Abstract
Ischemia is a common and deleterious secondary injury following traumatic brain injury (TBI). A great challenge for the treatment of TBI patients in the neurointensive care unit (NICU) is to detect early signs of ischemia in order to prevent further advancement and deterioration of the brain tissue. Today, several imaging techniques are available to monitor cerebral blood flow (CBF) in the injured brain such as positron emission tomography (PET), single-photon emission computed tomography, xenon computed tomography (Xenon-CT), perfusion-weighted magnetic resonance imaging (MRI), and CT perfusion scan. An ideal imaging technique would enable continuous non-invasive measurement of blood flow and metabolism across the whole brain. Unfortunately, no current imaging method meets all these criteria. These techniques offer snapshots of the CBF. MRI may also provide some information about the metabolic state of the brain. PET provides images with high resolution and quantitative measurements of CBF and metabolism; however, it is a complex and costly method limited to few TBI centers. All of these methods except mobile Xenon-CT require transfer of TBI patients to the radiological department. Mobile Xenon-CT emerges as a feasible technique to monitor CBF in the NICU, with lower risk of adverse effects. Promising results have been demonstrated with Xenon-CT in predicting outcome in TBI patients. This review covers available imaging methods used to monitor CBF in patients with severe TBI.
Introduction
Traumatic brain injury (TBI) is one of the leading causes of death and disability in young adults. Acute TBI is characterized by a primary and a secondary injury. Primary brain injury is the direct injury to the brain parenchyma at the time of the initial impact, which can be both focal and diffuse depending on the biomechanics of the impact. The secondary brain injury is caused by a combination of neuronal and vascular damage, proteolytic pathways, excitotoxicity, oxygen-free radicals, apoptosis, inflammatory processes, and ischemia (1). Secondary brain injury may also be caused by secondary clinical events, e.g., increased intracranial pressure (ICP), hypotension, hypoxemia, seizures, and pyrexia (2).
Ischemia plays a major role in the pathology of TBI; signs of ischemic brain damage are found on autopsy in more than 90% of TBI patients (3, 4). Astrup et al. demonstrated that the critical ischemic cerebral blood flow (CBF) threshold for electrical/functional disturbance was higher than the threshold for complete electrical failure/infarction, which was the foundation for the ischemic penumbra concept (5, 6). Jones et al. showed that the risk of infarction was dependent both of the CBF level and duration of time with decreased CBF (7). Furthermore, the degree and duration of decreased CBF was shown to be decisive of the outcome (8) and correlated with injury severity following TBI (9, 10).
Another important observation was the “luxury perfusion syndrome” originally described by Lassen (11). This syndrome was described as cerebral hyperemia or “over-abundant CBF relative to the metabolic needs of the brain tissue.” Cerebral hyperemia following brain injury has been demonstrated in several studies using intravenous Xenon-133 (12, 13). Normal and high CBF with narrow arteriojugular venous difference of oxygen (AVDO2) indicating “luxury perfusion” has been shown in comatose TBI patients (14).
Areas surrounding the focal regions of reduced CBF display milder reductions in flow following TBI (15, 16). It has been suggested that this area is at risk for secondary insults but most importantly, due to its viability, it is sensitive to therapeutic interventions (17).
The brain has almost no capacity to survive without oxygen. Its reserved oxygen capacity will only last for a few seconds. The brain adenosine triphosphate (ATP), the fuel crucial for neuronal functioning, will only last for 40 s during complete ischemia (18). Furthermore, the level of ATP in brain tissue following TBI has been shown to correlate to the severity of the brain injury (19).
Mean arterial pressure (MAP), ICP, PaCO2, and PaO2 are the physiologic variables that would influence CBF. The most important relationship, however, is the principle of flow-metabolism coupling whereby cerebral metabolic rate of oxygen (CMRO2) is directly related to CBF and AVDO2 (20).
Changes in CBF following TBI in patients have been described as a triphasic pattern. During the first and acute phase, there is a 50% decrease in CBF (21, 22). During the following initial 12 h post-injury, the second phase begins, marked by a rise in CBF that approaches or exceeds normal values in some patients and typically persists for the next 4–5 days (23). This phase is followed in turn by a third period of low CBF that lasts for up to 2 weeks post-injury. However, there is a strong heterogeneity of CBF among TBI patients. In some patients, the CBF may persist low while in others normal CBF values can be seen that remains for days to weeks. The assessment of CBF following TBI is important to detect episodes of ischemia. Ischemia in TBI patients regardless of when detected has shown to be correlated with poor outcome (21, 23, 24). It is important to relate CBF changes to the metabolic demand where both metabolic depression and transient hyperglycolysis following TBI have been observed (25–27). The episodes of high CBF paralleled the episodes of hyperglycolysis and the question was raised whether low CBF in patients following TBI always means an inadequate supply for metabolic demand. Combining CBF imaging with microdialysis could show that high lactate/pyruvate ratio, usually interpreted as ischemia, occurred despite that the CBF was not low (28). This suggested that the metabolic crises can be caused by mitochondrial dysfunction rather than inadequate CBF.
A great challenge for the treatment of TBI patients in the neurointensive care unit (NICU) is to detect early signs of secondary brain injury in order to prevent further advancement and deterioration of the brain tissue. Multimodality monitoring using focal and global methods provides valuable information but has its limitations. Imaging of the brain may add important information. An ideal imaging technique would enable continuous non-invasive measurement of regional blood flow and metabolism across the whole brain. Currently, there are several methods that offer snapshots of the CBF, and some also provides information about the metabolic state of the injured brain. The aim of this article is to give a short review of currently available brain imaging methods used in patients with severe TBI. Relevant references are summarized in Table 1.
