Patients with chronic obstructive pulmonary disease (COPD) are progressively limited in their ability to undertake normal everyday activities by a combination of exertional dyspnoea and peripheral muscle weakness. COPD is characterised by expiratory flow limitation, resulting in air trapping and lung hyperinflation. Hyperinflation increases acutely under conditions such as exercise or exacerbations, with an accompanying sharp increase in the intensity of dyspnoea to distressing and intolerable levels. Air trapping, causing increased lung hyperinflation, can be present even in milder COPD during everyday activities. The resulting activity-related dyspnoea leads to a vicious spiral of activity avoidance, physical deconditioning, and reduced quality of life, and has implications for the early development of comorbidities such as cardiovascular disease. Various strategies exist to reduce hyperinflation, notably long-acting bronchodilator treatment (via reduction in flow limitation and improved lung emptying) and an exercise programme (via decreased respiratory rate, reducing ventilatory demand), or their combination. Optimal bronchodilation can reduce exertional dyspnoea and increase a patient's ability to exercise, and improves the chance of successful outcome of a pulmonary rehabilitation programme. There should be a lower threshold for initiating treatments appropriate to the stage of the disease, such as long-acting bronchodilators and an exercise programme for patients with mild-to-moderate disease who experience persistent dyspnoea.
{"title":"No room to breathe: the importance of lung hyperinflation in COPD.","authors":"Mike Thomas, Marc Decramer, Denis E O'Donnell","doi":"10.4104/pcrj.2013.00025","DOIUrl":"10.4104/pcrj.2013.00025","url":null,"abstract":"<p><p>Patients with chronic obstructive pulmonary disease (COPD) are progressively limited in their ability to undertake normal everyday activities by a combination of exertional dyspnoea and peripheral muscle weakness. COPD is characterised by expiratory flow limitation, resulting in air trapping and lung hyperinflation. Hyperinflation increases acutely under conditions such as exercise or exacerbations, with an accompanying sharp increase in the intensity of dyspnoea to distressing and intolerable levels. Air trapping, causing increased lung hyperinflation, can be present even in milder COPD during everyday activities. The resulting activity-related dyspnoea leads to a vicious spiral of activity avoidance, physical deconditioning, and reduced quality of life, and has implications for the early development of comorbidities such as cardiovascular disease. Various strategies exist to reduce hyperinflation, notably long-acting bronchodilator treatment (via reduction in flow limitation and improved lung emptying) and an exercise programme (via decreased respiratory rate, reducing ventilatory demand), or their combination. Optimal bronchodilation can reduce exertional dyspnoea and increase a patient's ability to exercise, and improves the chance of successful outcome of a pulmonary rehabilitation programme. There should be a lower threshold for initiating treatments appropriate to the stage of the disease, such as long-acting bronchodilators and an exercise programme for patients with mild-to-moderate disease who experience persistent dyspnoea.</p>","PeriodicalId":48998,"journal":{"name":"Primary Care Respiratory Journal","volume":"22 1","pages":"101-11"},"PeriodicalIF":0.0,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442765/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31347840","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Chara Ntala, Panagiota Birmpili, Allison Worth, Niall H Anderson, Aziz Sheikh
The quality of reporting of randomised controlled trials in asthma: systematic review protocol
{"title":"The quality of reporting of randomised controlled trials in asthma: systematic review protocol.","authors":"Chara Ntala, Panagiota Birmpili, Allison Worth, Niall H Anderson, Aziz Sheikh","doi":"10.4104/pcrj.2013.00003","DOIUrl":"https://doi.org/10.4104/pcrj.2013.00003","url":null,"abstract":"The quality of reporting of randomised controlled trials in asthma: systematic review protocol","PeriodicalId":48998,"journal":{"name":"Primary Care Respiratory Journal","volume":"22 1","pages":"PS1-8"},"PeriodicalIF":0.0,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4104/pcrj.2013.00003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31179544","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Under-diagnosis of COPD remains an international problem. Less than one-third of the predicted three million people in the UK with COPD currently have a diagnosis. Furthermore, there is wide and unwarranted variation in the proportion of those who have a diagnosis versus those who remain undiagnosed, with deprived populations having both the highest prevalence and the