Pulmonary Flashcards

(273 cards)

1
Q

air trapping signs in asthma that are ominous

A

decreased lung sounds

hyperresonance

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2
Q

dx for asthma

A

decreased PFTs (decreased FEV1/FVC
reversible - with beta agonist - albuterol
inducible - with Ach agonist

ABG - increased A-a gradient

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3
Q

If PFTs in a pt suspected of asthma next step =

A

methacholine challenge

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4
Q

stages of asthma symptoms

A

day night FEV1
I <2/wk <2/mon 80%
II <1/day <1/wk . 80%
III . >1/day >1/wk . 60-80%
IV . >1/day >1/wk . <60%
V . refractory to everything so they get oral steroids

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5
Q

stages of asthma tx

A

I - SABA
II - SABA + ICS (or leukotriene antagonist)
III - SABA + ICS + LABA
IV - SABA + ICS(increase dose) + LABA

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6
Q

LABA without ICS

A

never ever do this and leukotrine antagonist = ICS

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7
Q

basics of overall asthma tx

A

always watch pt use their med and add a spacer to make sure meds get in lungs and not just mouth

make sure pts adhere to meds

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8
Q

initial steps during an asthma exacerbation

A

O2 to maintain SpO2>90%
nebulizers (ipatropium, albuterol)
oral steroids
peak expiration flow rate

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9
Q

Following an acute asthma exacerbation what criteria allows a pt to be discharged home

A

no O2 requirement
no wheezing
peak expiratory flow rate >70%

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10
Q

following an acute asthma exacerbation what criteria puts them in the ICU

A

increased O2 demand
rising CO2 on ABG
no wheezing (cant move air)
peak expiratory flow rate <50%

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11
Q

ICU tx of an asthma exacerbation

A

ventillators
IV methylprednisone
IV magnesium is third line agent

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12
Q

salvage therapy for an asthma exacerbation

A

racemic Epi
Sub Q Epi
Mg2+

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13
Q

presentation of a pt with lung cancer

A

fever
weight loss
hemopytosis
(smoking hx)

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14
Q

initial steps to dx cancer

A

CXR

  • if neg -> paraneoplastic syndrome -> if no -> no cancer
  • if effusion -> thoracentesis -> if fluid has malignant cells —-> cancer stage 4

if non dx -> CT scan -> 1st Stage with PET scan, 2nd PFs, 3rd Tx

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15
Q

dx techniques for lung cancer

  • large proximal lesion
  • peripheral lesion
  • lesion in the middle of the lung
  • large irregular mass in lung
A
  • large proximal -bronchoscopy - EBUS (see thru walls)
  • peripheral - CT guided percutaneous biopsy (needle)
  • middle of lung - cardiothoracic surgeon - video assisted thorascopic surgery (VATS)
  • large, irregular mass in lung - resection
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16
Q

primary prevention of lung cancer

A

avoid smoking

avoid 2nd hand smoke

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17
Q

what are the requirement for cancer screening with low dose CT scans

A

55-80
30 pack per year history
quite <15 years ago

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18
Q

nodule criteria that is non cancerous

A

Size <8mm
Surface - smooth
Smoking - never
Self (age) <45

calcified

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19
Q

nodule criteria that is cancer suspicious

A

Size >2cm
Surface - spiculated
Smoking - Hx +
Self (age) - >70

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20
Q

pulmonary nodule is found next step is

A

finding old films

  • if no change –> stable
  • if new or change –>
  • —–> low risk –> serial CT scans
  • —–> high risk –> biopsy
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21
Q

small cell lung cancer basics

A

smoking Hx
centrally located

paraneoplastic syndromes - ACTH (cushing) and SIADH and Lambert Eaton syndrome

tx - chemo and radiation (responds well)

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22
Q

Sqaumous cell cancer lung cancer basics

A

smoking Hx
centrally located with necrosis and cavitation
More common than small cell cancer

paraneoplastic syndromes - PTH-related peptide (high Ca)

