PNEUMONIA
BY Dr. BIRHANU A.
OUTLINES
• OBJECTIVES
• PNEUMONIA
– Ethiology,
– Epidemiology,
– C/Manifestation,
– Pathogenesis,
– Diagnosis And
– Management
Objectives
• At the end of this lecture you should
understand the etiology, epidemiology,
pathogenesis, c/manifestation, diagnosis and
management of pneumonia in children.
Pneumonia
• Is inflammation of the lung parenchyma
• Etiology
– Infectious
– Noninfectious and aspiration
– Hypersensitivity and reaction
– Drugs or radiation-induced pneumonitis
Bacteria
• S.pnuemonia-commonest 3wk-4yr
• C.pneumoniaeand M.pnuemoniae-
commonest above ≥5years of age
• S.aureus-commonest after influenza viruse
• S.pyogenes
Conti……….
AGE GROUP FREQUENT PATHOGENS (IN ORDER OF FREQUENCY)
Neonates (<3 wk) GBS, E.coli, other Gram-negative bacilli, S.pneumoniae,
H.influenzae (type b, nontypeable)
3 wk-3 mo RSV, other respiratory viruses (rhinoviruses, parainfluenza
viruses, influenza viruses, human metapneumovirus,
adenovirus), S. pneumoniae, H. influenzae (type b,
nontypeable); if patient is afebrile, consider C. trachomatis
4 mo-4yr RSV, other respiratory viruses (rhinoviruses, parainfluenza
viruses, influenza viruses, human metapneumovirus,
adenovirus), S. pneumoniae, H. influenzae (type b,
nontypeable), M.pneumoniae, group A streptococcus
≥5 yr M. pneumoniae, S. pneumoniae, C.pneumoniae, H. influenzae
(type b,* nontypeable), influenza viruses, adenovirus, other
respiratory viruses
• S. pneumoniae, H. influenzae, and S. aureus
are the major causes of hospitalization and
death from bacterial pneumonia.
• The incidence of pneumonia caused by H.
influenzae or S.pneumoniae has been
significantly reduced in areas where routine
immunization has been implemented.
EPIDEMIOLOGY
• Is the leading infectious cause of death globally
• Among children younger than 5 yr, accounting for
an estimated 920,000 deaths each year.
• Pneumonia mortality is closely linked to poverty.
• More than 99% of pneumonia deaths are in low-
and middle-income countries.
• The highest pneumonia mortality rate occurring
in poorly developed countries.
PATHOGENESIS
• Defence mechanisms of respiratory tract
– Mucociliary clearance
– Macrophages
– Secretory immunoglobulin A
– Coughing refelex
Viral pneumonia
• Usually results from spread of infection along the
airways.
• Then causes a direct injury of the respiratory
epithelium.
• Airway obstruction occurs from swelling, abnormal
secretions, and cellular debris.
• The small caliber of airways in young infants makes
such patients particularly susceptible to severe
infection.
• Atelectasis, interstitial edema, and hypoxemia from
ventilation–perfusion mismatch often accompany
airway obstruction.
• Viral infection of the respiratory tract can also
predispose to secondary bacterial infection by
– Disturbing normal host defence mechanisms
– Altering secretions
– Through disruptions in the respiratory microbiota.
Bacterial pneumonia
• Most often occurs when respiratory tract
organisms colonize the trachea and
subsequently gain access to the lungs
• Pneumonia may also result from direct
seeding of lung tissue after bacteremia.
• When bacterial infection is established in the
lung parenchyma, the pathologic process
varies according to the invading organism.
M. pneumoniae
• Attaches to the respiratory epithelium, inhibits ciliary
action, and leads to cellular destruction and an
inflammatory response in the submucosa.
• As the infection progresses, sloughed cellular debris,
inflammatory cells, and mucus cause airway obstruction,
with spread of infection occurring along the bronchial tree,
as is seen in viral pneumonia.
S. pneumoniae
• produces local edema that aids in the proliferation of
organisms and their spread into adjacent portions of lung,
often resulting in the characteristic focal lobar involvement.
Group A streptococcus
• Lower respiratory tract infection typically results
in more diffuse lung involvement with interstitial
pneumonia.
• The pathology includes
– Necrosis of tracheobronchial mucosa
– Formation of large amounts of exudate
– Edema and local hemorrhage, with extension into the
interalveolar septa; and involvement of lymphatic
vessels with frequent pleural involvement.
S. aureus pneumonia
• Manifests as confluent bronchopneumonia,
often unilateral and characterized by
– the presence of extensive areas of hemorrhagic
necrosis and irregular areas of cavitation of the
lung parenchyma, resulting in pneumatoceles,
empyema, and bronchopulmonary fistulas.
