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1992 citation(s) found for "Vu, Joshua".

Clinical Predictors of a Diagnosis of Common Variable Immunodeficiency-related Granulomatous-Lymphocytic Interstitial Lung Disease
Mannina, Amar, Swigris, Jeffrey J. , Solomon, Joshua J. , Huie, Tristan J. , Yunt, Zulma X., Truong, Tho Q., Brown, Kevin K. , Achcar, Rosane Duarte , Olson, Amy L. , Cox, Christian W. , Kligerman, Seth , Pérez, Evans R. Fernández , Chung, Jonathan Hero , Curran‐Everett, Douglas

Annals of the American Thoracic Society | April 11, 2016 | Volume: 13 | Issue: 7 | Pages: 1042-1049

10.1513/annalsats.201511-728oc | PMID 27064856 Get It

Abstract Rationale Granulomatous-lymphocytic interstitial lung disease (GLILD) has emerged as a major cause of morbidity in patients with common variable immunodeficiency (CVID). While GLILD is among the most serious noninfectious pulmonary complications of CVID, risk factors for this condition have not been reported. Objectives To identify clinical, physiologic, and serologic risk factors for GLILD in adults with CVID. Methods Of 345 consecutive adult patients with CVID, we identified 34 in the National Jewish Health research database who had a radiographic-pathologic diagnosis of GLILD evaluated between 2002 and 2014. Each case was age and sex matched to 52 CVID control subjects. We used logistic regression to determine independent predictors of GLILD. A mixed effects model was used to estimate the longitudinal change in percent predicted FVC. Measurements and Main Results: The mean time from CVID diagnosis to GLILD detection was 7.8 years. Compared with matched control subjects, cases were more likely to have a history of autoimmune cytopenia, hypersplenism, polyarthritis, lower marginal zone and switched memory B cells, and restrictive lung function. Multivariate analysis revealed that hypersplenism (odds ratio [OR], 24; 95% confidence interval [CI], 4.5–179.1), polyarthritis (OR, 19; 95% CI, 2.3–206.8), and percent predicted FVC (OR, 0.93; 95% CI, 0.87–0.98) were independently associated with the development of GLILD. The rate of change of percent predicted FVC (slope, P = 0.48) did not vary significantly in patients with GLILD over a mean follow-up of 7 years after diagnosis. Conclusions Hypersplenism and polyarthritis are strong risk factors for GLILD in patients with CVID. Percent predicted FVC remained stable over time in patients with GLILD.
Vascular specialist response to Medicare Evidence Development Coverage Advisory Committee (MEDCAC) panel on peripheral artery disease of the lower extremities
Shishehbor, Mehdi H. , Bartholomew, John R. , Beckman, Joshua A. , Froehlich, James B. , Lookstein, R. , Roberts, Anne C. , Misra, Sanjay , Aronow, Herbert D. , Misra, Sanjay, Rosenfield, Kenneth , Jaff, Michael R. , Misra, Sanjay , Beckman, Joshua A

Vascular Medicine | April 10, 2016 | Volume: 21 | Issue: 3 | Pages: 281-286

10.1177/1358863x16636955 | PMID 27063017 Get It

Vascular specialist response to medicare evidence development coverage advisory committee (MEDCAC) panel on peripheral artery disease of the lower extremities
Shishehbor, Mehdi H. , Bartholomew, John R. , Beckman, Joshua A. , Froehlich, James B. , Lookstein, R. , Roberts, Anne C. , Misra, Sanjay , Aronow, Herbert D. , Misra, Sanjay, Rosenfield, Kenneth , Jaff, Michael R. , Misra, Sanjay , Beckman, Joshua A

Catheterization and Cardiovascular Interventions | April 10, 2016 | Volume: 87 | Issue: 7 | Pages: 1181-1186

10.1002/ccd.26512 | PMID 27062192 Get It

Long‐term follow‐up after PFO device closure
Taggart, Nathaniel W. , Reeder, Guy S., Lennon, Ryan J. , Slusser, Joshua P. , Freund, Monique , Cetta, Frank , Hagler, Donald J. , Freund, Monique A, Cabalka, Allison K. , Taggart, Nathaniel W

Catheterization and Cardiovascular Interventions | March 31, 2016 | Volume: 89 | Issue: 1 | Pages: 124-133

