N/A
N=150
Intraoperative Pathway in DIEP Flap Breast Reconstruction
Breast Cancer
Bottom Line
View on ClinicalTrials.gov: NCT00543764 ↗Enrolled (actual)
150
Serious AEs
0.0%
Results posted
Jul 2012
Primary outcome: Primary: Operative Time — 8.2; 6.9 hours
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- pathway (Other)
- Age
- Pediatric, Adult, Older Adult
- Sex
- Female
- Sponsor
- Beth Israel Deaconess Medical Center
- Primary completion
- Dec 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Operative Time |
8.2; 6.9 | — |
Summary
Efficiency in the operating room can be difficult in long cases with multiple surgeons. We used a team based approach to develop an intraoperative pathway for microsurgical breast reconstruction with a deep inferior epigastric perforator flap.
Eligibility Criteria
Inclusion Criteria
- All cases prior to pathway
Exclusion Criteria
- None
Data sourced from ClinicalTrials.gov (NCT00543764). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.