Correlation between brain tissue oxygen tension and regional cerebral oximetry in uninjured human brain under conditions of changing ventilation strategy.

Controversy surrounds regional cerebral oximetry (rSO2) because extracranial contamination and unmeasured changes in cerebral arterial:venous ratio confound readings. Correlation of rSO2 with brain tissue oxygen (PbrO2), a "gold standard" for cerebral oxygenation, could help resolve this controversy but PbrO2 measurement is highly invasive. This was a prospective cohort study. The primary aim was to evaluate correlation between PbrO2 and rSO2 and the secondary aim was to investigate the relationship between changing ventilation regimens and measurement of PbrO2 and rSO2. Patients scheduled for elective removal of cerebral metastases were anesthetized with propofol and remifentanil, targeted to a BIS range 40-60. rSO2 was measured using the INVOS 5100B monitor and PbrO2 using the Licox brain monitoring system. The Licox probe was placed into an area of normal brain within the tumor excision corridor. FiO2 and minute ventilation were sequentially adjusted to achieve two set points: (1) FiO2 0.3 and paCO2 30 mmHg, (2) FiO2 1.0 and paCO2 40 mmHg. PbrO2 and rSO2 were recorded at each. Nine participants were included in the final analysis, which showed a positive Spearman's correlation (r = 0.50, p = 0.036) between PbrO2 and rSO2. From set point 1 to set point 2, PbrO2 increased from median 6.0, IQR 4.0-11.3 to median 22.5, IQR 9.8-43.6, p = 0.015; rSO2 increased from median 68.0, IQR 62.5-80.5 to median 83.0, IQR 74.0-90.0, p = 0.047. Correlation between PbrO2 and rSO2 is evident. Increasing FiO2 and PaCO2 results in significant increases in cerebral oxygenation measured by both monitors.

Introduction

Controversy surrounds the use of cerebral near infrared spectroscopy (NIRS) as a measure of true cerebral oxygenation because extracranial contamination has been demonstrated for cerebral oximeters from several manufacturers; saturation signals obtained from the scalp interfere with those obtained more exclusively from the brain [1]. Furthermore, cerebral arterial:venous ratio is assumed fixed within device software algorithms [2], thereby acting as an unmeasured confounder. Despite these concerns, cerebral oximetry is still used in multiple clinical settings [3]; decreases below an absolute measure of 50% or relative decreases of 20% appear to associate with cerebral ischemia [2] and low baseline values are associated with poor perioperative outcome [4].

The measurement of brain tissue oxygen (PbrO2) is used in routine neurosurgery [5] and has been shown to reliably demonstrate cerebral hypoxia following traumatic brain injury [6]. It is the most direct measure of cerebral oxygenation, but probe insertion is highly invasive and hence precludes use outside of the neurosurgical or neurocritical care setting. Correlation between rSO2 and jugular bulb monitoring has been demonstrated under conditions of varying inspired oxygen fraction (FiO2) in both uninjured [7] and injured human brain [8], but no study has been specifically designed to correlate PbrO2 (the most reliable) and rSO2 (the least invasive) as measures of cerebral oxygenation. Here, we test the hypothesis that PbrO2 and rSO2 correlate under conditions of varying FiO2 and partial pressure of carbon dioxide in arterial blood (PaCO2) in uninjured, human brain.

Methods

The primary aim of this prospective single center cohort study was to evaluate for correlation between PbrO2 and rSO2 under the conditions of varying FiO2 and PaCO2 in uninjured human brain. The secondary aim was to investigate the relationship between changing ventilation strategy with both PbrO2 and rSO2. The study was approved by the Institutional Review Board of the University of Michigan, Ann Arbor, prior to study initiation (HUM00105648, 1/14/2016) and registered with an appropriate clinical trials registry (ClinicalTrials.gov: NCT03128957, 25/4/2017). Following written informed consent, we recruited adult patients at Michigan Medicine who were scheduled for elective excision of secondary cerebral metastases under general anesthesia. Consent was obtained by a study team member during the surgical preoperative evaluation. Patients were excluded if they refused to give consent, required prone positioning, had clinical or radiological evidence of elevated intracranial pressure, coagulopathy, were taking therapeutic agents known to increase bleeding risk, a history of cardiovascular disease, cerebrovascular disease, suffered from respiratory failure, or were not fluent English speakers. Since skin pigmentation may impact rSO2 values [9] and the study was small, recruitment was limited to Caucasian patients. All patients were subject to the same two-step variation in ventilation strategy.

