TEE and Dysphagia in Lung Transplantation

Sponsor
University of California, Los Angeles (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06089434
Collaborator
(none)
116
1
2
24
4.8

Study Details

Study Description

Brief Summary

The primary outcome of this study is dysphagia (difficulty swallowing) on postoperative speech and swallow evaluation following lung transplantation.

Transesophageal echocardiography (TEE) (creates pictures of the heart from inside the participants body) is routinely performed for all lung transplantations at the University of California, Los Angeles (UCLA) and it is the standard of care. Patients are randomized to two groups. The intervention group would limit the number of TEE clips (# pictures taken) per case. The control group would leave the number of TEE clips to the discretion of the attending anesthesiologist.

The investigators hypothesize that reduction in TEE imaging during lung transplantation will reduce dysphagia.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Transesophageal Echocardiography (TEE) with limited number of TEE clips
  • Diagnostic Test: Transesophageal Echocardiography (TEE) with number of TEE clips per attending anesthesiologist
N/A

Detailed Description

Dysphagia is a common complication after cardiac surgery and specifically after lung transplantation. The incidence of dysphagia after lung transplantation is approximately 40-50%. Dysphagia after cardiac surgery leads to a significant increase in mortality, morbidity, cost, and length of stay. There are several risk factors that have been identified retrospectively including patient comorbidities, length of surgery, length of intubation, and number of TEE clips obtained during surgery. Many of these risk factors are not modifiable, however, the number of TEE clips obtained is a potential area for intervention. Retrospective studies demonstrate that a high number of TEE clips may be associated with dysphagia postoperatively. TEE should not be completely eliminated from these procedures because it adds value for patient management and the diagnosis of intraoperative complications.

This is a prospective, cluster randomized study for adult patients undergoing single and double lung transplantation. Groups will be randomized by month. The primary outcome of the study is dysphagia on postoperative speech and swallow evaluation.

TEE is routinely performed for all lung transplantation at UCLA and it is the standard of care. Patients would be randomized to two groups. The intervention group would be limited to fewer than 20 TEE clips per case. The control group would leave the number of TEE clips to the discretion of the attending anesthesiologist (average ~80-100 TEE clips per case). The current standard of care is to leave the number of TEE clips to the discretion of the attending anesthesiologist (the control arm). The attending anesthesiologist has the ability to obtain more TEE clips in the intervention arm if they feel it will be beneficial to patient care.

The postoperative speech and swallow evaluation is standard of care for all lung transplant recipients and would be done regardless of participation in the study. This is a bedside evaluation done by a speech/language therapist after the patient has been extubated, usually performed on postoperative day (POD) 1.

Data will also be collected and recorded from the medical record.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
116 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Transesophageal Echocardiography (TEE) and Dysphagia in Lung Transplantation (LT)
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
Oct 1, 2025
Anticipated Study Completion Date :
Nov 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Transesophageal Echocardiography (TEE) with limited number of TEE clips

The intervention group would limit the number of TEE clips per case.

Diagnostic Test: Transesophageal Echocardiography (TEE) with limited number of TEE clips
The intervention group would be limited to fewer than 20 TEE clips per case (versus the average of ~ 80-100 TEE clips per case).

Other: Transesophageal Echocardiography (TEE) with number of TEE clips per attending anesthesiologist

The control group would leave the number of TEE clips to the discretion of the attending anesthesiologist.

Diagnostic Test: Transesophageal Echocardiography (TEE) with number of TEE clips per attending anesthesiologist
The control group would leave the number of TEE clips to the discretion of the attending anesthesiologist.

Outcome Measures

Primary Outcome Measures

  1. Number of participants with dysphagia [POD1]

    Dysphagia on the postoperative speech and swallow evaluation. Dysphagia is classified into 3 major classifications: swallowing without limitations, swallowing with limitations, and inability to swallow.

Secondary Outcome Measures

  1. Mortality [POD0 until discharge from the hospital. An average of 5-10 days until discharge from the hospital. A maximum of 30 days for in-hospital mortality.]

    In-hospital mortality

  2. Length of Intubation [From time of intubation until time to extubation, in hours, on average POD0 or POD1.]

    Number of hours intubated from POD0 to extubation.

  3. Length of intensive care unit (ICU) Stay [From time of admission to the ICU (POD0) until discharge from the ICU. An average of 3-5 days.]

    Number of days in the ICU from POD0 to discharge from the ICU.

  4. Length of Hospital Stay [From time of admission to the ICU (POD0) until discharge from the hospital, An average of 5-10 days.]

    Number of days in the hospital from POD0 to discharge from the hospital.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Adult patients

  2. Single or double lung transplantation

Exclusion Criteria:
  1. Contraindications to TEE including:
  • perforated esophagus;

  • esophageal stricture;

  • esophageal tumor; and

  • history of an esophagectomy

  1. Patients that require a tracheostomy postoperatively.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ronald Reagan UCLA Medical Center, Department of Anesthesiology & Perioperative Medicine Los Angeles California United States 90095

Sponsors and Collaborators

  • University of California, Los Angeles

Investigators

  • Principal Investigator: J.Prince Neelankavil, MD, University of California, Los Angeles

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jacques Neelankavil, Principal Investigator and Professor of Clinical Anesthesiology, University of California, Los Angeles
ClinicalTrials.gov Identifier:
NCT06089434
Other Study ID Numbers:
  • 23-000600
First Posted:
Oct 18, 2023
Last Update Posted:
Oct 18, 2023
Last Verified:
Oct 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jacques Neelankavil, Principal Investigator and Professor of Clinical Anesthesiology, University of California, Los Angeles
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 18, 2023