This document discusses acute respiratory distress syndrome (ARDS). ARDS is defined as an acute, diffuse inflammatory lung injury caused by diverse pulmonary and non-pulmonary insults, characterized by increased vascular permeability and loss of aerated lung tissue. The main criteria are hypoxemia, bilateral opacities on chest x-ray, decreased lung compliance, and increased physiological dead space. Management involves treating the underlying cause while providing supportive care such as mechanical ventilation. Outcomes depend on severity but may include long-term pulmonary dysfunction or neurocognitive impairments.
3. ARDS DEFINITION
It is an acute, diffuse, inflammatory lung injury caused by diverse
pulmonary and non-pulmonary etiologies.
It is characterized by increased vascular permeability, increased lung
weight and loss of aerated tissue within the 7 days of insult.
4. ARDS DEFINITION
Hypoxemia, bilateral opacities on the chest x-ray, decreased lung
compliance and increased physiological dead space are the main
clinical signs.
Diffuse alveolar damage characterized by edema, inflammation,
hyaline membrane formation or pulmonary hemorrhage are the
pathological hallmark.
5. ARDS CRITERIA
The Pediatric Acute Lung Injury Consensus Conference Group PALICC
Pediatr Crit Care Med. 2015 Jun; 16(5): 428–4
7. ARDS EQUATION
Oxygenation Index (OI) = (FiO2 X mean airway pressure X 100)/PaO2
Oxygen Saturation Index (OSI) = FiO2 X mean airway pressure X 100 /
SPO2
The PaO2/FiO2 (P/F) ratio can be calculated using PaO2 in mm of Hg
and FiO2in decimal from 0.21 to 1.0.
Pediatr Crit Care Med. 2015 Jun; 16(5): 428–4
8. ARDS EXAMPLE
For example, a patient receiving mechanical ventilation with a mean
airway pressure of 20 cm H2O, FiO2 of 0.6 has SPO2 of 98% and
PaO2 of 85 mm Hg.
OI = (0.6 X 20 x 100)/85 = 14.11
OSI = (0.6 X 20 x 100)/98 = 12.24
P/F ratio = 85/0.6 = 141.66
This patient has moderate ARDS.
https://emedicine.medscape.com/article/803573-
11. ARDS PATHOPHYSIOLOGY
Initial phase: areas of normal lungs are more so PEEP works, Later
(>5-7days) abnormal lung increases so PEEP is less effective,
PaCo2 increases.
Fibroproliferative phase: slow recovery & ventilator dependency.
Resolution phase: gradual recovery of hypoxemia, compliance, X
ray resolution
12. ARDS CLINICAL FEATURES
Dyspnea, agitation, increased WOB
Hypoxemia refractory to supplemental O2 ➞ Hypercarbia ➞
Acidosis.
Lung:
scatter of normal alveoli along with various grades of severity of involvement
Xray:
B/l infiltrates – patchy, asymmetric, may associated with pleural effusion
In progressive fibrosing alveoli:
persistant hypoxemia, decreasing compliance, Pulmonary HT ➞ Rt ventricular
failure
18. ARDS OUTCOMES
Pulmonary Function
Screening for pulmonary function abnormalities within the first year after
discharge.
Spirometry for older children.
pulmonologist referral.
Neurocognitive Development
physical, neurocognitive, emotional, family, and social function be evaluated within
3 months
Onset: within one week of known insult or new/worsening respiratory symptoms
Chest imaging (a radiograph or a computed tomogram) showing bilateral opacities consistent with pulmonary edema. This must not be fully explainable by effusion, collapse or nodules.
Origin of edema: patient can be diagnosed with ARDS provided respiratory failure cannot be fully explained by cardiac failure or fluid overload as determined by treating physician based on available clinical information. If the risk factors for ARDS are not present, objective evidence (e.g. echocardiography) would be required to exclude cardiac failure or fluid overload.
Oxygenation impairment: presence of hypoxemia is essential to the diagnosis of ARDS. The subgroup stratification of ARDS is determined by the degree of hypoxemia as below.