Table 1
| Reference | Subject | Additional monitoring | Time post-injury | n | GCS |
|---|---|---|---|---|---|
| XENON-CT | |||||
| Yonas et al. (29, 30) | CBF and TBI | 1 | GCS ≤8 | ||
| Langfitt et al. (31) | Imaging pathology and neuropsychological tests (133Xe) | MRI, PET, CT, Xenon-133 | Acute and 6 months | 3 | GCS ≤13 |
| Latchaw et al. (32) | CBF in different types of TBI | During NIC stay | 35 | GCS ≤8 | |
| Marion et al. (21) | Xenon-CT and ICP | Within 7 days | 23 | GCS ≤8 | |
| Schalen et al. (33) | CBF and hyperventilation response (133Xe) | Jugbulb | During NIC stay | 38 | GCS ≤8 |
| Marion et al. (21) | CBF following TBI | 1 h–7 days | 32 | GCS ≤7 | |
| Bouma et al. (23) | Early measurement of CBF in TBI | Jugbulb | First 24 h | 186 | GCS ≤8 |
| Bouma et al. (22) | CBF in acute phase of severe TBI | 3 h | 35 | GCS ≤8 | |
| Bouma et al. (22) | Autoregulation test (133Xe) | First days | 47 | GCS ≤8 | |
| Stringer et al. (34) | CBF and hyperventilation | During NIC stay | 12 | ||
| Bouma and Muizelaar (35) | Xenon-CT evaluation in TBI | ||||
| McLaughlin and Marion (36) | CBF and vasoresponsivity in contusions | 24–48 h | 10 | GCS ≤8 | |
| Kelly et al. (37) | CBF and outcome (133Xe) | 1–5 days | 54 | GCS ≤12 | |
| Schroder et al. (38) | Relation of CBV and CBF to explain cause of ischemia | Dynamic CT imaging (CBV) | 24 h | 51 | GCS ≤8 |
| Bouma et al. (39) | Underlying cause of cerebral swelling | Dynamic CT imaging (CBV) | Early posttrauma | 37 | |
| Doppenberg et al. (40) | Relation of potassium, glutamate, lactate, and CBF | Microdialysis | 70 | GCS ≤8 | |
| Kushi et al. (41) | CBF, C02, pH and CMR02 as prognostic indicator | Jugbulb | 22 | GCS ≤8 | |
| Hoelper et al. (42) | rCBF and contusions | 29 and 94 h | 44 | GCS ≤8 | |
| von Oettingen et al. (43) | TBI and pulmonary trauma, xenon concentration and CBF | 5 | |||
| Schutt et al. (44) | Thermo-dye-dilution and Xenon-CT | Thermo-dye-dilution | 1–5 days | 16 | GCS ≤8 |
| Valadka et al. (45) | CBF and pbr02 | pbr02 | 18 | GCS ≤6 | |
| Furuya et al. (46) | CBF and hypodense area | 50 | GCS ≤8 | ||
| Chieregato et al. (47) | rCBF in traumatic hemorrhagic contusions | 14 | GCS ≤9 | ||
| Chieregato et al. (48) | CBF and hypertension | 7 | GCS ≤8 | ||
| Chieregato et al. (49) | Recovery of CBF in tICH | First 20 day | 22 | GCS ≤8 | |
| Inoue et al. (50) | CBF and 6 months outcome | 1,2, 3, 4, 6 weeks | 20 | GCS ≤8 | |
| Chieregato et al. (51) | CBF in hematomas and traumatic contusions | 43 | GCS ≤8 | ||
| Poon et al. (52) | C02 reactivity and cerebral hemodynamics | TCD, ICP, Microdialysis | 35 | GCS ≤12 | |
| Marmarou et al. (53) | Type of edema in diffuse and focal TBI | DWI, MR | 45 | GCS ≤8 | |
| Chieregato et al. (54) | CBF and CPP levels | Jugbulb | During NIC stay | 237 | GCS ≤8 |
| Masaoka (55) | CBF during hypothermia | Jugbulb | 1–4 days | 30 | GCS ≤8 |
| Robertson et al. (56) | Genetic polymorphism of N03 and CBF | 12 and 48 h | 51 | GCS ≤8 | |
| Kaloostian et al. (57) | Outcome prediction within 12 h following TBI | 12 h | 120 | GCS ≤8 | |
| Shafer et al. (58) | CBF and oxygen saturation | INVOS | During NIC stay | 22 | “Intubated” |
| PET | |||||
| Bergsneider et al. (27) | Cerebral hyperglycolysis in TBI patients | 1–24 h | 28 | GCS ≤8 | |
| Hattori et al. (59) | Metabolic rate of glucose and level of consciousness | 1–5 days | 23 | GCS ≤15 | |
| Coles et al. (60) | Measurement of ischemic lesion | 1–24 h | 12 | GCS ≤12 | |
| Coles et al. (61) | Ischemic brain volume and outcome | 1–72 h | 15 | GCS ≤12 | |
| Hattori et al. (62) | characterize contusional, pericontusional, and remote regions in TBI | 1–5 days | 21 | GCS 3-15 | |
| Wu et al. (63) | Metabolic rate of glucose in gray matter | 1–4 days | 14 | GCS ≤14 | |
| Cunningham et al. (64) | Threshold for irreversible tissue damage | 1–5 days | 14 | GCS ≤8 | |
| Vespa et al. (28) | Microdialysis and PET | Mean 36 h | 19 | GCS ≤14 | |
| SPECT | |||||
| Abdel-Dayem et al. (65) | SPECT correlated to CT | 24 h | 14 | GCS ≤8 | |
| Roper et al. (66) | SPECT correlated to CT | 72 h | 15 | GCS ≤15 | |
| Ito et al. (67) | Cerebral perfusion in diffuse brain injury and relationship to atrophy | Within 1 week and 1–6 months | 8 | GCS ≤8 | |
| PERFUSION CT | |||||
| Wintermark et al. (68) | Correlation of CPP and CBF | 61 | GCS ≤8 | ||
| Wintermark et al. (69) | Prognostic value of admission CBF | At admission | 130 | GCS ≤10 | |
| Soustiel et al. (70) | Prognostic value of admission CBF | At admission and l week | 30 | GCS ≤9 | |
| Huang et al. (71) | Progression of cerebral contusions | 1–6 h | 22 | GCS ≤8 | |
| Bendinelli et al. (72) | CBF within the first 48 h following TBI | 1–48 h | 30 | GCS ≤8 | |
| PERFUSION-MRI | |||||
| Garnett et al. (73) | rCVB in contusion | 2–19 days | 18 | GCS ≤8 vs. ≥9 | |
| COMPARATIV STUDIES | |||||
| Hagen et al. (74) | Comparison PW-MRI and Xenon-CT | 1–24 h | 10 | Stenosis, HCF, atrophy | |
| Rempp et al. (75) | PW-MRI and PET in healthy subjects | 12 | NC | ||
| Gillard et al. (76) | Comparison CTP and PET in AVM and gliomas | 8 | 8 AVM, 2 glioma | ||
| Campbell et al. (77) | Comparison PW-MRI and perfusion CT in ischemic stroke | 3–6 h | 49 | Acute stroke | |
Presents a summary of publications using Xenon-CT, PET, perfusion CT, perfusion-MRI, and comparative studies using different imaging modalities.
CBF, cerebral blood flow; ICP, intracranial pressure; CPP, cerebral perfusion pressure; CT, computer tomography; rCBV, regional cerebral blood flow; tICH, traumatic intracranial hematoma; pbrO2, partial brain oxygen tension; Jugbulb, jugular bulb; INVOS, brain tissue oxygen saturation.
