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1.
Medicine (Baltimore) ; 98(42): e17075, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31626080

ABSTRACT

Motion-induced artifacts have been a major drawback in bladder cancer imaging. This study is to evaluate the clinical utility of periodically rotated overlapping parallel lines with enhanced reconstruction (PROPELLER) acquisition in improving motion-induced artifacts in T2-weighted (T2W) magnetic resonance imaging (MRI) of bladder cancer at 3T.Sixteen patient MRI exams were included. Using a Likert scale, 2 radiologists independently scored T2W data without and with PROPELLER in terms of artifact severity and tumor visualization. Statistical analysis was done to assess the image quality improvement by PROPELLER and inter-observer variability.Without PROPELLER, the median scores of artifact severity and tumor visualization were 1.5 and 1.5 for reviewer 1, and 2.0 and 2.0 for reviewer 2. With PROPELLER, the scores increased to 3 and 3.5 for reviewer 1, and 3.5 and 3.5 for reviewer 2. Despite the inter-observer variability (κ scores < 0.2), both reviewers found significant improvement in artifacts and visualization (all P < .001).PROPELLER acquisition significantly improved the image quality of T2W-MRI. These initial findings indicate that this technique should be utilized in clinical MRI of the bladder.


Subject(s)
Artifacts , Carcinoma, Transitional Cell/diagnostic imaging , Magnetic Resonance Imaging/methods , Urinary Bladder Neoplasms/diagnostic imaging , Humans , Image Processing, Computer-Assisted/methods , Motion , Observer Variation , Prospective Studies , Quality Improvement , Urinary Bladder Neoplasms/pathology
2.
Invest Ophthalmol Vis Sci ; 58(13): 5636-5645, 2017 11 01.
Article in English | MEDLINE | ID: mdl-29094168

ABSTRACT

Purpose: To determine the intravitreal pharmacokinetic properties and to study the systemic biodistribution characteristics of I-124-labeled bevacizumab, ranibizumab, and aflibercept with positron emission tomography-computed tomography (PET/CT) imaging in a nonhuman primate model. Methods: Three groups with four owl monkeys per group underwent intravitreal injection with 1.25 mg/0.05 mL I-124 bevacizumab, 0.5 mg/0.05 mL I-124 ranibizumab, or 2.0 mg/0.05 mL I-124 aflibercept in the right eye of each subject. All subjects were imaged using PET/CT on days 0, 1, 2, 4, 8, 14, 21, 28, and 35. Serum blood draws were performed at hours 1, 2, 4, 8, 12 and days 1, 2, 4, 8, 14, 21, 28, and 35. Radioactivity emission measurements were used to determine the intravitreal half-lives of each agent and to study the differences of radioactivity uptake in nonocular organs. Results: The intravitreal half-lives were 3.60 days for I-124 bevacizumab, 2.73 days for I-124 ranibizumab, and 2.44 days for I-124 aflibercept. Serum levels were highest and most prolonged for bevacizumab as compared to both ranibizumab and aflibercept. All agents were primarily excreted through the renal and mononuclear phagocyte systems. However, bevacizumab was also found in significantly higher levels in the liver, heart, and distal femur bones. Conclusions: Among the three anti-VEGF agents used in clinical practice, bevacizumab demonstrated the longest intravitreal retention time and aflibercept the shortest. Significantly higher and prolonged levels of bevacizumab were found in the serum as well as in the heart, liver, and distal bones. These differences may be considered by clinicians when formulating treatment algorithms for intravitreal therapies with these agents.


Subject(s)
Bevacizumab/pharmacokinetics , Ranibizumab/pharmacokinetics , Recombinant Fusion Proteins/pharmacokinetics , Retinal Diseases/drug therapy , Vitreous Body/metabolism , Angiogenesis Inhibitors/administration & dosage , Angiogenesis Inhibitors/pharmacokinetics , Animals , Aotidae , Bevacizumab/administration & dosage , Disease Models, Animal , Female , Follow-Up Studies , Intravitreal Injections , Male , Positron Emission Tomography Computed Tomography , Ranibizumab/administration & dosage , Receptors, Vascular Endothelial Growth Factor/administration & dosage , Recombinant Fusion Proteins/administration & dosage , Retinal Diseases/diagnosis , Retinal Diseases/metabolism , Tissue Distribution , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Vitreous Body/diagnostic imaging
3.
J Magn Reson Imaging ; 31(5): 1272-6, 2010 May.
Article in English | MEDLINE | ID: mdl-20432367

ABSTRACT

PURPOSE: To investigate residual magnetization at different locations in the MRI suite at several time points prior, during and after field-rampdown with the goal to determine if the MRI suites could be reused in a clinical environment after the field-rampdown of MR scanners of different field strengths. MATERIALS AND METHODS: Residual magnetism was measured with two gaussmeters in the MRI suites of an 8 Tesla (T) and a 0.7T whole body magnet at several time points prior, during and after field-rampdown. RESULTS: Residual magnetism, in the MRI suite after controlled rampdown of an 8T superconducting magnet, was not significantly elevated compared with magnetic fields in the environment. Through 40 days, no significant changes in magnetism could be seen compared with initial measurements directly after rampdown, as both gaussmeters consistently measured. Similar findings were also observed after the quenched shutdown of a 0.7T system but a remanence was observed. CONCLUSION: A controlled rampdown of even an ultrahigh field MR system does not lead to retained magnetic contamination, while forced quenched rampdown of a mid-field system revealed temporary remanence. There is no need to degauss an MRI suite when an appropriate steel composition has been used in the iron shield.


Subject(s)
Magnetic Resonance Imaging/instrumentation , Radiometry , Electromagnetic Fields , Equipment Design , Equipment Failure Analysis , Radiation Dosage
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