[原发性纤毛运动障碍的物理治疗]。

IF 1.2 Q4 RESPIRATORY SYSTEM
Pneumologie Pub Date : 2025-04-01 DOI:10.1055/a-2502-8151
Christina Krämer, Jasmin Flock, Birgit Borges-Lüke, Johanna Raidt, Felix C Ringshausen
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引用次数: 0

摘要

原发性纤毛运动障碍(PCD)是由纤毛运动功能障碍引起的多系统疾病。它的特点是上、下气道的慢性粘液潴留。这导致破坏性的肺部疾病与支气管扩张的发展。针对PCD患者的循证治疗方法很少。大多数治疗概念是基于其他呼吸系统疾病或专家意见。这篇文章是关于PCD患者的物理治疗护理,并提供了从目前的文献建议和多年的经验,物理治疗的PCD患者的概述。目前,还没有治疗PCD的方法。以黏液管理为重点的对症治疗是相关的。这包括吸入、动员黏液、身体活动以及有针对性地使用医疗辅助设备进行清胸和康复。在可能的情况下,专业治疗师应提供物理治疗指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Physiotherapy in Primary Ciliary Dyskinesia].

Primary ciliary dyskinesia (PCD) is a multisystem disease caused by dysfunction of motile cilia. It is characterized by chronic mucus retention of the upper and lower airways. This results in a destructive lung disease with the development of bronchiectasis. There are a very few evidence-based therapies for patients with PCD. Most treatment concepts are based on other respiratory diseases or expert opinion. This article is about the physiotherapy care of patients with PCD and provides an overview of recommendations from the current literature as well as many years of experience in the physiotherapy treatment of patients with PCD. Currently, no curative therapy for PCD exists. Symptomatic treatment with a focus on mucus management is relevant. This includes inhalation, mobilization of mucus, physical activity and the targeted use of medical aids for chest clearance as well as rehabilitation. Whenever possible, specialized therapists should provide guidance for physiotherapy.

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来源期刊
Pneumologie
Pneumologie RESPIRATORY SYSTEM-
CiteScore
1.80
自引率
16.70%
发文量
416
期刊介绍: Organ der Deutschen Gesellschaft für Pneumologie DGP Organ des Deutschen Zentralkomitees zur Bekämpfung der Tuberkulose DZK Organ des Bundesverbandes der Pneumologen BdP Fachärzte für Lungen- und Bronchialheilkunde, Pneumologen und Allergologen
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