Salford COPD Treatment Pathway

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Salford COPD Treatment Pathway Development led by Helen Pyne with Salford Asthma and Respiratory Team (SART) Department Respiratory Medicine Salford Royal NHS Foundation Trust Hope Hospital, Stott Lane, Salford, M6 8HD Page 1 of 7

I II III Start at the level appropriate to the patient s symptoms Diagnosis of COPD Salbutamol / Terbutaline Aerosol 1-2 puffs PRN (MDI) (or equivalent) via appropriate device suited to the individual s lifestyle and preference Salbutamol Aerosol 2 puffs QDS (MDI) or Terbutaline Aerosol 2 puffs QDS (MDI). Plus 2 puffs PRN (or equivalent) via appropriate device suited to the individual s lifestyle and preference Salbutamol / Terbutaline Aerosol 2 puffs QDS (MDI) plus 2 puffs PRN (or equivalent) Plus ADD IN Ipratropium Bromide Aerosol 2 puffs QDS (MDI) via appropriate device suited to the individual s lifestyle and preference Note for COPD Diagnosis Post bronchodilator FEV 1 <80% predicted FVC/FEV 1 ratio <70% at 6 seconds or SVC Lung function that does not change markedly over several months Check Alpha 1 antitrypsin if severe COPD in individuals under 40-50yrs. If positive screen family Common symptoms Morning cough Recurrent respiratory infections Shortness of breath on vigorous exertion / manual labour Sputum production Smoking Cessation Provide advice, support and NRT or Zyban as appropriate. Refer to advisor if additional support required. Keep a record of the patients smoking history. Depression A large proportion of COPD patients experience depression at some time. Consider depression and appropriate management through counselling and/or prescription drugs Spirometry Recommended periodically establishing the speed of deterioration and stage of disease process and variability if any. Continued Page 3 Serial Peak Expiratory Flow Monitoring Recommended if reversible element to obstruction suspected Flu & Pneumonia Vaccinations Recommended Influenza vaccination every October / November to all COPD patients and single Pneumonia vaccine. Omit if the patient has an egg allergy or previous sensitivity. Page 2 of 7

IV From Page 2 Salbutamol Aerosol 4 puffs QDS (MDI) Plus 2 puffs PRN (or equivalent) Plus Ipratropium Bromide Aerosol to 4 puffs QDS (MDI) via inhaler device suited to the individual s lifestyle and preference Combined Therapies Are to be considered only when optimum therapies have been established. If these therapies are initiated before drug effectiveness has been established optimum therapy will be difficult to identify. Combined therapies may aid patient concordance because of, convenience and tolerability, therefore effectiveness of the drugs. Combined Therapies (During Trials of Treatment) Are only recommended during trials of treatment, if concordance, cost, convenience or tolerability is highlighted as a problem. V VI Salbutamol Aerosol 2-6 puffs PRN / QDS (MDI) (or equivalent) Via inhaler device most suited to the individuals lifestyle and preference STOP Ipratropium Bromide Aerosol 4 puffs QDS (MDI) Plus ADD IN Tiotropium Bromide 1 cap (18mcg) OD via handihaler STOP Tiotropium Bromide for a period of 4/52 ADD IN Salmeterol Aerosol 2 puffs BD (MDI) (or equivalent) Plus Ipratropium Bromide Aerosol 2-4 puffs QDS (MDI) Salbutamol Aerosol 2-6 puffs PRN / QDS (MDI) (or equivalent) Via inhaler device most suited to the individual s lifestyle and preference Continued Page 4 (CONSIDER AFTER VIII) Theophyllines May be considered for a trial period once all other therapies have been trialed. Uniphyllin Continuous 200mg BD for 1 week then increases to 300mg BD. Over 70kg can increase to 400mg BD. If effective continue and monitor levels annually. Measure PEAK blood level 6 hours post dose. Target range is 55-110 micromol/litre. Exacerbation of COPD At any stage exacerbation can occur Worsening of previously stable condition Sputum purulence Increased sputum volume Increased wheeze Increased dyspnoea Chest tightness Fluid retention Treatment Increase short acting Beta II agonist usage, upto 6 puffs QDS (MDI) + 2 PRN or equivalent Short course of oral steroids 30-40mgs for 5-14 days. Antibiotics : If fever, leukocytosis or purulent sputum. Amoxicillin 500mg TDS - 7 DAYS (21 capsules). If patient has an allergy to penicillin use Erythromycin 500mgs QDS - 7 DAYS (28 capsules) Page 3 of 7

