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    Palliative medicine andnon-malignant, end-stagerespiratory disease

    MADONNA R. BACORRO. M.D.SHPM fellow 2012UP-PGH

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    HIV-related respiratory diseases

    post-tuberculous

    bronchiectasis

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    USA and Europe

    COPD

    cystic fibrosis

    restrictive chest wall diseases (e.g. scoliosis,thoracoplasty)

    neuro-muscular disorders (e.g. muscular

    dystrophies, old poliomyelitis)

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    pathophysiological causes of dyspnoeaPathophysiological mechanism Typical causes

    Increased respiratory drive

    Hypoxaemia Many respiratory and cardiac diseases

    Metabolic acidosis Renal failure, cardiac failure

    Intrapulmonary receptor stimulation Infiltrative disease, pulmonary oedema

    Mechanical impedence

    Airflow obstruction Asthma, COPD, tumour, stenosis

    Mechanical chest wall restriction Kyphoscoliosis, obesity, pregnancy

    Reduced compliance (stiff lungs) Interstitial fibrosis, lymphangitiscarcinomatosis

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    pathophysiological causes of dyspnoeaPathophysiological mechanism Typical causes

    Respiratory muscle failure

    Muscle disease/paralysis Poliomyelitis, muscular dystrophy

    Mechanical disadvantage Hyperinflation, pneumothorax, pleuraleffusion

    Intrapulmonary receptor stimulation Hyperinflation, pneumothorax, pleuraleffusionInfiltrative disease, pulmonaryoedemaWasted ventilation

    Large vessel obstruction Pulmonary emboli, pulmonary vasculitis

    Capillary damage Interstitial lung disease, emphysema

    Psychological

    Anxiety, depression Hyperventilation syndrome

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    Assessment of dyspnoea

    good history and examination

    Diagnostic testing

    measurement of the severity of dyspnoea aidsdecision making and may indicate the success

    of a particular therapy

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    Table 7 Modified Borg Dyspnoea Scale(72)

    Intensity of sensation Rating

    Nothing at all 0Very, very slight 0.5

    Very slight 1

    Slight 2

    Moderate 3Somewhat severe 4

    Severe 5

    6

    Very severe 7

    8

    Very, very severe 9

    Maximal 10

    The visual analogue scale

    uses a 10 cm line, with nobreathlessness andmaximum breathlessnessat the two ends.

    Verbally reported

    intensity: reproducibleratings of dyspnoeaintensity can be made onlinear or numerical scales.

    Simple verbal numerical

    scales rate dyspnoea from0 to 10.

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    Clinical implications of

    cough

    preventing sleep interrupting communication causing social embarrassment

    Others:

    haemodynamic changes (e.g.arrhythmias, hypotension)

    ruptured vessels (e.g. eyes, nasal,bronchial)

    urinary incontinence hernia neurological problems (e.g. syncope,

    headache)

    lung barotrauma (e.g. pneumothorax), rib fractures

    Excessivecough

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    Treatment of the causeProtussive therapy:

    makes cough more

    effective

    Adequate hydration,steam inhalations, andnebulized saline.

    Physiotherapy

    Pharyngeal suctioning

    Mini-tracheostomy

    Pharmacological

    Antitussive therapy:prevents or eliminates

    cough

    Opioids

    Oral local anaesthetics Nebulized local

    anaesthetics

    Other antitussive agents

    Antimuscarinics

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    Oral local anaesthetics

    benzonate (200 mg 8 hourly) is related toprocaine and inhibits stretch receptors.

    Levodroproizine modulates C-fibre activity

    and suppresses cough as well asdihydrocodeine but with less sedation.

    Benzocaine and lignocaine lozenges may be

    useful for laryngeal, pharyngeal, or trachealirritation but the risk of aspiration must beconsidered.

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    Nebulized local anaesthetics

    lignocaine (5 mL of 2 per cent solution 6hourly) and bupivacaine (5 mL 0.25 per centsolution 6 hourly) have been used for

    intractable cough but they can causebronchospasm requiring bronchodilators.

    Efficacy has not been established

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    Other antitussive agents

    theophyllines and 2-agonists Sodium cromoglycate

    Steroids

    antihistamine-decongestant (e.g.pseudoephedrine, dexbrompheniramine) andexpectorant (e.g. guaifenesin) preparations

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    Antimuscarinic

    Antimuscarinic bronchodilators

    Hyoscine hydrobromide (0.4 mg sc prn) orglycopyrronium bromide (0.4 mg im prn) may be

    essential for the control of the distressing chestrattle due to loose secretions in the terminalphase of chronic lung disease.

    Both cause sedation and dysphoria and

    occasionally, in the elderly, central anticholinergicsyndrome with excitement, ataxia, andhallucinations.

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    chest radiography

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    Chest pain

    Musculoskeletal

    disorders

    Pleuropulmonary

    disorders

    Visceral and other

    disorders

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    Relatives should be warned and drugsimmediately available.

