Restrictive lung disease Flashcards

1
Q

Define restrictive lung disease

A

Reduced lung volumes (TLC, FRC and FVC)

These conditions cause trouble when fully expanding lung

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2
Q

Describe parenchymal lung disease.

Which four conditions cause restriction in the parenchyma?

A

Transient problems of alveoli filling processes (water, blood, pus etc)

  1. Pulmonary oedema
  2. Pulmonary haemorrhage
  3. Infection (e.g. pneumonia)
  4. Infiltrative cancer
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3
Q

Describe the types of interstitial disease (connective tissue) that can occur

A

Intralobular septa- surround individual alveoli where capillaries are found

Interlobular septa- outline the secondary lobes. This is where the lymphatics & veins of the lungs are
Usually not seen by CT, only when expanded by blood/pus etc
Thickened septa may be caused by left heart failure or lymphangtic spread of cancer

Normal interstitial structures can be affected by inflammation or fibrotic scarring

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4
Q

Outline the causes of interstitial lung disease

A

Environmental exposure

  1. Hypersensitivity pneumovitus (e.g. mould and bird protein)
  2. Occupational (e.g coal, silica, asbestos) PERMANENT PARTICLES

Idiopathic

  1. Vasculitis
  2. Idiopathic pulmonary fibrosis
  3. Lymphangioleiomyomatosis (LAM)

Systemic inflammatory disease

  1. Autoimmune disease- ILD (rh.arthiritis)
  2. Sarcoidosis (granulomatous)
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5
Q

Describe the pathophysiology of occupational interstitial lung disease, specifically coal.

A

Small coal dust particles reach air sac (Lasts forever in lung)

Engulfed by macrophages= inflammation

may trigger massive fibrosis

May lead to progressive lung fibrosis

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6
Q

What kind of disease does silica and coal dust cause?

A

Nodular disease is common

Areas of dense fibrosis

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7
Q

What does asbestos exposure look like on a CT?

A

Fine peripheral lines on CT

'’Honeycomb cysts”

Can also cause pleural plaques (calcified) which can turn into mesothelioma tumours

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8
Q

Describe what happens in hypersensitivity pneumonitis

A

Antigen-presenting cell expresses antigen on MHC complex

T cell becomes sensitised to antigen

Stimulates macrophages activation which leads to granuloma formation

Also causes inflammation along bronchioles and alveoli

Can be acute (weeks) or chronic, fibrotic teases which could lasts months/years. The fibrosis occurs as the body attempts to repair the problem

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9
Q

Describe a typical patient who might present with Idiopathic pulmonary fibrosis

What does the disease look like?

A

> 50, smoker or previous smoker

Mostly affects the lower and peripheral aspects of long
Fine peripheral lines
Honeycomb cysts
Lots of fibroblasts which make collagen type 3 which is not helpful n stretching, minimal inflammation

IT IS PROGRESSIVE

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10
Q

What is atelectasis?

Describe the different kinds

A

Incomplete expansion as alveolar are not able to fill with air properly

  1. Resorptive atelectasis endobronchial obstruction –> Dwindling alveolar size –> Eventual lung collapse
  2. Compressive atelactasis: pleural process or lung mass causes loss of transmural distending pressure promoting alveolar expansion (It is in this way that effusions cause restriction)

Can occur as a result of post-op pain –> less ventilation–> prone to alveolar collapse

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11
Q

Describe the normal contents of the pleural space.

A

Normally 1L of fluid cycles through pleural space/day
(At any one time scant/radiologically undetectable amount in pleural space)

It lubricates pleural surface

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12
Q

What is a pleural effusion?

A

Effusion occur when influx of fluid> efflux
It is the abnormal accumulation of >25ml

Influx comes from:

  1. Capillary leak
  2. Pulmonary interstitium
  3. Small holes in diaphragm allowing peritoneal fluid to enter the pleural space. E.G ascites(more common on RHS)

Efflux:
Lymphatics: resorptive stoma give the pleura large surge capacity (can increase absorption 20x)

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13
Q

What are the symptoms of pleural effusion?

