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首页> 外文期刊>BMC Pulmonary Medicine >A short-term evaluation of a prototype disposable Oscillating Positive Expiratory Pressure (OPEP) device in a cohort of children with cystic fibrosis
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A short-term evaluation of a prototype disposable Oscillating Positive Expiratory Pressure (OPEP) device in a cohort of children with cystic fibrosis

机译:囊性纤维化群体中的原型一次性振荡正呼气压力(OPEP)装置的短期评价

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Oscillating Positive Expiratory Pressure (OPEP) devices are important adjuncts to airway clearance therapy in patients with cystic fibrosis (CF). Current devices are typically reusable and require daily, or often more frequent, cleaning to prevent risk of infection by acting as reservoirs of potentially pathogenic organisms. In response, a daily disposable OPEP device, the UL-OPEP, was developed to mitigate the risk of contamination and eliminate the burdensome need for cleaning devices. A convenience sample of 36 participants, all current OPEP device users, was recruited from a paediatric CF service. For one month, participants replaced their current OPEP device with a novel daily disposable device. Assessment included pre- and post-intervention lung function by spirometry, as well as Lung Clearance Index. Quality of life was assessed using the Cystic Fibrosis Questionnaire – Revised, while user experience was evaluated with a post-study survey. 31 participants completed the study: 18 males; median age 10?years, range 4–16?years. Lung function (mean difference?±?SD, ?V1?=?1.69?±?11.93; %FVC?=?0.58?±?10.04; FEV1: FVC?=?0.01?±?0.09), LCI (mean difference?±?SD, 0.08?±?1.13), six-minute walk test, and CFQ-R were unchanged post-intervention. Participant-reported experiences of the device were predominantly positive. The disposable OPEP device maintained patients’ lung function during short term use (≤?1 month), and was the subject of positive feedback regarding functionality while reducing the risk of airway contamination associated with ineffective cleaning. The study was approved as a Clinical Investigation by the Irish Health Products Regulatory Authority (CRN-2209025-CI0085).
机译:振荡正呼气压力(OPEP)器件是囊性纤维化患者的气道清关治疗的重要辅助(CF)。目前的装置通常是可重复使用的,并且每天需要或通常更频繁地清洁,以防止作为潜在致病生物的储层来防止感染风险。作为回应,开发了一台每日一次性OPEP设备,UL-OPEP,以减轻污染的风险,并消除清洁装置的繁重需求。从儿科CF服务招募了36名参与者,所有当前OPEP设备用户的便利样本。一个月,参与者用新的日常一次性装置取代他们目前的OPEP装置。评估包括肺活量测定和肺部间隙指数的前干预后肺功能。使用囊性纤维化问卷评估的生活质量 - 修订,而用户体验是通过研究后调查评估的。 31名参与者完成了这项研究:18名男性;中位年龄10?年龄,范围为4-16岁?年。肺功能(平均差异?±αSD,?V1?=?1.69?±11.93;%FVC?=?0.58?±10.04; FEV1:FVC?=?0.01?±α09),LCI(平均差异? ±3,0.08?±1.13),六分钟的步伐,CFQ-R后介入后不变。报告的设备的经验主要是积极的。一次性OPEP器件在短期使用期间维持患者的肺功能(≤?1个月),并且是关于功能的正反馈的主题,同时降低与无效清洁相关的气道污染的风险。该研究被批准为爱尔兰保健品监管机构的临床调查(CRN-2209025-CI0085)。

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