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Practitioner 2010; 254 (1734): 19–24
Opportunistic case finding pivotal in diagnosing COPD
23 Nov 2010
AUTHORS
Dr Paul P Walker BMedSci (Hons) BM BS MD FRCP
Consultant in Respiratory Medicine, University Hospital Aintree, Liverpool
Article
Diagnosis, management and delivery of care for patients with chronic obstructive pulmonary disease (COPD) remains an important issue for clinicians. COPD accounts for more than 10% of emergency hospital admissions.
The 2008 National COPD Audit showed that the 90-day mortality rate after a COPD hospitalisation was 13.9% and almost one in three patients discharged from hospital were readmitted within three months.1
Over the past decade a huge number of publications have strengthened the evidence base which is the foundation for COPD management while the development of a National Clinical Strategy for COPD2 and the 2010 update to the NICE COPD guidelines3 should help implementation of an evidence-based approach to management. At the time of writing the consultation phase of the National Clinical Strategy had been completed but no publication date had been set.
Diagnosis
The principle of COPD diagnosis is based on establishing the presence of obstructive post-bronchodilator spirometry in an at-risk individual with appropriate symptoms (see figure 1). The case for screening the whole population for COPD has yet to be made so diagnosis is focused on opportunistic case finding.
In the UK, COPD is very rarely seen before 35 years of age and is rare below 45 unless there is an extensive history of opiate (heroin or crack) smoking.
In addition, most individuals diagnosed with COPD have substantial cigarette smoke exposure and while specific occupational factors may contribute to the development of COPD most people diagnosed have smoked more than 10 and usually 20 pack years.
Finally, individuals with COPD usually have symptoms of cough and phlegm, exertional breathlessness, wheezing, recurrent winter bronchitis or a combination of these symptoms. A current or ex-smoker, aged over 35, with respiratory symptoms should undergo spirometry testing.
The hallmark of COPD is the presence of airflow obstruction after administration of a bronchodilator (usually inhaled or nebulised salbutamol).3 Hence, if the ratio of forced expiratory volume in 1 second (FEV1) to forced vital capacity (FVC) is less than 0.7 after bronchodilation this suggests a diagnosis of COPD (see figure 2).
There are two important caveats. The first is that while normal spirometry excludes COPD, obstructive spirometry is seen in asthma and bronchiectasis emphasising the importance of clinical features. Second, older individuals, in particular men, may have marginally obstructive spirometry due to aging-related loss of lung elastic recoil.
Spirometry needs to be performed by an appropriately trained individual who is doing the test regularly. A variety of training courses exist including many supported by the Association of Respiratory Technology and Physiology.
Assessment of severity
A further significant change introduced in the 2010 NICE guideline is the new grading system for COPD severity.3 Since 2005 the UK has been out of step with other countries but the new severity classification (see table 1) brings us into line with the European, American and GOLD (global) guidelines.4
A system based on FEV1 alone oversimplifies disease severity and full clinical assessment should include symptoms, frequency of exacerbations and impact of disease on functioning and health status.
A variety of prognostication indices have been developed and two recently published indices, ADO5 and DOSE6, are potentially applicable in primary care as they no longer require a formal assessment of exercise capacity.
Treatment
Current treatment for COPD is listed in table 2. The most important single intervention is smoking cessation as this is proven to reduce decline in FEV1 and reduce mortality. There is clinical trial evidence for efficacy of nicotine replacement, bupropion, varenicline and nortriptyline in improving quit rates. In addition, there is also evidence that influenza vaccination improves outcomes in COPD. Pulmonary rehabilitation benefits patients with COPD who are functionally limited by breathlessness and is addressed in more detail below.
Guidance on inhaler therapy was recently updated by NICE and is summarised in figure 3.3 Long-acting bronchodilator therapy (tiotropium, salmeterol, formoterol and indacaterol) is recommended at an early stage for patients with an FEV1 of greater than 50% predicted with combination long-acting beta agonist/inhaled corticosteroid inhalers generally reserved for patients with an FEV1 of less than 50% predicted and/or frequent exacerbations.
The role of mucolytics is still unclear although there is evidence that the drugs reduce exacerbation rates in patients not taking inhaled corticosteroids.7,8 A therapeutic trial may be worthwhile in certain cases. The newly licensed PDE4 inhibitor roflumilast may benefit some patients, in particular those with symptoms of chronic bronchitis.9,10The current UK licence is for treatment in patients with an FEV1 of
The primary aims of treatment are to improve symptoms such as breathlessness, exercise capacity, activity and sleep quality and to reduce exacerbations. It should be noted that generally no single treatment is transformative and treatment usually involves a combination of multiple therapies.
Pulmonary rehabilitation
Pulmonary rehabilitation is based on the principle that peripheral muscle training can help reverse the effects of deconditioning usually associated with COPD (as well as a number of other respiratory conditions). The evidence base for rehabilitation is very strong with positive effects shown on breathlessness, exercise capacity, activity level, exacerbation rate, leg muscle strength and quality of life.11, 12 Efficacy has been shown in patients who are functionally limited (MRC grade 2-5). However, it is important to optimise treatment before rehabilitation as this may improve the benefit obtained.