highest under-diagnosis of COPD. This is important, since the diagnosis of COPD is often made late when significant lung function has been lost, when exacerbations and hospitalisations are more common, quality of life is notably affected, and the costs of managing the disease are significant. Given that awareness of COPD is low, both amongst primary care clinicians and patients, it is not surprising that the early identification of people with clinically relevant COPD is central to disease management guidelines and health policy. In this issue of the PCRJ, Falzon et al. describe the use of a locally enhanced service (LES) in one particular Primary Care Trust (PCT) in the UK that uses financial incentives to drive up COPD diagnosis rates. Evidence to support the use of financial incentives to improve performance in healthcare is so far modest and inconsistent. Critics have even suggested that such incentives are controlling and may undermine and even worsen performance, especially when intrinsic motivation is high to begin with. Yet, finding ways to motivate and engage over-burdened primary care clinicians in the management of chronic diseases remains challenging. In the UK National Health Service (NHS), the new Clinical Commissioning Groups (CCGs), led by primary care clinicians, will have the remit to drive improvement by setting priorities and influencing the provision of care in order to obtain positive health outcomes in their localities. Improvements in COPD care should be high on their agenda; CCGs are specifically tasked with reducing mortality in respiratory disease as well as reducing the time people with long-term conditions spend in hospital, both of which are more likely to be achieved if people are diagnosed early and treated appropriately. Critics of early diagnosis initiatives rightly highlight that smoking is the major cause of COPD and that almost all cases could be prevented, or disease progression lessened, by patients quitting. Furthermore, the ability of primary care to perform and interpret spirometry accurately has been questioned. However, although all smokers should be advised to quit, utilising lung function measures can enhance quit rates in those with COPD, and it is entirely possible to assure the quality of spirometry in primary care settings. Therefore, financial incentives for COPD case-finding should at least be tied to the provision of smoking cessation support and quality assured spirometry. But there is also opportunity to enhance care through other high value interventions, such as influenza vaccination and pulmonary rehabilitation. Falzon et al.
{"title":"Finding the 'missing millions': do we need incentives to optimise COPD outcomes?","authors":"June Roberts, Stephen Gaduzo","doi":"10.4104/pcrj.2013.00024","DOIUrl":"https://doi.org/10.4104/pcrj.2013.00024","url":null,"abstract":"Under-diagnosis of COPD remains an international problem. Less than one-third of the predicted three million people in the UK with COPD currently have a diagnosis. Furthermore, there is wide and unwarranted variation in the proportion of those who have a diagnosis versus those who remain undiagnosed, with deprived populations having both the highest prevalence and the highest under-diagnosis of COPD. This is important, since the diagnosis of COPD is often made late when significant lung function has been lost, when exacerbations and hospitalisations are more common, quality of life is notably affected, and the costs of managing the disease are significant. Given that awareness of COPD is low, both amongst primary care clinicians and patients, it is not surprising that the early identification of people with clinically relevant COPD is central to disease management guidelines and health policy. In this issue of the PCRJ, Falzon et al. describe the use of a locally enhanced service (LES) in one particular Primary Care Trust (PCT) in the UK that uses financial incentives to drive up COPD diagnosis rates. Evidence to support the use of financial incentives to improve performance in healthcare is so far modest and inconsistent. Critics have even suggested that such incentives are controlling and may undermine and even worsen performance, especially when intrinsic motivation is high to begin with. Yet, finding ways to motivate and engage over-burdened primary care clinicians in the management of chronic diseases remains challenging. In the UK National Health Service (NHS), the new Clinical Commissioning Groups (CCGs), led by primary care clinicians, will have the remit to drive improvement by setting priorities and influencing the provision of care in order to obtain positive health outcomes in their localities. Improvements in COPD care should be high on their agenda; CCGs are specifically tasked with reducing mortality in respiratory disease as well as reducing the time people with long-term conditions spend in hospital, both