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Dive into the research topics where John W. Karanian is active.

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Featured researches published by John W. Karanian.


Optics Express | 2010

A resource for the assessment of lung nodule size estimation methods: database of thoracic CT scans of an anthropomorphic phantom

Marios A. Gavrielides; Lisa M. Kinnard; Kyle J. Myers; Jennifer Peregoy; William F. Pritchard; Rongping Zeng; Juan Esparza; John W. Karanian; Nicholas Petrick

A number of interrelated factors can affect the precision and accuracy of lung nodule size estimation. To quantify the effect of these factors, we have been conducting phantom CT studies using an anthropomorphic thoracic phantom containing a vasculature insert to which synthetic nodules were inserted or attached. Ten repeat scans were acquired on different multi-detector scanners, using several sets of acquisition and reconstruction protocols and various nodule characteristics (size, shape, density, location). This study design enables both bias and variance analysis for the nodule size estimation task. The resulting database is in the process of becoming publicly available as a resource to facilitate the assessment of lung nodule size estimation methodologies and to enable comparisons between different methods regarding measurement error. This resource complements public databases of clinical data and will contribute towards the development of procedures that will maximize the utility of CT imaging for lung cancer screening and tumor therapy evaluation.


Journal of Vascular and Interventional Radiology | 2004

Radiofrequency cauterization with biopsy introducer needle.

William F. Pritchard; Diane Wray-Cahen; John W. Karanian; Stephen L. Hilbert; Bradford J. Wood

PURPOSE The principal risks of needle biopsy are hemorrhage and implantation of tumor cells in the needle tract. This study compared hemorrhage after liver and kidney biopsy with and without radiofrequency (RF) ablation of the needle tract. MATERIALS AND METHODS Biopsies of liver and kidney were performed in swine through introducer needles modified to allow RF ablation with the distal 2 cm of the needle. After each biopsy, randomization determined whether the site was to undergo RF ablation during withdrawal of the introducer needle. Temperature was measured with a thermistor stylet near the needle tip, with a target temperature of 70 degrees C-100 degrees C with RF ablation. Blood loss was measured as grams of blood absorbed in gauze at the puncture site for 2 minutes after needle withdrawal. Selected specimens were cut for gross examination. RESULTS RF ablation reduced bleeding compared with absence of RF ablation in liver and kidney (P <.01), with mean blood loss reduced 63% and 97%, respectively. Mean amounts of blood loss (+/-SD) in the liver in the RF and no-RF groups were 2.03 g +/- 4.03 (CI, 0.53-3.54 g) and 5.50 g +/- 5.58 (CI, 3.33-7.66 g), respectively. Mean amounts of blood loss in the kidney in the RF and no-RF groups were 0.26 g +/- 0.32 (CI, -0.01 to 0.53 g) and 8.79 g +/- 7.72 (CI, 2.34-15.24 g), respectively. With RF ablation, thermal coagulation of the tissue surrounding the needle tract was observed. CONCLUSION RF ablation of needle biopsy tracts reduced hemorrhage after biopsy in the liver and kidney and may reduce complications of hemorrhage as well as implantation of tumor cells in the tract.


American Journal of Physiology-heart and Circulatory Physiology | 2010

Prelesional arterial endothelial phenotypes in hypercholesterolemia: universal ABCA1 upregulation contrasts with region-specific gene expression in vivo

Mete Civelek; Gregory R. Grant; Chrysta R. Irolla; Congzhu Shi; Rebecca J. Riley; Oscar A. Chiesa; Christian J. Stoeckert; John W. Karanian; William F. Pritchard; Peter F. Davies

Atherosclerosis originates as focal arterial lesions having a predictable distribution to regions of bifurcations, branches, and inner curvatures where blood flow characteristics are complex. Distinct endothelial phenotypes correlate with regional hemodynamics. We propose that systemic risk factors modify regional endothelial phenotype to influence focal susceptibility to atherosclerosis. Transcript profiles of freshly isolated endothelial cells from three atherosusceptible and three atheroprotected arterial regions in adult swine were analyzed to determine the initial prelesional effects of hypercholesterolemia on endothelial phenotypes in vivo. Cholesterol efflux transporter ATP-binding cassette transporter A1 (ABCA1) was upregulated at all sites in response to short-term high-fat diet. Proinflammatory and antioxidative endothelial gene expression profiles were induced in atherosusceptible and atheroprotected regions, respectively. However, markers for endoplasmic reticulum stress, a signature of susceptible endothelial phenotype, were not further enhanced by brief hypercholesterolemia. Both region-specific and ubiquitous (ABCA1) phenotype changes were identified as early prelesional responses of the endothelium to hypercholesterolemia.


