Quiz #3 Flashcards

1
Q

does restrictive lung disease involve difficulty getting air in or out?

A

difficulty getting air in

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2
Q

does obstructive lung disease involve difficulty getting air in or out?

A

difficulty getting air out

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3
Q

what is ventilation?

A

air in and out

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4
Q

what is respiration?

A

gas exchange

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5
Q

what is RLD?

A

abnormal reduction in pulmonary ventilation due to restriction of chest wall or lung expansion

decreased air moving in and out

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6
Q

what is the pathogenesis of RLD?

A

decreased chest wall compliance (stiff and difficult to expand)

decreased lung volumes and capacities

increased work of breathing (need greater transpulmonary pressure)

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7
Q

what anatomy is affected by restrictive lung disease?

A

lung parenchyma

thoracic pump

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8
Q

what breathing difficulty is associated with restrictive lung disease?

A

inspiration

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9
Q

how is tidal volume maintained with restrictive disease?

A

increased respiratory rate

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10
Q

what inspiratory muscles need to work harder due to decreased compliance?

A

diaphragm, external intercostals, accessory muscles

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11
Q

what are the 6 classic signs of RLD?

A

1) tachypnea
2) hypoxemia
3) decreased breath sounds w/dry inspiratory crackles heard at the base of the lungs caused by ateletactic alveoli
4) decreased lung volumes and capacities
5) decreased DLCO
6) cor pulmonale

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12
Q

what is diffusing capacity of the lungs for carbon monoxide (DLCO)?

A

measures of integrity of the functional unit

measure CO bc Hgb has a higher affinity for it than O2

gas perfusion measurement

dysfunction of alveoli membrane

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13
Q

what is cor pulmonale?

A

R sided HF

fibrotic pulmonary capillary beds –> pulm HTN –> hypoxemia (low O2 in blood)

caused by pulmonary disease

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14
Q

t/f: <50% DLCO is predictive of restrictive lung disorder

A

true

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15
Q

what are the 3 symptoms of RLD?

A

1) dyspnea/SOB
2) dry, non-productive cough
3) muscle wasting (cachexia)

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16
Q

what is the treatment for RLD if the etiology is permanent?

A

supportive measures

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17
Q

what are supportive measures?

A

supplemental oxygen

antibiotic therapy for secondary infection

interventions to promote adequate ventilation

interventions to prevent accumulation of secretions

good nutritional support

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18
Q

what is the treatment for RLD if the etiology is reversible?

A

corrective (chest tube) and supportive (temporary mechanical ventilation)

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19
Q

what is the role of surfactant?

A

keeps the alveoli open and prevents them from collapsing in on itself

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20
Q

what is respiratory distress syndrome (RDS)?

A

hyaline membrane disease

lack of complete lung maturation

inadequate surfactant production in alveoli

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21
Q

how is RDS diagnosed?

A

chest radiograph will show diffuse hazy appear with low lung volumes

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22
Q

how is RDS treated?

A

CPAP

PEEP

ECMO

surfactant replacement therapy

corticosteroids to mother b4 brith

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23
Q

what should the lungs look like on a chest x-ray?

A

black

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24
Q

when does normal aging begin?

