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Vlies BH, Walker PP. Improving the diagnosis and management of COPD. Practitioner 2015; 259 (1787):15-19

Improving the diagnosis and management of COPD

25 Nov 2015

AUTHORS

Dr Ben H Vlies MB ChB MRCP(UK), Clinical Research Fellow, Respiratory Medicine

Dr Paul P Walker BMed Sci (Hons) BM BS MD FRCP, Consultant in Respiratory Medicine

Clinical Science Centre, University Hospital Aintree, Liverpool, UK

Article

Chronic obstructive pulmonary disease (COPD) remains important not only for people with the condition and their carers but also for the health economy because of the impact on resources and costs particularly related to hospitalisation where there has been a further 13% rise since 2008 despite greater use of admission prevention schemes.

Compared with the previous audit, the 2014 national COPD secondary care audit highlighted a reduction in mortality and length of stay with better use of non-invasive ventilation and early supported discharge.1

However, deficiencies were also evident with many patients not seeing a respiratory specialist while in hospital, and oxygen prescribing and documentation of spirometry were still well below expected levels. Ongoing management was often not well coordinated. Many patients were still failing to receive smoking cessation input while inpatients and there were deficiencies in post-discharge oxygen assessment and consideration of pulmonary rehabilitation; all of which are evidence-based treatments.

In time, increasing use of discharge care bundles, see figure 1, may help to address these shortcomings.2

A COPD discharge care bundle would commonly include confirmation that:

• Inhaler technique has been checked

• The patient has an individualised written self-management plan

• Smokers have been given help to quit

• Pulmonary rehabilitation has been offered

• Follow-up spirometry and oxygen assessment has been arranged where indicated.

Diagnosis

COPD is a progressive condition. Therefore, earlier diagnosis allows earlier intervention in particular smoking cessation. It is clear that smoking stopping in early middle age where an individual has relatively mild COPD is associated with a slower decline in lung function and reduced mortality.3

Spirometry should be performed in symptomatic (breathlessness, cough, phlegm and wheeze), current or former smokers (typically ≥ 10 pack years) who are aged at least 35 years where COPD is a likely differential diagnosis.

Spirometry should be performed by a healthcare professional who has received theoretical training, then supervised practice followed by regular performance. The Association for Respiratory Technology and Physiology (www.artp.org.uk) runs high quality spirometry training courses.

COPD can be diagnosed in a patient with the relevant clinical features where there is evidence of airflow obstruction after bronchodilation.

Traditionally, airflow obstruction has been based on a FEV1: FVC ratio < 0.7 but airflow obstruction occurs naturally with aging through loss of lung elastic recoil and so use of a ‘fixed’ ratio of 0.7 can lead to overdiagnosis of COPD in older people, particularly men, and underdiagnosis in younger people, particularly women.

Consequently, there is a strong move to use standardised residuals to determine airflow obstruction ‘in the individual’ according to the Global Lung Initiative 2012 recommendations.4

Once airflow obstruction is proven and a diagnosis of COPD established (remembering that airflow obstruction is not infrequently seen in patients with asthma and bronchiectasis) then a measure of COPD severity can be made based on FEV1 expressed as a percentage of predicted value5 as shown in table 1.

Risk factors and comorbidity

In the developed world, cigarette smoking is by far the most important risk factor for COPD although exposure to certain occupational inhalants and second-hand cigarette smoke may also increase risk.

The development of severe COPD is seen in many individuals who have smoked heroin regularly for five or more years; something that occurs at an early age, often 30-40 years, and is associated with a high mortality.6

When an individual with COPD is assessed it is vital that comorbid conditions are considered and management optimised.

Cardiovascular disease and diabetes were seen most commonly in people enrolled in the 2014 national COPD audit1 and it has long been recognised that many patients with COPD die from ischaemic heart disease, heart failure and lung cancer. Osteoporosis is also very important because many patients with COPD have multiple risk factors, the use of oral and inhaled steroids is high and rib and vertebral fractures can have such a symptomatic impact.

Evaluation and assessment

The most important factor to assess is the impact that COPD has on the patient’s symptoms and quality of life and treatment should aim to address this. Patients with COPD complain of disabling breathlessness that limits their ability to walk, be active and sometimes sleep.

Chronic cough and phlegm production is burdensome and patients feel particularly unwell when suffering from an acute exacerbation with a disproportionate impact in those with frequent exacerbations.

Dyspnoea is typically assessed using the MRC dyspnoea score and exacerbation rate recorded annually. Two or more exacerbations per year is classed as frequent, and treatments known to reduce exacerbation rate should be considered.

The COPD Assessment Tool (CAT) is a simple measure of health status (see figure 2) that takes under five minutes to complete. The score ranges from 0 to 40, with a change of two points considered clinically significant. It has been assessed for use in primary care consultations.7

There is a relationship between mortality and various measurable factors including FEV1 and this has led to the development of prognostication indices. The original ‘BODE Index’ has been shown to be useful in various clinical situations but the need to perform a six-minute walking test (requiring a 30 metre corridor) generally precludes its use in primary care.

