Final Test COPY Flashcards

(148 cards)

1
Q
  • Identify and discuss diagnostic considerations for evaluating pneumonia.*
  • Differentiate between typical and atypical pneumonia
A
  • Typical
    • Generally Lobar pattern, classic presentation, “typical” pathogens
  • Atypical
    • Generally Interstitial pattern, atypical presentation, “atypical” pathogens (no growth on standard culture media, nothing seen on Gram’s stain), Viral
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2
Q

Contrast clinical findings in presentations of restrictive and obstructive lung processes.

  • Does this describe obstructive or restrictive lung disease?
    • Blue is normal
A

obstructive

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3
Q

Identify types of pneumoconiosis and the compounds that initiate disease.

Chest XR finding: Large masses of dense fibrosis in the UPPER zones

  • State which pneumoconiosis is associated with the above Chest XR finding. Options are below
    1. Silicosis
    2. Coal workers’ pneumoconiosis
    3. Asbestosis
A

Identify types of pneumoconiosis and the compounds that initiate disease.

Chest XR finding: Large masses of dense fibrosis in the UPPER zones

  • State which pneumoconiosis is associated with the above Chest XR finding. Options are below
    1. Silicosis
    2. Coal workers’ pneumoconiosis
    3. Asbestosis
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4
Q
  • Recall and be able to perform the major components of the lung exam (inspection, palpation, percussion and auscultation).*
  • What order do you perform a lung exam in?
A

Recall and be able to perform the major components of the lung exam (inspection, palpation, percussion and auscultation).

  • What order do you perform a lung exam in?
    • Order Of Exam:
      • 1. Look
      • 2. Feel
      • 3. Listen (Includes percuss)
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5
Q
  • Discuss the typical clinical presentation and diagnostic findings of chronic obstructive lung disease including emphysema and chronic bronchitis.*
  • Describe COPD that is predominantly emphysema as it relates to everything listed
A
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6
Q
  • Know examples of how pathogens can evade immune responses and define a successful pathogen*
  • What are the 5 features of a successful pathogen?
A

Know examples of how pathogens can evade immune responses and define a successful pathogen

  • What are the 5 features of a successful pathogen?
    1. Gains access to a host
    2. Finds a unique site (niche)
    3. Avoids host protective mechanisms
    4. Multiplies in host
    5. Often causes disease
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7
Q

Describe the composition, synthesis, mechanism of action and function of lung surfactant.

  • What is the lipid and protein composition of surfactant?
  • What is the predominant lipid?
  • What cells secrete surfactant?
A
  • Surfactant production in humans begins in Type II alveolar cells during the alveolar sac stage of lung development.
  • Lamellar bodies appear in the cytoplasm at about 20 weeks gestation.
  • These lamellar bodies are secreted by exocytosis into the surface water layer lining the alveolar airspace, where the surfactant forms a meshwork of tubular myelin.
  • Term infants are estimated to have an alveolar storage pool of approximately 100 mg/kg of surfactant, while preterm infants have an estimated 4–5 mg/kg at birth.
    • ​Think IRDS
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8
Q
  • Describe the changes in lung smooth muscle and cellular infiltrates associated with asthma.*
  • What is shown in these pictures?
A
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9
Q

Discuss the pathophysiology, clinical presentation and treatment of bronchiolitis.

  • What are the signs/symptoms of bronchiolitis?
  • How do you Dx this?
  • How do you treat this?
  • What complications arise?
  • How do you prevent bronchiolitis?
A

Discuss the pathophysiology, clinical presentation and treatment of bronchiolitis.

  • What are the signs/symptoms of bronchiolitis?
    • Low grade fever
    • Irritability
    • Increased work of breathing
    • Very young infants may not have a prodrome, may have apnea as the first sign of infection
    • Prolonged expiratory phase
    • Nasal flaring
    • Intercostal retractions (Sometimes)
    • Suprasternal retractions (Sometimes)
    • Air trapping with hyper-expansion of the lungs
  • How do you Dx this?
    • Laboratory studies are not required but quick test in office is easily done
    • Pulse oximetry is adequate for monitoring oxygenation
    • Frequent regular assessments of cardiorespiratory status is necessary
    • Infants may develop respiratory failure quickly if they are very tired
  • How do you treat this?
    • Hospitalize if respiratory distress, hypoxia, under 4 months of age
    • Supportive care includes:
      • Cool, humidified oxygen
      • Nasopharyngeal suctioning
      • Chest physiotherapy
      • Elevate head of bed
      • IV fluids if unable to take oral feeds
  • What complications arise?
    • Short Term
      • Dehydration (water loss due to increased respiratory rate)
      • Acidosis
    • Late Term
      • Asthma later in childhood
      • Recurrence is common, tends to be mild, treatment same as the first episode
  • How do you prevent bronchiolitis?
    • Palivizumab (RSV monoclonal antibody) Initiate just before onset of RSV season
    • Monthly injections, 15mg/kg per dose
    • Indicated for those under 2 years with chronic lung disease, very low birth weight, hemodynamically significant cyanotic and cyanotic heart disease
    • Immunization with influenza vaccine over 6 months
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10
Q

Differentiate between community-acquired and hospital-acquired bacterial pneumonia.

  • Define HAP
  • What are some predisposing factors to CAP?
  • What are the common bacterial causes of CAP (differentiate between early onset and late onset)?
  • What is VAP?
A
  • VAP: Ventilator-Associated Pneumonia (≥ 48hrs after endotracheal intubation)
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11
Q

Differentiate between community-acquired and hospital-acquired bacterial pneumonias.

  • HAP Tx
    • If a patent has risk factors for MRSA, what do you do?
A
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12
Q

Differentiate between community-acquired and hospital-acquired bacterial pneumonias.

  • Outpatient CAP Tx
    • What can you give to a previously healthy patient who has not been on any antibiotics for the last 3 months?
A

3 options

  • A macrolide
    • Usually clarithromycin
  • Azithromycin
  • Doxycycline
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13
Q

Describe mutation analysis techniques and be able to recommend appropriate tests and interpret the results from that test.

  • Do you need to know the mutation you are looking for with the following lab tests:
    • • Sanger
    • • PyroSequence
    • • Next-Gen
  • What is each test above used for and name an advantage or disadvantage for each?
A
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14
Q

Summarize the various presentations of different types of lung cancers.

  • Malignant Mesothelioma
    • Where do these arise in the body?
    • How long is the latent period for this?
    • What are the three morphologic appearances of this?
    • What do signs/symptoms do patients present with?
    • Is metastasis common?
    • What is seen when the lungs are examined at autopsy?
    • How does asbestos relate to smoking?
A

Summarize the various presentations of different types of lung cancers.

  • Malignant Mesothelioma
    • Where do these arise in the body?
      • Usually in the parietal or visceral pleura
      • It also occurs much less commonly in the peritoneum and pericardium.
    • How long is the latent period for this?
      • The latent period for developing malignant mesothelioma after the initial exposure is long, often 25 to 40 years.
    • What are the three morphologic appearances of this?
      1. Epithelial,
        • Cuboidal cells with small papillary buds line tubular and microcystic spaces;
      2. Sarcomatous
        • Spindled, occasionally fibroblastic-appearing cells grow in sheets
      3. Biphasic
        • Both sarcomatous and epithelial areas.
    • What do signs/symptoms do patients present with?
      • The presenting complaints are chest pain, dyspnea, and recurrent pleural effusions.
      • Concurrent pulmonary asbestosis is present in only 20% of individuals.
    • Is metastasis common?
      • The lung is invaded directly, and there is often metastatic spread to the hilar lymph nodes and, eventually/rarely, to the liver and other distant organs.
    • What is seen when the lungs are examined at autopsy?
      • At autopsy, the affected lung typically is ensheathed by a layer of yellow-white, firm, variably gelatinous tumor that obliterates the pleural space.
    • How does asbestos relate to smoking?
      • Exposure to asbestos in nonsmokers increases the risk for developing lung cancer 5-fold, while in heavy smokers exposed to asbestos the risk is increased approximately 55-fold.
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15
Q

Identify types of pneumoconiosis and the compounds that initiate disease.

Chest XR finding: Multiple small nodules in the UPPER zones and Hilar “eggshell” calcifications

  • State which pneumoconiosis is associated with the above Chest XR finding. Options are below
    1. Silicosis
    2. Coal workers’ pneumoconiosis
    3. Asbestosis
A

Identify types of pneumoconiosis and the compounds that initiate disease.

Chest XR finding: Multiple small nodules in the UPPER zones and Hilar “eggshell” calcifications

  • State which pneumoconiosis is associated with the above Chest XR finding. Options are below
    1. Silicosis
    2. Coal workers’ pneumoconiosis
    3. Asbestosis
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16
Q

Explain the diagnostic strategies for pulmonary arterial hypertension (PAH) and sleep apnea (SA).

  • What are the 5 classes of PAH?
  • What is a Polysomnography?
  • What does chronic hypoxemia cause?
  • What are the classes of sleep apnea?
A
  • Polysomnography, also called a sleep study,
    • a test used to diagnose sleep disorders.
    • Polysomnography records your brain waves, the oxygen level in your blood, heart rate and breathing, as well as eye and leg movements during the study.
  • Chronic Hypoxemia can cause:
    • ▸ Pulmonary vasoconstriction
    • ▸ 2 ̊ polycythemia
    • ▸ Systemic hypertension
    • ▸ Cardiac arrhythmias
    • ▸ Sudden death
  • Sleep Apnea Classes
    • Obstructive (OSA)
      • Obese
      • Hypoxic
      • Hypercapneic
      • Excess parapharyngeal tissue = adults who snore loudly
      • Adenotonsillar hypertrophy = children who snore loudly
    • Central
      • Toxic (opiates/sedatives)
      • Trauma/infection/stroke
      • Advanced HF
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17
Q

Identify types of pneumoconiosis and the compounds that initiate disease.

  • What is notable about where asbestosis starts in the lungs?
  • In asbestosis, contraction of the fibrous tissue distorts the normal architecture, creating enlarged air spaces enclosed within thick fibrous walls. What is the notable term used to describe the way the regions look?
  • What is the most common manifestation of asbestos, and what are they made of /contain?
  • What is shown in the image?
  • How do patients with the asbestos present?
A

Identify types of pneumoconiosis and the compounds that initiate disease.

  • What is notable about where asbestosis starts in the lungs?
    • In contrast with CWP and silicosis, asbestosis begins in the lower lobes and subpleurally, spreading to the middle and upper lobes as the fibrosis progresses.​
  • In asbestosis, contraction of the fibrous tissue distorts the normal architecture, creating enlarged air spaces enclosed within thick fibrous walls. What is the notable term used to describe the way the regions look?
    • Honeycombing
  • What is the most common manifestation of asbestos, and what are they made of /contain?
    • Pleural plaques are the most common manifestation of asbestos exposure and are well-circumscribed plaques of dense collagen, often containing calcium.
    • They develop most frequently on the anterior and posterolateral aspects of the parietal pleura and over the domes of the diaphragm.
  • What is shown in the image?
    • Asbestos bodies
      • When asbestos fibers are inhaled, they become surrounded by alveolar macrophages and coated by a protein-iron complex, forming asbestos bodies.
      • These bodies eventually undergo fibrosis, causing the lung tissue to become diffusely fibrotic and rigid and the airways to become distorted.
  • How do patients with the asbestos present?
    • Progressively worsening dyspnea appears 10 to 20 years after exposure.
    • It is usually accompanied by a cough and production of sputum.
    • The disease may remain static or progress to CHF, cor pulmonale, and death.
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18
Q

Describe the differences between emphysema and bronchitis.