Following pre-oxygenation, anesthesia was induced using fentanyl (1-2mcg/kg) and propofol (0.5–2 mg/kg). Muscle relaxation was initiated and maintained as clinically indicated. The patient’s trachea was intubated, and their lungs ventilated to achieve an FiO2 and PaCO2 determined by the study protocol. General anesthesia was maintained by total intravenous anesthesia (TIVA) with a combination of propofol (80–150 mcg/kg/min) and remifentanil (0.05–0.1 mcg/kg/min) targeted to a Bispectral Index range 40–60 (BIS; Covidien, Boulder, CO).

Routine perioperative monitoring and invasive blood pressure monitoring was used for all patients. rSO2 was measured using the INVOS 5100B monitor (Somanetics Corporation, Troy, MI) and PbrO2 using the Licox brain tissue oxygen monitoring system (Integra LifeSciences Corporation, Plainsboro, NJ). BIS and rSO2 optodes were applied, before induction of anesthesia, by a single researcher on the patient’s forehead, as recommended by the manufacturer. Baseline rSO2 readings were recorded in the preoperative holding room with the patient sitting and breathing room air.

Licox probes are most typically placed and secured via a bolt inserted into the skull. Even with this highly invasive approach, the technique is reported to be safe [10], with hematoma as the main complication occurring in < 2% patients [11]. Here, a bolt was not used. The Licox probe was instead placed under direct vision into an area of normal brain within the future tumor excision corridor by the attending neurosurgeon, hence minimizing risk [5, 12, 13]. The probe was secured in place and allowed to equilibrate while maintaining close supervision of the surgical field to ensure that there was no undue edema or bleeding.

The starting tidal volume was set at 6–8 ml/kg and adjustments made by changing respiratory rate rather than tidal volume. During a pause in surgery, FiO2 and minute ventilation were sequentially adjusted to achieve the following pairs of ventilation set points:

FiO2 0.3 and PaCO2 30 mmHg

FiO2 1.0 and PaCO2 40 mmHg

Following a change in inspired gas composition, PaO2, PaCO2, PbrO2 and rSO2 were recorded at each set point, once both device readings had stabilized. Blood pressure, heart rate, hematocrit, BIS value, and propofol and remifentanil infusion rates were also recorded at each set point. The anesthesiologist and surgeon caring for the patient were blinded to the measures of cerebral oxygenation. N2O, a possible confounding factor, was not used. If bolus doses of phenylephrine were required, recording was delayed because this pressor is associated with a reduction in rSO2 of approximately 3% which is sustained for several minutes [14]. Demographic and intraoperative data were retrieved from the patient’s electronic medical records.

Statistical analysis

Exploratory data analysis was used to describe measures. Extreme values were identified using the Tukey Fences approach. Spearman’s correlation was used to test for correlation between PbrO2 and rSO2 under conditions of varying ventilation strategy. Given the small sample size, and to be conservative in our approach, the analysis was not adjusted for repeated measures. When comparing PbrO2 and rSO2, we also standardized both measures to a z-score. This transformation facilitates comparison across quantities with different measurement units. A pre-study power analysis and sample size determination indicated that a sample size of 15 would achieve an 80% power with a one-sided type I error of 5% to detect a positive correlation of 0.6 (from the null hypothesis of no correlation) between PbrO2 and rSO2 subsequent on alterations made in ventilation strategy. P values < 0.05 were considered statistically significant.

Results

COVID-19 disrupted neurosurgical case volume and, consequently, recruitment for this study. Nineteen patients were screened for eligibility, 4 failed to meet inclusion criteria, 3 declined to participate and 2 were excluded for logistical reasons. Ten patients completed the study, 1 was excluded from final analysis. All patients recovered well without complication.

Demographic characteristics and baseline data are shown in Table 1. Baseline rSO2 measured with the subjects sitting, fully awake and breathing room air, varied between 31% and 78%. The left cerebral oximetry optode was removed, at the time of surgical preparation, for 5 included subjects. Analysis was therefore limited to data obtained from the right. Males were more frequently represented, malignant melanoma was the most prevalent diagnosis, and left-sided lesions were more frequent than right-sided lesions. The average time between measurements recorded at set point 1 and set point 2 was 17 minutes.

