Non-invasive Monitoring of Intracranial Pressure Using Transcranial Doppler Ultrasonography: Is It Possible?

1Intracranial pressure (ICP) is an important monitoring modality in the clinical management of several neurological diseases carrying intrinsic risk of potentially lethal intracranial hypertension (ICH). ICP essentially consists of four components, driven by different physiological mechanisms: inflow and volume of arterial blood, venous blood outflow, cerebrospinal fluid (CSF) circulation, and brain volume. These components are responsible for different patterns of ICH.

2Although ICP can guide patient management in neurocritical care, it is not commonly monitored in many clinical conditions outside this environment. The invasive character of the standard methods for ICP monitoring (epidural, subdural, intraparenchymal, and intraventricular monitors) and their associated risks to the patient (infections, brain tissue lesions, and hemorrhage) contribute to this scenario. They have prevented ICP monitoring in a broad range of diseases like in patients with risk of coagulopathy, as well as in other conditions in which invasive monitoring is not considered or outweighed by the risks of the procedure. Another downside is related to costs and availability: invasive monitoring is an expensive technique, requires trained personnel and neurosurgical settings. Average cost of intraparenchymal microtransducer is US $600, additionally to US $6000–10,000 for the display monitor. Provided that knowledge of ICP can be crucial for the successful management of patients in many sub-critical conditions, non-invasive estimation of ICP (nICP) may be helpful when indications for invasive ICP monitoring are not met and when it is not immediately available or even contraindicated.

3Transcranial Doppler Ultrasonography (TCD) was first described by Aaslid et al.. Apart from many clinical applications, TCD waveform analysis has been investigated as a technique for nICP estimation, and this could represent one of its most useful applications outside the critical care environment. It is conceivable if one considers that increased ICP could affect the waveform of blood flow velocity in major cerebral vessels which have compliant walls. Such vessels are subjected to an external pressure (ICP) and an internal pressure (arterial blood pressure—ABP). Active tension of the arterial walls and the arterial wall compliance are another (and unknown) parameters, which undoubtedly fall into the equation. On top of this, not only all changes in FV waveform, like low diastolic cerebral blood flow velocity (FVd), peaked waveform, and higher pulsatility index (PI) values can be observed with TCD during elevated ICP, but also in arterial hypotension and hypocapnia.

4TCD-based nICP methods are mainly based on approximate semi-quantitative relationships between cerebrovascular dynamics and ICP. They can be divided into three categories: (I) methods based on the TCD-derived pulsatility index; (II) methods based on the calculation of non-invasive cerebral perfusion pressure (nCPP); and (III) methods based on mathematical models.

5Although derived from the same principle, there is a considerable variability in the reported accuracy of these methods inter- and intra-categories.

6Considering the wide range of TCD applications as a technique for nICP monitoring, the purpose of this review is to generally present these methods and their documented clinical or experimental applications with measures of accuracy.

7A review of the literature was performed on PUBMED database using the search keywords ‘Transcranial Doppler non-invasive intracranial pressure.’ Works from 1985 to 2015 were found, in a total of 98 studies. The inclusion criteria were the use of Transcranial Doppler as tool for non-invasive ICP with clinical or experimental applications of such methods. Excluded papers consisted of works using TCD, but with no application for non-invasive ICP estimation, or absence of clinical or experimental applications in papers describing methods using TCD for non-invasive ICP estimation. The selected articles were then subdivided into the three categories aforementioned. Only full-length available articles in the English language were considered (see flow diagram in Fig. 1). The total number of articles considered was 37, with occasional repetitions within each nICP category, i.e., certain articles presented assessments in more than one category.

8Results for each nICP category are presented in Tables 1, 2, and 3. They include main findings and measures of accuracy of the studies considered. Sections in Results present major attributes of the nICP categories.

9Pulsatility index describes quantitative and qualitative changes in the morphology of the TCD waveform resulting from cerebral perfusion pressure changes. It represents a relationship between the difference of systolic flow velocity (FVs) and FVd divided by mean flow velocity (FVm). All possible methods based on TCD-derived pulsatility index are based on observation that ICP and PI are positively correlated during increases of ICP. However, increase in PI is not specific for increase in ICP. In certain situations, such as a drop in CPP, PI presents an increasing trend, which can be related to increases in ICP or decreases in ABP (Fig. 2). The same behavior occurs during decrease in PaCO2 (partial pressure of carbon dioxide) or increase in pulsatility of ABP waveform. Mathematically, PI can be expressed as inversely proportional to mean CPP, directly proportional to pulse amplitude of arterial blood pressure and non-linearly proportional to the compliance of the arterial bed (Ca), cerebrovascular resistance (CVR), and heart rate (HR).