of which are more likely to be achieved if people are diagnosed early and treated appropriately. Critics of early diagnosis initiatives rightly highlight that smoking is the major cause of COPD and that almost all cases could be prevented, or disease progression lessened, by patients quitting. Furthermore, the ability of primary care to perform and interpret spirometry accurately has been questioned. However, although all smokers should be advised to quit, utilising lung function measures can enhance quit rates in those with COPD, and it is entirely possible to assure the quality of spirometry in primary care settings. Therefore, financial incentives for COPD case-finding should at least be tied to the provision of smoking cessation support and quality assured spirometry. But there is also opportunity to enhance care through other high value interventions, such as influenza vaccination and pulmonary rehabilitation. Falzon et al.","PeriodicalId":48998,"journal":{"name":"Primary Care Respiratory Journal","volume":"22 1","pages":"12-3"},"PeriodicalIF":0.0,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4104/pcrj.2013.00024","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31252598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The article by de Bot et al. in this issue of the PCRJ demonstrates that fractional exhaled nitric oxide (FeNO) does not correlate with symptoms or quality of life (QoL) in children with allergic rhinitis (AR) with and without asthma. Patients were assessed for FeNO, nasal and asthma symptom scores, rhinitis-related QoL and house dust mite-specific immunoglobulin E level. Cross-sectional and longitudinal correlations were sought between these parameters at baseline and after two years. The authors found no or very weak correlations between FeNO levels and nasal symptoms, asthma symptoms or QoL in both groups in both years, and concluded that FeNO is unlikely to be a useful biomarker of the clinical severity of upper or lower airway disease in primary care. These findings are not surprising. Nitric oxide (NO) is produced endogenously in cells by NO synthase. Its production is increased in response to inflammatory cytokines, and FeNO is thought to be an indirect measurement of airway eosinophilic inflammation. Initial enthusiasm about FeNO as a marker of airway inflammatory disease has now turned into a more balanced outlook, with it being seen as one of the many indirect outcome measures which still require much fine-tuning before they can find (if ever) broad clinical applicability in primary or secondary care. The advantages of FeNO testing are non-invasiveness, speed, simplicity, ease of tolerance by children and adult patients with severe airway obstruction, and lack of known risks to the patient. The disadvantages include the expense of purchasing and maintaining equipment, the variability of FeNO measurement between centres, and significant overlap of FeNO levels between populations with and without asthma, which thus far renders it as a research tool only. The American Thoracic Society (ATS) has approved a set of clinical practice guidelines of FeNO interpretation for clinical applications. There are recommendations concerning the use of FeNO in asthma, particularly for diagnosis and monitoring of eosinophilic airway inflammation and determining the likelihood of steroid responsiveness, whilst accounting for age and allergen exposure as factors. This contrasts with a limited role for the measurement of nasal NO levels, which, though altered in several diseases (e.g. cystic fibrosis, primary ciliary dyskinesia), cannot be recommended for routine clinical practice. A sample of recent literature supports the observations by de Bot et al. Ciprandi et al. evaluated children with AR or asthma and found a correlation between FeNO levels and change in forced expiratory volume in 1 second (FEV1) after bronchodilator testing (bronchial reversibility). The correlation was moderate for both asthma (r = 0.69) and rhinitis (r = 0.54). Levels of 34 parts per billion (ppb) of FeNO were predictive of bronchial reversibility. The same group also found a moderate negative correlation between FeNO levels and bronchial hyperreactivity in adult patients with per