10.1002/ccd.26518 | PMID 27027873 Get It

ObjectivesTo describe medium‐ to long‐term follow‐up of patients undergoing device closure of patent foramen ovale (PFO) for stroke or transient ischemic attack (TIA).BackgroundTranscatheter device closure of PFO continues to be used for secondary prevention of cryptogenic stroke or TIA, but data are lacking regarding long‐term outcomes.MethodsWe reviewed the Mayo Clinic Rochester PFO database for patients who underwent device closure of PFO for secondary prevention of stroke/TIA from December 2001 to June 2012. Demographic, clinical, procedural, and follow‐up data were reviewed. Recurrence rate of stroke/TIA were calculated. Data were analyzed to identify risk factors of recurrent neurologic events.ResultsSeven hundred and thirty patients (mean age 53 years; 40% female) were included in our study. Most patients (72%) had cryptogenic stroke as their qualifying event for PFO closure. There were no procedure‐related deaths or strokes. The most commonly used device was the Amplatzer Septal Occluder (82%). Median follow‐up was 6 years. A 3.9% of patients had documented residual right‐to‐left shunting at last echocardiogram. Recurrent stroke and/or TIA were reported in 45 patients, (6.3% of patients with follow‐up data). Patients who experienced recurrent stroke/TIA were older and had a higher rate of diabetes and hypertension than those who did not. The presence of residual shunt did not correlate with risk of recurrent events.ConclusionsDevice closure of PFO can be performed safely with very good long‐term resolution of atrial shunting. Recurrent neurologic events after PFO closure may reflect additional comorbid risk factors unrelated to the potential for paradoxical embolism. © 2016 Wiley Periodicals, Inc.
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability
Kirby, Jacqueline, Speltz, Peter, Rasmussen, Luke V. , Gottesman, Omri, Peissig, Peggy , Pacheco, Jennifer A. , Tromp, Gerard , Pathak, Jyotishman , Ellis, Stephen B. , Thompson, Will K, Savova, Guergana , Haines, Jonathan L. , Roden, Dan M. , Denny, Joshua C. , Basford, Melissa , Carrell, David , Lingren, Todd , Roden, Dan M. , Harris, Paul A. , Denny, Joshua C , Rasmussen, Luke V , Pacheco, Jennifer A

Journal of the American Medical Informatics Association | March 30, 2016 | Volume: 23 | Issue: 6 | Pages: 1046-1052

10.1093/jamia/ocv202 | PMID 27026615 Get It

Abstract Objective Health care generated data have become an important source for clinical and genomic research. Often, investigators create and iteratively refine phenotype algorithms to achieve high positive predictive values (PPVs) or sensitivity, thereby identifying valid cases and controls. These algorithms achieve the greatest utility when validated and shared by multiple health care systems. Materials and Methods We report the current status and impact of the Phenotype KnowledgeBase (PheKB, http://phekb.org ), an online environment supporting the workflow of building, sharing, and validating electronic phenotype algorithms. We analyze the most frequent components used in algorithms and their performance at authoring institutions and secondary implementation sites. Results As of June 2015, PheKB contained 30 finalized phenotype algorithms and 62 algorithms in development spanning a range of traits and diseases. Phenotypes have had over 3500 unique views in a 6-month period and have been reused by other institutions. International Classification of Disease codes were the most frequently used component, followed by medications and natural language processing. Among algorithms with published performance data, the median PPV was nearly identical when evaluated at the authoring institutions (n = 44; case 96.0%, control 100%) compared to implementation sites (n = 40; case 97.5%, control 100%). Discussion These results demonstrate that a broad range of algorithms to mine electronic health record data from different health systems can be developed with high PPV, and algorithms developed at one site are generally transportable to others. Conclusion By providing a central repository, PheKB enables improved development, transportability, and validity of algorithms for research-grade phenotypes using health care generated data.
Quantitative 3D magnetic resonance elastography: Comparison with dynamic mechanical analysis
Arunachalam, Shivaram P. , Rossman, Phillip J. , Arani, Arvin , Lake, David S. , Glaser, Kevin J. , Trzasko, Joshua D. , McGee, Kiaran P. , Araoz, Philip A. , Manduca, Armando , Ehman, Richard L. , Arunachalam, S P , Arani, Arvin

Magnetic Resonance in Medicine | March 26, 2016 | Volume: 77 | Issue: 3 | Pages: 1184-1192

