The Winnipeg Intraspinal Pressure Monitoring Study (WISP): A protocol for validation of fiberoptic pressure monitoring for acute traumatic spinal cord injury

被引:3
作者
Dhaliwal, Perry [1 ]
Wilkinson, Marshall [2 ]
Zeiler, Frederick A. [1 ,3 ,4 ,5 ,6 ]
机构
[1] Rady Fac Hlth Sci, Dept Surg, Sect Neurosurg, Winnipeg, MB, Canada
[2] Shared Hlth Manitoba, Hlth Sci Ctr, Winnipeg, MB, Canada
[3] Rady Fac Hlth Sci, Dept Human Anat & Cell Sci, Winnipeg, MB, Canada
[4] Univ Cambridge, Dept Med, Div Anaesthesia, Cambridge, England
[5] Fac Engn, Biomed Engn, Winnipeg, MB, Canada
[6] Univ Manitoba, Ctr Aging, Winnipeg, MB, Canada
基金
加拿大创新基金会; 美国国家卫生研究院; 加拿大健康研究院;
关键词
PERFUSION-PRESSURE;
D O I
10.1371/journal.pone.0263499
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Research efforts have been focused on limiting secondary injury after traumatic spinal cord injury by performing spinal decompression and early optimization of spinal cord perfusion. The Winnipeg Intraspinal Pressure Monitoring Study (WISP) was designed to validate the technique of intraspinal pressure monitoring at the site of injury using a fiberoptic pressure monitor placed at the site of injury. Objectives To describe the design of the WISP study. Study design Descriptive. Methods We explain the current limitations in the available scientific literature around the topic of blood pressure management for acute traumatic spinal cord injury and rational for the WISP study. Then, we describe the design of WISP including the patient selection criteria, study interventions, follow up schedules and outcome measurements. A multitude of future research avenues are also discussed. Results The WISP study is a single center pilot study designed to validate the technique of intraspinal pressure monitoring following acute traumatic spinal cord injury. The study involves the measurement of intraspinal pressure from within the subarachnoid space at the site of injury to derive a number of physiological parameters including spinal cord perfusion pressure, spinal cord blood volume, measures of spinal cord compliance and vascular reactivity indices. Twenty eligible patients will be recruited and followed for a period of 12 months with visits scheduled for the first 5 days and 1, 3, 6, and 12 months following surgical intervention. Conclusions The WISP study will provide the first attempt in North America at validation of intraspinal pressure monitoring with a fiberoptic pressure monitor at the site of injury. Successful validation will lead to future studies to define optimal spinal cord perfusion pressure, relationships of neural injury biomarkers and outcomes as well as epigenetic studies.
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页数:11
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