Pub Date : 2025-12-01Epub Date: 2025-06-13DOI: 10.1080/15412555.2025.2502671
R A Müller, F Klimeš, A Voskrebenzev, L Behrendt, T F Kaireit, M Wernz, M Zubke, A L Kern, M R Prince, W Shen, C B Cooper, R G Barr, J M Hohlfeld, J Vogel-Claussen
Hyperinflation in chronic obstructive pulmonary disease (COPD) patients worsens on exertion/exercise when breathing frequency increases. Fast breathing, paced at 40 breaths per minute using a metronome (metronome-paced tachypnea, MPT), induces dynamic hyperinflation (DH) and can be performed during MRI. MPT in combination with phase-resolved functional lung (PREFUL) MRI can be used to assess stress-driven ventilation dynamics globally and regionally. A 90 s time series of one coronal slice centered to the trachea was acquired for PREFUL MRI during 60 s of resting tidal breathing (RTB) and 30 s of MPT at 40 breaths per minute in COPD patients and healthy volunteers. MPT detected DH in 12 out of 15 COPD patients and in 1 out of 15 healthy controls. During MPT, the global fractional ventilation decreased by 20% in healthy subjects (p = 0.01) and by 48% in COPD patients (p < 0.001). The end-expiratory lung area remained stable in healthy subjects and increased significantly by 7% in COPD patients over the course of MPT (p = 0.004). Younger, healthy volunteers adapted to increase breathing frequency by reducing tidal volume (global fractional ventilation), while older healthy volunteers showed less tidal volume reduction (p = 0.036). The MPT-induced change of regional ventilation homogeneity (flow volume loop cross-correlation, FVL-CCMPT/RTB) increased with age in healthy volunteers (p = 0.039) likely due to the development of compensatory dystelectasis in younger volunteers leading to reduced homogeneity during MPT. In the future, the MPT test during MR imaging may be used for COPD treatment analysis and disease monitoring.
{"title":"Phase-Resolved Functional Lung MRI Evaluation of Dynamic Hyperinflation Induced by Metronome-Paced Tachypnea in Patients with Chronic Obstructive Pulmonary Disease.","authors":"R A Müller, F Klimeš, A Voskrebenzev, L Behrendt, T F Kaireit, M Wernz, M Zubke, A L Kern, M R Prince, W Shen, C B Cooper, R G Barr, J M Hohlfeld, J Vogel-Claussen","doi":"10.1080/15412555.2025.2502671","DOIUrl":"10.1080/15412555.2025.2502671","url":null,"abstract":"<p><p>Hyperinflation in chronic obstructive pulmonary disease (COPD) patients worsens on exertion/exercise when breathing frequency increases. Fast breathing, paced at 40 breaths per minute using a metronome (metronome-paced tachypnea, MPT), induces dynamic hyperinflation (DH) and can be performed during MRI. MPT in combination with phase-resolved functional lung (PREFUL) MRI can be used to assess stress-driven ventilation dynamics globally and regionally. A 90 s time series of one coronal slice centered to the trachea was acquired for PREFUL MRI during 60 s of resting tidal breathing (RTB) and 30 s of MPT at 40 breaths per minute in COPD patients and healthy volunteers. MPT detected DH in 12 out of 15 COPD patients and in 1 out of 15 healthy controls. During MPT, the global fractional ventilation decreased by 20% in healthy subjects (<i>p</i> = 0.01) and by 48% in COPD patients (<i>p</i> < 0.001). The end-expiratory lung area remained stable in healthy subjects and increased significantly by 7% in COPD patients over the course of MPT (<i>p</i> = 0.004). Younger, healthy volunteers adapted to increase breathing frequency by reducing tidal volume (global fractional ventilation), while older healthy volunteers showed less tidal volume reduction (<i>p</i> = 0.036). The MPT-induced change of regional ventilation homogeneity (flow volume loop cross-correlation, FVL-CC<sub>MPT/RTB</sub>) increased with age in healthy volunteers (<i>p</i> = 0.039) likely due to the development of compensatory dystelectasis in younger volunteers leading to reduced homogeneity during MPT. In the future, the MPT test during MR imaging may be used for COPD treatment analysis and disease monitoring.</p>","PeriodicalId":10704,"journal":{"name":"COPD: Journal of Chronic Obstructive Pulmonary Disease","volume":"22 1","pages":"2502671"},"PeriodicalIF":2.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12174575/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144282751","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2025-07-28DOI: 10.1080/15412555.2025.2531017
Tanja Sofie Hansen, Pia Søe Jensen, Vibeke Nørholm, Mia Ingerslev Loft, Ingrid Poulsen
Objective: To assess the feasibility and acceptability of a nurse-led COllective PErson-centred dialogue (COPE-Dialogue) intervention developed though co-production focusing on nutritional and physical activity support to hospitalised patients with Chronic obstructive pulmonary disease.