Positron Emission Tomography
Positron emission tomography (PET) is an imaging technique that provides quantitative measurement of cerebral perfusion and metabolism (78, 79). Positron emitting radionuclides are used either after incorporation into chemical compounds (e.g., C15O, C15O2, and H2150) or as molecular tracers (e.g., 15O2). After intravenous administration or inhalation, the isotopic tracer is distributed in the tissues according to the physiological properties, and the radioactive tracer concentration is measured regionally. The radioisotopes, which are produced by a cyclotron, have short half-life and must be used without delay. The detected regional tracer concentrations allows for mathematical quantification of CBF, cerebral blood volume (CBV), the oxygen extraction fraction (OEF), and CMRO2 (80–82).
O15-radioisotope has been used to measure CBF and OEF, while F19 deoxyglucose (FDG) assesses regional brain glucose metabolism. FDG is analogous to glucose in the body. It rapidly crosses the blood–brain barrier and is taken up into brain cells. Since FDG is not further metabolized, it can be imaged to produce metabolic maps for PET imaging. The images obtained are then generally co-registered with CT or magnetic resonance imaging (MRI) to obtain anatomic relationships (78, 79, 83).
Several studies have used PET in assessment of TBI (27, 28, 59, 60, 62–64, 84–86).
Regional brain ischemia was detected in TBI patients, who underwent PET within 24 h following injury according to CBF, OEF, and CMRO2 measurements, and an increase of the ischemic volume was correlated with poor outcome (61).
By using PET, both hypo- and hyperglycolysis have been demonstrated in TBI patients. In a study performed by Bergsneider et al., it was shown that both global and regional hyperglycolysis occur following severe TBI. Within 1 week following injury, 56% of the patients showed evidence of hyperglycolysis using FDG-PET (27). In a follow-up study, PET was performed within 4 days following TBI, and a depressed cerebral metabolic rate of glucose was observed (63).
Combining PET with microdialysis in TBI patients, Vespa et al. demonstrated high lactate/pyruvate ratio that indicates metabolic crises without presence of ischemia according to PET (28). It was suggested that high lactate/pyruvate ratio under those circumstances indicated mitochondrial dysfunction rather than ischemia (28, 87, 88).
One of the advantages of PET is that it can generate images of greater resolution. The main advantage is that PET provides the possibility to obtain quantitative regional measurements of both CBF and metabolism. The drawbacks are that the generation of isotopes requires a costly cyclotron and is labor intensive. In addition, the isotopes that are used have a shorter half-life thereby requiring that the radiopharmaceuticals must be readily available. Furthermore, PET provides a non-continuous measurement and the need for transfer of the patient to a radiology unit (61, 89).
Single-photon emission computed tomography
The principal of single-photon emission computed tomography (SPECT) is similar to PET in using radioactive material to detect gamma rays. The tracer usually used is the radioisotope 99mTc that crosses the blood–brain barrier and localize in the brain tissue in proportion to blood flow. SPECT is a semi-quantitative CBF measurement technique that is based on the calculation of tracer uptake ratios and an estimation of the relative regional CBF (rCBF) distribution within the brain (90).
An initial study lesions detected by SPECT in TBI patients during the first 72 h was compared to CT findings. It was shown that SPECT detected 40% more lesions than shown by CT scans (65). Similar results have been reported by Roper et al. (66). In a study of eight patients with severe diffuse TBI, SPECT revealed several lesions in all patients, even in non-depicted regions on MRI (67). Abnormalities in cerebral perfusion were also observed 1–6 months following injury.
There are numerous publications proving SPECT functional brain imaging as a powerful research tool, especially in the fields of cerebrovascular disease and cognitive disorders, and there is extensive development in receptor and molecular imaging (91). In a recent systematic review, Raji et al. concluded that SPECT imaging could be useful in evaluating patients with neurological and psychiatrically sequela after TBI (92).
Although SPECT provide images with lower resolution than PET, the radioisotope is significantly less expensive and longer lasting with no need of cyclotrons. Implementation of SPECT into clinical routine for estimation of rCBF in the acute phase of TBI is however lacking.
Stable Xenon Computed Tomography
Xenon computed tomography (Xenon-CT) utilizes inhalation of a gas mixture containing 28% (30–35% in older studies) non-radioactive xenon (131Xe) and oxygen. The Xenon gas is a radio opaque, highly lipid soluble and capable of crossing the BBB. The Kety–Schmidt equation is applied to measure regional and global CBF. It provides primarily measurements of rCBF in the cortex and has been used under a variety of clinical conditions to study the pathophysiology and guide therapy regarding blood pressure and ventilation management (29). The first report of Xenon-CT in a TBI patient demonstrated that this technique could be used to detect regions with loss of autoregulation and CO2 reactivity (30). In a following Xenon-CT study including 35 TBI patients, the feasibility of using Xenon-CT for detecting changes in CBF, for guidance of the degree of hyperventilation, and for the identification of brain death was evaluated (32). Higher incidence of ischemia (very low CBF) than previously assumed following TBI could be demonstrated by Xenon-CT (35), which also was shown to be associated to high early mortality (22). Studies on contusions following TBI have shown that the CBF is concentrically distributed, improving from the core to the periphery (47). In traumatic hematomas, it was shown that low rCBF levels seen in the perihematoma low-density area CBF recovered from day 2 and forward and persistence ischemia was only seen in the core (49). It appears that type of contusion is also determinant of rCBF, with lower values in mixed contusions compared to hamorrhagic and non-hamorrhagic contusions (42).
The Xenon-CT has also been used to evaluate the effect of different interventions performed in the NICU on CBF following TBI. Chieregato et al. observed that rCBF in the intracontusional low-density area having critically reduced initial values was marginally affected by norepinephrine induced increase in cerebral perfusion pressure (CPP). However, in subjects starting from non-critical baseline values, rCBF was significantly reduced (48). Stringer et al. reported that hyperventilation in patients with acute brain lesion reduced CBF substantially both within the lesion and in apparently normal brain regions (34). Furthermore, the CBF in contusions has been shown to be reduced but with preserved CO2 reactivity. It was suggested that this area and the surrounding parenchyma are hypersensitive to hyperventilation and hypotension and thus vulnerable to secondary injury (36). The CO2 reactivity has been suggested as a good early prognostic indicator (41). In the study by Kushi et al., jugular bulb catheters were used in combination with Xenon-CT. Xenon-CT with simultaneous multimodality monitoring have generated interesting results regarding CBF and metabolism following TBI. Combining Xenon-CT with cerebral microdialysis showed that loss of CO2 reactivity was associated with increased ICP and increased lactate, glutamate and glycerol dialyzate levels, and consistently a fatal outcome (52). In another study, areas with low CBF showed increased levels of glutamate (40).
Xenon computed tomography has also been combined with tissue oxygen tension monitoring in TBI, and it showed a linear relationship between pbrO2 and CBF (45).
Promising results have been demonstrated with Xenon-CT in predicting outcome in TBI patients. Patients with low CBF that returns to normal 2–3 weeks following severe TBI show better neurological outcome that the group who had sustained low CBF (50).