    Simple measures like the use of green towels

    and bed linen to mask the evidence of blood,nursing the patient with the affected chestside down, and the calming influence of acontrolled situation are invaluable. Palliative

    treatment should aim to reduce awarenessand fear. Both opioid and anxiolytic therapymay be required.

    Management of massive haemoptysis

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    Respiratory failure(COPD)

    (a) pharmacological therapies: to reduceairways obstruction, correct hypoxaemia, andrelieve dyspnoea

    (b) non-pharmacological therapies: toimprove respiratory musclefunction/ventilation and enhance gas

    exchange.

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    Palliative oxygen therapy In patients with refractory hypoxaemia despite

    high flow rate oxygen, a nasal reservoir (e.g.oximizer), which stores oxygen during

    expiration and delivers a larger bolus at theonset of inspiration, may be useful.

    A blood gas should be measured or end tidalCO2 checked to confirm hypercapnea and theoxygen flow rate reduced whilst monitoringCO2 and mental function.

    Drug treatment for the relief of

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    Drug treatment for the relief ofdyspnoea

    Anxiolytic agents and promethazine

    Antidepressant drugs

    Oral opioids Nebulized opioids

    Mucolytics

    Other drugs

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    Non-pharmacological therapies

    Vaccinations: Influenza and pneumococcal

    General nursing

    Nutrition

    Physiotherapy

    Controlled breathing techniques

    Non-invasive mechanical ventilation

    Lung reduction surgery and lungtransplantation

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    Interstitial/fibrotic lung disease

    Immunosuppressive therapy includingsteroids, cyclophosphamide, azothioprine, andpenicillamine

    It is rare for CO2 retention to occur and it issafe to use high inspired concentrations ofoxygen.

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    Neuromuscular, restrictive, and chestwall disease

    ventilatory support iffar advanced andhypercapnic respiratory failure is developingor already established

    Advances in respiratory care and theavailability of specialist respiratory facilitieshave made it possible for patients to live forlong periods with an acceptable quality of lifeon mechanical ventilation with or withouttracheostomy.

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    Bronchiectasis and cystic fibrosis

    Treatment involves management of infection,secretions, haemoptysis, and obstructiveairways disease and includes:

    Antimicrobial drugs, bronchodilator therapy,chest physical therapy, nebulized recombinanthuman deoxyribonuclease, anti-inflammatory

    therapy ,supplemental oxygen and mechanicalventilation, surgery

    HIV associated chronic infection

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    HIV-associated chronic infectionPulmonary complications Examples

    Infection

    Bacterial Streptococcus pneumoniae, Haemophilusspecies, Pseudomonas aeruginosa

    Mycobacterial M. tuberculosis, M. avian complex, M. kanasii

    Fungi Pneumocystis carinii, Cryptococcus neoformans,

    Histoplasma capsulatum, Aspergillus species,Blastomyces dermatitidis, Penicillium marneffei

    Viruses Cytomegalovirus

    Parasites Toxoplasma gondii

    Malignancies Kaposi's sarcoma, non-Hodgkin's lymphoma,bronchogenic carcinoma

    Interstitial pneumonitides Lymphocytic and non-specific interstitialpneumonitis

    Other COPD, PHT, diffuse alveolar damage, bronchiolitis

    obliterans organizing pneumonia, alveolarproteinosis

    T b l i

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    Tuberculosis

    Poorly treated tuberculosis with recurrentreactivation results in severe pulmonary scarring,cavitation, and secondary aspergillus infection.

    In deprived populations, these patients maydevelop respiratory failure, recurrent bacterial and

    tuberculosis-related infection, and massivehaemoptysis.

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    Respiratory terminal care and

    palliative sedation During the terminal phase of end-stage

    respiratory disease, simple nursing measuresincluding a constant draught from an openwindow or fan, regular sips of water to moisten

    the mouth (particularly when using oxygen), andsitting upright may be very beneficial.. In the terminal stages of end-stage respiratory

    disease, including the neuromuscular diseases,

    the emphasis of management changes fromactive interventions to purely supportive andsymptomatic measures.

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    Respiratory terminal care and

    palliative sedation Non-invasive ventilatory support and active

    physiotherapy may be withdrawn to facilitategreater comfort for the patient.

    Drug treatments aimed at palliating symptoms ofpain, breathlessness, constipation, andhaemoptysis are often unavoidable.

    If possible drugs should be given orally using

    sustained release preparations but subcutaneousinfusions or intermittent, intramuscular injectionsmay be necessary.

    R i t t i l d

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    Respiratory terminal care andpalliative sedation

    Use of nasal prongs facilitates communication withrelatives and carers. Similarly, nebulizers should becontinued as long as practically possible to provide

    bronchodilators, local anaesthetic, and opioids toalleviate

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    Respiratory terminal care and

    palliative sedation

    The use of palliative sedation for the relief ofrefractory dyspnoea is particularly difficultbecause of the perceived risk of respiratory

    depression Benzodiazepines, in particular midazolam and

    opioids, are the sedatives most frequently

    used and can be titrated to achieve thedesired level of sedation

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    E N D

    Thank You!!!!

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    Reference:

    Oxford Textbook of Palliative Medicine, 3rd

    Edition