A

in 20s

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25
what is the treatment for maturational cuases of restrictive lung dysfunction?
keep aerobically exercising (walk 10 min, 3x/day) strength training
26
what are some causes of RLD?
interstitial, infectious, neoplastic, pleural, cardiovascular, neuromuscular, connective tissues, maturational, immunologic, pregnancy, nutrition/metabolic, traumatic, therapeutic, pharmaceudical, radiologic
27
what are the 3 interstitial causes of RLD?
1) idiopathic pulmonary fibrosis 2) sarcoidosis 3) broncholitis obliterans
28
what is idiopathic pulmonary fibrosis?
chronic and irreversible respiratory dysfunction due to fibrotic repsonse driven by abnormally activated alveolar epithelial cells
29
what is the pathophysiology of idiopathic pulmonary fibrosis?
atypical reparative process after lung epithelium injury (excessive fibroblast activity)
30
what is the worst environmental factor affecting idiopathic pulmonary fibrosis?
smoking
31
what is seen on a chest x-ray or CAT scan of idiopathic pulmonary fibrosis?
patchy focal lesions scattered
32
what is the disease progression in idiopathic pulmonary fibrosis?
steady decline in fxn epithelial cells become more fibrotic inflammation followed by repair process followed by fibroblastic phase acute exacerbations characterized by rapid deterioration in lung fxn survival rate: 2-3 years after dx
33
what are the diagnostic tests for idiopathic pulmonary fibrosis?
hx (exclusion of other causes of interstitial lung disease) high res CT(patchy, peripheral, bibasilar reticular opacities) chest radiography (opacities/infiltrates)
34
t/f: chest radiography lacks diagnostic specificity for idiopathic pulmonary fibrosis
true
35
what is the characteristic appearance of variably sized cysts in a background of densely scarred lung tissue in idiopathic pulmonary fibrosis?
honeycomb
36
what are the symptoms of idiopathic pulmonary fibrosis?
dyspnea on exertion nonproductive cough weight loss fatigue sleep disturbances
37
what are the signs of idiopathic pulmonary fibrosis?
decreased lung capacities abnormal markings on chest x-ray inspiratory dry rales distal clubbing pulm HTN pedal edema
38
what is the treatment of idiopathic pulmonary fibrosis?
antifibrotic drugs supportive care (supplemental O2) pulm rehab (exercise)
39
what is sarcoidosis?
idiopathic multisystems granulomatous inflammatory disorder primarily affecting black women unknown etiology 20-40 y/o
40
what is the hilum?
the entrance of the major arteries and blood vessels from the heart and lungs
41
what are the 3 distinctive features of sarcoidosis?
1) inflammation: flu-like symptoms, night sweats, jt pain, fatigue 2) granulomas: masses of inflammed tissue 3) pulmonary sarcoidosis: scar tissue in lungs
42
what are the pulmonary causes of restrictive lung dysfunction?
bronchopulmonary dysplagia bronchiolitis obliternas necrosis of BRONCHIOLES fibrotic lung disease that affects small airways
43
what is bronchopulmonary dysplagia?
chronic pulmonary syndrome in neonates who've been ventilated and receiving high concentrations of O2
44
what is bronchiolitis obliternas?
infection causing restrictive and obstructive lung dysfunction
45
what causes bronchiolitis obliterans in children?
viral infection
46
what causes bronchiolitis obliterans in adults?
toxic fume inhalation, viral, basterial, RA, graft vs host rxn
47
what lung structure is affected by bronchiolitis obliterans?
bronchioles
48
what is pneumonia?
inflammation of lung parenchyma beginning in lower respiratory tract
49
what are the 2 categories of pneumonia?
community acquired hospital acquired (healthcare or ventilator associated)
50
what are the 4 types of pneumonia?
bacterial viral fungal chlamydial
51
what is community acquired pneumonia most often caused by?
staph aureus (bacterial pneumonia)
52
what are bacterial pneumonias?
streptococcus pneumoniae pseudomonas aeruginosa staphylococcus aureus
53
what bacterial pneumonia has a vaccine?
staph aureus
54
what bacterial pneumonia is the msot often occuring nosocomial infection?
pseudomonas aeruginosa
55
what is the most common pneumonia in young children?
viral pneumonia
56
what is mycoplasma pneumonia?
atypical bacterial pneumonia walking pneumonia
57
what pneumonia can emenate from air-conditioning equipment?
legionella pneumophila
58
what pneumonia is associated with AIDS?
fungal pneumonia
59
what are the symptoms of bacterial pneumonia?
high fever, chills, dyspnea, tachypnea, nonproductive cough, pleuritic pain
60
what are the symptoms of viral pneumonia?
moderate fever, dyspnea, tachypnea, nonproductive cough, myalgias
61
how is pneumonia treated?