In a recent study, Xenon-CT was used to monitor CBF in the first 12 h following injury in 120 TBI patients. It was shown that measurement of CBF within the first 12 h predicts 6 months outcome, and the best outcome prediction was obtained if Xenon-CT was measured within 6 h following TBI (57). In TBI, patient with pulmonary injury care should be taken in CBF analyses since end-tidal and arterial xenon concentration curves can be a source of error (43).
Previous studies indicate that endothelial nitric oxide synthase (NO3) activity is important in maintaining CBF after TBI. Using Xenon-CT, Robertson et al. studies the association of genetic polymorphism of NO3 and CBF following TBI. They showed that patients with the C/C genotype had lowest CBF values and worse outcome (56).
Xenon computed tomography is fast and provides quantitative measurements of CBF. The big advantage is that by using a mobile CT scanner there are no need to transport the patient to a different setting, which is always associated with increase risk of adverse events (93, 94). Other advantages are the short half-life and very low risk of side effects of inhaled Xenon, which makes repeated examinations more feasible. The very low risk of side effects was demonstrated in a recent multicentre evaluation study concluding that CBF measurements by Xenon-CT can be performed safely, with a very low risk of adverse events, and no risk of permanent morbidity or sequela could be detected (95). However, the brain is exposed to a small dose of radiation.
Wintermark et al. reported a radiation dose of 3.5–10 mSv for the whole xenon study (96). While Seifert et al. report that in the case of brain partially located in the region of primary radiation, a mean organ dose of 39 mSv was calculated, corresponding to an effective does of 1.6 mSv (97).
In our hands, the effective dose for a complete Xenon-CT examination is 2.7 mSv (in-house investigation, data not published). This dose can be compared to an annual mean background dose in Sweden of 3 mSv.
Brain Perfusion Imaging
Cerebral perfusion is defined as the steady-state delivery of blood to brain tissue per unit volume, measured in milliliters per 100 g of tissue per minute. Perfusion imaging uses intravascular tracers most commonly iodine or gadolinium contrasts depending on imaging method. These methods take advantage of signal changes that accompany the passage of tracer through the cerebrovascular system. Contrasts used in MRI, such as gadolinium, are compounds that work by altering the magnetic properties of nearby hydrogen nuclei, while CT perfusion uses iodine contrast agents, which are radiopaque (such as iohexol) (98, 99).
The data acquired can be used to generate color-coded maps and quantification of various perfusion parameters, including CBF, CBV, mean transit time (MTT), and time to peak (TTP; the time from the start of contrast agent injection to the time of maximum enhancement). The two commonly used methods are perfusion-MRI and CT perfusion and will be discussed below.
Perfusion-weighted MRI
The most common technique for measuring perfusion parameters with MRI is dynamic susceptibility contrast (DSC). DSC-MRI perfusion is also known as bolus-tracking MRI or perfusion-weighted MRI (PW-MRI). We chose PW-MRI throughout this review. In PW-MRI, a time series of fast T2-weighted images are acquired when gadolinium contrast agent is injected. As gadolinium passes through the tissues, it produces a reduction of T2 intensity depending on the local concentration. Curves showing intensity changes based on the concentration of gadolinium over time can be generated. This time-to-signal intensity alteration can be processed to extract parameters that reflect either CBF, CBV, or MTT. These are linked by the equation CBF = CBV/MTT, also known as the “central volume principle” (100, 101).
Studies on TBI using PW-MRI are limited. Garnett et al. used PWI during the subacute phase of TBI in a small group of patients and reported that regions of both normal-appearing and contused brain may have an abnormal regional CBV and had worse outcome (73). In a study including 10 patients with neurological illness, PW-MRI was compared with Xenon-CT and showed a good correlation of rCBF between these methods (74).
Perfusion-weighted MRI can be used together with diffusion-weighted MRI (DWI), then the ischemic penumbra can be identified (102, 103). It can assess vascular patency if magnetic resonance angiography (MRA) is added (104). PW-MRI was used in healthy subjects to measure absolute values of rCBF and rCBV and compares these to values obtained by PET. The values were in agreement with previous findings using PET both in white and gray matter (75). In a recent study, PW-MRI was compared with CT perfusion, and it was found that PW-MRI is superior in precision and accuracy in identifying ischemic core and salvageable tissue (77).
One of the advantages of PW-MRI is that the contrast agent used is gadolinium that has fewer contraindications than iodinated contrasts.
However, compared to CT scan the PW-MRI is relatively time-consuming and more expensive. MRI scans are also less available and more difficult to monitor patients in.
Computed tomography perfusion scan
In computed tomography perfusion (CTP), a native (unenhanced) CT is obtained followed by infusion of iodinated contrast. The concurrent acquisition of images after contrast injection allow for the measurement of changes in tissue attenuation that occur in the brain with time. Post processing of the data allows the generation of color-coded maps and quantification of various perfusion parameters, including CBF, CBV, MTT, and TTP. CTP has been mainly used in the management of patients with acute stroke and other cerebrovascular disorders since it provides an easy and practical way of obtaining both structural and CBF pictures. The first study performed with CTP in severe TBI included 130 patients and suggested that the number of arterial territories with low rCBV values was an independent prognostic factor regarding functional outcome (69). Same group examined the correlation of CPP and CTP findings. They could discriminate between two groups of patients; one without relationship between CBF and corresponding CPP values, considered as preserved autoregulation and the other group with strong correlation between CBF and CPP, interpreted as impaired autoregulation. Interestingly, the group with impaired autoregulation showed better clinical outcome (68).
Two studies have examined cerebral contusions using CTP in patients with TBI. In the first study, both contusional core and the surrounding brain tissue were examined. It was shown that early CBV and CBF maps corresponds better than an early native CT scan with the findings of non-contrast CT scans after 1 week, and therefore, CTP provides better early evaluation of tissue viability (70). In the second study, CTP was performed within 6 h of arrival, and contrast extravasation was predictive of hemorrhage progression (71). A recent study performed CTP during the first 48 h following severe TBI and confirmed abnormal perfusion following TBI and detected areas of hypoperfusion in 60% of patients that were not seen in conventional CT (72).
Measurement of CBF using CTP was compared with PET in patients with arteriovenous malformations and gliomas. Good correlation was found, although CTP had a tendency to overestimate CBF (76).
The advantages of CTP are that all units equipped with a CT scanner can obtain perfusion images and it is fast. Disadvantages include the exposure to radiation, potential for an allergic reaction to the iodine contrast, contraindication to use iodine contrast in case of renal insufficiency and the risk of inducing renal failure with repeated examinations, and the need to predetermine the regions of interest before the scan. Furthermore, although quantitative values can be acquired with perfusion CT, the accuracy of the flow values obtained has not been fully validated. It has not been determined if the references for normal CBF and critical CBF thresholds as measured with PET or Xenon-CT can be applied in perfusion CT. Perfusion CT uses an intravascular tracer to measure intravascular CBF, which likely reflects a different physiologic mechanism than that of PET and Xenon-CT, which employ a diffusible trace.