Methods: A non-randomised feasibility study according to the Medical Research Council framework for developing and testing a complex intervention. The intervention consisted of a dialogue tool with three components related to nutrition and physical activity: (1) A needs assessment, (2) Recommendations for support (3) Transitional information. Data from patients and nurses was collected from January through March 2024. Recruitment, fidelity, and acceptability were measured with qualitative and quantitative approaches including progression criteria. Qualitative content analysis and descriptive statistic were applied in the analysis.
Results: Recruitment was feasible, with 77% patients participating. Fidelity was high for the needs assessment and recommendations. Transitional information needs modification and should be combined with a relational contact. Patients and nurses found the dialogue tool acceptable and meaningful but faced time constraints.
Conclusions: The dialogue tool was feasible regarding recruitment and fidelity. The tool was acceptable and meaningful to both patients and nurses, while modification is required in the transitional information. However, there is a need to strengthen the quality of the fundamental care within nutritional and physical activity combined with clinical management support.
{"title":"Supporting Nutritional Status and Physical Activity in Patients with Chronic Obstructive Pulmonary Disease: A Feasibility Study of a Complex Intervention.","authors":"Tanja Sofie Hansen, Pia Søe Jensen, Vibeke Nørholm, Mia Ingerslev Loft, Ingrid Poulsen","doi":"10.1080/15412555.2025.2531017","DOIUrl":"10.1080/15412555.2025.2531017","url":null,"abstract":"<p><strong>Objective: </strong>To assess the feasibility and acceptability of a nurse-led COllective PErson-centred dialogue (COPE-Dialogue) intervention developed though co-production focusing on nutritional and physical activity support to hospitalised patients with Chronic obstructive pulmonary disease.</p><p><strong>Methods: </strong>A non-randomised feasibility study according to the Medical Research Council framework for developing and testing a complex intervention. The intervention consisted of a dialogue tool with three components related to nutrition and physical activity: (1) A needs assessment, (2) Recommendations for support (3) Transitional information. Data from patients and nurses was collected from January through March 2024. Recruitment, fidelity, and acceptability were measured with qualitative and quantitative approaches including progression criteria. Qualitative content analysis and descriptive statistic were applied in the analysis.</p><p><strong>Results: </strong>Recruitment was feasible, with 77% patients participating. Fidelity was high for the needs assessment and recommendations. Transitional information needs modification and should be combined with a relational contact. Patients and nurses found the dialogue tool acceptable and meaningful but faced time constraints.</p><p><strong>Conclusions: </strong>The dialogue tool was feasible regarding recruitment and fidelity. The tool was acceptable and meaningful to both patients and nurses, while modification is required in the transitional information. However, there is a need to strengthen the quality of the fundamental care within nutritional and physical activity combined with clinical management support.</p>","PeriodicalId":10704,"journal":{"name":"COPD: Journal of Chronic Obstructive Pulmonary Disease","volume":"22 1","pages":"2531017"},"PeriodicalIF":2.1,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144728489","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2025-01-29DOI: 10.1080/15412555.2025.2449889
Tyler Pitre, Daniel Lupas, Jasmine Mah, Matthew Stanbrook, Alina Blazer, Dena Zeraatkar, Terence Ho
Background: Despite limited breakthroughs in COPD pharmacotherapy, recent trials have shown promising results for biologics in COPD patients. However, robust evidence synthesis in this area is currently lacking.
Methods: We conducted a systematic review of MEDLINE, EMBASE, and Cochrane CENTRAL from inception to July 17, 2024, to identify randomized trials of biologic medications in patients with COPD. We performed a random effects frequentist network meta-analysis and present the results using relative risk (RR) and 95% confidence intervals (CI). We used the GRADE framework to rate the certainty of the evidence. Outcomes of interest included exacerbations, change in FEV1, change in quality of life, and serious adverse events.
Results: Dupilumab reduced exacerbations as compared to placebo (RR 0.68 [95% CI 0.59 to 0.79]) (high certainty). Benralizumab (RR 0.89 [95% CI 0.78 to 1]), itepekimab (RR 0.81 [95% CI 0.61 to 1.07]) and tezepelumab (RR 0.83 [95% CI 0.61 to 1.12]) may reduce exacerbations as compared to placebo (all low certainty). Dupilumab probably reduced exacerbations more than mepolizumab (RR 0.74 [95% CI 0.62 to 0.89]) (moderate certainty). Dupilumab may reduce exacerbations more than tezepelumab (RR 0.82 [95% CI 1.14]) (low certainty). For all patients, no treatment improved FEV1 above the pre-specified minimal clinically important difference (MCID) of 0.1 L. Dupilumab probably has no meaningful effect on FEV1 compared to placebo (MD 0.07 [95% CI 0.02 to 0.13]) (moderate certainty). However, in the subgroup of patients with blood eosinophils ≥300/mcL, both tezepelumab (MD 0.15 [95% CI 0.05 to 0.26]) and dupilumab (MD 0.13 [95% CI 0.06 to 0.19]) probably improved FEV1 above the MCID.
