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Underreporting of exacerbations of COPD 低报COPD加重
Pub Date : 2008-05-01 DOI: 10.1016/j.rmedu.2008.02.018
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引用次数: 0
Does the educational component of a pulmonary rehabilitation programme meet patients’ needs? 肺康复计划的教育部分是否满足患者的需要?
Pub Date : 2008-05-01 DOI: 10.1016/j.rmedu.2008.01.003

Aims

This study aimed to understand patient information needs and how best to meet them in order to improve rehabilitation provision and aid disease self-management by exploring experiences of people who had recently completed a pulmonary rehabilitation programme in a community hospital setting.

Methods

Qualitative research using focus groups was undertaken with 23 patients who had completed pulmonary rehabilitation within the previous four months. The focus groups were tape-recorded and contemporaneous notes made. The tapes were transcribed verbatim and template analysis was used to develop themes.

Findings

The key information needs were for a full understanding of the disease to be generated for patients, their families and the wider public much earlier in the disease process and preferably at the point of diagnosis. Patients perceived that they needed to come to terms with the condition. In order to improve disease self-management feelings of anxiety and frustration should be addressed with the suggestion that individual counseling might be made available through the rehabilitation programme. The need for continued support was highlighted with an emphasis on peer group support activities.

Conclusions

The findings have implications for primary care in terms of unmet needs in the early stages of the condition and pulmonary rehabilitation programmes in terms of providing individual counseling and ongoing peer group support to aid disease self-management.

Reproduced with permission from Sage Publications Ltd.

目的本研究旨在了解患者的信息需求,以及如何最好地满足他们,以改善康复提供和帮助疾病自我管理,通过探索最近在社区医院完成肺部康复计划的人的经历。方法采用焦点小组法对23例在4个月内完成肺部康复的患者进行定性研究。对焦点小组的讨论进行录音,并作同期笔记。磁带逐字转录,模板分析用于发展主题。研究结果需要的关键信息是在疾病过程的早期,最好是在诊断时,为患者、其家属和更广泛的公众充分了解这种疾病。病人们意识到他们需要接受这种情况。为了改善疾病自我管理,应解决焦虑和沮丧的感觉,并建议通过康复方案提供个人咨询。会议强调了继续提供支助的必要性,强调了同侪团体支助活动。结论:该研究结果对早期未满足需求的初级保健和肺部康复方案提供个人咨询和持续的同伴团体支持以帮助疾病自我管理具有启示意义。经Sage出版有限公司许可转载。
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引用次数: 0
Forthcoming events (Volume 4 Issue 2) 即将举行的活动(第四册第二期)
Pub Date : 2008-05-01 DOI: 10.1016/j.rmedu.2008.01.001
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引用次数: 0
Atherosclerosis, COPD and chronic inflammation 动脉粥样硬化、慢性阻塞性肺病和慢性炎症
Pub Date : 2008-05-01 DOI: 10.1016/j.rmedu.2008.01.007
Magnus Bäck

The prevalence of ischemic heart disease is approximately twofold higher in chronic obstructive pulmonary disease (COPD) cohorts compared to the general population. Likewise, cardiac patients with COPD have a reduced short- and long-term survival. This co-morbidity of COPD with atherosclerotic vessel disease is associated with common risk factors, such as smoking. However, atherosclerosis, in addition, shares many of the inflammatory mechanisms with those found in COPD. Atherosclerotsic lesions, as well as the COPD lung, are sites of local inflammation. Furthermore, a systemic inflammatory response, measured as increased CRP, has been reported in both patient populations. There are a number of inflammatory mediators produced in both the vessel wall and in the lungs, which potentially induce common pathological processes. For example, leukotriene B4, which induces chemotaxis of neutrophils, monocytes, T-lymphocytes and smooth muscle cells, has been suggested as a therapeutic target in both diseases. Furthermore, activation of smooth muscle cells may lead to a narrowing of the lumen in both airways and vessels. Finally, proteolytic activities of matrix metalloproteinases may be involved both in emphysema formation and in atherosclerotic plaque rupture, leading to myocardial infarction and stroke. Taken together, the associated co-morbidity of COPD with atherosclerosis and their potential common pathophysiological mechanisms support a notion of these, and other inflammatory diseases, as manifestations of chronic inflammation.

