Efficacy of Enhanced Recovery After Surgery Pathway for Total Mastectomy

NCT ID: NCT03181139

Last Updated: 2017-06-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

386 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-07-01

Study Completion Date

2016-04-30

Brief Summary

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Retrospective analysis of pre and post-Enhanced Recovery after Surgery for Total mastectomy pathway implementation.

Detailed Description

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Retrospective analysis of pre- and post-Enhanced Recovery after surgery for total mastectomy pathway implementation in patients at Mount Zion Hospital. We examined perioperative opioid consumption, pain scores, post-operative nausea and vomiting, benzodiazepine use, length of stay for the time period before and after implementation of an Enhanced Recovery after Surgery pathway for Total mastectomy. Pathway features included preoperative acetaminophen and gabapentin, minimizing opioids, postoperative NSAIDs, Pecs blocks, and aggressive postoperative nausea and vomiting prophylaxis.

Conditions

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Mastectomy Breast Cancer Female

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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pre-ERAS

Patients cared for prior to the implementation of the Enhanced Recovery after surgery for total mastectomy pathway

No interventions assigned to this group

post-ERAS

patients cared for after the implementation of the Enhanced Recovery after surgery for total mastectomy pathway. Pathway included preoperative acetaminophen and gabapentin, Pec blocks, multimodal analgesia postoperatively and aggressive PONV treatment.

ERAS pathway for Total Mastectomy

Intervention Type OTHER

Enhanced Recovery after Surgery (ERAS) pathway for Total Mastectomy

Interventions

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ERAS pathway for Total Mastectomy

Enhanced Recovery after Surgery (ERAS) pathway for Total Mastectomy

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* female patients at least 18 years old undergoing total skin sparing mastectomy at University of California San Francisco Mount Zion hospital

Exclusion Criteria

* patients undergoing concurrent bilateral salpingo-oophorectomy, flap reconstruction
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Mount Zion Health Fund

OTHER

Sponsor Role collaborator

Monica Harbell

OTHER

Sponsor Role lead

Responsible Party

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Monica Harbell

Assistant Professor

Responsibility Role SPONSOR_INVESTIGATOR

Other Identifiers

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ERASBreast

Identifier Type: -

Identifier Source: org_study_id

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