Respiratory System Flashcards

1
Q

Hypersenstivity Pneumonitis

A

Fever , Chills , Cough , Dyspnea
Bilateral interstitial opacities, crackles, restrictive pattern.
bronchial lavage has lymphocytic dominance >20% Often >50%.

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2
Q

Obstructive Lung Disease

A

Asthama, COPD, Old age.

PFT:

  • FEV1↓ , FVC ↓ ,
  • FEV1/FVC ↓(<70% ; Normal is 70%)
  • TLC ↑
  • RV ↑↑ , FRC (ERV-RV) ↑
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3
Q

Restrictive Lung Disease

A

Pulmonary Fibrosis, Pneumoconiosis etc

PFTs:

  • FEV1 ↓, FVC ↓,
  • FEV1/FVC ↑ (>70-80%)
  • TLC ↓, RV ↓, FRC ↓.
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4
Q

SVC syndrome

A

Superior vena cava syndrome
Flushing of face + Congestion of neck veins.
Caused by pancoast tumor (Adenocarcinoma of Lungs)

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5
Q

NRDS (Neonatal Respiratory Distress Syndrome)

A

Aka hyaline membrane disease

  • Due to insufficient surfactant production by type II pneumocytes due to decrease in lamellar bodies (the specialized organelles that produce surfactant).
  • Decrease lecithin/sphingomyelin ratio (i.e., <2.0).
  • ↓ surfactant production means ↓ alveolar compliance, ↓ FRC, ↑ Airway resistance &­ ↑ elastic recoil.
  • CXR shows a “reticulogranular” appearance.
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6
Q

Acute respiratory distress
syndrome (ARDS)

A

Bilateral exudative chest infiltrates and decr O2 sats
in patient following: pancreatitis; aspiration of vomitus; near-drowning episodes (aspiration of fresh/sea water); improper insertion of NG tube into the lungs with feeding initiated; toxic shock syndrome; or general trauma / sepsis.

  • Pulmonary decompensation associated with pancreatitis.
  • Patient can be ventilated as follows: prone positioning (patient on
    stomach) + low-tidal volume setting + permissive hypercapnia.
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7
Q

Pertussis

A
  • Classic whooping cough presents as succession of many coughs
    followed by an inspiratory stridor.
  • Can also present in adults Cough with hypoglycemia or post-tussive emesis, which means vomiting after coughing episodes.
  • Pertussis can cause super-high WBC counts in the 30-50,000-range, where there are >80% lymphocytes.
  • One way to prevent = vaccination (TDaP)
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8
Q

Cystic Fibrosis

A
  • Autosomal recessive mutation (∆F508) impairs - - CFTR function
  • ATP dependant Chloride channel defective
  • Chronic, productive cough
  • Recurrent sinopulmonary infections (eg,Staphylococcus aureus, Pseudomonas aeruginosa)
  • Pancreatic insufficiency (Def Fat Sol Vitamins)
  • Male infertility (bilateral absence of vasdeferens)
  • Elevated sweat chloride levels
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9
Q

Sarcoidosis

A

(noncaseating granulomas)
Female with lymphedonopathy
Bilateral hilar adenopathy, uveitis
Hypercalcemia is also seen
Complication:
Granuloma express increased activity of alpha-1 hydroixylase -> increase 1,25 hydroxy vit-D-> ca+2 reabsorbtion in GI lumen, this can cause Nephrolithiasis

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10
Q

Rubeola

A

High Fever & 3Cs ( Cough, Coryza, Conjuntivitis)
Koplik Spots (2-3days after symptoms)
As fever abates a Maculopapular rash starts at head and descends to cover whole body (like rubella)

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11
Q

Mumps

A

Classically presents as:

  • Parotidits
  • Orchitis
  • Meningitis

Caused by Paramyxovirus.

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12
Q

Pulmonary Fibrosis

A
  • Progressive dyspnea
  • Digital clubbing
  • Loud P2 (pulmonary hypertension due to lung disease).

Idiopathic pulmonary fibrosis affects individuals in late adulthood, and lung examination would reveal inspiratory crackles.

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13
Q

Septic Shock

A
  • Fever
  • Leukocytosis
  • Hypotension
  • Tachycardia
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14
Q

Predisposing conditions for aspiration pneumonia

A
  • Altered consciousness impairing cough reflex/glottic closure (eg, dementia, drug intoxication)
  • Dysphagia due to neurologic deficits (eg, stroke, neurodegenerative disease)
  • Upper gastrointestinal tract disorders (eg, GERD)
  • Mechanical compromise of aspiration defenses (eg, nasogastric & endotracheal tubes)
  • Protracted vomiting
    -Large volume tube feedings in recumbent position
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15
Q

Methhemoglobinemia

A
  • Methemoglobin has Fe+3 (ferric) instead of Fe+2 (ferrous)
  • Results usually after the use of oxidizing medications i.e Nitrites, Dapsone, Benzociane etc
  • Functional anemia > Cyanosis
  • Chocolate brown blood, doesn’t turn red with O2
  • Cyanosis with O2 sats showing 85-90%
  • Can be inherited in AR form, deficiency of Cytochrome b-5 reductase

Rx: Methylene blue (acquired form)

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16
Q

CO posioning

A
  • CO binds to Hb
  • CO has 200X more affinity for Hb than O2
  • Makes blood bright red
  • Cyanosis, but O2 sat may show 100%

Rx: 100% O2

17
Q

COPD

A
  • Blue Bloaters (Cyanotic & Swollen)
  • Hypertrophy of mucus glands in the bronchioles
  • Increased reid index >50%
  • Mucus & inflamation causes obstruction
  • Decrease Ventilation, Increase CO leads to V/Q mismatch
  • Decrease FEV1/FVC ratio
  • Wheezing, Crackles, Cyanosis & Dyspnea
  • Signs of RHF (Swollen bloated look)
  • Risk factor: Smoking
18
Q

Centriacinar Emphysema

A
  • Caused by smoking
  • Barrel shaped chest
  • Breathing through pursed lips
  • Decrease lung recoil & Increase lung compliance
  • Dyspnea, Tachycardia, Decreased breath sounds, Hypoxemia
  • Pink Puffers
19
Q

Panacinar Emphysema

A
  • Seen in Young patients
  • Caused by Alpha-1 antitrypsin deficiency
  • Can also cause liver cirhosis
  • Unexplained Emphysema + Abnormal LFT
  • Young patient + Liver problem + Lung problem
  • Imaging: Flat diaphragm, Increase CV angles, Thin mediastinum
20
Q

Asthama

A
  • Caused by bronchiole hyperresponsiveness leading to reversible bronchoconstriction
  • Type-I hypersentivity
  • Eosinophilia
  • Allergic asthama also has IL-4, IL-5, IL-10 & IL-13
  • Cough, Wheezing, Tachypnea, Dyspnea

Dx: Methacholine stress test

Rx: Bronchodilators, Steroids etc

21
Q

Bronchiectasis

A
  • Irreversible dilation of Bronchi
  • Purulent sputum, Infections, Hemoptysis
  • Caused by: Klebsiella, Bronchial Obstruction, Decrease Ciliary motility, Kartagner syndrome, CF, Aspergillosis
  • Recurrent & Chronic Pneumonia
  • Sparing of Rt lower lobe in imaging
22
Q

Respiratory Changes with Aging

A
  • ↑ V/Q mismatch
  • ↑ Dead Space ventilation
  • ↑ A-a gradient (↓ PaO2)
  • No Hypoventilation (Normal PaCO2)