10.1002/mrm.26207 | PMID 27016276 Get It

Purpose Magnetic resonance elastography (MRE) is a rapidly growing noninvasive imaging technique for measuring tissue mechanical properties in vivo. Previous studies have compared two‐dimensional MRE measurements with material properties from dynamic mechanical analysis (DMA) devices that were limited in frequency range. Advanced DMA technology now allows broad frequency range testing, and three‐dimensional (3D) MRE is increasingly common. The purpose of this study was to compare 3D MRE stiffness measurements with those of DMA over a wide range of frequencies and shear stiffnesses. Methods 3D MRE and DMA were performed on eight different polyvinyl chloride samples over 20–205 Hz with stiffness between 3 and 23 kPa. Driving frequencies were chosen to create 1.1, 2.2, 3.3, 4.4, 5.5, and 6.6 effective wavelengths across the diameter of the cylindrical phantoms. Wave images were analyzed using direct inversion and local frequency estimation algorithm with the curl operator and compared with DMA measurements at each corresponding frequency. Samples with sufficient spatial resolution and with an octahedral shear strain signal‐to‐noise ratio > 3 were compared. Results Consistency between the two techniques was measured with the intraclass correlation coefficient (ICC) and was excellent with an overall ICC of 0.99. Conclusions 3D MRE and DMA showed excellent consistency over a wide range of frequencies and stiffnesses. Magn Reson Med 77:1184–1192, 2017. © 2016 The Authors Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
International Myeloma Working Group Recommendations for the Diagnosis and Management of Myeloma-Related Renal Impairment
Dimopoulos, Meletios Α. , Sonneveld, Pieter , Merlini, Giampaolo , Kastritis, Efstathios , Goldschmidt, Hartmut , Joshua, Douglas, Orlowski, Robert Z. , Powles, Raymond, Vesole, David H., Garderet, Laurent, Palumbo, Antonio , Cavo, Michèle , Richardson, Paul G. , Moreau, Philippe , Miguel, Jesús F. San , Durie, Brian G.M. , Terpos, Evangelos , Bergsagel, P. Leif , Russell, Stephen J. , Rosiñol, Laura , Ocio, Enrique M. , García‐Sánz, Ramón , Beksaç, Meral , Zweegman, Sonja , Usmani, Saad Z. , Donk, Niels W.C.J. van de , Pratt, Guy , Chari, Ajai , Cook, Gordon , Rossi, Adriana , O’Dwyer, Michael , Paiva, Bruno , Larrea, Carlos Fernández de , Souza, Cármino Antônio De , Terragna, Carolina , Bergsagel, P. Leif , Dimopoulos, Meletios A, Ludwig, Heinz , San Miguel, Jesús, Leung, Nelson , Joshua, Douglas, Orlowski, Robert Z. , Einsele, Hermann , Richardson, Paul Gerard Guy , Rajkumar, S. Vincent , Zweegman, Sonja , Merlini, Giampaolo , Dimopoulos, Meletios A , Russell, Stephen J , Moreau, Philippe , Terpos, Evangelos , Chari, Ajai , San-Miguel, Jesus , Paiva, Bruno , Kastritis, Efstathios , Garcia-Sanz, Ramon , Beksac, Meral , Cook, Gordon , Usmani, Saad , Rossi, Adriana , Ocio, Enrique M

Journal of Clinical Oncology | March 14, 2016 | Volume: 34 | Issue: 13 | Pages: 1544-1557

10.1200/jco.2015.65.0044 | PMID 26976420 Get It

Purpose The aim of the International Myeloma Working Group was to develop practical recommendations for the diagnosis and management of multiple myeloma–related renal impairment (RI). Methods Recommendations were based on published data through December 2015, and were developed using the system developed by the Grading of Recommendation, Assessment, Development, and Evaluation Working Group. Recommendations All patients with myeloma at diagnosis and at disease assessment should have serum creatinine, estimated glomerular filtration rate, and electrolytes measurements as well as free light chain, if available, and urine electrophoresis of a sample from a 24-hour urine collection (grade A). The Chronic Kidney Disease Epidemiology Collaboration, preferably, or the Modification of Diet in Renal Disease formula should be used for the evaluation of estimated glomerular filtration rate in patients with stabilized serum creatinine (grade A). International Myeloma Working Group criteria for renal reversibility should be used (grade B). For the management of RI in patients with multiple myeloma, high fluid intake is indicated along with antimyeloma therapy (grade B). The use of high-cutoff hemodialysis membranes in combination with antimyeloma therapy can be considered (grade B). Bortezomib-based regimens remain the cornerstone of the management of myeloma-related RI (grade A). High-dose dexamethasone should be administered at least for the first month of therapy (grade B). Thalidomide is effective in patients with myeloma with RI, and no dose modifications are needed (grade B). Lenalidomide is effective and safe, mainly in patients with mild to moderate RI (grade B); for patients with severe RI or on dialysis, lenalidomide should be given with close monitoring for hematologic toxicity (grade B) with dose reduction as needed. High-dose therapy with autologous stem cell transplantation (with melphalan 100 mg/m 2 to 140 mg/m 2 ) is feasible in patients with RI (grade C). Carfilzomib can be safely administered to patients with creatinine clearance > 15 mL/min, whereas ixazomib in combination with lenalidomide and dexamethasone can be safely administered to patients with creatinine clearance > 30 mL/min (grade A).
Fecal Microbiome in Epidemiologic Studies—Response
Vogtmann, Emily , Amir, Amnon , Shi, Jianxin , Flores, Roberto , Knight, Rob , Chia, Nicholas , Sinha, Rashmi R. , Chen, Jun , Sampson, Joshua N. , Chia, Nicholas

