Benefit from regular versus leakage-related exchange of voice prostheses in patients post-laryngectomy considering complication rates and patient satisfaction feedback-a randomized case-controlled trial.

IF 3.5 3区 医学 Q2 ONCOLOGY Frontiers in Oncology Pub Date : 2025-01-24 eCollection Date: 2025-01-01 DOI:10.3389/fonc.2025.1468955
Michał Żurek, Małgorzata Czesak, Daniel Majszyk, Anna Rzepakowska
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Abstract

Objective: The complications related to voice prosthesis usage substantially affect the physical and social functioning of patients after total laryngectomy, which influences their quality of life. Leakage dysfunction is the most common, causing uncertainty and requiring unscheduled hospital visits. Our study was designed to estimate the benefit of regular versus leakage-related replacement of the voice prosthesis. Study Design. Randomized case-controlled trials. Setting. Tertiary hospital.

Methods: The study included patients who underwent total laryngectomy with primary voice prosthesis insertion between 2020 and 2021 and were randomly assigned to one of two arms: regular exchange (REA) every 3 months or leakage-dependent exchange (LEA). The control treatment was continued for 12 months. The primary outcome measure was the comparison of complication rates in both arms, including periprosthetic leakage, granulation or atrophy of mucosa around the fistula, and dislocation of the prosthesis. The secondary outcome measures were the mean number of exchanges per year and patient satisfaction.

Results: Thirty-six patients continued the study according to the protocol, with 16 in REA and 20 in LEA. A total of 153 voice prostheses were replaced during the study period, including 98 in REA and 55 in LEA. Comparative analysis of REA and LEA revealed a significantly longer time between replacements in the LEA group (p = 0.023) and a significantly lower rate of complications in the REA group (p = 0.029). Periprosthetic leakage was the most common complication associated with the use of voice prostheses, occurring in 3.06% of patients in REA and 9.09% in LEA, but this difference was statistically insignificant (p = 0.137). The analysis of factors predisposing patients to leakage failure revealed that treatment schemes, concomitant diseases, dental conditions, and diet or alcohol consumption significantly affect the longevity of voice prostheses. The relative and absolute risks (RRR and ARR) of complications in the REA group were reduced by 69.39% and 13.88%, respectively. The number of replacements (NNTs) that should be performed in the REA scheme to prevent one complication over the LEA scheme is 721.

Conclusion: The replacement of regular voice prostheses improved the overall complication rate over the scheme based on leakage demand; however, it did not yield superior benefits in terms of patient satisfaction or economic aspects.

Clinical trial registration: https://clinicaltrials.gov/study/NCT04268459, identifier NCT04268459.

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考虑并发症发生率和患者满意度反馈,喉切除术后患者定期与泄漏相关的置换声假体的获益——一项随机病例对照试验。
目的:假声术后并发症严重影响全喉切除术后患者的身体和社会功能,影响患者的生活质量。渗漏功能障碍是最常见的,造成不确定性和需要不定期的医院就诊。我们的研究旨在评估常规与泄漏相关的语音假体置换的益处。研究设计。随机病例对照试验。设置。三级医院。方法:该研究纳入了在2020年至2021年期间接受全喉切除术并植入声假体的患者,并随机分配到两组中的一组:每3个月定期交换(REA)或泄漏依赖性交换(LEA)。对照组治疗12个月。主要结局指标是比较双臂的并发症发生率,包括假体周围渗漏、瘘管周围粘膜肉芽肿或萎缩以及假体脱位。次要结局指标为每年平均换药次数和患者满意度。结果:36例患者按照方案继续研究,其中REA 16例,LEA 20例。研究期间共更换了153个假体,其中REA 98个,LEA 55个。REA组与LEA组的对比分析显示,LEA组的置换期间隔明显延长(p = 0.023), REA组的并发症发生率明显降低(p = 0.029)。假体周围渗漏是使用假体最常见的并发症,REA组为3.06%,LEA组为9.09%,但差异无统计学意义(p = 0.137)。分析导致患者漏声失败的因素表明,治疗方案、伴随疾病、牙齿状况、饮食或饮酒显著影响假体的寿命。REA组并发症的相对危险度(RRR)和绝对危险度(ARR)分别降低69.39%和13.88%。在REA方案中应该执行的替换(nnt)数量为721,以防止LEA方案中的一个并发症。结论:常规假体置换方案比基于漏音需求的方案总体并发症发生率提高;然而,就患者满意度或经济方面而言,它并没有产生优越的效益。临床试验注册:https://clinicaltrials.gov/study/NCT04268459,标识符NCT04268459。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Oncology
Frontiers in Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
6.20
自引率
10.60%
发文量
6641
审稿时长
14 weeks
期刊介绍: Cancer Imaging and Diagnosis is dedicated to the publication of results from clinical and research studies applied to cancer diagnosis and treatment. The section aims to publish studies from the entire field of cancer imaging: results from routine use of clinical imaging in both radiology and nuclear medicine, results from clinical trials, experimental molecular imaging in humans and small animals, research on new contrast agents in CT, MRI, ultrasound, publication of new technical applications and processing algorithms to improve the standardization of quantitative imaging and image guided interventions for the diagnosis and treatment of cancer.
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