Pulmonology Flashcards

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1
Q

Asthma characteristics

A

Chronic inflammation characterized by reversible airway obstruction and bronchospasm

Triggers: allergens, pollution, URI, exercise, beta blockers, aspirin (rare)

Presentation:
Cough
Wheezing
Chest tightness
Dyspnea
Tachypnea
Tachycardia
Prolonged expiratory duration
Decreased breath sounds
Accessory muscle use
Pulses paradoxus
Cyanosis

Labs:
Decreased peak flow, decreased FEV1/FVC ratio
ABG - mild hypoxia, respiratory alkalosis

CXR: hyper inflation - air trapping

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2
Q

Indications for home 02

A

Pulse ox symmetry less than 88%
Pulmonary hypertension
Peripheral edema
Polycythemia

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3
Q

COPD - features, dx, general management all stages

A
Clinical features:
Productive cough
Recurrent respiratory infections
Dyspnea
Wheezing
Rhonchi

FEV1/FVC less than 80% - obstructive lung disease
FEV1/FVC less than 70% - diagnostic of COPD

Tx:
stop smoking
yearly influenza vaccine
Pneumococcal vaccine - 19-65; single vaccine after 65 if more than 5 yrs from initial

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4
Q

COPD staging

A

GOLD 1: FEV1 > 80% predicted - mild
GOLD 2: FEV1 50-80% - moderate
GOLD 3: FEV1 30-50% - severe
GOLD 4: FEV1 less than 30% - very severe

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5
Q

COPD management - Category A

A

GOLD 1 or 2 with mild or infrequent symptoms
0-1 exacerbations per year

Short acting bronchodilator - albuterol, ipatropium

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6
Q

COPD management - Category B

A

GOLD 1 or 2 with moderate to severe symptoms
-stop to catch breath when walking on level ground, walk slowly

Short acting bronchodilator
Long-acting bronchodilator: B2-agonist or anticholinergic (tiotropium, ipratropium)

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7
Q

COPD management - Category C

A

GOLD 3 or 4 with mild or infrequent symptoms

Short acting bronchodilator
Long acting bronchodilator
inhaled steroid

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8
Q

COPD management - Category D

A

GOLD 3 and 4 with moderate to severe symptoms

Short acting bronchodilator
Long acting bronchodilator
inhaled steroid
\+/- theophylline
Home O2
\+/- phosphodiesterase-4 inhibitor - roflumilast
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9
Q

Emphysema

A

Destruction of alveoli and bronchioles

  • centriacinar - smoking
  • panacinar - alpha-1-antitrypsin deficiency
Features:
Dyspnea, productive cough, wheezing, rhonchi, decreased breath sounds
Barrel chest, use of accessory muscles
Prolonged expiratory duration
Pursed lip breathing (increases PEEP)
Morning headaches
Decreased heart sounds
JVD

Dx:
PFT: decreased FEV1/FVC, increased total lung capacity - air trapping
ABG: low O2, high CO2 - during exacerbations
CXR: flat diaphragm, hyperinflation, subpleural blebs/bullae, decreased vascular markings
DLCO decreased

Tx:
Stop smoking
Fast acting beta agonist, inhaled anticholinergics, inhaled corticosteroids
Home O2

A1-antitrypsin augmentation -> lung transplant

Complications
Chronic respiratory decompensation
Cor pulmonale
Frequent respiratory infection
Comorbid lung cancer common
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10
Q

Chronic bronchitis

A

Productive cough for three months in each of two successive years

Can proceed or follow development of airflow limitation

Tx:
Stop smoking
azithromycin, respiratory fluoroquinolone (levofloxacin), amoxicillin/clavulanate

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11
Q

Etiologies of bronchiectasis

A

Permanent dilation

unknown in 50%
Cystic fibrosis
Immunodeficiency
Dyskinetic cilia: Kartagener syndrome (dextrocardia, sinusitis, bronchiectasis), ADPKD
Pulmonary infections: TB, fungal infection, lung abscess
Obstruction: FB, tumor, LN