{"title":"Fractional exhaled nitric oxide (FeNO) measurement in asthma and rhinitis.","authors":"Artur Gevorgyan, Wytske J Fokkens","doi":"10.4104/pcrj.2013.00019","DOIUrl":"https://doi.org/10.4104/pcrj.2013.00019","url":null,"abstract":"The article by de Bot et al. in this issue of the PCRJ demonstrates that fractional exhaled nitric oxide (FeNO) does not correlate with symptoms or quality of life (QoL) in children with allergic rhinitis (AR) with and without asthma. Patients were assessed for FeNO, nasal and asthma symptom scores, rhinitis-related QoL and house dust mite-specific immunoglobulin E level. Cross-sectional and longitudinal correlations were sought between these parameters at baseline and after two years. The authors found no or very weak correlations between FeNO levels and nasal symptoms, asthma symptoms or QoL in both groups in both years, and concluded that FeNO is unlikely to be a useful biomarker of the clinical severity of upper or lower airway disease in primary care. These findings are not surprising. Nitric oxide (NO) is produced endogenously in cells by NO synthase. Its production is increased in response to inflammatory cytokines, and FeNO is thought to be an indirect measurement of airway eosinophilic inflammation. Initial enthusiasm about FeNO as a marker of airway inflammatory disease has now turned into a more balanced outlook, with it being seen as one of the many indirect outcome measures which still require much fine-tuning before they can find (if ever) broad clinical applicability in primary or secondary care. The advantages of FeNO testing are non-invasiveness, speed, simplicity, ease of tolerance by children and adult patients with severe airway obstruction, and lack of known risks to the patient. The disadvantages include the expense of purchasing and maintaining equipment, the variability of FeNO measurement between centres, and significant overlap of FeNO levels between populations with and without asthma, which thus far renders it as a research tool only. The American Thoracic Society (ATS) has approved a set of clinical practice guidelines of FeNO interpretation for clinical applications. There are recommendations concerning the use of FeNO in asthma, particularly for diagnosis and monitoring of eosinophilic airway inflammation and determining the likelihood of steroid responsiveness, whilst accounting for age and allergen exposure as factors. This contrasts with a limited role for the measurement of nasal NO levels, which, though altered in several diseases (e.g. cystic fibrosis, primary ciliary dyskinesia), cannot be recommended for routine clinical practice. A sample of recent literature supports the observations by de Bot et al. Ciprandi et al. evaluated children with AR or asthma and found a correlation between FeNO levels and change in forced expiratory volume in 1 second (FEV1) after bronchodilator testing (bronchial reversibility). The correlation was moderate for both asthma (r = 0.69) and rhinitis (r = 0.54). Levels of 34 parts per billion (ppb) of FeNO were predictive of bronchial reversibility. The same group also found a moderate negative correlation between FeNO levels and bronchial hyperreactivity in adult patients with per","PeriodicalId":48998,"journal":{"name":"Primary Care Respiratory Journal","volume":"22 1","pages":"10-1"},"PeriodicalIF":0.0,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4104/pcrj.2013.00019","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31252600","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The changing face of asthma in Finland: improved recognition and no further increase in symptoms
{"title":"The changing face of asthma in Finland: improved recognition and no further increase in symptoms.","authors":"Anders Bjerg","doi":"10.4104/pcrj.2013.00030","DOIUrl":"https://doi.org/10.4104/pcrj.2013.00030","url":null,"abstract":"The changing face of asthma in Finland: improved recognition and no further increase in symptoms","PeriodicalId":48998,"journal":{"name":"Primary Care Respiratory Journal","volume":"22 1","pages":"13-4"},"PeriodicalIF":0.0,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4104/pcrj.2013.00030","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31252601","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The role of primary care as part of the multidisciplinary team (MDT) in the management of lung cancer: the “Dream MDT” report — new guidance from the UK Lung Cancer Coalition
{"title":"The role of primary care as part of the multidisciplinary team (MDT) in the management of lung cancer: the \"Dream MDT\" report - new guidance from the UK Lung Cancer Coalition.","authors":"David Bellamy, Mick Peake, Andrea Williams","doi":"10.4104/pcrj.2013.00007","DOIUrl":"https://doi.org/10.4104/pcrj.2013.00007","url":null,"abstract":"The role of primary care as part of the multidisciplinary team (MDT) in the management of lung cancer: the “Dream MDT” report — new guidance from the UK Lung Cancer Coalition","PeriodicalId":48998,"journal":{"name":"Primary Care Respiratory Journal","volume":"22 1","pages":"3-4"},"PeriodicalIF":0.0,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4104/pcrj.2013.00007","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31194877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Minal R Patel, Smita Shah, Michael D Cabana, Susan M Sawyer, Brett Toelle, Craig Mellis, Christine Jenkins, Randall W Brown, Noreen M Clark
Background: Physician Asthma Care Education (PACE) is a programme developed in the USA to improve paediatric asthma outcomes.
