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Updated: Oct 19, 2025

Oxygenation-sensitive Cardiac MRI with Vasoactive Breathing Maneuvers for the Non-invasive Assessment of Coronary Microvascular Dysfunction
Published on: August 17, 2022
Association between tissue oxygenation and myocardial injury in patients undergoing major spine surgery: a
Katrine Feldballe Bernholm1,2, Christian S Meyhoff2,3,4, Philip Bickler5
1Department of Anesthesia and Perioperative Care, University of California, San Francisco, California, USA bernholm3@hotmail.com.
Objective:
To describe the association between intraoperative tissue oxygenation and postoperative troponin elevation in patients undergoing major spine surgery. We hypothesised that a decrease in intraoperative skeletal muscle tissue oxygenation (SmO2) was associated with the peak postoperative cardiac troponin value.
Design:
This is a prospective cohort study.
Setting:
Single-centre, University of California San Francisco Medical Center.
Participants:
Seventy adult patients undergoing major elective spine surgery.
Primary And Secondary Outcome Measures:
High-sensitivity troponin T (hsTnT) was measured in plasma preoperatively and on the first and second day after surgery to assess the primary outcome of peak postoperative hsTnT. Secondary outcomes included MINS and intensive care unit (ICU) admission within 30 days. Skeletal cerebral tissue oxygenation and SmO2 was measured continuously with near-infrared spectroscopy during surgery. The primary exposure variable was time-weighted area under the curve (TW AUC) for SmO2.
Results:
Mean age was 65 (33-85) years and 59% were female. No significant association was found between TW AUC for SmO2 and peak hsTnT (Spearman's correlation, rs=0.17, p=0.16). A total of 28 (40%) patients had MINS. ICU admission occurred in 14 (40%) in lower vs 25 (71%) in upper half of patients based on TW AUC for SmO2, p=0.008.
Conclusions:
Decrease in SmO2 was not a statistically significant predictor for peak troponin value following major spine surgery but is a potential predictor for other postoperative complications.
Trial Registration Number:
NCT03518372.
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