Respiratory Flashcards
Describe the Epidemiology of Asthma (2)
- Commonly presents in childhood/adolescence
- More common in developed countries
What are the two types of Asthma
- Allergic/Eosinophillic
- Non-Allergic/Non Eosinophillic
What are the 3 main characteristics of Asthma
- Airway hyper-responsiveness
- Airway obstruction
- Bronchial inflammation/fibrosis with smooth muscle hypertrophy, increased mucosal secretion and epithelial damage
What are the risk factors for Asthma (5)
- Atopy
- Family History
- Premature birth
- Obesity
- Poor socioeconomic status
What are the main precipitating factors for Asthma (6)
- Cold air
- Smoke (tobacco)
- Exercise
- Allergens
- Stress
- NSAIDs and Beta blockers
How might someone with Asthma present (6)
- Intermittent dyspnoea
- Wheeze
- Frequent exacerbation due to an identifiable factor
- Cough
- Symptoms worse at night
- Often a younger patient
What tests might you do in Asthma (4)
- RCP3
- Spirometry
- Obstructive pattern (FEV1/FVC <0.7) - PEFR diary with introduction of Salbutamol
- Skin prick test (for allergies)
What medication might you prescribe in Asthma (3)
- Beta agonists
- SABA (salbutamol)
- LABA (Salmeterol) - Muscarinic Antagonists
- SAMA (Ipratropium)
- LAMA (Tiotropium) - Inhaled Corticosteroids
- Prednisolone
- May be given systemically if ineffective
What is the medication Guideline regime in Asthma (4)
- SABA
- SABA and ICS
- SABA and LABA and ICS
- SABA and LABA and ICS plus 4th?
How would a patient having an acute Asthma attack present (3)
- Tachycardia
- Resp. Rate > 24
- Unable to finish sentences due to severe
breathlessness
How would you treat an acute Asthma attack (3)
- Oxygen (keep above 92%)
- Nebulised Salbutamol
- Prednisolone
What is COPD
- A disease state with progressive airway obstruction that is not fully reversible
What are the risk factors for COPD (3)
- Smoking
- Alpha 1 Antitrypsin defficiency
- Occupational factors (Coal dust, chemicals, etc.)
What are the two diseases in COPD
- Chronic Bronchitis
- Emphysema
Describe the pathophysiology of Chronic Bronchitis
- Airway narrowing and increased mucosal secretions in response to inhaled irritants
- Hypertrophy and Hyperplasia of mucus scereting glands of Bronchi
- Inflammation and fibrosis of Bronchial walls leading to airway narrowing
- Blue Bloaters
Describe the pathophysiology of Emphysema
- Dilatation and destruction of lung tissue distal to bronchioles in reponse to inhaled irritants
- inflammation leads to decreased elastic recoil and dilatation of alveoli
- This leads to alveolar collapse and decreased compliance/ decreased gas exchange
- pink puffers
How might someone with COPD present (6)
- Chronic productive (clear) cough
- Breathlessness
- Wheeze
- Frequent infections
- Symptoms worsened by cold/damp
- Usually older Smokers
What is the treatment for COPD (4)
- Smoking cessation (most effective)
- B2 Agonists
- LABA (salmeterol)
- SABA (salbutamol) - Corticosteroids
- 2 week prednisolone trial
- beclametasone ICS if improves symptoms - Oxygen therapy
What type of disease is Hypersensitivity Pneumonitis
- Autoimmune Interstitial Lung Disease (restrictive)
What is the epidemiology of Hypersensitivity Pneumonitis (2)
- Usually in Adults
- Acute, Sub-Acute and Chronic Forms
What are the causes/risk factors for hypersensitivity pneumonitis
- Farmers Lung (Mouldy Hay)
- Cheese Workers Lung (Mouldy Cheese)
- Pigeon Fanciers Lung (Proteins in droppings)
- Malt Worker (Mouldy Malt)
- Existing Lung Disease
Describe the Pathophysiology of Hypersensitivity Pneumonitis
- Type 3 hypersensitivity reaction
- Cellular immune response and immune complex deposition in response to inhaled allergen
- This leads to granulatomous inflammation and hence progressive fibrosis of the lung parenchyma
How might someone with acute Hypersensitivity Pneumonitis present (6)
- Fever, sweats, rigor
- Dyspnoea
- Dry cough
- Myalgia
- Crackling
- Tight chest
How might someone with sub-acute Hypersensitivity Pneumonitis present (8)
- Similar to acute but less pronounced and slower onset