10Table 1 presents the papers which studied the relationship between PI and ICP. Accuracy of nICP estimation varies from ±5 to ±43.8 mmHg. The most favorable results are from Bellner et al., in which the authors found a 95 % confidence interval for prediction of ±4.2 mmHg and strong correlation coefficient with ICP, R = 0.94 (p < 0.05). However, such results were never replicated by other authors.

11The second approach for nICP monitoring was primarily intended for estimating the nCPP. However, non-invasive ICP can be calculated based on the assumption that nICP = ABP − nCPP. Four methods are described in the literature (Table 2).

12Aaslid et al. have determined CPP based on the amplitudes of the fundamental frequency components of FV (F) and of the arterial blood pressure (A):

13Some studies have demonstrated that specific patterns of TCD waveform, such as a decrease in diastolic flow velocity, reflect impaired cerebral perfusion caused by a decrease in CPP (Fig. 3). Based on waveform analysis of FV, the proposed equation was14 mmHg is a calibration (zeroing) parameter established for traumatic brain injury patients.

14This method is based on the combination of the phasic values of both FV and ABP. The non-invasive CPP (nCPP) was calculated using the following formula:where ABPm and ABPd are the mean and diastolic ABP, respectively.

15Critical closing pressure (CrCP) represents a threshold of ABP, below which the blood pressure in the brain microvasculature is inadequate to prevent the collapse and cessation of blood flow. CrCP equals the sum of ICP and vascular wall tension (WT): CrCP = ICP + WT. Given the association of this parameter with the vasomotor tone of small blood vessels (i.e., wall tension), CrCP may be able to provide information regarding the state of cerebral haemodynamics in several neurological conditions and then could reflect changes in CPP (Fig. 4). The equation for nCPP estimation based on CrCP is Constant coefficients (0.734, 0.266, 7.026) were derived from analysis of database of 232 TBI retrospective cases. CaBV Amp represents the fundamental amplitude of the cerebral arterial blood volume. ABP Amp represents the fundamental amplitude of arterial blood pressure.

16The accuracy for these methods was mainly reported for nCPP estimations and varied from ±12 to 48.9 mmHg. Variability for nICP in this case ranged from ±9.19 to ±59.60 mmHg. Out of the four methods, the best accuracy for prediction ICP was reported by Cardim et al. elsewhere, using the nICP_CrCP, in which ICP could be predicted within a confidence interval of ±9.19 mmHg.

17In this model, the intracranial compartment was considered a black-box (BB) system, with ICP being a system response to the incoming signal ABP. The system response was described in terms of a transfer function between ABP and ICP. The transfer function was controlled by TCD and ABP derived parameters, the so-called TCD characteristics, which include ICP-related parameters and an ABP to TCD transfer function. The rules of this TCD-based linear control had been formerly determined using a multiple regression model between TCD characteristics and ABP-ICP transfer function on datasets of reference patients. The output data provide continuous full waveform of nICP (in mmHg) (Fig. 5).

18Application of this model is summarized in Table 3.

19This model-based nICP method focuses on the major intracranial compartments and their associated variables: brain tissue, cerebral vasculature, and cerebrospinal fluid (CSF). It continuously estimates and tracks ICP using measurements of peripheral ABP and FV in the middle cerebral artery (MCA). This physiological model of cerebrovascular dynamics is represented by a circuit analog and provides mathematical limits that relate the measured waveforms to ICP. Patient-specific ICP estimations are produced by an algorithm, with no calibration or training in specific populations needed. The dynamical model of CSF and cerebral blood circulation has been first published by Ursino and Lodi.

20Accuracy of this method is summarized in Table 3.

21The previously described black-box model for ICP estimation adopts a linear relationship among ABP, ICP, and FV. Xu et al. assuming that the relationships among these three signals are more complex than linear models, and consequently not adequate to depict the relationship between f and w coefficients (relationship between ABP and ICP and that between ABP and FV, respectively), investigated the adoption of several nonlinear regression approaches. Considering that nonlinear regressions such as support vector machines (SVMs), kernel spectral regression (KSR) have been proved to be more powerful for the prediction problem than the linear ones, the authors proposed to use these approaches to model the relationship between coefficients f and w.

22The ICP estimation showed that the mean ICP error by the nonlinear approaches can be reduced compared to the original approach (Table 3). Statistical tests also demonstrated that the ICP estimation error by the proposed nonlinear kernel approaches is statistically smaller than that obtained with nICP_BB.

