The value of b0 images obtained from diffusion-weighted echo planar sequences for the detection of intracranial hemorrhage compared with GRE sequence

Purpose

Our aim was to evaluate the clinical utility of b0EPI images obtained from diffusion sequence for the detection of the intracranial hemorrhagic lesions, especially acute intracerebral bleeds thereby shorten the scan time particularly in the critical acute cases of stroke.

Materials and methods

Among all consecutive MR brain studies performed in our department last year, we retrospectively selected those who followed the following criteria: (1) clinically suspected or radiographically confirmed acute infarction or hemorrhage. (2) MRI imaging including DWI and T2∗ images. Sensitivity of hemorrhage detection, conspicuity of lesions, and diagnostic certainty were compared between the b0EPI and GRE sequences.

Results

There were 77 hemorrhagic lesions with a variety of pathogeneses in various locations. 76/77 (98.7%) of these lesions were hemorrhagic (hypointense) on the GRE sequences, whereas 61 (79.2%) were characterized as hemorrhagic on b0EPI images, and 16 (20.8%) were not detected. The overall difference in hemorrhage conspicuity/diagnostic certainty between GRE and b0EPI sequences was statistically significant (P < .05).

Conclusion

b0EPI sequence, although shorter in acquisition time, was inferior to GRE imaging in the detection of acute and chronic intracerebral hemorrhage.     

Detection of intracranial hemorrhage: comparison between gradient-echo images and b0 images obtained from diffusion-weighted echo-planar sequences on 3.0T MRI

In this study, we compared the effectiveness of b0 echo-planar MR images (EPI) imaging with gradient recalled echo (GRE) in detecting acute hemorrhage. Brain images in 69 patients who suffered from acute infarction were reviewed. Nine of them had suffered from acute hemorrhage. Comparing b0EPI and GRE images side-by-side, we found no significant different effectiveness in detecting hemorrhage (P = .522, > or =.05). We concluded that b0EPI imaging could detect hemorrhagic lesions as effectively as GRE can without additional acquisition time.     

Detection of hyperacute parenchymal hemorrhage of the brain using echo-planar T2*-weighted and diffusion-weighted MRI

We investigated the usefulness of echo-planar imaging (EPI) as well as T2^*-weighted and diffusion-weighted MRI (DWI) to identify hyperacute hemorrhage (within 24 h after ictus) in the brain. Seven patients were examined 3.5 to 24 h after onset of symptoms using a whole-body 1.5-T MR system. Two diffusion-weighted sequences were run to obtain isotropic and anisotropic diffusion images. Apparent diffusion coefficients (ADC) were calculated from the isotropic diffusion images. All DWI images as well as the T2*-weighted EPI images showed the hematomas as either discrete, deeply hypointense homogeneous lesions, or as lesions of mixed signal intensity containing hypointense areas. We conclude that even in the early phase after hemorrhage, sufficient amounts of paramagnetic deoxyhemoglobin are present in intracerebral hemorrhages to cause hypointensity on EPI T2^*-weighted and DWI images; thus, use of ultrafast EPI allows identification of intracerebral hemorrhage. Received: 21 March 2000 Revised: 26 July 2000 Accepted: 27 July 2000     

MR imaging of acute hemorrhagic brain infarction

Six patients with acute hemorrhagic brain infarct were imaged using spin-echo (SE) pulse sequences on a 1.5 Tesla MR scanner. Including two patients with repeated MR imaging, a total of eight examinations, all performed within 15 days after stroke, were analyzed retrospectively. Four patients revealed massive hemorrhages in the basal ganglia or cerebellum and three cases demonstrated multiple linear hemorrhages in the cerebral cortex. On T1-weighted images, hemorrhages were either mildly or definitely hyperintense relative to gray matter, while varied from mildly hypointense to hyperintense on T2-weighted images. T1-weighted images were superior to T2-weighted images in detection of hemorrhage. CT failed to detect hemorrhages in two of five cases: indicative of MR superiority to CT in the diagnosis of acute hemorrhagic infarcts.     