Other etiologies: Young syndrome, RA, Sjogen syndrome, allergic bronchopulmonary aspergillosis, smoking

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12
Q

Bronchiectasis

A
features:
Persistent, productive cough
Hemoptysis
Frequent respiratory infections
Dyspnea
copious sputum
wheezing, rales
hypoxemia

CXR: multiple cysts and bronchial crowding
CT: dilation of bronchi, bronchial wall thickening, bronchial wall cysts, dilation and thickening of the airways

Tx:
pulmonary hygiene - hydration, sputum removal
Chest physiotherapy
Abx when sputum production increases
Inhaled b2-agonists and corticosteroids may reduce sxs
Resection of severely diseased regions - hemorrhage, substantial sputum production, inviability

Complications:
Cor pulmonale
Massive hemoptysis
frequent abscess formation

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13
Q

Characteristics of malignant pulmonary lesions

A
Smoker
Over 45
New or progress lesion
irregular or asymmetric calcifications
>2 cm
Irregular margins

Get PET, bx, immediate ressection

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14
Q

Characteristics of benign pulmonary lesions

A
Under 35
No change from prior films
Central/uniform lesion with smooth margins
Less than 2 cm
No evidence of LAD

Follow with CXR in 3-6 mo

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15
Q

Adenocarcinoma of lung

A

MC lung cancer, and in nonsmokers and females

Peripheral, on pre-existing parenchymal scars
Associated with smoking

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16
Q

Large cell carcinoma of lung

A

Peripheral
anaplastic, undifferentiated giant cells
Strongly associated with smoking
Poor prognosis

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17
Q

Squamous cell carcinoma of lung

A

2nd MC type of lung cancer

Central - hilar mass from bronchus
Associated with smoking

Hypercalcemia - paraneoplastic syndrome, PTH-r protein

CXR/CT: cavitated lesion

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18
Q

Small cell carcinoma of lung

A

Central
Associated with smoking
Paraneoplastic: ACTH (Cushing Sn), ADH (SIADH), antibodies against presynaptic calcium channels (Lambert-Eaton Sn)

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19
Q

Pancoast tumor

A

usually non-small cell
Apex of lung
Can compress cervical sympathetic ganglion
-> Horner syndrome (miosis, ptosis, anhidrosis)

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20
Q

Superior vena cava syndrome

A

Edema/ flushing a face and arms
SOB, dysphagia, HA
Compression by lung tumor

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21
Q

Lung cancer treatments

A

non-small cell - surgical resection if possible, radiation, chemotherapy

Small cell: chemotherapy primarily

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22
Q

Malignant mesothelioma

A

pleura or pericardium
heavily associated with asbestos exposure
No association with smoking

presentation:
Chest pain
Dyspnea
Dullness to percussion
Exudative pleural effusion
Chest wall mass
Tx:
Surgery - pleurectomy, decortication
Radiotherapy
Chemotherapy
Poor prognosis
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23
Q

Asbestos exposure cancer risk

A

more likely to get bronchogenic lung cancer than mesothelioma

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24
Q

Laryngeal cancer

A

Associated with tobacco use - smoking, smokeless tobacco; alcohol use

Presentation:
Hoarseness
Dysphasia
Ear pain
hemoptysis

Dx: larygnoscopy with bx

Tx: partial or total laryngectomy, radiation, chemo

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25
Q

Idiopathic pulmonary fibrosis

A

Ineffective repair of alveolar epithelial cells injured by smoking, pollutants, microaspirations

over 40 yo

Presentation:
Progressive exercise intolerance
Dyspnea
Dry crackles
JVD
Tachypnea
Possible digital clubbing

PFT: decrease lung volume, normal FEV1/FVC ratio

Radiology: honey come appearance - reticular
Bx: fibrosis with decreased parenchymal architecture

Tx:
pirfenidone
nintedanib
sildenafil
Corticosteroids
Antibiotics
One transplant

Only survive 3 to 5 years after diagnosis

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26
Q

Sarcoidosis

A
"A GRUELING Disease"
ACE elevated in serum
Gammaglobulinemia
RA
Uveitis
Erythema nodosum
LAD - b/l hilar LAD
Idiopathic
Noncaseating Grandulomas
D vitamin production by activated macrophages in granulomas -> hypercalcemia

