Background: End points used to determine treatment efficacy in eosinophilic esophagitis (EoE) have evolved over time. With multiple novel therapies in development for EoE, harmonization of outcomes measures will facilitate evidence synthesis and appraisal when comparing different treatments. Objective: We sought to develop a core outcome set (COS) for controlled and observational studies of pharmacologic and diet interventions in adult and pediatric patients with EoE. Methods: Candidate outcomes were generated from systematic literature reviews and patient engagement interviews and surveys. Consensus was established using an iterative Delphi process, with items voted on using a 9-point Likert scale and with feedback from other participants to allow score refinement. Consensus meetings were held to ratify the outcome domains of importance and the core outcome measures. Stakeholders were recruited internationally and included adult and pediatric gastroenterologists, allergists, dieticians, pathologists, psychologists, researchers, and methodologists. Results: The COS consists of 4 outcome domains for controlled and observational studies: histopathology, endoscopy, patient-reported symptoms, and EoE-specific quality of life. A total of 69 stakeholders (response rate 95.8%) prioritized 42 outcomes in a 2-round Delphi process, and the final ratification meeting generated consensus on 33 outcome measures. These included measurement of the peak eosinophil count, Eosinophilic Esophagitis Histology Scoring System, Eosinophilic Esophagitis Endoscopic Reference Score, and patient-reported measures of dysphagia and quality of life. Conclusions: This interdisciplinary collaboration involving global stakeholders has produced a COS that can be applied to adult and pediatric studies of pharmacologic and diet therapies for EoE and will facilitate meaningful treatment comparisons and improve the quality of data synthesis.

Development of a core outcome set for therapeutic studies in eosinophilic esophagitis (COREOS)

de Bortoli N.
Membro del Collaboration Group
;
2022-01-01

Abstract

Background: End points used to determine treatment efficacy in eosinophilic esophagitis (EoE) have evolved over time. With multiple novel therapies in development for EoE, harmonization of outcomes measures will facilitate evidence synthesis and appraisal when comparing different treatments. Objective: We sought to develop a core outcome set (COS) for controlled and observational studies of pharmacologic and diet interventions in adult and pediatric patients with EoE. Methods: Candidate outcomes were generated from systematic literature reviews and patient engagement interviews and surveys. Consensus was established using an iterative Delphi process, with items voted on using a 9-point Likert scale and with feedback from other participants to allow score refinement. Consensus meetings were held to ratify the outcome domains of importance and the core outcome measures. Stakeholders were recruited internationally and included adult and pediatric gastroenterologists, allergists, dieticians, pathologists, psychologists, researchers, and methodologists. Results: The COS consists of 4 outcome domains for controlled and observational studies: histopathology, endoscopy, patient-reported symptoms, and EoE-specific quality of life. A total of 69 stakeholders (response rate 95.8%) prioritized 42 outcomes in a 2-round Delphi process, and the final ratification meeting generated consensus on 33 outcome measures. These included measurement of the peak eosinophil count, Eosinophilic Esophagitis Histology Scoring System, Eosinophilic Esophagitis Endoscopic Reference Score, and patient-reported measures of dysphagia and quality of life. Conclusions: This interdisciplinary collaboration involving global stakeholders has produced a COS that can be applied to adult and pediatric studies of pharmacologic and diet therapies for EoE and will facilitate meaningful treatment comparisons and improve the quality of data synthesis.
2022
Ma, C.; Schoepfer, A. M.; Dellon, E. S.; Bredenoord, A. J.; Chehade, M.; Collins, M. H.; Feagan, B. G.; Furuta, G. T.; Gupta, S. K.; Hirano, I.; Jairath, V.; Katzka, D. A.; Pai, R. K.; Rothenberg, M. E.; Straumann, A.; Aceves, S. S.; Alexander, J. A.; Arva, N. C.; Atkins, D.; Biedermann, L.; Blanchard, C.; Cianferoni, A.; Ciriza de los Rios, C.; Clayton, F.; Davis, C. M.; de Bortoli, N.; Dias, J. A.; Falk, G. W.; Genta, R. M.; Ghaffari, G.; Gonsalves, N.; Greuter, T.; Hopp, R.; Hsu Blatman, K. S.; Jensen, E. T.; Johnston, D.; Kagalwalla, A. F.; Larsson, H. M.; Leung, J.; Louis, H.; Masterson, J. C.; Menard-Katcher, C.; Menard-Katcher, P. A.; Moawad, F. J.; Muir, A. B.; Mukkada, V. A.; Penagini, R.; Pesek, R. D.; Peterson, K.; Putnam, P. E.; Ravelli, A.; Savarino, E. V.; Schlag, C.; Schreiner, P.; Simon, D.; Smyrk, T. C.; Spergel, J. M.; Taft, T. H.; Terreehorst, I.; Vanuytsel, T.; Venter, C.; Vieira, M. C.; Vieth, M.; Vlieg-Boerstra, B.; von Arnim, U.; Walker, M. M.; Wechsler, J. B.; Woodland, P.; Woosley, J. T.; Yang, G. -Y.; Zevit, N.; Safroneeva, E.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1124704
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