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274
Table 14.2 (continued)
NCSE Non-invasive estimation of ICP
Perioperative cardiovascular and aortic counterpulsation balloon
Cerebral venous thrombosis (CVT) Non-invasive estimation of ICP
Sepsis Changes in the cerebral perfusion pressure (CPP) as a
BDD brain death diagnosis, NCSE non-convulsive epileptic status, VV venous-venous/VA veno- arterial, ARDS acute respiratory distress syndrome, CPP cerebral perfusion pressure, TCCS tran­scranial color-coded duplex sonography [4351]
Cerebral autoregulation
Changes in the cerebral perfusion pressure (CPP) and
blood ow velocities
Detection of intra-extra-axial space-occupying lesions
Non-invasive estimation of ICP
Cerebral autoregulation
Changes in the cerebral perfusion pressure (CPP) and
blood ow velocities
Detection of Intra-extra-axial collection
Middle line shift (MLS)
Assessment of the cerebral deep venous system and dural
sinuses
Detection of intra-axial space-occupying lesion
risk factor to develop sepsis-associated encephalopathy
Non-invasive estimation of ICP
C. N. Rodríguez and D. Pugin

14.9 TCCS Protocol: Hemodynamic Parameters

With the use of transcranial color-coded duplex sonography (TCCS), we can obtain information, in real time, about hemodynamic behavior and anatomical distribution of the basal cerebral arteries:
1. Visualize: Access the anatomical landmarks to identify the different basal cere­bral arteries to insonate
(B-Mode and color Doppler).
2. Flow Direction: Identify intracranial anatomical distribution of the basal cere­bral arteries and ow direction of each one (Color-coded Doppler).
3. Flow Patterns: Identify the blood ow velocities and spectral Doppler waveform of each insonated basal cerebral artery (PW Doppler) (Table14.3).
After identifying the vessel to insonate (Color Doppler), the pulsed wave Doppler (PW Doppler) is placed to obtain the signal corresponding to the Doppler spectrum. The hemodynamic parameters derived from the pulsed Doppler are as follows:
(a) Peak Systolic Velocity (PSV) (b) End-Diastolic Velocity (EDV) (c) Mean Flow Velocity (MFV) (d) Pulsatility Index (PI) (e) Resistance Index (RI)
14 Neurosonology in ICU: Transcranial Color-Coded Duplex Sonography (TCCS…
Table 14.3 Normal velocity values in the basal cerebral arteries [14, 16, 40, 5360]
Artery
Middle cerebral artery (MCA) 90±16 45±10 62±12 Anterior cerebral artery (ACA) 78±18 35±6 50±15 Posterior cerebral artery (PCA) 53±11 26±7 37±10 Vertebral artery (VA) 40±12 20±5 29±15 Basilar artery (BA) 52±9 31±9 39±9
Table 14.4 Flow direction and waveform
Artery Flow direction Spectral waveform
Middle cerebral artery (M1– M2) Toward to the probe (red color) Low resistance Anterior cerebral artery (A1) Away from the probe (blue color) Low resistance Posterior cerebral artery (P1) Toward to the probe (red color) Low resistance Posterior cerebral artery (P2) Away from the probe (blue color) Low resistance Vertebral artery (VA) Away from the probe (blue color) Low resistance Basilar artery (BA) Away from the probe (blue color) Low resistance Ophthalmic artery (OA) Toward to the probe (red color) High resistance
PSV (cm/s)
EDV (cm/s)
MFV (cm/s)
275
Table 14.5 Normal values of the hemodynamic indexes [54]
Artery Pulsatility index (PI)
Middle cerebral artery (MCA) 0.9±0.24 Anterior cerebral artery (ACA) 0.83±0.17 Posterior cerebral artery (PCA) 0.88±0.2 Vertebral artery (VA) 0.86±0.08 Basilar artery (BA) 0.86±0.09
As previously stated, if the blood ows toward the probe, it is color-coded red and is positive. On the opposite, if the ow moves away from the probe, it is color­coded blue and is negative (Table14.4). The shape of the ow curve gives an indica­tion of the system’s resistance. If the diastolic velocities are low, the resistances are high, while if the diastolic velocities are high, the resistances are low.
Using the velocities recorded for each vessel, a Pulsatility Index (PI) and Resistance Index (RI) can be calculated (Table 14.5). Only the PI is used in the TCCS analysis and is an indirect indication of the increased intracranial pressure. It is worth noting that the ow rates of intracerebral arterial vessels decrease with the age of the patient. On the contrary, pulsatility increases with the age of the patient [61].
Remember that to obtain a more accurate measurement of the ow velocity, the correction of the insonation angle with the positioning of the pulsed wave spectral Doppler cursor as parallel as possible to the ow is mandatory (< 60°) [62].
276
C. N. Rodríguez and D. Pugin