  • Both emphysema and bronchitis present with SOB. What are the other 2 main presentations for bronchitis?
A

Describe the differences between emphysema and bronchitis.

  • Both emphysema and bronchitis present with SOB. What are the other 2 main presentations for bronchitis?
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19
Q

Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.

  • Group A (Streptococcus pyogenes)
    • What can patients with a URI from this present with?
    • List and describe the 3 conditions that can happen if this is untreated?
A

Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.

  • Group A (Streptococcus pyogenes)
    • What can patients with a URI from this present with?
      • Intense acute pharyngitis
      • Glomerulonephritis
      • Tonsillitis
      • Redness and edema of mucus membranes
      • Purulent exudate
    • List and describe the 3 conditions that can happen if this is untreated?
      1. Scarlet fever
        • - High fever > 38.30C
        • Sandpaper rash
        • Strawberry tongue
        • Circumoral palor
      2. Rheumatic fever and Rheumatic heart disease
        • Antibodies to M protein and other cell wall components also bind human cardiac sarcolemma
      3. Post-Strep Glomerulonephritis
        • 1-5 weeks after acute pharyngitis or streptococcal skin infection
        • Blood and protein in urine, edema, hypertension, renal insufficiency, oliguria
        • Deposition of immune complexes in the kidneys
        • Majority of patients recover but it can be fatal or develop into chronic disease in rare cases.
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20
Q

Recall and be able to perform the major components of the lung exam (inspection, palpation, percussion and auscultation).

  • Describe these lung sounds
    • Tracheal
    • Bronchial
    • BC
    • Vesicular
    • Adventitious
A
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21
Q

Compare and contrast the causes of atopic (extrinsic) versus non-atopic (intrinsic) asthma.

  • For Atopic
    • ​How common is this?
    • What type of hypersensitivity is this, and what Ig molecule is it associated with?
    • When does it start in life?
    • Does it have a genetic component?
    • What often precedes asthma attacks?
    • What will a skin test show?
A

Compare and contrast the causes of atopic (extrinsic) versus non-atopic (intrinsic) asthma.

  • For Atopic
    • ​How common is this?
      • The most common form of asthma
    • What type of hypersensitivity is this, and what Ig molecule is it associated with?
      • A classic example of type I IgE–mediated hypersensitivity reaction.
    • When does it start in life?
      • Childhood
    • Does it have a genetic component?
      • Yes, a positive family history of atopy and/or asthma is common
    • What often precedes asthma attacks?
      • Allergic rhinitis, urticaria, or eczema.
    • What will a skin test show?
      • Wheal and Flare Rxn
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22
Q

Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.

  • Bordatella pertussis AKA Whooping Cough
    • Describe the catarrhal stage
    • Describe the paroxysmal stage
    • When is the initiation of treatment pointless?
A

Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.

  • Bordatella pertussis AKA Whooping Cough
    • Describe the catarrhal stage
      • 2 week incubation
      • Mild disease if anything but highly infectious
    • Describe the paroxysmal stage
      • After two weeks.
      • Explosive whooping cough
      • Whoop upon inhalation leading to rapid exhaustion -
      • Associated with vomiting, cyanosis, convulsions
      • Dangerous complications in infants
      • Rarely can lead to seizures and encephalopathy.
    • When is the initiation of treatment pointless?
      • Treatment initiated after the start of the paroxysmal stage rarely alters the clinical
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23
Q
  • Describe risk factors other than smoking that can lead to increased lung cancer risk.*
  • What are the common occupational exposures that have an increased risk of lung cancer?
A

Describe risk factors other than smoking that can lead to increased lung cancer risk.

  • What are the common occupational exposures that have an increased risk of lung cancer?
    • Uranium Mines
    • Work with asbestos
    • Inhalation of dust containing arsenic, chromium, nickel, or vinyl chloride.
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24
Q

Describe pathophysiology of cystic fibrosis and how this relates to morbidity and mortality. Explain clinical presentation and diagnosis of cystic fibrosis.​

