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Real-Time Assessment of Spinal Cord Microperfusion in a Porcine Model of Ischemia/Reperfusion
Published on: December 10, 2020
Echo-guided identification of key lumbar arteries for the spinal cord: preliminary study in the canine model
Kazumasa Orihashi1, Hajime Kumagai, Mitsuhiro Isaka
1Department of Surgery, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima 734-8551, Japan.
Insights
Identifying critical spinal cord arteries is vital to prevent paralysis during thoracoabdominal aortic surgery. This study shows echocardiography with lumbar artery saline injection is a feasible method for accurate artery identification in a canine model.
Area of Science:
- Vascular Surgery
- Interventional Radiology
- Surgical Anatomy
Background:
- Accurate identification of the artery of Adamkiewicz (or key spinal artery) is crucial to prevent paraplegia during thoracoabdominal aortic surgery.
- Current methods for identifying this artery are often complex or lack reliability.
Purpose of the Study:
- To evaluate the feasibility and adequacy of a novel echocardiography-guided method using saline injection into lumbar arteries for identifying the key spinal cord perfusor.
- To assess the accuracy of this technique in a canine model.
Main Methods:
- The abdominal aorta was accessed in canine models.
- Saline was injected into lumbar arteries while visualizing the spinal cord via echocardiography through the intervertebral disc.
- Lumbar arteries were classified as "positive" (echogenic/Doppler signal detected in spinal cord) or "negative" (no signal).
- Post-mortem resin injection (red for positive, blue for negative) confirmed artery perfusion.
Main Results:
- The echo-guided method correctly identified key arteries supplying the spinal cord in the canine model.
- "Positive" arteries, primarily on the left, accounted for about one-third of lumbar arteries and perfused the spinal cord.
- "Negative" arteries primarily supplied paravertebral muscles.
- Evidence of collateral circulation was observed among "positive" arteries, independent of "negative" arteries.
Conclusions:
- Echocardiography-guided identification of key spinal arteries using lumbar artery saline injection is technically feasible.
- This preliminary canine study demonstrates the technique's accuracy in determining critical spinal cord perfusion.
- This method holds potential as a reliable, non-complicated approach for pre-operative surgical planning.
Abstract:
Although identification of the key artery that perfuses the spinal cord is essential to avoid occurrence of paraplegia after surgery on the thoracoabdominal aorta, reliable and noncomplicated measures are not yet available. A new method of determining it by using echocardiography with a saline injection into the lumbar artery was evaluated for feasibility and adequacy in a canine model. In two mongrel dogs, the abdominal aorta was opened and saline was directly injected into the lumbar arteries while the spinal cord was visualized by echocardiography through the intervertebral disc. When the echogenic or Doppler signal was detected in the spinal cord, the particular lumbar artery was determined as "positive", or as "negative" when the signal was not detected. After the dog was sacrificed, red resin was injected into the "positive" arteries and blue resin into the "negative" arteries. In the extracted spinal cord, the anterior and posterior spinal arteries were filled with red resin, rather than with blue resin, to indicate that the key arteries were correctly identified. There were multiple "positive" arteries, which were mainly located on the left side and accounted for approximately one-third of the entire lumbar arteries. The "negative" arteries mainly perfused the muscles around the vertebra. Injected resin came out of the adjacent lumbar arteries of the same category, suggesting that communication is present among the positive arteries, but independently of that among the negative arteries. Echo-guided identification of key arteries is technically feasible and correctly determines the key arteries in this preliminary canine model.