23Hu et al. initially proposed an innovative data mining framework of nICP assessment. The proposed framework explores the rules of deriving ICP from ABP and FV that are captured implicitly by a signal database without using a mathematical model. The main strategy of the this framework is to provide a mapping function to quantify the uncertainty of an ICP estimate associated with each database entry, and to use this information to determine the best entry to build an ICP simulation model for an optimal ICP estimation. In comparison to Schmidt’s method (nICP_BB), for example, this model presented a smaller median normalized prediction error (bias), and a greater median correlation coefficient between estimated and measured normalized ICP (Table 3).

24In another work of the same group, Kim et al. aimed at adopting a new (linear and nonlinear) mapping functions into the previous data mining framework for nICP estimation to demonstrate that the performance of nICP assessment could be improved by utilizing proper mapping functions. Results are summarized in Table 3.

25As previously seen, FV waveform analysis has been frequently applied for non-invasive ICP assessment. Kim et al. introduced a non-invasive detection of intracranial hypertension method based on the TCD measurement of FV alone to demonstrate its performance both in the supervised and semisupervised learning settings (Table 3).

26Out of these five model-based methods, the best accuracy was reported by Kashif and Heldt et al., in which authors present a strong correlation between nICP and ICP of R = 0.90, sensitivity of 83 %, specificity of 70 %, with an AUC of 0.83 for detecting ICP ≥ 20 mmHg. In addition, a 95 % CI for prediction of ICP of ±14.9 mmHg (SDE of ±7.6 mmHg) was found for this method. Although other reviewed methods presented smaller 95 % CI, considering all measures of accuracy together, nICP_Heldt was the one showing the best performance.

27Intracranial pressure and its management have been considered of fundamental importance in the treatment of neurocritical patients. ICP monitoring has been available since 1951, but it is important to realize that the monitor itself contributes little to outcome without proper interpretation and secondary analysis of the observed signal. Instead, a positive outcome depends on how the data from the monitor are used and whether an effective treatments exists. In a recent study, Chesnut et al., demonstrated that there was no difference in primary outcome in TBI patients who received ICP monitoring. However, while this trial has internal validity, it has not been externally validated and did not test whether treatment of ICP per se makes a difference, but rather compared two management protocols (patients with or without ICP monitoring). Moreover, ICP should not be considered solely as a “number,” as waveform analysis of this parameter is also important. For instance, ICP waveform analysis can provide information on the state of cerebrovascular reactivity (PRx index), compensatory reserve (RAP index) and can be used to estimate individualized optimal cerebral perfusion pressure levels.

28Despite eventual complications that might raise from invasive monitoring, direct methods still remain as the gold standards. When direct ICP monitoring is contraindicated, a reliable non-invasive method would be helpful, at least in the early stages of treatment, when it could act as a screening tool. Such scenario would be beneficial to a wide range of neurological conditions in which ICP monitoring is not usually applied or is a neglected parameter, such as cerebral malaria, status epilepticus, mild or moderate TBI, brain tumors. For an example, TCD has been demonstrated to accurately screen patients with mild or moderate TBI at risk of secondary neurological deterioration.

29The advent of Transcranial Doppler Ultrasonography allowed the development of several methods dedicated to assess the cerebrovascular circulation and dynamics, particularly non-invasive assessment of ICP and CPP. Moreover, subject to good fixing of ultrasound probes, it allows monitoring of these parameters as they may change in time. TCD comprises most of the features a nICP method should contemplate: relatively low cost, risk-free, easily available, portable, high temporal resolution, repeatable and suitable for emergency and ambulatory settings. Nevertheless, as most of the non-invasive techniques, TCD also presents some intrinsic disadvantages which can negatively influence its accuracy. They are mainly represented by signal transmission attenuation through the cranial bones, linearity and stability of the signal in time. Furthermore, TCD measurements may be especially difficult in a certain percentage of the population (up to 8 %) which does not present an adequate acoustic window for artery insonation. On the other hand, accuracy may not be the primary performance measure in every clinical situation, and such downsides may be compensated for by the ability of the method to track changes and trends of ICP over time, rather than its absolute value.