tx - stage related chemo, radiation, resection

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23
Q

adenocarcinoma lung cancer basics

A

MC primary lung cancer in both smokers and nonsmoker

asbesostosis (non smokers)
peripherally located - can cause pleuritic pain

tx - stage related chemo, radiation, resection

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24
Q

carcinoid lung cancer basics

A

left sided fibrosis, flushing, wheezing, diarrhea

serotinin syndrome

dx - 5-HIAA in urine

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25
transudate pleural effusion pathophys
fluid falling out of the capillary space due to: - hydrostatic pressure - CHF - loss of oncotic pressure (hypoalbuminemia)
26
exudative pleural effusion pathophys
caused by inflammation - increased permeability of pleural spaces or decreased lymphatic flow from pleural surface because of damage to pleural membranes or vasculature
27
presentation of pleural effusion
orthopnea dyspnea on exertion decreased lung sounds dullness to percussion in the area of effusion
28
CXR of pleural effusion
blunting of the costophrenic angle horizontal meniscus
29
dx workup of pleural effusion imaging studies
Lateral Decubitus X-ray or US or CT if small < 1cm watch and wait if >1cm and no CHF hx --> Tap if pt has CHF - don't Tap --> diuresis --> if fails Tap
30
if pleural effusion suspected and septations/lobes (loculation) present next step =
thoracostomy (+/-) tPA --> if fails then --> thoractomy for debridment
31
thoracentesis: transudate vs exudate lights criteria
LDH of fluid ---> 2/3 upper nml limits LDHfluid : LDHserum --> ( >0.6) total protein (fluid): total protein (serum) --> ( >0.5) [if any (1) above is + then --> exudate] all (3) above negative = transudate
32
what tubes do you send after performing a thoracentesis
1) cell count with diff 2) cytology - cancer (if + stage 4) 3) ADA, glucose, pH, Total protein, LDH , TGL 4) blood cultures - gram stain culture, TB, fungi
33
breakdown of tube 1 sent s/p thoracentesis
PNA - leukocytosis with PMN (neutrophils) TB - WBCs with lymphocytosis RBC - hemothorax or cancer
34
breakdown of tube 3 sent s/p thoracentesis
ADA - TB | TGL - for chylothorax
35
DVT causes (vircows triad)
1 - venous stasis - immobility 2 - endothelial injury - central lines, plastics, smoking 3 - hypercoagable stages - hormone replacement therapy, OCPs, factor V leiden, malignancy
36
DVT presentation
unilateral leg swelling ( >2cm larger than other leg) | tenderness to palpation
37
dx and tx of DVT
US and anticoagulate
38
wedge infarct PE pathophys
necrosis dead lung --> hemopytosis ischemia of pleural --> pleuritic CP pulm HTN - due to right heart strain 0% perfusion but gas exchagne occurs 100% --> V/Q mismatch --> hypoxemia
39
platelet derived mediators pathophys on their destruction
vasodilation -> fluid leak out --> increased diffusion barrier for O2 which is diffusion limited -> decreased O2 --> tachypnea and tachycardia (too try and compensate by increasing CO) but since CO2 is perfusion limited -> pt still able to breath off CO2 which will be worsened by tachypnea due to poor hypoxia throughout lung --> massive vasoconstriction
40
ABG findings of PE
increased pH decreased CO2 decreased O2
41
CXR and ECG findings in a PE with right heart strain
CXR - nml ECG - S1, Q1, T3 = right heart strain and/or elevated troponin and/or elevated BNP
42
Wells criteria
<2 --> low probability --> D-dimer >4 --> CTA (must have good kidneys) or do V/Q >6 --> V/Q scan (must have nml CXR)
43
when is an IVC filter used for PE
when the next PE will kill the pt and/or if massive bleed (ex: GI bleed) is present and anticoagulants are C/I
44
cancer pts with PE tx
LMWH
45
management of an asymptomatic PE
home - LMWH bridge to Warfarin no right heart strain vital signs stable
46
management of a symptomatic PE
admit to floor - LMWH --> warfarin no right heart strain vital signs are stable
47
management of submassive PE
ICU - heparin drip --> warfarin right heart strain is present vital signs are stable
48
management of massive PE
ICU - TPA (if C/I --> thrombectomy) abnormal vital signs right heart strain is present
49
how to assess if there is right heart strain in a PE
``` elevated troponin or elevated BNP or 2D echo - dilated RV, big RA ```
50
chronic thromboembolic pulmonary HTN
pulm HTN with multiple PEs diagnosed tx - thrombectomy
51
COPD CXR
barrel shaped chest Flat Diaphragm increased radiolucency of lung parenchyma elongated and narrow heart shadows
52
COPD pathophys and PFTs
decreased alveolar elasticity in COPD --> lung hyperinflation --> increased TLC, increased FRC, increased RV --> increased work of breathing reduced inspiratory and expiratory flow rates
53
ADR of systemic glucocorticoids
leukocytosis with neutrophilic predominance decreased lymphocytes decreased eosinophils
54
MCC of secondary clubbing are
lung malignancy cystic fibrosis R->L cardiac shunt
55
COPD exacerbation management
- O2 - SpO2 target 88-92% - inhaled bronchodilators - systemic glucorticoids - ABX if >1 cardinal sign - Oseltamavir - if evidence of influenza - NPPV if ventilatory failure - Intubate if NPPV fails or if it is contraindicated
56
cardinal signs of an infectious cause of a COPD exacerbation
``` increased dyspnea increased cough (frequency or severity) increased sputum production (change in color or volume) ```
57
indications for long term home O2 therapy
resting arterial oxygen tension (PaO2) <55mmHg SaO2 < 88% on room air pts with cor pulmonale or hematocrit >55% requirements - SaO2 <89 - PaO2 <59
58
what are the . most common etiologies of chronic cough
upper airway cough syndrome (post nasal drip) GERD Asthma
59
When can a methachline challenge be given
if no bronchodilator response seen
60
Lung dz in pts with ankylosing spondylitis
can develop restrictive lung dz due to diminished chest wall and spinal movement PFTs - decreased VC, decreased TCLl, nml FEV1/FVC
61
apical cavitary lesion on CXR
reactivation of TB | - fever, night sweats, blood tinged sputum
62
young pt with SOB, productive cough, evidence of destruction of lower lung lobes
alpha 1 antitrypsin deficiency panacinar (panlobular) ephysema <45 y/o association with liver dz
63
clinical presentation of interstitial lung dz
