What we already know about this topic
• NIRS tissue oximetry enables noninvasive estimation of the hemoglobin oxygen saturation in a regional vascular bed.
• In vivo validation of NIRS tissue oximetry depends on a fixed arterial-to-venous blood volume ratio for the calculation of a reference value from co-oximetry on arterial and regional venous blood.
• Cerebral arterial-to-venous blood volume ratio changes with hypoxia and hypercapnia, due to regulatory vasoreactivity.
What this study adds that is new
• When arterial hypotension was induced by obstruction of blood flow in the inferior vena cava, the drop in cerebral oxygenation as measured by NIRS was significantly less than the drop measured by co-oximetry.
• This relative insensitivity of cerebral oximetry to ischemic hypoxia may at least partly be due to an increase in the AV ratio during hypotension.
The immature cardiovascular system of preterm infants puts them at risk for low blood pressure (hypotension); a condition known to be associated with cerebral injury.12.–3 However, the lower threshold of blood pressure leading to reduced brain perfusion has not yet been established in preterm infants4,5 and it might very well vary both within and between infants. Consequently, more direct methods of monitoring the sufficiency of oxygen supply to the brain are under investigation. Near-infrared spectroscopy (NIRS) is a noninvasive method that allows for measurement of cerebral oxygenation.6 Continuous monitoring with NIRS to guide treatment has been demonstrated to reduce the hypoxic burden on the brain in extremely preterm infants.7 The optical properties of hemoglobin change with the binding of oxygen. NIRS illuminates tissue with near-infrared light and detects the reflected light at some distance from the light source.8 Since hemoglobin in all vascular compartments within the illuminated tissue contributes to the attenuation of the reflected light, a reference for in vivo validation from co-oximetry, i.e., direct blood gas analysis from blood samples, must be a weighted average reflecting the distribution between venous and arterial volume. A cerebral arterial-to-venous volume ratio (AV-ratio) of 1 to 3 (0.25) is widely accepted in humans under normal physiological conditions.6,9 However, the cerebral blood volume (CBV) distribution might change over time due to cerebral autoregulation; the ability of blood vessels to regulate arterial resistance to maintain a stable perfusion despite blood pressure changes, through chemical, metabolic, and neurogenic mechanisms.10 Accordingly, pathophysiological conditions known to effect cerebral perfusion, such as low tissue oxygenation (hypoxia), elevated blood levels of carbon dioxide (hypercapnia), or hypotension (low arterial blood pressure) may change the AV-ratio. Previously, NIRS oximetry validation against arterial and cerebral venous blood oxygenation measured by co-oximetry during hypoxia has suggested changes in the AV-ratio.11 The change in AV-ratio estimated by NIRS during hypotension has not yet been examined. Improving our knowledge about changes in the cerebral AV-ratio during pathologic states could strengthen the interpretation of data obtained by NIRS, as well as improve the accuracy when validated against cerebral blood co-oximetry.
We used a dataset obtained during a previous study on the effects of dopamine on the cerebral autoregulation in hypotensive newborn piglets. We used the dataset to compare the values of cerebral oxygenation obtained by NIRS and co-oximetry. Accordingly, the piglets had continuous dopamine infusion during half of the experiment, as described in Sec. 2.5.
Anesthesia and Monitoring
Anesthesia was induced by 3% isoflourane, supplemented with propofol and fentanyl. Induction of anesthesia was followed by continuous infusion of propofol 15 to and fentanyl . The fentanyl infusion was stopped 1 h prior to the start of planned blood pressure manipulations, as described in Sec. 2.5. Piglets were tracheostomized and connected to a pressure-controlled mechanical ventilator. was maintained between 4 to 6 kPa and arterial saturation above 95%. Arterial saturation and heart rate were monitored by pulse oximetry on the foreleg (Radical 7, Masimo, Irvine, California). Piglets were kept on a heating pad to maintain rectal temperature at 38.5°C to 39.5°C.
The femoral artery was cannulated with an arterial line placed in the thoracic aorta for mean arterial blood pressure (MABP) monitoring and arterial blood sampling. The femoral veins were cannulated with a 4 FR double lumen catheter for infusion of glucose and dopamine and a 4 FR embolectomy catheter with a balloon at its tip (LeMaitre Vascular, Sulzbach, Germany). The balloon was placed in the inferior vena cava (16 cm mark) to decrease cardiac preload and MABP when inflated. Control of placement of the embolectomy catheter was done by making sure that MABP was easily manipulated during inflation/deflation. Cerebral venous blood samples were retrieved by cannulating the superior sagittal sinus. The piglets recovered for 1 h after preparation and cannulation.