- May have a history of acute attacks
- Fever, sweats, rigor
- Dyspnoea
- Dry cough
- Myalgia
- Crackling
- Tight chest
How might someone with Chronic Hypersensitivity Pneumonitis present (5)
- Unlikely to have history of acute attack
- Progressive dyspnoea
- Weight loss
- Cyanosis
- Finger clubbing
What tests might you do on someone with Hypersensitivity Pneumonitis (3)
- Bloods
- Raised ESR/CRP
- Raised WCC
- Chest X-Ray
- Diffuse Nodular Shadowing
- Fibrotic Shadowing in upper zone
- Spirometry
- Reversible Restriction
How would you treat someone with Acute/ Subacute Hypersensitivity Pneumonitis (3)
- Remove Allergen
- Oxygen
- Prednisolone
How would you treat someone with Chronic Hypersensitivity Pneumonitis (2)
- Avoid exposure to allergen
- Prednisolone
Describe the Epidemiology of Brochiectasis (3)
- More common in Females
- Often caused by infection
- Incidence increases with age
What are the causes of Bronchiectasis (3)
- Infection
- Pneumonia/TB
- Congenital
- Cystic Fibrosis/Primary Ciliary Dyskinesia
- Mechanical bronchial obstruction
- Tumour
Describe the Pathophysiology of Bronchiectasis
- Decreased Mucociliary clearance and impaired immune function lead to recurrent lung infections
- This results in constant bronchial wall inflammation and fibrosis
- In response to this the airways permanently dilate
How might someone with Bronchiectasis present (6)
- Chronic productive cough with green smelly sputum
- Dyspnoea
- Chest pain
- Recurrent infection
- Wheeze
- Finger clubbing
What tests might you run for Bronchiectasis (5)
- Chest X-Ray
- Dilated Airways - Sputum Culture
- Look for bacterial colonisation - Spirometry
- Restrictive pattern - Test for Cystic Fibrosis
- Bronchoscopy
What is the treatment for Bronchiectasis (3)
- Mucus Drainage
- Antibiotics to treat infections
- Bronchodilator
- ICS
Describe the Epidemiology of Cystic Fibrosis (3)
- More common in Caucasians
- Multi-System mostly affects lungs and pancreas
- Autosomal recessive
Describe the pathophysiology of Cystic Fibrosis
- Mutation of Cystic Fibrosis gene on chromosome 7
- Codes for Cystic Fibrosis Transmembrane regulator
- CFTR tranports Cl which is followed by Na then water into mucus
- in CF this means that less water moves into mucus resulting in thicker secretions
- Leads to Obstruction/ Bronchiectasis and Pancreatic insufficiency
How might someone with Cystic Fibrosis present (9)
- Thicc mucus
- Cough
- Shortness of breath
- Anorexia/ Weight loss
- Bowel obstruction
- Wheeze
- Recurrent infection
- Diabetes
- Weight loss
What tests might you run for Cystic Fibrosis (3)
- Genetic screening
- Sweat test (Salt >60mmol/L)
- Clinical/Family History
What is the treatment for Cystic Fibrosis (7)
- Education
- Vaccination/Antibiotics
- Pancreatic replacement therapy
- ADEK vitmain suplements
- B2 agonists and ICS to relive symptoms
- Stop Smoking
- Amiloride (reduces Na transport)
Describe the Epidemiology of Sarcoidosis (4)
- Type of Interstitial lung disease
- Commonly affects adults 20-40
- More common in women
- Multi-system granulatomous disease mostly affects lungs and Lymph nodes
How might someone with Sacrcoidosis present (6)
- Fever, Fatigue, Weight loss
- Erythema Nodosum (red lumps on skin)
- Cough
- Progressive dyspnoea
- Lymphadenopathy
- Chest pain
- plus so many others i cba fucking learning
What tests might you run for Sarcoidosis (3)
- Chest X-Ray
- Bilateral Hilar Lymphadenopathy
- Lung infiltrates/fibrosis - Biopsy
- Non Caseating Granulomas (DIAGNOSTIC)
- Bronchoscopy
How would you treat Sarcoidosis (2)
- Acute attack
- Bed rest and NSAIDs - Steroids
- Prednisolone (IV Methylprednisolone if severe)
Describe the epidemiology of Idiopathic pulmonary fibrosis (IPF) (3)
- More common in Males, Inc. with age
- Most common cause of interstitial lung disease
- Progressive lung fibrosis of unknown cause
Describe the pathophysiology of IPF
- Progressive fibrosis of lung parenchyma
- Leads to decreased lung compliance and impaired gas exchange due to thicker alveolar membrane