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Dive into the research topics where Kamlesh Kukreja is active.

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Featured researches published by Kamlesh Kukreja.


Journal of Vascular and Interventional Radiology | 2015

Endovascular Thrombolysis in the Management of Iliofemoral Thrombosis in Children: A Multi-Institutional Experience.

Marian Gaballah; Junzi Shi; Kamlesh Kukreja; Leslie Raffini; Cristina Tarango; Marc S. Keller; Ganesh Krishnamurthy; John M. Racadio; Manish N. Patel; Anne Marie Cahill

PURPOSE To evaluate technical feasibility, complications, and clinical outcomes of endovascular thrombolysis for iliofemoral thrombosis at two tertiary-care childrens hospitals. MATERIALS AND METHODS Institutional review board-approved retrospective review from March 2003 through June 2013 showed that venous thrombolysis for iliofemoral thrombosis was performed in 57 children (64 limbs) with a median age of 16.1 years (mean age, 14.5 y; range, 1.0-17.8 y). Techniques included catheter-directed thrombolysis (CDT), percutaneous mechanical thrombectomy (PMT), and pharmacomechanical catheter-directed thrombolysis (PCDT) with adjunctive angioplasty and/or stent placement. Villalta and modified Villalta scales were applied retrospectively to follow-up data to assess postthrombotic syndrome (PTS). RESULTS Technical success (≥ 50% thrombolysis) rate was 93.7%: grade III (100%) in 19 limbs, grade II (50%-99%) in 41 limbs, and grade I (< 50%) in four limbs. Techniques included CDT with PCDT (32.8%) or PMT (35.9%), CDT alone (26.6%), PCDT alone (4.7%) or with adjunctive angioplasty (54.7%), and stent placement (6.3%). Mean duration of CDT was 36.5 hours (range, 2.9-89.6 h). There was one major complication (1.8%) of bleeding requiring transfusion. Minor complications (ie, bleeding) occurred in seven patients (12.2%). Median follow-up was 1.5 years (range, 30 d to 7 y). Seven patients underwent repeat thrombolysis for recurrent thrombosis. The PTS rate was 59.3% per modified Villalta scale but only 2.1% per Villalta scale. CONCLUSIONS Endovascular thrombolysis is technically feasible and safe for iliofemoral thrombosis in children. Variable results were seen with two scales to assess PTS, suggesting an acute need for standardization of outcome measurement in children.


Journal of Vascular and Interventional Radiology | 2014

Endovascular venous thrombolysis in children younger than 24 months.

Kamlesh Kukreja; Matthew P. Lungren; Manish N. Patel; Neil D. Johnson; John M. Racadio; Christopher E. Dandoy; Cristina Tarango

PURPOSE To evaluate the technical feasibility and safety of percutaneous endovascular thrombolysis for extremity deep venous thrombosis (DVT) in children < 24 months old. MATERIALS AND METHODS A retrospective chart review of a clinical and imaging database was performed for pediatric patients who underwent endovascular therapy for DVT between January 2010 and July 2013. Indications, techniques, technical and clinical success, and complications were reviewed. Techniques for thrombolysis included catheter-directed therapy (CDT) using alteplase infusion via a multi-side hole catheter, mechanical thrombectomy, and angioplasty. Short-term outcomes were assessed using surgical and imaging follow-up examinations for patency of the targeted vessel. Patients included 11 children (mean age, 9 mo; range, 3 wk-23 mo) who consecutively underwent endovascular thrombolysis for upper extremity (n = 6) or lower extremity (n = 5) DVT. The most common indication was preservation of venous access for future cardiac surgery or medical therapy. RESULTS The most common risk factor was the presence of a central venous catheter (10 of 11 patients). All patients with upper extremity DVT had congenital heart disease. CDT and angioplasty were performed in all patients. Venous patency was established in all patients. A grade III (95%-100%) thrombolysis response was achieved in seven patients, and a grade II (50%-95%) thrombolysis response was achieved in four patients. A major complication of pulmonary embolism occurred in one patient with upper extremity thrombolysis and was managed by intravenous systemic alteplase and heparin. No recurrence of thrombosis was found on average follow-up of 11.8 months (range, 1-41 mo). CONCLUSIONS Percutaneous endovascular thrombolysis for extremity DVT is safe and technically feasible in children < 24 months old.