14.10 TCCS Protocol: Limitations

The TCCS is not a perfect technique. Many aspects (technical and interpretative) must be considered in order to obtain a reliable examination. Therefore, we should keep in mind operator dependency and a 10–20% of patients having inadequate transtemporal acoustic window.
14.10.1 Limitations
14.10.1.1 Acoustic Windows
The effectiveness of the transcranial color-coded duplex sonography (TCCS) depends on the good penetrance of the ultrasound through the temporal bone and/or through the suboccipital window:
Transtemporal Acoustic Window
There is a 10–30% of patients, in middle age, in which the study cannot be carried out due to the lack of an adequate acoustic window. These values are decreasing as the quality of the TCCS improves. Sometimes, the A2 segment of ACA is not pos­sible insonated. Then, we should elect another acoustic window (Frontal bone window).
Suboccipital Acoustic Window
Sometimes, the anatomical morphology of the vertebro-basilar arterial system is tortuous where the insonation is difcult.
In the cervical syndromes, especially in the spinal cord injury, a neck exion to access the suboccipital acoustic window to insonate the vertebro-basilar system is not possible. Then, the submandibular acoustic window can be selected.
14 Neurosonology in ICU: Transcranial Color-Coded Duplex Sonography (TCCS…
277
14.10.1.2 Middle-Line Shift Measurement
This technique allows to measure the midline shift changes at bedside. It is impor­tant to keep in mind that a little tilt of the probe may alter the results [6366]. This ultrasound measure is difcult in case of subdural or epidural hematomas and in clinical situations where the temporal window is temporarily (post-operative) blocked or absent [48, 67].
On the other hand, the hydrocephalus should not alter the measurement [68, 72].
14.10.1.3 Limitations inSpecic Clinical Situations
Intra-/Extra-Axial Space-Occupying Lesions: Diagnosis andMonitoring
The TCCS is useful in the diagnosis and monitoring of intra- or extra-axial collec­tions, which can be seen on the B-Mode. In case of subdural and epidural hema­toma, a midline shift could be observed. This bedside exam may limit the use of brain CT scan and their repetition. The suspicion of the location of the intra-axial space-occupying lesions is important in determining the usefulness of brain ultra­sound. Frontal and parietal collections may be the most difcult to detect.

14.11 Conclusion

The increase of ICU specialists with ultrasound abilities and availability of ultra­sound machines in the ICU creates the best condition for a wider use of transcranial color-coded duplex sonography (TCCS). As discussed in this chapter, this technique provides many relevant clinical information at bedside that directly impact the ther­apeutic strategies in the acute neurological patients. TCCS allows intensivists to provide an immediate evaluation next at patient’s bedside (24hours a day, 7days a week) in both acute neurological injury (TBI, SAH, etc.) and non-neurological criti­cal pathology (Sepsis, Acute liver failure, ARDS, RRT, etc.). Therefore, it is expected and necessary that the use of the TCCS becomes a very valuable comple­ment in the routine clinical investigations of the intensive care units.
278

Algorithm

C. N. Rodríguez and D. Pugin
ICPn
ESTIMATION
Transtemporal Window Transorbital Window
Mesencephalic
Plane
MEASUREMENT TRENDS
Pulsatility Index (PI)
MCA / ACA Oxygenation? Pupillary Diameter
PCA / BA CBFV -OA
Neurological
Monitoring
TRANSCRANIAL COLOR-CODED DUPLEX SONOGRAPHY (TCCS)
CEREBRAL HEMODYNAMIC BRAIN PARENCHYMA
FRONTAL BONE
WINDOW
1. Paramedian Zone Anterior Triangle
2. Supraorbital Zone Circle of Willis Mesencephalic Plane
3. Laterofrontal Zone Diencephalic Plane Mesencephalon
1. A1-ACA 2. ECA 3. A2-ACA 3. PICA 3th Ventricle
2. A2-ACA 3. ICA Ventricular Plane Thalamus
3. Circle of Willis M3-MCA Pineal Gland
SUBMANDIBULAR
WINDOW
Of Neck
1. CCA 2. M3-MCA 2. BA Diecenphalic Plane
CBFVs Spectral Doppler Waveform Sphenoid bone
Lindegaard Index Pulsatility Index Petrosal bone
Cerebral Autoregulation: Mx / PRx / Sx Anterior Coronal Plane
CONSIDER: Trendof the Measurements Frontal horns of LV
INTENSIVE CARE UNIT (ICU)
EMERGENCY DEPARTMENT (ED)
Clinical Status of the Patient
ABCD MI < 2.3 Level of Consciousness (GCS) TI < 2.0
Bilateral Pupillary Reactivity. Hemodynamic Stability? ONSD
DIAGNOSIS
CRITICALLY ILL
PATIENT
TRANSTEMPORAL
WINDOW
Mesencephalic Plane Foramen Magnum
1. M2-MCA 1. V4-VA Perimesencephalic Cisterns
Upper PontinePlane Midline Shift (MLS)
Siphon-ICA Ventricular Plane
OA Frontal horns of LV
Lower Pontine Plane Upper Pontine Plane
C1-ICA Sphenoid bone
Anterior Coronal Plane Petrosal bone
C1-ICA Medial Cerebral Fossa
MEASUREMENTS Lower Pontine Plane
TRANSFORAMINAL
WINDOW
NEURO-ORBITAL
ULTRASOUND
SAFETY
ALARA
MEASUREMENT TRENDS
CBFV -CRA
Neurological Compromise
ULTRASOUND
(B-Mode)
TRANSTEMPORAL
WINDOW
Cerebellum
ABCD Airway-breathing-circulation-disability, GCS Glasgow coma scale, FVs Peak systolic velocity, FVm Mean velocity, MCA Middle cerebral artery, ACA Anterior Cerebral Artery, PCA Posterior Cerebral Artery, BA Basilar Artery, VA Vertebral Artery, OA Ophthalmic artery, ONSD optic nerve sheath diameter, CRA Central retinal artery, ICPn Non-invasive intracranial pressure,
CBFV Cerebral blood ow velocity, LV Lateral ventricle, PICA Postero- inferior cerebellar artery, TI Thermal index, MI Mechanical index, Mx Mean ow index, Sx systolic ow index, PRx Pressure
reactivity index.

