N339 Exam 5: Respiratory Disorders Flashcards
What are two types of Fibrotic Interstitial Lung Diseases?
- Diffuse Intersitial Lung Disease (Restrictive lung disease)
- Sarcoidosis
With _____ tissue becomes fibrotic and restricts the contraction of the lungs.
fibrotic interstitial lung disease
Diffuse Interstitial Lung Disease is also known as?
Diffuse Intersittial Pulmonary Fibrosis
Diffuse Interstitial Lung Disease is characterized by and related to?
characterized by Inflammation and thickening of the alveolar interstitium. “scarring down tissue”
Related to an immune reaction that begins with injury to the alveolar epithelial or capillary endothelial cells, leading to infiltration by immune cells.
Excess fibrin deposits from Diffuse Interstitial lung disease result in ? (6)
- stiff, noncompliant lungs
- Decreased vital capacity
- decreased tital volume
- decreased function residual capacity
- decreased diffusion capacity
- increased respiratory rate to compensate for tidal volume.
What are the most common patient complaints with Diffuse Interstitial lung disease? what is the contributing factor?
- Progressive Dyspnea
- Non-productive cough
- SOB
Smoking
With Pulmonary Fibrosis:
- An unknown antigen triggers ___ & ___ lymphocytes.
- B and T Cells activate ____.
- Activated ____ recruit Neutrophils and activate _____.
- _____ lay down collagen and _____ tissue
- _____ release oxidant _____.
- Excess fibrin deposition results in stiff, _____ lungs.
- B and T
- Macrophages
- macrophages, fibroblasts
- Fibroblastas, connective
- Neutrophils, proteases
- noncompliant
- Type II pneumocytes usually release ____.
2. With pulmonary fibrosis, ____ of type II pneumocytes occurs b/c of the inflammatory process.
- Surfactants
2. deactivation
With pumonary fibrosis, increased connective tissue causes poor _____. Additionally, since type II pneumocytes are deactivated, surfactant ____ results in alveoli that can’t ____.
diffusion.
decrease
stay open
Treatment of pulmonary fibrosis (diffuse interstitial lung disease) centers on administration of drugs to depress immune system activity, such as ____.
corticosteroids
Fibrotic interstitial Lung Disorders include:
- Diffuse ____ lung disease
- Sarcoidosis
- Hypersensitivity _____
- _____ Lung Disease
- interstitial
- Pneumonitis
- Occupational
Sarcoidosis is ____ or chronic of unknown cause but ____ cause is likely.
acute
immunologic
Sarcoidosis is characterized by development of multiple _____ of 1-2mm in diameter that affect _____ organs but most commonly the _____ and lung tissue.
granulomas
multiple
lymph nodes
Sypmtoms of Saroidosis include:
dyspnea
fever
enlarged lymph nodes
Hypersensitivity Pneumonitis is caused by exposure of lung tissue to inhaled _____ agents. This leads to a type ____ hypersensitivity reaction (ie ___ ___ complexes)
organic
III
antigen-antibody
What organic agents cause hypersensitivity Pneumonitis?
Mold
Bird Poop
Fungal Infections
In advanced cases of Hypersensitivity Pneumonitis, ____ lung changes occur (_____ lesions and _____ alveolar walls)
fibrotic
granulomatous
thickened
Symptoms of Hypersensitiviity Pneumonitis include?
Fever Chills Malaise Dyspnea Dry cough Tachypnea
Occupational Lung Disease is caused by inhalation of ____ substances (toxic gases) and foreign particles.
Inorganic
An example of Occupational Lung Disease caused by inhalation of inorgaic dust particles is _____.