antibiotic therapy O2 (supplemental of vent) may be necessary with refractory hypoxemia (PaO2<60) postural drainage, percussion, vibration, and assisted coughing
62
what is refractory hypoxemia?
O2 levels stay the same despite use of supplemental O2
63
what are neoplastic causes of RLD?
bronchiogenic carcinoma
64
what is bronchiogenic carcinoma?
malignant growth of abnormal epithelial cells in the tracheobronchial tree
65
is the risk of lung cancer more closely related to when someone starts smoking or how much someone smokes?
when someone starts smoking
66
what are the 2 main types of bronchogenic carcinomas?
1) small cell 2) non-small cell
67
what are the 3 types of non-small cell cancers?
1) adenocarcinoma 2) squamous cell carcinoma 3) large cell carcinoma
68
what is the most common type of lung cancer?
adenocarcinoma
69
what lung cancer starts in the bronchi and could present like obstructive lung disease?
squamous cell carcinoma
70
what lung cancer is rare, but rapidly growing and often not known until it is widespread?
large cell carcinoma
71
what is the most common lung cancer type in smokers?
small cell cancer
72
what type of lung cancer metastasizes very quickly to lymph nodes and vascular channels and is already metastatic at diagnosis?
small cell cancer
73
t/f: 75% of small cell cancers metastasize to the CNS
true
74
where is small cell cancer located?
bronchial epithelium near the hilar region
75
where is squamous cell carcinoma located?
bronchial epithelium near the hilar and projects to the bronchi
76
where is adenocarcinoma located?
mucous glands tracheobronchial tree
77
where is large cell carcinoma located?
central or peripheral but often in trachea/large airways
78
what is the growth rate of small cell cancer?
very rapid
79
what is the growth rate of adenocarcinoma?
moderate
80
what is the growth rate of squamous cell carcinoma?
slow
81
what is the growth rate of large cell carcinoma?
rapid
82
what are the diagnoistic tests for bronchiogenic carcinoma?
chest x-ray and PET scans
83
what are the treatment options for bronchiogenic carcinoma?
surgery, radiation, chemo, immunotherapy
84
what is the most radiosensitive bronchiogenic carcinoma?
small cell followed by squamous
85
what is the treatment of choice for small cell cancer?
chemo
86
chemo has a low effect on what type of bronchiogenic carcinoma?
non-small cell
87
what is pleural effusion?
abnormal amount of pleural fluid in the pleural space
88
what are the 3 main etiologies of pleural effusion?
cardiac failure, pneuomnia, and malignant neoplasms
89
what is transudative effusion?
associated with HYDROSTATIC PRESSURE in pleural capillaries LOW protein content CARDIOGENIC increased pulmonary capillary pressures--> fluid in pulmonary interstitium fluid enters the pleural space, exceeding the drainage capacity of the lymphatics
90
what is exudative effusion?
INFLAMMATORY PROCESSES produce increased PERMEABILITY of pleural surfaces, allowing proteins and excessive fluid to move into pleural space HIGH protein content NON-CARDIOGENIC
91
what is the most common cardiogenic origin of transudative effusions?
CHF
92
what is the purpose of the pleural cavity?
lubrication for movement
93
what is the fluid in the pleural cavity made of?
filtrate from capillaries and lymphatics
94
what is the difference b/w pleural effusion and pulmonary edema?
pulmonary edema involved fluid int he alveoli pleural effusion involved fluid in the pleural space
95
is the parietal pleura high or low pressure?
high pressure
96
is the visceral pleura high or low pressure?
low pressure
97
fluid moves from the ___ pleura capillaries into the pleural space and is then reabsorbed into the ___ pleural capillaries
parietal, visceral
98
t/f: more blood flows from the parietal pleura towards the lungs
true
99
what is oncotic pressure?
pressure from amount of protein fluid into capillaries
100
what is hydrostatic pressure?
fluid out of capillaries
101
what pleural diseases can cause pleural effusion?
pleuritis fibrothorax pneumothorax emphysema hemothorax
102
what is pleuritis?
inflammation of pleura (visceral or parietal)
103
what is fibrothorax?
visceral pleura becomes fibrotic and destroys pleural cavity pleural cavity becomes connective tissue
104
what is pneumothorax?
air in the lungs
105
what is emphysema?
pus in the lungs
106
what is hemothorax?
blood in the lungs
107
what are the 3 types of pneumothorax?
1) closed 2) open 3) tension
108
what is a closed pneuomothorax?
the amount of air entering the pleural cavity doesn't increase collapsed lung lung or bronchus rupture
109
what is an open pneumothorax?
air goes in and out chest wound
110
what is a tension pneumothorax?
