiologists. The online based survey will include a specific scenario and details on the scenario represented in image format and a brief description of the patient to aid with their analysis of the situation.

Condition or Disease Intervention/Treatment Phase
  • Device: LIDCO Rapid, Pulmonary artery catheter

Detailed Description

Data from PA catheter such as PA pressure, pulmonary wedge pressure and cardiac output has been widely used in the various clinical situations warranting advance hemodynamic monitoring. It is considered as gold standard but unfortunately there is always risk associated with PA catheter and time lag between the clinical events and interpretation. Lidco Rapid is one of the non-invasive hemodynamic tools to measure various parameters. It is widely used in the intensive care set up for goal directed therapy but unfortunately there is not enough data to show whether it is useful in various peri-operative clinical conditions. In the online based survey, responses from the participants are recorded in the nominal scale ( 1 to 5 where 3 represents near normal). This survey will help to determine whether Investigators can replace the Lidco in any clinical situation warranting advance hemodynamic monitoring.

No previous study was done to specifically find out the hemodynamic component that differs between these tools intraoperatively in varying hemodynamic conditions during cardiac surgery although there were few studies compared the trend in the cardiac output with difference in opinion on their accuracy.

Study Design

Study Type:
Observational
Actual Enrollment :
64 participants
Time Perspective:
Prospective
Official Title:
Comparative Hemodynamic Assessment Between Lidco Rapid and Pulmonary Artery Thermodilution
Study Start Date :
Aug 1, 2015
Actual Primary Completion Date :
May 1, 2016
Actual Study Completion Date :
May 1, 2016

Outcome Measures

Primary Outcome Measures

  1. To expect difference is within 1 unit ( scale of 1 to 5) in the hemodynamic assessment preferably preload , afterload and contractility between Lidco and data from PA catheter in different cardiac surgical patient scenarios. [intraoperative]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Must be a certified Anesthesiologist with cardiac fellowship training
Exclusion Criteria:
  • none

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Iowa

Investigators

  • Principal Investigator: Sudhakar Subramani, M.D., University of Iowa

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Sudhakar Subramani, M.D., University of Iowa
ClinicalTrials.gov Identifier:
NCT02529033
Other Study ID Numbers:
  • 201504777
First Posted:
Aug 19, 2015
Last Update Posted:
Oct 25, 2016
Last Verified:
Oct 1, 2016
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 25, 2016