resp failure Flashcards
what is type 1 resp failure
Type 1: Oxygen Problem (Hypoxemic)
• Definition: Low oxygen (PaO₂ < 8 kPa or 60 mmHg) but normal or low CO₂.
• Think: 1 Gas (O₂) is the problem.
• Cause: A problem with oxygenation (e.g., pneumonia, pulmonary edema, ARDS).
• Key Feature: Ventilation is still working, but oxygen cannot get in.
what is type 2 resp failure
Type 2: Ventilation Problem (Hypercapnic)
• Definition: High CO₂ (PaCO₂ > 6.5 kPa or 50 mmHg) with or without low O₂.
• Think: 2 Gases (CO₂ and O₂) are involved.
• Cause: A problem with ventilation (e.g., COPD, chest wall deformities ,neuromuscular disorders).
• Key Feature: Lungs cannot remove CO₂ effectively.
what are signs of resp failure
use of accessory muscles
tachypnea
sweating
signs of Co2 retention (asterixis, bounding pulse
what is used as a guide in deterioratiom in acute neuromuscular problems
FVC
RR and TV are insensitibe indicators of RF
what will ABG show in type 1 and type 2 RF
type 1: resp alkolosis
type 2: resp acidosis
what is acute respiratory distress syndrome
type of resp failure characterized by rapid onset of spread of inflammation in the lungs
what would show in chest x ray of ARDS
new bilateral diffuse patchy or homogenous pulmonary infiltrates
stiff lungs no comliance more dead space
what are causes ARDS
direct lung injury: pneumonia, gastric aspiration, inhalation injury
secondary to severe systemic illness: shock,sepsis,hemorrhage
what can cause death in ARDS
multiorgan failure
hemodynamic instability
what is a diagnostic criteria of ARDS
4 must exist:
1)Timing: acute onset, symptoms occur within 1 wk
2)bilateral infiltrates
3)pulmonary capillary wedge pressure < 18 or lack of clinical congestive heart failure
4) refractory hypoxemia with Pao2 : fio2 <200 (berlin definition )
management of ARDS
admit to icu
sepsis: identify organism
early prone positioning
limit pulmonary edema
resp support: mechanical ventilation
what are symptoms of ILD
exertional dysnea
nonproductive cough
what does examination in ILD pt show
fine crackles
pulmonary htn
clubbing
chest x ray in ILD would show what pattern
reticular or reticulonodulary pattern (ground glass appearance )
pft in ILD would show what
restrictive pattern
upper lobe fibrosis distribution of ILD include
sarcoidosis
hypersensitiving pnemonitis
silicosis
radiation
ankylosing spondilitis
lower lobe fibrosis iclude
idiopathic pulmonary fibrosis
asbestosis
idiopathic pulmonary fibrosis features
men in late 60s
no known cause
progressive breathlessness
non- productive cough
on examination of pulmonary fibrosis
clubbing in 50%
fine end inspiratory basal crackles
tx of IPF
disease is life limiting shoud consider transplanation , survival without transplant is 5 yrs
pirfenidone : anti fibrotic agent slow rate of decline
nintedanib: TK inhibitor that blocks fibrogenic growth factor
treat GERD if present
what causes formation of non- caseating granulomas in multiple organs , most common lungs and LN
sarcoidosis
diagnosis of sarcoidosis in chest x ray and lab test
xray: bilateral hilar lymphadenopathy
lab test: elevated serum ACE , hypercalcemia , elevated inflam markers
what are other organs affected in sarcoidosis
eyes: ant and post uveitis
skin: erythema nodusm , maculopapular lesions, lupus, alopecia
lofgren syndrome: erythema nodusm , arthritis , hilar adenopathy
Heerfordt syndrome: fever, parotid enlargement, uveitis, facial palsy
tx of sarcoidosis
first line: CORTICOSTEROIDS
if pt needs long term tx –> steroid sparing agents ( methotrexate, azathioprine, cyclophosphamide)