Conclusion
Cerebral hypoperfusion and other CBF disturbances are common after TBI and play an important role in the development of secondary brain injury. It has been difficult to integrate methods for quantitative rCBF measurements in neurointensive care, which relies mainly on uni-focal or global monitoring methods to detect cerebral ischemia or to evaluate different treatments aimed at increasing CBF. There is a need of a rapid assessment of CBF in the NIC unit without transportation of the patient. Currently, bedside Xenon-CT is the only method fulfilling these criteria. All other methods discussed above require transfer of TBI patients to the radiological department. However, Xenon-CT can only provide quantitative measurements of CBF. In order to assess parameters such as CBV, CMRglu, and CMRO2, it is necessary to use perfusion imaging and PET. PET is a complex and costly procedure with a need of cyclotron, which has limited its use to few TBI centers. None of the current available methods provide continuous measurements of CBF.
Bedside Xenon-CT emerges as an economical and more accessible imaging technique with few adverse effects that can be used in the routine NIC to measure CBF following TBI.
Statements
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
1
WernerCEngelhardK. Pathophysiology of traumatic brain injury. Br J Anaesth (2007) 99:4–9.10.1093/bja/aem131
2
RoseJValtonenSJennettB. Avoidable factors contributing to death after head injury. Br Med J (1977) 2:615–8.10.1136/bmj.2.6087.615
3
GrahamDIAdamsJHDoyleD. Ischaemic brain damage in fatal non-missile head injuries. J Neurol Sci (1978) 39:213–34.10.1016/0022-510X(78)90124-7
4
GrahamDIFordIAdamsJHDoyleDTeasdaleGMLawrenceAEet alIschaemic brain damage is still common in fatal non-missile head injury. J Neurol Neurosurg Psychiatry (1989) 52:346–50.10.1136/jnnp.52.3.346
5
AstrupJSymonLBranstonNMLassenNA. Cortical evoked potential and extracellular K+ and H+ at critical levels of brain ischemia. Stroke (1977) 8:51–7.
6
AstrupJSiesjoBKSymonL. Thresholds in cerebral ischemia – the ischemic penumbra. Stroke (1981) 12:723–5.
7
JonesTHMorawetzRBCrowellRMMarcouxFWFitzgibbonSJDegirolamiUet alThresholds of focal cerebral ischemia in awake monkeys. J Neurosurg (1981) 54:773–82.10.3171/jns.1981.54.6.0773
8
HeissWDRosnerG. Functional recovery of cortical neurons as related to degree and duration of ischemia. Ann Neurol (1983) 14:294–301.10.1002/ana.410140307
9
GrahamDIAdamsJH. Ischaemic brain damage in fatal head injuries. Lancet (1971) 1:265–6.10.1016/S0140-6736(71)91003-8
10
DietrichWDAlonsoOBustoRPradoRZhaoWDewanjeeMKet alPosttraumatic cerebral ischemia after fluid percussion brain injury: an autoradiographic and histopathological study in rats. Neurosurgery (1998) 43:585–93; discussion 593–84.10.1097/00006123-199809000-00105
11
LassenNA. The luxury-perfusion syndrome and its possible relation to acute metabolic acidosis localised within the brain. Lancet (1966) 2:1113–5.10.1016/S0140-6736(66)92199-4
12
BruceDALangfittTWMillerJDSchutzHVapalahtiMPStanekAet alRegional cerebral blood flow, intracranial pressure, and brain metabolism in comatose patients. J Neurosurg (1973) 38:131–44.10.3171/jns.1973.38.2.0131
13
EnevoldsenEMColdGJensenFTMalmrosR. Dynamic changes in regional CBF, intraventricular pressure, CSF pH and lactate levels during the acute phase of head injury. J Neurosurg (1976) 44:191–214.10.3171/jns.1976.44.2.0191
14
ObristWDLangfittTWJaggiJLCruzJGennarelliTA. Cerebral blood flow and metabolism in comatose patients with acute head injury. Relationship to intracranial hypertension. J Neurosurg (1984) 61:241–53.10.3171/jns.1984.61.2.0241
15
DeWittDSJenkinsLWWeiEPLutzHBeckerDPKontosHA. Effects of fluid-percussion brain injury on regional cerebral blood flow and pial arteriolar diameter. J Neurosurg (1986) 64:787–94.10.3171/jns.1986.64.5.0787
16
DietrichWDAlonsoOBustoRPradoRDewanjeeSDewanjeeMKet alWidespread hemodynamic depression and focal platelet accumulation after fluid percussion brain injury: a double-label autoradiographic study in rats. J Cereb Blood Flow Metab (1996) 16:481–9.10.1097/00004647-199605000-00015
17
BramlettHMGreenEJDietrichWD. Exacerbation of cortical and hippocampal CA1 damage due to posttraumatic hypoxia following moderate fluid-percussion brain injury in rats. J Neurosurg (1999) 91:653–9.10.3171/jns.1999.91.4.0653
18
SiesjoBK. Brain Energy Metabolism. New York, NY: John & Wiley (1978).
19
MarklundNSalciKRonquistGHilleredL. Energy metabolic changes in the early post-injury period following traumatic brain injury in rats. Neurochem Res (2006) 31:1085–93.10.1007/s11064-006-9120-0
20
ReillyPLBullockR. Head Injury, Pathophysiology and Management. London: Hodder Education (2005).
