Key result
Patients with orthostatic intolerance but normal tilt table test results showed a significant delay in the return to cerebral homeostasis compared to healthy controls (383.5 vs 127.8 seconds, p=0.004).
Why the study?
Blood pressure and heart rate monitoring during head-up tilt table tests provide indirect measurements of cerebral perfusion that can lead to inaccurate evaluation of orthostatic intolerance.
Does cerebral perfusion monitoring using near-infrared spectroscopy during head-up tilt table test detect differences in cerebral hemodynamic changes between patients with orthostatic intolerance and healthy controls?
Cross-Sectional (n=42)
No
Does cerebral perfusion monitoring using near-infrared spectroscopy during head-up tilt table test detect differences in cerebral hemodynamic changes between patients with orthostatic intolerance and healthy controls?
Absolute Event Rate: 383.5% vs 127.8%
p-value: p=0.004
Near-infrared spectroscopy during head-up tilt table testing reveals that patients with orthostatic intolerance experience delayed recovery of cerebral oxygenation and blood volume compared to healthy controls, offering a direct measure of cerebral perfusion.
NIRS may enhance HUT sensitivity for cerebral hypoperfusion in OI; leaves open whether it should alter clinical protocols pending prospective trials.
The head-up tilt table test (HUT) is one of the primary clinical examinations for evaluating orthostatic intolerance (OI). HUT can be divided into three phases: dynamic tilt phase (supine to tilt up), static tilt phase (remain tilted at 70°), and post tilt phase (tilt down back to supine position). Commonly, blood pressure (BP) and heart rate (HR) are monitored to observe for OI symptoms, but are indirect measurements of cerebral perfusion and can lead to inaccurate HUT evaluation. In this study, we implemented a 108-channel near-infrared spectroscopy (NIRS) probe to characterize HUT performance by monitoring cerebral hemodynamic changes for healthy controls (HCs), OI patients with normal HUT results, and OI patients with positive HUT results: vasovagal syncope (VS), postural orthostatic tachycardia syndrome (POTS), orthostatic hypotension (OH), and orthostatic hypertension (OHT). By the end of the static tilt phase, OI patients typically did not show a complete recovery back to baseline cerebral oxygenation and total blood volume compared to HCs. We characterized the return to cerebral homeostasis by polynomial fitting total blood volume changes and determining the inflection point. The OI patients with normal HUT results, VS, OH, or OHT showed a delay in the return to cerebral homeostasis compared to the HC group during HUT.
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Kim et al. (2019) conducted a cross-sectional in Orthostatic Intolerance (n=42). Orthostatic intolerance vs. Healthy controls was evaluated on Inflection point of total hemoglobin (HbT) changes representing return to cerebral homeostasis (seconds after tilt up) (p=0.004). Patients with orthostatic intolerance but normal tilt table test results showed a significant delay in the return to cerebral homeostasis compared to healthy controls (383.5 vs 127.8 seconds, p=0.004).
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