W5 COPD and Cystic Fibrosis (AG) Flashcards

(AG Wed 25.10)

1
Q

Why do we need to do spirometry?

A

To assess lung function
Look at airway limitation using GOLD guidelines

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2
Q

Main difference between Asthma and COPD?

A

Asthma- Reversible, Eosinophilic disease
COPD- Progressive and Non-reversible

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3
Q

Treatment Guidelines GOLD:
What is the layout of GOLD like?

A

ABCD cube

  • Spirometrically confirmed diagnosis
  • Assessment of airflow limitation
  • Assessment of symptoms/risk of exacerbation (whether they have led to hosp admissions)
  • Post-bronchodilator measure FEV1/FVC ratio= should be >70% to be classed as good.
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4
Q

GOLD- pharmacological treatment- what is given to the groups?

A

Group A= Bronchodilator
Group B= LABA or LAMA
Group C= LAMA
Group D= LAMA OR LAMA + LABA OR ICS + LABA (COPD with asthmatic features- as ICS as LABA only works in the presence of ICS in asthma patients will work with good levels eosinophil levels)

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5
Q

What is CAT Score?
What is mMRC?

A

COPD Assessment Test
- Higher scores denote a more severe impact of COPD on a patient’s life

Modified Medical Research Council Dyspnoea scale
- Assesses the degree of dyspnoea in patients.

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6
Q

GOLD Treatment guidelines for COPD:
Dyspnea:

A
  1. LABA or LAMA
  2. LABA + LAMA OR LABA + ICS then LABA +LAMA + ICS
  3. Consider switching inhaler device or molecules
    Investigate and treat other causes of dyspnea
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7
Q

GOLD Treatment guidelines for COPD:
Exacerbations:

A
  1. LABA or LAMA
  2. LABA + LAMA
    IF eos <100= Roflumilast, FEV1 <50% & chronic bronchitis OR Azithromycin in fromer smokers
    IF eos >100= LABA + LAMA + ICS
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8
Q

What are the 5 Fundamentals of COPD care?

A

After confirmed diagnosis of COPD:

Offer Pulmonary Rehabilitation if indicated
Offer pneumococcal and influenza vaccinations
Offer smoking cessation
Co-develop a personalised self-management plan
Optimise treatment for co-morbidities

These treatments and plans should be revisited at every review

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9
Q

NICE Guidlines COPD:
On what conditions should inhaled therapies be started? (3)
Which Inhaled therapies?

A

Only if:
- All the 5 fundamentals have been offered (if appropriate) and
- inhaled therapies are needed to relieve breathlessness and exercise limitation and
- people have been trained to use inhalers and can demonstrate satisfactory technique

Offer SABA or SAMA To use as needed

Review medication and assess inhaler technique and adherence regularly for all inhaled therapies

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10
Q

NICE Guidelines COPD

A
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11
Q

Risk of giving ICS to a patient with COPD and asthmatic features with low eosinophil levels (means they don’t have asthma only features)

A

= Risk of PNEUMONIA
= Leads to hosp admission
= They already have high risk of chest infection.

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12
Q

Example of
SABA?
SAMA?
LABA?
LAMA?

A

Salbutamol
Ipratropium
Formeterol/Salmeterol
Tiotropium

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13
Q

What are the types of Inhaled antimuscarinics + examples?

MHRA advice?
Cautions?
SE?
Contraindications?

A
  • SAMA: Ipratropium bromide (paramedics often use in a nebulised form)
  • LAMA: Tiotropium, Umeclidinium, Glycopyronnium
  • MHRA/CHM advice: risk of inhalation of capsule if placed in the mouthpiece of the inhaler
  • Cautions: bladder outflow obstruction, paradoxical bronchospasm, prostatic hyperplasia, angle-closure glaucoma, cystic fibrosis
  • S/E: constipation, arrhythmia, cough, dizziness, dry mouth, headache, nausea
  • Contra-indicated in patients with hypersensitivity to atropin
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14
Q

Management of exacerbation:
What are 3 things that increase during an exacerbation?

A

increased dyspnea, increased sputum volume, increased sputum purulence

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15
Q

Management of exacerbation:
How does this happen?
What o2 levels should be aimed for?

A
  • Short-acting (SAMA, SABA) usually at higher doses through nebuliser
  • Withhold LAMA treatment if a SAMA is given
  • Hydrocortisone was traditionally the drug of choice in severe life-threatening asthma
  • Short course of oral prednisolone along with other therapies
  • Antibiotics where there are signs of infections, in immunocompromised, co-morbidities

Oxygen
* Aim for 94-98% oxygen saturation- not too high!
* 88-92% oxygen saturation for patients at risk of hypercapnic respiratory failure

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16
Q

Prevention of exacerbations:

A
  1. Pulmonary exacerbations
    - improved dyspnea, health status and exercise tolerance
    - reduces hospitalisation among pts who have had a recent exacerbation
    - leads to a reduction in symptoms of anxiety and depression
    - leads to a reduction in symptoms of anxiety and depression
  2. Education and self-management
    - both together improves health status and decreases hospitalisations and emergency department visits
  3. Integrated Care programs
    -have no demonstrated benefit at this time
17
Q

What is a description of Cystic Fibrosis?
What are the main clinical signs?
What do its complications include?

A
  • It is a genetic disorder affecting the lungs, pancreas, liver, intestine, and reproductive organs.
  • Main clinical signs: pulmonary disease, with recurrent infections and the production of copious viscous sputum, and malabsorption due to pancreatic insufficiency.
  • Complications include hepatobiliary disease, osteoporosis, cystic fibrosis-related diabetes, and distal intestinal obstruction syndrome.
18
Q

What are the aims of treatment in Cystic Fibrosis? (4)

A
  • Preventing and managing lung infections
  • Loosening and removing thick, sticky mucus from the lungs
  • Preventing or treating intestinal obstruction
  • Providing sufficient nutrition and hydration

Lung function is a key predictor of life expectancy in people with cystic fibrosis and optimising lung function is a major aim of care.

19
Q

What is the non-drug treatment for COPD?

A
  • Provide advice on airway clearance, nebuliser use, musculoskeletal disorders,
    physical activity, and urinary incontinence (by specialist physiotherapists).
  • Regular exercise improves both lung function and overall fitness
20
Q

What is the drug treatment for COPD?

A
  • Treatment is based on the
    prevention of lung infection and the maintenance of lung function.
  • Patients, who have clinical
    evidence of lung disease, the frequency of routine review should
    be based on their clinical
    condition.
  • Adults should be reviewed at leastevery 3 months.
  • More frequent review is required immediately after diagnosis.
21
Q

What mucolytics are offered for COPD patients?

A
  • Patients with cystic fibrosis who have evidence of lung disease should be offered a mucolytic.
  • Dornase alfa is the first choice mucolytic.
  • If there is an inadequate response, dornase alfa and hypertonic sodium chloride, or hypertonic sodium chloride alone should be considered.
  • Mannitol dry powder for inhalation is recommended as an option when dornase alfa is unsuitable, when lung function is rapidly declining, and if other osmotic drugs are not considered appropriate.
22
Q

What are examples of a Pulmonary Infection?

A

Staphylococcus aureus: Offer an antibacterial oral or IV

Pseudomonas aeruginosa: Offer an oral antibacterial in combination with an inhaled antibacterial.

Aspergillus fumigatus complex: Offer an antifungal drug only to
suppress chronic complex respiratory infection in patients with
declining pulmonary status

23
Q
A