Conclusion: Dupilumab is effective at improving patient-relevant outcomes in COPD with higher eosinophil levels. Other biological therapies, including tezepelumab, have no important effect on patient-relevant outcomes.
背景:尽管COPD药物治疗方面的突破有限,但最近的试验显示生物制剂治疗COPD患者的结果很有希望。然而,目前在这一领域缺乏强有力的证据综合。方法:我们对MEDLINE、EMBASE和Cochrane CENTRAL从启动到2024年7月17日进行了系统回顾,以确定生物药物治疗COPD患者的随机试验。我们进行了随机效应频率网络荟萃分析,并使用相对风险(RR)和95%置信区间(CI)呈现结果。我们使用GRADE框架来评估证据的确定性。关注的结局包括急性加重、FEV1改变、生活质量改变和严重不良事件。结果:与安慰剂相比,Dupilumab减少了恶化(RR 0.68 [95% CI 0.59至0.79])(高确定性)。与安慰剂相比,Benralizumab (RR 0.89 [95% CI 0.78至1])、itepekimab (RR 0.81 [95% CI 0.61至1.07])和tezepelumab (RR 0.83 [95% CI 0.61至1.12])可能减少恶化(均为低确定性)。Dupilumab可能比mepolizumab更能减少恶化(RR 0.74 [95% CI 0.62至0.89])(中等确定性)。Dupilumab可能比tezepelumab更能减少恶化(RR 0.82 [95% CI 1.14])(低确定性)。对于所有患者,没有任何治疗方法使FEV1的改善高于预先规定的最小临床重要差异(MCID) 0.1 L。与安慰剂相比,Dupilumab可能对FEV1没有显著影响(MD为0.07 [95% CI为0.02至0.13])(中度确定性)。然而,在血嗜酸性粒细胞≥300/mcL的患者亚组中,tezepelumab (MD 0.15 [95% CI 0.05至0.26])和dupilumab (MD 0.13 [95% CI 0.06至0.19])可能改善MCID以上的FEV1。结论:Dupilumab可有效改善嗜酸性粒细胞水平较高的COPD患者相关结局。其他生物疗法,包括tezepelumab,对患者相关结果没有重要影响。
{"title":"Biologic Therapies for Chronic Obstructive Pulmonary Disease: A Systematic Review and Network Meta-Analysis of Randomized Controlled Trials.","authors":"Tyler Pitre, Daniel Lupas, Jasmine Mah, Matthew Stanbrook, Alina Blazer, Dena Zeraatkar, Terence Ho","doi":"10.1080/15412555.2025.2449889","DOIUrl":"10.1080/15412555.2025.2449889","url":null,"abstract":"<p><strong>Background: </strong>Despite limited breakthroughs in COPD pharmacotherapy, recent trials have shown promising results for biologics in COPD patients. However, robust evidence synthesis in this area is currently lacking.</p><p><strong>Methods: </strong>We conducted a systematic review of MEDLINE, EMBASE, and Cochrane CENTRAL from inception to July 17, 2024, to identify randomized trials of biologic medications in patients with COPD. We performed a random effects frequentist network meta-analysis and present the results using relative risk (RR) and 95% confidence intervals (CI). We used the GRADE framework to rate the certainty of the evidence. Outcomes of interest included exacerbations, change in FEV1, change in quality of life, and serious adverse events.</p><p><strong>Results: </strong>Dupilumab reduced exacerbations as compared to placebo (RR 0.68 [95% CI 0.59 to 0.79]) (high certainty). Benralizumab (RR 0.89 [95% CI 0.78 to 1]), itepekimab (RR 0.81 [95% CI 0.61 to 1.07]) and tezepelumab (RR 0.83 [95% CI 0.61 to 1.12]) may reduce exacerbations as compared to placebo (all low certainty). Dupilumab probably reduced exacerbations more than mepolizumab (RR 0.74 [95% CI 0.62 to 0.89]) (moderate certainty). Dupilumab may reduce exacerbations more than tezepelumab (RR 0.82 [95% CI 1.14]) (low certainty). For all patients, no treatment improved FEV1 above the pre-specified minimal clinically important difference (MCID) of 0.1 L. Dupilumab probably has no meaningful effect on FEV1 compared to placebo (MD 0.07 [95% CI 0.02 to 0.13]) (moderate certainty). However, in the subgroup of patients with blood eosinophils ≥300/mcL, both tezepelumab (MD 0.15 [95% CI 0.05 to 0.26]) and dupilumab (MD 0.13 [95% CI 0.06 to 0.19]) probably improved FEV1 above the MCID.</p><p><strong>Conclusion: </strong>Dupilumab is effective at improving patient-relevant outcomes in COPD with higher eosinophil levels. Other biological therapies, including tezepelumab, have no important effect on patient-relevant outcomes.</p>","PeriodicalId":10704,"journal":{"name":"COPD: Journal of Chronic Obstructive Pulmonary Disease","volume":"22 1","pages":"2449889"},"PeriodicalIF":2.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143058441","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: To investigate whether chronic obstructive pulmonary disease (COPD) and asthma increase the risk of gallstones based on the National Health and Nutrition Examination Survey (NHANES) and Mendelian randomization (MR).
