p1 Flashcards

(88 cards)

1
Q

preop management of COPD?

A

smoking cessation(4-6) wk prior to surgery decreases post-op pulmonary complications(pneumonia and RF) significantly even if small cigarette consumption.

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2
Q

Long-term oxygen therapy in COPD?

A

Given if resting O2 saturation <88%

have mortality benefit

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3
Q

what about preop corticosteroid, methylxanthine, and antibiotic?

A

No benefit

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4
Q

future and approach of a patient with RLD?

A
Decreased VC
Normal or increased FEV1/FVC ratio
First, do DLCO
If normal--CW abnormality and RM weakness
if decreased --ILD
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5
Q

Cause for CW abnormality and RM weakness?

A
CW abnormality
Obesity hypoventilation syndrome
Scoliosis
           RM weakness
Myasthenia gravis
ALS
Polio
Gulian barre syndrome
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6
Q

ILD future?

A

Progressive dry cough, fatigue, and dyspnea
Crackles, clubbing
Imaging shows peripheral reticular opacities with traction bronchiectasis +/– “honeycomb” appearance of the lung (advanced disease).
Histologic pattern: usual interstitial pneumonia.

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7
Q

cause of ILD?

A

Dust
Drug
Radiation
Systemic CTD

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8
Q

Dust?

A

Asbestos
Beryllium
Silicon
Coal worker pneumoconiosis

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9
Q

Drug?

A
Amiodarone
Bleomycin
Nitrofurantoin
Methotrexate
Busulfan
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10
Q

Systemic CTD?

A

RA
Scleroderma
Sjögrens syndrome

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11
Q

Pathophysiology of ILD?

A

May involve multiple cycles of lung injury-
inflammation, and fibrosis.
Fibrosis affects the airway, alveoli, and interstitium

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12
Q

Pulmonary HTN symptom?

A

Progressive dyspnea, fatigue, and weakness
Exertional angina and syncope due to Dec RVO
Abdominal pain and distension

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13
Q

Physical examination?

A

left the parasternal lift and RV heave
Loud P2 and right side s3
pansystolic murmur due to TR
RSHF sign

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14
Q

Classification?

A

primary PHTN
due to LSHF
due to chronic lung disease(ILD

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15
Q

Normal FVC and FVC1/FVC ratio?

A

FVC:80-120%
FVC1/FVC ratio–>80%
In COPD ratio usualy <70

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16
Q

GERD and asthma?

A

GERD–microaspiration–bronchial hyperactivity and increase vagal tone.
Asma exacerbation during the night and after a meal
Treat with PPI

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17
Q

Normal pH range?

A

7.35 to 7.45

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18
Q

Normal values for PaCO2?

A

are usually 35-45 mmHg.

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19
Q

Partial pressure of oxygen (PaO2)?

A

75 to 100 millimeters

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20
Q

PE and (A-a) oxygen gradient?

A

increase due to VQ mismatch

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21
Q

(A-a) oxygen gradient?

A
  • 2.5 + 0.21xage
  • Patient age/4 + 4
  • Between 5–14 inage < 40
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22
Q

How to calculate PA02?

A

150-PaCO2/0.8

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23
Q

Exercise-induced asthma pathophysiology?

A

High volume gas and cold air entery—mast cell degranulation–bronchospasm

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24
Q

Management?

A

Beta agonist-10-15 min prior exercise(first line), should be used in whom require less than daily
Antilukatrine agent 15-20 min before exercise–second line, not tolerate beta-blocker
Both can be used together in the case of high performing athletes
Antiukatrine and steroid for patient daily exercise practice

