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Featured researches published by N. Gutta.


Journal of Vascular and Interventional Radiology | 2013

Comparison of simulation-based treatment planning with imaging and pathology outcomes for percutaneous CT-guided irreversible electroporation of the porcine pancreas: a pilot study.

Thomas Wimmer; Govindarajan Srimathveeravalli; N. Gutta; Paula C. Ezell; Sebastien Monette; T. Peter Kingham; Majid Maybody; Jeremy C. Durack; Yuman Fong; Stephen B. Solomon

PURPOSE To investigate the reliability of simulations for planning pancreatic irreversible electroporation (IRE) ablations compared with computed tomography (CT) and pathology outcomes in an animal model. MATERIALS AND METHODS Simulations were performed varying treatment parameters, including field strength (1.5-2.5 kV/cm), pulse number (70-90 pulses), and pulse length (70-100 µs). Pancreatic IRE was performed in six pigs under CT guidance. Two animals each were sacrificed for histology after 1 day, 14 days, and 28 days. Follow-up CT scans were performed on day 0, day 1, day 14, and day 28. Biochemical markers were collected before the procedure, 1 day after the procedure, and 14 days after the procedure. RESULTS All ablation zones could be visualized on CT scan immediately after the procedure and on day 1 follow-up CT scan, and all animals survived until the designated endpoints. Histopathology revealed necrosis and edema on day 1 and fibrosis and glandular atrophy after 28 days. Blood vessels close to the ablation zone appeared normal. Laboratory analysis indicated mild to moderate amylasemia and lipasemia with normalization after 14 days. The ablation size on CT scan measured a mean (± SD) 146% ± 18 (day 0, P < .126) and 168% ± 18 (day 1, P < .026) of the simulation and on pathology measured 119% ± 10 (day 1, not significant) of the simulation. CONCLUSIONS Results from simulations for planning IRE ablations, CT, and pathology may differ from each other. Ablation zones on CT and pathology appear larger than simulated, suggesting that clinically used treatment planning may underestimate the ablation size in the pancreas.


Regional Anesthesia and Pain Medicine | 2014

Novel use of noninvasive high-intensity focused ultrasonography for intercostal nerve neurolysis in a swine model.

Amitabh Gulati; Jeffrey Loh; N. Gutta; Paula C. Ezell; Sebastien Monette; Joseph P. Erinjeri; Majid Maybody; Stephen B. Solomon

Background High-intensity focused ultrasound (HIFU) is a noninvasive thermal ablation technique. High-intensity focused ultrasound has been used in small-animal models to lesion neural tissue selectively. This study aimed to evaluate the efficacy of HIFU in a large-animal model for ablation of nerves similar in size to human nerves. Methods Twelve acute magnetic resonance–guided HIFU ablation lesions were created in intercostal nerves in a swine model. In a second pig, as a control, 4 radiofrequency ablation and 4 alcohol lesions were performed on intercostal nerves under ultrasound guidance. Preprocedural and postprocedural magnetic resonance imaging was then performed to evaluate radiologically the lesion size created by HIFU. Animals were euthanized 1 hour postprocedure, and necropsy was performed to collect tissue samples for histopathologic analysis. Results On gross and histological examination of the intercostal nerve, acute HIFU nerve lesions showed evidence of well-demarcated, acute, focally extensive thermal necrosis. Four intercostal nerves ablated with HIFU were sent for histopathologic analysis, with 2 of 4 lesions showing pathologic damage to the intercostal nerve. Similar results were shown with radiofrequency ablation technique, whereas the intercostal nerves appeared histologically intact with alcohol ablation. Conclusions High-intensity focused ultrasound may be used as a noninvasive neurolytic technique in swine. High-intensity focused ultrasound may have potential as a neuroablation technique for patients with chronic and cancer pain.


Technology in Cancer Research & Treatment | 2016

Feasibility of a Modified Biopsy Needle for Irreversible Electroporation Ablation and Periprocedural Tissue Sampling.