21
MarionDWDarbyJYonasH. Acute regional cerebral blood flow changes caused by severe head injuries. J Neurosurg (1991) 74:407–14.10.3171/jns.1991.74.3.0407
22
BoumaGJMuizelaarJPStringerWAChoiSCFatourosPYoungHF. Ultra-early evaluation of regional cerebral blood flow in severely head-injured patients using xenon-enhanced computerized tomography. J Neurosurg (1992) 77:360–8.10.3171/jns.1992.77.3.0360
23
BoumaGJMuizelaarJPChoiSCNewlonPGYoungHF. Cerebral circulation and metabolism after severe traumatic brain injury: the elusive role of ischemia. J Neurosurg (1991) 75:685–93.10.3171/jns.1991.75.5.0685
24
OvergaardJMosdalCTweedWA. Cerebral circulation after head injury. Part 3: does reduced regional cerebral blood flow determine recovery of brain function after blunt head injury?J Neurosurg (1981) 55:63–74.10.3171/jns.1981.55.1.0063
25
JaggiJLObristWDGennarelliTALangfittTW. Relationship of early cerebral blood flow and metabolism to outcome in acute head injury. J Neurosurg (1990) 72:176–82.10.3171/jns.1990.72.2.0176
26
HovdaDALeeSMSmithMLVon StuckSBergsneiderMKellyDet alThe neurochemical and metabolic cascade following brain injury: moving from animal models to man. J Neurotrauma (1995) 12:903–6.10.1089/neu.1995.12.903
27
BergsneiderMHovdaDAShalmonEKellyDFVespaPMMartinNAet alCerebral hyperglycolysis following severe traumatic brain injury in humans: a positron emission tomography study. J Neurosurg (1997) 86:241–51.10.3171/jns.1997.86.2.0241
28
VespaPBergsneiderMHattoriNWuHMHuangSCMartinNAet alMetabolic crisis without brain ischemia is common after traumatic brain injury: a combined microdialysis and positron emission tomography study. J Cereb Blood Flow Metab (2005) 25:763–74.10.1038/sj.jcbfm.9600073
29
YonasHGurDWolfsonSKJrGoodWFGoodBCLatchawRE. Xenon-enhanced computerised tomographic cerebral blood flow mapping. Lancet (1984) 1:1357.10.1016/S0140-6736(84)91856-7
30
YonasHSnyderJVGurDGoodWFLatchawREWolfsonSKJret alLocal cerebral blood flow alterations (Xe-CT method) in an accident victim. J Comput Assist Tomogr (1984) 8:990–1.10.1097/00004728-198410000-00038
31
LangfittTWObristWDAlaviAGrossmanRIZimmermanRJaggiJet alComputerized tomography, magnetic resonance imaging, and positron emission tomography in the study of brain trauma. Preliminary observations. J Neurosurg (1986) 64:760–7.10.3171/jns.1986.64.5.0760
32
LatchawREYonasHDarbyJMGurDPenthenySL. Xenon/CT cerebral blood flow determination following cranial trauma. Acta Radiol Suppl (1986) 369:370–3.
33
SchalenWMesseterKNordstromCH. Cerebral vasoreactivity and the prediction of outcome in severe traumatic brain lesions. Acta Anaesthesiol Scand (1991) 35:113–22.10.1111/j.1399-6576.1991.tb03258.x
34
StringerWAHassoANThompsonJRHinshawDBJordanKG. Hyperventilation-induced cerebral ischemia in patients with acute brain lesions: demonstration by xenon-enhanced CT. AJNR Am J Neuroradiol (1993) 14:475–84.
35
BoumaGJMuizelaarJP. Evaluation of regional cerebral blood flow in acute head injury by stable xenon-enhanced computerized tomography. Acta Neurochir Suppl (Wien) (1993) 59:34–40.
36
McLaughlinMRMarionDW. Cerebral blood flow and vasoresponsivity within and around cerebral contusions. J Neurosurg (1996) 85:871–6.10.3171/jns.1996.85.5.0871
37
KellyDFMartinNAKordestaniRCounelisGHovdaDABergsneiderMet alCerebral blood flow as a predictor of outcome following traumatic brain injury. J Neurosurg (1997) 86:633–41.10.3171/jns.1997.86.4.0633
38
SchroderMLMuizelaarJPFatourosPKutaAJChoiSC. Early cerebral blood volume after severe traumatic brain injury in patients with early cerebral ischemia. Acta Neurochir Suppl (1998) 71:127–30.
39
BoumaGJMuizelaarJPFatourosP. Pathogenesis of traumatic brain swelling: role of cerebral blood volume. Acta Neurochir Suppl (1998) 71:272–5.
40
DoppenbergEMReinertMZaunerAMassieTSBullockR. Determinants of cerebral extracellular potassium after severe human head injury. Acta Neurochir Suppl (1999) 75:31–4.
41
KushiHMoriyaTSaitoTKinoshitaKShibuyaTHayashiN. Importance of metabolic monitoring systems as an early prognostic indicator in severe head injured patients. Acta Neurochir Suppl (1999) 75:67–8.
42
HoelperBMReinertMMZaunerADoppenbergEBullockR. rCBF in hemorrhagic, non-hemorrhagic and mixed contusions after severe head injury and its effect on perilesional cerebral blood flow. Acta Neurochir Suppl (2000) 76:21–5.
43
von OettingenGBergholtBOstergaardLJensenLCGyldenstedCAstrupJ. Xenon CT cerebral blood flow in patients with head injury: influence of pulmonary trauma on the input function. Neuroradiology (2000) 42:168–73.10.1007/s002340050039
44
SchuttSHornPRothHQuintelMSchillingLSchmiedekPet alBedside monitoring of cerebral blood flow by transcranial thermo-dye-dilution technique in patients suffering from severe traumatic brain injury or subarachnoid hemorrhage. J Neurotrauma (2001) 18:595–605.10.1089/089771501750291837
45
ValadkaABHlatkyRFuruyaYRobertsonCS. Brain tissue PO2: correlation with cerebral blood flow. Acta Neurochir Suppl (2002) 81:299–301.
46
FuruyaYHlatkyRValadkaABDiazPRobertsonCS. Comparison of cerebral blood flow in computed tomographic hypodense areas of the brain in head-injured patients. Neurosurgery (2003) 52:340–5; discussion 345–6.10.1227/01.NEU.0000043931.83041.AA
47
ChieregatoAFainardiETanfaniAMartinoCPransaniVCoccioloFet alMixed dishomogeneous hemorrhagic brain contusions. Mapping of cerebral blood flow. Acta Neurochir Suppl (2003) 86:333–7.
48
ChieregatoAFainardiETanfaniASabiaGMartinoCPascarellaRet alInduced acute arterial hypertension and regional cerebral flow in intracontusional low density area. Acta Neurochir Suppl (2003) 86:361–5.
49
ChieregatoAFainardiEServadeiFTanfaniAPuglieseGPascarellaRet alCentrifugal distribution of regional cerebral blood flow and its time course in traumatic intracerebral hematomas. J Neurotrauma (2004) 21:655–66.10.1089/0897715041269669
50
InoueYShiozakiTTasakiOHayakataTIkegawaHYoshiyaKet alChanges in cerebral blood flow from the acute to the chronic phase of severe head injury. J Neurotrauma (2005) 22:1411–8.10.1089/neu.2005.22.1411
51
ChieregatoACompagnoneCTanfaniARavaldiniMTagliaferriFPascarellaRet alCerebral blood flow mapping in two different subtypes of intraparenchymal hemorrhagic traumatic lesions. Acta Neurochir Suppl (2005) 95:159–64.
52
PoonWSNgSCChanMTLamJMLamWW. Cerebral blood flow (CBF)-directed management of ventilated head-injured patients. Acta Neurochir Suppl (2005) 95:9–11.10.1007/3-211-32318-X_2
53
MarmarouASignorettiSAygokGFatourosPPortellaG. Traumatic brain edema in diffuse and focal injury: cellular or vasogenic?Acta Neurochir Suppl (2006) 96:24–9.10.1007/3-211-30714-1_6
54
ChieregatoATanfaniACompagnoneCTurriniCSarpieriFRavaldiniMet alGlobal cerebral blood flow and CPP after severe head injury: a xenon-CT study. Intensive Care Med (2007) 33:856–62.10.1007/s00134-007-0604-4
55
MasaokaH. Cerebral blood flow and metabolism during mild hypothermia in patients with severe traumatic brain injury. J Med Dent Sci (2010) 57:133–8.