Particular benefit has been shown for rehabilitation early after a COPD exacerbation13 and there is evidence that repeat rehabilitation is helpful in the majority of patients.14
Referral
The vast majority of patients with COPD are managed in primary and/or intermediate care but there are circumstances where secondary care assessment should be sought. In 2008 the BTS issued a statement on criteria for specialist referral, admission, discharge and follow-up for adults with respiratory disease (see table 3, p23).15
End of life care
Death is a common outcome for patients with COPD, approximately 25,000 COPD patients in England and Wales die each year. Around 1 in 12 patients hospitalised because of COPD die in hospital. It is increasingly recognised that many patients with COPD could benefit from improved end of life care; however, it is difficult to predict mortality risk in COPD patients. A number of factors are associated with higher mortality including lower FEV1, older age, severe breathlessness, lower body mass index and poorer exercise capacity. However, even where a number of poor prognostic features are present at the time of assessment there remains up to a 30% chance that the patient will be alive after five years. End of life care is recognised as an area that would benefit from greater study.
Conclusions
Accurate diagnosis remains vital in patients with COPD and opportunistic case finding is advocated. Recent research has clarified the role of a variety of therapies with the cornerstones of treatment remaining smoking cessation, pharmacological treatment and pulmonary rehabilitation. The National Clinical Strategy for COPD should clarify a framework covering prevention, diagnosis, treatment and end of life care.
REFERENCES
1 Report of the National Chronic Obstructive Pulmonary Disease Audit 2008: Clinical audit of COPD exacerbations admitted to acute NHS units across the UK. Available at: www.rcplondon.ac.uk/clinical-standards/ceeu/Currentwork/ncrop/Pages/audit.aspx.
2 www.dh.gov.uk/prod_consum_dh/groups/dh_digitalassets/@dh/@en/documents/digitalasset/dh_113279.pdf
3 National Institute for Health and Clinical Excellence. CG101. Chronic obstructive pulmonary disease: Management of chronic obstructive pulmonary disease in adults in primary and secondary care (partial update). NICE. London. 2010
4 Global Strategy for Diagnosis, Management, and Prevention of COPD 2009 Update. www.goldcopd.com/Guidelineitem.asp?l1=2&l2=1&intId=2003
5 Puhan MA, Garcia-Aymerich J, Frey M et al. Expansion of the prognostic assessment of patients with chronic obstructive pulmonary disease: the updated BODE index and the ADO index. Lancet 2009;374(9691):704-11
6 Jones RC, Donaldson GC, Chavannes NH et al. Derivation and validation of a composite index of severity in chronic obstructive pulmonary disease: the DOSE Index. Am J Respir Crit Care Med 2009;180:1189-95
7 Decramer M, Rutten-van Mölken M, Dekhuijzen PN. Effects of N-acetylcysteine on outcomes in chronic obstructive pulmonary disease (Bronchitis Randomized on NAC Cost-Utility Study, BRONCUS): a randomised placebo-controlled trial. Lancet 2005; 365(9470):1552-60
8 Zheng JP, Kang J, Huang SG et al. Effect of carbocisteine on acute exacerbation of chronic obstructive pulmonary disease (PEACE Study): a randomised placebo-controlled study. Lancet 2008;371(9629):2013-8
9 Calverley PM, Rabe KF, Goehring UM et al. M2-124 and M2-125 study groups. Roflumilast in symptomatic chronic obstructive pulmonary disease: two randomised clinical trials. Lancet 2009;374(9691):685-94
10 Fabbri LM, Calverley PM, Izquierdo-Alonso JL et al. M2-127 and M2-128 study groups. Roflumilast in moderate-to-severe chronic obstructive pulmonary disease treated with longacting bronchodilators: two randomised clinical trials. Lancet 2009; 374(9691):695-703
11 Griffiths TL, Burr ML, Campbell IA et al. Results at 1 year of outpatient multidisciplinary pulmonary rehabilitation: a randomised controlled trial. Lancet 2000; 355(9201):362-8
12 Walker PP, Burnett A, Flavahan PW et al. Lower limb activity and its determinants in COPD. Thorax 2008;63(8):683-9
13 Seymour JM, Moore L, Jolley CJ et al. Outpatient pulmonary rehabilitation following acute exacerbations of COPD. Thorax 2010;65(5):423-8
14 Ries AL, Make BJ, Lee SM et al. National Emphysema Treatment Trial Research Group. The effects of pulmonary rehabilitation in the national emphysema treatment trial. Chest 2005;128(6):3799-809
15 BTS statement on criteria for specialist referral, admission, discharge and follow-up for adults with respiratory disease. Thorax 2008;63(Suppl I):i1-i16
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