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Prolonged mucolytic therapy in patients with diagnosed COPD

Working Party – Rudolf, Bellamy, Burrill, Scullion & Thomas

  • This guideline is intended to complement the NICE COPD guideline’s recommendations on mucolytic therapy and provide further guidance on its use in patients with COPD who have the common symptoms of chronic, troublesome cough and sputum production
  • Underdiagnosis of COPD is a problem in the UK. Patients who present with frequent cough and sputum, or frequent ‘respiratory infections’, should be assessed for the presence of underlying COPD (including the use of spirometry), particularly if they have a significant smoking history
  • Cough and sputum production can affect the patient’s quality of life
  • The primary aims of mucolytic therapy are to improve cough and ease sputum expectoration. Associated benefits, e.g. less breathlessness and less frequent coughing, may also be noticed

Assessment

  • Assessment is subjective and should aim to identify those patients in whom cough and sputum are troublesome
  • It may be helpful to ask about:
    • colour/consistency and amount of sputum
    • difficulty of expectoration
    • timing and duration of symptoms
    • quality of life issues, e.g. embarrassment
    • willingness to consider drug treatment
    • history and frequency of COPD exacerbations
  • Management with mucolytic therapy can be considered for adult patients who:
    • have a confirmed diagnosis of COPD
    • have cough and sputum on most days for 3 months, in 2 consecutive years
    • are in a chronic, stable but symptomatic state
  • Mucolytic therapy is not suitable if patients:
    • have COPD but do not have long-standing, troublesome cough and sputum
    • have copious, watery sputum
  • Consider differential diagnoses:
    • lung cancer
    • bronchiectasis
    • rhinitis or post-nasal drip

Managing cough and sputum

  • Symptoms should be managed according to their duration:
    • year-round symptoms may require year-round treatment
    • seasonal symptoms normally require treatment only for the duration of the symptomatic period

Initial trial of therapy

  • Trial carbocisteine/mecysteine therapy for 4–6 weeks, at the recommended initial fixed dose
  • Discuss points to consider during the trial period with the patient:
    • quantity and colour of sputum
    • ease of expectoration
    • amount of coughing

Review at 4–6 weeks

  • Review criteria are subjective, based on the patient’s perception of how their cough and sputum have changed
  • It may be helpful to ask the following:
    • is your sputum easier to cough up?
    • has the amount or colour changed?
    • is your cough less bothersome?
    • have you noticed improvement in any other COPD-related symptom?
    • have you noticed any new problems that might be related to the drug?
    • are you happy to continue with therapy?

Continuing therapy

  • Continue therapy if:
    • patient reports improvement in cough and sputum production/expectoration
    • no unacceptable side-effects
    • patient perceives benefit in mucolytic therapy
  • Therapy for seasonal symptoms:
    • repeat annually, if still of benefit and acceptable to the patient
  • Therapy for year-round symptoms
    • less well supported by evidence, but reasonable to continue treatment on long-term basis
    • reduce dose to minimum required for effective symptom control
    • assess continuing benefits of therapy annually

Prolonged mucolytic therapy in patients with diagnosed COPD continued

Reducing COPD exacerbations

  • Treatment with mucolytics may be associated with a reduction in acute exacerbations of COPD
  • Long-term treatment with mucolytics can therefore be useful in patients who have repeated, prolonged or severe exacerbations of COPD
  • Exacerbation reduction is seen especially in patients not already taking inhaled corticosteroids. Thus, patients who are not tolerant of, or do not wish to take, inhaled corticosteroids (which NICE guidance recommends should always be given in a combination inhaler together with a long-acting β2-agonist) could be considered for prophylactic treatment with mucolytic therapy if they have:
    • chronic, troublesome cough and sputum production
    • frequent exacerbations (at least two per year)
  • Patients who experience frequent exacerbations require additional interventions, in keeping with the NICE COPD guideline, and mucolytic therapy should not routinely be used to prevent exacerbations

Trial of therapy

  • Carbocisteine/mecysteine therapy for prophylaxis of COPD exacerbations should be trialled at the initial fixed dose recommended by the individual product’s SPC, and only continued if there is a documented reduction in exacerbation frequency and/or improvement in patient symptoms

Continuing therapy

  • Mucolytic therapy for prophylaxis of exacerbations should be continued at the initial fixed dose for the duration of the normal exacerbation period (usually 3–6 months), provided that the patient is willing to continue with therapy, and that there are no unacceptable side-effects
  • Therapy should be repeated annually, if still acceptable and of benefit to the patient

Mucolytic therapy in patients with diagnosed COPD and troublesome cough and sputum

mucolytic

about this working party guideline…
sponsor— The development of this working party guideline has been sponsored by Teva UK Limited. This consensus guideline is an update to a previous version published in October 2007. Both versions of the guideline have has been developed by MGP Ltd, the publishers of Guidelines, and the Working Party was convened by them. Teva UK Limited was able to recommend experts for the working party group and comment on the scope and title, with final decisions resting with the Chair. Teva UK Limited had the opportunity to comment on the technical accuracy of both versions of the guideline but the content is independent of and not influenced by Teva UK Limited
working party members— Dr Michael Rudolf (chair, consultant physician), Dr David Bellamy (general practitioner), Peter Burrill (specialist pharmaceutical adviser for public health), Jane Scullion (respiratory nurse consultant), Dr Mike Thomas (general practitioner)
further information— call MGP Ltd (01442 876100) for further information and a copy of the full guideline
September 2010
MUC/10/013a

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eGuidelines.co.uk (22 May 2012)
© 2012 MGP Ltd
Updated guideline: Oct 10
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