Conspicuity of diffuse axonal injury lesions on diffusion-weighted MR imaging

OBJECTIVE: (1) To detect diffuse axonal injury (DAI) lesions by diffusion-weighted imaging (DWI), as compared with fluid-attenuated inversion recovery (FLAIR) imaging and (2) to evaluate hemorrhagic DAI lesions by b0 images obtained from DWI, as compared with gradient-echo (GRE) imaging. METHODS: We reviewed MR images of 36 patients with a diagnosis of DAI. MR imaging was performed 20 h to 14 days (mean, 3.7 days) after traumatic brain injury. We evaluated: (1) conspicuity of lesions on DWI and FLAIR and (2) conspicuity of hemorrhage in DAI lesions on b0 images and GRE imaging. RESULTS: DWI clearly depicted high-signal DAI lesions. The sensitivity of DWI to lesional conspicuity in DAI lesions was almost equal to that of FLAIR. The sensitivity of b0 images to identification of hemorrhagic DAI lesions was inferior to that of GRE. CONCLUSION: DWI is as useful as FLAIR in detecting DAI lesions. GRE imaging is still the superior tool for the evaluation of hemorrhagic DAI.     

PROPELLER FSE磁共振扩散加权技术在诊断超急性和急性脑梗死中的价值

目的比较螺旋桨扫描技术(PROPELLER FSE)和平面回波成像(EPI)两种扩散加权成像(DWI)序列,探讨PROPELLER技术在DWI的应用价值。资料与方法选取67例临床疑诊急性脑梗死的患者分别行PROPEL-LER FSE DWI、EPI DWI和常规T1WI、T2WI、T2WI液体衰减反转恢复序列(FLAIR)检查,比较两种不同的DWI序列的图像质量,病灶检出率和对病变的显示程度。结果67例EPI DWI图像均不同程度地存在磁化率伪影,67例PROPELLER FSE DWI图像未见明显伪影及变形。67例中共发现并确诊46个急性脑梗死灶(4例为颅内多发病灶),其中病灶位于颅底区域12个,非颅底区域34个。PROPELLER FSE DWI和EPI DWI均可分辩出所有非颅底区域梗死灶。对12个颅底病灶PROPELLER FSE DWI检出率达100%,而EPI DWI可以明确诊断的7个,检出率达58.3%,病灶形态显示不充分或变形者3个,占25%,漏诊2个,漏诊率为16.7%。所有颅底区域病灶EPI DWI上信噪比(SNR)低于相应PROPELLER FSE DWI的SNR(t=-2.874,P<0.05)。结论PROPELLER FSE DWI能提高图像SNR,有效消除颅底磁化率伪影,改善图像质量,提高颅底病变的检出率。     

MR imaging of acute intracranial hemorrhage: findings on sequential spin-echo and gradient-echo images in a dog model

Seven intraparenchymal hematomas (four venous and three arterial) were placed in the brains of six dogs in order to study the MR appearance of acute hemorrhage and to evaluate the effects of several variables on the signal intensity of the hematoma. MR imaging at 0.6 and 1.5 T was performed by using standard short and long TR spin-echo and low-flip-angle gradient-echo sequences. Sequential examinations were performed during the first week following hematoma creation. MR findings were compared with CT and postmortem examinations. Three patterns of signal intensity were observed, which varied according to the size (small vs large) and location (parenchymal vs intraventricular) of the hematomas. The small parenchymal hematomas did not undergo evolutionary changes. On short TR scans they were isointense at both field strengths, and therefore not detectable; on long TR scans these hematomas were of variable intensity at 1.5 T and were hyperintense at 0.6 T. On gradient-echo scans, they were hypointense at all times at both field strengths. The large parenchymal hematomas underwent evolutionary changes typical of those seen in clinical imaging. On short TR scans they were initially isointense and became hyperintense 1-3 days later. Long TR scans demonstrated initial hyperintensity, followed by the development of hypointensity within 12 hr in the venous hematomas and within 60 hr in the arterial hematoma. The intensity changes on long TR scans were seen at both 0.6 and 1.5 T, but occurred sooner and to a greater degree at 1.5 T. Gradient-echo imaging of these large lesions demonstrated hypointensity at all times at both field strengths. The intraventricular hemorrhages demonstrated more rapid development of hyperintensity on short TR scans and slower and less pronounced development of hypointensity on long TR scans compared with the parenchymal clots in the same animal. Gradient-echo imaging of the intraventricular hemorrhages demonstrated hypointensity at all times at both field strengths. A multifactorial hypothesis is proposed to explain the differences in intensity between venous, arterial, and intraventricular blood. Gradient-echo sequences should prove to be highly useful in detecting and delineating hemorrhages and are recommended for the MR protocol of patients with acute neurologic ictus and suspected hemorrhage.     