Journal of Vascular and Interventional Radiology | 2010

Efficiency of Drug Delivery to the Coronary Arteries in Swine Is Dependent on the Route of Administration: Assessment of Luminal, Intimal, and Adventitial Coronary Artery and Venous Delivery Methods

John W. Karanian; Jennifer Peregoy; O. Alberto Chiesa; Tracy L. Murray; Chul Ahn; William F. Pritchard

PURPOSE To compare the efficiency of five different drug delivery methods to the coronary artery in swine. MATERIALS AND METHODS A nanoparticle-albumin-bound, nonradioactive isotopic marker was administered within the left anterior descending coronary artery (LAD) through a microinfusion catheter (MIC: adventitial, n = 8, and luminal, n = 4), a porous drug infusion balloon (DIB: intimal, n = 4), and a straight catheter (SC: luminal, n = 2) and within the superior vena cava (SC: intravenous, luminal, n = 2). The distribution of the marker in heart, lung, liver, kidney, muscle, blood, urine, and bile was determined 68-84 minutes after delivery. The heart was sectioned into six axial slices and each slice divided into four quadrants. The marker content was assayed by neutron bombardment and the total counts of disintegrations per minute (DPM) expressed as a percentage of the control for each device delivery control. RESULTS After luminal delivery with the nonactuated MIC (MIC-NA) or intimal delivery with the DIB, 0.17% ± 0.07 and 0.39% ± 0.09, respectively, less than 0.39% of the total marker was detected in the heart. After adventitial delivery with the actuated MIC (MIC-A), 63.1% ± 9.9 of the total marker was detected in the heart. Marker was only detected in quadrants containing the coronary LAD, with the highest level in the middle slice and lower marker levels in consecutive proximal and distal heart slices. The nonactuated MIC-NA and DIB drug infusion balloon patterns of marker distribution were similar to those of actuated MIC-A, although with reduced levels. These delivery methods were also associated with considerably more marker detected in the lungs and liver: at least 22% compared with 1.34% ± 1.34 for the actuated MIC-A There was one delivery failure with the actuated MIC. CONCLUSIONS Catheter-based adventitial delivery with the MIC-A represents a more efficient delivery method for retention of vascular therapeutics.


Journal of Vascular and Interventional Radiology | 2012

Pulsed High–Intensity-focused US and Tissue Plasminogen Activator (TPA) Versus TPA Alone for Thrombolysis of Occluded Bypass Graft in Swine

Nadine Abi-Jaoudeh; William F. Pritchard; Hayet Amalou; Marius George Linguraru; Oscar A. Chiesa; J.D. Adams; C. Gacchina; Robert Wesley; Subha Maruvada; Briana McDowell; Victor Frenkel; John W. Karanian; Bradford J. Wood

PURPOSE Prosthetic arteriovenous or arterial-arterial bypass grafts can thrombose and be resistant to revascularization. A thrombosed bypass graft model was created to evaluate the potential therapeutic enhancement and safety profile of pulsed high-intensity-focused ultrasound (pHIFU) on pharmaceutical thrombolysis. MATERIALS AND METHODS In swine, a right carotid-carotid expanded polytetrafluoroethylene bypass graft was surgically constructed, containing a 40% stenosis at its distal end to induce graft thrombosis. The revascularization procedure was performed 7 days after surgery. After model development and dose response experiments (n = 11), two cohorts were studied: pHIFU with tissue plasminogen activator (TPA; n = 4) and sham pHIFU with TPA (n = 3). The experiments were identical in both groups except no energy was delivered in the sham pHIFU group. Serial angiograms were obtained in all cases. The area of graft opacified by contrast medium on angiograms was quantified with digital image processing software. A blinded reviewer calculated the change in the graft area opacified by contrast medium and expressed it as a percentage, representing percentage of thrombolysis. RESULTS Combining pHIFU with 0.5 mg of TPA resulted in a 52% ± 4% increase in thrombolysis on angiograms obtained at 30 minutes, compared with a 9% ± 14% increase with sham pHIFU and 0.5 mg TPA (P = .003). Histopathologic examination demonstrated no differences between the groups. CONCLUSIONS Thrombolysis of occluded bypass grafts was significantly increased when combining pHIFU and TPA versus sham pHIFU and TPA. These results suggest that application of pHIFU may augment thrombolysis with a reduced time and dose.