Two other indices, the DOSE index (dyspnoea, airflow obstruction, smoking and exacerbation rate) and ADO index (age, dyspnoea and airflow obstruction), have been developed and are more suited to use outside hospital.8,9

Prognostication is important when considering palliation and end of life care. It can link very effectively with the Gold Standards Framework (www.goldstandardsframework.org.uk).

Patients with COPD should expect an annual review and many of the assessments mentioned could reasonably be carried out at such a review. Performing spirometry each year can usefully identify patients with a rapid, progressive decline in lung function and allow this to be addressed. Inhaler technique should be checked at this review and also when a new type of inhaler is commenced.

This also provides an opportunity to discuss pulmonary rehabilitation, which can be repeated after a year as per guideline recommendations.10

An audit of pulmonary rehabilitation in England and Wales Pulmonary Rehabilitation: Time to breathe better was carried out in 2015 and the initial organisational results show that most programmes are delivering care consistent with national quality standards.11 However, improving referral and completion rates, ensuring availability of pulmonary rehabilitation after hospitalisation and ensuring security of funding for programmes are all areas highlighted as needing improvement. The patient outcome results are due to be published in February 2016.

Management

A review of all treatment options is beyond the scope of this article but there are multiple evidence-based COPD treatment guidelines including NICE5 and the recently updated GOLD (The Global Initiative for Chronic Obstructive Lung Disease) guidelines.12 The single most important factor is still helping patients who continue to smoke to quit.

Bronchodilator therapy

As emphasised in the 2010 NICE COPD guideline update, use of long-acting bronchodilators is recommended at an early stage for any patient with at least moderate COPD (FEV1 < 80% predicted) and symptoms, including exacerbations.

There are now multiple licensed long-acting beta-agonists (LABA) and long-acting antimuscarinic (LAMA) drugs. Both classes have been shown to be superior to their short-acting relatives with a combination providing additional benefit. There are multiple different combinations of long-acting beta agonist/inhaled corticosteroid (LABA/ICS) and more recently four new LABA/LAMA combinations have been licensed. The existing evidence base precludes broad recommendation of one particular agent over another, something which may become clearer over the following years.

One additional challenge this creates is the increase in number of different inhaler devices used to deliver these agents and it is more important than ever to check inhaler technique regularly to ensure the individual is able to use the device prescribed. An argument can be made for striving for consistency of device where possible.

Corticosteroids

For many years corticosteroids, both orally (given acutely) and inhaled (prescribed chronically), have been used to treat COPD albeit with the recognition that their efficacy is much less than when treating asthma.

Large clinical trials have shown that inhaled corticosteroids both reduce exacerbation rate and improve health status in COPD.

However, the same trials and others have shown an increased incidence of pneumonia in those prescribed inhaled corticosteroids13 though this does not lead to increased mortality. This risk is higher with inhalers containing fluticasone. This has created management challenges on how best to use these therapies in the context of an evolving evidence base.

It is important that this risk is discussed with patients and inhaled corticosteroids should only be commenced where there are clear indications. They should not be prescribed in those with mild to moderate COPD who do not have frequent exacerbations.

What to do where people are already prescribed inhaled corticosteroids is more challenging although, as with new prescriptions, it is reasonable to stop these drugs where there is no indication for their use.

If the patient has more frequent exacerbations there is evidence from the recent WISDOM trial that inhaled steroids can be gradually withdrawn with careful clinical observation for a deterioration of symptoms.14 This appears to result in a small fall in FEV1 which may or may not be progressive.

In the acute situation, a recent Cochrane review has confirmed a similar benefit from using 5-7 rather than 10-14 days of oral prednisolone at the time of an acute exacerbation15 and a five-day course is commonly prescribed.

 

Long-term antibiotics

Evidence from a large, randomised controlled trial shows that use of low-dose azithromycin, in this case taken daily, leads to a reduction in exacerbations.16 This is a potential therapeutic option in those who have frequent exacerbations and many clinicians choose to prescribe azithromycin thrice weekly.

However, the use of antibiotics is not universally accepted and the GOLD guideline does not recommend their use.12 Care should be taken to ensure no interaction with cardiac medication and patients should be warned about the rare side-effect of hearing impairment.

There remains concern about the impact of widespread prescribing on macrolide resistance, particularly with pneumococcus, and it has been suggested that this has occurred in the USA.17

Self-management and home care

Self-management remains a vital part of COPD care but it is evident from a large study from Glasgow that, according to predetermined criteria, only 40-50% of patients self-manage their condition optimally.18

Successful self-management was more common in younger people who did not live alone and in this group there was a reduction in healthcare use.

Telemonitoring appears to be suited to monitoring COPD but studies so far have been disappointing with little effect on individual quality of life or use of healthcare resources.19 In part this may relate to the day-to-day variability in COPD symptoms and consequent difficulty differentiating this from an exacerbation. Other studies are ongoing and may provide further insight as to how to use this monitoring tool.

The evidence base for use of early supported discharge schemes is robust and their use is increasing although wider expansion was a specific recommendation from the 2014 secondary care audit.1

Conclusions

COPD remains a frequent and important condition that impacts significantly upon primary care. Increasingly COPD care is delivered outside hospital in an integrated service model.

