Hemorrhage Elimination During Lumbar Puncture Using Ultrasound Measurements (HELPUS) (HELP)
研究概览
详细说明
Lumbar puncture (LP) is a frequently performed procedure in pediatric emergency departments, most often to evaluate meningitis in hyperthermic, hypothermic, or ill-appearing neonates, infants and children. Older children often present with headaches, meningismus, and/or altered mental status.
The risks of LP include introduction of pathogens, pain, the need for multiple attempts, and failure to obtain interpretable CSF. The latter frequently leads to a spine ultrasound study the following day and, if this does not demonstrate an epidural blood clot, repeat lumbar puncture using fluoroscopic guidance by interventional radiologists.
In evaluating the management of infant sepsis, one study found that the success of the initial LP plays a significant role: infants with unsuccessful initial LPs have longer hospital stays and require more resources. Therefore, ensuring successful LPs on the first attempt is critical for minimizing healthcare utilization, optimizing patient care, and decreasing the emotional burden of this procedure on parents and patients.
Unfortunately, epidural hematoma (EDH) is not uncommon after LP, with U/S diagnosed EDH identified among 40% of patients < 6 months with a traumatic LP and among 31% of unsuccessful but nontraumatic LP's, with complete effacement of the thecal sac in 17%. The spinal canal is wide enough to accommodate EDH with only rare sequelae. However, intramedullary hemorrhage of the conus medullaris resulting in paraplegia in a neonate has been reported.
Since the introduction of the revised febrile neonate guidelines in 2021,4 the number of lumbar punctures performed in young infants has decreased substantially. A consequence of performing fewer lumbar punctures is that clinicians-particularly trainees and early-career practitioners-have fewer opportunities to maintain procedural competence. As procedural skill and confidence decline, the risk of obtaining non-interpretable or traumatic samples increases.
Clearly, improvement of the traditional approach to LP in neonates and infants and young children is needed to prevent these complications. Ultrasound is an imaging modality that is frequently used in the emergency department and does not involve ionizing radiation. Ultrasound can be used prior to lumbar punctures to identify critical anatomical landmarks and needle-insertion distances to avoid the posterior epidural venous plexus and to increase the proportion of LP's with non-traumatic, interpretable CSF. However, an ultrasound technique that is easily learned and that can be applied accurately and efficiently in the emergency department is lacking. Incorporating ultrasound (U/S) into LP training or performance may help clinicians who perform the procedure infrequently to improve success rates and obtain interpretable cerebrospinal fluid samples through identifying optimal intervertebral spaces, visualizing spinal anatomy, and guiding needle placement.
This study employs a standardized, ultrasound-assisted LP approach that integrates pre-procedural identification of spinal anatomy and measurement of the optimal needle insertion distance along the angled trajectory to potentially minimize traumatic taps. Unlike traditional LP methods, this approach provides objective, reproducible guidance that can be given and applied by clinicians. The study is novel in its prospective assessment of ultrasound-guided LP outcomes. By evaluating interpretable CSF yield, this research advances pediatric procedural methodology and has the potential to establish a new standard of care for LP in young infants.
The overarching aim of this research is to determine whether U/S-assisted LP increases the rate of interpretable CSF from the current, approximately 65% to at least 80%.
Primary Aim: To determine the extent to which ultrasound-assisted lumbar puncture using a standardized procedure, including use of ultrasound to ascertain the presence of cerebrospinal fluid (CSF) at L3 - L5 and the optimal needle insertion distance, increases the acquisition rate of CSF that is interpretable for patient management.
Hypothesis: The standardized, ultrasound-assisted procedure for lumbar puncture in neonates and infants is associated with yield of interpretable CSF of at least 85%.
A Sufficient U/S study includes visualization of the following with each reported by the proceduralist on the data report form:
- Lower lumbar and S1 spinous processes visualized
- S1 drop-off
- L4-5 and/or L3-5 interspaces visualized
- Presence of CSF sufficient for LP
- Cauda Equina
Inclusion of lumbar punctures for which U/S was not performed:
We will review and record the results of studies performed without U/S guidance, the technique used by clinicians not participating in this study provide a prospectively acquired control group with which to compare outcomes after U/S measurement. This data will be used in the multivariable regression models described below.
Use of Previously Obtained Ultrasound Images:
As part of this study, investigators may utilize ultrasound images that were obtained as part of routine clinical care prior to the performance of lumbar puncture. These ultrasound images will have been acquired independently of, and prior to, study enrollment and will not require any additional imaging procedures for research purposes. When used for research analysis, ultrasound images will be limited to those relevant to the study objectives. Images will be accessed only by authorized study personnel and will be de-identified prior to analysis whenever feasible. No additional risk to participants is anticipated as a result of using these previously obtained clinical images.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Donald H Arnold, MD, MPH
- 电话号码:615-936-4498
- 邮箱:don.arnold@vumc.org
学习地点
-
-
Tennessee
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Nashville、Tennessee、美国、37232
- 招聘中
- Vanderbilt University Medical Center
-
接触:
- Donald H Arnold, MD, MPH
- 电话号码:615-936-4498
- 邮箱:don.arnold@vumc.org
-
接触:
-
-
参与标准
资格标准
适合学习的年龄
- 孩子
接受健康志愿者
描述
Inclusion Criteria:
- - Neonates and infants (< 12 months)
- Hemodynamically stable
- Undergoing a lumbar puncture for diagnostic testing
Exclusion Criteria:
- - Infants > 12 months and 1 day
- Signs of clinical instability
- Known spinal anomalies (e.g., spina bifida, meningomyelocele) or previous spinal surgery
学习计划
研究是如何设计的?
设计细节
- 主要用途:诊断
- 分配:非随机化
- 介入模型:并行分配
- 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
Intervention: Ultrasound of spinal canal
|
Ultrasound of spinal canal without contrast.
We included the term "ultrasound contrast" because the choices were limited.
|
|
无干预:Control Group
Infants undergoing lumbar puncture without ultrasound assist
|
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 |
|---|---|---|
|
Successful LP rate
大体时间:Time from lumbar puncture to results of CSF returned by lab, approximately 1 hour.
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Acquisition of CSF sufficient for cell count, culture and meningoencephalitis PCR panel (MEP).
|
Time from lumbar puncture to results of CSF returned by lab, approximately 1 hour.
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Unsuccessful ultrasound attempt
大体时间:Immediately after intervention
|
Ultrasound attempt in which the ultrasound operator could not complete the study and, as a result, did not attempt to use ultrasound images to inform LP.
Potential causes include but are not limited to infant fussiness, inability to maintain positioning sufficient for ultrasound, and malfunction of the ultrasound machine.
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Immediately after intervention
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Traumatic LP rate
大体时间:Time from lumbar puncture to results of CSF returned by lab, approximately 1 hour
|
CSF RBC count > 500 cells/mm, the most widely accepted definition of traumatic LP. 10-12 The rate of traumatic LPs using this definition is 35 - 47% in neonates and 22 - 26% in infants (< 13 months).
|
Time from lumbar puncture to results of CSF returned by lab, approximately 1 hour
|
|
Number of attempts/ Number of Fluoroscopy-guided lumbar puncture (LP)
大体时间:Immediately after intervention
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Number of attempts required for CSF acquisition or need for fluoroscopy-guided LP
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Immediately after intervention
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
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
- IRB #251901 HELP Study
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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