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


N/A
18 Years
75 Years
Open (Enrolling by invite only)
Female
Breast Diseases

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Trial Information

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


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.


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

- BMI>35

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

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

Outcome Description:

The patient will be met with by the study coordinator, just before discharge to administer the Quality of Recovery Questionnaire (QoR27)

Outcome Time Frame:

On average between 18 and 24 hours postoperatively

Safety Issue:

No

Principal Investigator

John L Semple, MD, MSc, FRCSC, FACS

Investigator Role:

Principal Investigator

Investigator Affiliation:

Women's College Hospital

Authority:

Canada: Ethics Review Committee

Study ID:

2010-0050-E

NCT ID:

NCT01438268

Start Date:

July 2011

Completion Date:

December 2012

Related Keywords:

  • Breast Diseases
  • Breast Diseases

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