progressive exertional dyspnea or persistent cough half of pts have smoking hx fine crackles heard during mid to late inspiration possible digital clubbing
64
labs/imaging of interstitial lung disease
CXR - reticular or nodular opacities CT - fibrosis, honeycombing, traction bronchiectasis PFTs - increased FEV1/FVC decreased DLCO2, TLC, RV signficant hypoxemia with exertion due to V/Q mismatch ---> increased Alveolar-arterial gradient (A-a)
65
idiopathic pulmonary fibrosis pathophys
excess collagen deposition in the extracellular matrix around the alveoli --> resultant scarring --> affected PFTs decrease
66
predisposing factors for aspiration pneumonia
AMS - impaired cough reflex, glottic issues Dysphagia - due to neuro deficits GERD Protracted vomiting NG-ET tubes Large volume tube feedings in the recumbent position
67
Bilateral hilar adenopathy on CXR increased Ca erythema nodosum
Sarcoidosis pts can also have anterior uveitis, arthralgias, arthritis, bells palsy, papilledema, peripheral neuropathy
68
emphysema presentation | pink puffer
pts are thin - due to increased energy during breathing which is through pursed lips pts lean forward when sitting using accesory muscles
69
bronchitis | blue bloater
overweight and cyanotic (secondary to hypercapnia and hypoxemia) chronic cough and sputum production inflammation of airways -> decreased O2 cyanosis and hypoxemia --> vasoconstriction in lungs -> increased resistance in pulmonary arteries -> pulmonary HTN -> RHF --> edema
70
dx workup of COPD
PFTs | decreased FEV1/FVC
71
tx of COPD (not an exacerbation)
1 - SABA 2- SABA + LAMA (tiatropium) 3 - SABA + LAMA + LABA 4 - SABA + LAMA + LABA + ICS 5 - SABA + LAMA + LABA +ICS + PDE 4inhbitor 6 - SABA + LAMA + LABA + ICS + PDE4-I + Steroids
72
tx of chronic COPD
Corticosteroids - inhaled, oral (prednisone), IV (methylprednisolone) O2 if SpO2 <88%, PaO2 <55 Prevention (vaccines: flu, streptococcal, smoking cessation) Dilators (Short acting - albuterol, tiatropium, long acting LABA, LAMA, Theophyline, PDE4-I) Experimental Rehab
73
what 2 things decrease mortality in a COPD pt
O2 and smoking cessation
74
signs and symptoms of a COPD exacerbation
wheezing - especially on forced expiration cough sputum production tachycardia, tachypnea, decreased breath sounds prolonged expiratory time
75
pt discharged home on what meds following COPD exacerbations
PO steroids - prednisone | Metered dose inhalers - albuterol
76
Pathophys behind ARDS
noncardiogenic pulmonary edema leaky capillaries -> crushes the alveoli --> fluid causes an increased diffusion barrier --> O2 = diffusion limited = less O2 getting in stiff lungs, increased A-a gradient
77
presentation of ARDS
sick as shit patient,hypoxemic acute hypoxemic resp failure = P/A <200 septic shock, transfusion related lung injury , near drowning victim
78
ARDS CXR
pulmonary edema will be evident
79
differentiating between ARDS vs HF
CHF - increased PCWP and decreased LV function ARDS - decreased PCWP and nml to increased LV function
80
ARDS management
intubation keep tidal volume low to reduce pressure keep respiratory rate high so theres no accumulation of CO2 PEEP treat underlying condition and try diuresis
81
PEEP pathophys
applies back pressure to maintain recruitment of alveoli which has a small diffusion barrier which allows O2 to get in easier
82
presentation of diffuse parenchymal lung disease (DPLD) also called interstitial lung disease
chronic and insidious development of hypoxemia dry hacking cough dry crackles restrictive PFTs
83
tx of DPLD (interstitial lung dz)
steroids DMARDS biologics
84
Idiopathic causes of interstitial lung disease (DPLD)
< 6 wks = acute interstitial pneumonitis > 6months = idiopathic pulmonary fibrosis
85
drug induced causes of interstitial lung disease
``` bleomycin amiodarone radiation nitrofurantoin phenytoin ```
86
rheumatological disease that cause interstitial lung disease
SLE RA systemic sclerosis
87
sarcoidosis interstitial lung disease
autoimmune, younger black women asymptomatic bilateral hilar lymphadenopathy insidious hypoxemia, blurred vision heart block, bellsy palsy erythematous nodosum
88
dx of sarcoidosis
CXR - bilateral hilar lymphadenopathy CT - (high resolution) - ground glass PFTs - restrictive pattern Biopsy = noncasseating granulomas
89
Trying to rule in cardiac sarcoidosis without pulmonary involvement work up
Cardiac MI followed by a biopsy of endomyocardium with sarcoid in it conduction disturbances - heart block, arrhythmias it is the most common cause of death
90
abestosis interstitial lung disease
increased cancer risk exposure: shipyard, constructions >30yrs CXR - pleural plaques on CXR
91
mesothelioma is dx of
abestosis biopsy - barbell bodies indicative of abestosis
92
silicosis of interstitial lung disease
sandblasting, rock quaries, mining, glass manufacturing upper lungs - looks like TB pts are at increased risk for TB so need annual TB checks egg shell calcifications - CXR
93
berryliosis interstitial lung disease
aeronautic professions | ppl who build or manufacture electronics
94
coal interstitial lung disease
``` coal miners caplan syndrome - arthralgias - pulmonary fibrosis ----> check rhematoid factor ```
95
hypersensitivity pneumonitis
antigen mediated person goes to work during week and has pneumonitis symptoms but these disappear over long weekend or on vacation regional or temporal DPLD
96
intrapulmonary shunting
examples: pulm edema, PNA, atelectasis increased A-a gradient V/Q = O (no ventilation)
97
diffuse alveolar hypoventilation
uniform fall in ventilation throughout lung causes: narcotic overdose and neuromuscular weakness
98
prolonged High FiO2 risks
oxygen toxicity - > formation of proinflammatory oxygen free radicals and predispose atlectasis as nitrogen is displaced
99
target PaO2 for COPD exacerbation
PaO2 55-80% once this target is reached lower FiO2 <60% which is the safe zone
100
pt with sick contact, cough, and no upper respiratory symptoms (rhinorrhea, etc) and has right lower lobe cracles on exam
indicates possibly pulmonary consolidation - must do CXR to r/o non viral etiology
101
pt with an underyling malignancy who presents with acute dyspnea, chest pain, tachycardia, hypoxia, and clear lungs is suggestive of
