Diagnostic criteria and core outcome set development for necrotising otitis externa: the COSNOE Delphi consensus study

Author:

Lodhi SiratORCID,Dodgson Kirsty,Dykes Michael,Vishwanath Veena,Bazaz Rohit,Mathur Sachin,Watson Glen,Cartwright Katherine,Pearson Amy,Wearmouth Deborah,List Richard,Yates Phillip,Dixon Joanna,Puveendran Arullendran,Wilson Margarita,Watson Katherine,Cullinan Milo,Mentias Youssef,Capper Ruth,Jewes Linda,Wallis Sebastian,Hamilton David,Adams Brook,Khalid-Raja Mamoona,Faris Barzo,Khan Maha,Linton Stefan,Abrar Rohma,Owen Eloise,Bisbinas Vasiliki,Ijaz Ali,Lau Kimberley,Timms Sara,Bruce Jack,Stapleton EmmaORCID

Abstract

Abstract Objective Evidence for necrotising otitis externa (NOE) diagnosis and management is limited, and outcome reporting is heterogeneous. International best practice guidelines were used to develop consensus diagnostic criteria and a core outcome set (COS). Methods The study was pre-registered on the Core Outcome Measures in Effectiveness Trials (COMET) database. Systematic literature review identified candidate items. Patient-centred items were identified via a qualitative study. Items and their definitions were refined by multidisciplinary stakeholders in a two-round Delphi exercise and subsequent consensus meeting. Results The final COS incorporates 36 items within 12 themes: Signs and symptoms; Pain; Advanced Disease Indicators; Complications; Survival; Antibiotic regimes and side effects; Patient comorbidities; Non-antibiotic treatments; Patient compliance; Duration and cessation of treatment; Relapse and readmission; Multidisciplinary team management. Consensus diagnostic criteria include 12 items within 6 themes: Signs and symptoms (oedema, otorrhoea, granulation); Pain (otalgia, nocturnal otalgia); Investigations (microbiology [does not have to be positive], histology [malignancy excluded], positive CT and MRI); Persistent symptoms despite local and/or systemic treatment for at least two weeks; At least one risk factor for impaired immune response; Indicators of advanced disease (not obligatory but mut be reported when present at diagnosis). Stakeholders were unanimous that there is no role for secondary, graded, or optional diagnostic items. The consensus meeting identified themes for future research. Conclusion The adoption of consensus-defined diagnostic criteria and COS facilitates standardised research reporting and robust data synthesis. Inclusion of patient and professional perspectives ensures best practice stakeholder engagement.

Publisher

Cambridge University Press (CUP)

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