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281
Chapter 15
Fc
()
Transcranial Color-Coded Duplex Sonography (TCCS): Importance ofAngle Correction
PiergiorgioLochner, AntonioSiniscalchi, andAndreaNaldi
Key Points
1. Angle correction can be performed by TCCS, allowing a more real measurement
of cerebral vessels’ ow velocity compared to not angle-corrected ones.
2. TCCS angle-corrected velocity is proportional but not equal to the true velocity.
3. Angle correction should be performed when the Doppler sample volume identi-
es a sufcient straight vessel segment (at least 15mm in length) in order to ensure a correct assessment.
4. Angle correction should be performed when the angle between the ultrasonic
beam and the vessel is small, in other way be likely to produce signicant errors.
5. The angle-corrected velocity with TCCS is signicantly higher as compared to
the uncorrected velocity of the same system or to conventional TCD.

15.1 Introduction

Based on the Doppler equation (Eq.15.1)
Fv
=
P. Lochner (*) Department of Neurology, Saarland University Medical Center, Homburg, Germany e-mail: piergiorgio.lochner@uks.eu
A. Siniscalchi Department of Neurology and Stroke Unit, Annunziata Hospital, Cosenza, Italy
A. Naldi Department of Neuroscience Rita Levi Montalcini, University of Turin, Turin, Italy
C. N. Rodríguez et al. (eds.), Neurosonology in Critical Care,
https://doi.org/10.1007/978-3-030-81419-9_15
2• •cos /
α
(15.1)
283© Springer Nature Switzerland AG 2022
284
(incident frequency)
r
P. Lochner et al.
where ΔF is the Doppler shift, F is the frequency of incident wave, and c is the propagation speed. Flow velocity (v) of a target vessel depends on the cosine of the angle (α) between the ultrasonic beam and blood ow (Fig.15.1).
Thus, in ideal circumstances, if the ultrasound (US) beam is parallel to ow direction (angle α=0), the cos α=1 and ow velocity will correspond to reality. On contrary, when the US beam is perpendicular to ow direction (angle α=90°), the cos α =0, resulting in a weak receiving signal and false ow velocity. Therefore, one of the most important limiting factors for the estimation of correct blood ow velocity is represented by the angle of insonation. The impact of the angle insonation on ow velocities is relatively low in a range of 0–30°, and it is still considered acceptable until 60°. On contrary, angle >60° generates large variation in the cosine used for the correction, resulting in signicant errors of measurements [1] (Fig.15.2).
Moreover, we should keep in mind that the arteries of circle of Willis can have a different angle of insonation of ultrasound and angle of vessel. In 10%, the insonation angle of anterior cerebral artery (ACA) is more than 40° and in 33% the angle of posterior cerebral artery (PCA) is between 31° and 40° [2].
Two techniques are currently available for the assessment of intracranial vessel ow velocity: transcranial Doppler (TCD) (Fig.15.3) and transcranial color-coded duplex sonography (TCCS).
In conventional TCD, the identication of cerebral arteries is based on the posi­tion of transducer, ow direction, and insonation depth. Introduced since the 80s, this technique was also dened as “blind sonography,” because it does not allow a direct visualization of brain vessels. Even if the insonation angle is uncertain, it is assumed to be 0 degree, or anyway small enough (range 0–30°) to not determine signicant errors of measurements [3, 4]. On this basis, normative values of intra­cranial arteries blood velocity have been proposed and widely used (Table15.1).
On the other hand, the more recent TCCS allows the combination of B-mode and color Doppler imaging, permitting the real-time visualization of parenchymal
Fig. 15.1 The alpha angle (α) of the Doppler equation is determined by the intersection between the incident frequency emitted by the ultrasound transducer and the direction of blood ow
Blood flow
Receiving frequency
Ultrasonic beam
Transduce
α