ESPBs vs TAPs for Pain Relief After Breast Reconstruction Surgery
Trial Summary
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. However, if you are using opioids regularly, you may not be eligible to participate.
What data supports the effectiveness of this treatment for pain relief after breast reconstruction surgery?
Research shows that both the erector spinae plane (ESP) block and the transversus abdominis plane (TAP) block are effective in reducing pain after various surgeries, including abdominal and breast surgeries. The ESP block, in particular, has been successfully used for pain control in breast surgery, which suggests it could be effective for breast reconstruction surgery as well.12345
Are ESPB and TAP blocks safe for humans?
How does the ESPB treatment differ from other treatments for pain relief after breast reconstruction surgery?
The erector spinae plane block (ESPB) is a newer regional anesthesia technique that is simpler and potentially safer than other methods like the paravertebral block, and it provides effective pain relief by targeting nerves in the back. This makes it unique compared to traditional pain relief methods, which may not offer the same ease of administration or safety profile.12356
What is the purpose of this trial?
Breast cancer is the second most common cancer diagnosed in American women . For patients who have undergone surgical mastectomy, autologous breast reconstruction is an alternative option to breast implants. Deep Inferior Epigastric Perforator (DIEP) flaps are the gold standard for autologous breast reconstruction . Effective pain control following surgery is imperative and ultrasound-guided bilateral transversus abdominis plane blocks (TAPs) with the infiltration of local anesthetics, such a bupivacaine are a common regional technique of choice . A newer described technique, bilateral Erector Spinae Plane blocks (ESPBs) (which also are an infiltration of local anesthetic) present as an alternative approach for post-operative analgesia. ESPBs have been proven efficacious in reducing intra- and post-operative opioid requirements, lessening the need for rescue analgesics in other similar surgical procedures.The hypothesis is that preoperative bilateral ESPBs could provide equivalent pain control as a regional analgesic for patients undergoing DIEP flap surgery when compared to preoperative bilateral TAPs
Eligibility Criteria
This trial is for adult women with breast cancer, who are in good to moderate health (ASA 1-3), and are scheduled for DIEP flap surgery. It's not open to those who regularly use opioids, have allergies to local anesthetics, or can't describe their pain level using a number scale.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive either Erector Spinae Plane blocks or Transversus Abdominis Plane blocks for post-operative analgesia following DIEP flap surgery
Follow-up
Participants are monitored for pain control and opioid requirements post-surgery
Treatment Details
Interventions
- Pre-operative Erector Spinae Plane block
- Pre-operative Transversus Abdominus Plane blocks
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Kansas Medical Center
Lead Sponsor