Archive | 2010

Quantitative Mapping of Vascular Geometry for Implant Sites

John W. Karanian; O. Lopez; D. Rad; Briana McDowell; M. Kreitz; J. Esparza; J. Vossoughi; Oscar A. Chiesa; William F. Pritchard

In vivo characterization of the complex dynamic forces and repetitive deformations experienced by pelvic and leg vasculature is important to improve the evaluation of safety and effectiveness of implantable interventional devices such as stents [1]. The goal of this study was to use image based geometric modeling and analytical techniques to characterize the vascular deformations that occur with pelvic-hind limb motion in swine.


Archive | 2010

The Role of Imaging Tools in Biomedical Research: Preclinical Stent Implant Study

William F. Pritchard; M. Kreitz; O. Lopez; D. Rad; Briana McDowell; S. Nagaraja; M. L. Dreher; J. Esparza; J. Vossoughi; Oscar A. Chiesa; John W. Karanian

Imaging tools are used at the bedside for diagnostic and interventional procedures. The use of more than one modality (including fused modalities) can provide information from diverse sources during different stages of imageguided interventional procedures such as diagnosis, delivery of a stent to treat vascular disease and subsequent evaluation. Multi-modality interventions use an array of tools including ultrasound, fluoroscopy, angiography, endoscopy, electromagnetic tracking, robotics and computed tomographic (CT) imaging, alone or in combination, together with analytical tools during preclinical vascular and therapeutic procedures. Explant analysis includes specimen radiography (Faxitron) and scanning electron microscopy (SEM)).


Journal of Vascular and Interventional Radiology | 2012

Radiopaque Drug-Eluting Beads for Transcatheter Embolotherapy: Experimental study of Drug Penetration and Coverage in Swine

Matthew R. Dreher; Karun V. Sharma; David L. Woods; Goutham Reddy; Yiqing Tang; William F. Pritchard; Oscar A. Chiesa; John W. Karanian; Juan Esparza; Danielle Donahue; E. Levy; Sean Willis; Andrew L. Lewis; Bradford J. Wood


Journal of Vascular and Interventional Radiology | 2010

Electromagnetic navigation for thoracic aortic stent-graft deployment: a pilot study in swine.

Nadine Abi-Jaoudeh; Neil Glossop; Michael D. Dake; William F. Pritchard; Alberto Chiesa; Matthew R. Dreher; Thomas Shu Yin Tang; John W. Karanian; Bradford J. Wood


Biochemical and Biophysical Research Communications | 2005

Regional determinants of arterial endothelial phenotype dominate the impact of gender or short-term exposure to a high-fat diet

Anthony G. Passerini; Congzhu Shi; Nadeene M. Francesco; Peiying Chuan; Elisabetta Manduchi; Gregory R. Grant; Christian J. Stoeckert; John W. Karanian; Diane Wray-Cahen; William F. Pritchard; Peter F. Davies

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William F. Pritchard

Center for Devices and Radiological Health

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Bradford J. Wood

National Institutes of Health

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Oscar A. Chiesa

Center for Devices and Radiological Health

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David L. Woods

National Institutes of Health

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E. Levy

National Institutes of Health

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Ivane Bakhutashvili

National Institutes of Health

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J. Esparza-Trujillo

National Institutes of Health

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Matthew R. Dreher

National Institutes of Health

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Venkatesh Krishnasamy

National Institutes of Health

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Andrew S. Mikhail

National Institutes of Health

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