Pulmonary involvement: cough dyspnea and chest pain

Radiology: noncaseating granulomas, b/l hilar LAD, pulmonary infiltrate, skin lesions

Tx: Glucocorticoids, cytotoxic drugs, +/- lung transplant

Frequently show anergy to skin test or PPD

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27
Q

Silicosis

A

mining, demolition of concrete, stonecutting, sandblastng

Upper lobes
“eggshell” calcifications of hilar LN
Increased susceptibility to TB
risk of lung CA increased x2

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28
Q

Coal workers disease

A

mining coal

Anthracosis - generally asx or mild
-urban dwellers, tobacco smokers

Simple coal workers disease - small fibrotic lung nodules

Complicated: progressive massive fibrosis and necrosis

Presents as chronic bronchitis

No increased lung cancer risk, unless radon or smoking exposure

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29
Q

Berylliosis

A

aerospace manufacturing
Noncaseating granulomas
Increased risk of lung cancer

30
Q

Goodpasture’s syndrome

A

progressive autoimmune disease of lungs and kidneys

Anti-glomerular basement membrane Ab

Presentation:
hemoptysis
dyspnea
Respiratory infection
proteinuria
granular casts
hematuria

Dx:
anti-GBM ab
Bx: crescentic GN and IgG deposits along glomerular capillaries

Tx:
plasmapheresis, corticosteroids, immunosuppressive agents

31
Q

Granulomatosis with polyangiitis (Wegner)

A

Triad:
Necrotizing granulomas of the upper and/or lower respiratory tract
Necrotizing or granulomatous vasculitis in lungs and upper airways
Focal necrotizing, often crescentic, glomerulonephritis

Presentation:
hemoptysis
dyspnea
myalgias
chronic sinusitis
ulcerations of nasopharynx
saddle nose deformity

c-ANCA

Tx:
corticosteroids, cyclophosphamide
methotrexate
rituximab
plasma exchange
32
Q

A-a gradient

A

Compares O2 status of alveoli to arterial blood
Normal 5-15
increased in PE, pulmonary edema, right to left shunt

PAlvO2 - PartO2

713 x 0.21 - (PaCO2/0.8) - PaO2

33
Q

Pulmonary embolism

A
Risk factors:
Immobilization
Malignancy
Recent surgery
Pregnancy
OCP use
Smoking
Obesity
Fractures
Prior DVT
Severe burns

Presentation:
dyspnea, pleuritic chest pain, cough, hemoptysis (rare)
DVT symptoms (swollen leg)
Abrupt AMS

Dx:
D dimer - r/o DVT/PE in low probability situations
CTA - best test
CXR: Hampton’s Hump - wedge shaped opacification at distal lung fields; usually normal, may have atelectasis, pleural efusions
ABG - elevated A-a gradient

ECG - sinus tach - classic but rare: S1Q3T3
V/Q scan - if can’t use contrast for CTA
-ventilatory defects suggest PNA or other parenchymal lung disease
-perfusion defects suggest PE

Tx:
Unstable - thrombolysis (tPA, streptokinase, urokinase)
Stable - anticoagulation
-state LMWH, heparin or fondaparinux -> warfarin or rivaroxaban, apixaban, edoxaban or dabigatran

34
Q

Pulmonary hypertension

A
Causes:
PE
Valvular disease - MS, MR
Left to right shunt
COPD (MC)
Idiopathic

Presentation: dypsnea, fatigue, CP, cough, syncope

Exam:
cyanosis
Digital clubbing
loud S2
JVD
Hepatomegaly

Dx:
ECG - RVH - cor pulmonale
CXR: pulmonary vascular congestion, enlarged RV
ECHO or cath to measure pressure

Tx:
CCB (nifedipine)
endothelin receptor antagonists (ambrisentan, bosentan)
cGMP phosphodiesterase inhibitors (sildenafil, tadalafil)
Prostanoids (ilprost, treprostinil)