慢性阻塞性肺疾病(COPD)队列中缺血性心脏病的患病率大约是普通人群的两倍。同样,患有慢性阻塞性肺病的心脏病患者的短期和长期生存率都较低。慢性阻塞性肺病与动脉粥样硬化性血管疾病的合并症与吸烟等常见危险因素有关。然而,此外,动脉粥样硬化与COPD中发现的炎症机制有许多相同之处。动脉粥样硬化病变,以及慢性阻塞性肺病,都是局部炎症的部位。此外,在两组患者中均报道了以CRP升高为指标的全身性炎症反应。在血管壁和肺中都有许多炎症介质产生,它们可能诱发常见的病理过程。例如,白三烯B4可诱导中性粒细胞、单核细胞、t淋巴细胞和平滑肌细胞趋化,已被认为是这两种疾病的治疗靶点。此外,平滑肌细胞的激活可能导致气道和血管的管腔狭窄。最后,基质金属蛋白酶的蛋白水解活性可能参与肺气肿形成和动脉粥样硬化斑块破裂,导致心肌梗死和中风。综上所述,COPD与动脉粥样硬化的相关合并症及其潜在的共同病理生理机制支持了这些以及其他炎症性疾病作为慢性炎症表现的概念。
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引用次数: 15
COPD news 慢性阻塞性肺病的新闻
Pub Date : 2008-05-01 DOI: 10.1016/j.rmedu.2008.02.009
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引用次数: 0
Atherosclerosis, COPD and chronic inflammation 动脉粥样硬化、慢性阻塞性肺病和慢性炎症
Pub Date : 2008-05-01 DOI: 10.1016/J.RMEDU.2008.01.007
M. Bäck
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引用次数: 16
Change in patient health status following an acute COPD exacerbation 慢性阻塞性肺病急性加重后患者健康状况的变化
Pub Date : 2008-05-01 DOI: 10.1016/j.rmedu.2008.01.004

The current study aimed to assess the impact on patient health status during an acute exacerbation of chronic obstructive pulmonary disease (AECOPD). A total of 421 COPD patients were enrolled in a multicentre, single-arm study with a 6-month observational follow-up period. Patients received two inhalations of Symbicort 200 Turbuhaler(R) twice a day. Patients were assessed before the run-in period, at baseline and at 1, 3 and 6 months. Patients were instructed to report a change in respiratory symptoms lasting >24 h. This defined an AECOPD. In addition to the initial call, the St George's Respiratory Questionnaire (SGRQ), COPD Control Questionnaire (CCQ), Medical Research Council (MRC) dyspnoea scale and activities of daily living (ADL) were completed at 5–7 and 12–14 days. A group of 176 patients reported at least one AECOPD. Exacerbations were associated with statistically significant mean changes (worsening) in the SGRQ activity and impact domains at onset (mean+/−sd 12.1+/−18.1 and 14.0+/−15.2), during the first (9.8+/−19.0 and 9.4+/−16.6) and second weeks (3.1+/−15.5 and 3.3+/−14.7). Clinically significant deterioration in SGRQ impact scores was shown in 71% of patients following early identification, with 55 and 37% during the first and second weeks of an AECOPD, respectively. Acute exacerbation severely impacts on health status. The current study provides valuable information on the change in health status during an acute exacerbation of chronic obstructive pulmonary disease that can be utilised for future trials that evaluate therapeutic intervention.

Reproduced with permission from European Respiratory Society Journals Ltd.