Methods: Data from the NHANES 2017-2023 were included in the cross-sectional study. Diagnoses of COPD, asthma and gallstones were obtained from self-report questionnaires. Multivariate logistic regression, subgroup analyses and interaction tests were applied to explore these associations. Data for MR analysis were obtained from the Finnish cohort and the Integrative Epidemiology Unit (IEU). The inverse variance weighting (IVW) estimate was applied as the main approach to determine the causality of associations.
Results: A total of 8,728 participants were enrolled in the cross-sectional study. Both COPD (OR 1,842, 95% CI 1.144, 2.968, p = 0.015) and asthma (OR 1.434, 95% CI 1.093, 1.883, p = 0.012) were associated with increased gallstone risk before and after covariate adjustments, and diabetes history may interact with the COPD-gallstone association (p = 0.020). In MR analysis, although a causal association was observed between COPD and gallstones (OR 1.216, 95% CI 1.023, 1.445; p = 0.026), leave-one-out analysis suggested that the causal association disappeared without serpin family A member 1 (SERPINA1). No causal association was observed between asthma and gallstones (OR 1.016, 95% CI 0.932, 1.108; p = 0.718).
Conclusions: Although both COPD and asthma were positively associated with gallstones based on NHANES, the COPD-gallstone association was largely driven by SERPINA1, and no causality was observed in asthma-gallstone association. The available evidence provided limited support for causal associations between obstructive lung diseases and gallstones.
目的:通过全国健康与营养调查(NHANES)和孟德尔随机化(MR),探讨慢性阻塞性肺疾病(COPD)和哮喘是否会增加胆结石的发生风险。方法:横断面研究纳入NHANES 2017-2023的数据。COPD、哮喘和胆结石的诊断通过自述问卷获得。应用多元逻辑回归、亚组分析和交互作用检验来探讨这些关联。磁共振分析的数据来自芬兰队列和综合流行病学单位(IEU)。采用逆方差加权(IVW)估计作为确定关联因果关系的主要方法。结果:共有8728名参与者参加了横断面研究。在协变量调整前后,COPD (OR 1,842, 95% CI 1.144, 2.968, p = 0.015)和哮喘(OR 1.434, 95% CI 1.093, 1.883, p = 0.012)与胆结石风险增加相关,糖尿病史可能与COPD-胆结石相关(p = 0.020)。在MR分析中,尽管COPD与胆结石之间存在因果关系(OR 1.216, 95% CI 1.023, 1.445;p = 0.026),留一分析表明,没有serpin家族成员1 (SERPINA1),因果关系消失。哮喘与胆结石无因果关系(OR 1.016, 95% CI 0.932, 1.108;p = 0.718)。结论:尽管基于NHANES, COPD和哮喘与胆结石均呈正相关,但COPD-胆结石的关联主要由SERPINA1驱动,哮喘-胆结石的关联未观察到因果关系。现有证据对阻塞性肺病和胆结石之间的因果关系提供了有限的支持。
{"title":"Linking Chronic Obstructive Pulmonary Disease and Asthma with Gallstones: Evidence from a Cross-Sectional Study and Mendelian Randomization.","authors":"Dongru Du, Jiangyue Qin, Lijuan Gao, Xueru Hu, Suli Liu, Yanqiu Wu, Xiaohua Li, Fengming Luo, Yongchun Shen","doi":"10.1080/15412555.2025.2502118","DOIUrl":"https://doi.org/10.1080/15412555.2025.2502118","url":null,"abstract":"<p><strong>Objective: </strong>To investigate whether chronic obstructive pulmonary disease (COPD) and asthma increase the risk of gallstones based on the National Health and Nutrition Examination Survey (NHANES) and Mendelian randomization (MR).</p><p><strong>Methods: </strong>Data from the NHANES 2017-2023 were included in the cross-sectional study. Diagnoses of COPD, asthma and gallstones were obtained from self-report questionnaires. Multivariate logistic regression, subgroup analyses and interaction tests were applied to explore these associations. Data for MR analysis were obtained from the Finnish cohort and the Integrative Epidemiology Unit (IEU). The inverse variance weighting (IVW) estimate was applied as the main approach to determine the causality of associations.</p><p><strong>Results: </strong>A total of 8,728 participants were enrolled in the cross-sectional study. Both COPD (OR 1,842, 95% CI 1.144, 2.968, <i>p</i> = 0.015) and asthma (OR 1.434, 95% CI 1.093, 1.883, <i>p</i> = 0.012) were associated with increased gallstone risk before and after covariate adjustments, and diabetes history may interact with the COPD-gallstone association (<i>p</i> = 0.020). In MR analysis, although a causal association was observed between COPD and gallstones (OR 1.216, 95% CI 1.023, 1.445; <i>p</i> = 0.026), leave-one-out analysis suggested that the causal association disappeared without serpin family A member 1 (<i>SERPINA1</i>). No causal association was observed between asthma and gallstones (OR 1.016, 95% CI 0.932, 1.108; <i>p</i> = 0.718).</p><p><strong>Conclusions: </strong>Although both COPD and asthma were positively associated with gallstones based on NHANES, the COPD-gallstone association was largely driven by <i>SERPINA1</i>, and no causality was observed in asthma-gallstone association. The available evidence provided limited support for causal associations between obstructive lung diseases and gallstones.</p>","PeriodicalId":10704,"journal":{"name":"COPD: Journal of Chronic Obstructive Pulmonary Disease","volume":"22 1","pages":"2502118"},"PeriodicalIF":2.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144076435","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2025-02-24DOI: 10.1080/15412555.2024.2444663