Table 1

Demographic characteristics and baseline data

Variable	N	Percent	Mean (Std)	Range
Age	9		61.4(9.6)	(45–72)
Gender
F	2	22.2
M	7	77.8
ASA status
2	1	11.1
3	7	77.8
4	1	11.1
rSO2 (L)	9		68.6(13.5)	(34–78)
rSO2(R)	9		67.8(14.7)	(31–78)
BP
Systolic	9		134.7(18)	(117–173)
Diastolic	9		77.7(11.5)	(67–106)
Diagnosis
History of systemic malignant melanoma	6	66.7
History of renal cell carcinoma	2	22.2
Adenocarcinoma of breast	1	11.1
Location (lobe)
Frontal	4	44.4
Parietal	1	11.1
Temporal	3	33.3
Occipital	1	11.1
Location (laterality)
Left	8	88.9
Right	1	11.1

Demographic characteristics and baseline data. rSO: Regional cerebral oximetry, BP Blood pressure, Std: Standard deviation

Correlation between PbrO2and rSO2

Positive Spearman’s correlation (r = 0.50, p = 0.036) was measured between rSO2 and PbrO2 (Fig. 1). Computation of z-scores of rSO2 and PbrO2, allowing for ventilation strategies, showed no statistically significant differences.

Fig. 1

Scatter plot illustrating the relationship between brain tissue oxygen tension (PbrO2) and cerebral oximetry (rSO2) at each ventilation set point

Influence of ventilation strategy on PbrO2

PbrO2 increased from median 6.0, IQR 4.0–11.3 at set point 1 (FiO2 0.3 and PaCO2 30 mmHg) to median 22.5, IQR 9.8–43.6 at set point 2 (FiO2 1.0 and PaCO2 40 mmHg) p = 0.015. PbrO2 increased in all subjects with the change in ventilation strategy.

Influence of ventilation strategy on rSO2

rSO2 increased from median 68.0, IQR 62.5–80.5 at set point 1 to median 83.0, IQR 74.0–90.0 at set point 2, p = 0.047. rSO2 increased in all subjects with the change in ventilation strategy.

Outliers

A single outlier exhibited a PbrO2 of 162.2 mmHg at FiO2 1.0 and PaCO2 40 mmHg, more than 100 mmHg and 3 times greater than the nearest subject. This subject was identified as an extreme value using the Tuckey Fences approach and was excluded from final analysis. The patient was a 67-year-old male who underwent right temporal craniotomy for metastatic melanoma excision and displayed unremarkable baseline readings. Arterial gas tensions were within range displayed by other subjects and responded similarly to the change in ventilation strategy. Placement of the Licox probe followed standard processes. rSO2 increased from 49% at set point 1 to 69% at set point 2.

Arterial gas tension, hemodynamics, hematocrit, BIS, and anesthesia

The changes in ventilation strategy resulted in significant increases in PaO2 and PaCO2 while the potential confounders of heart rate, arterial blood pressure and hematocrit remained unchanged. BIS and the infusion rate of anesthetic drugs was measured within target range; there was no difference between values at the study set points 1 and 2 (Table 2).

Table 2

Arterial gas tensions, hemodynamics, hematocrit and depth of anesthesia

N = 9	FIO2 0.3 and paCO2 30 mmHg		FIO2 1.0 and paCO2 40 mmHg		Kruskal–Wallis test by ranks
Variable	Mean (Std)	Range	Mean (Std)	Range	p-value
PaCO2	28.7 (2.9)	(2–34)	41.3 (3)	(38–47)	0.0003
PaO2	92.3 (27.3)	(62–150)	343.3 (67.9)	(273–462)	0.0003
Systolic BP	125.4 (24.5)	(82–170)	124.9 (20.5)	(101–154)	0.8944
Diastolic BP	69.9 (11.8)	(51–91)	68.6 (11)	(53–88)	0.8597
HR	68.0 (17.7)	(47–100)	64.1 (16.8)	(43–100)	0.6269
HCT	36.0 (3.7)	(29–41)	35.7 (4.8)	(27–42)	0.9645
BIS	38.5 (8.9)	(21–47)	41.1 (5.2)	(33–50)	0.9157
Propofol mcg/kg/min	78.3 (14.6)	(60–100)	80.6 (11.8)	(60–100)	0.651
Remifentanil mcg/kg/min	0.1 (0)	(0.05–0.15)	0.1 (0)	(0.05–0.15)	0.7814