VII From Page 3 Stop Ipratropium Bromide Aerosol 2-4 puffs QDS (MDI). Reintroduce Tiotropium Bromide 1 cap (18mcgs) OD Plus continue Salmeterol Aerosol 2 puffs BD (MDI) (or equivalent) Plus continue Salbutamol Aerosol 2-6 puffs PRN (MDI) (or equivalent) Via inhaler device most suited to the individual s lifestyle and preference Inhaled Steroids Are not routinely recommended for COPD patients. Nonetheless are recommended for prevention of recurrent exacerbation. FEV 1 <50% predicted with TWO exacerbations of COPD requiring antibiotics and oral steroids over the previous 12 months. Discontinue Tiotropium Bromide. Continue Salmeterol Aerosol 2 puffs BD (MDI) (or equivalent) if previous benefit noted. Via inhaler device most suited to the individual s lifestyle and preference VIII Inhaled Steroid If FEV 1 <50% predicted with 2 exacerbations of COPD requiring antibiotics and oral steroids over the previous 12 months. A minimum effective dose of inhaled steroid Beclomethasone Dipropionate 1000mcgs or equivalent. DAILY IN TWO DIVIDED DOSES Via inhaler device most suited to the individuals lifestyle and preference. Advise the patient to rinse their mouth after use. For patient on inhaled steroid and LABA it is cost effective to use Seretide 500/50 Accuhaler 1 puff BD WEEKS 1 AND 2 This stage based in dedicated clinic Salbutamol 2.5mg nebule 1 QDS Plus Ipratropium Bromide Aerosol 4 puffs QDS Plus Salbutamol Aerosol 2 puffs PRN Plus Salmeterol Aerosol 2 puffs BD if previous benefit noted WEEKS 3 AND 4 This stage based in dedicated clinic Salbutamol 5mg nebule 1 QDS Plus Ipratropium Bromide Aerosol 4 puffs QDS Plus Salbutamol Aerosol 2 puffs PRN Plus Salmeterol Aerosol 2 puffs BD if previous benefit noted WEEKS 5 AND 6 This stage based in dedicated clinic Combivent nebule 1 QDS Plus Salbutamol Aerosol 2 puffs PRN Plus Salmeterol Aerosol 2 puffs BD if previous benefit noted Decide with the patient which treatment has been most effective Nebulised Drug Therapies It is recommended that nebulised drugs should not be prescribed for any COPD patient that has purchased their own nebuliser until assessment completed at the hospital. Discourage any COPD patients from purchasing his or her own compressor and nebuliser unit. It is important not to compromise appropriate drug assessment, machine servicing, disposables replacement, education and condition monitoring Mucolytics Should be discussed with the patient by the hospital team if more than three exacerbations requiring antibiotics and oral steroids within a twelve-month period, despite inhaled steroids. Nebuliser Assessment Referral Any patient diagnosed with COPD that experience symptoms affecting their activities of living. Patients treated at Stage III and above. Optimisation of therapies must be established through trials of treatment. They may or may not require nebulised therapies. Nebulised Therapies If Nebulised Therapies are required the hospital will provide the compressor unit (with replacement filters) on long-term loan. The unit will be serviced annually. Durable nebuliser sets will be provided and replenished annually. Back up Inhalers Will be required for emergency use if compressor unit or nebuliser set are not working effectively and for PRN doses. Page 4 of 7

Consultant Referral 3 exacerbations in 12 month period Stridor Symptoms disproportionate to lung function deficit Rapid decline in FEV 1 Uncertain diagnosis / dysfunctional breathing Supervised withdrawal from long-term oral steroids for COPD Onset cor-pulmonale Assessment for pulmonary rehabilitation Severe COPD Assessment for Long Term Oxygen Therapy Assessment for nebuliser therapy Pulmonary Rehabilitation Exclusion Cognitive impairment Unstable angina Unstable cardiac disease Inclusion Agree to attend programme bi-weekly for 6 weeks Respiratory diagnosis Seen within last 12 months by respiratory physician or Respiratory Nurse Specialist (refer as appropriate) Therapy optimised Outcome Assessments for Trials of Treatments Start the patient at level appropriate to their lung function and symptoms. All trials of treatment must be assessed with both objective and subjective outcome measures. If neither an objective nor subjective improvement noted the treatment should be discontinued. If symptoms persist then continue down the pathway until optimum therapy established. At any stage of the pathway if symptoms are controlled then optimum therapy has been established. If little or no response to treatment consider concurrent or alternative diagnosis. Provide a written self-management plan to all patients with contact number. Page 5 of 7