Kaiqi Ren, Lu Zou, Jingjing Yang, Yuxiu Wang, Lingfeng Min
Chronic obstructive pulmonary disease (COPD) is characterized by restricted airflow that leads to significant respiratory difficulties. This progressive disease often results in diminished pulmonary function and the onset of additional respiratory conditions. Autophagy, a critical cellular homeostasis mechanism, plays a significant role in the exacerbation of COPD. In this study, we utilized various bioinformatics tools to identify autophagy-related genes activated by smoking in individuals with COPD. Furthermore, we explored the immune landscape of COPD through these genes, analyzing cell communication patterns using scRNA-seq data. This analysis focused on key pathways between epithelial cells and other cellular subpopulations with different autophagy scores, essential for understanding the initiation and progression of COPD.
{"title":"The Role of Autophagy and Cell Communication in COPD Progression: Insights from Bioinformatics and scRNA-seq.","authors":"Kaiqi Ren, Lu Zou, Jingjing Yang, Yuxiu Wang, Lingfeng Min","doi":"10.1080/15412555.2024.2444663","DOIUrl":"10.1080/15412555.2024.2444663","url":null,"abstract":"<p><p>Chronic obstructive pulmonary disease (COPD) is characterized by restricted airflow that leads to significant respiratory difficulties. This progressive disease often results in diminished pulmonary function and the onset of additional respiratory conditions. Autophagy, a critical cellular homeostasis mechanism, plays a significant role in the exacerbation of COPD. In this study, we utilized various bioinformatics tools to identify autophagy-related genes activated by smoking in individuals with COPD. Furthermore, we explored the immune landscape of COPD through these genes, analyzing cell communication patterns using scRNA-seq data. This analysis focused on key pathways between epithelial cells and other cellular subpopulations with different autophagy scores, essential for understanding the initiation and progression of COPD.</p>","PeriodicalId":10704,"journal":{"name":"COPD: Journal of Chronic Obstructive Pulmonary Disease","volume":"22 1","pages":"2444663"},"PeriodicalIF":2.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143482414","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2025-09-26DOI: 10.1080/15412555.2025.2563218
Meera Srinivasan, David Touma, Kaj E C Blokland, Katrina O Tonga, David G Chapman, Gregory G King
Rationale: The incremental shuttle walk test (ISWT) correlates closely with peak oxygen uptake in COPD and relates to important outcomes such as mortality, response to treatment and hospital readmission. Despite this, there is limited data on the physiological determinants of ISWT distance (ISWD) in COPD. Methods: In this exploratory, prospective observational study, spirometry, lung volumes, diffusion capacity (DLCO) and oscillometry were performed in patients with confirmed COPD. Patients then completed two ISWT with the results of the best test, measured by distanced walked taken. The determinants of ISWD and dyspnoea measured by BORG score were evaluated. Results: 25 COPD patients, mean (SD) age 71 (8.82) years, 48% female with a mean (SD) FEV1 Z-score -2.54 (0.83) were recruited. Median (IQR) ISWD was 350 (210-440) metres (mean (SD) 66.4 (27.9)% predicted distance). Most patients (85%) stopped due to inability to maintain walking speed with submaximal mean heart rate of 77.3 (10.1)% predicted and BORG dyspnoea score of 'severe' (median 5/10 (IQR 4-5.5)). Inspiratory capacity to TLC ratio (IC/TLC) correlated strongly with ISWD, even when corrected for age and height (rs = 0.59 p = 0.02). Oscillatory reactance (Xrs5) and DLCO were also correlated with ISWD. There were no oscillometric or spirometric predictors of dyspnoea. Conclusion: Resting hyperinflation measured by IC/TLC, predicted ISWD despite submaximal dyspnoea, suggesting that hyperinflation may not be the mechanism that limits exercise performance, but rather reflects overall impairment in COPD.
