Side Effects of Transesophageal Echocardiography

Sponsor
Medical University of Vienna (Other)
Overall Status
Completed
CT.gov ID
NCT03432559
Collaborator
(none)
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Study Details

Study Description

Brief Summary

Transesophageal echocardiography is commonly used during cardiac surgery. Complications of transesophageal echocardiography are rare (1,2%), but are often underestimated and can lead to unrecognized blood loss and site of infection.

This study wants to assess the mucosa of pharynx, upper larynx, esophagus and stomach prior to and after echo probe insertion during cardiac surgery with endoscopy.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: endoscopy
N/A

Detailed Description

Transesophageal echocardiography is commonly used during cardiac surgery. Main reasons for its use are the evaluation of cardiac function and valve morphology previous to and after cardiac surgery.

Complications of transesophageal echocardiography are rare (1,2%). Described complications may involve the gastrointestinal, cardiovascular or respiratory system.

The major complication of transesophageal echocardiography is local injury of the GI tract. Only massive bleeding and perforation were reported, minor injuries are not noticed in the early postoperative period but may play an important role, especially in patients discomfort, source of minor unrecognized blood loss and site of infection. As oropharyngeal bacteria are known to cause endocarditis and graft infection, this site of infection may be of special interest in cardiac surgery.

Study objectives:

To assess the mucosa of pharynx, upper larynx, esophagus and stomach prior to and after TEE probe insertion during cardiac surgery using flexible endoscopy.

Design:

Open, not randomized, observer blinded, pilot study. Inclusion criteria

  • Planned cardiac surgery

  • Age above 18 years

  • Signed informed consent

  • Clinical need for intraoperative use of transesophageal echocardiography Exclusion criteria

  • Recent gastrointestinal pathologies (3-6 months)

  • Recent operations of the upper gastrointestinal tract (3-6 months)

  • Subjects not able to understand study procedures

  • No signed informed consent

  • Contraindications for transesophageal echocardiography

After induction of anesthesia and insertion of all needed catheters (arterial catheter, central venous catheter, bladder catheter, and pulmonary artery catheter, if indicated) an expert physician will perform the endoscopy (Olympus; Hamburg, Germany) of pharynx, esophagus, and stomach in order to exclude (respectively map) any alteration of the mucosa.

Immediately after endoscopy the transesophageal probe (6T, 6T-RS, 6Tc, 6Tc-RS Vivid GE; USA; X7-2T, S7-2omni, Philips), covered with a special condom, will be inserted. The TOE probe will remain 7-8 hours in the GI tract.

Two standard echocardiographic examinations are routinely performed during cardiac operation; the first (prior to skin incision) is assigned as baseline evaluation of cardiac morphology and function; the second (after weaning from cardiopulmonary bypass) is performed to check the result of the surgical procedure respectively to determine cardiac function for decision-making of medical treatment. A routine TEE - examination follows guidelines for standard TEE views and examination workflow and includes a minimum of 11 views up to a maximum of 28 views, depending on the type of pathology. Average time needed to perform a standard TEE examination varies from 5-15minutes.

For these reasons the number of TEE views per examination, the length of each examination, and the different probe positions (upper esophageal, mid esophageal, transgastric and deep transgastric) during examination and the length of stay of the probe in each position will be reported. As soon as the TEE probe has been removed the second endoscopy it will be performed in the same order as the baseline endoscopy.

Possible lesions of the mucosa will be classified as described by Geene et al. (Greene 1999, #9) as follows: erythema, edema, hematoma, mucosal erosion, petechiae, and perforation. In particular pharynx, upper esophagus, mid esophagus, cardia, gastric fundus, und gastric body will be examined.

The analysis of filmed examination will be performed by the endoscopist in a second time off-line, in a blind manner.

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
endoscopy of pharynx, upper esophagus, mid esophagus, cardia, gastric fundus, and gastric bodyendoscopy of pharynx, upper esophagus, mid esophagus, cardia, gastric fundus, and gastric body
Masking:
None (Open Label)
Masking Description:
the investigator doing the transesophageal examination will not be informed about the results of the endoscopy
Primary Purpose:
Diagnostic
Official Title:
Local Side Effects of Transesophageal Echocardiography
Actual Study Start Date :
Jul 1, 2009
Actual Primary Completion Date :
Mar 31, 2010
Actual Study Completion Date :
Jan 31, 2018

Arms and Interventions

Arm Intervention/Treatment
Other: endoscopy

endoscopy of the upper GI tract

Diagnostic Test: endoscopy
endoscopy of pharynx, upper esophagus, mid esophagus, cardia, gastric fundus, und gastric body

Outcome Measures

Primary Outcome Measures

  1. incidence of endoscopic mild mucosal injury [7-8 hours]

    erythema, edema, hematoma, mucosal erosion, petechiae, or perforation of the upper GI mucosa

Secondary Outcome Measures

  1. length of examination [1 day]

    Duration of the actual TEE examination

  2. incidence of postoperative complications [up to 1 week]

    GI bleeding, Perforation, swallowing difficulties

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Planned cardiac surgery

  • Age above 18 years

  • Signed informed consent

  • Clinical need for intraoperative use of transesophageal echocardiography

Exclusion Criteria:
  • Recent gastrointestinal pathologies (3-6 months)

  • Recent operations of the upper gastrointestinal tract (3-6 months)

  • Subjects not able to understand study procedures

  • No signed informed consent

  • Contraindications for transesophageal echocardiography

  • Antibiotic treatment within three months prior to surgery

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of Vienna Vienna Austria 1090

Sponsors and Collaborators

  • Medical University of Vienna

Investigators

  • Principal Investigator: Ulrike Weber, M.D.Ph.D., Medical University of Vienna

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ulrike Weber, Ass.Prof.Dr., Medical University of Vienna
ClinicalTrials.gov Identifier:
NCT03432559
Other Study ID Numbers:
  • 164/2009
First Posted:
Feb 14, 2018
Last Update Posted:
Feb 14, 2018
Last Verified:
Feb 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ulrike Weber, Ass.Prof.Dr., Medical University of Vienna
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 14, 2018