  • How do each of the following characteristics of CF present?
    • Acute Pulmonary exacerbation
    • Chronic Pulmonary Clinical Complications
    • Exocrine Clinical complications
    • GI Clinical complications
    • Reproductive Clinical Complications
    • Integumentary Clinical Complications ​
A
  • Acute Pulmonary exacerbation
    • • Increase in cough
    • • Fever
    • • Change in sputum
    • • Decreased activity, lethargy
    • • Hemoptysis
  • Chronic Pulmonary Clinical Complications
    • • Recurrent pulmonary infections
    • • Sinusitis
    • • Pneumonia
    • • Bronchiectasis
  • Exocrine Clinical complications
    • • Pancreatic insufficiency
    • • Pancreatitis
    • • Malabsorption of fat-soluble vitamins
    • • 30% develop diabetes mellitus
    • • Failure to thrive
  • GI Clinical complications
    • • Meconium ileus in newborns
    • • Malabsorption with steatorrhea of fat-soluble vitamins
    • • Rectal prolapse
    • • Prolonged neonatal jaundice
  • Reproductive Clinical Complications
    • • 99% of males struggle with fertility
    • • Increased difficulties with fertility for females
  • Integumentary Clinical Complications
    • • “salty” skin
    • • clubbing of fingers
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25
* Describe how virulence factors impact the pathogenesis of bacterial pneumonia.* * What is a virulence factor?
*Describe how virulence factors impact the pathogenesis of bacterial pneumonia.* * What is a virulence factor? * **Virulence factors are molecules produced by bacteria, viruses, fungi, and protozoa that add to their effectiveness**
26
*Discuss the signs, symptoms and pathophysiology of pulmonary embolism.* * What are the common signs/symptoms of PE? * What do 20% of patients present with? * Why do strokes occur? * What cardiac symptoms occur?
*Discuss the signs, symptoms and pathophysiology of pulmonary embolism.* * What are the common signs/symptoms of PE? * **Prolonged Sitting** * **Nothing makes it better** * **DOE, SOB, and cough, LE swelling and calf pain (Homan’s positive).** * What do 20% of patients present with? * **• Classic triad of pleuritic CP, SOB and hemoptysis is present in \<20%** * **• 4% present with syncope and 2% present with new seizure** * Why do strokes occur? * **Increase pulmonary pressure due to PE. 20% of people have a PFO.** * **Can send thrombotic material back into the LA and LV and into the carotid circulation** * **Paroxysmal embolism syndrome** * What cardiac and respiratory symptoms occur? * **Tachycardia is common; fever occurs in 10%, but only 2% are above 102.5** * **Resp - typically clear but can hear: wheezes, crackles bilaterally** * **Card - new RBBB; can have atrial fibrillation or if massive PE can have cardiac arrest and arrhythmias (PEA, asystole)**
27
*Discuss special considerations when evaluating and treating pneumonia in regard to patients of high-risk groups (influenza, tuberculosis, HIV, Legionella and pertussis).* * HIV * ​If a patient has this, what other infx's can occur that can cause pneumonia.
* Pneumocystis jirovecii (PCP) * Fungal pathogens, parasites, and less common: cytomegalovirus
28
* Discuss the pathophysiology of ARDS and contrast the three phases of ARDS.* * How does direct injury cause ARDS?
* What causes the damage: Direct injury * • Alveoli are directly injured * • Release of proinflammatory cytokines which include tumor necrosis factor and interleukin * • Cytokines recruit neutrophils that release toxic mediators – destructive enzymes and O2 free radicals * • Results in damage to the capillary endothelium and alveolar epithelium
29
*Describe the initial treatment of a patient presenting to the emergency department with a critical respiratory illness.* * HYPERCAPNIC RESPIRATORY FAILURE * What happens to serum CO2? * What is wrong with ventilation? * What the reading for PaCO2? * Respiratory acidosis: What is the rule of thumb for pH changes and PaCO2?
*Describe the initial treatment of a patient presenting to the emergency department with a critical respiratory illness.* * HYPERCAPNIC RESPIRATORY FAILURE * What happens to serum CO2? * **Increases** * What is wrong with ventilation? * **Unable to VENTILATE alveoli, problem with the air pump** * What the reading for PaCO2? * **Under 45** * Respiratory acidosis: What is the rule of thumb for pH changes and PaCO2? * **Every change of 10 in the PaCO2, pH changes by 0.08** * **As PaCO2 decreases, pH increases.**
30
*Recall and be able to perform the major components of the lung exam (inspection, palpation, percussion and auscultation).* * What are the accessory muscles? * What things can you "feel" for?
* "Feel" * A minor aspect of the exam and clinically not extremely useful * Can feel for tactile fremitus * Percuss
31
Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis. * Bordatella pertussis AKA Whooping Cough * Are these gram negative or positive? * What shape do they have? * Are these bacteria encapsulated? * Describe the test results for * Oxidase * Catalase * Nitrate * Citrate * Urea
Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis. * Bordatella pertussis AKA Whooping Cough * Are these gram negative or positive? * **Gram-negative** * What shape do they have? * **Coccobacilli** * Are these bacteria encapsulated? * **Encapsulated** * Describe the test results for * **Oxidase and catalase positive** * **Think oxygen = positive** * **Nitrate, citrate and urea negative**
32
* Predict the routine and emergency medical treatment of chronic obstructive lung disease presentations.* * Look at the different groups that COPD Tx recommendations can be classified as. What are the treatment options for each group?
33
*Describe mutation analysis techniques and be able to recommend appropriate tests and interpret the results from that test.* * Do you need to know the mutation you are looking for with the following lab tests: * PCR-Sizing * ARMS-PCR * Oligonucleotide Ligation * What is each test above used for and name an advantage or disadvantage for each?
34
*Discuss the clinical presentation, mechanisms of pathogenicity, diagnosis, prevention/treatment and epidemiology of the following bacterial respiratory pathogens: Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Mycoplasma pneumoniae, Klebsiella pneumoniae .* * Mycoplasma pneumoniae​ * ​What conditions can prolonged infection cause? * What tests are used to diagnose this?
*Discuss the clinical presentation, mechanisms of pathogenicity, diagnosis, prevention/treatment and epidemiology of the following bacterial respiratory pathogens: Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Mycoplasma pneumoniae, Klebsiella pneumoniae .* * Mycoplasma pneumoniae​ * ​What conditions can prolonged infection cause? * **Steven Johnson Syndrome** * **Hemolytic Anemia** * What tests are used to diagnose this? * **Complement fixation test (CFT)** * **IgM by latex agglutination or ELISA**
35
*Describe the viral pathogens, physical exam, and pharmacologic interventions of croup.* * How do patients present? * What is the home treatment for it? * What is the Rx treatment for it? * What do you use for significant airway compromise? * What sign will you see on x-ray?
*Describe the viral pathogens, physical exam, and pharmacologic interventions of croup.* * How do patients present? * **Most patients have an upper respiratory infection with some combination of rhinorrhea, pharyngitis, mild cough, and low grade fever for 1-3 days before signs of upper airway obstruction become apparent.** * **Child then develops the classic “barking” cough, hoarseness, and inspiratory stridor.** * **Fever can reach 39-40 degrees C (102.2-104 F), some are afebrile** * **Symptoms are worse at night and recur for several days.** * **Lasts about 5 days with the 3rd night being the worst** * What is the home treatment for it? * **Warm humidified air is helpful to decrease the swelling of the subglottis, this can be done in a closed bathroom with the hot shower running** * **If warm mist fails, breathe cool air by standing near an open refrigerator or freezer. You can also go outside with the child if weather is cold** * What is the Rx treatment for it? * **Best: Dexamethasone phosphate (0.6 mg/kg) orally x 1 dose. Can be given intramuscularly if child will not take the oral medication** * **Alternative: Prednisilone 2mg/kg per day orally in 2 divided doses/day for 3 days** * What do you use for significant airway compromise? * **Racemic epinephrine reduces subglottic edema. Because of rebound, this should be administered in an Emergency Department** * **​An inhaled alpha adrenergic agent that decreases subglottic edema** * **Takes effect in 10-30 minutes and fades within 60-90 minutes** * **Under age 4 yrs - 0.05 mL/kg/dose up to max dose of 0.5mL/dose diluted with 3mL NS via nebulizer over 15 min** * **Over 4 years - 0.5mL/dose diluted with 3mL NS via nebulizer over 15 min** * **Rebound effect may occur, with worsening of symptoms as the effect of the drug dissipates.** * **Aerosol treatment may be repeated every 20 minutes for 1-2 hours in severe cases** * What sign will you see on x-ray?
36
*Describe the differences between emphysema and bronchitis.* Between the green and orange squares: * Which is associated with bronchitis and which is associated with emphysema?
*Describe the differences between emphysema and bronchitis.* Between the green and orange squares: * Which is associated with bronchitis and which is associated with emphysema? * CB= Chronic bronchitis=Green * Emphysema=Orange
37
* Recognize and contrast normal lung exam vs abnormal lung exam.* * Differentiate between barrel chest, pigeon chest, and pectus excavatum and list how they may cause an abnormal lung exam
38
*Discuss the pathophysiology of ARDS and contrast the three phases of ARDS.* * What is shown here? * What are the 2 most common causes of ARDS?
* What are the 2 most common causes of ARDS? * Pneumonia * Sepsis
39
*Describe the role of IgA in mucosal immunity* * What cell produces mucus? * What cell produces IgA? * When is IgA the first line of defense for the body?
*Describe the role of IgA in mucosal immunity* * What cell produces mucus? * **Goblet cells produce mucus** and protect the airway and lung tissue from inspired particles. * Goblet cells extend to the end of the bronchi. * What cell produces IgA? * **Mostly B-Cells** * When is IgA the first line of defense for the body? * **Secretory IgA serves as the first line of defense in protecting the intestinal epithelium from enteric toxins and pathogenic microorganisms.**
40
*Understand the differences between panacinar and centriacinar emphysema.* * Panacinar * Are the acini uniformly enlarged, or are only parts of them enlarged? * What lung zone is usually affected? * What protein are patients deficient in? What is the function of this protein?
*Understand the differences between panacinar and centriacinar emphysema.* * Panacinar * Are the acini uniformly enlarged, or are only parts of them enlarged? * **Acini are uniformly enlarged, from the level of the respiratory bronchiole to the terminal blind alveoli.** * What lung zone is usually affected? * **It occurs more commonly in the lower lung zones,** * What protein are patients deficient in? What is the function of this protein? * **Patients have a α1-anti-trypsin deficiency** * **Normally present in serum, tissue fluids, and macrophages, is a major inhibitor of proteases (particularly elastase) secreted by neutrophils during inflammation. α1-anti-trypsin is encoded by a gene in the proteinase inhibitor (Pi) locus on chromosome 14.**
41
*Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.* * Chlamydia pneumoniae * Is this gram negative or positive? * Where does this bacterium live? * What URI's are common? * How do you Dx this as the causative pathogen?
*Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.* * Chlamydia pneumoniae * Is this gram negative or positive? * **Gram-Negative** * Where does this bacterium live? * **Obligate intracellular bacterium** * What URI's are common? * **Mild URI's** * **Pharyngitis, otitis media, rhinitis, low fever, laryngitis** * How do you Dx this as the causative pathogen? * **Microimmunofluorescence or ELISA using species- specific antigens**
42
*Identify types of pneumoconiosis and the compounds that initiate disease.* * This pneumoconiosis is associated with increased susceptibility to tuberculosis. * Imaging shows fine nodularity in the upper zones of the lung. What do these nodules contain? * What eventually occurs as the nodules coalesce into hard, collagenous scars?
*Identify types of pneumoconiosis and the compounds that initiate disease.* * This pneumoconiosis is associated with increased susceptibility to tuberculosis. * **Silicosis** * Imaging shows fine nodularity in the upper zones of the lung. What do these nodules contain? * **The nodules demonstrate concentrically arranged (whorled) hyalinized collagen fibers surrounding an amorphous center.** * **Examination by polarized microscopy reveals weakly birefringent silica particles in the nodules.** * What eventually occurs as the nodules coalesce into hard, collagenous scars? * **Many patients develop progressive massive fibrosis aka PMF and further develop pulmonary HTN and cor pulmonale as a result of chronic hypoxia-induced vasoconstriction and parenchymal destruction.**
43
Differentiate between community-acquired and hospital-acquired bacterial pneumonias. * Inpatient CAP Tx * What are the options for tx?
44