{"title":"Resting Hyperinflation Predicts Incremental Shuttle Walk Distance in Chronic Obstructive Pulmonary Disease.","authors":"Meera Srinivasan, David Touma, Kaj E C Blokland, Katrina O Tonga, David G Chapman, Gregory G King","doi":"10.1080/15412555.2025.2563218","DOIUrl":"10.1080/15412555.2025.2563218","url":null,"abstract":"<p><p><b>Rationale:</b> The incremental shuttle walk test (ISWT) correlates closely with peak oxygen uptake in COPD and relates to important outcomes such as mortality, response to treatment and hospital readmission. Despite this, there is limited data on the physiological determinants of ISWT distance (ISWD) in COPD. <b>Methods:</b> In this exploratory, prospective observational study, spirometry, lung volumes, diffusion capacity (DLCO) and oscillometry were performed in patients with confirmed COPD. Patients then completed two ISWT with the results of the best test, measured by distanced walked taken. The determinants of ISWD and dyspnoea measured by BORG score were evaluated. <b>Results:</b> 25 COPD patients, mean (SD) age 71 (8.82) years, 48% female with a mean (SD) FEV1 Z-score -2.54 (0.83) were recruited. Median (IQR) ISWD was 350 (210-440) metres (mean (SD) 66.4 (27.9)% predicted distance). Most patients (85%) stopped due to inability to maintain walking speed with submaximal mean heart rate of 77.3 (10.1)% predicted and BORG dyspnoea score of 'severe' (median 5/10 (IQR 4-5.5)). Inspiratory capacity to TLC ratio (IC/TLC) correlated strongly with ISWD, even when corrected for age and height (r<sub>s</sub> = 0.59 <i>p</i> = 0.02). Oscillatory reactance (Xrs<sub>5</sub>) and DLCO were also correlated with ISWD. There were no oscillometric or spirometric predictors of dyspnoea. <b>Conclusion:</b> Resting hyperinflation measured by IC/TLC, predicted ISWD despite submaximal dyspnoea, suggesting that hyperinflation may not be the mechanism that limits exercise performance, but rather reflects overall impairment in COPD.</p>","PeriodicalId":10704,"journal":{"name":"COPD: Journal of Chronic Obstructive Pulmonary Disease","volume":"22 1","pages":"2563218"},"PeriodicalIF":2.1,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145148177","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2025-02-27DOI: 10.1080/15412555.2024.2441184
Yabing Chen, Jiale Sang, Lingbo Fu, Ying Zhang
Objective: To analyze the status of research on treating chronic obstructive pulmonary disease (COPD) combined with respiratory failure internationally to reveal its development trends through visualization methods and to provide a reference and suggestions for future research directions.
Methods: Literature on the treatment of COPD combined with respiratory failure published from the year of inception of the Web of Science database to December 31, 2023, was searched. CiteSpace 6.2.R7 software was used to visualize and analyze the published articles. A bibliometric analysis of the publications, keyword co-occurrence analysis, keyword clustering analysis, and keyword emergence analysis were performed to draw a correlation map and analyze the results.
Results: A total of 369 articles were analyzed. An overall increasing trend was observed in the number of publications. The network of researchers was relatively dense, and a core team was clearly observed. The researchers' affiliations were mainly European universities and hospitals, and close cooperation between institutions was observed. The keyword analysis obtained high-frequency keywords such as "noninvasive ventilation", "mechanical ventilation", and "positive pressure ventilation". The keyword clustering analysis revealed 10 clusters, and the keyword emergence analysis yielded 20 keywords.
Conclusions: The focus of attention internationally has been on respiratory failure classification and types of ventilation support, such as high-flow oxygenation and noninvasive positive pressure ventilation. Future directions should include clinical research on high-flow oxygen administration to improve patient prognosis and the application of extracorporeal carbon dioxide removal technology to enhance patients' quality of life.