PE - underlying malignancy (prothrombic state) they can present with syncope and hemodynamic collapse (RV dysfunction) if massive PE - along with RBBB on ECG pts with PE can also develop small pleural effusions
102
new onset LBBB
suggest an acute MI dyspnea/hypoxia due to pulm edema (crackles on exam)
103
MCC of orthostatic hypotension in elderly
hypovolemia -> due to decreased renal perfusion -> activation of renin angiotensin aldosterone system -> decreased urine sodium concentration
104
aspirin exacerbated respiratory dz
non IgE mediated pseudoallergic drug rxn to an imbalance between prostaglandins/ leukotrienes pts have hx of asthma or chronic rhinosinusitis with nasal polyps bronchospasm and nasal congestion following aspirin ingestion tx - montelukast (leukotriene receptor antagonist)
105
goodpastures disease
lung affects - cough, dyspnea, hemopytosis renal affects - nephritic range proteinuria, acute renal failure, dysmorphic red cells/red cell casts on UA pathophys - linear . IgG antibodies along glomerular basement membrane (alpha 3 chain type IV collagen antibodies)
106
management of ARDS involves avoiding complications of mechanical ventilation such as using lung protective strategies =
low tidal volume ventilation --> lower pulmonary pressures --> decrease likelihood of overdistending alveoli and improve mortality
107
Pathophys behind ARDS being a complication of pancreatitis
increase serum [ ] of pancreatic enzymes such as phospholipase A2 --> cross pulm capillaries --> damaging lungs and cause inflammatory cascade --> leakage of blood and proteinaceous fluid into alveoli --> alveolar collapse due to surfactant loss and diffuse alveolar damage
108
complication during the post ictal state
hypoventilation - leading to respiratory acidosis
109
pancoast tumor (superior pulmonary sulcus tumor)
shoulder pain C8-T2 neuro issues: weakness and/or atrophy of intrinsice hand muscles, pain and parethesias of 4th and 5th digit, medial forearm and arm weight loss, supraclavicular lymph node enlargement horners syndrome association usually squamous cell cancers
110
primary pulmonary hypertension | presentation
middle aged patients exertional breathlessness lungs clear to auscultation
111
dx of primary pulmonary hypertension
CXR - enlargement of pulmonary arteries with rapid tapering of distal vessels, enlargement of RV ECG - Right axis deviation
112
centrilobular emphysema
MC type seen in smokers predilection for upper lung zones destruction limited to respiratory bronchioles
113
panlobular emphysema
pts with alpha 1 antitrypsin deficiency destruction involves both proximal and distal acini predilection for lung bases
114
spirometry values in COPD
FEV1/FVC <0.70 (70%) FEV1 is decreased TLC is increased residual volume is increased
115
chronic bronchitis timeline
chronic cough productive of sputum for at least 3 months per year for at least 2 consecutive years
116
alpha 1 antitrypsin pathophys
destruction of alveolar walls is due to relative excess in protease (elastase) which is released from PMNs and macrophages and is usually blocked by alpha 1 antitrypsin tobacco smoke increases number of activated PMNs and macrophages as well as inhibits alpha 1 antitrypsin
117
emphysema pathophys | pink puffer
permanent enlargement of air spaces distal to the terminal bronchioles due to destruction of alveolar walls No change in oxygen, no hypoxemia CO2 retention - compensate by: - increased AP diameter (barrel chested) - prolonged expirations
118
airway obstruction spirometry values
nml or increased TLC with decreased FEV1 (amount of air that can be forced out of lungs in 1 sec) the lower the FEV1 the more difficulty one has breathing
119
restrictive lung dz spirometry values
FEV1//FVC = nml to high ``` TLC = low RV = low to normal ```
120
COPD - affect on body pH
leads to chronic resp acidosis with compensatory metabolic alkalosis also FEV1 measurements for COPD pts have the highest predictive value
121
what are the only interventions in COPD known to decreased mortality
home oxygen therapy | smoking cessation
122
what drugs are contraindicated in either a COPD exacerbation or asthma exacerbation
beta blockers
123
complications of COPD
secondary polycythemia (Hct >55% in men or >47% in women)
124
signs of acute severe asthma attacks
``` tachypnea diaphoresis wheezing speaking in incomplete sentences use of accessory muscles ```
125
paradoxic movement of abd and diaphragm on inspiration is a sign of
impending respiratory failure
126
PFTs in asthma
decrease FEV1 decreased FVC decreased FEV1/FVC ratio increased FEV1 of 12% with albuterol decreased FEV1 <20% with methacholine or histamine
127
In an acute setting (ED) what is the quickest method for dx asthma when a pt is SOB
measuring peak flow (peak expiratory flow rate)
128
during an acute asthma exacerbation if the PaO2 is nml or elevated
pt is getting fatigued and is no longer performing gas exchange since typically asthmatics hyperventilate and blow off CO2 so respiratory failure is imminent
129
ADR of inhaled corticosteroids
due to oropharnygeal deposition - sore throat - oral candidiasis (thrush) - hoarseness tx - using a spacer and rinsing the mouth after use
130
uses for montelukast and cromolyn sodium/nedocromil sodium
prophylaxis for mild exercise induce asthma
131
complications of asthma
satus asthmaticus - does not respond to standard meds acute resp failure - due to resp muscle fatigue pneumothroax, atelectasis, pneumomediastinum
132
bronchiectasis basics
permanent, abnormal dilation and destruction of the bronchial walls chronic inflammation airway airway collapse ciliary loss/ dysfunction leading to impaired clearance of secretion
133
causes of bronchiectasis
recurrent infections cystic fibrosis kartagnener syndrome autoimmune dzs
134
clinical features of bronchiectasis
cough with large amounts of mucopurulent, foul smelling sputum dyspnea hemoptysis - due to ruptured blood vessels near bronchial wall surfaces
135
dx and tx of bronchiectasis
dx - high res CT, obstructive PFT pattern tx - abx, bronchial hygiene - hydration and chest physiotherapy, inhaled bronchodilators
136
the main goal of treating bronchiectasis is to
prevent the complications of PNA and hemoptysis
137
what type of dx is necessary to differentiate non small cell lung cancer to small cell lung cancer t
