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Dive into the research topics where Jeffrey M. Pollock is active.

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Featured researches published by Jeffrey M. Pollock.


American Journal of Neuroradiology | 2008

Arterial Spin-Labeling in Routine Clinical Practice, Part 1: Technique and Artifacts

A. R. Deibler; Jeffrey M. Pollock; Robert A. Kraft; Huan Tan; Jonathan H. Burdette; Joseph A. Maldjian

SUMMARY: The routine use of arterial spin-labeling (ASL) in a clinical population has led to the depiction of diverse brain pathologic features. Unique challenges in the acquisition, postprocessing, and analysis of cerebral blood flow (CBF) maps are encountered in such a population, and high-quality ASL CBF maps can be generated consistently with attention to quality control and with the use of a dedicated postprocessing pipeline. Familiarity with commonly encountered artifacts can help avoid pitfalls in the interpretation of CBF maps. The purpose of this review was to describe our experience with a heterogeneous collection of ASL perfusion cases with an emphasis on methodology and common artifacts encountered with the technique. In a period of 1 year, more than 3000 pulsed ASL cases were performed as a component of routine clinical brain MR evaluation at both 1.5 and 3T. These ASL studies were analyzed with respect to overall image quality and patterns of perfusion on final gray-scale DICOM images and color Joint Photographic Experts Group (JPEG) CBF maps, and common artifacts and their impact on final image quality were categorized.


American Journal of Neuroradiology | 2008

Arterial Spin-Labeling in Routine Clinical Practice, Part 3: Hyperperfusion Patterns

A. R. Deibler; Jeffrey M. Pollock; Robert A. Kraft; Huan Tan; Jonathan H. Burdette; Joseph A. Maldjian

SUMMARY: Arterial spin-labeled (ASL) perfusion imaging can be implemented successfully into a routine clinical neuroimaging protocol and can accurately demonstrate alterations in brain perfusion. We have observed patterns of focal, regional, and global hyperperfusion in a wide variety of disease processes. The causes of hyperperfusion at clinical ASL have not been previously characterized. Focal lesions such as brain tumors and vascular malformations with increased perfusion can be well depicted by ASL. More global causes of hyperperfusion, including postanoxia vasodilation and hypercapnia, may go undetected on conventional MR images, whereas the regional hyperperfusion, which may occur in reversible encephalopathies and luxury perfusion, has been consistently illustrated on ASL cerebral blood flow maps at our institution.


Magnetic Resonance Imaging Clinics of North America | 2009

Arterial spin-labeled MR perfusion imaging: clinical applications.

Jeffrey M. Pollock; Huan Tan; Robert A. Kraft; Christopher T. Whitlow; Jonathan H. Burdette; Joseph A. Maldjian

Arterial spin labeling (ASL) imaging soon will be available as a routine clinical perfusion imaging sequence for a significant number of MR imaging scanners. The ASL perfusion technique offers information similar to that provided by conventional dynamic susceptibility sequences, but it does not require the use of an intravenous contrast agent, and the data can be quantified. The appearance of pathology is affected significantly by the ASL techniques used. Familiarity with the available sequence parameter options and the common appearances of pathology facilitates perfusion interpretation.


American Journal of Neuroradiology | 2008

Migraine Associated Cerebral Hyperperfusion with Arterial Spin-Labeled MR Imaging

Jeffrey M. Pollock; A. R. Deibler; Jonathan H. Burdette; Robert A. Kraft; Huan Tan; A. B. Evans; Joseph A. Maldjian

SUMMARY: We present a case series demonstrating abnormal regional cerebral hyperperfusion associated with migraine headache using arterial spin-labeling (ASL). In 3 of 11 patients, regional cortical hyperperfusion was demonstrated during a headache episode that corresponded to previous aura symptoms.


American Journal of Neuroradiology | 2008

Hypercapnia-Induced Cerebral Hyperperfusion: An Underrecognized Clinical Entity

Jeffrey M. Pollock; A. R. Deibler; Christopher T. Whitlow; Huan Tan; Robert A. Kraft; Jonathan H. Burdette; Joseph A. Maldjian

BACKGROUND AND PURPOSE: The incidence of cerebral hyperperfusion and hypoperfusion, respectively, resulting from hypercapnia and hypocapnia in hospitalized patients is unknown but is likely underrecognized by radiologists and clinicians without routine performance of quantitative perfusion imaging. Our purpose was to report the clinical and perfusion imaging findings in a series of patients confirmed to have hypercapnic cerebral hyperperfusion and hypocapnic hypoperfusion. MATERIALS AND METHODS: Conventional cerebral MR imaging examination was supplemented with arterial spin-labeled (ASL) MR perfusion imaging in 45 patients during a 16-month period at a single institution. Patients presented with an indication of altered mental status, metastasis, or suspected stroke. Images were reviewed and correlated with arterial blood gas (ABG) analysis and clinical history. RESULTS: Patients ranged in age from 1.5 to 85 years. No significant acute findings were identified on conventional MR imaging. Patients with hypercapnia showed global hyperperfusion on ASL cerebral blood flow (CBF) maps, respiratory acidosis on ABG, and diffuse air-space abnormalities on same-day chest radiographs. Regression analysis revealed a significant positive linear relationship between cerebral perfusion and the partial pressure of carbon dioxide (pCO2; β, 4.02; t, 11.03; P < .0005), such that rates of cerebral perfusion changed by 4.0 mL/100 g/min for each 1-mm Hg change in pCO2. CONCLUSIONS: With the inception of ASL as a routine perfusion imaging technique, hypercapnic-associated cerebral hyperperfusion will be recognized more frequently and may provide an alternative cause of unexplained neuropsychiatric symptoms in hospitalized patients. In a similar fashion, hypocapnia may account for a subset of patients with normal MR imaging examinations with poor ASL perfusion signal.