本研究旨在评估慢性阻塞性肺疾病(AECOPD)急性加重期对患者健康状况的影响。共有421名COPD患者参加了一项多中心、单臂研究,随访6个月。患者每天两次吸入辛比柯200 Turbuhaler(R)。在磨合期前、基线和1、3、6个月时对患者进行评估。指示患者报告持续24小时的呼吸系统症状变化。这定义为AECOPD。除了最初的呼叫外,还在5-7天和12-14天完成了圣乔治呼吸问卷(SGRQ)、COPD控制问卷(CCQ)、医学研究委员会(MRC)呼吸困难量表和日常生活活动(ADL)。一组176例患者报告了至少一例AECOPD。在第一周(9.8+/ - 19.0和9.4+/ - 16.6)和第二周(3.1+/ - 15.5和3.3+/ - 14.7)期间,发作时SGRQ活性和影响域的平均变化(恶化)与统计学上显著相关(平均+/ - sd 12.1+/ - 18.1和14.0+/ - 15.2)。在早期诊断后,71%的患者SGRQ影响评分出现临床显著恶化,其中55%和37%分别出现在AECOPD的第一周和第二周。急性加重严重影响健康状况。目前的研究为慢性阻塞性肺疾病急性加重期间健康状况的变化提供了有价值的信息,可用于未来评估治疗干预的试验。经欧洲呼吸学会期刊有限公司许可转载。
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引用次数: 0
Do PaO2 and adverse social circumstances affect outpatient treatment of COPD exacerbations? PaO2和不良的社会环境是否影响门诊治疗COPD加重?
Pub Date : 2008-05-01 DOI: 10.1016/j.rmedu.2008.01.006

The current British Thoracic Society guidelines on COPD recommend that patients with COPD exacerbations should be admitted to hospital if they either have partial pressure of arterial oxygen of <7.0 kilopascals (kPa) or if they are living alone. This study was carried out to see if either of these factors have any effect on the outcome in patients presenting with COPD exacerbation in the setting of well established COPD services. This study was to see if patients with PaO(2) <7.0 kPa or those living alone were readmitted more frequently or had higher mortality than other patients discharged through the same scheme. A retrospective analysis was carried out on 1078 patients with acute exacerbation of COPD who were discharged home through Wigan “hospital at home” scheme in the period between November 1999 and February 2004 prior to the introduction of the new guidelines. This study found that there was no statistically significant difference in the rates of readmissions in patients with low PaO(2) or those living in adverse social circumstances compared to other groups of patients. The number of patients dying in this period was too small to analyse with adequate power. This study indicates that such patients can be safely managed at home in the context of well established COPD services.

Reproduced with permission from Sage Publications Ltd.

目前的英国胸科学会COPD指南建议,如果COPD加重患者的动脉氧分压为7.0千帕(kPa)或独居,则应入院治疗。本研究旨在观察这些因素中是否有任何一个对在完善的COPD服务环境中出现COPD恶化的患者的预后有影响。本研究旨在观察PaO(2) <7.0 kPa患者或独居患者是否比通过相同方案出院的其他患者更频繁地再次入院或有更高的死亡率。对1999年11月至2004年2月期间通过Wigan“家庭医院”计划出院的1078名慢性阻塞性肺病急性加重患者进行了回顾性分析,这些患者在引入新指南之前。本研究发现,与其他组患者相比,低PaO患者(2)或生活在不良社会环境中的患者再入院率无统计学差异。在此期间死亡的患者数量太少,无法进行足够的分析。这项研究表明,在建立良好的慢阻肺服务的背景下,这些患者可以在家中安全管理。经Sage出版有限公司许可转载。
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引用次数: 0
Are we unjustifiably denying intensive care support to patients suffering severe COPD exacerbation? 我们是否不合理地拒绝重症监护支持严重COPD加重患者?
Pub Date : 2008-05-01 DOI: 10.1016/j.rmedu.2008.02.004

Objective

To determine whether clinicians’ prognoses in patients with severe acute exacerbations of obstructive lung disease admitted to intensive care match observed outcomes in terms of survival.

Design

Prospective cohort study.

Setting

92 intensive care units and three respiratory high dependency units in the United Kingdom.

Participants

832 patients aged 45 years and older with breathlessness, respiratory failure, or change in mental status because of an exacerbation of COPD, asthma, or a combination of the two.

Main outcome measures

Outcome predicted by clinicians. Observed survival at 180 days.

