Respiratory Flashcards
Chronic bronchitis Dx requirements
Chronic productive cough lasting 3 months over a minimum of 2 years
COPD changes in FEV, FVC, TLC (spirometry)
Decrease FVC, MORE decrease in FEV1, decrease in FEV1/FVC ratio, increase in TLC
Chronic bronchitis is associated with
Smoking
% of wall is mucous glands in CHronic bronchitis
> 50%, measures in Reid index, hypertrophy of bronchial mucinous glands
The excess mucous goes where in chronic bronchitis
Coughed up or can plug parts of lung
What is Reid index?
Measure of the thickness of the glands in the bronchial wall
Clinical features of chronic bronchitis
Productive cough, cyanosis, inc. PaCO2, dec. PaO2, inc. risk of infection and cor pulmonale
Emphysema mechanism of disease
loss of elasticity, destruction of the alveolar air sacs, the many air sacs now act as one (one reason for obstructive disease), air drag and loss of elasticity allows for some “collapse” of the walls of bronchioles (second reason for obstruction)
EMphysema cause
imbalance of proteases and anti-proteases; smokers cause the increase in protease activity; alpha 1 anti trypsin def. leads to less antiprotease protection
what is most common cause of emphysema
smoking
2 categories of emphysema
panacinar and centriacinar
smoking causes which kind of emphysema
centriacinar, mainly upper lobes
alpha 1 anti trypsin def causes which emphysema
pan-acinar, lower lobes mainly
A1AT def also involves
liver, causing cirrhosis
most clinically relevent allele muattions for A1AT
PiZ allele, now protein accumulates in ER
PiMZ heterozygotes
higher risk for emphysema with smoking but otherwise assyptomatic
clinical features of emphysema
dyspnea, cough, no sputum, pursed lips with prolonged expiration, lbs loss, inc. AP diameter (barrel chest)
functional residual capacity is what in empysema
increased and in a fibrosis of lung then the FRC will decrease
late complications of emphysema
hypoxemia, cor pulmonale
Asthma descript
revrsible airway bronchoconstrict, usually from a type 1 hypersensitivity rxn
Asthma pathogenesis
allergins induce TH2 phenotype CD4 t cells of genetically susceptible individuals, the TH2 cells secrete IL-4,5,10
IL 4 important for what
IgE shift
IL5 important for
eosinphil
IL10 important for
Th2 dif and block Th1 form
early phase of asthma
mast cell activation leading to contriction, from the leukotrienes
late phase of asthma
inflammation and major basic protein potentiate the bronchoconstriction
clinical features of asthma
dyspnea, wheezing, productive cough with curschmann spirals with charcot leyden crystals, severe unrelenting attack can lead to status asthmaticus and death
non allergic causes of asthma
exercise, viral infection, aspirin (aspirin intolerant asthma), occupational exposure
nasal polyps associations
chronic rhinitis
adults+asthma + polyps = aspirin intolerant asthma
child + polyps = CF
Bronchiectasis definition
permant dilation of bronchioles and bronchi causing loss of airway tone and results in air trapping
Bronchiectasis causes
CF, kartagener syndrome, tumor or foreign body, nectrotizing infection, allergic bronchopulmonary aspergillosis—–all in all its due to inflammation eith damage to the air way walls
clinical features of bronchiectasis
cough, dyspnea, foul smelling sputum, with complications of hypoxemia with cor pulmonale and 2ndary amyloidosis
restrictive diseases spirometry findings
cant fill lung thus dec. TLC, decreased more FVC, decreased FEV1, increased FEV1/FVC ratio
causes of restrictive diseases
interstital diseases causing fibrosis of the interstitium or even a chest wall issue (ex obesity)
Idiopathic pulmonary fibrosis is what kind of disease
restrictive disease with fibrosis of the lung interstitium
etiology of idiopathic pulm. fibrosis
cyclical lung injury, TGF-Beta thought to be agent causing the fibrosis….must exclude other causes to be able to give this Dx
clinical features of IPF
progressive dyspnea, cough, fibrosis seen on lung CT leads to a honey comb lung, Tx is lung transplant
Pneumoconioses def.
interstitial fibrosis due to occupational exposure, requires chronic exposure to fibrogenic small particles
Coal workers pneumoconiosis
carbon dust is the causeitive agent
Coal workers pneumoconiosis pathologic findings
diffuse fibrosis (black lung), assoc. with RA (Caplan syndrome)
Anthracosis def.
mild exposure to carbon from pollution, not clinically relevant
Silicosis
exposure to silica, as in using a sandblaster or working in a silica mine
silicosis pathologic findings
fibrotic nodules in upper lobes of lungs
which pneumocosis inc. risk for TB?
silicosis, the silica impairs the phagolysosome formation by macrophages
Berylliosis
beryllium, miners and also from the aerospace industry
berylliosis path. finsdings
non-caseating granulomas in lung, hilar nodes, systemic organs
berylliosis increases risk for what
lung cancer
Asbestosis
asbestos fibers, seen in construct workers, plumbers, shipyard workers
asbestosis path. findings
fibrosis of lung and pleura with inc. risk for lung cancers and mesothelioma. lung cancer has higher incidence
asbestosis lesions characteristics
lesions has long golden brown fibers with associated iron (asbestos bodies)
WHat pneumoconiosis is similar to sarcoidosis
berylliosis
Sarcoidosis is what type of lung issue
restrictive disease
Sarcoidosis def
systemic disease characterized by non-caseating granulomas in multiple organs
Sarcoidosis most common population
african american females
sarcoidosis etiology
unknown, likely due to CD4 T-helper response
characteristic findsing in sarcoidosis
asteroid bodies
granulomas from sarcoidosis generally involve
hilar nodes and lung
other tissues involved in sarcoidosis
Uveitis, cutaneous nodules or erythema nodosum, salivary/lacrimal glands (may mimic sjogren syndrome),
clinical features of sarcoidosis
dyspnea, cough, elvated serum ACE, hypercalcemia, Tx is steroids, but can spontaneously regress
non-caseating granulomas have what activity
1 alpha hydroxylase activity
Hypersensitivity pneumonitis is what class
restrictive disease
hypersensitivity pneumonitis has what patholgy
granulomatous rxn to inhaled oragnic antigens
hypersensitivity oneumonitis clinical features
fever, cough, dyspnea that resolves with removal of exposure…chronic exposure can lead to interstitial fibrosis, remember also there will be eosinophils also
pulmonary mean arterial P, normal and what dictatses pulm. HTN
10 is normal and over 25 is HTN