*Summarize the various presentations of different types of lung cancers.* * Squamous cell carcinomas * Who gets this more: men or women? * ​Where do they usually arise? Where do they often spread to? * Large Squamous cell carcinomas may undergo central necrosis. What does this give rise to? * What often precedes the development of Squamous cell carcinoma? * How would you describe what the tumor looks like and its location when patients reach the symptomatic stage?
*Summarize the various presentations of different types of lung cancers.* * Squamous cell carcinomas * Who gets this more: men or women? * **Men** * ​Where do they usually arise? Where do they often spread to? How is this different compared to other types? * **​They tend to arise centrally in major bronchi and eventually spread to local hilar nodes, but they metastasize outside the thorax later than other histologic types.** * Large Squamous cell carcinomas may undergo central necrosis. What does this give rise to? * **​Large SCCAs may undergo central necrosis, giving rise to cavitation.** * What often precedes the development of Squamous cell carcinoma? * **Squamous cell carcinomas often are preceded by the development, over years, of squamous metaplasia or dysplasia in the bronchial epithelium, which then transforms to carcinoma in situ, a phase that may last for several years.** * How would you describe what the tumor looks like and its location when patients reach the symptomatic stage? * **Eventually, when the neoplasm reaches the symptomatic stage, a well-defined tumor mass begins to obstruct the lumen of a major bronchus, often producing distal atelectasis and infection.**
45
* Contrast clinical findings in presentations of restrictive and obstructive lung processes.* * Does this describe obstructive or restrictive lung disease?
restrictive
46
* Describe the differences between emphysema and bronchitis.* * Does the following describe emphysema or bronchitis? Defined by morphologic and radiologic features and affects the acinus
* Describe the differences between emphysema and bronchitis.* * Does the following describe **emphysema** or bronchitis? Defined by morphologic and radiologic features and affects the acinus
47
*Compare and contrast the lung capacity of restrictive versus obstructive lung diseases.* * In obstructive lung diseases, state whether the following values or increased, normal, or decreased compared to normal. * FEV-1 * FVC * FEV1/FVC ratio
*Contrast clinical findings in presentations of restrictive and obstructive lung processes.* * In obstructive lung diseases such as COPD * FEV-1 is **decreased** * Forced vital capacity (FVC) is near **normal or only slightly decreased** * FEV-1/FVC ratio is **\< 70% of predicted**
48
* Describe the three levels of severity of ARDS based on the PaO2/FiO2 ratio.* * How do you define mild, moderate, and severe ARDS?
* ARDS severity is defined by the ratio, PaO2/FiO2 * Mild, PaO2/FiO2 \>200 but \<300 mmHg * Moderate, PaO2/FiO2 \>100 but \<200 mmHg * Severe, PaO2/FiO2 \<100 mmHg
49
*Understand that secondary lung cancer (metastatic cancer from a distal site) is more common than primary lung cancer.* * What is the most common site of metastatic neoplasms? * How do these neoplasms get there? * What is a distinct feature seen in the parenchyma of this organ?
*Understand that secondary lung cancer (metastatic cancer from a distal site) is more common than primary lung cancer.* * What is the most common site of metastatic neoplasms? * **The lung is the most common site of metastatic neoplasms.** * How do these neoplasms get there? * **Both carcinomas and sarcomas arising anywhere in the body may spread to the lungs via** * **The blood** * **Lymphatics** * **Direct continuity** * What is a distinct feature seen in the parenchyma of this organ? * **Multiple discrete nodules (cannonball lesions) are scattered throughout all lobes, more at the periphery.**
50
* Know anatomical locations of mucosal-associated lymphoid tissues.* * ​What are the 6 areas of the body where mucosal-associated lymphoid tissues are located?
* Know anatomical locations of mucosal-associated lymphoid tissues.* * ​What are the 6 areas of the body where mucosal-associated lymphoid tissues are located? 1. **GI tract** 2. **Respiratory tract** 3. **Urogenital tract** 4. **Salivary glands** 5. **Lacrimal glands** 6. **Mammary glands** **Mr. Slug**
51
*Discuss special considerations when evaluating and treating pneumonia in regard to patients of high-risk groups (influenza, tuberculosis, HIV, Legionella and pertussis).* * Influenza virus * What does this increase the risk of? * How do you treat it?
* Influenza virus * Higher risk of secondary bacterial pneumonia with Staph/MRSA) * Tx: Neuraminidase inhibitor (oseltamivir) within 48-72hrs or combined with for hospitalized: secondary bacterial pneumonia.
52
*Recognize and contrast normal lung exam vs abnormal lung exam.*​ "An abnormal pattern of breathing characterized by progressively deeper, and sometimes faster, breathing followed by a gradual decrease that results in a temporary stop in breathing called an apnea." * What breathing pattern is described above? Your choices are below. * Kussmaul * Biot * Ataxic * Cheyne Stokes
Cheyne Stokes
53
* Describe the changes in lung smooth muscle and cellular infiltrates associated with asthma.* * What are the 4 hallmarks of asthma?
*Describe the changes in lung smooth muscle and cellular infiltrates associated with asthma.* * What are the 4 hallmarks of asthma? * **The hallmarks of asthma are** 1. **intermittent, reversible airway obstruction** 2. **chronic bronchial inflammation with eosinophils;** 3. **bronchial smooth muscle cell hypertrophy and hyperreactivity;** 4. **increased mucus secretion.**
54
*Identify the common pathogens for community acquired pneumonia (COP) and healthcare associated pneumonia (HCAP).* * What is the most common cause of CAP? * What is the most common bacterial cause of CAP? * List the 4 main bacterial causes of atypical pneumonia
55
Differentiate between community-acquired and hospital-acquired bacterial pneumonias. * HAP Tx * If a patent has no risk factors for resistant gram-negative pathogens, what do you use?
56
*Summarize the various presentations of different types of lung cancers.* * This cancer accounts for about 30% of lung cancers. * These tumors may be mucus-secreting, especially when it has an acinar growth pattern. What lung cancer is it?
Adenocarcinoma
57
Differentiate between community-acquired and hospital-acquired bacterial pneumonias. * MRSA CAP Tx * What tx options are preferred?
58
* Explain clinical presentation and diagnosis of cystic fibrosis.​* * How do you Dx cystic fibrosis?
*Explain clinical presentation and diagnosis of cystic fibrosis.​* * How do you Dx cystic fibrosis? * ***_Clinical symptoms_*** * ***_Family history_*** * ***_Immunoreactive trypsinogen_*** * ***_Sweat test_*** * ***_Genetic testing_***
59
* Describe the composition, synthesis, mechanism of action and function of lung surfactant.* * What are the three main functions of lung surfactant?
*Describe the composition, synthesis, mechanism of action and function of lung surfactant.* * What are the three main functions of lung surfactant? 1. **• To increase pulmonary compliance.** 2. **• To prevent atelectasis (collapse of the lung) at the end of expiration.** 3. **• To facilitate recruitment of collapsed airways.​**
60
*Describe the composition, synthesis, mechanism of action and function of lung surfactant.* What does the following describe? * This is involved with innate host defense, has antimicrobial properties, and helps regulate inflammation. 1. SP-A 2. SP-B 3. SP-C 4. SP-D 5. Both 1 and 2 6. Both 1 and 4
*Describe the composition, synthesis, mechanism of action and function of lung surfactant.* What does the following describe? * This is involved with innate host defense, has antimicrobial properties, and helps regulate inflammation. 1. SP-A 2. SP-B 3. SP-C 4. SP-D 5. Both 1 and 2 6. **Both 1 and 4**
61
* Discuss the pathophysiology of ARDS and contrast the three phases of ARDS.* * How does indirect injury cause ARDS?
* What causes the damage: Indirect injury * • can involve some type of systemic problem (sepsis) * • release of a substance into the circulation (fat emboli from fracture) * • some type of stress, burns or multiple trauma • antigens from a blood transfusion * • common pathway for both direct and indirect causes of ARDS seems to involve an inflammatory response that causes damage to the alveoli
62
*Identify factors that may affect the disease expressing genes and explain their contribution to human diseases utilizing specific examples.* * What does the image describe? The answer choices are below. 1. Locus Heterogeneity 2. Mosaicism 3. Pleiotropy 4. Penetrance - Incomplete 5. Penetrance - Age-dependent 6. Variable expression 7. New mutations (de novo)
Mosaicism (germline)
63
*Discuss special considerations when evaluating and treating pneumonia in regard to patients of high-risk groups (influenza, tuberculosis, HIV, Legionella and pertussis).* * Aspiration pneumonia * What types of bacteria are associated with this? * Where do they reside?
* Aspiration pneumonia * Includes Anaerobes and gram-negative bacteria * Usually polymicrobial pathogens isolated! R sided lobar infiltrates, but can also present bilateral and diffuse/interstitial pattern.
64
Describe the differences between emphysema and bronchitis. * Does the following describe emphysema or bronchitis? _Air space enlargement, alveolar wall destruction_
Describe the differences between emphysema and bronchitis. * Does the following describe **emphysema** or bronchitis? _Air space enlargement, alveolar wall destruction_
65
*Discuss the clinical presentation, mechanisms of pathogenicity, diagnosis, prevention/treatment and epidemiology of the following bacterial respiratory pathogens: Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Mycoplasma pneumoniae, Klebsiella pneumoniae .* * Haemophilus influenzae * What gram stain does this have? * What shape does this have? * Is it encapsulated? * What do patients present with? * How do you dx this specific pathogen? * What vaccine exits?
*Discuss the clinical presentation, mechanisms of pathogenicity, diagnosis, prevention/treatment and epidemiology of the following bacterial respiratory pathogens: Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Mycoplasma pneumoniae, Klebsiella pneumoniae .* * Haemophilus influenzae * What gram stain does this have? * **Gram-Negative** * What shape does this have? * **Rod** * Is it encapsulated? * **Yes** * What do patients present with? * **Epiglottitis, meningitis, otitis media, pneumonia** * How do you dx this specific pathogen? * **Growth on chocolate agar with factors V and X** * **No hemolysis** * What vaccine exits? * **Vaccine that uses a type B capsular antigen**
66
*Describe the changes in lung smooth muscle and cellular infiltrates associated with asthma.* * Which Ig molecule and which granulocyte are associated with asthma? * Describe the early and late phase of asthma-related reactions. Which one is associated with inflammation?
*Describe the changes in lung smooth muscle and cellular infiltrates associated with asthma.* * Which Ig molecule and which granulocyte are associated with asthma? * **IgE coats submucosal mast cells, which on exposure to allergen release their granule contents and secrete cytokines and other mediators.** * Describe the early and late phase of asthma-related reactions * **Mast cell-derived mediators produce two waves of reaction: an early (immediate) phase and a late phase.** * **The early-phase reaction** * **Dominated by bronchoconstriction, increased mucus production, and vasodilation.** * **Bronchoconstriction is triggered by mediators released from mast cells, including histamine, prostaglandin D2, and leukotrienes LTC4, D4, and E4, and by reflex neural pathways.** * **The late-phase reaction** * **Inflammatory in nature.** * **Inflammatory mediators stimulate epithelial cells to produce chemokines that promote the recruitment of TH2 cells, eosinophils, and other leukocytes, amplifying an inflammatory reaction initiated by resident immune cells.**
67
*Identify factors that may affect the disease expressing genes and explain their contribution to human diseases utilizing specific examples.* * What does the image describe? The answer choices are below. 1. Locus Heterogeneity 2. Mosaicism 3. Pleiotropy 4. Penetrance - Incomplete 5. Penetrance - Age-dependent 6. Variable expression 7. New mutations (de novo)
Penetrance - Incomplete
68
# *Define toxic shock and explain the mechanism behind it.* ​Toxic Shock can lead to septic shock * What are the two big hallmarks of septic shock? * How does septic shock relate to deaths in the ICU * In high concentrations, what molecule will lead to: * Fever * Induces macrophages to release the inflammatory cytokines IL-1 and IL-6 * Activates coagulation pathways * Suppresses bone marrow proliferation * Cachexia (wasting of muscle/fat)
# *Define toxic shock and explain the mechanism behind it.* ​Toxic Shock can lead to septic shock * What are the two big hallmarks of septic shock? * **Disseminated intravascular coagulation and vascular collapse which is hallmark of septic shock** * How does septic shock relate to deaths in the ICU * **Septic Shock #1 cause of death in ICUs** * In high concentrations, what molecule will lead to: * Fever * Induces macrophages to release the inflammatory cytokines IL-1 and IL-6 * Activates coagulation pathways * Suppresses bone marrow proliferation * Cachexia (wasting of muscle/fat) * **TNF-ALPHA is the answer**
69