56
RobertsonCSGopinathSPValadkaABVanMSwankPRGoodmanJC. Variants of the endothelial nitric oxide gene and cerebral blood flow after severe traumatic brain injury. J Neurotrauma (2011) 28:727–37.10.1089/neu.2010.1476
57
KaloostianPRobertsonCGopinathSPStipplerMKingCCQuallsCet alOutcome prediction within twelve hours after severe traumatic brain injury by quantitative cerebral blood flow. J Neurotrauma (2012) 29:727–34.10.1089/neu.2011.2147
58
ShaferRBrownATaylorC. Correlation between cerebral blood flow and oxygen saturation in patients with subarachnoid hemorrhage and traumatic brain injury. J Neurointerv Surg (2011) 3:395–8.10.1136/jnis.2010.004184
59
HattoriNHuangSCWuHMYehEGlennTCVespaPMet alCorrelation of regional metabolic rates of glucose with glasgow coma scale after traumatic brain injury. J Nucl Med (2003) 44:1709–16.
60
ColesJPFryerTDSmielewskiPRiceKClarkJCPickardJDet alDefining ischemic burden after traumatic brain injury using 15O PET imaging of cerebral physiology. J Cereb Blood Flow Metab (2004) 24:191–201.10.1097/01.WCB.0000100045.07481.DE
61
ColesJPFryerTDSmielewskiPChatfieldDASteinerLAJohnstonAJet alIncidence and mechanisms of cerebral ischemia in early clinical head injury. J Cereb Blood Flow Metab (2004) 24:202–11.10.1097/01.WCB.0000103022.98348.24
62
HattoriNHuangSCWuHMLiaoWGlennTCVespaPMet alAcute changes in regional cerebral (18)F-FDG kinetics in patients with traumatic brain injury. J Nucl Med (2004) 45:775–83.
63
WuHMHuangSCHattoriNGlennTCVespaPMYuCLet alSelective metabolic reduction in gray matter acutely following human traumatic brain injury. J Neurotrauma (2004) 21:149–61.10.1089/089771504322778613
64
CunninghamASSalvadorRColesJPChatfieldDABradleyPGJohnstonAJet alPhysiological thresholds for irreversible tissue damage in contusional regions following traumatic brain injury. Brain (2005) 128:1931–42.10.1093/brain/awh536
65
Abdel-DayemHMSadekSAKourisKBaharRHHigaziIErikssonSet alChanges in cerebral perfusion after acute head injury: comparison of CT with Tc-99m HM-PAO SPECT. Radiology (1987) 165:221–6.
66
RoperSNMenaIKingWASchweitzerJGarrettKMehringerCMet alAn analysis of cerebral blood flow in acute closed-head injury using technetium-99m-HMPAO SPECT and computed tomography. J Nucl Med (1991) 32:1684–7.
67
ItoHIshiiKOnumaTKawashimaRFukudaH. Cerebral perfusion changes in traumatic diffuse brain injury; IMP SPECT studies. Ann Nucl Med (1997) 11:167–72.10.1007/BF03164829
68
WintermarkMChioleroRVan MelleGRevellyJPPorchetFRegliLet alRelationship between brain perfusion computed tomography variables and cerebral perfusion pressure in severe head trauma patients. Crit Care Med (2004) 32:1579–87.10.1097/01.CCM.0000130171.08842.72
69
WintermarkMVan MelleGSchnyderPRevellyJPPorchetFRegliLet alAdmission perfusion CT: prognostic value in patients with severe head trauma. Radiology (2004) 232:211–20.10.1148/radiol.2321030824
70
SoustielJFMahamidEGoldsherDZaaroorM. Perfusion-CT for early assessment of traumatic cerebral contusions. Neuroradiology (2008) 50:189–96.10.1007/s00234-007-0337-7
71
HuangAPLeeCWHsiehHJYangCCTsaiYHTsuangFYet alEarly parenchymal contrast extravasation predicts subsequent hemorrhage progression, clinical deterioration, and need for surgery in patients with traumatic cerebral contusion. J Trauma (2011) 71:1593–9.10.1097/TA.0b013e31822c8865
72
BendinelliCBivardANebauerSParsonsMWBaloghZJ. Brain CT perfusion provides additional useful information in severe traumatic brain injury. Injury (2013) 44:1208–12.10.1016/j.injury.2013.03.039
73
GarnettMRBlamireAMCorkillRGRajagopalanBYoungJDCadoux-HudsonTAet alAbnormal cerebral blood volume in regions of contused and normal appearing brain following traumatic brain injury using perfusion magnetic resonance imaging. J Neurotrauma (2001) 18:585–93.10.1089/089771501750291828
74
HagenTBartyllaKPiepgrasU. Correlation of regional cerebral blood flow measured by stable xenon CT and perfusion MRI. J Comput Assist Tomogr (1999) 23:257–64.10.1097/00004728-199903000-00015
75
RemppKABrixGWenzFBeckerCRGuckelFLorenzWJ. Quantification of regional cerebral blood flow and volume with dynamic susceptibility contrast-enhanced MR imaging. Radiology (1994) 193:637–41.
76
GillardJHMinhasPSHayballMPBearcroftPWAntounNMFreerCEet alAssessment of quantitative computed tomographic cerebral perfusion imaging with H2(15)O positron emission tomography. Neurol Res (2000) 22:457–64.
77
CampbellBCChristensenSLeviCRDesmondPMDonnanGADavisSMet alComparison of computed tomography perfusion and magnetic resonance imaging perfusion-diffusion mismatch in ischemic stroke. Stroke (2012) 43:2648–53.10.1161/STROKEAHA.112.660548
78
SokoloffLReivichMKennedyCDes RosiersMHPatlakCSPettigrewKDet alThe [14C]deoxyglucose method for the measurement of local cerebral glucose utilization: theory, procedure, and normal values in the conscious and anesthetized albino rat. J Neurochem (1977) 28:897–916.10.1111/j.1471-4159.1977.tb10649.x
79
ReivichMKuhlDWolfAGreenbergJPhelpsMIdoTet alThe [18F]fluorodeoxyglucose method for the measurement of local cerebral glucose utilization in man. Circ Res (1979) 44:127–37.10.1161/01.RES.44.1.127
80
Ter-PogossianMMEichlingJODavisDOWelchMJ. The measure in vivo of regional cerebral oxygen utilization by means of oxyhemoglobin labeled with radioactive oxygen-15. J Clin Invest (1970) 49:381–91.10.1172/JCI106247
81
FrackowiakRSLenziGLJonesTHeatherJD. Quantitative measurement of regional cerebral blood flow and oxygen metabolism in man using 15O and positron emission tomography: theory, procedure, and normal values. J Comput Assist Tomogr (1980) 4:727–36.10.1097/00004728-198012000-00001
82
HerscovitchPMarkhamJRaichleME. Brain blood flow measured with intravenous H2(15)O. I. Theory and error analysis. J Nucl Med (1983) 24:782–9.