Aims: To examine translation of PACE to Australia.
Methods: The RE-AIM framework was used to assess translation. Demographic characteristics and findings regarding clinical asthma outcomes from PACE randomised clinical trials in both countries were examined. Qualitative content analysis was used to examine fidelity to intervention components.
Results: Both iterations of PACE reached similar target audiences (general practice physicians and paediatric patients with asthma); however, in the USA, more children with persistent disease were enrolled. In both countries, participation comprised approximately 10% of eligible physicians and 25% of patients. In both countries, PACE deployed well-known local physicians and behavioural scientists as facilitators. Sponsorship of the programme was provided by professional associations and government agencies. Fidelity to essential programme elements was observed, but PACE Australia workshops included additional components. Similar outcomes included improvements in clinician confidence in developing short-term and long-term care plans, prescribing inhaled corticosteroids, and providing written management instructions to patients. No additional time was spent in the patient visit compared with controls. US PACE realised reductions in symptoms and healthcare use, results that could not be confirmed in Australia because of limitations in follow-up time and sample sizes. US PACE is maintained through a National Heart, Lung, and Blood Institute website. Development of maintenance strategies for PACE Australia is underway.
Conclusions: Based on criteria of the RE-AIM framework, the US version of PACE has been successfully translated for use in Australia.
{"title":"Translation of an evidence-based asthma intervention: Physician Asthma Care Education (PACE) in the United States and Australia.","authors":"Minal R Patel, Smita Shah, Michael D Cabana, Susan M Sawyer, Brett Toelle, Craig Mellis, Christine Jenkins, Randall W Brown, Noreen M Clark","doi":"10.4104/pcrj.2012.00093","DOIUrl":"https://doi.org/10.4104/pcrj.2012.00093","url":null,"abstract":"<p><strong>Background: </strong>Physician Asthma Care Education (PACE) is a programme developed in the USA to improve paediatric asthma outcomes.</p><p><strong>Aims: </strong>To examine translation of PACE to Australia.</p><p><strong>Methods: </strong>The RE-AIM framework was used to assess translation. Demographic characteristics and findings regarding clinical asthma outcomes from PACE randomised clinical trials in both countries were examined. Qualitative content analysis was used to examine fidelity to intervention components.</p><p><strong>Results: </strong>Both iterations of PACE reached similar target audiences (general practice physicians and paediatric patients with asthma); however, in the USA, more children with persistent disease were enrolled. In both countries, participation comprised approximately 10% of eligible physicians and 25% of patients. In both countries, PACE deployed well-known local physicians and behavioural scientists as facilitators. Sponsorship of the programme was provided by professional associations and government agencies. Fidelity to essential programme elements was observed, but PACE Australia workshops included additional components. Similar outcomes included improvements in clinician confidence in developing short-term and long-term care plans, prescribing inhaled corticosteroids, and providing written management instructions to patients. No additional time was spent in the patient visit compared with controls. US PACE realised reductions in symptoms and healthcare use, results that could not be confirmed in Australia because of limitations in follow-up time and sample sizes. US PACE is maintained through a National Heart, Lung, and Blood Institute website. Development of maintenance strategies for PACE Australia is underway.</p><p><strong>Conclusions: </strong>Based on criteria of the RE-AIM framework, the US version of PACE has been successfully translated for use in Australia.</p>","PeriodicalId":48998,"journal":{"name":"Primary Care Respiratory Journal","volume":"22 1","pages":"29-36"},"PeriodicalIF":0.0,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4104/pcrj.2012.00093","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31036750","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
David Price, Barbara Yawn, Guy Brusselle, Andrea Rossi
