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RESPIRATORY SYSTEM
DR. JASASHREE CHOUDHURY
PROFESSOR
DEPT OF PEDIATRICS
IMS & SUM HOSPITAL
Etiopathogenesis , clinical features,complications, investigations
Differential diagnosis and management of Acute URI,
Pneumonia with emphasis on bronchopneumonia
Bronchiolitis
Bronchitis
Bronchial asthma
Etiopathogenesis, c/f ,diagnosis, classification, management
t/t of Ac. Severe Asthma
Fb aspiration diagnosis ,management
Pathogenesis c/f & management of pneumothorax,
Pleural effusion, empyema
Etiology,C/F,diagnosis of
bronchiolitis
Management of bronchiolitis
Acute bronchitis-clinical
features,treatment
Common cause of hospitalization in young
children,<2yrs (severe in 2m-6m)
May be associated with future development
of bronchial hyper reactivity
May be associated with significant morbidity
though mortality is only 1 – 2%
INTRODUCTION
MICROBIOLOGY
Typically caused by viruses
RSV-most common
Parainfluenza
Human Metapneumovirus
Influenza
Rhinovirus
Coronavirus
Occasionally associated with Mycoplasma
pneumonia infection
RISK FACTORS OF SEVERITY
Prematurity
Low birth weight
Age less than 12months
Hemodynamically significant cardiac disease
Immunodeficiency
Neurologic disease
Anatomical defects of the airways
PATHOGENESIS
Viruses penetrate terminal bronchiolar cells—
directly damaging
also via inflammatory mediators
Pathologic changes begin 18-24 hours after
infection
Bronchiolar cell necrosis, ciliary disruption,
peribronchial lymphocytic infiltration
Edema, excessive mucus, sloughed epithelium
lead to airway obstruction and atelectasis
CLINICAL FEATURES
Begin with upper respiratory tract
symptoms: nasal congestion,
 rhinorrhea, mild cough, low-grade fever
Progress in 3-6 days to rapid respirations,
chest retractions, wheezing
CLINICAL FEATURES
Tachypnoea,low grade fever
Prolonged expiratory phase, rhonchi,
wheezes and crackles throughout
Severe distress,grunting
 Dehydration
 Conjunctivitis or otitis media
 Cyanosis or apnea(very young infants)
DIAGNOSIS
Clinical diagnosis based on history and
physical exam
Usually child is active alert apart from f/o
resp distress no toxic look
Supported by CXR:
hyperinflation, flattened diaphragms,
air bronchograms, peribronchial cuffing,
patchy infiltrates, atelectasis
Most useful in children with complicating
symptoms
CBC,Routine urine test--to help determine
bacterial illness
Blood gas--evaluate respiratory failure
CXR--evaluate pneumonia, heart disease
INVESTIGATION
DIFFERENTIAL DIAGNOSIS
Viral-triggered asthma
Bronchitis or pneumonia
Chronic lung disease
Foreign body aspiration
Gastroesophageal reflux or dysphagia leading to
aspiration
Congenital heart disease or heart failure,cardiac
asthma
Vascular rings, bronchomalacia, complete tracheal
rings or other anatomical abnormalities
RISK FOR SEVERE DISEASE
Toxic or ill-appearing
Oxygen saturation < 95% on room air
Age less than 3 months
Respiratory rate > 70
Atelectasis on CXR
HOSPITALIZATION
Children with severe disease
Toxic with poor feeding, lethargy,
dehydration
Moderate to severe respiratory
distress
(RR > 70, dyspnea, cyanosis)
Severe Hypoxemia,Apnea
Parent unable to care for child at
home
TREATMENT
Supportive care
Pharmacologic therapy
 Oxygen supplement,respiratory support
 Adequate fluid intake(Isotonic
fluid),antipyretics
 Hypertonic saline nebulization
 Adrenaline nebulization
 Saline nasal drop,bulb suctioning
 Aerosolised Ribavirin in special
situations
 Bronchodilators are controversial
 Aviod deep suctioning
Oxygen saturations to maintain above 90-
92%
Keep saturations higher in the presence of
fever, acidosis, Hemoglobinopathies
Wean carefully in children with heart
disease,
 chronic lung disease, prematurity
Mechanical ventilation for pCO2 > 55 or
apnea
ANTIBIOTICS
Not useful in bronchiolitis per se
Should be used if there is evidence of
concomitant
bacterial infection
Positive urine culture
Acute otitis media
Consolidation on CXR
 Follows upper respiratory infection
 Viral infection to bacterial invasion of upper
airways
 Inflammation of airways
 Increased mucus production
Clinical presentation
Fever
Tachypnea
Mild dyspnea
Cough with clear to purulent
sputum production
Diffuse ronchi & crepitation
X ray - rule out pneumonia
No evidence of lung infiltration
Management
Chest physiotherapy to mobilize secretion
Hydration to liquefy secretion
Pharmacologic intervention
1)Bronchodilators – reduce bronchospasm
and promote sputum expectoration
2) Oral antibiotics
3) Symptomatic treatment
Respiratory system.pptx

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Respiratory system.pptx