air continually going into the pleural space wound air accumulates in the pleural cavity
111
how is a pleural effusion diagnosed?
hx/exam chest radiography (white fluid) thoracoscopy (thoracentesis-analysis of fluid-exudate) opacity of atelectactic segment/lobe (large hematogenous opacity of fluid) elevation of hemidiaphragm on affected side blunting of costophrenic angle shift of mediastenum toward the affected side
112
what is the costophrenic angle?
where the diaphragm meets the ribs
113
what lung sound is indicative of pleural inflammation?
pleural rub
114
where are bronchial breath sounds normally heard?
normally heard b/w 1st and 2nd rib; anywhere else is abnormal
115
what is egophany?
e sounds like ah
116
when is abnormal bronchial breath sounds, pleural rub, and/or egophany heard?
in pleural effusions/inflammation
117
how is pleural effusion treated?
based off the underlying cause thoracentesis (needle extracts fluid) thoracoscopy (scope explores hemithorax) pleural space chest tube
118
what are chest drains?
one-way mechanism that lets air/fluid out of the pleural space and prevents outside air/fluid from entering
119
___ pressure during inspiration causes the water level in the chest tube to rise slightly
negative
120
____ pressure during expiration pushes air and fluid out of the pleural space and into the chest tube and collection bottle
positive
121
what helps with fluid drainage in chest tubes?
gravity
122
t/f: pleural effusion is an indication for bronchopulmonary hygiene techniques
false
123
why don't drainage positions work to treat pleural effusions?
bc the fluid is in the pleural space, not the alveoli
124
what is atelectasis?
incomplete expansion of the lungs or loss of volume collapsed, nonaerated lung parenchyma
125
what are the 6 types of atelectasis?
1) obstruction (resorptive) 2) passive 3) adhesive 4) compressive 5) cicatrization 6) congestive
126
what 2 types of atelectasis can best be treated by pT
obstructive and passive
127
what types fo atelectasis are most associated with bedrest and surgery?
obstructive and passive
128
what is obstruction atelectesis?
the most common due to a tumor, mucus plug, or foreign body
129
what is passive atelectasis?
simple pneumothorax associated with bedrest, sedation, anesthesia, and not taking deep breaths
130
what is adhesive atelectasis?
surfactant deficiency
131
what is compressive atelectasis?
space occupying lesion pleural effusion
132
what is cicatrization atelectasis?
fibrosis
133
what is congestive atelectasis?
edema and hemorrhage into lung parenchyma from PE
134
how is atelectasis diagnosed?
chest radiograph
135
what is the treatment for atelectesis?
manage the underlying cause deep breathing or incentive spirometry, coughing
136
what does incentive spirometry measure?
max inspiration with a single breath
137
what is ARDS?
inflammation causing an increase in pulmonary vascular permeability, lung weight, and loss of aerated tissue a form of non-cardiogenic pulmonary edema, due to alveolar injury secondary to an inflammatory process, that can be either pulmonary or systemic (extra pulmonary) in origin
138
what syndrome is described as a"leaky bucket" where excessive fluid is leaking out of endothelial capillary and alveolar membrane?
ARDS
139
what is a milder case of ARDS?
ALI
140
what are the pulmonary origins of ARDS?
pneumonia inhalation injury aspiration or gastric contents chest trauma/pulmonary contusion near drowning
141
what are the non-cardiogeneic causes of ARDS?
sepsis major trauma burns pancreatitis fat embolism hypovolemia transfusion-related acute lung injury cardiopulmonary bypass
142
what is the 3 stage process of ARDS?
1) exudative 2) proliferative 3) fibrotic
143
what is the exudative stage of ARDS?
inflammatory phase with release of inflammatory mediators causing edema in the lungs ventilation-perfusion mismatch reduced compliance thrombus formation w/in pulmonary capillaries
144
what is the proliferative stage of ARDS?
synthesis of scarring
145
what is the fibrotic stage of ARDS?
scars mature into fibrotic tissue
146
what are the signs of ARDS?
decreased pulmonary capacities and compliance decreased DLCO chest x ray shows bilateral opacities (DEFINING CRITERIA) decreased ABGs decreased breath sounds over fluid filled areas, wet rales, wheezing, rhonci tachycardia and maybe arryhthmias due to hypoxemia
147
what are the symptoms of ARDS?
appearn acutely ill dyspnic at rest and w/activity fast, labored breathing cyanotic may have impaired mental status, restlessness, headache, anxiety
148
what are the treatments for ARDS?
treat precipitating cause mechanical ventilation (lung protective vent, PEEP, and proning) supportive prevent/treat complications
149