While the pharmacological management of chronic obstructive pulmonary disease (COPD) has evolved from the drugs used to treat asthma, the treatment models are different and the two diseases require clear differential diagnosis in order to determine the correct therapeutic strategy. In contrast to the almost universal requirement for anti-inflammatory treatment of persistent asthma, the efficacy of inhaled corticosteroids (ICS) is less well established in COPD and their role in treatment is limited. There is some evidence of a preventive effect of ICS on exacerbations in patients with COPD, but there is little evidence for an effect on mortality or lung function decline. As a result, treatment guidelines recommend the use of ICS in patients with severe or very severe disease (forced expiratory volume in 1 second <50% predicted) and repeated exacerbations. Patients with frequent exacerbations - a phenotype that is stable over time - are likely to be less common among those with moderate COPD (many of whom are managed in primary care) than in those with more severe disease. The indiscriminate use of ICS in COPD may expose patients to an unnecessary increase in the risk of side-effects such as pneumonia, osteoporosis, diabetes and cataracts, while wasting healthcare spending and potentially diverting attention from other more appropriate forms of management such as pulmonary rehabilitation and maximal bronchodilator use. Physicians should carefully weigh the likely benefits of ICS use against the potential risk of side-effects and costs in individual patients with COPD.
{"title":"Risk-to-benefit ratio of inhaled corticosteroids in patients with COPD.","authors":"David Price, Barbara Yawn, Guy Brusselle, Andrea Rossi","doi":"10.4104/pcrj.2012.00092","DOIUrl":"10.4104/pcrj.2012.00092","url":null,"abstract":"<p><p>While the pharmacological management of chronic obstructive pulmonary disease (COPD) has evolved from the drugs used to treat asthma, the treatment models are different and the two diseases require clear differential diagnosis in order to determine the correct therapeutic strategy. In contrast to the almost universal requirement for anti-inflammatory treatment of persistent asthma, the efficacy of inhaled corticosteroids (ICS) is less well established in COPD and their role in treatment is limited. There is some evidence of a preventive effect of ICS on exacerbations in patients with COPD, but there is little evidence for an effect on mortality or lung function decline. As a result, treatment guidelines recommend the use of ICS in patients with severe or very severe disease (forced expiratory volume in 1 second <50% predicted) and repeated exacerbations. Patients with frequent exacerbations - a phenotype that is stable over time - are likely to be less common among those with moderate COPD (many of whom are managed in primary care) than in those with more severe disease. The indiscriminate use of ICS in COPD may expose patients to an unnecessary increase in the risk of side-effects such as pneumonia, osteoporosis, diabetes and cataracts, while wasting healthcare spending and potentially diverting attention from other more appropriate forms of management such as pulmonary rehabilitation and maximal bronchodilator use. Physicians should carefully weigh the likely benefits of ICS use against the potential risk of side-effects and costs in individual patients with COPD.</p>","PeriodicalId":48998,"journal":{"name":"Primary Care Respiratory Journal","volume":"22 1","pages":"92-100"},"PeriodicalIF":0.0,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6548052/pdf/pcrj201292.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31036008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Marc Miravitlles, Juan José Soler-Cataluña, Myriam Calle, Jesús Molina, Pere Almagro, José Antonio Quintano, Juan Antonio Trigueros, Pascual Piñera, Adolfo Simón, Juan Antonio Riesco, Julio Ancochea, Joan B Soriano
After the development of the COPD Strategy of the National Health Service in Spain, all scientific societies, patient organisations, and central and regional governments formed a partnership to enhance care and research in COPD. At the same time, the Spanish Society of Pneumology and Thoracic Surgery (SEPAR) took the initiative to convene the various scientific societies involved in the National COPD Strategy and invited them to participate in the development of the new Spanish guidelines for COPD (Guía Española de la EPOC; GesEPOC). Probably the more innovative approach of GesEPOC is to base treatment of stable COPD on clinical phenotypes, a term which has become increasingly used in recent years to refer to the different clinical forms of COPD with different prognostic implications. The proposed phenotypes are: (A) infrequent exacerbators with either chronic bronchitis or emphysema; (B) overlap COPD-asthma; (C) frequent exacerbators with emphysema predominant; and (D) frequent exacerbators with chronic bronchitis predominant. The assessment of severity has also been updated with the incorporation of multidimensional indices. The severity of the obstruction, as measured by forced expiratory volume in 1 second, is essential but not sufficient. Multidimensional indices such as the BODE index have shown excellent prognostic value. If the 6-minute walking test is not performed routinely, its substitution by the frequency of exacerbations (BODEx index) provides similar prognostic properties. This proposal aims to achieve a more personalised management of COPD according to the clinical characteristics and multidimensional assessment of severity.