Hemorrhagic shearing lesions in children and adolescents with posttraumatic diffuse axonal injury: improved detection and initial results

PURPOSE: To compare the effectiveness of a high-spatial-resolution susceptibility-weighted (SW) magnetic resonance (MR) imaging technique with that of a conventional gradient-recalled-echo (GRE) MR imaging technique for detection of hemorrhage in children and adolescents with diffuse axonal injury (DAI). MATERIALS AND METHODS: Seven young patients with a mean Glasgow Coma Scale score of 7 +/- 4 (SD) at admission were imaged a mean of 5 days +/- 3 after injury. High-spatial-resolution three-dimensional GRE imaging performed with postprocessing by using a normalized phase mask was compared with conventional GRE MR imaging. The total and mean values of lesion number and apparent hemorrhage volume load determined with both examinations were compared. Mean values were compared by using paired t test analysis. Differences were considered to be significant at P < or =.05. RESULTS: Hemorrhagic lesions were much more visible on SW MR images than on conventional GRE MR images. SW MR imaging depicted 1,038 hemorrhagic DAI lesions with an apparent total hemorrhage volume of 57,946 mm3. GRE MR imaging depicted 162 lesions with an apparent total hemorrhage volume of 28,893 mm3. SW MR imaging depicted a significantly higher mean number of lesions in all patients than did GRE MR imaging, according to results of visual (P =.004) and computer (P =.004) counting analyses. The mean hemorrhage volume load for all patients also was significantly greater (P =.014) by using SW MR imaging according to computer analysis. SW MR imaging appeared to depict much smaller hemorrhagic lesions than GRE MR imaging. The majority (59%) of individual hemorrhagic DAI lesions seen on SW MR images were small in area (<10 mm(2)), whereas the majority (43%) of lesions seen on GRE images were larger in area (10-20 mm(2)). CONCLUSION: SW MR imaging depicts significantly more small hemorrhagic lesions than does conventional GRE MR imaging and therefore has the potential to improve diagnosis of DAI.     

急性期脑内血肿3.0T MR扩散加权成像表现

目的:探讨3.0T MR设备中平面回波扩散加权成像(EPI-DWI)和表观扩散系数(ADC)图对急性脑内血肿的诊断价值及与脑梗死的鉴别诊断能力。方法:对18例急性期脑内血肿患者行EPI-DWI检查,获得ADC图并与CT及常规MRI进行对比。同期选择发病时间、病变体积相近的急性脑梗死患者18例,比较急性期脑内血肿与脑梗死的MRI表现。结果:所有急性期脑内血肿在EPI-DWI及ADC图上均为混杂信号,尤其是较大血肿;不同大小血肿周边均可见低信号环。所有急性脑梗死病变均未见周边环状低信号。结论:血肿周边低信号环为急性期脑内血肿的特异性DWI表现,可资与急性脑梗死相鉴别。     

Experimental acute intracerebral hemorrhage. Value of MR sequences for a safe diagnosis at 1.5 and 0.5 T

