COPD: Basics + Epidemiology + Clinical manifestations Flashcards

1
Q

What is COPD?

A
  • Heterogeneous disease characterized by chronic, persistent respiratory symptoms resulting from airflow obstruction and alveolar gas exchange abnormalities, with little or no reversibility
  • COPD includes emphysema (an anatomically defined condition), chronic bronchitis (clinically defined condition), and small airway disease
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2
Q

What are exogenous risk factors for COPD?

A

*Tobacco use:
- Smoking is the major and most common risk factor for COPD (80% of cases are due to smoking but only one in five smokers is affected, so it is likely that a genetic predisposition also plays a role in the development of the disease), but those who have quit ≥ 10 years ago are not at increased risk
- Passive smoking
*Exposure to air pollution or fine dusts:
- Nonorganic dust: such as industrial bronchitis in coal miners
- Organic dust: ↑ incidence of COPD in areas where biomass fuel (e.g., wood, animal dung) is regularly burned indoors

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3
Q

What are endogenous risk factors for COPD?

A

*Lung growth and development abnormalities:
- Recurrent pulmonary infections and tuberculosis
- Premature birth (The lower the birth weight, the higher the risk of poor lung growth and developing COPD)
*α1-antitrypsin deficiency
*Airway hyperresponsiveness
*Antibody deficiency syndrome (e.g., IgA deficiency)
*Primary ciliary dyskinesia (e.g., Kartagener syndrome)

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4
Q

What is chronic bronchitis?

A

Productive cough for at least 3 months per year for 2 consecutive years that cannot be explained by an alternative diagnosis

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5
Q

Presence of chronic bronchitis, emphysema, and small airway disease in COPD patients

A
  • Emphysema, chronic bronchitis, and small airway disease are present in varying degrees in different COPD patients
  • Chronic bronchitis is common in patients with COPD, especially in young, male patients who are exposed to tobacco smoke or pollution
  • Chronic bronchitis and emphysema often occur simultaneously in patients with COPD
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6
Q

What is emphysema?

A

Permanent dilatation of pulmonary air spaces distal to the terminal bronchioles that is caused by the destruction of the alveolar walls and pulmonary capillaries required for gas exchange

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7
Q

COPD epidemiology

A
  • COPD will typically present in adulthood, primarily present in smokers and those greater than age 40, often during winter months
  • Prevalence increases with age, with a prevalence of 10–20% of the over-40s;
  • 3:2 male/female ratio (Formerly, COPD was significantly more prevalent in men, but the incidence has gradually been reaching parity between genders)
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8
Q

Symptoms and physical findings of COPD

A
  • The three cardinal symptoms of COPD are dyspnea, chronic cough, and sputum production (morning is usually when symptoms are worse)
  • The most common early symptom is exertional dyspnea
  • Less common symptoms include wheezing and chest tightness
  • Other findings can include pursed lip breathing, prolonged expiratory phase, crackles, muffled breath sounds, and/or coarse rhonchi on auscultation, cyanosis due to hypoxemia, and tachycardia
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9
Q

What are features of advanced COPD

A
  • Congested neck veins
  • Barrel chest (Increased anterior-posterior chest wall diameter): This deformity is most commonly seen in individuals with emphysema.
  • Asynchronous movement of the chest and abdomen during respiration
  • Use of accessory respiratory muscles due to diaphragmatic dysfunction
  • Hyperresonant lungs, reduced diaphragmatic excursion, and relative cardiac dullness on percussion
  • Decreased breath sounds on auscultation: “silent lung”
  • Peripheral edema (most often ankle edema)
  • Right ventricular hypertrophy with signs of right heart failure and cor pulmonale
  • Hepatomegaly
  • Often weight loss and cachexia
  • Secondary polycythemia
  • Confusion: due to hypoxemia and hypercapnia
  • Nail clubbing in the case of certain comorbidities (e.g., bronchiectasis, pulmonary fibrosis, lung cancer) [15]
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10
Q

Nail clubbing in COPD

A

Nail clubbing is not a finding specific to COPD; its presence usually suggests comorbidities such as bronchiectasis, pulmonary fibrosis, or lung cancer.

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11
Q

What can COPD patients be categorized into based on their clinical appearance?

A

Often categorized as either “Pink Puffer” or “Blue Bloater”

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12
Q

Describe a pink puffer COPD patient

A
  • Main pathomechanism: emphysema
  • Clinical features: Noncyanotic, cachectic, pursed lip breathing, mild cough
  • PaO2: Slighlty reduced
  • PaCO2: Normal (or low possibly in late hypercapnia)
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13
Q

Describe a blue bloater COPD patient

A
  • Main pathomechanism: chronic bronchitis
  • Clinical features: Productive cough, overweight, peripheral edema
  • PaO2: Markedly reduced
  • PaCO2: Increased (early hypercapnia)
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14
Q

Features of COPD due to α1-antitrypsin deficiency

A
  • Age of onset is generally younger (< 60 years)
  • Often have hepatic signs and symptoms (jaundice) related to hepatitis or cirrhosis
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15
Q

What can emphysema be divided into?

A

Emphysema can be divided into the following subtypes:
* Centrilobular/centriacinar emphysema
* Panlobular/panacinar emphysema
* Other subtypes: Cicatricial emphysema, giant bullous emphysema, and age related emphysema (

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16
Q

Which type of emphysema is the most common?

A

Centriacinar is the most common form, constituting more than 95% of clinically significant cases

17
Q

What is centrilobular emphysema characterized by and who does it affect?