Cancer Epidemiology, Biomarkers & Prevention | March 10, 2016 | Volume: 25 | Issue: 5 | Pages: 870-871

10.1158/1055-9965.epi-16-0161 | PMID 26961994 Get It

Evaluation of Immune-Related Response Criteria and RECIST v1.1 in Patients With Advanced Melanoma Treated With Pembrolizumab
Hodi, F. Stephen , Hwu, Wen-Jen , Kefford, Richard , Weber, Jeffrey S. , Daud, Adil , Hamid, Omid , Patnaik, Amita , Ribas, Antoni , Robert, Caroline , Gangadhar, Tara C., Joshua, Anthony M. , Hersey, Peter , Dronca, Roxana , Joseph, Richard W. , Hille, Darcy A., Xue, Dahai, Li, Xiaoyun , Kang, Sunyu , Ebbinghaus, Scot, Perrone, Andrea , Joseph, Richard, Hille, Darcy, Li, Xiaoyun Nicole, Kang, S Peter, Wolchok, Jedd D, Hwu, Wen‐Jen , Wolchok, Jedd D. , Daud, Adil I , Weber, Jeffrey

Journal of Clinical Oncology | March 8, 2016 | Volume: 34 | Issue: 13 | Pages: 1510-1517

10.1200/jco.2015.64.0391 | PMID 26951310 Get It

Purpose We evaluated atypical response patterns and the relationship between overall survival and best overall response measured per immune-related response criteria (irRC) and Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST v1.1) in patients with advanced melanoma treated with pembrolizumab in the phase Ib KEYNOTE-001 study (clinical trial information: NCT01295827). Patients and Methods Patients received pembrolizumab 2 or 10 mg/kg every 2 weeks or every 3 weeks. Atypical responses were identified by using centrally assessed irRC data in patients with ≥ 28 weeks of imaging. Pseudoprogression was defined as ≥ 25% increase in tumor burden at week 12 (early) or any assessment after week 12 (delayed) that was not confirmed as progressive disease at next assessment. Response was assessed centrally per irRC and RECIST v1.1. Results Of the 655 patients with melanoma enrolled, 327 had ≥ 28 weeks of imaging follow-up. Twenty-four (7%) of these 327 patients had atypical responses (15 [5%] with early pseudoprogression and nine [3%] with delayed pseudoprogression). Of the 592 patients who survived ≥ 12 weeks, 84 (14%) experienced progressive disease per RECIST v1.1 but nonprogressive disease per irRC. Two-year overall survival rates were 77.6% in patients with nonprogressive disease per both criteria (n = 331), 37.5% in patients with progressive disease per RECIST v1.1 but nonprogressive disease per irRC (n = 84), and 17.3% in patients with progressive disease per both criteria (n = 177). Conclusion Atypical responses were observed in patients with melanoma treated with pembrolizumab. Based on survival analysis, conventional RECIST might underestimate the benefit of pembrolizumab in approximately 15% of patients; modified criteria that permit treatment beyond initial progression per RECIST v1.1 might prevent premature cessation of treatment.
Creation of the Prevention of Organ Failure Checklist. A Multidisciplinary Approach Using the Modified Delphi Technique
Pearl, Joshua, Dong, Yue , Herasevich, Vitaly , Gong, Michelle N. , Gajic, Ognjen , Herasevich, Vitaly , Dong, Yue

Annals of the American Thoracic Society | March 2, 2016 | Volume: 13 | Issue: 6 | Pages: 910-916

10.1513/annalsats.201509-626bc | PMID 26933899 Get It

Abstract Rationale Respiratory failure represents a major risk for morbidity and mortality. Although generally managed in the intensive care unit (ICU), respiratory failure often begins elsewhere. Checklists of care processes to minimize the duration of mechanical ventilation and adverse events are routinely used in the ICU, but are uncommonly used outside the ICU. Objectives To develop consensus among a multidisciplinary expert panel on care practices to include in a checklist of best practices for critically ill patients with respiratory failure before and after ICU admission. Methods A multidisciplinary expert panel was assembled. The panel was tasked with creating a checklist of care processes aimed at decreasing progression to respiratory failure, duration of mechanical ventilation, mortality in mechanical ventilation, and adverse events. Over the course of multiple teleconferences and e-mail communications, the Prevention of Organ Failure Checklist list was reviewed, refined, and voted upon. Items that received greater than 75% of the vote were included in the final checklist. Measurements and Main Results: Using a modified Delphi process, the expert panel was able to compile Prevention of Organ Failure Checklist into 20 items that aimed to decrease mechanical ventilation by assessing the causes of acute respiratory failure, ventilation strategies, sedation, and general critical care processes, as well as to avoid unwanted or nonbeneficial interventions. Conclusions The modified Delphi process identified readily available preventative interventions suitable for checklist implementation in patients with or progressing to respiratory failure even before ICU admission.