For further information the NICE5 and GOLD12 guidelines provide a comprehensive evidence-based review.

REFERENCES

1 COPD: Who Cares Matters. Royal College of Physicians of London. London. 2015. www.rcplondon.ac.uk/projects/ outputs/copd-who-cares-matters-clinical-audit-2014

2 Laverty AA, Elkin SL, Watt HC et al. Impact of a COPD discharge care bundle on readmissions following admission with acute exacerbation: interrupted time series analysis. PLoS One 2015; 10(2): e0116187. doi: 10.1371/journal.pone.0116187

3 Anthonisen NR, Skeans MA, Wise RA et al. Lung Health Study Research Group. The effects of a smoking cessation intervention on 14.5-year mortality: a randomized clinical trial. Ann Intern Med 2005;142(4): 233-39

4 Quanjer PH, Stanojevic S, Cole TJ et al. ERS Global Lung Function Initiative. Multi-ethnic reference values for spirometry for the 3-95-yr age range: the global lung function 2012 equations. Eur Respir J 2012;40(6):1324-43. doi: 10.1183/09031936.00080312

5 National Institute for Health and Clinical Excellence. CG101. Chronic obstructive pulmonary disease in over 16s: Diagnosis and management. NICE. London. 2010 www.nice.org.uk

6 Walker PP, Thwaite E, Amin S et al. The association between heroin smoking and early onset emphysema. Chest 2015 May 28. doi: 10.1378/chest.15-0236 [Epub ahead of print]

7 Gruffydd-Jones K, Marsden HC, Holmes S et al. Utility of COPD Assessment Test (CAT) in primary care consultations: a randomised controlled trial. Prim Care Respir J 2013; 22(1): 37-43. doi: 10.4104/pcrj.2013.00001

8 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. doi: 10.1016/S0140-6736(09)61301-5

9 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(12):1189-95. doi: 10.1164/rccm.200902-0271OC

10 British Thoracic Society. Guideline on Pulmonary Rehabilitation in Adults. BTS. London. 2013 www.brit-thoracic.org.uk/guidelines-and-quality-standards/pulmonary-rehabilitation-guideline

11 www.rcplondon.ac.uk/projects/outputs/pulmonary-rehabilitation-time-breathe-better

12 Global strategy for diagnosis, management, and prevention of COPD, Updated January 2015 www.goldcopd.org/Guidelines/guidelines-resources.html

13 Kew KM, Seniukovich A. Inhaled steroids and risk of pneumonia for chronic obstructive pulmonary disease. Cochrane Database Syst Rev 2014 Mar 10;3:CD010115. doi:

10.1002/14651858.CD010115.pub2.

14 Magnussen H, Disse B, Rodriguez-Roisin R et al. WISDOM Investigators. Withdrawal of inhaled glucocorticoids and exacerbations of COPD. N Engl J Med 2014;371(14):1285-94. doi:10.1056/NEJMoa1407154

15 Walters JA, Tan DJ, White CJ, Wood-Baker R. Different durations of corticosteroid therapy for exacerbations of chronic obstructive pulmonary disease. Cochrane Database Syst Rev 2014;12:CD006897. doi:10.1002/14651858.CD006897.pub3

16 Albert RK, Connett J, Bailey WC et al. COPD Clinical Research Network. Azithromycin for prevention of exacerbations of COPD. N Engl J Med 2011;365(8): 89-98. doi:10.1056/NEJMoa1104623. Erratum in: N Engl J Med 2012;366(14): 1356

17 Serisier DJ. Risks of population antimicrobial resistance associated with chronic macrolide use for inflammatory airway diseases. Lancet Respir Med 2013; 1(3): 262-74. doi:10.1016/S2213-2600(13)70038-9

18 Bucknall CE, Miller G, Lloyd SM et al. Glasgow supported self-management trial (GSuST) for patients with moderate to severe COPD: randomised controlled trial. BMJ 2012;344:e1060. doi: 10.1136/bmj.e1060

19 Pinnock H, Hanley J, McCloughan L et al. Effectiveness of telemonitoring integrated into existing clinical services on hospital admission for exacerbation of chronic obstructive pulmonary disease: researcher blind, multicentre, randomised controlled trial. BMJ 2013;347:f6070

PRESET SEARCHES

NICE evidence search

COPD treatment

PubMed

COPD primary care review

Global Initiative for Chronic Obstructive Lung Disease: 2017 Pocket guide

GOLD (2017) Pocket Guide

The 2017 GOLD guide states a refinement of their established ABCD GOLD grade assessment tool in which ABCD groups will be derived exclusively from patient symptoms and their history of exacerbation.(see pages 7-8)

In the GOLD refined assessment scheme, patients should undergo spirometry to determine the severity of airflow obstruction (GOLD 1-4). They should then undergo assessment of either dyspnoea (using MRC) or symptoms (CAT) and  their history of exacerbations (including prior hospitalisations) should be recorded.

This classification scheme may facilitate consideration of individual therapies (exacerbation prevention vs symptom relief) and also help guide escalation and de-escalation treatment strategies for individual patients. (see pages 23-24 especially)