Abstract

Introduction: We postulate a relationship between a transcutaneous hepatic NIRS measurement and a directly obtained hepatic vein saturation. If true, hepatic NIRS monitoring (in conjunction with the current dual-site cerebral-renal NIRS paradigm) might increase the sensitivity for detecting shock since regional oxygen delivery changes in the splanchnic circulation before the kidney or brain. We explored a reliable technique for hepatic NIRS monitoring as a prelude to rigorously testing this hypothesis. This proof-of-concept study aimed to validate hepatic NIRS monitoring by comparing hepatic NIRS measurements to direct hepatic vein samples obtained during cardiac catheterization.Method: IRB-approved prospective pilot study of hepatic NIRS monitoring involving 10 patients without liver disease who were already undergoing elective cardiac catheterization. We placed a NIRS monitor on the skin overlying liver during catheterization. Direct measurement of hepatic vein oxygen saturation during the case compared with simultaneous hepatic NIRS measurement.Results: There was no correlation between the Hepatic NIRS values and the directly measured hepatic vein saturation (R = −0.035; P = 0.9238). However, the Hepatic NIRS values correlated with the cardiac output (R = 0.808; P = 0.0047), the systolic arterial blood pressure (R = 0.739; P = 0.0146), and the diastolic arterial blood pressure (R = 0.7548; P = 0.0116).Conclusions: Using the technique described, hepatic NIRS does not correlate well with the hepatic vein saturation. Further optimization of the technique might provide a better measurement. Hepatic NIRS does correlate with cardiac output and thus may still provide a valuable additional piece of hemodynamic information when combined with other non-invasive monitoring.

Highlights

  • We postulate a relationship between a transcutaneous hepatic Near Infra-Red Spectroscopy (NIRS) measurement and a directly obtained hepatic vein saturation

  • Dual-site NIRS monitoring can be helpful during shock, when regional blood flow redistributes to maximize oxygen delivery to the brain and heart [5], because changes in local cardiac output to organs will likely result in changes in their measured tissue oxygenation

  • The Hepatic NIRS value was strongly correlated with the cardiac output (R = 0.808; P = 0.0047), the systolic arterial blood pressure (R = 0.739; P = 0.0146), and the diastolic arterial blood pressure (R = 0.7548; P = 0.0116), indicating that it may reflect systemic perfusion over a discrete range of blood pressure measurements Interestingly, Hepatic NIRS was related to the height (R = 0.772; P = 0.009), body surface area (R = 0.705; P = 0.023), and was borderline statistically significant for relationship to age at intervention (R = 0.632; P = 0.050)

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Summary

Introduction

We postulate a relationship between a transcutaneous hepatic NIRS measurement and a directly obtained hepatic vein saturation. Transcutaneous Near Infra-Red Spectroscopy (NIRS) technology allows for non-invasive, real-time monitoring of regional tissue oxygenation saturation (rS02). This technology has demonstrated utility in pediatric critical care, especially in the perioperative period, and many centers in the United States consider dual-site organ centric NIRS monitoring (brain and kidney) an important component of Intensive Care Unit (ICU) care [4]. Dual-site NIRS monitoring can be helpful during shock, when regional blood flow redistributes to maximize oxygen delivery to the brain and heart [5], because changes in local cardiac output to organs will likely result in changes in their measured tissue oxygenation. Dual-site NIRS monitoring provides an incomplete picture, since decreases to gut flow precede significant decreases to kidney or brain flow [5]

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