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Clinical Trials/NCT01438268
NCT01438268
Unknown
Not Applicable

Expedited Discharge of Patients Undergoing Pedicled TRAM Flap Breast Reconstruction Procedure in Ambulatory Surgical Facility: Quality of Recovery Outcomes

Women's College Hospital1 site in 1 country60 target enrollmentJuly 2011
ConditionsBreast Diseases

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Diseases
Sponsor
Women's College Hospital
Enrollment
60
Locations
1
Primary Endpoint
The primary outcome measure is the quality of recovery at discharge as assessed by the QoR27
Last Updated
12 years ago

Overview

Brief Summary

Specific Aim: To assess the quality of recovery of patients following early discharge (18 hrs) after pedicled TRAM flap breast reconstruction. Quality of recovery will be assessed using a 27-item validated questionnaire, QoR-27 at discharge, and on Post Operative Days (POD) 2, 4 and 7. In addition a 100 mm Visual Analog Score (VAS) for Pain will be completed on discharge from the recovery room, discharge from hospital and on POD 2, 4 and 7.

Clinical Relevance: Postoperative recovery is a complex process related to various outcomes such as physiological endpoints, incidence of adverse events and change in psychological status. Previous studies of recovery after surgery and anesthesia have focused primarily on the physiological endpoints and the incidence of adverse events. Much of the work has occurred in specialties dealing with chronic disease states such as cancer, rheumatology and musculoskeletal disorders. There is clearly a need to focus on recovery outcome measures in the ambulatory population for postoperative recovery. Here the investigators propose to measure postoperative recovery outcomes within the first week following a TRAM flap reconstructive procedure using a validated postoperative quality of recovery instrument (QoR-27) and a 100 mm VAS for pain.

Detailed Description

Women's College Hospital is the first and only independent ambulatory care hospital in Ontario, and the only hospital in Ontario with a primary focus on women's health. Patients undergoing breast reconstruction following breast cancer at our institution are now undergoing expedited discharge at 18 hrs postoperatively. To facilitate next day discharge, a multidisciplinary group was formed to determine the best evidence for perioperative care to ensure patient safety and excellent postoperative recovery. Minimizing length of stay has obvious cost savings for hospitals, but for patients the advantages include minimizing exposure to hospital-acquired infections and an earlier return to their more familiar home environment. The need to balance the advantage of early discharge to patient complications, however, must be addressed. As other hospitals across the country face the same length of stay constraints as has been our experience, this study will provide important data on the quality of recovery of patients undergoing early discharge following breast reconstructive surgery.

Registry
clinicaltrials.gov
Start Date
July 2011
End Date
January 2014
Last Updated
12 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Women undergoing any type of TRAM flap
  • Age\<75 yrs
  • Non-smoker

Exclusion Criteria

  • History of chronic pain or psychiatric disturbance
  • History of chronic use of opioid medications
  • Allergy to local anesthesia or opioid medication
  • Inability to communicate in English

Outcomes

Primary Outcomes

The primary outcome measure is the quality of recovery at discharge as assessed by the QoR27

Time Frame: On average 72-96 hours post operatively

The patient will be contacted by the study coordinator, 4 days following their surgery to administer the Quality of Recovery Questionnaire (QoR27)

The primary outcome measure is the quality of recovery post operatively, as assessed by the QoR27

Time Frame: on average between 48-72 hours postoperatively

The patient will be contacted by the study coordinator, 2 days following their surgery to administer the Quality of Recovery Questionnaire (QoR27)

The primary outcome measure is the quality of recovery post operatively as assessed by the QoR27

Time Frame: On average 7-8 days postoperatively

The patient will be contacted by the study coordinator, 7 days following their surgery to administer the Quality of Recovery Questionnaire (QoR27)

Secondary Outcomes

  • The secondary outcome measure is the quality of recovery as assessed by the VAS pain score(This outcome will be done at the exact same time as the measurements of Quality of Recovery listed above)

Study Sites (1)

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