We used the NIRO 300 (Hamamatsu Phototonics, Hamamatsu City, Japan) with an NIRS probe consisting of two aligned photodetectors and a light-source, which emits near-infrared light at four different wavelengths. The photodetectors were placed 4 cm from the emission probe in a nontransparent probe holder. The NIRS probe was placed above the left frontal and parietal cortex. The position of the NIRS probe was secured with a self-adhesive bandage and, once placed, the NIRS probe was not relocated. The device estimates change in oxy-hemoglobin and deoxy-hemoglobin through spatially resolved spectroscopy by measuring light attenuation at the two source–detector separations.8 Regional tissue oxygenation (), i.e., the regional oxygenated hemoglobin to total hemoglobin in percentage was estimated at 2 Hz. is labeled “tissue oxygenation index” by the manufacturer; Hamamatsu Phototonics.
MABP was manipulated by inflating or deflating the balloon in the inferior vena cava. Changes in blood pressure were induced gradually in steps of . At each stable MABP level, gas analysis (ABL-500, Radiometer, Copenhagen, Denmark) was done on blood drawn from the arterial line and superior sagittal sinus. The sampled blood volume was replaced with saline. Piglets were randomized to start with either baseline, i.e., blood pressure with a completely deflated balloon, or with low blood pressure. Hence, all piglets had a phase of gradual increase and a phase of gradual decrease of MABP, but the order of the phases was randomized. If the piglet was randomized to start with baseline blood pressure, MABP was lowered to a minimum of . Subsequently, MABP was returned to baseline blood pressure. If piglets were randomized to start with low blood pressure, MABP was gradually returned to baseline blood pressure and, subsequently, gradually lowered to a minimum of . Between the two phases of either increase or decrease in MABP, the piglet was allowed to stabilize with the balloon fully deflated for 30 min.
As part of a larger experimental design, the piglets were randomized to receive continuous dopamine infusion during either the phase of increase or decrease in MABP.
Changes in Cerebral Blood Volume
Changes in CBV from baseline () were calculated by dividing changes in hemoglobin from baseline measured by NIRS () with total hemoglobin measured with arterial co-oximetry (HBT).12 NIRS measurements were converted to by using a differential path length factor (DPF) of 4.99.13 in ml per 100 g was calculated according to the following equation:1415 and is the brain tissue .16
We used the mean of 15 s of measurements after arterial and venous sampling. Assuming an AV-ratio of 0.25, the reference was calculated by the following equation:
Assuming to be the true regional cerebral oxygenation and that all blood exists in either the arterial or venous compartment, it is possible to calculate arterial and venous volume fractions by solving the following equation for and :11
Piglets and Descriptive Statistics
Twenty-one piglets were studied with a median age of 60 h (range 4 to 66) and mean weight . A total of 246 paired measurements were analyzed. The number of data pairs in each piglet ranged from 10 to 13. A total of five pairs of measurements were excluded; one due to erroneous NIRS-measurement, and four due to failed blood gas analysis. For all piglets, was kept above 95%. was stable at during the phases with changing MABP.
Relationship, AV-Ratio, and
An example of concurrent changes in MABP, , and during the experiment is given in Fig. 1. The average change in was 25% of the corresponding change in (Fig. 2). CBV decreased with per 100 g per mmHg decrease in MABP (Fig. 3). Median AV-ration at baseline was 0.17. The AV-ratio was inversely correlated to MABP increasing by (Fig. 4). Estimates of the AV-ratio were above 1 or below 0 in 81 out of 246 data points with 79 being below 0.
None of the outcome variables; , the AV-ratio, or , were affected by whether or not the piglet started with low or baseline MABP. Similarly, it made no difference if dopamine was infused in the first or second half of the experiment (Table 1).
Descriptive statistics and regression statistics.
|MABP (mmHg)||61.6 (57.9 to 69.7)||21.1 (18.9 to 21.5)|
|rStO2,NIRS (%)||47.8 (43.8 to 53.2)||39.9 (37.3 to 42.1)|
|rStO2,COX (%)||56.4 (49.2 to 61.2)||38.9 (34.1 to 44.6)|
|rStO2,NIRS versus rStO2,COX (fraction)||0.25±0.02||p<0.001|
|CBV versus MABP (ml·100 g−1·mmHg−1)||0.008±0.001||p<0.001|
|AV-ratio versus MABP (mmHg−1)||0.007±0.002||p<0.001|
Note: MABP, rStO2,NIRS, and rStO2,COX data described with median (IQR). Regression slopes±SEM during hypotension. The slope is different from 0 if p<0.05. MABP, mean arterial blood pressure.
This is, to our knowledge, the first study to investigate the influence of hypotension on apparent blood volume redistribution with cerebral NIRS oximetry. During a wide range of blood pressures, our data showed that NIRS oximetry poorly reflect changes in reference cerebral oximetry. The apparent AV-ratio increased as the MABP was reduced. This may in part explain the inaccuracy of the cerebral NIRS estimates of .