tissue diagnosis
138
local invasion signs for lung cancer
``` Superior vena cava syndrome phrenic nerve palsy recurrent laryngeal nerve palsy horner syndrome pancoast tumor ```
139
superior vena cava syndrome
Most commonly occurs with small cell lung cancer facial fullness facial and arm edema dilated veins over anterior chest , arms and face JVD
140
phrenic nerve palsy
courses through the mediastinum where it can be destroyed by a tumor hemidiaphragmtic paralysis
141
recurrent laryngeal palsy
causes hoarseness
142
tx of NSCLC and SCLC
NSCLC - surgery if not metastatic along with adjunct radiation SCLC - combo os chemo and radiation surgery is not indicated as masses are unresectable
143
calcification signs in lung cancer
eccentric asymmetric calcification - malignancy dense central calcification - benign
144
mediastinal masses
MCC in older pts = metastatic masses anterior - 4 T's = thyroid, teratogenic tumors, thymoma, terrible lymphoma middle - lung cancer, lymphoma, aneurysms posterior - neurogenic tumors, esophageal masses, enteric cysts, bochdalek hernia
145
clinical features of mediastinal masses
usually asymptomatic unless compressing adjacent structures - cough - trachea or bronchi compression - dysphagia - esophagus compression - SVC syndrome - hoarseness - laryngeal - horners - sympathetic ganglia - diaphragm paralysis - phrenic
146
dx of mediastinal mass
CT scan is test of choice | if CT suggests benign and pt is asymptomatic - observation is appropriate
147
causes of transudative pleural effusions
``` CHF cirrhosis PE Nephrotic syndrome Peritoneal Dialysis hypoalbuminemia atelectasis ```
148
causes of exudative pleural effusions
``` bacterial pneumonia TB (MCC in developing countries) malignancy, Metastatic dz viral infection PE collagen vascular dzs ```
149
elevated pleural fluid amylase
esophageal rupture | pancreatitis malignancy
150
milky, opalescent fluid seen on thoracentesis drainage of pleural effusion
chylothorax - lymph in the pleural space
151
frankly purulent fluid seen on thoracentesis
empyema - complication of untreated exudative pleural effusion or bacterial pna tx - aggressive drainage of pleura and abx - recurrence rate is high if severe and persistent rib resection and open drainage might be necessary
152
bloody effusion seen with thoracentesis
suspect malignancy
153
parapneumonic effusion
noninfected pleural effusion secondary to bacterial pneumonia seen as a complication of rheumatoid pleurisy low pleural fluid glucose pH < 7.2 - since its exudative
154
if pleural fluid on thoracentesis has a glucos elevel < 60 suspect
rheumatoid arthritis in your differential
155
tx of transudative pleural effusion
diuretics and sodium restriction | therapeutic thoracentesis only if massive effusion is causing dyspnea
156
pneumothorax
air in the pleural space | 2 categories: spontaneous and traumatic
157
spontaneous pneumothorax
without trauma primary - healthy persion, spontaneous rupture of subpleural blebs (tall, lean, men), high recurrence rate secondary (complicated) - underlying lung dz (asthma, interstitial lung dz, CF) life threatening due to lack of pulm reserve
158
presentation of pneumothorax
sudden onset of ipsy chest pain dypsnea cough decreased breath sounds hyperresonance over chest decreased or absent tactile fremitus on affected side
159
clinical features of a tension pneumothorax
hypotension - due to impaired filling of great veins distended neck veins trachea shifted decreased breath sounds
160
histiocytosis X | interstitial lung disease
caused by abnormal proliferation of histiocytes (related to langerhans cells of the skin) smokers dyspnea and nonproductive cough spontaneous pneumo, lytic bone lesions, diabetes insipidus
161
wegener granulomatosis | interstitial lung disease
characterized by necrotizing granulomatous vasculitis upper and lower resp infections glomerulonephritis and pulmonary nodules + c-ANCA
162
churg strauss syndrome | interstitial lung disease
granulomatous vasculitis seen in pts with asthma pulmonary infiltrates, rash, and eosinophilia + p-ANCA tx - systemic glucocrticoids
163
abestosis increases risk for
bronchogenic carcinoma and malignant mesothelioma
164
causes of hypersenstivity pneumonitis
farmers lung - moldy hay bird breeders lung - avian droppings air condition lug bagassosis lung - moldy sugar cane mushroom workers lung - compost
165
severe hypercapnia (and resp acidosis) can lead to
dyspnea vasodilation of cerebral vessels (with increased intracranial pressure and subsequent papilledema, HA, and coma)
166
criteria for respiratory failure
hypoxia - PaO2 <60mmHg | hypercapnia - PCO2 >50mmHg
167
hypoxemic resp failure
low PaO2 with a PaCO2 that is nml or low - present when O2 sat < 90% despite FiO2 > 0.6 Causes; - ARDS, severe pna and pulm edema
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hypercapnic resp failure
failure of alveolar ventilation decrease in mute ventilation or increase in physiologic dead space leads to CO2 retention --> hypoxemia Causes: CF, asthma, COPD, severe bronchitis
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ventilation is monitored by
PaCO2 - to decrease PaCO2 either increase RR or Tidal volume
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oxygenation is monitored by
PaO2 - to decrease PaO2 either decrease FiO2 or decrease PEEP
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shunting in resp failure
little or no ventilation in perfused areas (due to collapsed or fluid filled alveoli) venous blood shunted into arterial circulation without being oxygenated increased CO2 production: DKA, sepsis, hyperthermia
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causes of shunting in resp failure
atelectasis or fluid buildup in alveoli (pneumonia or pulmonary edema), direct R --> L shunt
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supplemental oxygen effect on shunt in resp failure
hypoxia due to a shunt is not responsive to supplemental oxygen
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clinical features of respiratory failure
dyspnea - first symptom maybe cough inability to speak in complete sentences use of accessory muscles of respiration tachypnea, tacycardia cyanosis AMS
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preferred oxygen delivery system in COPD patients