Purpose: To determine the detectability of intracerebral hematomas with MR imaging at 1.5 T and 0.5 T with fluid attenuated inversion recovery turbo spin-echo (FLAIR) and gradient-echo sequences.Material and Methods: Twenty-seven intracerebral hematomas were created in 25 piglets by injection of venous blood into the brain through a burr hole. All were imaged with T2*-weighted gradient echo sequences (fast field echo, FFE), T2-weighted fluid attenuated inversion recovery turbo spin-echo sequences (FLAIR), T2-weighted turbo spin-echo (TSE) and T1-weighted spin-echo sequences. Follow-up was performed on the 2nd, 4th and 10th postoperative days. Ten animals were additionally investigated with similar sequences at 0.5 T. Histologic correlation was obtained in all cases.Results: T2* FFE sequences detected all acute intracerebral hematomas and demonstrated the size correctly at 1.5 T and 0.5 T. The conspicuity was better at 1.5 T. FLAIR sequences were unreliable in the hyperacute phase at 1.5 T. However, subarachnoid and intraventricular extension was best appreciated with FLAIR images. T2 TSE images were incapable of detecting paraventricular and subarachnoid hemorrhages, but clearly demonstrated intracerebral blood in other locations. T1-weighted images were insensitive to hemorrhage in the acute state but very useful in subacute and chronic hematomas.Conclusion: The safe and reliable diagnosis of intracerebral hemorrhage is probably possible with MR imaging at 1.5 T and 0.5 T even of hematomas less than 90 min old, but requires the application of at least FLAIR, T2* FFE and T1 sequences and is therefore time consuming.     

MR imaging of experimentally induced intracranial hemorrhage in rabbits during the first 6 hours.

PURPOSE: To evaluate the MR appearance of intracranial, especially intraparenchymal, hemorrhage during the first 6 hours after bleeding with various pulse sequences in an animal model. MATERIAL AND METHODS: Intracerebral hematomas and subarachnoid hemorrhage were created by injecting autologous blood in 9 rabbits. MR studies were performed using a 1.5 T scanner with pixel size and slice thickness comparable to those used in clinical practice before blood injection, immediately after injection, and at regular intervals during 6 hours. The images were compared with the hematoma sizes on formalin-fixed brain slices. RESULTS: In every animal, susceptibility-weighted gradient-echo (GRE) pulse sequences depicted the intraparenchymal hematomas and blood escape in the ventricles or subarachnoid space best as areas of sharply defined, strong hypointensity. The findings remained essentially unchanged during follow-up. The sizes corresponded well to the post-mortem findings. Gradient- and spin-echo (GRASE) imaging revealed some hypointensities, but these were smaller and less well defined. Spin-echo (SE) sequences (proton density-, T1- and T2-weighted) as well as a fluid-attenuated inversion recovery turbo spin-echo sequence (fast FLAIR) depicted the hemorrhage sites as mostly isointense to brain. CONCLUSION: Susceptibility-weighted GRE imaging at 1.5 T is highly sensitive to both hyperacute hemorrhage in the brain parenchyma and to subarachnoid and intraventricular hemorrhage.     

Diffusion-Weighted MR Imaging of Intracerebral Hemorrhage

Objective

To document the signal characteristics of intracerebral hemorrhage (ICH) at evolving stages on diffusion-weighted images (DWI) by comparison with conventional MR images.

Materials and Methods

In our retrospective study, 38 patients with ICH underwent a set of imaging sequences that included DWI, T1-and T2-weighted imaging, and fluid-attenuated inversion recovery (FLAIR). In 33 and 10 patients, respectively, conventional and echo-planar T2* gradient-echo images were also obtained. According to the time interval between symptom onset and initial MRI, five stages were categorized: hyperacute (n=6); acute (n=7); early subacute (n=7); late subacute (n=10); and chronic (n=8). We investigated the signal intensity and apparent diffusion coefficient (ADC) of ICH and compared the signal intensities of hematomas at DWI and on conventional MR images.

Results

DWI showed that hematomas were hyperintense at the hyperacute and late subacute stages, and hypointense at the acute, early subacute and chronic stages. Invariably, focal hypointensity was observed within a hyperacute hematoma. At the hyperacute, acute and early subacute stages, hyperintense rims that corresponded with edema surrounding the hematoma were present. The mean ADC ratio was 0.73 at the hyperacute stage, 0.72 at the acute stage, 0.70 at the early subacute stage, 0.72 at the late subacute stage, and 2.56 at the chronic stage.

