The Pneumothorax And Symptom Evaluation (PASE) study: Bendopnoea in patients with pneumothorax.

IF 0.8 Q4 RESPIRATORY SYSTEM Respirology Case Reports Pub Date : 2024-08-06 eCollection Date: 2024-08-01 DOI:10.1002/rcr2.1443
Bianca M Iacopetta, Michaela Donaghy, Chloe Charlesworth, Carolyn J Peddle-McIntyre, Ai Ling Tan, Y C Gary Lee
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Abstract

Background: Pneumothorax can cause distressing breathlessness, however the effect of the accumulated air in the pleural space and its association with diaphragmatic function and symptoms of breathlessness is not well understood. Bendopnoea is an evolving clinical symptom that has been demonstrated as clinically useful in some heart and lung conditions. Whether bendopnoea is present in patients with pneumothorax, and its potential clinical usefulness has not yet been investigated. The PASE study is a pilot study to explore the incidence and clinical relevance of bendopnoea in patients with pneumothorax and may provide better understanding of pneumothorax related dyspnoea.

Methods: PASE is a prospective study. Eligible patients are assessed at baseline (pre air drainage/lung reinflation) and in patients whose pneumothorax resolves once the lung has re-expanded (post conservative management or air drainage procedure). Outcome measures include the incidence of bendopnoea, correlation of the associated symptoms (pain and breathlessness) to the severity of bendopnoea and the size of pneumothorax; and correlation with clinical outcome (i.e., response to air drainage/lung reinflation). The study will recruit 50 participants.

Discussion: This is the first study to explore bendopnoea in patients with pneumothorax. The presence and significance of bendopnoea in relation to clinical and physiological parameters in patients with pneumothorax requires investigation. The findings of this study may further current understanding of dyspnoea related pneumothorax.

Trial registration: Name of the registry: Australia New Zealand Clinical Trial Registry Trial registration number : ACTRN12623001109695p. URL of the trial registry record for this trial : https://anzctr.org.au/Trial/Registration/TrialReview.aspx?id=386631&isReview=true Date of registration : Registered on 24 October 2023. Funding of the trial : This study has not received grant support. The study is sponsored by the Institute for Respiratory Health, a not-for-profit organisation. Name and contact information for the trial sponsor : Mr Bi Lam; Finance manager. Level 2, 6 Verdun Street, Nedlands, WA 6009. Role of sponsor : The funder is not involved in the planning of the study, gathering, analysing, and interpreting the data, or in preparing the manuscript. Protocol version : 1.

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气胸和症状评估(PASE)研究:气胸患者的憋气症状
背景:气胸可导致呼吸困难,但胸膜腔内积聚空气的影响及其与横膈膜功能和呼吸困难症状的关系尚不十分清楚。憋气是一种不断发展的临床症状,已被证明对某些心肺疾病有临床作用。至于气胸患者是否会出现弯腰呼吸及其潜在的临床用途,目前尚未进行研究。PASE 研究是一项试验性研究,旨在探讨气胸患者弯腰呼吸困难的发生率和临床相关性,从而更好地了解与气胸相关的呼吸困难:PASE 是一项前瞻性研究。方法:PASE 是一项前瞻性研究,对符合条件的患者进行基线评估(空气引流前/肺重新充气),并在肺重新扩张后对气胸消退的患者进行评估(保守治疗或空气引流术后)。结果测量包括气胸发生率、相关症状(疼痛和呼吸困难)与气胸严重程度和气胸大小的相关性,以及与临床结果(即对空气引流/肺复张的反应)的相关性。该研究将招募 50 名参与者:讨论:这是第一项探讨气胸患者肺动脉弯曲的研究。需要对气胸患者气胸的存在及其与临床和生理参数的关系进行研究。这项研究的结果可能会进一步加深目前对与气胸相关的呼吸困难的理解:注册名称:澳大利亚新西兰临床试验登记处试验登记号:ACTRN12623001109695p。该试验登记记录的 URL : https://anzctr.org.au/Trial/Registration/TrialReview.aspx?id=386631&isReview=true 登记日期 :注册日期 : 2023 年 10 月 24 日。试验资助:本研究未获得资助。本研究由非营利组织呼吸健康研究所赞助。试验发起人姓名和联系方式:Bi Lam 先生;财务经理。Level 2, 6 Verdun Street, Nedlands, WA 6009.赞助者的角色:赞助者不参与研究的计划、数据的收集、分析和解释,也不参与手稿的撰写。协议版本 : 1.
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来源期刊
Respirology Case Reports
Respirology Case Reports RESPIRATORY SYSTEM-
CiteScore
1.40
自引率
0.00%
发文量
178
审稿时长
8 weeks
期刊介绍: Respirology Case Reports is an open-access online journal dedicated to the publication of original clinical case reports, case series, clinical images and clinical videos in all fields of respiratory medicine. The Journal encourages the international exchange between clinicians and researchers of experiences in diagnosing and treating uncommon diseases or diseases with unusual presentations. All manuscripts are peer-reviewed through a streamlined process that aims at providing a rapid turnaround time from submission to publication.
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