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临床试验/NCT03656679
NCT03656679终止不适用

A Comparison of the Paravertebral Block Versus Pectoralis Block in Controlling Bilateral Post-mastectomy Pain in Setting of Tissue Expander Placement

University of Wisconsin, Madison2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2018年10月18日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
18
试验地点
2
主要终点
Total Opioid Consumption

研究概览

简要总结

Post-mastectomy pain affects more than half of patients undergoing the procedure and can last for years. It has been well established that development of chronic pain is related to experienced pain in the perioperative period. This study therefore aims to assess if both acute and chronic post-operative mastectomy pain can be better managed by a novel regional anesthesia nerve block known as the pectoralis block (PECs). The PECs block is easier for patients to position for placement, has less risk of harm to nearby structures, and less risk for systemic uptake of local anesthetic in comparison to the paravertebral block. The PECs block has a strong safety profile. Standard of care at University of Wisconsin (UW) hospital is to utilize regional anesthesia for post op pain management. While PVB is performed on a regular basis at UW per surgeon request, Surgeon can request for PECS block in patients where a PVB was contraindicated (ie. coagulation issues). PECS is in fact the standard of care at other hospitals. This study will assess outcomes in the post anesthetic care unit (PACU), post-operative day 1, 7 and 30.

详细描述

Post-mastectomy pain occurs in up to 55% of patients and can last for months. The development of chronic pain is related to experienced perioperative pain. The development of chronic pain is related to experienced perioperative pain. There is great potential to enhance the quality of life for breast surgery patients if the hospital can improve our perioperative pain prevention techniques. New to the spectrum of multimodal analgesia is the pectoralis block (PECs), which provides anesthesia to the anterior and anterior lateral chest wall as well to the axilla. This study is about aims to compare the pectoralis block to paravertebral block with benefits of ease placement, less risk for harm to nearby structures including pneumothorax, spinal cord trauma, sympathetic block and hypotension.

Literature reveals that the pectoralis block has provided improved pain scores as well as decreases post-operative nausea and vomiting, longer block duration, and subsequent pain relief in patient. Despite these promising preliminary studies, there remains a paucity on the effectiveness of the PECs Block, particularly regarding long term outcomes for patients.

Furthermore, there is no literature to date which has evaluated the best regional anesthetic technique for patients who receive breast tissue expanders, which can cause a significant amount of muscle pain and spasm due to the intended muscle disruption during surgical placement. The primary outcomes of this study is to compare total opioid consumption during the post-surgical period limited to 24 hrs beginning at PACU admission between patients who receive bilateral pectoralis plane versus bilateral paravertebral blocks and subsequently undergo bilateral mastectomy with tissue expanders.

The secondary outcomes includes post-operative pain scores on PACU arrival and discharge, post-operative days (POD) 1, 7, and 30, presence/absence of axillary pain, muscle relaxant consumption, presence of severity of muscle spasm, total antiemetic consumption 24-hrs beginning at PACU admission, presence of chronic opioid use (Defined as consumption at 30 days), time to perform block, and PACU duration.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

Assessor will be provided with de-identified data for analysis

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • The clinical decision has been made that the patient will have a bilateral mastectomy with tissue expander placement
  • The participant is ≥ 18 years and ≤ 80 years
  • Weight ≥ 60 kg and ≤ 90 kg
  • The participant's primary anesthesia care team has planned for general anesthesia
  • The participant agrees to receive a regional block
  • American Society of Anesthesiologists class 1-3

排除标准

  • 18 years of age or >80 years of age
  • < 60 kg or > 90 kg
  • Non-English speaking
  • Known or believed to be pregnant
  • Participant is a prisoner
  • Participant has impaired decision-making capacity per discretion of the Investigator
  • Standard contraindications to regional blocks (coagulopathy including abnormal INR after discontinuation of warfarin, baseline INR (international normalized ratio) >1.5, platelets <100,000, elevated PTT (prothrombin time), failure to discontinue anticoagulant medication, or infection at site)
  • Significant renal, cardiac or hepatic disease per discretion of the investigator
  • A clinical decision made that indicates need for a partial or complete axillary node dissection
  • American Society of Anesthesiologists class 4-5
  • Known hypersensitivity and/or allergies to local anesthetics
  • Chronic Opioid Use (daily or almost daily use of opioids for > 3 months)
  • Participant refusal

结局指标

主要结局

Total Opioid Consumption

时间窗: 24 hours

Primary outcome will be total opioid consumption in 24 hours for Paravertebral Nerve Block vs. Pectoralis Nerve Block.

次要结局

  • time to perform the block(4 hours)
  • Pain score(30 days)
  • Opioid consumption at POD 7 and 30(30 days)
  • Total muscle relaxant consumption(30 days)
  • Total antiemetic consumption(48 hours)
  • Presence and severity of muscle spasm(30 days)
  • Time in PACU and hospital duration(48 hours)
  • Location of most severe pain(30 days)
  • Presence or absence of axillary pain(30 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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