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25
trigger of anaphylaxis?
FOOD DRUG INSECT STING
26
CM?
hypotension, tachycardia, and tissue edema strider,horsnesnes and bronchospasm Urticarial rash, pruritis, and flushing nausea, vomiting, and abdominal pain
27
management?
``` intramuscular epinephrine airway management and resuscitation adjuvant therapy(antihistamin and glucocorticoid) ```
28
How to differentiate asthma fromCOPD?
spirometry plus bronchodilator therapy asthma --reversible COPD --not reversible/partially reversible
29
Old patient with lower lobe infiltration?
CAP due to S.pnumonia | If cavity--Lung abscess due to anaerobes(associated foul-smelling sputum, dysphagia and common in alcoholic)
30
Assist-Control (AC) mode?
Most common methods of mechanical ventilation in the intensive care unit AC ventilation is a volume-cycled mode of ventilation. It works by setting a fixed Tidal Volume (VT) that the ventilator will deliver at set intervals of time or when the patient initiates a breath.
31
How much TV should be adjusted?
6ml/kg
32
Bird fancier lung and farmer's lung?
Type of Hypersensitivity pneumonitis due to exposure of bird dropping and mold respectively.
33
clinical manifestation?
cough, fever, malaise, and breathlessness after 4-6 hr of antigen exposure. If chronic--restrictive lung disease
34
CXR?
Ground-glass opacity/heaviness on CXR.
35
pathophysiology?
chronic inflammation--lung fibrosis
36
management?
Avoid exposure | Systemic corticosteroid--severe manifestation and acute exacerbation
37
myasthenic crisis CM?
Increase generalized or oropharyngeal paralysis | respiratory insuficieny
38
precipitating factor?
Infection and surgery Pregnancy or childbirth tapering corticosteroid medication(aminoglycoside,fluoroquinolone,BB and CCB)
39
management?
intubation if deteriorating respiratory status(impeding RF) | plasmapheresis, IV Ig, and corticosteroid
40
impeding RF sign?
tachypnea shallow breath respiratory muscle paralysis choking
41
alpha 1 antitrypsin deficiency?
Family history of COPD and Liver disease COPD Smoking exacerbates Minimal LFT abnormality
42
Diagnosis?
Serum A1A level Pulmonary spirometry Liver function test
43
for a patient who presents with subacute/chronic cough | w/o apparent cause and absent parenchymal lesion what first to do?
Emperic 1st generation antihistamin Combined antihistamines and decongestants If not respond for 3-4 wk-- Immaging
44
Atelectasis feutcher?
Decrease/absent BS Decrease TF Dullness on percussion The trachea will deviate to the side of the lesion?
45
What is a solitary lung nodule?
round opaque <=3 CM normal surrounding lung parenchyma no LDP, surrounding PE and athelectasis
46
How we approach if it is found on routine x-Ray?
ask for previous X-ray >2 years back--If the same-No further test but patient have not/changed size CT
47
After CT?
Depend on the presence of malignancy fetcher (low density, large, onion skin calcification and speculated border) Also consider CM suggesting of malignancy(age >40, smoking, previous malignancy, and weight loss)
48
no malignancy future?
serial CT follow-Up
49
Borderline?
Biopsy | PET
50
malignancy future?
Surgical excision
51
cause of recurrent pneumonia?
depend on region involvement
52
On the same field?
``` Local airway obstruction due to intrinsic(tumor, bronchiectasis) or extrinsic cause(tumor or LDP) Recurrent aspiration(alcohol,drug,GERD,dysphagia and seizure) If the patient has a risk of Ca do CT ```
53
On different religions?
Immunosuppression sinopulmonary disease(ISS and CF) Non-Infectious(Vasculitis, BOOP)
54
Location of aspiration pneumonia in supine?
posterior segment of UL | the upper segment of LL
55
How stroke is a risk?
cause dysphagia and impaired cough reflex
56
Good pasture syndrome CM
 Renal—nephritic syndrome |  Pulmonary---Cough, SOB, and hemoptysis
57
Pathophysiology?
Ab against alpha 3 type chain of collagen type 4 in BM of glomeruli and alveoli
58
Diagnosis of pneumonia requires?
 CXR |  CM have sensitivity < 50%
59
Cause of acidosis in seizure patients?
 Prolonged muscle contraction—LA—M.Acidosis |  Aspiration/muscle spasm---hypoventilation –R.Acidosis
60
Acid-base disturbance in PE?
 Hypoxia/V/Q mismatch—Hypervantlasion-R.Alkalosis
61
CM of asbestosis?
 Develop prolonged asbestos exposure(e,g shipyard, mining)  Develop after 20 years of exposure  Dyspnea, Clubbing, and inspiratory crackle  Increase the risk of L, Ca, and mesothelioma plural plaqe in CXR
62
Imaging (CXR) other diagnosis modality?
