Clinical Trials Logo

Clinical Trial Summary

The pedicled latissimus dorsi flap is a piece of tissue taken from the back that is used to reconstruct the breast after cancerous tissue is removed. Over the years, improvements in surgical technique and pain control have decreased the length of stay in hospital after this procedure. Recently, early discharge after breast reconstruction using another very similar pedicled flap, called the transverse rectus abdominis flap, was shown to be safe, patient-centered, and associated with significant hospital cost-savings by another Canadian group.

With increasing pressure from hospital administrators to weigh financial considerations into treatment decision making, doctors must test cost-saving strategies in order to ensure patient satisfaction and safety. Here, we plan to evaluate patient safety, satisfaction and cost efficacy in breast reconstruction using the pedicled latissimus dorsi myocutaneous flap.

We hypothesize that patient care planning can allow for safe and cost-effective same-day discharge and improved patient satisfaction after autologous breast reconstruction using the pedicled latissimus dorsi flap. After nearly 10 successful same-day discharges using this flap, our experience at the Ottawa Hospital suggests that this practice is safe, has increased patient satisfaction scores, decreased narcotic use, no short or long term complications and is more cost effective compared to patients who stay overnight.

In the present study, we hope to quantify our results by demonstrating that same day discharge is a cost effective strategy that does not compromise patient safety and satisfaction.


Clinical Trial Description

The pedicled latissimus dorsi myocutaneous flap is a reliable option for autologous breast reconstruction after mastectomy. Improvements in technique and postoperative analgesia have decreased the length of hospital stay required after this procedure. Early discharge following a range of procedures has been consistently shown to increase patient satisfaction, decrease perioperative complication rates, and improve hospital cost-effectiveness. Specifically, early discharge after breast reconstruction using another pedicled myocutaneous flap, the transverse rectus abdominis myocutaneous flap, was shown to be safe, patient-centered, and associated with significant hospital cost-savings by another Canadian group.

The balance between financial savings and patient safety/comfort has been studied vigorously across many medical disciplines. With increasing pressure from hospital administrators to weigh financial considerations into treatment decision making, clinicians must empirically test cost-saving strategies in order to ensure patient satisfaction and safety.

Here, we evaluate patient safety, satisfaction and cost efficacy in ambulatory breast reconstruction using the pedicled latissimus dorsi myocutaneous flap. ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02791672
Study type Observational
Source Ottawa Hospital Research Institute
Contact Michael J Stein, MD
Phone 6132864646
Email micstein@toh.on.ca
Status Not yet recruiting
Phase N/A
Start date June 2016
Completion date June 2017

See also
  Status Clinical Trial Phase
Completed NCT04329819 - Satisfaction and QUality of Life After Breast REconstruction
Completed NCT04919317 - Combination Dexamethasone and Bupivacaine Pain Control in Reduction Mammaplasty Phase 2
Completed NCT03016663 - Volumetric Study of Fat Resorption After Breast Lipofilling N/A
Completed NCT00227084 - Effect of Arista Powder on Bleeding in Reductive Mammary Surgery Phase 2
Not yet recruiting NCT03240900 - Electrical Stimulation for Improving Postoperative Breast Sensation N/A
Recruiting NCT05171179 - The Use of Pecs Blocks in Combination With Exparel in Breast Reconstruction Surgery Phase 3
Terminated NCT00432328 - Juvista (Avotermin) in Breast Reduction Surgery Scars Phase 2
Active, not recruiting NCT04715802 - Options on the Breast Reconstruction Timing and Method After Removal of Polyacrylamide Hydrogel
Recruiting NCT03488888 - PEC Block II in Mammoplasty Surgeries N/A
Completed NCT03744273 - Capsule Biopsy in Acellular Dermal Matrix-based Prosthetic Breast Reconstruction: a Prospective Pilot Study N/A
Enrolling by invitation NCT03069885 - iNPWT in Immediate Breast Reconstruction N/A
Withdrawn NCT00310882 - Involvement of Endogenous Digitalis-like Compounds in Breast Cancer N/A
Recruiting NCT04891510 - A Comparative Analysis of REVOLVE, LipoGrafter, and Viality in Autologous Fat Grafting During Breast Surgery N/A
Recruiting NCT03118024 - Perioperative Management of DIEP Flaps N/A
Completed NCT04854525 - Breast Reconstruction in Previously Irradiated Breast
Completed NCT04783818 - Adjuvant Radiotherapy's Effect on One and Two Stages Prosthetic Breast Reconstruction and on Autologous Reconstruction
Not yet recruiting NCT06420323 - NovoX®Cup as Primary Dressing After Breast Reduction
Completed NCT04273464 - Breast Reconstruction With Autologous Tissue: Microsurgery or Fat Grafting? N/A
Completed NCT00616135 - Study of Autologous Fat Enhanced w/ Regenerative Cells Transplanted to Reconstruct Breast Deformities After Lumpectomy Phase 4
Completed NCT00466765 - Breast Reconstruction and Augmentation With Brava Enhanced Autologous Fat Micro Grafting N/A