what is the goal of lung protective ventilation?
adequate gas exchange and low TV
150
what is positive end expiratory pressure (PEEP)?
keeps the alveoli open PREVENTS alveolar collapse 5-15 cm H2O higher cm H2O=worse condition
151
what is proning?
delivery of mechanical ventilation with pt in prone to IMPROVE OXYGENATION and IMPROVE LUNG PERFUSION
152
what are the cardiovascular causes of RLD?
pulmonary edema pulmonary emboli
153
what is pulmonary edema?
increased fluid int eh lungs from pulmonary vascular systems starting int he interstitial space and progressing to alveolar space
154
what are the 2 main categories of pulmonary edema?
cardiogenic and noncardiogenic
155
what is the primary cause of cardiogenic pulmonary edema?
left ventricular failure
156
what are causes of cardiogenic pulmonary edema?
LEFT VENTRICULAR FAILURE ARDS renal failure high altitude pulmonary edema heart disease
157
how does L ventricular failure result in cardiogenic pulmonary edema?
increased L atrial pressure --> pressure back on pulmonary circulation--> increased microcirculation (hydrostatic pressure)-->fluid spills into interstitial space
158
the lymphatics don't work when the pulmonary vascular hydrostatic pressure is >___mmHg
30
159
pulmonary edema of cardiac origin has ___ protein content
low (transudative)
160
what are Kerly B lines and what are they indicative of?
short, thin horizontal lines extedning inward from pleural space indicative of cardiogenic pulmonary edema
161
what breath sounds are heard in cardiogenic pulmonary edema?
wet rales with decreased breath sounds bronchospasms and wheezing
162
are arrythmias common in cardiogenic pulmonary edema?
yes
163
what are the symptoms of cardiogenic pulmonary edema?
appear in respiratory distress report sense of suffication SOB orthopnea cough with pink frothy sputum cynaptic increased RR labored breathing pallor diaphoresis
164
how is cardiogenic pulmonary edema managed?
decrease cardiac prelaod (GET FLUID OUR OF HEART) with diuretics, vasodialtors, decreased sodium, and physical activity maintain oxygenation of tissues with supplemental O2 and mechanical vent as needed
165
what is a pulmonary emboli?
complication of venous thrombosis that travels from systemic vein (mostly from the legs) to pulmonary circulation
166
t/f: 1/3 of pulmonary emboli end with death w/in an hour
true
167
what fraction of ppl with a DVT/PE will have another one within 10 years?
1/3
168
t/f: PE are clinically silent
true
169
what are the classical traid of symptoms with PE?
pleuritic chest pain, hemoptosis, and DVT
170
what % of orthopeadic pts will have a PE w/o blood thinners
80%
171
what are the pathophysiologic changes associated with PE?
occlusion of pulmonary artery branch leads to edema and hemorrhage lack of blood flow-->necrosis of alveolar walls--> inflammatory response a portion of the lung is ventilated but no longer perfused
172
what is the clinical presentation of PE?
dyspnea chest pain hemoptysis
173
what are the risk factors for DVT?
immobilization injuries to leg increased age inherited clotting disorders infectious and inflammatory diseases pregnancy/contraceptives cancer smoking obesity burns thrombocytosis sickle cell anemia orthopedic pts
174
how is a PE diagnosed?
CT pulmonary angiography
175
what 4 things should be involved in DVT risk assessment?
1) advocate for a culture of mobility 2) assess for risk during hx and exam 3) when pts present with conditions that increase their risk, we should be highly suspicious of DVT 4) promote preventative measures for those with high risk
176
what is the medical intervention for PE?
prevention anticoagulants some kind of filtration device
177
what are the neuromuscular causes of RLD?
SCI ALS GBS myasthenia gravis duchenne's muscular dystrophy
178
what muscles are involved in inspiration?
external intercostals
179
what muscles are involved in expiration?
internal intercostals
180
what can cervical SCI cause?
decreased VC and MVV weak/paralyzed expiratory muscles weak/absent diaphragm
181
what can weak/paralyzed expiratory muscles and weak/absent diaphragm lead to?
inability to cough pulmonary infection alveolar hypoventilation, hypoxemia, and hypercapnia
182
what can alveolar hypoventilation, hypoxemia, and hypercapnia lead to?
atelectasis
183
what is paradoxical breathing?
diaphragm goes up and chest wall goes in with inspiration; diaphragm goes down and chest wall flares with expiration chest expands and abdomen draws in with inspiration; abdomen pushes out with expiration
184
how is cervical SCI treated?
strengthen and increase the endurance of any remaining ventilatory muscles - inspiratory muscle training - resistance exercise training - incentive spirometry secretion clearance techniques - postural drainage, percussion, vibration, assisted cough, suctioning