Conclusion

DWI showed that the signal intensity of an ICH may be related to both its ADC value and the magnetic susceptibility effect. In patients with acute stroke, an understanding of the characteristic features of ICH seen at DWI can be helpful in both the characterization of intracranial hemorrhagic lesions and the differentiation of hemorrhage from ischemia.     

MR imaging of intracerebral blood: diversity in the temporal pattern at 0.5 and 1.0 T

MR scans were obtained at 0.5 and 1.0 T in 40 patients with 46 intracerebral hematomas categorized as hyperacute (0-2 days), acute (3-7 days), subacute (8-14 days), and chronic (15 days to 6 years). In a retrospective review, the signal intensity of the lesions was compared with that of normal white matter of the brain on spin-density, T1-, and T2-weighted spin-echo and T1-weighted gradient-echo sequences. The classic appearance and evolution of hematomas described in the literature at 1.5 T were not found in a significant number of the cases reviewed. In the hyperacute group, only five of eight hematomas had signal intensities that were hypointense relative to brain on T2-weighted images. Two of eight hyperacute hematomas were hyperintense relative to brain on the T1-weighted spin-echo images. However, T1-weighted gradient-echo images reliably demonstrated a hypointense signal in some portion of the hematoma in 45 of 46 cases. We conclude that while there is no constant temporal pattern on spin-echo or gradient-echo sequences, there are signal-intensity changes suggestive of hemorrhage in nearly all hematomas imaged at 0.5 and 1.0 T. Although the inconsistency may be frustrating from a diagnostic standpoint, this variability may reveal important individual differences in hematomas and the brain that surrounds them, and thus be clinically significant. Before these data can be mechanistically analyzed, the reason for contrast on MR scans of hematoma must be better understood.     

MRI diffusion-weighted imaging in intracranial hemorrhage (ICH)

Purpose

To assess the role of MRI DWI in detection and characterization of ICH.

Patients and methods

61 patients with intracranial hemorrhage who underwent MRI (including DWI, ADC, and GRE) and CT were retrospectively included in this study. MRI DWIs were analyzed for age, type, (primary parenchymal hemorrhage or hemorrhagic lesion) and location of the hemorrhage. The results were compared with conventional MRI sequences, GRE, and CT to assess the diagnostic accuracy of DWI in assessment of patients with intracranial hematoma.

Results

We had 61 patients with intracranial hemorrhage, six cases were missed by DWI. MRI DWI was accurate for the detection of hyperacute, medium, large sized acute, early and late sub acute, subdural, hemorrhagic components of arterial and venous infarction, intraventricular hemorrhage. DWI showed low sensitivity in detection of subarachnoid and small intraparenchymal hemorrhage The ADC measurements in hyperacute, acute, early and late subacute hematoma were statistically equivalent and were significantly less than the late subacute hematoma as well as the contralateral white matter.

Conclusion

MRI DWI was accurate in detection, characterization and staging hyperacute, acute, subacute hemorrhage as well as hemorrhagic components of arterial and venous infarctions and of low diagnostic accuracy in subarachnoid and small parenchymal hemorrhage.     

MR detection of hyperacute parenchymal hemorrhage of the brain.

BACKGROUND AND PURPOSEThe detection of hemorrhage in acutely ill patients is crucial to clinical management. The MR features that allow diagnosis of intracerebral hematomas of less than 24 hours'' duration are described and the mechanistic basis of these features is investigated.METHODSThe clinical MR features of seven confirmed hyperacute intracerebral hematomas were compared with those of experimentally induced hematomas in a rat model in which detailed analyses of iron metabolism and morphometry were performed.RESULTSIn all patients and all animals, a hypointense rim on T2-weighted spin-echo images that was less marked on T1-weighted spin-echo images was seen surrounding a central isointense or heterogeneous region of hyperacute hematoma. Histologically, the clot showed interdigitation of intact erythrocytes and tissue at the hematoma-tissue interface without significant hemosiderin, ferritin, or phagocytic activity. Biochemically, the iron from the extravasated blood was present only as heme proteins within the first 24 hours.CONCLUSIONThe hypointense rim on T2-weighted images, and to a lesser extent on T1-weighted images, is a distinctive feature of hyperacute hematoma. This pattern is consistent with magnetic susceptibility variations of paramagnetic deoxygenated hemoglobin within intact erythrocytes at a microscopically irregular tissue-clot interface. The detection of hemorrhage is important in the management of patients with acute stroke.     

