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Variation in Endoscopic Activity Assessment and Endoscopy Score Validation in Adults With Eosinophilic Esophagitis.
Schoepfer, Alain M; Hirano, Ikuo; Coslovsky, Michael; Roumet, Marie C; Zwahlen, Marcel; Kuehni, Claudia E; Hafner, David; Alexander, Jeffrey A; Dellon, Evan S; Gonsalves, Nirmala; Leung, John; Bussmann, Christian; Collins, Margaret H; Newbury, Robert O; Smyrk, Thomas C; Woosley, John T; Yang, Guang-Yu; Romero, Yvonne; Katzka, David A; Furuta, Glenn T; Gupta, Sandeep K; Aceves, Seema S; Chehade, Mirna; Spergel, Jonathan M; Falk, Gary W; Meltzer, Brian A; Comer, Gail M; Straumann, Alex; Safroneeva, Ekaterina.
Afiliação
  • Schoepfer AM; Division of Gastroenterology and Hepatology, Centre Hospitalier Universitaire Vaudois/CHUV, Lausanne, Switzerland. Electronic address: alain.schoepfer@chuv.ch.
  • Hirano I; Division of Gastroenterology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Coslovsky M; Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
  • Roumet MC; Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
  • Zwahlen M; Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
  • Kuehni CE; Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
  • Hafner D; Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
  • Alexander JA; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
  • Dellon ES; Center for Esophageal Diseases and Swallowing, Division of Gastroenterology and Hepatology, University of North Carolina School of Medicine, Chapel Hill, North Carolina.
  • Gonsalves N; Division of Gastroenterology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Leung J; Center for Food Related Diseases, Division of Pediatric Allergy and Immunology, Division of Gastroenterology, Tufts Medical Center and Floating Hospital for Children, Boston, Massachusetts.
  • Bussmann C; Viollier AG, Institute for Pathology, Basel, Switzerland.
  • Collins MH; Division of Pathology and Laboratory Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Newbury RO; Department of Pathology, Rady Children's Hospital, University of California, San Diego, San Diego, California.
  • Smyrk TC; Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, Rochester, Minnesota.
  • Woosley JT; Department of Pathology and Laboratory Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina.
  • Yang GY; Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Romero Y; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota; Department of Otolaryngology, Mayo Clinic, Rochester, Minnesota; GI Outcomes Unit, Mayo Clinic, Rochester, Minnesota.
  • Katzka DA; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
  • Furuta GT; Gastrointestinal Eosinophilic Diseases Program, Department of Pediatrics, University of Colorado School of Medicine; Digestive Health Institute, Children's Hospital Colorado, Aurora, Colorado.
  • Gupta SK; Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Riley Hospital for Children, Indiana University School of Medicine, Indianapolis, Indiana.
  • Aceves SS; Division of Allergy and Immunology, Rady Children's Hospital, University of California, San Diego, San Diego, California.
  • Chehade M; Departments of Pediatrics and Medicine, Mount Sinai Center for Eosinophilic Disorders, Jaffe Food Allergy Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Spergel JM; Divisions of Allergy and Immunology, Department of Pediatrics, The Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Falk GW; Division of Gastroenterology, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Meltzer BA; Adare Pharmaceuticals, Inc, Lawrenceville, New Jersey.
  • Comer GM; Kimberton Drug Development Consulting, LLC, Phoenixville, Pennsylvania.
  • Straumann A; Swiss EoE Clinic, Division of Gastroenterology, University Hospital Zurich, Zurich, Switzerland.
  • Safroneeva E; Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Clin Gastroenterol Hepatol ; 17(8): 1477-1488.e10, 2019 07.
Article em En | MEDLINE | ID: mdl-30476587
ABSTRACT
BACKGROUND &

AIMS:

Eosinophilic esophagitis (EoE) is assessed endoscopically (endoscopic activity), based on grades of edema, rings, exudates, furrows, and strictures (EREFS). We examined variations in endoscopic assessments of severity, developed and validated 3 EREFS-based scoring systems, and assessed responsiveness of these systems using data from a randomized placebo-controlled trial of patients with EoE.

METHODS:

For the development set, 5 gastroenterologists reviewed EREFS findings from 266 adults with EoE and provided endoscopist global assessment scores (EndoGA, scale of 0 to 10); variation (ΔEndoGA) was assessed using linear regression. We evaluated simple scores (features given arbitrary values from 0 to 3) and developed 2 scoring systems (adjusted score range, 0-100). We then fitted our linear regression model with mean EndoGA to data from 146 adults recruited in centers in Switzerland and the United States between April 2011 and December 2012. For the validation set, we collected data from 120 separate adults (recruited in centers in Switzerland and the United States between May 2013 and July 2014), assessing regression coefficient-based scores using Bland-Altman method. We assessed the responsiveness of our scoring systems using data from a randomized trial of patients with EoE given fluticasone (n=16) or placebo (n=8).

RESULTS:

The distribution of EndoGA values differed among endoscopists (mean ΔEndoGA, 2.6±1.8; range 0-6.6). We developed 2 regression-based scoring systems to assess overall and proximal and distal esophageal findings; variation in endoscopic features accounted for more than 90% of the mean EndoGA variation. In the validation group, differences between mean EndoGA and regression-based scores were small (ranging from -4.70 to 2.03), indicating good agreement. In analyses of data from the randomized trial, the baseline to end of study change in patients given fluticasone was a reduction of 24.3 in simple score (reduction of 4.6 in patients given placebo, P=.052); a reduction of 23.5 in regression-based overall score (reduction of 6.56 in patients given placebo, P=.12), and a reduction of 23.8 (reduction of 8.44 in patients given placebo, P=.11).

CONCLUSION:

Assessments of endoscopic activity in patients with EoE vary among endoscopists. In an analysis of data from a randomized controlled trial, we found that newly developed scoring systems are no better than simple scoring system in detecting changes in endoscopic activity. These results support the use of a simple scoring system in evaluation of endoscopic activity in patients with EoE. clinicaltrials.gov no NCT00939263 and NCT01386112.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esofagoscopia / Esôfago / Esofagite Eosinofílica / Fluticasona Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Gastroenterol Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esofagoscopia / Esôfago / Esofagite Eosinofílica / Fluticasona Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Gastroenterol Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2019 Tipo de documento: Article