  • 1. RESPIRATORY SYSTEM DR. JASASHREE CHOUDHURY PROFESSOR DEPT OF PEDIATRICS IMS & SUM HOSPITAL
  • 2. Etiopathogenesis , clinical features,complications, investigations Differential diagnosis and management of Acute URI, Pneumonia with emphasis on bronchopneumonia Bronchiolitis Bronchitis Bronchial asthma Etiopathogenesis, c/f ,diagnosis, classification, management t/t of Ac. Severe Asthma Fb aspiration diagnosis ,management Pathogenesis c/f & management of pneumothorax, Pleural effusion, empyema
  • 3. Etiology,C/F,diagnosis of bronchiolitis Management of bronchiolitis Acute bronchitis-clinical features,treatment
  • 4. Common cause of hospitalization in young children,<2yrs (severe in 2m-6m) May be associated with future development of bronchial hyper reactivity May be associated with significant morbidity though mortality is only 1 – 2% INTRODUCTION
  • 5. MICROBIOLOGY Typically caused by viruses RSV-most common Parainfluenza Human Metapneumovirus Influenza Rhinovirus Coronavirus Occasionally associated with Mycoplasma pneumonia infection
  • 6. RISK FACTORS OF SEVERITY Prematurity Low birth weight Age less than 12months Hemodynamically significant cardiac disease Immunodeficiency Neurologic disease Anatomical defects of the airways
  • 7. PATHOGENESIS Viruses penetrate terminal bronchiolar cells— directly damaging also via inflammatory mediators Pathologic changes begin 18-24 hours after infection Bronchiolar cell necrosis, ciliary disruption, peribronchial lymphocytic infiltration Edema, excessive mucus, sloughed epithelium lead to airway obstruction and atelectasis
  • 8. CLINICAL FEATURES Begin with upper respiratory tract symptoms: nasal congestion,  rhinorrhea, mild cough, low-grade fever Progress in 3-6 days to rapid respirations, chest retractions, wheezing
  • 9. CLINICAL FEATURES Tachypnoea,low grade fever Prolonged expiratory phase, rhonchi, wheezes and crackles throughout Severe distress,grunting  Dehydration  Conjunctivitis or otitis media  Cyanosis or apnea(very young infants)
  • 10. DIAGNOSIS Clinical diagnosis based on history and physical exam Usually child is active alert apart from f/o resp distress no toxic look Supported by CXR: hyperinflation, flattened diaphragms, air bronchograms, peribronchial cuffing, patchy infiltrates, atelectasis
  • 11. Most useful in children with complicating symptoms CBC,Routine urine test--to help determine bacterial illness Blood gas--evaluate respiratory failure CXR--evaluate pneumonia, heart disease INVESTIGATION
  • 12.
  • 13. DIFFERENTIAL DIAGNOSIS Viral-triggered asthma Bronchitis or pneumonia Chronic lung disease Foreign body aspiration Gastroesophageal reflux or dysphagia leading to aspiration Congenital heart disease or heart failure,cardiac asthma Vascular rings, bronchomalacia, complete tracheal rings or other anatomical abnormalities
  • 14. RISK FOR SEVERE DISEASE Toxic or ill-appearing Oxygen saturation < 95% on room air Age less than 3 months Respiratory rate > 70 Atelectasis on CXR
  • 15. HOSPITALIZATION Children with severe disease Toxic with poor feeding, lethargy, dehydration Moderate to severe respiratory distress (RR > 70, dyspnea, cyanosis) Severe Hypoxemia,Apnea Parent unable to care for child at home
  • 17.  Oxygen supplement,respiratory support  Adequate fluid intake(Isotonic fluid),antipyretics  Hypertonic saline nebulization  Adrenaline nebulization  Saline nasal drop,bulb suctioning  Aerosolised Ribavirin in special situations  Bronchodilators are controversial  Aviod deep suctioning
  • 18. Oxygen saturations to maintain above 90- 92% Keep saturations higher in the presence of fever, acidosis, Hemoglobinopathies Wean carefully in children with heart disease,  chronic lung disease, prematurity Mechanical ventilation for pCO2 > 55 or apnea
  • 19. ANTIBIOTICS Not useful in bronchiolitis per se Should be used if there is evidence of concomitant bacterial infection Positive urine culture Acute otitis media Consolidation on CXR
  • 20.  Follows upper respiratory infection  Viral infection to bacterial invasion of upper airways  Inflammation of airways  Increased mucus production
  • 21. Clinical presentation Fever Tachypnea Mild dyspnea Cough with clear to purulent sputum production Diffuse ronchi & crepitation X ray - rule out pneumonia No evidence of lung infiltration
  • 22. Management Chest physiotherapy to mobilize secretion Hydration to liquefy secretion Pharmacologic intervention 1)Bronchodilators – reduce bronchospasm and promote sputum expectoration 2) Oral antibiotics 3) Symptomatic treatment