35
Q

Pulmonary edema

A

Increased pulmonary venous pressure -> fluid leaks from vessels into lung interstitial and airspaces

Causes:
Left-sided heart failure
MI
Valvular disease
Arrhythmias
ARDS
Features:
dyspnea
orthopnea
paroxysymal noctural dyspnea
frothy pink sputum
tachycardia
\+/- wheezing

Dx:
BNP elevated
ECG: T wave abnormalities or QT prolongation
CXR: diffuse interstitial fluid, cephalization of the vessels, Kerley B lines

Tx: NOLIP
Nitrates - redistribute blood outside pulmonary vasculature, decreased preload
Oxygen - if hypoxemic
Loop diuretics
Inotropic drugs - dobutamine, milrinone (not first line, increased mortality)
Positioning

36
Q

Pleural effusion

A

Excess fluid in the pleural space

Presentation:
Sob, dyspnea with exertion
\+/- pleuritic chest pain
Fatigue
dullness to percussion (over 300 ml)
Decreased breath sounds
Decreased tactile fremitus
egophony
\+/- tracheal deviation

CXR: fluid level or blunting of costophrenic angles

Transudate: CHF, cirrhosis, nephrotic sn

  • Pleural to serum protein less than 0.5 - OR-
  • Pleural to serum LDH less than 0.6

Exudative: cancer, infection, vasculitis

  • Pleural to serum protein >0.5
  • Pleural to serum LDH >0.6

Tx: underlying pathology
Thoracentesis, chest tube
Pleurodesis - talc or chemo to scar space

Complications: take off too much fluid too quickly -> reexpansion pulmonary effusion

37
Q

Pneumothorax

A

Air in the pleural space

Closed PTX: COPD, TB, blunt trauma, spontaneous (thin tall male)

Open PTX: penetrating trauma, iatrogenic (central line, thoracentesis)

Tension PTX: open with ball valve mechanism, increasing pressure

Small PTX - asx

Tension PTX sxs:
Decrease wall movement
Decreased breath sounds
Increased resonance to percussion
Decreased tactile fremitus
hypoxemia
JVD
Decreased blood pressure
Tracheal deviation away from side

Tx:
less than 15%: O2 and monitoring
>15% - chest tube

Tension: needle decompression
Recurrent - pleurodesis

38
Q

Hemothorax

A

blood in the pleural space
like pleural effusion presentation

Complication: clotting blood -> fibrosis pleural space

Dx: thoracentesis - grossly bloody

Tx: O2, chest tube
Tx underlying cause

39
Q

CENTOR criteria

A

Strep pharyngitis

Cough absent +1
Exudates, tonsillar +1
Nodes- tender anterior cervical +1
Temperature +1
under 15 +1 OR over 44 -1

0-1 no treatment no cx
2-3: get cx and treat if positive
4-5: tx empirically

Tx: b-lactam abx - PCN, amox

40
Q

Ludwig angina

A

cellulitis of floor of mouth, extending into submandibular area

Causes:
dental ifnection
polymicrobial - GAS, staph, Bacteroides

Tx: abx
I&D
protect airway

41
Q

Peritonsillar abscess

A

Infection between the tonsil and pharyngeal constrictors

Causes: strep, S. aureus, Bacteroides

Presentation:
Fever, severe sore throat, muffled “hot potato” Voice
Tonsil or uvula deflection to the opposite side
Trismus (lockjaw)
Drooling

Tx: needle aspiration, I&D, abx

42
Q

Mononucleosis

A

EBV

Presentation
Fatigue 3-6 mo
Sore throat
malaise
LAD - posterior cervical
Splenomegaly
Fever
Tonsillar exudates
Labs:
heterophil Ab - monospot
EBV serology
elevated LFTs
Hemolytic anemia (rare)
thrombocytopenia (rare)

Tx: supportive
no noncontact supports x3 weeks
no contact sports x4 weeks

43
Q

Viral influenza

A
Presentation:
arthralgias, myalgias (severe)
nasal congestion
cough
V/D
high fevers
LAD