在西班牙国家卫生服务局制定了《慢性阻塞性肺病战略》后,所有科学学会、患者组织以及中央和地区政府结成了伙伴关系,以加强对慢性阻塞性肺疾病的护理和研究。与此同时,西班牙肺病和胸外科学会(SEPAR)主动召集了参与国家COPD战略的各个科学学会,并邀请它们参与制定新的西班牙COPD指南(Guía Española de la EPOC;GesEPOC)。GesEPOC更具创新性的方法可能是将稳定型COPD的治疗建立在临床表型的基础上,近年来,该术语越来越多地用于指代具有不同预后意义的不同临床形式的COPD。提出的表型是:(A)罕见的慢性支气管炎或肺气肿加重者;(B) 重叠型COPD哮喘;(C) 以肺气肿为主的频繁加重;和(D)以慢性支气管炎为主的频繁发作。对严重程度的评估也进行了更新,纳入了多层面指数。阻塞的严重程度,通过1秒内的用力呼气量来衡量,是必要的,但还不够。BODE指数等多维指标显示出良好的预后价值。如果不定期进行6分钟步行测试,用恶化频率(BODEx指数)代替它可以提供类似的预后特性。该提案旨在根据临床特征和严重程度的多维评估,实现更个性化的COPD管理。
{"title":"A new approach to grading and treating COPD based on clinical phenotypes: summary of the Spanish COPD guidelines (GesEPOC).","authors":"Marc Miravitlles, Juan José Soler-Cataluña, Myriam Calle, Jesús Molina, Pere Almagro, José Antonio Quintano, Juan Antonio Trigueros, Pascual Piñera, Adolfo Simón, Juan Antonio Riesco, Julio Ancochea, Joan B Soriano","doi":"10.4104/pcrj.2013.00016","DOIUrl":"10.4104/pcrj.2013.00016","url":null,"abstract":"<p><p>After the development of the COPD Strategy of the National Health Service in Spain, all scientific societies, patient organisations, and central and regional governments formed a partnership to enhance care and research in COPD. At the same time, the Spanish Society of Pneumology and Thoracic Surgery (SEPAR) took the initiative to convene the various scientific societies involved in the National COPD Strategy and invited them to participate in the development of the new Spanish guidelines for COPD (Guía Española de la EPOC; GesEPOC). Probably the more innovative approach of GesEPOC is to base treatment of stable COPD on clinical phenotypes, a term which has become increasingly used in recent years to refer to the different clinical forms of COPD with different prognostic implications. The proposed phenotypes are: (A) infrequent exacerbators with either chronic bronchitis or emphysema; (B) overlap COPD-asthma; (C) frequent exacerbators with emphysema predominant; and (D) frequent exacerbators with chronic bronchitis predominant. The assessment of severity has also been updated with the incorporation of multidimensional indices. The severity of the obstruction, as measured by forced expiratory volume in 1 second, is essential but not sufficient. Multidimensional indices such as the BODE index have shown excellent prognostic value. If the 6-minute walking test is not performed routinely, its substitution by the frequency of exacerbations (BODEx index) provides similar prognostic properties. This proposal aims to achieve a more personalised management of COPD according to the clinical characteristics and multidimensional assessment of severity.</p>","PeriodicalId":48998,"journal":{"name":"Primary Care Respiratory Journal","volume":"22 1","pages":"117-21"},"PeriodicalIF":0.0,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442753/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31266844","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pedro Azevedo, Jaime Correia de Sousa, Jean Bousquet, António Bugalho-Almeida, Stefano R Del Giacco, Pascal Demoly, Tari Haahtela, Tiago Jacinto, Vanessa Garcia-Larsen, Thys van der Molen, Mário Morais-Almeida, Luis Nogueira-Silva, Ana M Pereira, Miguel Román Rodríguez, Bárbara G Silva, Ioanna G Tsiligianni, Hakan Yaman, Barbara Yawn, João A Fonseca
