Current Practice, Safety and Efficacy of Interventions for Recurrent Respiratory Papillomatosis: Evidence From a UK Registry

医学 复发性呼吸道乳头状瘤病 心理干预 儿科 恶性肿瘤 病人登记处 辅助治疗 疾病 急诊医学 内科学 癌症 精神科
作者
Adam J. Donne,Kim Keltie,Julie Burn,Emma Belilios,Steven Powell,Paola Cognigni,Iain J. Nixon,Neil Bateman,Haytham Kubba,Owen Judd,Andrew Sims
出处
期刊:Clinical Otolaryngology [Wiley]
被引量:1
标识
DOI:10.1111/coa.14245
摘要

ABSTRACT Objectives To determine the current practice, safety and efficacy of interventions used in the management of recurrent respiratory papillomatosis (RRP) in the UK NHS. Design Prospective registry (recruitment between 1st April 2018 and 31st August 2022, retrospective data from 1st January 2015 permitted with consent). Sub‐group data‐linked to Hospital Episode Statistics for additional follow‐up (until 31st July 2022). Setting UK NHS hospitals treating RRP patients. Participants Children and adults diagnosed with RRP and managed in an NHS hospital. Main Outcome Measures Disease severity (Derkay, voice handicap and GRBAS scores), management (type and frequency of surgical and adjuvant intervention) and complications (cancer, death). Results Three hundred and thirty patients were entered into the registry; 304 (including 65 children) were eligible for analysis. Children had more severe disease than adults (median Derkay score 10 vs. 5). Microdebrider was the most common surgical intervention, particularly in children (86% of children, 49% of adults). Additionally, lasers (CO 2 , KTP and pulsed dye) were used in 34% of adults. Gardasil was the most common adjuvant therapy (21 children, 23 adults). Procedural complications were rare (10.8% children, 5.9% adults). Five patients developed laryngeal malignancy; there were six deaths during follow‐up period. Conclusions This is the largest UK RRP study to date. RRP is more aggressive in children than adults, and treatment choice differs between age groups. Overall, management was safe with minimal complications reported, and generally effective in maintaining a safe airway. Standardised reporting is required to objectively monitor disease progression and safety over time. Trial Registration: NCT03465280, ISRCTN36100560
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