American Journal of Neuroradiology | 2008

Anoxic Injury-Associated Cerebral Hyperperfusion Identified with Arterial Spin-Labeled MR Imaging

Jeffrey M. Pollock; Christopher T. Whitlow; A. R. Deibler; Huan Tan; Jonathan H. Burdette; Robert A. Kraft; Joseph A. Maldjian

BACKGROUND AND PURPOSE: Anoxic brain injury is a devastating result of prolonged hypoxia. The goal of this study was to use arterial spin-labeling (ASL) to characterize the perfusion patterns encountered after anoxic injury to the brain. MATERIALS AND METHODS: Sixteen patients with a history of anoxic or hypoxic-ischemic injury ranging in age from 1.5 to 78.0 years (mean, 50.3 years) were analyzed with conventional MR imaging and pulsed ASL 1.0–13.0 days (mean, 4.6 days) after anoxic insult. The cerebral perfusion in each case was quantified by using pulsed ASL as part of the standard stroke protocol. Correlation was made among perfusion imaging, conventional imaging, clinical history, laboratory values, and outcome. RESULTS: Fifteen of the 16 patients showed marked global hyperperfusion, and 1 patient showed unilateral marked hyperperfusion. Mean gray matter (GM) cerebral blood flow (CBF) in these patients was 142.6 mL/100 g of tissue per minute (ranging from 79.9 to 204.4 mL/100 g of tissue per minute). Global GM CBF was significantly higher in anoxic injury subjects, compared with age-matched control groups with and without infarction (F2,39 = 63.11; P < .001). Three patients had global hyperperfusion sparing areas of acute infarction. Conventional imaging showed characteristic restricted diffusion in the basal ganglia (n = 10) and cortex (n = 13). Most patients examined died (n = 12), with only 4 patients surviving at the 4-month follow-up. CONCLUSION: Pulsed ASL can dramatically demonstrate and quantify the severity of the cerebral hyperperfusion after a global anoxic injury. The global hyperperfusion probably results from loss of autoregulation of cerebral vascular resistance.


Journal of Magnetic Resonance Imaging | 2009

A fast, effective filtering method for improving clinical pulsed arterial spin labeling MRI

Huan Tan; Joseph A. Maldjian; Jeffrey M. Pollock; Jonathan H. Burdette; Lucie Y. Yang; A. R. Deibler; Robert A. Kraft

To evaluate the effectiveness of a fully automated postprocessing filter algorithm in pulsed arterial spin labeling (PASL) MRI perfusion images in a large clinical population.


Journal of Computer Assisted Tomography | 2008

Arterial spin-labeled magnetic resonance imaging in hyperperfused seizure focus: a case report.

Jeffrey M. Pollock; A. R. Deibler; Thomas West; Jonathan H. Burdette; Robert A. Kraft; Joseph A. Maldjian

We present a case of a clinically suspected cerebral infarction that was diagnosed as a seizure focus on pulsed arterial spin labeling. The finding of hyperperfusion with perfusion imaging significantly impacted clinical management of the patient.


American Journal of Roentgenology | 2011

Response of Arteriovenous Malformations to Gamma Knife Therapy Evaluated With Pulsed Arterial Spin-Labeling MRI Perfusion

Jeffrey M. Pollock; Christopher T. Whitlow; Justin Simonds; E. Andrew Stevens; Robert A. Kraft; Jonathan H. Burdette; Joseph A. Maldjian

OBJECTIVE The goal of this study was to use pulsed arterial spin-labeling (PASL) MRI to evaluate the effect of gamma knife treatment on arteriovenous malformation (AVM) blood flow by measuring perfusion of the AVM nidus and nearby vascular territories. CONCLUSION PASL can show and quantify the steal phenomena and the relative flow rates within the AVM nidus and may be used to follow AVM perfusion over time to assess treatment efficacy.


Journal of Neuroimaging | 2009

Ruptured Anterior Spinal Artery Aneurysm: A Case Report

Jeffrey M. Pollock; Alexander K. Powers; E. Andrew Stevens; Amit N. Sanghvi; John A. Wilson; Pearse Morris

We present a case of a subarachnoid hemorrhage and vasospasm secondary to a ruptured anterior spinal artery aneurysm associated with a Chiari 1 malformation. To our knowledge this is the first reported spinal artery aneurysm with this association.

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Huan Tan

Wake Forest University

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Thomas West

Wake Forest University

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A. B. Evans

Wake Forest University

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