venturi mask - since you can more precisely control oxygenation
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NPPV - noninvasive positive pressure ventilation
BIPA or CPAP indicated in pts in impending resp failure in an attempt to avoid intubation and mechanical ventilation pts must be neurologically intact, awake, cooperative and able to protect their airway
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dx of ARDS
CXR - bilateral infiltrates on imaging pulm edema not explained by fluid overload or CHF PCWP < 18mmHg PaO2/FiO2 ration: - 200 to 300 - mild ARDS - 100 - severe ARDS
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complications of ARDS
permanent lung injury - lung scarring or honeycomb lung barotrauma secondary to high pressure mechanical ventilation - pneumothorax or pneumomediastinum renal failure - may be due to nephrotoxic medications, sepsis with hypotension
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always confirm correct ET placement by
listening for bilateral breath sounds checking post intubation CXR - tip of ET should be 2-5cm above the carina
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two major goals of mechanical ventilation
maintain alveolar ventilation | correct hypoxemia
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pts who require mechanical ventilation
significant resp distress impaired or reduced LOC with inability to protect airway = absent cough or gag reflex metabolic acidosis - unable to compensate with ventilation resp muscle fatigue significant hypoxemia = PaO2 < 70mmHg or hypercapnia PaCO2 >50mmHg
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acceptable ABG ranges with mechanical ventilation
``` PaO2 = 50 - 60 PaCO2 = 40-50 ``` pH = 7.35 - 7.50
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criteria for weaning off from ventilator or extubation
``` intact cough PaO2/FiO2 >200 PEEP of < 5cm FiO2 <40% RR < 35 minute ventilation < 12 ```
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high levels of PEEP increase the risk for
barotrauma (injury to airway = pneumothorax) + decreased cardiac output (decreased venous return form increased intathoracic pressure
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complications of mechanical ventilation
agitation, anxiety, discomfort difficulty with tracheal secretions ventilator associated PNA barotrauma tracheomalacia (softening of the tracheal cartilage) due to prolonged presence of ET
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when a pt is ventilator dependent for 2 or more weeks a
tracheostomy is performed to prevent tracheomalacia
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pulmonary HTN
mean pulmonary arterial pressure > 25mmHg at rest
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causes of pulmonary HTN
passive - due to resistance in pulm venous system (LHF, mitral stenosis, atrial myxoma) hyperkinetic (L --> R cardiac shunt, ASD, PDA) obstruction (PE, pulm artery stenosis) pulmonary vascular obliteration (collage vascular dz)
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pulmonary arterial HTN
idiopathic, familial young or middle aged women abnormal increase in pulmonary arteriolar resistance leads to thickening of pulmonary arteriolar walls
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clinical features of pulmonary HTN
dyspnea on exertion fatigue chest pain - exertional syncope - exertional
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dx of Pulmonary HTN
loud P2 ECG - RVH and RAD CXR - enlargend pulm arteries echo - dilated pulm artery, dilated RA, hypertrophied RV increase pulmonary artery pressure > 25mmHg
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dx of cor pulmonale
CXR - enlargement of RA, RV, and pulm arteries ECG - RAD, RVH echo - RV dilatation, nml LV size and function
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sources of emboli to the lungs other than the traditional traveling thrombus
fat embolism - long bone fx amniotic fluid embolism - during or after delivery air embolism - trauma to thorax, indwelling venous/arterial lines septic embolism - IV drug use schistosomniasis
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complications of PE
recurrent PEs | pulmonary HTN - in 2/3 of pts
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risk factors for PE
age >60 malignancy prior DVT/PE hereditary hypercoagulable states - factor V Leidin, protein C and S def, antithrombin III deficiency ``` prolonged immobilization obesity major surgery (especially pelvic) major trauma pregnancy (OCPs) ```
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sources of emboli
LE - DVTs - iliofemoral DVT UE - DVT - rare - may be seen in IV drug users
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clinical features of a PE
dyspnea pleuritic chest pain cough/ hemoptysis tachypnea, tachycardia (leads to resp alkalosis) rales
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dx of PE
CTA - showing intraluminal filling defects in central, segmental, or lubular pulmonary arteries [cant be used if pt has renal insufficiency] + pulmonary angiogram - definitively proves PE
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what dx test and results can rule out a PE
negative (-) D-dimer and low clinical suspicion low probability V/Q scan and low clinical suspicion negative pulmonary angiogram (definite)
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modified wells criteria
symptoms and sign of DVT = 3.0 alternative dx less likely than PE = 3.0 heart rate > 100 bpm = 1.5 immobilization (>3days) or surgery in prev 4wks = 1.5 previous DVT/PE = 1.5 hemoptysis = 1.0 malignancy = 1.0 score < 5 = unlikely PE score > 4 = PE likely
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contraindications to heparin
active bleeding uncontrolled HTN recent stroke Heparin induced thrombocytopenia (HIT)
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tx of aspiration pneumonia
clindamycin (has anaerobic activity)
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differential dx of hemopytsis
bronchitis lung cancer (bronchogenic carcinoma) TB bronchiectasis goodpasture syndrome Aspergilloma within cavities