Reactivity of Cerebral NIRS Oximetry Assuming a Fixed AV-Ratio
A volume-weighted mean of the arterial and venous oxygenation is used for in vivo calibration of cerebral NIRS oximetry.17 Pollard et al.6 showed that cerebral NIRS oximetry reflected cerebral oxygenation in an AV-ratio of 0.25 in healthy adult volunteers. This fixed AV-ratio is widely accepted in literature, although some studies suggest wide interindividual variation.18,19 Assuming this fixed AV-ratio of 0.25 to calculate a reference value of tissue saturation from co-oximetry, we found that changed considerably less than expected: At low cerebral oxygenation, measured higher than , and at high oxygenation measurements were lower than . The NIRO-300 used in this study has previously been seen to react less to changes in oxygenation than the INVOS 5100 instrument (INVOS, Covidien, Boulder), which utilize the same spatially resolved NIRS technology and has a comparable source–detector separation, so it might to some extent be an issue of the specific NIRS instrument.20,21 In a study on newborn lambs subjected to hypoxia, Wong et al.11, also using the NIRO-300 instrument and assuming a fixed AV-ratio of 0.25, found that cerebral NIRS reflected 51% of the changes in weighted arterial and venous cerebral oxygenation. This study indicates that NIRS is sensitive to changes in AV-ratio. Wong et al. used the NIRO-300 device and measured reference co-oximetry in the extremes (range 13.7 to 74.4) as in our study. Anatomical differences between species may only partly explain the different accuracy with the NIRS-probe on lambs at 3 to 6 days possibly having a better fit than on piglets.
The most significant difference between the study from Wong et al. and our study may be that we used hypotension to reduce cerebral oxygenation. We minimized the potential vasoactive effects of arterial and on arterioles by keeping and stable during the phases with manipulation of MABP, and thus the physiological effects in play are most likely related to arterial and venous pressures. The vena cava balloon was inflated until MABP was reduced to the level required. The most likely mode of action of this intervention is through decreased venous return from the lower body leading to reduced preload of the heart. However, we did not measure the central venous pressure to confirm this or quantify the effect. We speculate that the reduced preload lowered the venous volumes of the upper limbs and the head, while cerebral arteries actively dilate as a response to the arterial hypotension due to the myogenic response.10,18 Thus, arterial blood volume dominates the CBV at low MABP. This may explain the poor response of NIRS in terms of cerebral volume-weighted oxygenation when assuming a fixed AV-ratio, because NIRS increasingly reflects arterial blood, leading to higher results compared to fixed AV-ratio, as blood pressure is reduced. The accuracy of NIRS-oximeters is not possible to determine in vivo, due to the uncertainty of the AV-ratio. Therefore, the in vitro accuracy is important. In the original paper describing the method of spatially resolved spectroscopy, very good accuracy in a blood–lipid phantom was demonstrated over oxygenation ranging from less than 20% to nearly 100%.22 In a more recent study using the same phantom, however, different NIRS-devices differed significantly as regard to their response to deoxygenation, e.g., the NIRO300 change was only 53% of the INVOS5100 change,20 whereas the INVOS5100 change came close to that of a reference standard.23 Another study reported a relative sensitivity to deoxygenation induced by a range of stimuli in young swine of using NIRO-300 compared to the INVOS.21 Thus, if we assume that the NIRO300 underestimates true deoxygenation by 50%, then the underestimation found in the present data must include yet another factor. We suggest that this is an increase in the AV-ratio.
CBV in newborn piglets has previously been found to measured by radiolabeled erythrocytes.24 While we did not attempt to measure CBV in absolute terms, we were able to calculate changes over time from the trends of oxy- and deoxyhemoglobin concentrations that are provided by the NIRO device in (brain tissue). These changes were small, but in the expected direction during physiological challenges. For example, lowering MABP by 40 mmHg resulted in a reduction of or 10% of total CBV. A lowering of MABP by 40 mmHg equals an increase of 0.28 in the AV-ratio. Previously, Lee et al.25 reported a comparable increase in the arterial volume fraction from 0.25 to 0.40 in response to hypercapnia, as the volume increase in the venous compartment was only approximately half of that in the arterial compartment. The lower threshold of the autoregulatory compensative capacity has been reported as an MABP of 30 mmHg or less in newborn children26 and 29 to 48 mmHg in newborn piglets,27,28 although wide interindividual variations are likely to exist.18 MABP below the lower threshold of autoregulation would result in a pressure-passive reduction of cerebral blood flow. Our results suggest that cerebral autoregulation is able to buffer the loss of CBV until the lower threshold of the autoregulation is reached. This could explain why the reduction in CBV was small compared to the increase of the AV-ratio. The variability of the data, most likely due to the low precision of cerebral oximetry by NIRS, made it impossible to examine any nonlinear relation between CBV and AV-ratio changes, which could have illustrated a possible change in vascular behavior below the autoregulatory threshold.