Asthma frequently occurs in association with allergic rhinitis and a combined management approach has been suggested. The Control of Allergic Rhinitis and Asthma Test (CARAT) is the first questionnaire to assess control of both diseases concurrently. However, to have an impact on healthcare it needs to be disseminated and adopted. In this paper we discuss the dissemination of CARAT in different countries and its possible applications in primary care. At present, the adaptation of CARAT for use in different languages and cultures is being led by volunteer researchers and clinicians in 15 countries. Website and smartphone applications have been developed, and a free open model of distribution was adopted to contribute to the dissemination of CARAT. Examples of dissemination activities include distribution of leaflets and posters, educational sessions on the use of the questionnaire in the follow-up of patients, development of clinical studies, collaborations with professional organisations and health authorities, and the inclusion of CARAT in clinical guidelines. The adoption of innovations is an important challenge in healthcare today, and research on the degree of success of dissemination strategies using suitable methods and metrics is much needed. We propose that CARAT can be used in a range of settings and circumstances in primary care for clinical, research and audit purposes, within the overall aim of increasing awareness of the level of disease control and strengthening the partnership between patients and doctors in the management of asthma and rhinitis.
{"title":"Control of Allergic Rhinitis and Asthma Test (CARAT): dissemination and applications in primary care.","authors":"Pedro Azevedo, Jaime Correia de Sousa, Jean Bousquet, António Bugalho-Almeida, Stefano R Del Giacco, Pascal Demoly, Tari Haahtela, Tiago Jacinto, Vanessa Garcia-Larsen, Thys van der Molen, Mário Morais-Almeida, Luis Nogueira-Silva, Ana M Pereira, Miguel Román Rodríguez, Bárbara G Silva, Ioanna G Tsiligianni, Hakan Yaman, Barbara Yawn, João A Fonseca","doi":"10.4104/pcrj.2013.00012","DOIUrl":"https://doi.org/10.4104/pcrj.2013.00012","url":null,"abstract":"<p><p>Asthma frequently occurs in association with allergic rhinitis and a combined management approach has been suggested. The Control of Allergic Rhinitis and Asthma Test (CARAT) is the first questionnaire to assess control of both diseases concurrently. However, to have an impact on healthcare it needs to be disseminated and adopted. In this paper we discuss the dissemination of CARAT in different countries and its possible applications in primary care. At present, the adaptation of CARAT for use in different languages and cultures is being led by volunteer researchers and clinicians in 15 countries. Website and smartphone applications have been developed, and a free open model of distribution was adopted to contribute to the dissemination of CARAT. Examples of dissemination activities include distribution of leaflets and posters, educational sessions on the use of the questionnaire in the follow-up of patients, development of clinical studies, collaborations with professional organisations and health authorities, and the inclusion of CARAT in clinical guidelines. The adoption of innovations is an important challenge in healthcare today, and research on the degree of success of dissemination strategies using suitable methods and metrics is much needed. We propose that CARAT can be used in a range of settings and circumstances in primary care for clinical, research and audit purposes, within the overall aim of increasing awareness of the level of disease control and strengthening the partnership between patients and doctors in the management of asthma and rhinitis.</p>","PeriodicalId":48998,"journal":{"name":"Primary Care Respiratory Journal","volume":"22 1","pages":"112-6"},"PeriodicalIF":0.0,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4104/pcrj.2013.00012","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31239834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}