*Summarize the various presentations of different types of lung cancers.* * Carcinoid Tumors * What is notable about the contents secretions of these cancer cells? * What is MEN syndrome? * Who usually gets bronchial carcinoid tumors? * Compare and contrast the 2 classes of Carcinoid Tumors
*Summarize the various presentations of different types of lung cancers.* * Carcinoid Tumors * What is notable about the contents secretions of these cancer cells? * **These are malignant tumors composed of cells that contain dense-core neurosecretory granules in their cytoplasm and, rarely, may secrete hormonally active polypeptides.** * What is MEN syndrome? * **These tumors can occasionally occur as part of the multiple endocrine neoplasia (MEN) syndrome.** * **MEN Syndrome: Characterized by several endocrine glands develop noncancerous (benign) or cancerous (malignant) tumors or grow excessively without forming tumors.** * Who usually gets bronchial carcinoid tumors? * **Young Adults** * Compare and contrast the 2 classes of Carcinoid Tumors * **Think of these as low-grade neuroendocrine carcinomas. They are subclassified as typical or atypical; both are often resectable and curable.** * **Typical carcinoids** * **Like those in the intestinal tract, are composed of nests of uniform cells that have regular round nuclei with “salt-and-pepper” chromatin, absent/rare mitoses and little pleomorphism.** * **Atypical carcinoid tumors** * **Display a higher mitotic rate and small areas of necrosis.**
70
*Summarize the various presentations of different types of lung cancers.* * Small cell lung carcinomas * Describe the shape/appearance of these tumors, as well as where they are located? * Are these tumors very fragile or very hard? * What is nuclear molding a result of? * What has usually occurred by the time this cancer has been diagnosed? * What kind of markers are often seen with this cancer?
*Summarize the various presentations of different types of lung cancers.* * Small cell lung carcinomas * Describe the shape/appearance of these tumors, as well as where they are located? * **Masses generally appear as pale gray, centrally located masses that extend into the lung parenchyma.** * **Masses are composed of relatively small tumor cells with a round to fusiform shape, scant cytoplasm, and finely granular chromatin with a salt and pepper appearance.** * Are these tumors very fragile or very hard? How do you know? * **Fragile** * **They often show fragmentation and “crush artifact” in small biopsy specimens.** * What is nuclear molding a result of? * **Nuclear molding results from close apposition of tumor cells that have scant cytoplasm** * What has usually occurred by the time this cancer has been diagnosed? * **By the time of diagnosis, most will have metastasized to hilar and mediastinal lymph nodes.** * What kind of markers are often seen with this cancer? * **Express a variety of neuroendocrine markers and may secrete polypeptide hormones that can result in paraneoplastic syndromes.**
71
Differentiate between community-acquired and hospital-acquired bacterial pneumonias. * HAP Tx * If a patent has risk factors for resistant gram-negative pathogens, what do you use?
72
Be able to describe the pathogenesis, prevention, and therapies of diphtheria. * Corynebacterium diphtheriae * Who is Infx by this prevented? * How is Infx by this treated?
Be able to describe the pathogenesis, prevention, and therapies of diphtheria. * Corynebacterium diphtheriae * Who is Infx by this prevented? * **There are four vaccines used to prevent diphtheria: DTaP, Tdap, DT, and Td.** * **Each of these vaccines prevents diphtheria and tetanus; DTaP and Tdap also help prevent pertussis (whooping cough).** * **Healthcare professionals give DTaP and DT to children younger than seven years old, while older children, teens, and adults get Tdap and Td.** * How is Infx by this treated? * See pic
73
* List risk factors of pulmonary arterial hypertension (PAH) and sleep apnea (SA).* * do what is says
Risk factors: BMI, neck circumference, congenital, HTN
74
*Discuss the etiology and treatment of infant respiratory distress syndrome.* * How does IRDS relate to neonatal mortality and premature births? * What is it caused by? * What are the 3 options for supportive care?
*Discuss the etiology and treatment of infant respiratory distress syndrome.* * How does IRDS relate to neonatal mortality and premature births? * **The most common cause of neonatal mortality** * **High incidence in premies** * What is it caused by? * **It is caused by insufficient lung surfactant** * What are the 3 options for supportive care? 1. **Oxygenation** 2. **Ventilation aka CPAP** 3. **Surfactant replacement therapy**
75
*Understand why toxins and superantigens can cause severe host damage and/or death* * What cells are continually activated by superantigen? What is released? * What is the difference between the following: * Exotoxin * Enterotoxin * Endotoxin
*Understand why toxins and superantigens can cause severe host damage and/or death* * What cells are continually activated by superantigen? What is released? * **It causes binding between host T-cells and MHC II receptors. Helper T cells express CD4 molecules, which bind to MHCII on antigen-presenting cells.** * **This interaction leads to the release of cytokines and further immune system activation.** * What is the difference between the following: * Exotoxin * **Found outside bacteria, heat-labile** * **Cytotoxins and Neurotoxins** * Enterotoxin * **An exotoxin that affects cell lining of GI tract** * Endotoxin * **In bacterial cell wall, heat-stable**
76
Summarize the various presentations of different types of lung cancers. * Large cell carcinomas * Which cell layer do these tumors occur in? * What cytologic features do these tumors lack? * What is notable about the nuclei, nucleoli, and cytoplasm of this cancer type?
Summarize the various presentations of different types of lung cancers. * Large cell carcinomas * Which cell layer do these tumors occur in? * **Large cell carcinomas are undifferentiated malignant *_epithelial_* tumors** * What cytologic features do these tumors lack? * **Cells lack the cytologic features of neuroendocrine carcinoma** * **Cells show no evidence of glandular or squamous differentiation.** * What is notable about the nuclei, nucleoli, and cytoplasm of this cancer type? * **The cells typically have large nuclei, prominent nucleoli, and moderate amounts of cytoplasm.**
77
* Describe the initial treatment of a patient presenting to the emergency department with a critical respiratory illness.* * What are the criteria for Dx for Acute Respiratory Failure?
78
*Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.* * Neisseria gonorrhoeae * Are these gram negative or positive? * What shape do these have? * What kind of URI's do patients present with? * What is unique about the identification of these bacteria?
*Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.* * Neisseria gonorrhoeae * Are these gram negative or positive? * **Gram-Negative** * What shape do these have? * **Diplococci** * What kind of URI's do patients present with? * ***_Pharyngitis_*** * **Tonsillitis** * **Most cases resolve spontaneously** * What is unique about the identification of these bacteria? * **Thayer-martin media with 5% sheep blood** * **Selective for Neisseria spp**
79
*Describe the composition, synthesis, mechanism of action and function of lung surfactant.* What does the following describe? * This strongly interacts with phospholipids, is involved with adsorption and spreading of the surfactant on the surface of lungs, and prevents the collapse of the alveolus. It is required for life. 1. SP-A 2. SP-B 3. SP-C 4. SP-D 5. Both 1 and 2 6. Both 2 and 3
*Describe the composition, synthesis, mechanism of action and function of lung surfactant.* What does the following describe? * This strongly interacts with phospholipids, is involved with adsorption and spreading of the surfactant on the surface of lungs, and prevents the collapse of the alveolus. It is required for life. 1. SP-A 2. **SP-B** 3. SP-C 4. SP-D 5. Both 1 and 2 6. Both 2 and 3
80
*Recognize and contrast normal lung exam vs abnormal lung exam.*​ "An abnormal pattern of breathing characterized by groups of quick, shallow inspirations followed by regular or irregular periods of apnea." * What breathing pattern is described above? Your choices are below. * Kussmaul * Biot * Ataxic * Cheyne Stokes
Biot
81
*Describe the types of infection that can lead to bronchiectasis* * What bacteria can cause this? * What viruses can cause this?
*Describe the types of infection that can lead to bronchiectasis* * What bacteria can cause this? * **Necrotizing, or suppurative, pneumonia, will predispose affected patients to the development of bronchiectasis. Particularly with virulent organisms such as** * ***_Staphylococcus aureus_*** * ***_Klebsiella spp.,_*** * What viruses can cause this? * **HIV, or other viruses that induce an immunocompromised state**
82
* Contrast clinical findings in presentations of restrictive and obstructive lung processes.* * Does this describe obstructive or restrictive lung disease?
restrictive
83
*Know examples of how pathogens can evade immune responses and define a successful pathogen* * Evasion of Immune Response * How do Neisseria gonorrhoeae, Hemophilus influenza & Neisseria meningitides mess with IgA? * How does Streptococcus pneumonia evade phagocytosis? * What does Pseudomonas secrete to evade the complement pathway? * What do Mycobacterium tuberculosis, M. leprae, and Brucella all have in common?
*Know examples of how pathogens can evade immune responses and define a successful pathogen* * Evasion of Immune Response * How do Neisseria gonorrhoeae, Hemophilus influenza & Neisseria meningitides mess with IgA? * **Neisseria gonorrhoeae, Hemophilus influenza & Neisseria meningitides secrete *_proteases cleaving IgA._*** * How does Streptococcus pneumoniae evade phagocytosis? * **Streptococcus pneumoniae has a polysaccharide capsule that resists phagocytosis.** * What does Pseudomonas secrete to evade the complement pathway? * **Pseudomonas secretes elastase that inactivates C3a and C5a.** * What do Mycobacterium tuberculosis, M. leprae, and Brucella all have in common? * **Mycobacterium tuberculosis, M. leprae, and Brucella escape phagolysosome formation.**
84
*Be able to describe the pathogenesis, prevention, and therapies of diphtheria.* * Corynebacterium diphtheriae * What shape do these have? * Are they gram negative or positive? * What does the Diphtheria toxin do to the epithelium of the upper respiratory tract? * What is usually seen on the tonsils, pharynx, and larynx?
*Be able to describe the pathogenesis, prevention, and therapies of diphtheria.* * Corynebacterium diphtheriae * What shape do these have? * **Clubbed or irregular shape** * **"Coryneforms"** * Are they gram negative or positive? * **Gram-Positive** * What does the Diphtheria toxin do to the epithelium of the upper respiratory tract? * **Causes a necrotic epithelium that becomes embedded with exuding fibrin, red, white cells** * What is usually seen on the tonsils, pharynx, and larynx? * **Grayish pseudomembrane**
85
*Discuss special considerations when evaluating and treating pneumonia in regard to patients of high-risk groups (influenza, tuberculosis, HIV, Legionella and pertussis).* * Tuberculosis * What part of the lung is usually affected? * Why would a patient get this?
* Usually upper lobe- apical consolidates with cavitation) * Exposures or secondary due to immunosuppression therapies (anti-TNF agents for RA)
86
*Differentiate between community-acquired and hospital-acquired bacterial pneumonia.* * Define CAP * What are some predisposing factors to CAP? * How are patients infected? * What are the common bacterial causes of CAP?
87
*Differentiate between community-acquired and hospital-acquired bacterial pneumonias.* * Outpatient CAP Tx * What can you give to patient who has commodities or has used antibiotics in the last 3 months?
* Options * Fluoroquinolone * Beta-Lactam * Amoxicillin * Amoxicillin/Clavulanate * Alternatives * Cephalosporin + macrolide
88
*Identify factors that may affect the disease expressing genes and explain their contribution to human diseases utilizing specific examples.* * What does the image describe? The answer choices are below. 1. Locus Heterogeneity 2. Mosaicism 3. Pleiotropy 4. Penetrance - Incomplete 5. Penetrance - Age-dependent 6. Variable expression 7. New mutations (de novo)
Locus Heterogeneity
89
Compare and contrast the causes of atopic (extrinsic) versus non-atopic (intrinsic) asthma. * Non-Atopic Asthma * What allergy history do patients have? * Do patients usually have a positive skin test? * What type of air pollutants can cause this? * What type of infections can cause this? What is thought to be the reason for this?
Compare and contrast the causes of atopic (extrinsic) versus non-atopic (intrinsic) asthma. * Non-Atopic Asthma * What allergy history do patients have? * **Patients with nonatopic forms of asthma do not have evidence of allergen sensitization.** * Do patients usually have a positive skin test? * **Skin test results usually are negative.** * What type of air pollutants can cause this? * **Air pollutants (e.g., sulfur dioxide, ozone, nitrogen dioxide)** * What type of infections can cause this? What is thought to be the reason for this? * **Respiratory infections due to viruses (e.g., rhinovirus, parainfluenza virus)** * **It is thought that virus-induced inflammation of the respiratory mucosa lowers the threshold of the subepithelial vagal receptors to irritants.​**
