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Mayo Clinic

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Endoscopic assessment of the oesophageal features of eosinophilic oesophagitis: validation of a novel classification and grading system
Hirano, Ikuo , Moy, Nelson, Thomas, Colleen S. , Gonsalves, Nirmala , Achem, Sami R., Heckman, Michael G.

Gut | May 22, 2012 | Volume: 62 | Issue: 4 | Pages: 489-495

10.1136/gutjnl-2011-301817 | PMID 22619364 Get It

Objective Abnormalities are commonly identified during endoscopy in eosinophilic oesophagitis (EoE). There is no standardised classification to describe these features. This study aimed to evaluate the interobserver agreement of a grading system for the oesophageal features of EoE. Method The proposed system incorporated the grading of four major oesophageal features (rings, furrows, exudates, oedema) and the presence of additional features of narrow calibre oesophagus, feline oesophagus, stricture and crepe paper oesophagus. Endoscopic videos from 25 patients with EoE and controls were reviewed by 21 gastroenterologists. Interobserver agreement was assessed by estimating multi-rater κ and the proportion of pairwise agreement. Results Using the original grading system, agreement for rings, furrows and exudates was moderate (κ=0.38–0.46, 56–65% agreement) but poor for oedema (κ=0.23, 51% agreement). Identification of narrow calibre oesophagus had fair agreement (κ=0.30, 74% agreement) while feline oesophagus had poor agreement (κ=0.15, 68% agreement). After collapsing the severity grading for oedema and furrows and eliminating poorly performing features of feline oesophagus and narrow calibre oesophagus, a modified grading system demonstrated good agreement for the four major features of EoE (κ=0.40–0.54, 71–81% agreement) and additional features of stricture and crepe paper oesophagus (κ=0.52 and 0.58, 79% and 92% agreement). Conclusions The proposed system for endoscopically-identified oesophageal features of EoE defines common nomenclature and severity scores for the assessment of EoE disease activity. The system has good interobserver agreement among practising and academic gastroenterologists.
Panel Discussion: Pulmonary Embolism Imaging and Outcomes
Araoz, Philip A. , Haramati, Linda B. , Mayo, John R. , Barbosa, Eduardo Jose Mortani , Rybicki, Frank J. , Colletti, Patrick M. , Haramati, Linda B

American Journal of Roentgenology | May 22, 2012 | Volume: 198 | Issue: 6 | Pages: 1313-1319

10.2214/ajr.11.8461 | PMID 22623543 Get It

RadCases: Nuclear Medicine
DeBenedetti, Maria

American Journal of Roentgenology | May 22, 2012 | Volume: 198 | Issue: 6 | Pages: W623-W623

10.2214/ajr.11.8318 Get It

Can Sarcoidosis and Metastatic Bone Lesions Be Reliably Differentiated on Routine MRI?
Moore, Sandra, Kransdorf, Mark J. , Schweitzer, Mark E. , Murphey, Mark D. , Babb, James S. , Babb, James S

American Journal of Roentgenology | May 22, 2012 | Volume: 198 | Issue: 6 | Pages: 1387-1393

10.2214/ajr.11.7498 | PMID 22623553 Get It

CT Findings and Long-Term Mortality After Pulmonary Embolism
Morris, Michael F. , Gardner, Bruce, Thomsen, Kristine M., Harmsen, William S. , Araoz, Philip A. , Hanson, Kristine T. , Gotway, Michael B. , Hanson, Kristine

American Journal of Roentgenology | May 22, 2012 | Volume: 198 | Issue: 6 | Pages: 1346-1352

10.2214/ajr.11.6801 | PMID 22623547 Get It

The Sodium Iodide Symporter (NIS) as an Imaging Reporter for Gene, Viral, and Cell-based Therapies
Penheiter, Alan R. , Russell, Stephen J. , Carlson, Stephanie K., Russell, Stephen J

Current Gene Therapy | May 22, 2012 | Volume: 12 | Issue: 1 | Pages: 33-47

10.2174/156652312799789235 | PMID 22263922 Get It

Reply to S.A. Kesikli et al
Franko, Jan , Sargent, Daniel J. , Grothey, Axel , Sargent, Daniel J

Journal of Clinical Oncology | May 22, 2012 | Volume: 30 | Issue: 18 | Pages: 2288-2289

10.1200/jco.2012.42.9712 Get It

Choosing the Best Trastuzumab-Based Adjuvant Chemotherapy Regimen: Should We Abandon Anthracyclines?
Burstein, Harold J. , Piccart, Martine , Perez, Edith A. , Albain, Kathy S. , Norton, Larry , Hudis, Clifford A. , Hortobágyi, Gabriel N. , Wolmark, Norman , Winer, Eric P. , Norton, Larry