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nml ABG values
``` pH = 7.35 - 7.45 PaO = 90 (decreases with age) PaCO2 = 35-45 ```
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DLco mechanism
measures the surface area of the alveolar capillary membrane useful in monitoring conditions such as sarcoidosis and emphysema
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causes of low DLco
emphysema sarcoidosis interstitial fibrosis pulmonary vascular dz lower with anemia
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causes of high DLco
``` asthma obesity intracardiac L --> R shunt exercise pulmonary hemorrhage ```
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if hemoptysis is severe consider
bronchial artery embolization or balloon tamponade of the airway
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bronchogenic cysts
middle mediastinum masses benign best seen on CT scan
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thymoma
anterior mediastinum mass young male or female strong association with myasthenia gravis
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neurogenic tumors | esophageal leiomyomas
located in posterior mediastinum
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indications for noninvasive positive pressure ventilation
COPD (severe exacerbation) Cardiogenic pulmonary edema acute resp failure
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contraindications for NPPV
``` inability to protect airway cardiac or respiratory arrest severe acidosis pH < 7.10 ARDS recent esophageal aneursym ```
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pulmonary contusion presentation and dx
< 24hrs after blunt thoracic trauma tachycardia, tachypnea, hypoxia dx - rales, decreased breath sounds, CT or CXR - with patchy, alveolar infiltrates not restricted by anatomical borders
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fat embolism
develop resp distress neurological abnormalities petechial rash following a latent period of 12-72hrs after injury
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invasive aspergillosis | risk factors and presentation
risk factors - immunocompromised (neutropenias, glucocorticoids, HIV) triad - fever, cp, hemoptysis
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invasive aspergillosis | dx and tx
dx - CXR/ CT - pulmonary nodule with surrounding ground glass opacities (halo sign) + cultures + cell wall biomarkers (galactomannan, beta D glucan) tx - voriconazole +/- capsofungin
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chronic aspergillosis | risk factors and findings
risk factors - lung dz/damage [cavitary TB] findings = > 3months - weight loss, cough, hemoptysis, fatigue
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chronic aspergillosis | dx and tx
dx - cavitary lesions +/- fungus ball + aspergillosis IgG serology tx - resect, azole meds, embolization if hemoptysis is severe
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what decreases the mortality rate of an acute PE
early and affective anticoagulation - should be initiated prior to dx tests being performed - unless a contraindication is present
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interstitial lung dz PFTs TLC FEV1/FVC DLco
TLC - decreased FEV1/FVC - nml or increased DLco - decreased
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COPD PFTs TLC FEV1/FVC DLco
TLC - increased FEV1/FVC - decreased DLco - decreased
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ASTHMA PFTs TLC FEV1/FVC DLco
TLC - nml/increased FEV1/FVC - decreased DLco - nml/increased
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Restrictive PFTs TLC FEV1/FVC DLco
TLC - decreased FEV1/FVC - increased or nml DLco - nml
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DLco in pulmonary artery HTN
decreased
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why is the glucose [ ] in an empyema low
due to high metabolic activity and/or leukocytes (and/or) bacteria in the fluid that metabolize the glucose
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3 mechanisms for transudative pleural effusion
increased hydrostatic pressure decreased oncotic pressure decreased intrapleural pressures
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compensatory metabolic alkalosis can lead to what lab affects
decreased Cl- concentration due to bicarbonate retention
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both nonallergic rhinitis and allergic rhinitis are managed with
intranasal glucocorticoids difference between the 2 is that allergic rhinitis pts can ID their trigger and present earlier
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exudative pleural effusion mechanisms
increased capillary permeability pleural membrane permeability disruption of the lymphatic outflow
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chlorpheniramine
H1 antihistamine receptor blocker decreases allergic response anti inflammatory -> reduced nasal secretions by limited the secretory response to inflammatory cytokines
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histoplasma capsulatum
central, midwestern, and northeastern US ppl who go in caves who are at increased risk for bat and bird droppings
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Coccidiomycosis
Arizona CP, fatigue, cough and fever CXR - nml unilateral infiltrate with ipsy hilar lymphadenopathy biopsy endospores and spherules
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bronchiectasis confirmed via
high resolution CT scan cough with daily mucopurelent sputum production
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empiric tx of CAP | outpatient
macrolide or doxycycline (healthy pt) | floroquinolone or beta lactam + macrolide (pt with comorbidities)
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empiric tx of CAP (inpatient) + (inpatient in ICU)
inpatient - fluoroquinolone (IV) or beta lactam + macrolide (IV for both) ICU pt - beta lactam + macrolide (IV) or beta lactam + flouroquinolone (IV)
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management of SIADH
fluid restriction +/- salt tablets | hypertonic (3%) saline
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granulomatosis with polyangitis presentation
