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Introduction
Pathophysiology & Types
Clinical Presentation
Assessment & Diagnosis
Management
Monitoring & Complications
Specific Conditions
Introduction to Pediatric Respiratory Failure
Definition
Respiratory failure occurs when the respiratory system fails in oxygenation and/or ventilation functions. In children, this represents a significant emergency requiring prompt recognition and intervention.
Key Concepts
Type I (Hypoxemic) Respiratory Failure:
PaO2 < 60 mmHg on FiO2 > 0.6
Normal or low PaCO2
Primarily oxygenation failure
Type II (Hypercapnic) Respiratory Failure:
PaCO2 > 50 mmHg
May have associated hypoxemia
Primarily ventilation failure
Epidemiology
Leading cause of cardiopulmonary arrest in children
Most common in children under 5 years
Higher incidence during respiratory virus seasons
Increased risk in children with chronic conditions
Risk Factors
Age-Related:
Smaller airway diameter
More compliant chest wall
Immature immune system
Higher metabolic demands
Anatomical:
Chronic lung disease
Airway anomalies
Chest wall deformities
Medical Conditions:
Neuromuscular disorders
Immunodeficiency
Cardiac disease
Genetic syndromes
Pathophysiology and Types
Basic Respiratory Physiology
Ventilation Components:
Neural drive
Respiratory muscles
Airways and alveoli
Chest wall mechanics
Gas Exchange:
Ventilation-perfusion matching
Diffusion capacity
Cardiac output
Pathophysiologic Mechanisms
Mechanism
Causes
Examples
Upper Airway Obstruction
Anatomic or functional obstruction
Croup, epiglottitis, foreign body
Lower Airway Disease
Bronchial obstruction or restriction
Asthma, bronchiolitis
Alveolar Disease
Inflammation or filling
Pneumonia, pulmonary edema
Chest Wall Dysfunction
Mechanical or neurological
Flail chest, muscular dystrophy
Control of Breathing
Central or peripheral
Brain injury, drug overdose
Types of Respiratory Failure
Type I (Hypoxemic):
V/Q mismatch
Right-to-left shunt
Diffusion impairment
Common in ARDS, pneumonia
Type II (Hypercapnic):
Decreased minute ventilation
Increased dead space
Increased CO2 production
Common in neuromuscular disease
Mixed:
Combined oxygenation and ventilation failure
Common in severe asthma
Poor prognostic indicator
Clinical Presentation
Early Warning Signs
Respiratory:
Tachypnea
Increased work of breathing
Nasal flaring
Use of accessory muscles
Retractions
Behavioral:
Agitation
Anxiety
Poor feeding
Decreased activity
Signs of Severe Respiratory Distress
Immediate Concerns:
Lethargy or decreased consciousness
Cyanosis
Poor muscle tone
Bradypnea or irregular breathing
Grunting
Compensatory Mechanisms:
Tachycardia
Sweating
Pallor
Poor peripheral perfusion
Age-Specific Presentations
Age Group
Key Features
Common Causes
Neonates
Apnea, poor feeding, temperature instability
RDS, sepsis, CHD
Infants
Nasal flaring, head bobbing, poor feeding
Bronchiolitis, pneumonia
Toddlers
Tripod positioning, drooling, stridor
Croup, foreign body
School-age
Chest pain, anxiety, speak in phrases
Asthma, pneumonia
Adolescents
Fatigue, decreased exercise tolerance
Asthma, PE, pneumothorax
Assessment and Diagnosis
Initial Assessment
Vital Signs:
Age
Normal RR
Warning RR
Normal SpO2
0-3 months
30-60
>60 or <30
>95%
3-12 months
24-40
>50 or <24
>95%
1-4 years
20-30
>40 or <20
>95%
4-12 years
18-25
>30 or <18
>95%
>12 years
12-20
>25 or <12
>95%
Diagnostic Studies
Laboratory:
Blood gas analysis (arterial preferred)
Complete blood count
Basic metabolic panel
Inflammatory markers
Blood cultures if indicated
Imaging:
Chest X-ray (AP and lateral)
Point-of-care ultrasound
CT chest if indicated
Additional Studies:
ECG
Echocardiogram
Viral studies
Pulmonary function tests (if stable)
Management
Initial Stabilization
Airway:
Position optimization
Airway clearance
Consider early intubation if indicated
Breathing:
Oxygen supplementation
Non-invasive ventilation when appropriate
Mechanical ventilation parameters
Circulation:
IV access
Fluid management
Cardiovascular support if needed
Respiratory Support
Support Type
Indications
Settings
High-Flow Nasal Cannula
Mild-moderate distress
1-2 L/kg/min up to 60 L/min
CPAP
Upper airway support
5-10 cmH2O
BiPAP
Type II failure
IPAP 10-20, EPAP 5-10
Mechanical Ventilation
Severe failure
Age/condition specific
Medication Therapy
Bronchodilators:
Albuterol: 2.5-5 mg nebulized
Epinephrine: 0.01 mg/kg IM
Anti-inflammatories:
Steroids: 1-2 mg/kg/day
Duration based on condition
Antibiotics:
If bacterial infection suspected
Choice based on likely pathogens
Monitoring and Complications
Continuous Monitoring
Clinical Parameters:
Work of breathing
Mental status
Perfusion
Urine output
Device Monitoring:
Pulse oximetry
Capnography
Cardiac monitoring
Blood pressure
Laboratory Monitoring:
Serial blood gases
Electrolytes
Lactate
Inflammatory markers
Complications
Respiratory:
Atelectasis
Ventilator-associated pneumonia
Pneumothorax
Post-extubation stridor
Cardiovascular:
Right heart failure
Shock
Arrhythmias
Pulmonary hypertension
Other Systems:
Neurological deterioration
Renal dysfunction
GI complications
Nosocomial infections
Prevention Strategies
Ventilator-Associated:
Head elevation 30-45 degrees
Oral care protocol
Daily sedation interruption
Ventilator bundle compliance
General Measures:
Early mobilization when appropriate
Stress ulcer prophylaxis
DVT prophylaxis in adolescents
Nutrition optimization
Specific Conditions
Status Asthmaticus
Assessment:
Severe bronchospasm
Poor response to initial therapy
Air trapping
Risk of respiratory failure
Management:
Continuous albuterol nebulization
IV magnesium sulfate
Systemic corticosteroids
Consider ketamine or heliox
ARDS
Diagnostic Criteria (PARDS):
Acute onset
Bilateral infiltrates
PaO2/FiO2 ratio ≤ 300
No evidence of left heart failure
Management Strategy:
Lung-protective ventilation
Permissive hypercapnia
Conservative fluid management
Prone positioning if severe
Bronchiolitis
Risk Factors:
Age < 12 months
Prematurity
Chronic conditions
Environmental exposure
Management Approach:
Supportive care
Oxygen supplementation
Hydration maintenance
HFNC if needed
Neuromuscular Weakness
Considerations:
Progressive weakness
Poor secretion clearance
Sleep-disordered breathing
Recurrent aspirations
Management:
NIV support
Airway clearance techniques
Prevention of complications
Early mobilization
Prognostic Factors
Factor
Good Prognosis
Poor Prognosis
Response to Therapy
Rapid improvement
Persistent deterioration
Underlying Condition
Reversible cause
Progressive disease
Organ Dysfunction
Single system
Multiple organ failure
Nutritional Status
Well-nourished
Malnourished
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