90
*Recognize and contrast normal lung exam vs abnormal lung exam.*​ "An abnormal pattern of breathing characterized by complete irregularity of breathing, with irregular pauses and increasing periods of apnea. As the breathing pattern deteriorates, it merges with agonal respirations." * What breathing pattern is described above? Your choices are below. * Kussmaul * Biot * Ataxic * Cheyne Stokes
Ataxic
91
* Identify and discuss diagnostic considerations for evaluating pneumonia.* * What 2 systems are used to define the severity of CAP?
92
* Identify and discuss diagnostic considerations for evaluating pneumonia.* * What tests are used to find the definitive pathogen/etiology of pneumonia?
* Tests * Cultures * Lab/Test Results * Gram’s Stain and Culture of Blood and/or Sputum * Typical pathogens * Urinary Antigen Tests (UAT): * Legionella, Pneumococcal * PCR ($$) * Atypical pathogens (16 viral + Legionella species, Mycoplasma pneumoniae, Chlamydia pneumoniae, and mycobacteria)
93
* Identify the types of obstructions that can cause bronchiectasis.* * What conditions, aside from Infx, cause bronchiectasis*?*
*Identify the types of obstructions that can cause bronchiectasis.* * What conditions, aside from Infx, cause bronchiectasis*?* * ***​*Common causes are tumors, foreign bodies, and impaction of mucus.** * **Cystic fibrosis, in which widespread severe bronchiectasis results from obstruction caused by abnormally viscid mucus and secondary infections.** * **When bronchiectasis is associated with situs inversus and chronic rhinosinusitis, the triad of indings is referred to as Kartagener syndrome aka Primary ciliary dyskinesia (the immotile cilia syndrome)**
94
* Summarize the various presentations of different types of lung cancers.* * Which 2 cancer types have the strongest association with smoking?
*Summarize the various presentations of different types of lung cancers.* * Which 2 cancer types have the strongest association with smoking? * **Squamous cell and small cell carcinomas have the strongest association with smoking, but there is also an association with adenocarcinoma.**
95
*Summarize the various presentations of different types of lung cancers.* * Carcinoid Tumors * Most masses originate in the main bronchi and follow 2 types of growth patterns. What are they? * Is metastasis at the time of diagnosis common? * Whare the signs and symptoms of this cancer? * What is carcinoid syndrome?
*Summarize the various presentations of different types of lung cancers.* * Carcinoid Tumors * Most masses originate in the main bronchi and follow 2 types of growth patterns. What are they? * **1. An obstructing polypoid, intraluminal mass** * **2. A mucosal plaque penetrating the bronchial wall, to fan out in the peribronchial tissue.** * Is metastasis at the time of diagnosis common? * **5 - 15% have metastasized to the hilar nodes at presentation, but distant metastases are rare.** * Whare the signs and symptoms of this cancer? * Most carcinoid tumors present with signs and symptoms related to their intraluminal growth. This include: * **Cough** * **Hemoptysis** * **Recurrent bronchial and pulmonary infections.** * What is carcinoid syndrome? * **Carcinoid syndrome is characterized by intermittent attacks of diarrhea, flushing, and cyanosis.** * **Only rarely do pulmonary carcinoids cause the carcinoid syndrome**
96
*Discuss the pathophysiology of ARDS and contrast the three phases of ARDS.* * In ARDS, what happens to the alveoli and hyaline membrane? * What does this lead to?
*Discuss the pathophysiology of ARDS and contrast the three phases of ARDS.* * In ARDS, what happens to the alveoli and hyaline membrane? * **The result of ARDs is diffuse alveolar damage and hyaline membrane disease** * What does this lead to? * **Hypoxemia and respiratory failure**
97
* Contrast clinical findings in presentations of restrictive and obstructive lung processes.* * Are these associated with an increased or decreased DLCO?
98
Discuss the signs, symptoms and pathophysiology of pulmonary embolism. * Where do most PE's come from? * What is Virchow's triad?
Discuss the signs, symptoms and pathophysiology of pulmonary embolism. * Where do most PE's come from? * PE is most commonly a thrombus (blood clot), but can be other things * **80% come from DVT in the lower extremities** * **15% from the pelvis** * **Rest from other sources (fat, air, amniotic fluid, foreign body such at talc, septic emboli, tumor emboli)** * What is Virchow's triad? * **Endothelial injury - surgery (most common risk), injury, infection** * **Stasis or turbulent flow - varicosities, edema/CHF, immobility (travel, bed rest, obstruction), pregnancy** * **Hypercoagulable state - cancer, smoking, hemophilias (protein C/S and antithrombin deficiency), ?pregnancy (PE typical in the weeks After delivery)**
99
*Summarize the various presentations of different types of lung cancers.* * A subset of adenocarcinomas (about 10% in whites and 30% in Asians), particularly those arising in nonsmoking women, harbor mutations that activate what molecule? What does this molecule do and what growth pathways are associated with it? * What are these types of tumors sensitive to?
*Summarize the various presentations of different types of lung cancers.* * A subset of adenocarcinomas (about 10% in whites and 30% in Asians), particularly those arising in nonsmoking women, harbor mutations that activate what molecule? What does this molecule do and what growth pathways are associated with it? * **Epidermal growth factor receptor (EGFR)** * **A receptor tyrosine kinase that stimulates downstream pro-growth pathways involving RAS, PI3K, and other signaling molecules.** * What are these types of tumors sensitive to? * **These tumors are sensitive to drugs that inhibit EGFR signaling, although the response is often short-lived.**
100
*Describe the relationship between pulmonary arterial hypertension (PAH) and sleep apnea (SA) and other illnesses (eg. depression, dementia, cardiovascular disease).* * What is OSA? * What is OHS/Pickwickian syndrome?
* Definition OSA aka Obstructive sleep apnea * recurrent nocturnal cessation of breathing \>10 seconds * Sublcass is OHS (obesity hypoventilation syndrome), OHS = Pickwickian Syndrome
101
*Contrast clinical findings in presentations of restrictive and obstructive lung processes.* * Does this describe obstructive or restrictive lung disease? * Blue is normal
restrictive
102
Differentiate between community-acquired and hospital-acquired bacterial pneumonias. * Pseudomonas CAP Tx * What tx options are preferred?
103
*Discover why lack of wheezes does not necessarily mean that a patient does not have asthma* * Does an extreme acute asthma attack have to have wheezing? * If someone has asthma without wheezing, what symptom will they most likely have? * Why could someone have asthma without wheezing?
*Discover why lack of wheezes does not necessarily mean that a patient does not have asthma* * Does an extreme acute asthma attack have to have wheezing? * **No** * **During a most extreme asthma attack, wheezing may be absent because almost no air is passing through the airways** * If someone has asthma without wheezing, what symptom will they most likely have? * **Dry, non-productive cough. aka atypical asthma** * Why could someone have asthma without wheezing? * **Coughing may start after people are exposed to allergens, or when they are breathing in cold air. Coughing may also follow an upper respiratory infection.** * **A cough that begins after a person has begun taking beta-blockers is likely to be cough-variant asthma.** * **Think Drug-Induced Asthma or Occupational Asthma**
104
*Be able to describe a typical immune response to an extracellular bacteria, intracellular bacteria, and fungus.​* ***_extracellular bacteria_*** * What 2 cells phagocytose extracellular bacteria? * What two molecules from gram (-) and gram (+) activate the lectin complement cascade? * What Ig molecule opsonizes extracellular bacteria?
*Be able to describe a typical immune response to an extracellular bacteria, intracellular bacteria, and fungus.​* ***_extracellular bacteria_*** * What 2 cells phagocytose extracellular bacteria? * **Phagocytosis by neutrophils and macrophages​** * What two molecules from gram (-) and gram (+) activate the lectin complement cascade? * **Gram (-) = peptidoglycan** * **Gram (+) = LPS** * What Ig molecule opsonizes extracellular bacteria? * **IgG opsonizes bacteria enhancing phagocytosis**
105
*Describe the relationship between pulmonary arterial hypertension (PAH) and sleep apnea (SA) and other illnesses (eg. depression, dementia, cardiovascular disease).* * What is the definition of pulmonary arterial hypertension? * What sequence does it have?
* PAH is Mean pulmonary artery pressure \> 25 mm Hg at REST * Sequelae * ▸ Athersclerotic vascular disease * ▸ Arterial narrowing and hypertension * ▸ Right heart strain * ▸ Respiratory compromise * ▸ Hypertrophy * ▸ Cor pulmonale
106
*Compare and contrast the lung capacity of restrictive versus obstructive lung diseases.* * In restrictive lung diseases, state whether the following values or increased, normal, or decreased compared to normal. * Vital capacity aka VC * Total lung capacity aka TLC * FEV1/FVC ratio
*Contrast clinical findings in presentations of restrictive and obstructive lung processes.* * In restrictive lung disease * **Decreased vital capacity** * **Decreased total lung capacity** * FEV1/FVC **ratio of \> 80%.**
107
# *Define toxic shock and explain the mechanism behind it.* * What does extracellular bacterial infection produce that causes a toxic shock? * What do T-Cells bind to because of the superantigen? What does this lead to? Is this specific binding, or non-specific binding? * What do patients usually present with? * What organism is the usual cause?
# *Define toxic shock and explain the mechanism behind it.* * What does extracellular bacterial infection produce that causes a toxic shock? * **Results from the production of a superantigen.** * What do T-Cells bind to because of the superantigen? What does this lead to? Is this specific binding, or non-specific binding? * **Superantigen causes binding between host T-cells and MHC II receptors. Helper T cells express CD4 molecules, which bind to MHCII on antigen-presenting cells.** * **This interaction leads to the release of cytokines and further immune system activation.** * **This nonspecific binding between host T cells and MHC II receptors by the superantigen leads to *_massive T cell activation._*** * What do patients usually present with? * **Massive T cell activation with the release of cytokines leads to *_fever, hypotension, and a defuse sunburn-like rash._*** * **Classically the nidus for infection is from a forgotten tampon in the vagina, but the most common presentation to clinics is from nasal packing after a nosebleed that has been kept in for too long.​** * What organism is the usual cause? * **Staphylococcus aureus is the most common cause, although β-hemolytic group A streptococci can cause a similar presentation.**
108
Contrast clinical findings in presentations of restrictive and obstructive lung processes. * Does this describe obstructive or restrictive lung disease?
obstructive
109
*Identify and discuss diagnostic considerations for evaluating pneumonia.* * What pattern do you see on an X-ray for: * Nosocomial (hospital(VAP), or hospital-acquired(HAP)) * Bacterial CAP * Viral and PCP (immune suppressed patients)
*Identify and discuss diagnostic considerations for evaluating pneumonia.* * What pattern do you see on an X-ray for: * Nosocomial (hospital(VAP), or hospital-acquired(HAP)) * **Bronchopneumonia pattern** * Bacterial CAP * **Lobar pattern:** * Viral and PCP (immune suppressed patients) * **Interstitial patterns**
110
*Discuss the pathophysiology, clinical presentation and treatment of bronchiolitis.* * What is bronchiolitis? * What are the common patients/infection characteristics? * What pathogens cause this? * What is the pathogenesis of this? * Describe severe RSV Infx.
*Discuss the pathophysiology, clinical presentation and treatment of bronchiolitis.* * What is bronchiolitis? * **It is a disease of the small bronchioles with increased mucus production and occasional bronchospasm, sometimes leading to airway obstruction** * **Hand carriage is the most frequent method of transmission** * What are the common patients/infection characteristics? * **Most common in infants and young children first 2 years of life** * **Males to females 1.5 :1** * **Most severe in young infants** * **100,000-126,000 infants are hospitalized yearly with Bronchiolitis** * **More common in winter and early spring** * What pathogens cause this? * **#1 Respiratory Syncytial Virus** * **Human metapneumovirus** * **Parainfluenza** * **Influenza** * **Adenoviruses** * **Rhinoviruses** * **Coronaviruses** * What is the pathogenesis of this? * **RSV has an incubation period of 4-6 days** * **Bronchiolitis presents as a progressive respiratory illness** * **Presents similarly to a common cold in the early phase with cough and rhinorrhea** * **Progresses over 3-7 days to noisy, raspy breathing and audible wheezing** * Describe severe RSV Infx. * **1 to 2 out of 100 children younger than 6 months of age with RSV infection may need to be hospitalized** * **They may require oxygen, intubation, and/or mechanical ventilation** * **Most improve in 2-5 days but cough can linger up to 21-30 days** * **1-2% mortality rate**