upper resp issues - sinusitis, saddle nose lower resp issues - lung nodules/ cavitations + renal issues - rapidly progressing glomerulonephritis skin - non healing ulcers
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granulomatosis with polyangitis | dx and tx
dx - CXR - necrotizing pulmonary vasculitis ANCA - PR3, MPO leukocytoclastic vasculitis pauci immune GN granulomatous vsculitis tx - corticosteroids + immunomodulators
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CO2 retentions leads to what affect on cerebral vasculature
cerebral vasodilation --> seizures, stroke, AMS
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complication of pneumocysitis in HIV pts
SIADH - --> decreased Na which can be further worsened by nml saline bolus
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CREST syndrome Scleroderma
``` C- calcinosis R- raynauds phenomenom E- esophageal dysmotility S-sclerodacytl T- telengiectasias ```
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pathophys of PAH
intimal hyperplasia of pulmonary arteries progressive dyspnea, exertional syncope, lighthedness --> due to RV failure
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alveolar spaces filled with fibroblasts are consistent with
interstitial lung dz
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bronchial wall thickening with mucous plugs is consistent with what dx
bronchiectasis
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drug induced SLE meds
procainamide isoniazide hydralazine
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during an acute asthma attack if the PaCO2 begins to normalize or increase
it is a sign of impending resp failure because typically these pts are tachypneic and should be breathing off a lot of CO2 but now they are fatigued and their breaths are not performing gas exchange
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exercise induced asthma tx
SABA - such as albuterol 10-20 min before exercise
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pH of transudative pleural effusion vs exudative pleural effusion
transudative pleural effusion - pH 7.40 - 7.55 exudative pleural effusion - pH 7.30-.7.45
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physical exam findings of lobar pneumonia
increased breath sounds (Crackles and egophony) increased tactile fremitus dullness to percussion
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physical exam findings of a pleural effusion
decreased breath sounds decreased tactile fremitus dullness to percussion
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physical exam findings of emphysema
decreased breath sounds decreased tactile fremitus hyperresonant to percussion
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mediastinum shifting affected by atelectasis
mediastinum will shift towards the side with a large amount of atelectasis decreased breath sounds decreased tactile fremitus dullness to percussion
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how does alveolar consolidation in PNA causes hypoxemia
due to R --> L intrapulmonary shunting
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dead space ventilation
ventilation of areas of the lung that are not perfused with blood (ex: PE)
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high PaCO2 and low PaO2 levels are suggestive of
alveolar hypoventilation
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alveolar gradient formula =
PAO2 - PaO2
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CXR showing loculation -->
parapneumonic effusion and empyemas - exudative pleural effusion high protein - <60 glucose - low pH
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development of clubbing and sudden onset joint arthropathy in a chronic smoker is suggestive of
hypertrophic osteoarthropathy - typically associated with cancer so need to perform a CXR to r/o malignancy
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Oxygenation of a pt with PaO <60 can be improved by
Increasing FiO2 - usually weaned <60% to avoid O2 toxicity increased PEEP - improves mortality in pts with ARDS dont increase tidal volume as it can lead to increased risk of barotrauma
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tx of PE in pts with GFR <30
unfractionated heparin - preferred over LMWH this is because in renal insufficiency there is reduced clearance of anti Xa leading to increased activity --> increased bleeding risk
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mainstay tx of COPD
inhaled antimuscarinic agents
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tx of post nasal drip (upper airway cough syndrome)
oral first generation antihistamines
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theophylline toxicity
CNS - HA, insomnia, Szs GI - N/V Cardiac - arrhythmias, palpitations
265
Most Common ADR of inhaled corticosteroids therapy
oropharyngeal thrush (oral candidiasis)
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complications of positive pressure ventilation
alveolar damage pneumothorax hypotension
267
MCC of cor pulmonale
COPD
268
causes of increased plateau pressure
pneumothroax pulm edema PNA atelectasis
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ADR of beta 2 agonists (albuterol)
reduce K+ levels by driving K+ into cells --> hypokalemia - - --> muscle weakness, arrhythmias, - --> EKG changes, tremors, palpitations, HA
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Acute PE - pressures
NML PCWP increased RA pressure increased pulmonary artery pressure
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causes of recurrent PNA in the same location
extrinsic bronchial compression (neoplasm, adenopathy) intrinsic bronchial obstruction (bronchiectasis, FB) recurrent aspirations: szs, alcohol, drug use, GERD, dysphagia workup = CT scan
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acute bronchitis
cough > 5days to 3wks (+/- purulent sputum) preceding resp illness (90% viral) absent systemic findings (fever, chills) wheezing or ronchi chest wall tenderness
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dx and tx of acute bronchitis
CXR only if PNA suspected tx - symptomatic tx - NSAIDs and/or bronchodilators