目的:分析慢性阻塞性肺疾病(COPD)合并呼吸衰竭治疗的国际研究现状,通过可视化方法揭示其发展趋势,为今后的研究方向提供参考和建议。方法:检索Web of Science数据库自建立之年至2023年12月31日发表的COPD合并呼吸衰竭治疗的文献。CiteSpace 6.2。采用R7软件对已发表文章进行可视化分析。通过文献计量学分析、关键词共现分析、关键词聚类分析和关键词涌现分析,绘制相关图并对结果进行分析。结果:共分析369篇文献。出版物数量总体呈增加趋势。研究人员网络相对密集,核心团队清晰可见。研究人员主要来自欧洲的大学和医院,研究机构之间的合作密切。关键词分析得到“无创通气”、“机械通气”、“正压通气”等高频关键词。关键词聚类分析得到10个聚类,关键词涌现分析得到20个关键词。结论:国际上关注的焦点一直是呼吸衰竭的分类和通气支持的类型,如高流量氧合和无创正压通气。未来的发展方向应包括临床研究高流量给氧以改善患者预后和体外二氧化碳去除技术的应用,以提高患者的生活质量。
{"title":"Knowledge Domain and Emerging Trends in the Treatment of Patients with Chronic Obstructive Pulmonary Disease Combined with Respiratory Failure: A Scientometric Review Based on CiteSpace Analysis.","authors":"Yabing Chen, Jiale Sang, Lingbo Fu, Ying Zhang","doi":"10.1080/15412555.2024.2441184","DOIUrl":"10.1080/15412555.2024.2441184","url":null,"abstract":"<p><strong>Objective: </strong>To analyze the status of research on treating chronic obstructive pulmonary disease (COPD) combined with respiratory failure internationally to reveal its development trends through visualization methods and to provide a reference and suggestions for future research directions.</p><p><strong>Methods: </strong>Literature on the treatment of COPD combined with respiratory failure published from the year of inception of the Web of Science database to December 31, 2023, was searched. CiteSpace 6.2.R7 software was used to visualize and analyze the published articles. A bibliometric analysis of the publications, keyword co-occurrence analysis, keyword clustering analysis, and keyword emergence analysis were performed to draw a correlation map and analyze the results.</p><p><strong>Results: </strong>A total of 369 articles were analyzed. An overall increasing trend was observed in the number of publications. The network of researchers was relatively dense, and a core team was clearly observed. The researchers' affiliations were mainly European universities and hospitals, and close cooperation between institutions was observed. The keyword analysis obtained high-frequency keywords such as \"noninvasive ventilation\", \"mechanical ventilation\", and \"positive pressure ventilation\". The keyword clustering analysis revealed 10 clusters, and the keyword emergence analysis yielded 20 keywords.</p><p><strong>Conclusions: </strong>The focus of attention internationally has been on respiratory failure classification and types of ventilation support, such as high-flow oxygenation and noninvasive positive pressure ventilation. Future directions should include clinical research on high-flow oxygen administration to improve patient prognosis and the application of extracorporeal carbon dioxide removal technology to enhance patients' quality of life.</p>","PeriodicalId":10704,"journal":{"name":"COPD: Journal of Chronic Obstructive Pulmonary Disease","volume":"22 1","pages":"2441184"},"PeriodicalIF":2.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143522794","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2025-03-24DOI: 10.1080/15412555.2025.2476435
Jiwoo Sohn, Eleanor Rochester, Adejoke O Oluyase
COPD is a highly stigmatised condition. To develop effective measures to reduce COPD-related stigma, it is important to understand patients' experiences and identify contributing factors. This systematic review explores qualitative evidence regarding the features of COPD leading to stigmatisation and how it can potentially influence health outcomes. Electronic databases were searched to identify primary qualitative studies focussing on stigma-related experiences of adults with COPD, published between January 1988 to August 2024. Data were synthesised using framework synthesis. Twenty-nine studies with 427 participants were included in this review. Findings fit well into six themes identified from Jones et al.'s framework of stigma dimensions and provide rich description. Smoking habit was not the only factor of stigma but also factors that contributed to disability of individuals. Patients experience COPD-related stigma mainly from themselves and healthcare professionals. Potential consequences of stigma identified are mental distress, isolation, reduced help-seeking behaviour and non-compliance to management. Collective effort by society and healthcare systems will be necessary to alleviate the stigma associated with chronic symptoms and smoking behaviour of COPD and to promote the benefit of pulmonary rehabilitation and available mental health support.
