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慢性阻塞性肺疾病急性加重期住院患者对结局和体验测量的接受度:一项西塞罗临床研究协作组-欧洲肺脏基金会在线患者调查

Patients' acceptance of outcome and experience measurements during hospitalisation for COPD exacerbations: a CICERO Clinical Research Collaboration-European Lung Foundation online patient survey.

作者信息

Gyselinck Iwein, Ramakrishnan Sanjay, Vermeersch Kristina, Halner Andreas, Pott Hendrik, Dobbels Fabienne, Coleman Courtney, Collis Philip, Watz Henrik, Greulich Timm, Franssen Frits M E, Burgel Pierre-Régis, Bafadhel Mona, Janssens Wim

机构信息

Clinical Department of Respiratory Diseases, University Hospitals Leuven, Leuven, Belgium.

BREATHE Lab, CHROMETA Department, KU Leuven, Leuven, Belgium.

出版信息

ERJ Open Res. 2023 Jul 3;9(4). doi: 10.1183/23120541.00148-2023. eCollection 2023 Jul.

Abstract

BACKGROUND

The lack of standardised outcome assessments during hospitalisation and follow-up for acute COPD exacerbations has hampered scientific progress and clinical proficiency. The objective of the present study was to evaluate patients' acceptance of selected outcome and experience measurements during hospitalisations for COPD exacerbations and follow-up.

METHODS

An online survey was held amongst COPD patients in France, Belgium, The Netherlands, Germany and the UK. The European Lung Foundation COPD Patient Advisory Group was involved in the conceptualisation, development and dissemination of the survey. The survey was complementary to a previously obtained expert consensus. We assessed patients' views and acceptance of selected patient-reported outcomes or experiences and corresponding measurement instruments (for dyspnoea, frequent productive cough, health status and hospitalisation experience), and of selected clinical investigations (blood draw, pulmonary function test, 6-min walk test, chest computed tomography, echocardiography).

FINDINGS

200 patients completed the survey. All selected outcomes and experiences were deemed important, and acceptance of their methods of assessment was high. The modified Medical Research Council scale and a numerical rating scale to address dyspnoea, the COPD Assessment Test for quality of life and frequent productive cough, and the Hospital Consumer Assessment of Healthcare Providers and Systems for hospital experiences were the instruments preferred by patients. Consensus on importance of blood draw and spirometry was higher compared with the other investigations.

INTERPRETATION

The survey results endorse the use of the selected outcome and experience measurements during hospitalisations for COPD exacerbations. They can be used to optimise standardised and patient-centred care and facilitate multicentric data collection.

摘要

背景

急性慢性阻塞性肺疾病(COPD)加重期住院及随访期间缺乏标准化的结局评估,阻碍了科学进步和临床水平的提高。本研究的目的是评估患者对COPD加重期住院及随访期间选定的结局和体验测量方法的接受程度。

方法

在法国、比利时、荷兰、德国和英国的COPD患者中进行了一项在线调查。欧洲肺病基金会COPD患者咨询小组参与了该调查的概念化、开发和传播。该调查是对先前获得的专家共识的补充。我们评估了患者对选定的患者报告结局或体验以及相应测量工具(用于呼吸困难、频繁咳痰、健康状况和住院体验),以及选定的临床检查(抽血、肺功能测试、6分钟步行试验、胸部计算机断层扫描、超声心动图)的看法和接受程度。

结果

200名患者完成了调查。所有选定的结局和体验都被认为很重要,并且对其评估方法的接受度很高。改良的医学研究委员会量表和用于评估呼吸困难的数字评分量表、用于评估生活质量和频繁咳痰的慢性阻塞性肺疾病评估测试,以及用于评估住院体验的医疗服务提供者和系统医院消费者评估是患者首选的工具。与其他检查相比,患者对抽血和肺活量测定重要性的共识更高。

解读

调查结果支持在COPD加重期住院期间使用选定的结局和体验测量方法。它们可用于优化标准化的以患者为中心的护理,并促进多中心数据收集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c7/10316033/fb13a24fe534/00148-2023.01.jpg

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