What does it look like on a CXR?

A

In effusion, patient complaints of dyspnoea, dullness to percussion

Fuzzy diaphragm borders

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14
Q

What are the causes of pleural effusion?

A
  1. Congestive heart disease
  2. Liver disease with portal hypertension and cirrhosis
  3. Low albumin states (e.g nephrotic syndrome)
  4. Infection (TB, parapneumonia, empyema)
  5. Malignant cancer
  6. Sterile inflammation/autoimmune: pleurisy
  7. Chylothorax
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15
Q

A pleural effusion can either be described as transudate or exudate. Describe each.

A

TRANSUDATE
Most common
Imbalance in hydrostatic/oncotic capillary pressures
Not harmful, dyspnoea
Caused by non-pleural disease primary process
Resolved if primary process fixed
SOMETHING WRONG WITH NORMAL FLUID BALANCE

EXUDATE
Will not resolve alone (drain)
Needle aspiration OR (chest) tube thoracotomy 
Caused by primary pleural disease
Varies by subtype 
SOMETHING WRONG WITH PLEURA
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16
Q

By which mechanisms may a exudative effusion occur?

A
  1. Altered pleural membrane permeability: infection, cancer, autoimmune disease
  2. Altered capillary membrane permeability: pneumonia -> vasodilation
  3. Blood in p.space: penetrating trauma
  4. Retrograde spillage of lymphatic materials into p.space: thoracic duct injury
  5. Entry of tumour cells via lymphatics: cancer
17
Q

What is a thoracentesis?

A

Procedure using a needle to sample or drain the effusion
Necessary where cause is unknown
Prevent re-expansion pulmonary oedema by limiting drainage to 1.5L/day

18
Q

What would you do with a sample obtained by thoracentesis?

A

Check:

pH
Cell count with WBC differential
Microbial stain with culture study
Cytriobiology: investigate cancer cells
Protein, LDH, glucose, cholesterol levels
\+/- triglyceride

less commonly: adenosine deaminase (ADA), RF filler, lupus erythematiesis cells

19
Q

Describe the three criterion required by Lights criteria to determine a exudative effusion

A
  1. Protein in pleural fluid/protein in serum >0.5
  2. Lactate dehydrogenase level (LDH) in pleural fluid/serum >0.6
  3. LDH in pleural fluid > 2/3 upper limit of normal serum level
20
Q

What is empyema?

A

Infected pleural space (pus)

21
Q

Describe the different types of effusions

A

Parapneumonic effusion (uncomplicated): sterile inflammation, pH>7.2. Heals as pneumonia resolves

Haemothorax: pleural fluis Het>50% blood Het

Hepatic hydrothorax: Cirrhotic fluid transverse diaphragm –> pleural space

Malignant effusion: cancer cells present in effusion

Chylothorax: triglyceride > 110mg/dL, milky

EMPYEMA AND HAEMOTHORAX REQUIRE COMPLETE EVACUATION TO PREVENT DEVELOPMENT FIBROUS PLEURAL PEEL—> TRAPPED LUNG (UNEXPANDABLE)

22
Q

What is pneumothorax?

What procedure is contraindicated by the presence of pneumothorax?

A

Air collection in pleural space due to rupture of alveoli near pleural space

  1. Spontaneous- swings in intrapleural pressure and blebs are often invoked
  2. Traumatic- procedural, penetrating trauma, rib fracture, baurotrauma

Restrictive because it prevents full expansion of affected lung as distending pressure increased.

Performing a PULMONARY FUNCTION TEST (PFF) -you’ll push more air into space

23
Q

Chest wall disease can be divided into skeletal and CT restrictions, and weakness/myopathy. Give examples for both

A

Skeletal/CT restrictions

  1. Extensive circumferential burns
  2. Kyphoscohosis

Weakness/myopathy

  1. Global weakness
  2. Myasthernia gravis
  3. Degenerative spinal disease (MND, polio)

RESTRICTION leads to DECREASED RV, FRC, TLC