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Ann Vasc Surg ; 49: 191-205, 2018 May.
Article in English | MEDLINE | ID: mdl-29518504

ABSTRACT

BACKGROUND: Paraplegia due to spinal cord ischemia (SCI) is a serious complication after repair of thoracoabdominal aortic aneurysms. For prevention and early treatment of spinal ischemia, intraoperative monitoring of spinal cord integrity is essential. This study was intended to improve recognition of SCI through a combination of transcranial motor-evoked potentials (tc-MEPs), serum markers, and innovative breath analysis. METHODS: In 9 female German Landrace pigs, tc-MEPs were captured, markers of neuronal damage were determined in blood, and volatile organic compounds (VOCs) were analyzed in exhaled air. After thoraco-phrenico-laparotomy, SCI was initiated through sequential clamping (n = 4) or permanently ligating (n = 5) SAs of the abdominal and thoracic aorta in caudocranial orientation until a drop in the tc-MEPs to at least 25% of the baseline was recorded. VOCs in breath were determined by means of solid-phase microextraction coupled with gas chromatography-mass spectrometry. After waking up, clinical and neurological status was evaluated (Tarlov score). Spinal cord histology was obtained in postmortem. RESULTS: Permanent vessel ligature induced a worse neurological outcome and a higher number of necrotic motor neurons compared to clamping. Changes of serum markers remained unspecific. After laparotomy, exhaled acetone and isopropanol showed highest concentrations, and pentane and hexane increased during ischemia-reperfusion injury. CONCLUSIONS: To mimic spinal ischemia occurring in humans during aortic aneurysm repair, animal models have to be meticulously evaluated concerning vascular anatomy and function. Volatiles from breath indicated metabolic stress during surgery and oxidative damage through ischemia reperfusion. Breath VOCs may provide complimentary information to conventional monitoring methods.


Subject(s)
Aorta, Abdominal/surgery , Aorta, Thoracic/surgery , Biomarkers/blood , Breath Tests/methods , Evoked Potentials, Motor , Intraoperative Neurophysiological Monitoring/methods , Spinal Cord Ischemia/diagnosis , Volatile Organic Compounds/metabolism , Animals , Constriction , Disease Models, Animal , Female , Gas Chromatography-Mass Spectrometry , Ligation , Motor Neurons/metabolism , Motor Neurons/pathology , Oxidative Stress , Predictive Value of Tests , Solid Phase Microextraction , Spinal Cord Ischemia/blood , Spinal Cord Ischemia/etiology , Spinal Cord Ischemia/physiopathology , Sus scrofa , Time Factors
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