111
Describe the differences between emphysema and bronchitis. * Does the following describe emphysema or bronchitis? Defined by clinical features and initially involves the large airways
Describe the differences between emphysema and bronchitis. * Does the following describe emphysema or **bronchitis**? Defined by clinical features and initially involves the large airways
112
*Describe the viral pathogens, physical exam, and pharmacologic interventions of croup.* * What is croup? * What are the common patients/infection characteristics? * What pathogens cause this? * What are the signs/symptoms of this?
*Describe the viral pathogens, physical exam, and pharmacologic interventions of croup.* * What is croup? * **Most common infection of the middle respiratory tract** * **Disproportionally affects children** * **Mucosal edema and inflammation exponentially increases airway resistance and the work of breathing** * **Viral infection of the glottic and subglottic regions** * What are the common patients/infection characteristics? * **Infx rates peak in fall and early winter** * **Most common in children 3 months to 5 years** * **Spread by secretions** * **Males \> females** * What pathogens cause this? * **Parainfluenza virus 1,2,3,4 (most common)** * **Respiratory syncytial virus** * **Influenza Adenovirus** * **Enteroviruses** * **Human metapneumovirus** * What are the signs/symptoms of this? * **Cough-barky or brassy, seal like** * **Hoarseness** * **Low grade fever** * **Occasional respiratory distress with retractions** * **Sometimes can have Stridor** * **Inspiratory sound when calm** * **Walls of subglottic space are drawn together making an obstruction that causes the sound** * **Turbulent airflow is usually inspiratory but may be biphasic**
113
Compare and contrast the lung capacity of restrictive versus obstructive lung diseases. * Which row shows obstructive lung disease and which shows restrictive?
Compare and contrast the lung capacity of restrictive versus obstructive lung diseases. * Which row shows obstructive lung disease and which shows restrictive?
114
*Discuss the clinical presentation, mechanisms of pathogenicity, diagnosis, prevention/treatment and epidemiology of the following bacterial respiratory pathogens: Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Mycoplasma pneumoniae, Klebsiella pneumoniae .* * Klebsiella pneumoniae * Are these gram negative or positive? * What shape do they have? * Are they aerobic or anaerobic? * What 2 populations are this common in, and what is notable about the spit of patients?
*Discuss the clinical presentation, mechanisms of pathogenicity, diagnosis, prevention/treatment and epidemiology of the following bacterial respiratory pathogens: Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Mycoplasma pneumoniae, Klebsiella pneumoniae .* * Klebsiella pneumoniae * Are these gram negative or positive? * **Gram-negative** * What shape do they have? * **rod** * Are they aerobic or anaerobic? * **anaerobic** * What 2 populations are this common in, and what is notable about the spit of patients? * **Alcoholics and diabetics** * **"Currant jelly” sputum (Blood and mucus)**
115
*Identify types of pneumoconiosis and the compounds that initiate disease.* * What is the difference between Simple coal worker's pneumoconiosis and Complicated coal worker's pneumoconiosis? * What is Pulmonary anthracosis?
*Identify types of pneumoconiosis and the compounds that initiate disease.* * What is the difference between Simple coal worker's pneumoconiosis and Complicated coal worker's pneumoconiosis? * **Simple coal worker's pneumoconiosis (CWP)** * **Macrophages accumulate with little to no pulmonary dysfunction** * **Characterized by the presence of coal macules and larger coal nodules.** * **The coal macule consists of dust-laden macrophages and small amounts of collagen fibers.** * **The upper lobes and upper zones of the lower lobes are more heavily involved.** * **Complicated coal worker's pneumoconiosis** * **Progressive massive fibrosis (PMF)** * **Fibrosis is extensive and lung function is compromised (** * **Occurs on a background of simple CWP by coalescence of coal nodules and generally develops over many years** * **It is characterized by multiple, dark black scars larger than 2 cm and sometimes up to 10 cm in greatest diameter, that consist of dense collagen and pigment.** * What is Pulmonary anthracosis? * **The most innocuous coal-induced pulmonary lesion in coal miners, and also is commonly seen in urban dwellers and tobacco smokers.** * **Inhaled carbon pigment is engulfed by alveolar or interstitial macrophages, which then accumulate in the connective tissue along the pulmonary and pleural lymphatics and in draining lymph nodes.**
116
* Discuss special considerations when evaluating and treating pneumonia in regard to patients of high-risk groups (influenza, tuberculosis, HIV, Legionella and pertussis).* * What are the important things to when considering Legionella Infx?
* Legionella * Remember to consider travel history * Diarrhea and most areas
117
*Understand the differences between panacinar and centriacinar emphysema.* * Centracinar * Is this more common than Panacinar? Which one is associated more with smoking? * Does this affect all of the acini or only parts of it? * What lung zone are lesions most common in?
*Understand the differences between panacinar and centriacinar emphysema.* * Centracinar * Is this more common than Panacinar? Which one is associated more with smoking? * **Centracinar is more common and associated with smoking** * Does this affect all of the acini or only parts of it? * **Central or proximal parts of the acini, formed by respiratory bronchioles, are affected, while distal alveoli are spared.** * What lung zone are lesions most common in? * **Upper lobes**
118
*Identify factors that may affect the disease expressing genes and explain their contribution to human diseases utilizing specific examples.* * What does the image describe? The answer choices are below. 1. Locus Heterogeneity 2. Mosaicism 3. Pleiotropy 4. Penetrance - Incomplete 5. Penetrance - Age-dependent 6. Variable expression 7. New mutations (de novo)
New mutations (de novo)
119
* Contrast clinical findings in presentations of restrictive and obstructive lung processes.* * Does this describe obstructive or restrictive lung disease?
obstructive
120
*Describe the initial treatment of a patient presenting to the emergency department with a critical respiratory illness.* * What is respiratory failure defined as? * What are the two main types of respiratory failure * What are the signs of respiratory failure?
*Describe the initial treatment of a patient presenting to the emergency department with a critical respiratory illness.* * What is respiratory failure defined as? * **Defined as an inadequate gas exchange due to malfunction of one or more components of the respiratory system** * What are the two main types of respiratory failure * **Two main types: hypoxemic and hypercapnic/hypercarbic** * **BOTH can be present in a patient** * What are the signs of respiratory failure? * **Mental status changes, fatigue, retractions, ineffective chest wall movements, cyanosis**
121
*Discuss the clinical presentation, mechanisms of pathogenicity, diagnosis, prevention/treatment and epidemiology of the following bacterial respiratory pathogens: Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Mycoplasma pneumoniae, Klebsiella pneumoniae .* * Streptococcus pneumoniae * Are these gram positive or negative? * What shape does it have? * What 3 main virulence factors does it have? * What is notable about the spit of patients? * What tests are used to Dx this? * What are the 3 vaccines and who is each one suited for? * What factors are associated with an increased incidence of pneumococcal pneumonia?
*Discuss the clinical presentation, mechanisms of pathogenicity, diagnosis, prevention/treatment and epidemiology of the following bacterial respiratory pathogens: Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Mycoplasma pneumoniae, Klebsiella pneumoniae .* * Streptococcus pneumoniae * Are these gram positive or negative? * **Gram-positive** * What shape does it have? * **Diplococci** * What 3 main virulence factors does it have? * **Capsule** * **Hyaluronidase** * **Pneumolysin** * What is notable about the spit of patients? * **Rusty sputum** * What tests are used to Dx this? * **Alpha-hemolytic** * **Optochin sensitive** * **Catalase negative** * What are the 3 vaccines and who is each one suited for? * **PPSV23: over 65 or immunocompromised** * **PCV13: over 65, immunocompromised** * **PCV7: pediatric** * What factors are associated with an increased incidence of pneumococcal pneumonia? * **Primary viral infection** * **Alcohol or drug intoxication can reduce phagocytosis and depress the cough reflex** * **Abnormal circulatory dynamics** * **Malnutrition, age, complement deficiency**
122
*Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.* * Group A (Streptococcus pyogenes) * Is this gram negative or gram positive? * What shape does it have? * Describe the following virulence factors: * Hyaluronic acid capsule * M Protein * What kind of hemolysis does this have?
*Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.* * Group A (Streptococcus pyogenes) * Is this gram negative or gram positive? * What shape does it have? * Describe the following virulence factors: * Hyaluronic acid capsule * **Resists phagocytosis** * **Binds to CD44 on epithelial cells which disrupts intercellular junctions allowing invasion of the epithelium.** * M Protein * **Major virulence factor** * **If absent, virulence is lost** * **Fimbriae** * **Inhibits complement** * **Maybe inhibits IgA** * What kind of hemolysis does this have? * **β-Hemolysis (Clear/Complete Hemolysis)**
123
* Identify types of pneumoconiosis and the compounds that initiate disease.* * What is ILD and what are the common causes?
*Identify types of pneumoconiosis and the compounds that initiate disease.* * What is ILD and what are the common causes? * The term “ILD” is generically used to describe a collection of diseases that involve diffuse scarring and/or inflammation of lung tissue. Common causes of ILD are as follows: * **Prolonged exposure to occupationally inhaled inorganic agents such as silicone, coal, asbestos, talc, mica, aluminum, and beryllium** * Idiopathic pulmonary fibrosis * Connective tissue disease (eg, Wegener granulomatosis, systemic lupus erythematosus, scleroderma, Sjögren disease) * **Sarcoidosis** * Hypersensitivity pneumonitis, such as “farmer’s lung” or “bird breeder's lung,” in which an immune reaction to organic dust induces a type III or type IV hypersensitivity reaction * Radiation-induced disease * Antitumor drugs (eg, bleomycin)
124
* Recognize and contrast normal lung exam vs abnormal lung exam.* * What is pursed lip breathing associated with?
125
* Contrast clinical findings in presentations of restrictive and obstructive lung processes.* * Are these associated with an increased or decreased DLCO?
126
*Discuss special considerations when evaluating and treating pneumonia in regard to patients of high-risk groups (influenza, tuberculosis, HIV, Legionella and pertussis).* * Fungal * What location is associated with Coccidiomycosis? * What location is associated with Histoplasmosis?
* Coccidiomycosis- Southwestern US * Histoplasmosis- Ohio River valley; Mississippi
127
*Summarize the various presentations of different types of lung cancers.* * Adenocarcinoma * Who gets this more: men or women? Do non-smokers get this? * Where do they usually occur? * Are they fast-growing or slow-growing? * What are the different growth patterns that this has?
*Summarize the various presentations of different types of lung cancers.* * Adenocarcinoma * Who gets this more: men or women? Do non-smokers get this? * **Adenocarcinomas also are by far the most common primary tumors arising in women, in never-smokers, and in individuals younger than 45 years of age.** * Where do they usually occur? * **Adenocarcinomas are usually peripherally located, but also may occur closer to the hilum.** * Are they fast-growing or slow-growing? * **In general, adenocarcinomas grow slowly and form smaller masses than do the other subtypes, but they tend to metastasize widely at an early stage.​** * What are the different growth patterns that this has? 1. **Acinar (gland- forming)** 2. **Papillary** 3. **Mucinous which is often multifocal and may manifest as pneumonia-like consolidation** 4. **Solid types.**
128
*Identify factors that may affect the disease expressing genes and explain their contribution to human diseases utilizing specific examples.* * What does the image describe? The answer choices are below. 1. Locus Heterogeneity 2. Mosaicism 3. Pleiotropy 4. Penetrance - Incomplete 5. Penetrance - Age-dependent 6. Variable expression 7. New mutations (de novo)
Penetrance - Age-dependent
129
*Discuss the pathophysiology of ARDS and contrast the three phases of ARDS.* * Describe each phase * Exudative * Proliferative * Fibrotic
130