185
what is ALS?
progressive degenerating NS disease involving demyelinated UMNs and LMNs
186
what are the phases of respiratory involvement in ALS?
phase 1: minimal complications phase 2: risk for complications phase 3: respiratory failure with signs of disease progression phase 4: continuous non-invasive ventilation (NIV) phase 5: trach, QOL
187
what lung fxn tests are used in ALS phase 2?
forced vital capacity max inspiratory pressure
188
what NIF/MIP is indicative of impaired diaphragm fxn?
above 60
189
what FVC is indicative of impaired diaphragm fxn?
less than 50%
190
what is BiPAP?
bilevel positive assisted airway pressure opens up alveoli and prevents them from collapsing
191
what is the difference b/w BiPAP and PEEP?
PEEP just keeps the alveoli from collapsing, BiPAP also opens them up many different mask options
192
what are these examples of: mechanical insufflation-exsufflation device suction devices
cough assist devices
193
what is GBS?
demyelination of peripheral motor neurons idiopathic polyneuritis linked to the immune system
194
what is the treatment for GBS?
heat for pain, PROM, active exercise including breathing
195
what is myasthenia gravis?
chronic neuromuscular disease characterized by progressive muscular weakness on exertion autoimmune attack on acetylcholine receptors at the postsynaptic neuromuscular junction weakness and fatigue of voluntary muscles, SOB, weak and ineffective cough
196
what is Duchenne's muscular dystrophy?
genetically determined progressive degenerative myopathy involvement of diaphragm late in disease
197
what is the treatment of DMD?
supportive, preserving mobility, and prevention of respiratory infection
198
what are the s/s of the neuromuscular causes of RLD?
respiratory muscle weakness decreased breath sounds SOB/dyspnea at rest inability to cough ineffective clearning of secretions poor voice volume decrease in life activities
199
what are connective tissue causes of RLD?
rheumatoid arthritis systemic lupus erythematosus scleraderma polymyositis
200
what is rheumatoid arthritis?
chronic inflammation of peripheral jts resulting in progressive destruction of articular and periarticular structures strong correlation with smoking lung PARENCHYMA changes decreased chest wall compliance and decreased inspiratory power pain from pleurisy
201
how is RA treated?
corticosteroids and immunosuppressant drugs
202
what is systemic lupus erythematosus (SLE)?
chronic inflammatory connective tissue disorder most in black women antigen-antibody reactions pleurisy diaphragmatic weakness BUTTERFLY RASH
203
how is SLE treated?
reverse autoimmune and inflammatory changes prevent complications
204
what is scleroderma?
progressive fibrosing disorder that causes degenerative changes in skin, small blood vessels, esophagus, intestinal tract, lung, heart, kidney, and articular structures FIBROSIS idiopathic more common in women
205
how is scleroderma treated?
treat specific symptoms supportive
206
what are musculoskeletal causes of RLD?
kyphoscoliosis ankylizing spondylitis pectus excavatum pectus carinatum pregnancy obesity
207
what is kyphoscoliosis?
combo of excessive AP and lat curvature of thoracic spine only 3% have lung dysfxn
208
how is hyphoscoliosis treated?
orthotic devices exercise surgery pulmonary compromise (immunizations, good hydration, aggressive treatment of pulm infections, avoidance of sedatives, supplemental O2, and resp musc training)
209
what is ankylosing spondylitis?
chronic inflammatory disease of the spine characterzied by immobility of SI and vertebral jts and ossification of paravertebral ligs low chest compliance
210
how is ankylosing spondylitis treated?
maintain good body alignment, thoracic mobility
211
what is pectus excavatum?
funnel chest sternal depression and decreased AP diameter decreased TLC, VC, and max voluntary ventilation
212
what is pectus carinatum?
pigeon breast sternum protruding anteriorly associated with prolonged childhood asthma
213
how does pregnancy lead to RLD?
decreased chest wall compliance due to downward excursion of diaphragm closing small airways ventilation-perfusion mismatch increased work of breathing
214
how does obesity lead to RLD?
decreased lung capacities, lung volumes, and respiratory musc strength increased airway resistance pulmonary diffusion heterogeneity of ventilation distribution hypercapnic resp failure
215
what are traumatic causes of RLD?
crush injuries penetrating wounds
216
how does surgical therapy lead to RLD?
pulm dysfxn due to anesthetic agent, surgical incision, pain post-op