{"title":"Features of COPD That Lead to Stigmatisation and Its Consequences: A Framework Synthesis.","authors":"Jiwoo Sohn, Eleanor Rochester, Adejoke O Oluyase","doi":"10.1080/15412555.2025.2476435","DOIUrl":"10.1080/15412555.2025.2476435","url":null,"abstract":"<p><p>COPD is a highly stigmatised condition. To develop effective measures to reduce COPD-related stigma, it is important to understand patients' experiences and identify contributing factors. This systematic review explores qualitative evidence regarding the features of COPD leading to stigmatisation and how it can potentially influence health outcomes. Electronic databases were searched to identify primary qualitative studies focussing on stigma-related experiences of adults with COPD, published between January 1988 to August 2024. Data were synthesised using framework synthesis. Twenty-nine studies with 427 participants were included in this review. Findings fit well into six themes identified from Jones et al.'s framework of stigma dimensions and provide rich description. Smoking habit was not the only factor of stigma but also factors that contributed to disability of individuals. Patients experience COPD-related stigma mainly from themselves and healthcare professionals. Potential consequences of stigma identified are mental distress, isolation, reduced help-seeking behaviour and non-compliance to management. Collective effort by society and healthcare systems will be necessary to alleviate the stigma associated with chronic symptoms and smoking behaviour of COPD and to promote the benefit of pulmonary rehabilitation and available mental health support.</p>","PeriodicalId":10704,"journal":{"name":"COPD: Journal of Chronic Obstructive Pulmonary Disease","volume":"22 1","pages":"2476435"},"PeriodicalIF":2.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143691405","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2025-07-23DOI: 10.1080/15412555.2025.2534002
Omotayo Olaoye, Sophie Dell'Aniello, Pierre Ernst, Samy Suissa, Christel Renoux
Evidence on the risk of adverse respiratory outcomes associated with gabapentinoids in patients with chronic obstructive pulmonary disease (COPD) remains limited. Thus, we aimed to assess the risk of severe COPD exacerbation associated with gabapentinoids. We assembled a base cohort of patients aged ≥ 55 years newly diagnosed with COPD between 1993 and 2021 using the UK's Clinical Practice Research Datalink, linked to the Hospital Episode Statistics, and Office for National Statistics datasets. Using a time-conditional propensity score (TCPS)-matched, new-user design, patients prescribed gabapentinoids with an indication of epilepsy, neuropathic pain, or other chronic pain were matched 1:1 with non-users with the same indication on age, sex, calendar year, COPD duration, and TCPS. Cox proportional hazards models were used to estimate the hazard ratios (HR) and 95% confidence intervals (CIs) of severe exacerbation associated with gabapentinoid use compared to non-use in the overall cohort, and by indication. The study cohort comprised 29,882 gabapentinoid users, including 1,256 with epilepsy, 19,155 patients with neuropathic pain, and 9,471 with other chronic pain matched 1:1 with non-users. Compared with non-use, gabapentinoid use was associated with an increased risk of severe exacerbation in the overall cohort (HR 1.43; 95% CI: 1.35-1.52), and among patients with epilepsy (HR 1.39; 95% CI: 1.11-1.74), neuropathic pain (HR 1.43; 95% CI: 1.32-1.54), and other chronic pain (HR 1.45; 95% CI: 1.31-1.60). These findings suggest that gabapentinoid use is associated with an increased risk of severe exacerbation among patients with COPD, consistent among patients with neuropathic pain, epilepsy, and other chronic pain.
{"title":"Risk of Severe Exacerbation Associated with Gabapentinoid Use in Patients with Chronic Obstructive Pulmonary Disease: A Population-Based Cohort Study.","authors":"Omotayo Olaoye, Sophie Dell'Aniello, Pierre Ernst, Samy Suissa, Christel Renoux","doi":"10.1080/15412555.2025.2534002","DOIUrl":"https://doi.org/10.1080/15412555.2025.2534002","url":null,"abstract":"<p><p>Evidence on the risk of adverse respiratory outcomes associated with gabapentinoids in patients with chronic obstructive pulmonary disease (COPD) remains limited. Thus, we aimed to assess the risk of severe COPD exacerbation associated with gabapentinoids. We assembled a base cohort of patients aged ≥ 55 years newly diagnosed with COPD between 1993 and 2021 using the UK's Clinical Practice Research Datalink, linked to the Hospital Episode Statistics, and Office for National Statistics datasets. Using a time-conditional propensity score (TCPS)-matched, new-user design, patients prescribed gabapentinoids with an indication of epilepsy, neuropathic pain, or other chronic pain were matched 1:1 with non-users with the same indication on age, sex, calendar year, COPD duration, and TCPS. Cox proportional hazards models were used to estimate the hazard ratios (HR) and 95% confidence intervals (CIs) of severe exacerbation associated with gabapentinoid use compared to non-use in the overall cohort, and by indication. The study cohort comprised 29,882 gabapentinoid users, including 1,256 with epilepsy, 19,155 patients with neuropathic pain, and 9,471 with other chronic pain matched 1:1 with non-users. Compared with non-use, gabapentinoid use was associated with an increased risk of severe exacerbation in the overall cohort (HR 1.43; 95% CI: 1.35-1.52), and among patients with epilepsy (HR 1.39; 95% CI: 1.11-1.74), neuropathic pain (HR 1.43; 95% CI: 1.32-1.54), and other chronic pain (HR 1.45; 95% CI: 1.31-1.60). These findings suggest that gabapentinoid use is associated with an increased risk of severe exacerbation among patients with COPD, consistent among patients with neuropathic pain, epilepsy, and other chronic pain.</p>","PeriodicalId":10704,"journal":{"name":"COPD: Journal of Chronic Obstructive Pulmonary Disease","volume":"22 1","pages":"2534002"},"PeriodicalIF":2.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144689140","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}