Lab: rapid swab

Tx: zanamivir or oseltamivir within 48 hr of sxs

ppx: vaccine - takes 2-4 weeks to kick in

44
Q

Sinusitis

A

associated with allergic rhinitis, barotrauma, viral infection, prolonged NG tube, asthma

Bacterial causes: S. pneumo, H flu, Moraxella catarrhalis

Rare spread to CNS -> meningitis

Chronic - over 3 mo - obstruction (polyps, deviated septum) or anaerobic infection

Presentation:
purulent nasal discharge
maxillary toothache
tendernes of affected sinus
foul smell
Tx:
nasal irrigation
analgesics
oral decongestants
intranasal steroids
amox-clav, doxy, levofloxacin

DM - mucormycosis

severe/chronic - get CT sinuses

45
Q

Acute bronchitis

A

features:
Cough lasting longer than five days - often productive +/- purulent sputum
usually not associated with fever

Dx: sputum cx not recommended
CXR r/o PNA (fever, abnl V/S, abnl lung exam)

Tx: supportive, usually viral

46
Q

Causes of pneumonia in neonates

A

GBS

E. coli

47
Q

Causes of pneumonia in under 5 yo

A

RSV
S. pneumo
S. aureus

48
Q

Causes of pneumonia in 5-20 yo

A

S. pneumo
Mycoplasma pneumoniae
Chalmydophilla pneumoniae

49
Q

Causes of pneumonia in >20 yo

A
S. pneumo
Mycoplasma penumoniae
Chlamydophila pneumoniae
Haemophilus influenzae
Influenza virus
Legionella pneumophila (+ diarrhea)
50
Q

Causes of pneumonia in ederly

A

S. pneumo
Haemophilus influenzae
S. aureas

51
Q

Typical pneumonia presentation, pathogens, empiric tx

A
presentation:
Fever
Cough
Sputum production
SOB

CXR: lobar consolidation

Pathogens:
S. pneumo
H flu
S. aureus

Tx: B-lactams

52
Q

Atypical pneumonia presentation, pathogens, empiric tx

A
Presentation:
Prolonged illness
Dry cough
Headache
Fatigue

CXR: interstitial infiltrates

Pathogens:
Mycoplasma pneumoniae
Chlamydophila pneumoniae
Legionella pneumophilia
Chlamydophila psittaci

Tx: macrolides, fluoroquinolones

53
Q

Empiric treatment for neonates with CAP

A

hospitalize

ampicillin + gentamicin
or
vancomycin + gentamicin

54
Q

empiric treatment for children with CAP

A

often outpt tx

amox or amox-clav for typical

azithromycin for atypical or pcn allergy

55
Q

Outpatient treatment of CAP in otherwise healthy individual with no antibiotics in last 3 mo

A

Azithromycin or doxycycline alone

56
Q

Outpatient treatment of CAP in patient who received antibiotics in the last three months or has chronic medical problems (DM, lung dz, immunosuppression)

A

b-lactam - amox or cefuroxime PLUS macrolide (azith)
OR
Respiratory fluoroquinolone - levo or moxi

57
Q

Inpatient treatment for CAP

A

B-lactam PLUS macrolide - ceftriaxone + azithromycin

Respiratory fluoroquinolone

58
Q

ICU treatment for CAP

A

b-lactam PLUS macrolide or respiratory fluoroquinolone

59
Q

Pneumococcal vaccine

A

PCV-13 - conjugate - 4 doses before 2 yo

PPSV-23 - polysaccharide
19-64 yo: smoker, alcoholic, chronic heart, lung, liver disease, DM
Over 65, CSF leak, asplenic, cochlear implant, or immunocompromised

60
Q

Pneumocystis jirovecii (PCP)

A

Immunocompromised

  • HIV CD4 less than 200
  • Chronic glucocorticoid use

Slow progression to respiratory failure

CXR: diffuse, B/L interstitial infiltrates
Elevated LDH
Sputum with Pneumocystis on stain