Results

517 patients (62%) survived to 180 days. Clinicians’ prognoses were pessimistic, with a mean predicted survival of 49% at 180 days. For the fifth of patients with the poorest prognosis according to the clinician, the predicted survival rate was 10% and the actual rate was 40%. Information from a database covering 74% of intensive care units in the UK suggested no material difference between units that participated and those that did not. Patients recruited were similar to those not recruited in the same units.

Conclusions

Because decisions on whether to admit patients with COPD or asthma to intensive care for intubation depend on clinicians’ prognoses, some patients who might otherwise survive are probably being denied admission because of unwarranted prognostic pessimism.

Reproduced with permission from BMJ Publishing Group Ltd.

目的确定临床医生对入住重症监护的严重急性加重期阻塞性肺疾病患者的预后是否与观察到的生存结果相匹配。前瞻性队列研究。英国共有92个重症监护病房和3个呼吸高度依赖病房。参与者832名年龄在45岁及以上的患者,由于COPD、哮喘或两者的加重而出现呼吸困难、呼吸衰竭或精神状态改变。主要结果测量:临床医生预测的结果。观察180天存活率。结果517例(62%)患者存活至180 d。临床医生的预后很悲观,平均预测180天的生存率为49%。临床医生认为预后最差的1 / 5患者,预测生存率为10%,实际生存率为40%。从涵盖英国74%重症监护病房的数据库中获取的信息表明,参与和未参与的病房之间没有实质性差异。招募的患者与未在同一单位招募的患者相似。结论:由于决定是否让COPD或哮喘患者接受插管重症监护取决于临床医生的预后,一些原本可能存活的患者可能因为毫无根据的预后悲观而被拒绝入院。经英国医学杂志出版集团有限公司许可转载。
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引用次数: 0
Can COPD patients benefit from treatment with infliximab? 慢性阻塞性肺病患者能从英夫利昔单抗治疗中获益吗?
Pub Date : 2008-05-01 DOI: 10.1016/j.rmedu.2008.02.017

Rationale

Chronic obstructive pulmonary disease (COPD) is a progressive, smoking-related, inflammatory lung disease in which tumor necrosis factor-alpha is overexpressed and has been suggested to play a pathogenic role.

Objectives

To determine if infliximab, an anti-TNF-alpha antibody, results in clinical benefit and has an acceptable safety profile in patients with moderate to severe COPD. METHODS: In a multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose-finding study, subjects with moderate to severe COPD received infliximab (3 mg/kg [n=78] or 5 mg/kg [n=79]) or placebo (n=77) at Weeks 0, 2, 6, 12, 18, and 24. Efficacy, health status, and safety were assessed through Week 44.

Measurements and main results

Infliximab was generally well tolerated, but showed no treatment benefit as measured by the primary endpoint, Chronic Respiratory Questionnaire total score. Similarly, there was no change in secondary measures, including prebronchodilator FEV(1), 6-min walk distance, SF-36 physical score, transition dyspnea index, or moderate-to-severe COPD exacerbations. Post hoc analysis revealed that subjects who were younger or cachectic showed improvement in the 6-min walk distance. Malignancies were diagnosed during the study in 9 of 157 infliximab-treated subjects versus 1 of 77 placebo-treated subjects. No opportunistic infections were observed, and there were no differences in the occurrence of antibiotic-requiring infections, although the incidence of pneumonia was higher in infliximab-treated subjects. No infection-related mortality was observed. Higher proportions of infliximab-treated subjects discontinued the study agent due to adverse events (20-27%) than did placebo-treated subjects (9%).

Conclusions

Subjects with moderate to severe COPD did not benefit from treatment with infliximab. Although not statistically significant, more cases of cancer and pneumonia were observed in the infliximab-treated subjects. The impact of infliximab on malignancy risk in patients with COPD needs to be further elucidated.