 Lower lob infiltration  Plural plaque  Spirometer show a restrictive pattern  Decrease DLCO
63
Pulmonary embolism cardiac catheterization evidence?
 Elevated RA pressure  Elevated pulmonary artery pressure  Normal or low capillary wage pressure
64
Cardiac tamponed finding in cardiac catheterization?
 Increase with equalization of RA, PA, and PCW pressure
65
Archnodinic acid metabolism?
 First PLA2m metabolize membrane PL to AA | AA metabolize to leukotriene and prostaglandin and thromboxane by LOX and COX respectively
66
Function?
 LT C4E4D4—Bronchoconstriction and increase vascular permeability, inflammatory  B4—chemotaxis and inflammatory  TXA2 and PGD2—bronchospasm and inflammatory  PGE2 and PGI2  Bronchodilator and vasodilation, anti-inflammatory
67
Did aspirin exacerbate respiratory disease(AERD) CM?
 Constellation of morbid obesity, chronic rhinosinusitis, nasal polyposis, or urticarial with AERD  Non-IGE mediated pseudo drug allergic reaction  Patient present with the asthmatic symptom, sinusitis symptom, and facial flushing after 30min-3 Hr of aspirin ingestion  Is due to an imbalance of pro-inflammatory leukotrienes and anti-inflammatory prostaglandins
68
Management?
 Management chronic sinusitis and asthma  Avoidance of NSAID  Desensitize if NSAID is necessary  Anti-leukotriene for respiratory and sinus symptom
69
The most common diagnostic criteria of anaphylaxis?
 Acute illness involving skin |  Respiratory or CVS compromise
70
A drug that exacerbates anaphylaxis?
 NSAID and beta-blocker |  By increasing non-immunologic mast cell degranulation and unopposed alpha effect
71
CM of pneumothorax?
 Hyper resonant lung  Decrease air entry  Decrease TF  Hypotension/shock— impairing RV preload due to media sternal venous obstruction
72
Positive end-expiration MV mechanism, benefit, and complication?
 Provide above AP pressure at end of expiration  Prevent alveolar collapse, increase FRC and decrease work of breathing  Alveolar injury, pneumothorax, and hypotension
73
Cause of atelectasis in MV patient?
 Mucus plugging  A shift of the ETT to one bronchus thus the other will be atelectatic --Normally the ET tube should be 2-4 CM above carina
74
How do ET intubation, bronchoscopy, and endoscopy, and NGT increase the risk of aspiration pneumonia?
 Blocking epiglottis closure
75
Bacteriology profile of AP?
 Mixed aerobic, anaerobic, G+ and G- rods and streptococcus
76
S/E of inhaled corticosteroid?
 In both high and low dose—MC oral thrush |  High dose-Cushing
77
Bronchiectasis signs and symptoms?
Cough with daily mucopurulent sputum production Rhinosinusitis, dyspnea, and hemoptysis Crackles and wheezing suspect specially in non smoker patient with chronic cough
78
pathophysiology?
Infectious insult with impaired clearance
79
Etiology?
``` airway obstruction rheumatic disease(RA and Sjogren) chronic or prior infection(aspergillosis and TB) immunodeficiency (hypogammaglobulinemia) congenital(CF and alpha 1 antitrypsin defriciency) ```
80
Evaluation?
HRCT for initial diagnosis Immunoglobulin quantification CF testing Sputum culture and pulmonary function testing
81
Symptom of B-agonist S/E?
* Hypokalemia related (increase cellular k uptake)—weakness, arrhythmia, and ECG change * Tremor * Headache * Palpitation
82
Drug induced lung injury future?
* Present acutely as hypersensitivity pneumonitis or chronic ILD * Fever, dry cough and SOB * Mid lung and lower lung interstitial infiltration with unilateral effusion * Leukocytosis and eosinophilia
83
Granulomatosis with polyangiitis(wegners) CM?
 Arthralgia, fever, Weight loss, and fatigue  Sinusitis, otitis media, and saddle nose deformity  Bloody or purulent nasal discharge and hearing loss  Lung nodule and cavitation  Dyspnea, cough, and hemoptysis  Rapidly progressive granulomatosis Livedo reticularis and skin ulceration
84
Diagnosis?
 ANCA—PR3(70)-C-ANCA and MPO(20)-P-ANCA  Leukocytoclastic vasculitis in skin biopsy  Pausini glomerulonephritis in renal biopsy  Granulomatous vasculitis in lung biopsy
85
Management?
Corticosteroid and immunomodulator
86
feucher of bronchiectasis?
Cough and mucopurulent sputum production Rhinosinusitis, dyspnea, and hemoptysis Crackles and wheezing
87
risk factors?
``` Airway obstruction Rheumatic disease(RA and sjhorgen), toxic inhalation Chronic and prior infection(aspergillosis and Tb) Immunodeficiency(hypoglobulinimia) Congenital(CF and alphal1 antitrypsin deficiency) ```
88
Evaluation?
High-resolution CT imunoglobulin quantification CF testing and sputum culture PFT