MR imaging of intracranial hemorrhage in neonates and infants at 2.35 Tesla

Summary The variations of the relative signal intensity and the time dependent changing contrast of intracranial hemorrhages on high-field spin-echo magnetic resonance images (MRI) were studied in 28 pediatric patients. For T1-weighted images, a repetition time (TR) of 500 ms and an echo time (TE) of 30 or 23 ms was used. The corresponding times for T2-weighted images were TR 3000 ms and TE 120 ms. Intracranial hematomas, less than 3 days old, were iso- to mildly hypointense on short TR/TE scans and markedly hypointense on long TR/TE scans (acute stage). In the following four days the signal of the hematomas became hyperintense on short TR/TE scans, beginning in the periphery and proceeding towards the center. On long TR/TE scans the signal remained markedly hypointense (early subacute stage). 7–14 days old hematomas were of high signal intensity on short TR/TE scans. On long TR/TE scans they appeared hypointense in the center and hyperintense in the periphery (late subacute stage). By the end of the second week the hematomas were of high signal intensity on all pulse sequences (chronic stage). Chronic hematomas were surrounded by a parenchymal rim of hypointensity on long TR/TE scans. 28 neonates and infants (with 11 follow-up examinations) of 31.5–70.6 weeks postconceptional age (PCA), with an intracranial hemorrhage were examined. The etiologies of the hemorrhages were: asphyxia (17 cases), brain infarct (2), thrombocytopenia (1), clotting disorder (1) and unknown origin (7). The aim of this study was to describe the appearance of intracranial hemorrhages inneonates and infants with MRI at2.35 Tesla using spine-cho sequences.     

MR imaging of hyperacute subarachnoid and intraventricular hemorrhage at 3T: a preliminary report of gradient echo T2*-weighted sequences

We describe MR imaging findings applying gradient echo (GRE) T2*-weighted and fluid-attenuated inversion recovery (FLAIR) MR images at 3T to three patients with hyperacute subarachnoid and intraventricular hemorrhage from ruptured aneurysms. Hyperacute subarachnoid and intraventricular hemorrhages (SAH and IVH) were more clearly visualized as an area of decreased signal intensity on GRE T2*-weighted sequences than on FLAIR sequences in all three patients. These preliminary results suggest that acute SAH and IVH with GRE T2*-weighted imaging can be reliably diagnosed at 3T.     

3.0T磁共振磁敏感加权成像对出血性脑梗死的诊断和鉴别诊断价值

目的探讨3.0T磁共振磁敏感加权成像(SWI)对出血性脑梗死的诊断和鉴别诊断价值。方法对430例脑梗死患者行MR的T1WI、T2WI、DWI与SWI扫描,分析T1WI、T2WI、DWI和SWI对出血性脑梗死检出率的差异和SWI对于出血性脑梗死的鉴别诊断价值。结果 SWI检出出血性脑梗死45例,T1WI检出20例,T2WI检出28例,DWI检出31例。结论 SWI较MR常规序列(T1WI和T2WI)和DWI序列可检出更多的出血性脑梗死病例;可早期发现脑梗死中的出血灶,明显优于MR常规序列(T1WI和T2WI)和DWI序列;具有一定的鉴别诊断价值;可作为出血性脑梗死检查的一线方法或常规序列。     