Thomas Wimmer; Govindarajan Srimathveeravalli; Mikhail Silk; Sebastien Monette; N. Gutta; Majid Maybody; Joseph P. Erinjery; Jonathan A. Coleman; Stephen B. Solomon; Constantinos T. Sofocleous

Objectives: To test the feasibility of modified biopsy needles as probes for irreversible electroporation ablation and periprocedural biopsy. Methods: Core biopsy needles of 16-G/9-cm were customized to serve as experimental ablation probes. Computed tomography-guided percutaneous irreversible electroporation was performed in in vivo porcine kidneys with pairs of experimental (n = 10) or standard probes (n = 10) using a single parameter set (1667 V/cm, ninety 100 µs pulses). Two biopsy samples were taken immediately following ablation using the experimental probes (n = 20). Ablation outcomes were compared using computed tomography, simulation, and histology. Biopsy and necropsy histology were compared. Results: Simulation-suggested ablations with experimental probes were smaller than that with standard electrodes (455.23 vs 543.16 mm2), although both exhibited similar shape. Computed tomography (standard: 556 ± 61 mm2, experimental: 515 ± 67 mm2; P = .25) and histology (standard: 313 ± 77 mm2, experimental: 275 ± 75 mm2; P = .29) indicated ablations with experimental probes were not significantly different from the standard. Histopathology indicated similar morphological changes in both groups. Biopsies from the ablation zone yielded at least 1 core with sufficient tissue for analysis (11 of the 20). Conclusions: A combined probe for irreversible electroporation ablation and periprocedural tissue sampling from the ablation zone is feasible. Ablation outcomes are comparable to those of standard electrodes.


CardioVascular and Interventional Radiology | 2015

Planning irreversible electroporation in the porcine kidney: are numerical simulations reliable for predicting empiric ablation outcomes?

Thomas Wimmer; Govindarajan Srimathveeravalli; N. Gutta; Paula C. Ezell; Sebastien Monette; Majid Maybody; Joseph P. Erinjery; Jeremy C. Durack; Jonathan A. Coleman; Stephen B. Solomon


computer assisted radiology and surgery | 2013

A study of porcine liver motion during respiration for improving targeting in image-guided needle placements

Govindarajan Srimathveeravalli; J. Leger; Paula C. Ezell; Majid Maybody; N. Gutta; Stephen B. Solomon


CardioVascular and Interventional Radiology | 2015

Feasibility Study on MR-Guided High-Intensity Focused Ultrasound Ablation of Sciatic Nerve in a Swine Model: Preliminary Results.

Elena A. Kaye; N. Gutta; Sebastien Monette; Amitabh Gulati; Jeffrey Loh; Govindarajan Srimathveeravalli; Paula C. Ezell; Joseph P. Erinjeri; Stephen B. Solomon; Majid Maybody


Journal of Vascular and Interventional Radiology | 2013

Prediction model, pathology and imaging correlation of acute and chronic outcomes following irreversible electroporation of the pancreas

Thomas Wimmer; Govindarajan Srimathveeravalli; N. Gutta; Sebastien Monette; Paula C. Ezell; Joseph P. Erinjeri; Majid Maybody; Stephen B. Solomon


Journal of Vascular and Interventional Radiology | 2013

Prediction model and imaging correlation in acute and chronic outcomes following irreversible electroporation of the kidney

Thomas Wimmer; Govindarajan Srimathveeravalli; N. Gutta; Paula C. Ezell; Sebastien Monette; Raymond H. Thornton; Joseph P. Erinjeri; Jeremy C. Durack; Majid Maybody; Stephen B. Solomon


Journal of Vascular and Interventional Radiology | 2013

New device and technique for application of irreversible electroporation for focal rectal ablation

Govindarajan Srimathveeravalli; N. Gutta; Paula C. Ezell; Sebastien Monette; P. Paty; Stephen B. Solomon


Journal of Vascular and Interventional Radiology | 2012

Abstract No. 398: CO2 rotational wedge portography with augmented fluoroscopy for TIPS placement: feasibility in a swine model

R. Ryan; C. Stevenson; Paula C. Ezell; N. Gutta; Raymond H. Thornton; George I. Getrajdman; Stephen B. Solomon

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Stephen B. Solomon

Memorial Sloan Kettering Cancer Center

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Paula C. Ezell

Memorial Sloan Kettering Cancer Center

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Majid Maybody

Memorial Sloan Kettering Cancer Center

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Sebastien Monette

Memorial Sloan Kettering Cancer Center

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Govindarajan Srimathveeravalli

Memorial Sloan Kettering Cancer Center

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Joseph P. Erinjeri

Memorial Sloan Kettering Cancer Center

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Thomas Wimmer

Medical University of Graz

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Amitabh Gulati

Memorial Sloan Kettering Cancer Center

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Jeremy C. Durack

Memorial Sloan Kettering Cancer Center

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Jeffrey Loh

Memorial Sloan Kettering Cancer Center

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