Tx:
21 days of TMP-SMX (IV or PO) or Pentamidine (IV) or Primaquine (PO) + clindamycin (IV or PO)
steroids if pO2 less than 70 on room air or A-a gradient greater than 35

61
Q

Primary tuberculosis

A

Local infection in the lung
Fever
+/- cough and chest pain
LAD

Forms granulomas with central caseous necrosis (Ghon focus)

Ghon complex: Ghon focus + hilar LAD

10% untreated -> PNA or disseminated TB
90% -> latent

62
Q

Reactivation of tuberculosis

A

5-10% with latent TB

Risk:
Recent primary infection
Immunosuppression
DM
Kidney disease
Older age
HIV
TNF-a inhibitors

Lung apices

Features:
Fever
Night sweats
Weight-loss
Cough and hemoptysis

Disseminated involves: bones, CNS, GI, GU

63
Q

Diagnosis of TB

A

Sputum x3 8 hours apart

  • Acid fast stain
  • AFB cx - takes 4-6 weeks, needed for susceptibility

TB NAAT - rapid, but no susceptibility info

64
Q

TB screening

A

PPD

Interfereon gamma release assay
-quantiferon TB- GOLD
-T-spot
Evaluates release of IFN-gamma by T cells presented with M. tuberulosis antigens
positive result - previous immune response to TB
Immunosuppression -> unreliable results

65
Q

PPD positive criteria

A

5 mm: HIV, close contact with TB, CXR suggestive of TB, immunosuppression

10 mm: homeless, IV drug use, prison, health care, immigrants from endemic areas, DM, HD, kids under 4

15 mm: always considered positive (low risk individuals)

66
Q

Treatment of active vs latent TB

A

Latent:
Isoniazid daily x 9 mo OR Rifapentine + isoniazid q1 wk x3 mo

Active:
2 months of RIPE then 4 mo of Rifampin + isoniazid

RIPE:
Rifampin
Isoniazid + B6
Pyrazinamide
Ethambutol
67
Q

Acute respiratory distress syndrome

A

Respiratory failure following a severe acute injury to lung
-sepsis, trauma, aspiration

Features:
Acute dyspnea and respiratory decompensation
Cyanosis
Tachypnea
Wheezing, rales, Rhonchi

Dx:
ABG: respiratory alkalosis
Wedge pressure less than 18 (if pulm edema w/ CHF over 20)
PaO2:FiO2 less than 200 (under 100 severe)
CXR: diffuse pulmonary densities

Tx:
Admit ICU - supportive care and treat underlying cause
Mechanical ventilation with low tidal volumes (minimize injury) and adequate PEEP (recruit collapse alveoli)
Conservative fluids - goal CVP 4-6 mmHg
Furosemide and albumin to prevent pulmonary edema
Prone positioning - improves oxygenation (not survival)

Minimize O2 consumption:

  • prevent fever
  • minimize anxiety and pain
  • limit respiratory muscle use- paralytics

Transfuse blood only if Hgb below 7 - transfusion may increase risk of death in ARDS patient

68
Q

Oxygen delivery methods

A

NC - 24-40% FiO2 (FiO2 increases 3% every 1L/min up to 6 L/min)

Face mask- 50-60% FiO2

Non-rebreather - 60-95% FiO2

CPAP -> 80% FiO2

Mechanical vent up to 100% FiO2

69
Q

Prevention of post operative atelectasis

A

Incentivive spirometry
Early postop ambulation
Upper airway suctioning
Bronchoscopic suctioning

70
Q

Intubation

A

Pre-oxygenate - 100% O2 several minutes

Pretreat

  • Lidocaine for increased ICP
  • Fentanyl for pain
  • Atropine for secretions, prevent bradycardia

Induction agents:
Sedatives: etomidate, propofol, midazolam, ketamine
Paralytics: succinylcholine, rocuronium

Cricoid pressure (Sellick technique)

Placement:
Watch tube pass vocal cords
-Check end tidal CO2
-look for bilateral lung expansions
-listen for air sounds in stomach
-CXR for positioning

Complications: tube misplacement, aspiration, dental injuries

Tracheostomy if ET tube in place for few weeks