Journal of Clinical Oncology | May 22, 2012 | Volume: 30 | Issue: 18 | Pages: 2179-2182

10.1200/jco.2012.42.0695 | PMID 22614986 Get It

The United States Registry for Fibromuscular Dysplasia
Olin, Jeffrey W. , Froehlich, James B. , Gu, Xiaokui, Bacharach, J. Michael, Gray, Bruce H. , Kim, Esther S.H. , Mace, Pam, Matsumoto, Alan H. , McBane, Robert D. , Kline‐Rogers, Eva , Gornik, Heather L. , Eagle, Kim A. , Jaff, Michael R. , White, Christopher J. , McBane, Robert

Circulation | May 21, 2012 | Volume: 125 | Issue: 25 | Pages: 3182-3190

10.1161/circulationaha.112.091223 | PMID 22615343 Get It

Background— Fibromuscular dysplasia (FMD), a noninflammatory disease of medium-size arteries, may lead to stenosis, occlusion, dissection, and/or aneurysm. There has been little progress in understanding the epidemiology, pathogenesis, and outcomes since its first description in 1938. Methods and Results— Clinical features, presenting symptoms, and vascular events are reviewed for the first 447 patients enrolled in a national FMD registry from 9 US sites. Vascular beds were imaged selectively based on clinical presentation and local practice. The majority of patients were female (91%) with a mean age at diagnosis of 51.9 (SD 13.4 years; range, 5–83 years). Hypertension, headache, and pulsatile tinnitus were the most common presenting symptoms of the disease. Self-reported family history of stroke (53.5%), aneurysm (23.5%), and sudden death (19.8%) were common, but FMD in first- or second-degree relatives was reported only in 7.3%. FMD was identified in the renal artery in 294 patients, extracranial carotid arteries in 251 patients, and vertebral arteries in 82 patients. A past or presenting history of vascular events were common: 19.2% of patients had a transient ischemic attack or stroke, 19.7% had experienced arterial dissection(s), and 17% of patients had an aneurysm(s). The most frequent indications for therapy were hypertension, aneurysm, and dissection. Conclusions— In this registry, FMD occurred primarily in middle-aged women, although it presents across the lifespan. Cerebrovascular FMD occurred as frequently as renal FMD. Although a significant proportion of FMD patients may present with a serious vascular event, many present with nonspecific symptoms and a subsequent delay in diagnosis.
Benefits and Adverse Events in Younger Versus Older Patients Receiving Adjuvant Chemotherapy for Colon Cancer: Findings From the Adjuvant Colon Cancer Endpoints Data Set
Thomas, David M. , Yothers, Greg , Green, Erin , Blanke, Charles D. , Labianca, Roberto , Shi, Qian , Gramont, Aimery de , Sargent, Daniel J. , Hubbard, Joleen M. , O’Connell, Michael J. , Bleyer, Archie , Sargent, Daniel J , Shi, Qian , Yothers, Greg

Journal of Clinical Oncology | May 21, 2012 | Volume: 30 | Issue: 19 | Pages: 2334-2339

10.1200/jco.2011.41.1975 | PMID 22614981 Get It

Purpose Limited data exist regarding the outcomes of adjuvant therapy in younger patients with stage II and III colon cancer. We examined disease-free survival (DFS), overall survival (OS), recurrence-free interval (RFI), and grade 3+ adverse events (AEs) in younger patients in the 33,574 patient Adjuvant Colon Cancer Endpoints Group data set. Patients and Methods Individual patient data from 24 randomized phase III clinical trials were obtained for survival outcomes, which included 10 clinical trials for AE outcomes. Two age-based cutoff points were used to define younger patients: age younger than 40 years and younger than 50 years. Adjuvant therapy benefit analyses were limited to the nine clinical trials in which the investigational chemotherapeutic arm demonstrated benefit. Results One thousand seven hundred fifty-eight patients (5.2%) were younger than 40 years, 5,817 patients (17.3%) were younger than 50 years, and only 299 patients (0.9%) were younger than 30 years. No meaningful differences in sex or stage were noted in younger versus older patients. Younger and older patients did not differ in RFI (age, < 40 years: hazard ratio [HR], 1.0; P = .62 and age < 50 years: HR, 1.02; P = .35). Younger patients (both cutoff points), had longer OS and DFS than older patients. In trials demonstrating adjuvant therapy benefit, similar DFS benefit was observed by age. Younger patients experienced less leukopenia and stomatitis, but more frequent nausea/vomiting. Conclusion Among patients on clinical trials, younger and older patients with stage II and III colon cancer had similar RFI and adjuvant therapy benefit. Younger patients have longer OS and DFS, which is likely primarily because of fewer competing causes of death. Adjuvant therapy is beneficial for colon cancer in patients younger than 50 years who meet typical clinical trial eligibility criteria.