Pediatric Radiology | 2016

Use of cone-beam CT and live 3-D needle guidance to facilitate percutaneous nephrostomy and nephrolithotripsy access in children and adolescents

C. Matthew Hawkins; Kamlesh Kukreja; Timothy Singewald; Eugene Minevich; Neil D. Johnson; Pramod Reddy; John M. Racadio

BackgroundGaining access into non-dilated renal collecting systems for percutaneous nephrolithotripsy, particularly in patients with prohibitive body habitus and/or scoliosis, is often challenging using conventional techniques.ObjectiveTo evaluate the feasibility of cone-beam CT for percutaneous nephrostomy placement for subsequent percutaneous nephrolithotripsy in children and adolescents.Materials and methodsA retrospective review of percutaneous nephrostomy revealed use of cone-beam CT and 3-D guidance in 12 percutaneous nephrostomy procedures for 9 patients between 2006 and 2015. All cone-beam CT-guided percutaneous nephrostomies were for pre-lithotripsy access and all 12 were placed in non-dilated collecting systems.ResultsTechnical success was 100%. There were no complications.ConclusionCone-beam CT with 3-D guidance is a technically feasible technique for percutaneous nephrostomy in children and adolescents, specifically for nephrolithotripsy access in non-dilated collecting systems.


CardioVascular and Interventional Radiology | 2018

Trans-splenic Access for Portal Venous Interventions in Children: Do Benefits Outweigh Risks?

Sheena Pimpalwar; Ponraj Chinnadurai; Alberto Hernandez; Kamlesh Kukreja; Shakeel Siddiqui; Henri Justino

BackgroundThe primary concern of trans-splenic access for portal interventions is the risk of life-threatening intraperitoneal bleeding.ObjectiveTo review the clinical indications and efficacy and evaluate the risk factors for intraperitoneal bleeding during trans-splenic portal interventions in children.Materials and MethodsA retrospective review of consecutive patients who underwent trans-splenic portal interventions at a tertiary care pediatric institution between March 2011 and April 2017 was performed. Forty-four procedures were performed in 30 children with a median age of 5 (0.3–18) years. Clinical indications, technical success, procedural success, and incidence of complications were recorded. Potential risk factors for intraperitoneal bleeding were evaluated using Wilcoxon rank and Fisher’s exact tests.ResultsTrans-splenic access was 100% successful. In 35/44 (79%) procedures, the subsequent intervention was successful including recanalization of post-transplant portal vein occlusion in 10/13, embolization of bleeding Roux limb varices in 8/8, recanalization of chronic portal vein thrombosis in native liver in 7/13, splenoportography and manometry in 6/6, and occlusion of portosystemic shunts in 4/4 procedures. Intraperitoneal bleeding occurred during 12/44 (27%) procedures and was managed with analgesics, blood transfusion, and peritoneal drainage without the need for splenectomy or splenic artery embolization. Statistically significant correlation of bleeding was found with intraprocedural anticoagulation, but not with patient age, weight, platelet count, INR, ascites, splenic length, splenic venous pressure, vascular sheath size, or tract embolization technique.ConclusionTrans-splenic access is a useful technique for successful pediatric portal interventions. Although it entails a substantial risk of intraperitoneal bleeding, this can be managed conservatively.


Urology | 2018

Nephrolithiasis in a 17-Year-Old Male With Seckel Syndrome and Horseshoe Kidneys: Case Report and Review of the Literature

Matthew Jung; Arun Rai; Lily C. Wang; Kathleen T. Puttmann; Kamlesh Kukreja; Chester J. Koh

We report the case of a 17-year-old male with Seckel syndrome and horseshoe kidneys which had a 7 mm kidney stone in the lower pole calyx of the right moiety. The patient had a history of rotoscoliosis with 60° dextroconvex curvature and hepatic steatosis. Attempted ureteroscopy was unsuccessful due to stone location and anatomy. Percutaneous nephrolithotomy was ultimately required. This case highlights the difficulties of endoscopic treatments of renal calculi in patients with abnormal renal anatomy and dysmorphia. To our knowledge, this is the first reported case of nephrolithiasis in a patient with Seckel syndrome and horseshoe kidneys.


Journal of Vascular and Interventional Radiology | 2017

Percutaneous Anterior Ureterostomy for Double J Ureteral Stent Placement in an 18-Month-Old Patient

Christopher Yen; Kamlesh Kukreja; Chester J. Koh

An 18-month-old boy presented with tachycardia and purulent drainage from a vesicostomy stoma. He had a prior history of obstructive uropathy from posterior urethral valves, with complications including end-stage renal disease and recent multidrug-resistant Escherichia coli bacteremia. Ultrasound demonstrated new layering debris in a severely dilated right ureter suggesting pyoureter and unchanged bilateral atrophic kidneys with nondilated pelves (Figs 1, 2). Urine culture was positive for Stenotrophomonas maltophilia. Right ureterovesical junction stenosis prevented cystoscopic stent placement, and percutaneous urinary decompression was required. Nephrostomy access was not possible because of the nondilated renal pelvis in an atrophic kidney. An anterior direct ureteral approach was chosen. With the patient in supine position and under general anesthesia, an 18-gauge needle was used to access the dilated distal right ureter with ultrasound guidance (Figs 3, 4). A 0.035-inch Glidewire (TerumoMedical Corp, Somerset, New Jersey)wasmaneuvered past the distal obstruction, into the bladder, and through the vesicostomy to obtain through-and-through access (Fig 5). A 4-F sheath (Cook, Inc, Bloomington,