Validation of cerebral NIRS against blood oxygenation in adults and infants has predominantly focused on situations of hypoxia and low- or high-blood content (hypo- or hypercapnia).11,19 However, as hypotension is a condition commonly treated in sick infants,29 validation under conditions resembling hypotension are also highly relevant. In healthy adult volunteers, cerebral oxygenation measured by NIRS during hypovolemia has been studied experimentally by applying lower body negative pressure.30,31 Literature on the effects of hypotension on NIRS oximetry measures in neonatal populations is limited. In preterm infants, mild short-term hypotensive episodes did not lower the cerebral oxygenation estimated by NIRS.32 Our study indicates that changes in the AV-ratio during hypotension should be taken into account and that we might underestimate the true reduction in tissue oxygenation by NIRS in this situation, as NIRS increasingly reflects arterial blood. Ideally, validation between NIRS oximetry and cerebral blood oxygenation should be adjusted by simultaneous and independent estimations of changes in the AV-ratio. This is not currently possible, therefore, the alternative is to investigate changes in the AV-ratio during pathophysiological conditions that are relevant in sick infants and take this knowledge into account when using cerebral oximetry in clinical practice.
Strengths and Limitations of the Study
Our piglet model allowed blood sampling from the superior sagittal sinus, draining the cerebral cortex, and thus minimizing the risk of contamination from the extracerebral veins.33 Once placed, the NIRS probe was secured by nontransparent bandage and not repositioned. This prevented reposition noise, where optic heterogeneity in the tissue as well as heterogeneity of blood flow in the brain would add within-subject variation. We were able to decrease MABP to very low levels, allowing an examination of NIRS in extreme situations of potential clinical relevance. In Eq. (1), we used human DPF due to lack of piglet data. DPF is a measure of the time it takes the light to travel through the tissue relative to what would be expected from a direct flight from source to detector. It depends on the optical characteristics of the tissue. We do know that the piglet brain is more mature at the time of birth with more developed myelination. This will increase DPF. Using too low DPF will not influence the estimate of rStO2, but will lead to an underestimation of the absolute changes in CBV.
Approximately 1/3 of the calculated AV-ratios were above 1 or below 0. The data were retained in our analysis to avoid statistical bias. In our calculation, the AV-ratio is determined by , , and [Eq. (3)]. The estimate of NIRO-300 has been shown to estimate lower baseline values compared to other devices in neonates34 and on the adult forearm.35 Also, a study in a blood–lipid phantom revealed significant difference in estimates between three commercial devices, including the NIRO-300.20,21 Errors in the measurement of would equally be able to estimate AV-ratios below 0 if the venous samples were not taken strictly anaerobically. Air in the syringe was carefully avoided and, if present, quickly removed when blood samples were drawn and the blood samples were analyzed immediately after sampling. The procedure did not differ from that in clinical practice. Although air-contamination cannot be ruled out in some samples, it is unlikely to be the sole cause of the large number of data points outside the physiological range. Wong et al.11 excluded eight nonphysiological values out of 49 during the analysis of the AV-ratio and . Finally, imprecision of NIRS oximetry may explain some of the nonphysiological data. It has been well-documented that irrespective of the NIRS instrument the precision of the estimate is about 5% to 6%.36,37 This means that a single estimate could be from the “true” oxygenation, thus NIRS values below could simply be due to random noise in the NIRS signal. Another limitation of our study is the fact that it was performed in newborn piglets. There are obvious differences between piglets and neonates. Newborn piglet brains average weight is 30 g, whereas extremely preterm infant brains weigh at least 100 g. The NIRS sensor was designed for human use and a source–detector distance of 4 cm might probe beyond the brain when used in a piglet including extracerebral tissue, such as tongue and basis cranii. Finally, the study was part of a larger setup where the effect of dopamine-infusion on cerebral autoregulation was studied. The piglets received dopamine when half of the blood samples were drawn. Dopamine is an inotrope affecting vascular resistance and cardiac output through dopaminergic, - and -adrenoceptors in arteries and the heart.38 Thus, dopamine has the potential to change cerebral blood flow. Importantly, dopamine did not affect the relationship between and , between and MABP, nor between the AV-ratio and MABP. Dopamine did not affect autoregulation (manuscript submitted). We are, therefore, confident that our results are relevant in a wider context.
NIRS oximetry had a poor response to cerebral hypoxia during hypotension when compared to a reference co-oximetry value assuming a fixed AV-ratio. This may partly be explained by the inaccuracy of the NIRS-device, but our data indicate that the AV-ratio changes during hypotension and affects NIRS estimates of cerebral oxygenation. Further research in NIRS oximetry in pathophysiological states is needed to help interpret future results for clinical use.
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