Acute intracranial hemorrhage: intensity changes on sequential MR scans at 0.5 T

Thirty-seven patients underwent MR imaging at 0.5 T within 7 days of a CT-documented intracranial hemorrhage. A total of 57 hematomas were evaluated. Twelve patients underwent serial scanning and 12 patients had multiple hemorrhages into different intracranial compartments. The appearances of the hematomas on spin-echo (SE) images with a short repetition time (TR) of 500 msec and short echo time (TE) of 32 msec (SE 500/32), long TR/intermediate TE (SE 2000/60), and long TR/long TE (SE 2000/120) were carefully evaluated with specific attention to the precise time after ictus. Hematomas showed heterogeneous, complex, rapidly changing intensities. There was a significant amount of variation among patients, especially between the third and seventh days. Hematomas studied between 12 and 24 hr after hemorrhage were mildly hyperintense on short TR scans and markedly hyperintense on long TR (intermediate and long TE) scans (stage I). These findings in acute hemorrhage have received little prior attention. Over the next 1-2 days, hematomas became iso- to mildly hypointense on short TR scans and markedly hypointense on long TR scans (stage II). Hypointensity on long TR scans has previously been described at high field strengths; our communication demonstrates that this phenomenon is seen routinely at intermediate field strengths as well. Hematomas became markedly hyperintense on short TR scans beginning on approximately the fourth day postictus and redeveloped hyperintensity on long TR scans approximately 5-6 days after ictus (stage III). By the end of the first week they were hyperintense on all pulse sequences (stage IV). MR findings on the first day after intracranial hemorrhage (in particular, subtle hyperintensity on short TR scans) probably allow for a specific diagnosis, while the variable, hetergeneous, and rapidly changing intensities noted between days 2 and 7 are often less specific.     

High-b-value diffusion-weighted MR imaging of suspected brain infarction

BACKGROUND AND PURPOSE: Recent technological advances in MR instrumentation allow acquisition of whole-brain diffusion-weighted MR scans to be obtained with b values greater than 1,000. Our purpose was to determine whether high-b-value diffusion-weighted MR imaging improved contrast and detection of signal changes in acute and chronic brain infarction. METHODS: We prospectively evaluated the MR scans of 30 subjects with a history of possible brain infarction on a 1.5-T MR imager with 40 mT/meter gradients (slew rate 150 T/m/s) by use of the following single-shot echo-planar diffusion-weighted MR sequences: 1) 7,999/ 71.4/1 (TR/TE/excitations, b = 1,000; 2) 999/ 88.1/3, b = 2,500; and 3) 7,999/ 92.1/4, b = 3,000. Diffusion-weighted MR imaging was performed in three orthogonal directions during all sequences. All subjects were scanned with fast fluid-attenuated inversion recovery (FLAIR) (10,006/145/2,200/1 [TR/TE/TI/excitations]) and fast spin-echo T2-weighted (3,650/95/3 [TR/TE/excitations], echo train length, 8). The diagnosis of brain infarction was established by clinical criteria. RESULTS: Twenty women and 10 men with a mean age of 67.7 years were enrolled in the study. One subject was excluded owing to poor image quality. Twelve of 29 subjects had a clinical diagnosis of acute infarction. All 12 had lesions that were hyperintense on diffusion-weighted images at all three b values; five were cortical and seven subcortical. There was increased contrast of all lesions on high-b-value scans (b = 2,500 and 3,000). Lesions that were hypointense on diffusion-weighted images were identified and evaluated at the three different b values. At b = 1,000, there were 19 hypointense lesions, whereas at b = 2,500 and 3,000 there were 48 and 55 lesions, respectively. On FLAIR and T2-weighted images, these low-signal lesions were predominantly chronic, subcortical, ischemic lesions and lacunar infarcts, but four chronic cortical infarcts, one porencephalic cyst, and one primary brain tumor were also found. Low-signal lesions were also noted to have increased contrast on high-b-value diffusion-weighted scans. CONCLUSION: High-b-value diffusion-weighted MR imaging (b = 2,500 or b = 3,000) had no impact on diagnosis of acute infarction. High-b-value diffusion-weighted MR imaging (b = 2,500) combined with diffusion-weighted MR imaging at b = 1,000 improves tissue characterization by increasing the spectrum of observed imaging abnormalities in patients with suspected brain infarction.