Pneymoconiosis
3 major types of ocuupational lung Pneumoconiosis include? and what is source of particles?
anthracosis: coal dust
silicosis: inhaling sand (sandblasting community)
asbestosis: wall insulation
With Occupational lung disease, lung ____ occurs as disease progresses. In late stage, ____ occurs (i.e. can’t get enough oxygen to support perfusion to the body).
fibrosis
hypoxemia
Common Atmosheric Pollutants that contribute to lung disease include? (5)
- Carbon monoxide (cars)
- Sulfar oxides (factories)
- Photochemical oxidants (byproduct of hydrocarbon exposure, ozone etc)
- Cigarette smoke (nicotine)
- Particulate Matter (factories)
What is the common pathology with exposure to atmospheric pollutants?
They all paralyze the mucociliary escalator.
What are two types of Atelectatic Disorders?
- Acute Respiratory distress Syndrome (ARDS)
2. Infant Respiratory Distress Syndrome
ARDS is characterized by damage to the ____-capillary membrane and has a mortality rate of ___%. Because of _____, patients that recover may have continued respiratory problems.
alveolar
50
scarring
ARDS is associated with? (5)
- Severe trauma
- Sepsis (40% of cases)
- Aspiration of gastric acid (30% of cases)
- Fat emboli syndrome (from fractured long bone)
- Shock (any cause of)
Characteristic findings of ARDS:
- Injury to ____
- Changes in Alveolar ____
- Injury to _____ circulation
- Disruption of oxygen ____ and utilization
- alveoli
- diameter
- pulmonary
- transport
With injury to Alveoli in ARDS, injury includes? (3)
- direct injury to wall
- aspiration of gases
- indirect shock
With changes in alveolar diameter and ARDS, decrease in diameter occurs b/c?
inactivation of surfactant
What are symptoms of ARDS?
- severe hypoxemia
- decreased lung compliance
- decreased functional residual compliance
- diffuse alveolar infiltrates
- non-cardiogenic pulmonary edema (not from heart failure)
Does oxygen therapy help ARDS patients?
No: can’t exchange gas thru alveolar walls due to hyaline membrane. Plus, capillary wall endothelial is thickened.
What are 4 conditions in whcih ARDS can develop?
- Aspiration
- Drugs, Toxins, Therpeutic Agents
- Infections
- Trauma and Shock
What are two events that can cause Aspiration leading to ARDS?
Near drowning
and
Aspiration of gastric contents
What are 4 types of chemicals that can lead to ARDS?
- heroin
- Inhaled gases (ex smoke or ammonia)
- Oxygen
- Radiation
What are 3 types of infections that can lead to ARDS
Gram negative septicemia
Bacterial and viral infections
What are 3 types of trauma or shock that cause ARDS
Burns
Fat embolism
Chest Trauma
What are 3 major pathophysiologic processes associated with ARDS?
- Non-cardiogenic pulmonary edema
- atelectasis from lack of surfactant
- fibrosis from inflammatory deposition of proteins.
With ARDS, increased ____ of the pulmonary vasculature and flooding of the alveoli with proteinaceous fluid, leading to the development of protein-rich pulmonary ____. The acute lung injury triggers the____ to activate the complement system and to initiate _____ sequestration in the lung
permeability
edema
immune system
neutrophil
Pathologenesis of ARDS:
Triggering agents has effect on vasculature (I.e. 1). Causes (2) due to inflamm response. With increased permeability, dumping of (3) cause non-cardiogenic edema. At same time, infection everywhere, activate alveloar macrophage that kick out (4), recruits (4), injures alveolar cap walls, leave cap bed, goes to alveolus. All released in alveolus cause damage, slough off of Type I (5). Type II hypertrophy become (6). All cellular debris and protein rich fluid forms (7) that lines inside of alveolus. Now alveolus begins to (8). Surfactant/exudate now referred to as (9) memrane. Oxygen that does get thru from capillaries can’t get into alveolus.
- Alveolar Capillary
- dilation
- plasma proteins
- cytokines, neutrophils
- alveolar cells
- inactivated
- exudate
- collapse
- hyaline
Surfactant normally decreases _______in small alveoli and prevents them from ____.
surface tension
collapsing
Infant Respiratory Distress Syndrome (IRDS) is also known as _____.
hyaline membrane disease