This is a prospective, randomized study evaluating the efficacy of bedside ultrasound assisted lumbar puncture in pediatric patients
Comparison of bedside ultrasound assisted lumbar puncture to traditional anatomical landmark approach in neonates and young infants requiring lumbar puncture
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
An investigator will perform beside ultrasound on the spinal area using a bedside ultrasound device. Attempts will be made to visualize the spinous processes and vertebral bodies in the general lumbarsacral area, as well as the presence of CSF in the thecal space below the conus medullaris, and identify the optimal location to perform the LP. This will be marked with a skin marker (If no CSF or abnormal anatomy is visualized, the LP will be advised to be postponed or cancelled). The treating physician will then proceed with the LP guided by the skin markings.
Advocate Christ Medical Center
Oak Lawn, Illinois, United States
Traumatic lumbar puncture
RBC\>10,000/ mm3 on spinal fluid analysis
Time frame: up to 24 hours
Unsuccessful lumbar puncture
failure to yield enough fluid for cerebrospinal fluid cell count as indicated by operator report on data collection sheet
Time frame: average of <1hour
Hospital length of stay
as reported in the subjects' medical record
Time frame: average of <7days
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