Arterial gas tensions, hemodynamics, hematocrit, bispectral index, and anesthesia infusion rates at each ventilation set point. HR: Heart rate, HCT: Hematocrit, BIS Bispectral index

Discussion

We found evidence of positive correlation between PbrO2 and rSO2 measured in human brain, under the conditions of changing ventilation strategy. In addition, the combined intervention of increasing FiO2 and PaCO2 result in consistent and significant increases in both PbrO2 and rSO2. Our data provide evidence to support the rationale for changing ventilation strategy in response to measured or anticipated cerebral hypoxemia, for example during periods of cerebral hypoperfusion. Selection and recruitment proved to be extremely difficult, and progress was further impeded by the COVID-19 pandemic; the study was therefore discontinued early. However, the findings, which were statistically significant, can be regarded as hypothesis-generating and provide the basis for future investigation. Additionally, the experimental model developed for this study is novel, with wider implications for other related correlations (e.g., scalp electroencephalography and intracortical neurophysiology).

The limitations of cerebral NIRS techniques are well described [3]; it is very unlikely that all changes in rSO2 reflect true changes in brain tissue oxygen, necessitating confirmatory investigation against a more reliable and invasive measure of cerebral oxygenation for each separate effector of rSO2. Our model does, however, provide an experimental paradigm within which such hypotheses could be tested.

The findings of a Spearman’s correlation of 0.5 without a demonstrable difference between z-scores suggest a potential proxy relationship between monitors. However, at study set point 1, while median PbrO2 was measured to be markedly low (6 mmHg), median rSO2 was 68%, a reading that would not alert anesthesiologists to the cerebral hypoxia detected invasively. The absolute value of rSO2 is difficult to interpret without context. Indeed, we have reported catastrophic ischemic neurological injury without noteworthy perturbation in cerebral oximetry values [15] and, despite meta-analysis, the effect of perioperative NIRS monitoring of the brain remains uncertain [16]. Trend monitoring has been previously suggested as the most appropriate application for cerebral oximetry [3]; our data support no more than this use.

It is concerning subjects displayed low brain tissue oxygen tensions (median 6 mmHg) with hematocrit and hemodynamics considered normal and, at FiO2 0.3 and PaCO2 30 mmHg; anesthesiologists should be aware that such a ventilation strategy may result in cerebral hypoxemia for some patients. Sampling location in proximity to a metastatic lesion may be contributory. Increasing FiO2 and PaCO2 was found to be an effective strategy to improve brain tissue oxygen tension. It is likely that studies proving the influence of ventilation strategy on cerebral oximetry [17] reflect true oxygenation increments in the brain. This is especially important for studies conducted in patients at risk of cerebral hypoperfusion, for example, those undergoing carotid endarterectomy [18, 19] or surgery in the beach chair position [20].

The study has limitations. Most notably, the sample size was small and adversely impacted by difficult recruitment. The study was single center and limited to Caucasian subjects to minimize the variability of rSO2 findings due to differing skin pigmentation. It would have been of great interest to measure the effect of FiO2 and PaCO2 separately. However, by doing so, the period of cessation of surgery would have been unacceptably prolonged. We chose the combined intervention of increasing FiO2 and PaCO2 known to result in significant and clinically relevant increases in rSO2 [20]. Future study may allow FiO2 and PaCO2 to be considered independently. Other highly selective criteria for study inclusion inadvertently resulted in a predominantly male population with a predominant diagnosis of metastatic melanoma. The generalizability of the conclusions is thus limited. However, every patient regardless of gender, site of surgery, or presenting diagnosis responded with the same positive trajectory of cerebral oxygenation with increasing FiO2 and PaCO2, including the subject excluded for extreme values.

In conclusion, correlation between rSO2 and PbrO2 is evident but rSO2 is limited to detect marked cerebral hypoxemia. Increasing FiO2 and PaCO2 results in significant increases in cerebral oxygenation measured by both monitors; rSO2 can likely function as an effective trend monitor during changes in ventilation strategy. Finally, this novel model of non-invasive and invasive measurement of uninjured brain physiology may have wider applications.