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Necessity of Using Pleural Drainage Tubes After IMA Harvesting During Cardiac Surgery

U

University of Calgary

Status

Completed

Conditions

Pleural Effusions Post Coronary Artery Bypass Graft

Treatments

Procedure: No Pleural Chest Tube

Study type

Interventional

Funder types

Other

Identifiers

NCT02147821
REB13-1374

Details and patient eligibility

About

This prospective randomized controlled trial will examine the efficacy of reducing the number of chest tubes used in the postoperative cardiac surgery patient. Typically used are three chest tubes - two in the mediastinum and one in the pleural space, if opened. The investigators propose that removal of the pleural tube will not impact the rates of clinically significant pleural effusions post cardiac surgery. Patients will be randomized into two groups - one receiving the standard three chest tubes (standard), and the other receiving only mediastinal drains (experimental). The primary outcome will be rates of post-operative pleural effusions as determined by defined interventions, including insertion of a chest tube, thoracentesis, or return to the operating room for primary evacuation of pleural effusion or hemothorax. Secondary outcomes include length of hospital stay, length of mechanical ventilation, postoperative respiratory status, and presence/size of pleural effusions, as well as readmission for pleural effusion.

Enrollment

162 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients must be undergoing CABG at our institution with the attempted harvest of a LIMA and/or RIMA
  • pleura must be entered in order for patients to be included.

Exclusion criteria

  • cardiac surgery where the pleura is not entered
  • previous surgery where the pleura was entered
  • other pre-existing pleural diseases or fibrosis
  • Patients currently participating in other studies
  • Patients presenting with emergent need for bypass

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Single Blind

162 participants in 2 patient groups

Standard
No Intervention group
Description:
Standard treatment will be defined as current practice whereby two mediastinal chest tubes are used for drainage, as well as an additional pleural tube if the pleura is opened during surgery. As part of current standard practice, the pleural and mediastinal spaces will be suctioned during the achievement of hemostasis prior to the insertion of chest tubes.
Intervention
Experimental group
Description:
The treatment arm of the study will involve standard placement of the mediastinal tubes with the exclusion of the pleural tube.
Treatment:
Procedure: No Pleural Chest Tube

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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