Research Appraisals

Diving and hyperbaric medicine

Evidence-informed decision aid for fitness-to-dive assessment after otologic surgery

INTRODUCTION: Fitness-to-dive after otologic surgery is often approached conservatively, with some procedures historically labelled as absolute contraindications despite limited empirical evidence. The available literature is heterogeneous and includes clinical reports, experimental pressure studies, guidance documents, and manufacturer specifications, leading to uncertainty in clinical counseling. We aimed to characterise the available evidence regarding fitness-to-dive after otologic surgery and to develop an evidence-informed clinical decision aid. METHODS: A scoping review was conducted in accordance with PRISMA-ScR guidance. PubMed/MEDLINE, Embase, Scopus, and relevant non-indexed sources were searched. Eligible sources included clinical reports and series, experimental or hyperbaric chamber studies, guidance or consensus documents, and manufacturer statements providing explicit pressure- or depth-related information. Data were charted descriptively by procedure type and evidence stream. RESULTS: The search identified 324 records; after removal of duplicates and screening, 40 sources were included. The evidence base was predominantly non-comparative. Across procedures, recommendations emphasised postoperative stability and reliable pressure equalisation rather than surgical history alone. Canal wall down mastoidectomy was consistently portrayed as incompatible with diving, whereas selected middle ear reconstructions and stapes surgery were commonly described as potentially compatible in appropriately selected individuals. For cochlear implantation, guidance was mainly conditional and based on hyperbaric testing, limited clinical diving reports, and manufacturer-specified pressure or depth limits. Communication emerged as an additional practical consideration in cases of significant hearing loss. CONCLUSIONS: Relevant evidence is limited and heterogeneous, and does not consistently support blanket prohibitions for all otologic procedures. A function-based, individualised approach is supported, while specific higher-risk scenarios warrant restriction. Prospective registries and standardised outcome reporting are needed to refine procedure-specific recommendations.