30In addition, a possible disadvantage about TCD is related to its principle of working. It is known that this technique is limited to detecting changes in the arterial bed of vasogenic origin (i.e., changes of arterial blood volume). Considering that ICP consists of several components (i.e., inflow and volume of arterial blood, venous blood outflow, CSF circulation and brain parenchyma volume), it is expected that a TCD-based method would present lower accuracy if changes in ICP were caused, for example, by derangements in the CSF circulation or by increase in parenchyma volume, rather than if they were purely of vasogenic origin. This is mainly because changes in the CSF and brain parenchyma compartments would not be promptly transmitted to the arterial bed as of those of vasogenic origin. Such characteristic can be exemplified by the fact that in certain situations where changes of ICP related to vasogenic fluctuations (plateau waves, B waves) overlaps the changes of ICP related to CSF circulation (for instance during CSF infusion test), there is a strong correlation in time domain between real and TCD-estimated ICP (as seen in Fig. 6, obtained from Cardim et al.), even showing reliable replications of vasogenic waves patterns.

31According to the revision of the presented methods, the measures of accuracy for each method varied substantially within and among nICP categories as observed in Tables 1, 2 and 3. For the approaches based on mathematical models, for instance, the most frequent measures were the ‘Bias’ and ‘SDE’ (standard deviation of the error [bias]), and MAD (mean absolute difference).

32Over measures of accuracy, a standard statistical assessment would be interesting for works on non-invasive intracranial pressure methods. For instance, at least for a clinical point of view, an assessment should contain the following statistical indicators: (I) correlation between nICP and measured ICP considering mean values of ICP and changes of ICP in time domain; (II) Bias and 95 % CI for prediction of ICP; (III) ROC analyses including the nICP method prediction ability at a certain threshold (usually around 20 mmHg for intracranial hypertension), sensitivity and specificity. Altogether, these parameters should provide the clinician a comprehensive picture of the qualities and downsides of a method.

33Another aspect that might confuse interpretation and comparisons is how the nICP averages were obtained, i.e., every work present with different average calculation windows. The number of samples should also be considered when comparing such results. Moreover, information about sensitivity and specificity, confidence intervals for prediction or any of the above mentioned parameters is not systematically available in the majority of the reviewed papers. Some of the studies also include a small number of patients, making a quantitative comparison unfeasible. This variability illustrates the importance and necessity of studies applying the same number of samples, calculation methods and measures of accuracy in order to compare different nICP methods consistently.

34The several degrees of approximation for ICP monitoring (i.e., epidural, subdural, intraparenchymal and intraventricular) could also contribute to a misleading interpretation when validating nICP methods against different invasive techniques. This is due to the presence of multiple intracranial compartments of variable deformability and ability to transmit pressure. Thus, ICP needs to be considered as an anisotropic parameter rather than a global isotropic pressure equally distributed in all intracranial compartments. Over this concept, each invasive method would then be specific to measuring compartmental pressures according to where they are located in the intracranial system. As proofs of this concept, simultaneous measurement of ICP by intraparenchymal and intraventricular probes showed a bias of −1.2 and a 95 % CI of ±6.8 mmHg (SDE of ±3.4 mmHg). In another study, simultaneous measurements of ICP using intraparenchymal and epidural probes presented a bias of 4.3 mmHg, with 95 % CI of ±17 mmHg (SDE of ±8.5 mmHg). Under these circumstances, the characteristics of invasive ICP monitoring should also be considered in the standard nICP assessment.

35Nevertheless, qualitative-wise, TCD-based nICP methods generally presented a positive degree of agreement and acceptable correlations with measured ICP (or with CPP for nCPP-based methods), with exceptions for PI-based methods. For this category, even though most of the studies indicated a direct, or at least indirect, correlation between PI and ICP, there is a divergence whether PI can predict ICP reliably, with some studies showing rather weak or even inexistent correlations between these two parameters. Such a controversy might originate from the different conditions in which PI can increase independently of increases in ICP.

36Considering the 95 % CI for the presented methods, there is a wide variability for the different method categories (from ±4.2 to ±59.60 mmHg). The authors’ personal experience on working with TCD-based methods suggests there is an overall intrinsic confidence interval of around ±12 mmHg, which still needs to be extensively validated in different patient populations and clinical conditions. Provided that the clinically relevant range of ICP is about 10 or 20 mmHg, TCD-based methods at the current state of development are not able to predict mean values of ICP with great confidence. However, the cerebral circulation dynamics can be observed with such methods as nICP changes in time domain, and tracked in real-time in the clinical setting (as observed in Fig. 6, for instance). This is one of the advantages of Transcranial Doppler Ultrasonography and may become particularly useful as a primary assessment tool in centres where ICP measurements are not routinely applied, or in patients in whom ICP monitoring is unavailable or may not be clearly indicated.

37In conclusion, although Transcranial Doppler Ultrasonography consists of a technique with various possibilities for nICP estimation, there is still a necessity of studies to systematically compare them in different clinical conditions, in order to determine which approach offers the best reliability to monitor ICP dynamics non-invasively.