A
  • Classically seen in smokers
  • Characterized by the destruction of the respiratory bronchiole (central portion of the acinus); spares distal alveoli
  • Usually affects the upper lobes
18
Q

What is panlobular emphysema characterized by and who does it affect?

A
  • Rare type of emphysema
  • Associated with AATD
  • Characterized by the destruction of the entire acinus (respiratory bronchiole and alveoli)
  • Usually affects the lower lobes
19
Q

What is pursed lip breathing?

A
  • The patient breathes in through the nose and breathes out slowly through pursed lips (as if you were going to whistle or blow out a candle)
  • This style of breathing increases airway pressure and prevents bronchial collapse during the last phase of expiration.
  • More commonly seen in patients with emphysema
20
Q

Types of GOLD classification of COPD

A

Two classifications:
- GOLD spirometric grades which inform on the severity of airflow obstruction and the prognosis of a patient
- GOLD groups which guide pharmacological management

21
Q

What are the possible grades a COPD patient may receive based on GOLD grades?

A

In all of them, FVC<0.7

22
Q

What are the possible groups a COPD patient may be put in based on GOLD group classification?

A

Extra notes:
- The number and severity of past exacerbations are good predictors for future exacerbations
- Symptom severity is evaluated using the modified British Medical Research Council (mMRC) questionnaire and the COPD Assessment Test (CAT)

23
Q

When is evaluation for COPD warranted?

A
  • COPD is often evaluated in patients with relevant symptoms and risk factors
  • Adults without any symptoms should not undergo further testing for COPD
24
Q

Diagnostic approach for COPD patients

A
  • Obtain spirometry to confirm significant airflow limitation and diagnosis (FEV1:FVC < 70%)
  • At the time of their initial diagnostic evaluation in addition to spirometry
    all patients should have: a chest radiograph to exclude other pathologies, a full blood count to identify anaemia, infection, or polycythaemia, and body mass index (BMI) calculated
  • In those with a confirmed diagnosis of COPD, screen them all for alpha 1 antitrypsin deficiency
  • ABG (if assessing for resp failure)
  • Additional investigations in different contexts is in a separate flashcard in this deck
25
Q

Spirometry in COPD

A
  • Spirometry is required to establish the diagnosis of COPD
  • FEV1:FVC < 70% after bronchodilator inhalation confirms the diagnosis.
  • Decreased FEV1 is seen (FEV1 % of the predicted value determines the GOLD spirometric grade)
  • Normal or ↓ FVC
26
Q

Differential diagnosis for COPD

A

Differential diagnoses:
- Asthma
- Heart failure
- Bronchiectasis
- Tuberculosis
- Bronchiolitis

27
Q

What is the mMRC dyspnea scale and how is it scored

A
  • The modified British Medical Research Council (mMRC) questionnaire is an assessment tool used to evaluate the extent of a patient’s functional disability caused by dyspnea (e.g., secondary to chronic obstructive pulmonary disease)
  • Its scale ranges from 0 (dyspnea only with strenuous exercise) to 4 (too dyspneic to leave the house or breathless when dressing)
28
Q

What is the CAT and how is it scored?

A
  • The COPD Assessment Test (CAT) provides a score on eight functional parameters to measure the impact of the disease on a patient’s daily life
  • Patients rate the following symptoms on a scale from 0 (best) to 5 (worst): cough, phlegm production, chest tightness, breathlessness walking uphill, limitation of daily activities at home, limitation of activities outside the home, quality of sleep, and level of energy
29
Q

How can differentiate between asthma and COPD?

A
  • Untreated COPD and asthma are frequently distinguishable on the basis of history (and examination) in people presenting for the first time
  • Whenever possible, use features from the history and examination (such as those in the table in this flashcard) to differentiate COPD from asthma
  • When diagnostic uncertainty remains, or both COPD and asthma are present, use the following findings to help identify asthma:
  • a large (over 400 ml) response to bronchodilators
  • a large (over 400 ml) response to 30 mg oral prednisolone daily for 2 weeks
  • serial peak flow measurements showing 20% or greater diurnal or day-to-day variability
  • Clinically significant COPD is not present if the FEV1 and FEV1/FVC ratio return to normal with drug therapy
  • Reconsider the diagnosis of COPD for people who report a marked
    improvement in symptoms in response to inhaled therapy
30
Q

Additional investigations in COPD patients

A

Perform additional investigations when needed as detailed in this table (NICE guidelines)

31
Q

Describe giant bullae emphysema

A
  • Characterized by large congenital or acquired bullae that extrude into the surrounding tissue
  • Bullae may rupture, leading to pneumothorax.
  • Depending on the shape of the bullae, resection should be considered.
32
Q

What is a pulmonary bullae?

A

An air-filled space, greater than 1 cm in diameter, that develops within the lung due to emphysematous damage of the lung)

33
Q

What is cicatricial emphysema caused by and what does it lead?

A
  • Mainly caused by exposure to quartz dust
  • Results in chronic inflammation and nodular scar formation
34
Q

What is an acute exacerbation in COPD?

A
  • An acute worsening of the manifestations of chronic obstructive pulmonary disease (typically characterized by increased frequency or severity of cough, increased sputum volume or change in sputum consistency, and/or increased dyspnea). - Caused by an underlying infection (e.g., viral or bacterial pneumonia) in ~ 80% of cases
35
Q

How is AATD tested?

A

A blood test can check the level of AAT protein in your blood. If the level is lower than normal, it is likely that you have AAT deficiency. A genetic test is the most certain way to check for AAT deficiency and should be done to confirm the results of the blood test and find the mutation in the AAT gene