Reproduced with permission from the American Thoracic Society

慢性阻塞性肺疾病(COPD)是一种进行性、吸烟相关的炎症性肺部疾病,肿瘤坏死因子- α过度表达,已被认为在致病中起作用。目的确定抗tnf - α抗体英夫利昔单抗在中重度COPD患者中是否具有临床获益和可接受的安全性。方法:在一项多中心、随机、双盲、安慰剂对照、平行组、剂量发现研究中,中度至重度COPD患者在第0、2、6、12、18和24周接受英夫利昔单抗(3mg /kg [n=78]或5mg /kg [n=79])或安慰剂(n=77)治疗。疗效、健康状况和安全性评估持续到第44周。测量和主要结果英夫利昔单抗总体耐受性良好,但根据主要终点慢性呼吸问卷总分测量,没有显示出治疗益处。同样,次要指标也没有变化,包括支气管扩张剂前FEV(1)、6分钟步行距离、SF-36身体评分、过渡性呼吸困难指数或中重度COPD加重。事后分析显示,年龄较小或体质较差的受试者在6分钟步行距离上表现出改善。在研究期间,157名英夫利昔单抗治疗的受试者中有9人被诊断出恶性肿瘤,而77名安慰剂治疗的受试者中有1人被诊断出恶性肿瘤。虽然英夫利昔单抗治疗组的肺炎发病率较高,但未观察到机会性感染,需要抗生素的感染发生率也没有差异。未观察到感染相关的死亡率。英夫利昔单抗治疗的受试者因不良事件而停药的比例(20-27%)高于安慰剂治疗的受试者(9%)。结论:中至重度COPD患者不能从英夫利昔单抗治疗中获益。虽然没有统计学意义,但在英夫利昔单抗治疗的受试者中观察到更多的癌症和肺炎病例。英夫利昔单抗对COPD患者恶性肿瘤风险的影响有待进一步阐明。经美国胸科学会许可转载
{"title":"Can COPD patients benefit from treatment with infliximab?","authors":"","doi":"10.1016/j.rmedu.2008.02.017","DOIUrl":"https://doi.org/10.1016/j.rmedu.2008.02.017","url":null,"abstract":"<div><h3>Rationale</h3><p>Chronic obstructive pulmonary disease (COPD) is a progressive, smoking-related, inflammatory lung disease in which tumor necrosis factor-alpha is overexpressed and has been suggested to play a pathogenic role.</p></div><div><h3>Objectives</h3><p>To determine if infliximab, an anti-TNF-alpha antibody, results in clinical benefit and has an acceptable safety profile in patients with moderate to severe COPD. METHODS: In a multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose-finding study, subjects with moderate to severe COPD received infliximab (3<!--> <!-->mg/kg [<em>n</em>=78] or 5<!--> <!-->mg/kg [<em>n</em>=79]) or placebo (<em>n</em>=77) at Weeks 0, 2, 6, 12, 18, and 24. Efficacy, health status, and safety were assessed through Week 44.</p></div><div><h3>Measurements and main results</h3><p>Infliximab was generally well tolerated, but showed no treatment benefit as measured by the primary endpoint, Chronic Respiratory Questionnaire total score. Similarly, there was no change in secondary measures, including prebronchodilator FEV(1), 6-min walk distance, SF-36 physical score, transition dyspnea index, or moderate-to-severe COPD exacerbations. Post hoc analysis revealed that subjects who were younger or cachectic showed improvement in the 6-min walk distance. Malignancies were diagnosed during the study in 9 of 157 infliximab-treated subjects versus 1 of 77 placebo-treated subjects. No opportunistic infections were observed, and there were no differences in the occurrence of antibiotic-requiring infections, although the incidence of pneumonia was higher in infliximab-treated subjects. No infection-related mortality was observed. Higher proportions of infliximab-treated subjects discontinued the study agent due to adverse events (20-27%) than did placebo-treated subjects (9%).</p></div><div><h3>Conclusions</h3><p>Subjects with moderate to severe COPD did not benefit from treatment with infliximab. Although not statistically significant, more cases of cancer and pneumonia were observed in the infliximab-treated subjects. The impact of infliximab on malignancy risk in patients with COPD needs to be further elucidated.</p><p>Reproduced with permission from the American Thoracic Society</p></div>","PeriodicalId":101083,"journal":{"name":"Respiratory Medicine: COPD Update","volume":"4 2","pages":"Page 80"},"PeriodicalIF":0.0,"publicationDate":"2008-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedu.2008.02.017","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91678313","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Respiratory Medicine: COPD Update
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