* Identify and discuss diagnostic considerations for evaluating pneumonia.* * List the symptoms and signs of bacterial pneumonia
* Symptoms of Bacterial Pneumonia * Productive cough * SOB * Trouble Swallowing * Fever, Fatigue * Tachycardia * Increased RR * Signs of Pneumonia * Egophony * Dull to percussion * Accessory Muscle * Sputum
131
*Describe the initial treatment of a patient presenting to the emergency department with a critical respiratory illness.* * HYPOXEMIC RESPIRATORY FAILURE ​ * What O2 saturation is associated with this? * What is characterized by, relative to the alveolar membrane? * What are the causes of this?
*Describe the initial treatment of a patient presenting to the emergency department with a critical respiratory illness.* * HYPOXEMIC RESPIRATORY FAILURE ​ * What O2 saturation is associated with this? * **Hypoxemia, inability to oxygenate, arterial oxygen saturation less than 90% while receiving increased inspired oxygen fraction** * What is characterized by, relative to the alveolar membrane? * **Impaired alveolar diffusion, inflammation or fluid affecting diffusion across alveolar membrane** * What are the causes of this? * **Pneumonia, ARDS, pulmonary embolism, pulmonary edema, alveolar hemorrhage** * **Ventilation-perfusion mismatch and intrapulmonary shunting**
132
*Be able to describe a typical immune response to an extracellular bacteria, intracellular bacteria, and fungus.​* ***_Fungus_*** Innate, Humoral, and Cell-mediated immunity are important for a protective immune response to fungal infections * What 2 molecules, secreted by CD4 T-h cells, play a role in the adaptive immune response against fungi? * What interleukin signal is responsible for the secretion of defensins and antifungal molecules? * What part of the fungi usually triggers the alternative and lectin complement pathways * What three things signal the end of an infection?
*Be able to describe a typical immune response to an extracellular bacteria, intracellular bacteria, and fungus.​* ***_Fungus_*** Innate, Humoral, and Cell-mediated immunity are important for a protective immune response to fungal infections * What 2 molecules, secreted by CD4 T-h cells, play a role in the adaptive immune response against fungi? * **IFN-Gamma (TH1) and IL-17 (TH17) secreted by CD4 T-Helper** * What interleukin signal is responsible for the secretion of defensins and antifungal molecules? * **Signaling through IL-17R leads to the secretion of defensins, antifungal molecules** * What cells have increased killing activity because of the answer above? * **These cytokines also enhance killing and ingestion by innate effector cells like macrophages and neutrophils** * What part of the fungi usually triggers the alternative and lectin complement pathways * **The alternative and lectin complement pathways can be triggered by fungal cell wall components** * What three things signal the end of an infection? * **Presence of T-reg cells, IL-10, and M2-cells usually signal an infection has resolved.**
133
*Describe the composition, synthesis, mechanism of action and function of lung surfactant.* What does the following describe? * This strongly interacts with phospholipids, is involved with adsorption and spreading of the surfactant on the surface of lungs, and prevents the collapse of the alveolus. Not required for life. 1. SP-A 2. SP-B 3. SP-C 4. SP-D 5. Both 1 and 2 6. Both 2 and 3
*Describe the composition, synthesis, mechanism of action and function of lung surfactant.* What does the following describe? * This strongly interacts with phospholipids, is involved with adsorption and spreading of the surfactant on the surface of lungs, and prevents the collapse of the alveolus. Not required for life. 1. SP-A 2. SP-B 3. **SP-C** 4. SP-D 5. Both 1 and 2 6. Both 2 and 3
134
*Identify factors that may affect the disease expressing genes and explain their contribution to human diseases utilizing specific examples.* * What does the image describe? The answer choices are below. 1. Locus Heterogeneity 2. Mosaicism 3. Pleiotropy 4. Penetrance - Incomplete 5. Penetrance - Age-dependent 6. Variable expression 7. New mutations (de novo)
Variable expression
135
*Discuss the clinical presentation, mechanisms of pathogenicity, diagnosis, prevention/treatment and epidemiology of the following bacterial respiratory pathogens: Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Mycoplasma pneumoniae, Klebsiella pneumoniae .* * Legionella pneumophila * What gram stain does this have? * Is it aerobic or anaerobic? * Is it extracellular or intracellular? * What locations have common infection rates? * What Virulence factors does it have? * What do patients present with? * What tests are used to dx this?
*Discuss the clinical presentation, mechanisms of pathogenicity, diagnosis, prevention/treatment and epidemiology of the following bacterial respiratory pathogens: Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Mycoplasma pneumoniae, Klebsiella pneumoniae .* * Legionella pneumophila * What gram stain does this have? * **Gram-negative** * Is it aerobic or anaerobic? * **aerobic** * Is it extracellular or intracellular? * **intracellular** * What locations have common infection rates? * **Hot tubs, Air conditioning, Showers** * What Virulence factors does it have? * **Major secretory protein: *_metalloprotease_*** * **DNase, Rnase** * **Lipase, phosphatase** * **Inhibits phago-lysosome fusion** * What do patients present with? * **Diarrhea** * **Hemolytic Anemia** * **Severe pneumonia with little or no inflammation of bronchioles or upper airways** * **Pontiac Fever: less severe, fever and muscle aches over 2-5 days, self-limiting** * What tests are used to dx this? * ***_Urinary antigen test_* or rapid microagglutination test** * **Slow growth on *_BCYE_***
136
* Discuss the typical clinical presentation and diagnostic findings of chronic obstructive lung disease including emphysema and chronic bronchitis.* * Describe COPD that is predominantly chronic bronchitis as it relates to everything listed
137
*Identify types of pneumoconiosis and the compounds that initiate disease.* ​ **Chest XR finding: Pleural thickening, plaques, effusions, and Nodules in the LOWER zones** * State which pneumoconiosis is associated with the above Chest XR finding. Options are below 1. Silicosis 2. Coal workers’ pneumoconiosis 3. Asbestosis
*Identify types of pneumoconiosis and the compounds that initiate disease.* ​ **Chest XR finding: Pleural thickening, plaques, effusions, and Nodules in the LOWER zones** * State which pneumoconiosis is associated with the above Chest XR finding. Options are below 1. Silicosis 2. Coal workers’ pneumoconiosis 3. **Asbestosis**
138
*Describe the changes in lung smooth muscle and cellular infiltrates associated with asthma.* * What leads to the structural changes in the bronchial wall? * What kind of changes happen to the bronchial wall?
Describe the changes in lung smooth muscle and cellular infiltrates associated with asthma. * What leads to the structural changes in the bronchial wall? * **Repeated bouts of inflammation lead to structural changes in the bronchial wall referred to as airway remodeling.** * What kind of changes happen to the bronchial wall? * **These changes include hypertrophy of bronchial smooth muscle and mucus glands and increased vascularity and deposition of subepithelial collagen, which may occur as early as several years after initiation of symptoms.**
139
*Differentiate between community-acquired and hospital-acquired bacterial pneumonias.* * NON-ICU, Inpatient CAP Tx * What are the two options for tx?
140
* Describe pathophysiology of cystic fibrosis and how this relates to morbidity and mortality.* * Why do people have the clinical manifestations of CF?
141
* Describe the differences between emphysema and bronchitis.* * Does the following describe emphysema or bronchitis? _Mucous gland hypertrophy and hyperplasia with hypersecretion_
* Describe the differences between emphysema and bronchitis.* * Does the following describe emphysema or **bronchitis**? _Mucous gland hypertrophy and hyperplasia with hypersecretion_
142
*Describe the types of infection that can lead to bronchiectasis.* * What is bronchiectasis*?* * What is seen on CT scans in bronchiectasis?
*Describe the types of infection that can lead to bronchiectasis.* * What is bronchiectasis*?* * ***​*Bronchiectasis is a disease state in which bronchi become inflamed and dilated, causing obstructed airflow (wide airways impair laminar outlaw) and impaired clearance of secretions.** * **It is often associated with AIDS, cystic fibrosis, and Kartagener syndrome.** * What is seen on CT scans in bronchiectasis? * **In bronchiectasis, a “tree-in-bud” pattern is commonly seen on high-resolution CT scans**
143
*Identify factors that may affect the disease expressing genes and explain their contribution to human diseases utilizing specific examples.* * What does the image describe? The answer choices are below. 1. Locus Heterogeneity 2. Mosaicism 3. Pleiotropy 4. Penetrance - Incomplete 5. Penetrance - Age-dependent 6. Variable expression 7. New mutations (de novo)
Pleiotropy
144
*Recognize and contrast normal lung exam vs abnormal lung exam.*​ "Deep and labored breathing pattern often associated with severe metabolic acidosis, particularly diabetic ketoacidosis but also kidney failure." * What breathing pattern is described above? Your choices are below. * Kussmaul * Biot * Ataxic * Cheyne Stokes
* Kussmaul
145
*Be able to describe a typical immune response to an extracellular bacteria, intracellular bacteria, and fungus.​* ***_Intracellular bacteria_*** * What pathway processes pathogens and their products found in the cytosol for MHC presentation? * What kind of T-cell activation is associated with MHC Class I? * How do these T-Cells kill cells? * What happens when T-h cells secrete a large amount of IFN-Gamma?
*Be able to describe a typical immune response to an extracellular bacteria, intracellular bacteria, and fungus.​* ***_Intracellular bacteria_*** * What pathway processes pathogens and their products found in the cytosol for MHC presentation? * **Pathogens and their products found in the cytosol (i.e. intracellular bacteria) are processed for MHC presentation by the endogenous pathway.** * What kind of T-cell activation is associated with MHC Class I? * **CD8 T cells.** * How do these T-Cells kill cells? * **CD8 T cells then kill infected cells via FAS/FASL or perforin.** * What happens when T-h cells secrete a large amount of IFN-Gamma? * **T-h cells secreting large amounts of IFN-Gamma which further activate the CD8 T cells**
146
*Explain how the mucosal immune system can both prevent responses to moral flora and also effectively respond to potential pathogens.* * Why we don’t have immune responses to these commensal bacteria? * In order to initiate appropriate adaptive immune responses to pathogens in the GI tract, antigens need to cross the intestinal mucosa and enter the underlying secondary lymphatic tissues. What are the two main ways in which this occurs? * What T cells are elicited by commensal bacteria? by pathogens?
*Explain how the mucosal immune system can both prevent responses to moral flora and also effectively respond to potential pathogens.* * Why we don’t have immune responses to these commensal bacteria? * **Dendritic Cells in the Lamina Propria only are weakly activated in the presence of commensal bacteria and so induce Tregs.** * In order to initiate appropriate adaptive immune responses to pathogens in the GI tract, antigens need to cross the intestinal mucosa and enter the underlying secondary lymphatic tissues. What are the two main ways in which this occurs? * **1. Transcytosis of antigens through M cells to be delivered to immune cells within Peyer’s patches.** * **2. Dendritic cells can capture antigens and transport them to secondary lymphatic tissue. Dendritic cells extend projections between adjacent epithelial cells, without disrupting the tight junctions. Process and present antigens to T cells within the secondary lymphatic tissues.** * What T cells are elicited by commensal bacteria? by pathogens? * **Commensals will most likely elicit Tregs** * **Pathogens should elicit Th1, Th2, or Th17 and CTLs**
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*Discuss the typical clinical presentation and diagnostic findings of chronic obstructive lung disease including emphysema and chronic bronchitis.* * List the spirometry findings and symptoms associated with * ​Stage 1 COPD aka mild * ​Stage 2 COPD aka moderate * ​Stage 3 COPD aka severe * ​Stage 4 COPD aka very severe
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*Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.* * Haemophilus influenzae * Are these gram negative or positive? * What shape do they have? * Are they encapsulated? * What emergency situation is this the most common cause of? * Does this have hemolysis?
*Understand and be able to discuss common bacterial pathogens responsible for upper respiratory tract infections, including those that present as sinusitis, pharyngitis, epiglottitis.* * Haemophilus influenzae * Are these gram negative or positive? * **Gram-negative** * What shape do they have? * **Rods** * Are they encapsulated? * **Yes** * What emergency situation is this the most common cause of? * ***_Epiglottitis_* due to Hib is rare BUT it remains the most common cause in both immunized and unimmunized individuals in the absence of trauma.** * Does this have hemolysis? * **No (gamma)**