Journal of Applied Clinical Medical Physics | 2015

Comparison of pediatric radiation dose and vessel visibility on angiographic systems using piglets as a surrogate: antiscatter grid removal vs. lower detector air kerma settings with a grid — a preclinical investigation

Keith J. Strauss; John M. Racadio; Todd Abruzzo; Neil D. Johnson; Manish N. Patel; Kamlesh Kukreja; Mark den Hartog; Bart Pierre Antoine Jozef Hoornaert; Rami Nachabe

The purpose of this study was to reduce pediatric doses while maintaining or improving image quality scores without removing the grid from X‐ray beam. This study was approved by the Institutional Animal Care and Use Committee. Three piglets (5, 14, and 20 kg) were imaged using six different selectable detector air kerma (Kair) per frame values (100%, 70%, 50%, 35%, 25%, 17.5%) with and without the grid. Number of distal branches visualized with diagnostic confidence relative to the injected vessel defined image quality score. Five pediatric interventional radiologists evaluated all images. Image quality score and piglet Kair were statistically compared using analysis of variance and receiver operating curve analysis to define the preferred dose setting and use of grid for a visibility of 2nd and 3rd order vessel branches. Grid removal reduced both dose to subject and imaging quality by 26%. Third order branches could only be visualized with the grid present; 100% detector Kair was required for smallest pig, while 70% detector Kair was adequate for the two larger pigs. Second order branches could be visualized with grid at 17.5% detector Kair for all three pig sizes. Without the grid, 50%, 35%, and 35% detector Kair were required for smallest to largest pig, respectively. Grid removal reduces both dose and image quality score. Image quality scores can be maintained with less dose to subject with the grid in the beam as opposed to removed. Smaller anatomy requires more dose to the detector to achieve the same image quality score. PACS numbers: 87.53.Bn, 87.57.N‐, 87.57.cj, 87.59.cf, 87.59.DjThe purpose of this study was to reduce pediatric doses while maintaining or improving image quality scores without removing the grid from X-ray beam. This study was approved by the Institutional Animal Care and Use Committee. Three piglets (5, 14, and 20 kg) were imaged using six different selectable detector air kerma (Kair) per frame values (100%, 70%, 50%, 35%, 25%, 17.5%) with and without the grid. Number of distal branches visualized with diagnostic confidence relative to the injected vessel defined image quality score. Five pediatric interventional radiologists evaluated all images. Image quality score and piglet Kair were statistically compared using analysis of variance and receiver operating curve analysis to define the preferred dose setting and use of grid for a visibility of 2nd and 3rd order vessel branches. Grid removal reduced both dose to subject and imaging quality by 26%. Third order branches could only be visualized with the grid present; 100% detector Kair was required for smallest pig, while 70% detector Kair was adequate for the two larger pigs. Second order branches could be visualized with grid at 17.5% detector Kair for all three pig sizes. Without the grid, 50%, 35%, and 35% detector Kair were required for smallest to largest pig, respectively. Grid removal reduces both dose and image quality score. Image quality scores can be maintained with less dose to subject with the grid in the beam as opposed to removed. Smaller anatomy requires more dose to the detector to achieve the same image quality score. PACS numbers: 87.53.Bn, 87.57.N-, 87.57.cj, 87.59.cf, 87.59.Dj.


Pediatric Radiology | 2009

Head and neck lymph nodes in children: the spectrum from normal to abnormal

Ricardo Restrepo; Julieta Oneto; Kathleen Lopez; Kamlesh Kukreja


Pediatric Radiology | 2007

Differentiation between pediatric spinal arachnoid and epidermoid-dermoid cysts: is diffusion-weighted MRI useful?

Kamlesh Kukreja; Glen Manzano; John Ragheb; L. Santiago Medina


Pediatric Radiology | 2015

Outcomes in children with deep vein thrombosis managed with percutaneous endovascular thrombolysis.

Christopher E. Dandoy; Kamlesh Kukreja; Ralph A. Gruppo; Manish N. Patel; Cristina Tarango

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Daniel Ashton

Boston Children's Hospital

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Sheena Pimpalwar

Baylor College of Medicine

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J. Hernandez

Boston Children's Hospital

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Manish N. Patel

Cincinnati Children's Hospital Medical Center

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John M. Racadio

Cincinnati Children's Hospital Medical Center

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Cristina Tarango

Cincinnati Children's Hospital Medical Center

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H. Cleveland

Boston Children's Hospital

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Neil D. Johnson

Cincinnati Children's Hospital Medical Center

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