N.B. OXYGEN PRESCRIBING WILL CHANGE IN 2006 Long Term Oxygen Therapy (LTOT) High Usage PRN Oxygen Therapy (Concentrator) (Concentrator) Diagnosis of COPD Breathless at rest or on exertion Refer to the hospital for assessment If SaO 2 <92% on room air at rest when condition stable or 6 weeks post exacerbation. Arterial or Earlobe Blood Gas Sample obtained PaO 2 <7.3kPa (or with right-sided heart failure <8kPa) on room air at rest when condition stable or 6 weeks post exacerbation Obtain informed consent and complete order form NB Back-up cylinder will be required for emergency use if electrical power failure or concentrator break-down Assessment Overnight assessment on the Medical Investigation Unit to establish appropriate percentage and flow rate Diagnosis of severe COPD, FEV 1 <30% Breathless at rest Refer to the hospital for assessment If SaO 2 >92% on room air at rest when condition stable or 6 weeks post exacerbation. Arterial Blood Gas (ABG) Sample obtained to identify CO 2 levels PaO 2 >7.3kPa (or with right-sided heart failure >8kPa) on room air at rest when condition stable or 6 weeks post exacerbation Using more than 5 cylinders of oxygen per month Unable to tolerate even short periods without oxygen Obtain informed consent and refer to the fire brigade NB Back-up cylinder will be required for emergency use if electrical power failure or concentrator break-down Assessment Overnight assessment on the Medical Investigation Unit to establish appropriate percentage and flow rate Guidelines for O 2 assessment will be circulated when available LTOT / High Use PRN Oxygen Therapy Back-up cylinder will be required for emergency use if electrical power cut or concentrator breakdown Ambulatory Oxygen Assessment Diagnosis of COPD Breathlessness on exertion when stable condition (6 weeks post exacerbation). Exercise oximetry proves significant desaturation (<90% for >30 seconds) Physical ability to mobilise Independently outside the house for more than 2 hours on more than 2 occasions a week SaO 2 >92% at rest, if 92% or below refer for LTOT assessment Assessment is required Differentiating Between LTOT and High Use PRN Oxygen Therapy Long Term Oxygen Therapy (LTOT) is a term used for oxygen administered to hypoxic patients (PaO 2 <7.3kPa) for a minimum of 15 hours per day. Some patients may benefit from improved symptoms and others may benefit from extended life expectancy. High use PRN oxygen is administered to patients experiencing disabling breathlessness with PaO 2 above 7.3kPa. PRN Oxygen Assessment Diagnosis of COPD Breathlessness on exertion even when condition is stable (6 weeks post exacerbation). PaO 2 >92% at rest, if 92% or below assess for LTOT Assessment is required. Advise when to clean and replace mask / mouth-piece Advice sheet available Note that the evidence-base for PRN oxygen therapy is very weak at present Obtain informed consent and complete order form PRN O 2 not advised for patients who continue to smoke Page 6 of 7

Hospital Referrals All general referrals will be pooled to Respiratory s. Nonetheless, referrals for patients with specific respiratory conditions will be passed onto the consultant physician with expertise in that area e.g. interstitial lung disease, cancer, TB, bronchiectasis, sleep apnoea. Dr Ronan O Driscoll Clinical Director for Respiratory Medicine Secretary : Kath Rayson - 206 5154 Fax - 206 4328 Dr Peter Turkington Respiratory & General Medicine Consultant Secretary : Jane Browne - 206 5155 Dr Murad Ghrew Respiratory & Intensive Care Consultant Secretary : Jane Brown - 206 5155 Dr Simon Taggart Respiratory & General Medicine Consultant Secretary : Win Duffy - 206 4039 Dr Paul Sullivan Respiratory & Acute Medicine Consultant Secretary : Tina Smethurst - 206 2020 Helen Pyne Lead Respiratory Nurse & Advanced Practitioner Telephone - 206 1604 Bleep Number - 3496 Norma Linaker, Vicky Sharples, Viv Johnson & Tom Woodrow Respiratory Nurse Specialists Telephone - 206 4423 Fax - 206 4691 Elaine Myers Respiratory Pharmacist. Bleep Number - 3115 Liz Bradshaw TB Nurse Specialist. Telephone - 0161 212 4167 Jeanette Murray Lung Cancer Nurse Specialists. Telephone - 206 1498 Melanie Bainbridge Smoking Cessation. Telephone - 0161 212 4050 Page 7 of 7