Does Use of Ultrasound Reduce the Rate of Sham Caudal Block in Children
研究概览
详细说明
Caudal blocks are one of the most commonly performed regional anesthetics in children and are performed daily for a host of infra-umbilical surgical procedures. A caudal block is an epidural injection, most commonly of local anesthetic into the epidural space as accessed via the sacral hiatus. In children, the sacral hiatus is a normally occurring aperture in which the epidural space may be accessed with extremely minimal risk; as neural tissue ends more proximally. Due to this measure of safety, caudal blocks are preferred in children when compared with standard lumbar epidurals. Caudal blocks are performed blindly using palpation and tactile feedback to assess if the medication is being administered in the correct location. As a result of blind injection, administration of local anesthetic totally or partially outside of the correct site can often be unnoticed or identified after a significant volume has already been injected. With the potential for toxicity of local anesthetic, this may result in either the inability to give a complete dose or an unintentional and often unnoticed sham block "incorrect site of injection".
Use of ultrasound has been proposed for identification of caudal block placement and correct medication spread. However, a recent review of the Pediatric Regional Anesthesia Network database reveals that ultrasound is reportedly only used in less that 3% of blocks. The benefit of ultrasound is safe and real-time confirmation of injection. Ultrasound allows the provider to determine with minimal local anesthetic or even saline injection if the correct space is accessed. Without ultrasound, failed blocks are either identified after significant percentage of the total dose of local anesthetic is incorrectly administered or intra or post operatively when the patient demonstrates a significant opioid requirement. This is problematic given that one of the primary benefits of a caudal block in children is the ability to avoid opioids.
Review of local practice here at Texas Children's Hospital for quality improvement purposes revealed a failure rate of caudal blocks to be 18%. Failure was defined as a heart rate increase with incision of >20% despite a caudal block and >1MAC of gas for the patient age. These patients all required opioids both intra and post operatively in addition to surgical levels of inhaled anesthetic agent.
研究类型
阶段
- 不适用
联系人和位置
学习地点
-
-
Texas
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Houston、Texas、美国、77030
- Texas Childrens Hospital
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Children ages 0-84 months
- Infra-umbilical procedure for which a caudal block is already planned
- American Society of Anesthesiology classifications of 1,2 or 3
Exclusion Criteria:
- Incarcerated hernias
- Emergency procedures
- Local Anesthetic allergy
- Sacral dimple
- Rash over sacrum
- Parents/legal guardians unable to consent for surgical procedure in English language Foster Care/Child protective services as guardians
- Parental Refusal for caudal block or study participation
- American Society of Anesthesiology classifications other than 1,2 or 3
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Ultrasound
The attending anesthesiologist will perform or instruct the placement of a caudal block according to their standard of practice. At the time of administration of local anesthetic into the caudal space, the study collaborator (SC) will ultrasound the caudal space keeping the provider placing the block blinded to the imaging. The provider placing the block will inject 0.5mL of saline. The provider will then be asked to state if they are correctly in the caudal space or not. If the provider feels they are not in the caudal space, they will re-do the procedure. If the provider fails to identify incorrect location and this is noted by ultrasound, the SC will inform the provider to re-do the procedure. All study participants will have ultrasound used for caudal block. |
The attending anesthesiologist will perform or instruct the placement of a caudal block according to their standard of practice.
At the time of administration of local anesthetic into the caudal space, the study collaborator (SC) will ultrasound the caudal space keeping the provider placing the block blinded to the imaging.
The provider placing the block will inject 0.5mL of preservative free saline.
The provider will then be asked to state if they are correctly in the caudal space or not.
If the provider feels they are not in the caudal space, they will re-do the procedure.
If the provider fails to identify incorrect location and this is noted by ultrasound, the SC will inform the provider to re-do the procedure
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Identify the rate at which blindly placed caudal blocks are not within the epidural space
大体时间:15 minutes
|
Assess the percentage of providers not recognizing wrong site of injection without ultrasound
|
15 minutes
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Identify the rate at which ultrasound can guide a wrong block into the correct location
大体时间:15 minutes
|
Assess the number of blocks that are require the use of ultrasound to redirect needle into caudal space
|
15 minutes
|
|
Identify if lack of heart rate change on incision can predict successful placement when medication administration is successfully confirmed with ultrasound
大体时间:15 minutes
|
With ultrasound identification of correct caudal injection, (successful block), does lack of heart rate change correlated with successful block
|
15 minutes
|
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Identify if after using ultrasound to visualize placement, if concentrations of inhaled agents may be reduced in children
大体时间:30 minutes to 3 hours
|
With demonstration of successful caudal injection, can inhaled agent concentration be reduced as calculated by MAC hours
|
30 minutes to 3 hours
|
合作者和调查者
调查人员
- 首席研究员:Adam C Adler, MD, FAAP、Texas Childrens Hospital
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- H-40844
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
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