83
ReivichMKuhlDWolfAGreenbergJPhelpsMIdoTet alMeasurement of local cerebral glucose metabolism in man with 18F-2-fluoro-2-deoxy-d-glucose. Acta Neurol Scand Suppl (1977) 64:190–1.
84
PickardJDHutchinsonPJColesJPSteinerLAJohnstonAJFryerTDet alImaging of cerebral blood flow and metabolism in brain injury in the ICU. Acta Neurochir Suppl (2005) 95:459–64.10.1007/3-211-32318-X_94
85
MenonDK. Brain ischaemia after traumatic brain injury: lessons from 15O2 positron emission tomography. Curr Opin Crit Care (2006) 12:85–9.10.1097/01.ccx.0000216572.19062.8f
86
KatoTNakayamaNYasokawaYOkumuraAShinodaJIwamaT. Statistical image analysis of cerebral glucose metabolism in patients with cognitive impairment following diffuse traumatic brain injury. J Neurotrauma (2007) 24:919–26.10.1089/neu.2006.0203
87
ClausenTZaunerALevasseurJERiceACBullockR. Induced mitochondrial failure in the feline brain: implications for understanding acute post-traumatic metabolic events. Brain Res (2001) 908:35–48.10.1016/S0006-8993(01)02566-5
88
NielsenTHBindslevTTPedersenSMToftPOlsenNVNordstromCH. Cerebral energy metabolism during induced mitochondrial dysfunction. Acta Anaesthesiol Scand (2013) 57:229–35.10.1111/j.1399-6576.2012.02783.x
89
NortjeJGuptaAK. The role of tissue oxygen monitoring in patients with acute brain injury. Br J Anaesth (2006) 97:95–106.10.1093/bja/ael137
90
LevinCS. Primer on molecular imaging technology. Eur J Nucl Med Mol Imaging (2005) 32:S325–45.10.1007/s00259-005-1973-y
91
DevousMDSr. Single-photon emission computed tomography in neurotherapeutics. NeuroRx (2005) 2:237–49.10.1602/neurorx.2.2.237
92
RajiCATarzwellRPavelDSchneiderHUszlerMThorntonJet alClinical utility of SPECT neuroimaging in the diagnosis and treatment of traumatic brain injury: a systematic review. PLoS One (2014) 9:e91088.10.1371/journal.pone.0091088
93
HillmanJSturnegkPYonasHHeronJSandborgMGunnarssonTet alBedside monitoring of CBF with xenon-CT and a mobile scanner: a novel method in neurointensive care. Br J Neurosurg (2005) 19:395–401.10.1080/02688690500389898
94
SturnegkPMellergardPYonasHTheodorssonAHillmanJ. Potential use of quantitative bedside CBF monitoring (Xe-CT) for decision making in neurosurgical intensive care. Br J Neurosurg (2007) 21:332–9.10.1080/02688690701411574
95
CarlsonAPBrownAMZagerEUchinoKMarksMPRobertsonCet alXenon-enhanced cerebral blood flow at 28% xenon provides uniquely safe access to quantitative, clinically useful cerebral blood flow information: a multicenter study. AJNR Am J Neuroradiol (2011) 32:1315–20.10.3174/ajnr.A2522
96
WintermarkMSesayMBarbierEBorbelyKDillonWPEastwoodJDet alComparative overview of brain perfusion imaging techniques. Stroke (2005) 36:e83–99.10.1161/01.STR.0000177884.72657.8b
97
SeifertHBlassGLeetzHKVogesM. The radiation exposure of the patient from stable-xenon computed tomography. Br J Radiol (1995) 68:301–5.10.1259/0007-1285-68-807-301
98
BarbierELLamalleLDecorpsM. Methodology of brain perfusion imaging. J Magn Reson Imaging (2001) 13:496–520.10.1002/jmri.1073
99
GrandinCB. Assessment of brain perfusion with MRI: methodology and application to acute stroke. Neuroradiology (2003) 45:755–66.10.1007/s00234-003-1024-y
100
RosenBRBelliveauJWVeveaJMBradyTJ. Perfusion imaging with NMR contrast agents. Magn Reson Med (1990) 14:249–65.10.1002/mrm.1910140211
101
LiaTQGuang ChenZOstergaardLHindmarshTMoseleyME. Quantification of cerebral blood flow by bolus tracking and artery spin tagging methods. Magn Reson Imaging (2000) 18:503–12.10.1016/S0730-725X(00)00137-5
102
SorensenAGBuonannoFSGonzalezRGSchwammLHLevMHHuang-HellingerFRet alHyperacute stroke: evaluation with combined multisection diffusion-weighted and hemodynamically weighted echo-planar MR imaging. Radiology (1996) 199:391–401.
103
BairdAEBenfieldASchlaugGSiewertBLovbladKOEdelmanRRet alEnlargement of human cerebral ischemic lesion volumes measured by diffusion-weighted magnetic resonance imaging. Ann Neurol (1997) 41:581–9.10.1002/ana.410410506
104
StaroselskayaIAChavesCSilverBLinfanteIEdelmanRRCaplanLet alRelationship between magnetic resonance arterial patency and perfusion-diffusion mismatch in acute ischemic stroke and its potential clinical use. Arch Neurol (2001) 58:1069–74.10.1001/archneur.58.7.1069
Summary
Keywords
cerebral blood flow, brain injury, neurointensive care, Xenon-CT, imaging
Citation
Rostami E, Engquist H and Enblad P (2014) Imaging of Cerebral Blood Flow in Patients with Severe Traumatic Brain Injury in the Neurointensive Care. Front. Neurol. 5:114. doi: 10.3389/fneur.2014.00114
Received
07 April 2014
Accepted
16 June 2014
Published
07 July 2014
Volume
5 - 2014
Edited by
Ibolja Cernak, University of Alberta, Canada
Reviewed by
Sonia Villapol, Georgetown University, USA; Bridgette D. Semple, University of California San Francisco, USA
Copyright
© 2014 Rostami, Engquist and Enblad.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Elham Rostami, Section of Neurosurgery, Department of Neuroscience, Uppsala University, Uppsala SE-751 85, Sweden e-mail: elham.rostami@neuro.uu.se
This article was submitted to Neurotrauma, a section of the journal Frontiers in Neurology.
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