Recurrent pneumonia
• Is defined as 2 or more episodes in a single
year or 3 or more episodes ever, with
radiographic clearing between occurrences.
• An underlying disorder should be considered if
a child experiences recurrent pneumonia.
• Differential diagnosis of recurrent pneumonia
are the following
HEREDITARY DISORDERS
– Cystic fibrosis
– Sickle cell disease
DISORDERS OF IMMUNITY
– HIV/AIDS
– Primary immunodeficiencies
DISORDERS OF CILIA
– Primary ciliary dyskinesia
– Kartagener syndrome
ANATOMIC DISORDERS
– Pulmonary sequestration
– Lobar emphysema
– Congenital cystic adenomatoid malformation
– Gastroesophageal reflux
– Foreign body aspiration
– Tracheoesophageal fistula (H type)
– Bronchiectasis
– Aspiration (oropharyngeal incoordination)
– Aberrant bronchus
CLASSIFICATION
Criteria used for classification
• Etiologic
• Anatomic
• severity
Anatomic
• Lobar
• Bronchial
• interstitial
Severity
• Sever pneumonia
• Pneumonia
• No pneumonia
Ethiology
• Viral
• Bacterial
• Fungal
COMPLICATIONS
LOCAL COMPLICATIONS
• Pleural effusion,
• empyema, abscess,
• Bronchopleural fistula,
• Necrotizing pneumonia,
acute
• Acute respiratory
distress syndrome
• Respiratory failure
DISTANT COMPLICATIONS
• Meningitis
• Arthritis
• Pericarditis
• Osteomyelitis
• Endocarditis
• Haemolytic uremic
syndrome
• Sepsis
Clinical Manifestations
• Frequently preceded by several day symptoms of URTI
• Cough: chief symptom
• Increased respiratory rate:
– > 60/minute infants younger than 2 months old
– >50/minute infants 2-12 months old
– > 40/minute children 1-5 years old
• Grunting (keeps narrow airways open)
• Sign of severe distress and impending respiratory
failure
• Nasal flaring (air hunger)
• In infants
– vomiting, anorexia, diarrhea, and abdominal
distention secondary to a paralytic ileus.
– may have a prodrome of URTI and poor feeding,
leading to the abrupt onset of fever, restlessness,
apprehension, and respiratory distress.
• In older children sudden onset high fever,
cough, and chest pain may presentation.
• Retractions: intercostal, supraclavicular,
subcostal
• Increased effort to breathe, decreased lung
compliance
• Hypoxemia: normal >95%
• Fever
Diagnosis
• Chet x-ray
• Chest U/S
• CBC
• ESR/CRP
• PCR
• Blood culture (fail to improve, have clinical
deterioration, complicated pneumonia, or require
hospitalization)
• ASO and anti-DNase B titers
MANAGEMENT
• INDICATION FOR ADMISSION
– Age <6 mo
– Immunocompromised state
– Toxic appearance
– Moderate to severe respiratory distress
– Hypoxemia (oxygen saturation <90% breathing room air, sea level)
– Complicated pneumonia
– Sickle cell anemia with acute chest syndrome
– Vomiting or inability to tolerate oral fluids or medications
– Severe dehydration
– No response to appropriate oral antibiotic therapy
– Social factors (e.g., inability of caregivers to administer medications at
home or follow-up appropriately)
1. Oxygen Therapy: IN o2, CPAP, MV
2. Fluid Therapy: MF, dehydration mgt.
3. Antipyretics: paracetamol
4. Antibiotics
5. Oral Zinc for 7days
ANTIBIOTICS
• Empiric antibiotic choice for hospitalised
suspected pneumonia patient depends on
– local epidemiology,
– the immunization status of the child, and
– the clinical manifestations at the time of
presentation
Ampicillin or penicillin G for inpatient
GIVEN
– without substantial high-level penicillin resistance for
s.pneumoniae
– Fully immunized for H.influenzae type b and
s.pneumoniae
– Not severely ill child
– Ceftriaxone or cefotaxime can be given for those that
don’t fulfil the above criteria.
– Total duration continued upto 10days
• Outpatient
– High dose amoxacillin
– Macrolides for pencillin allegy and suspected
antipical bacteria
– Total duration 5-7days if azithromycin for 5days
PROGNOSIS
• Tachycardia and hypotension- Within two days
• Fever, tachypnea, chest and arterial
oxygenation (PaO2)- Within three days
• Cough and fatigue- ≥14 days
• Radiographic improvement up to 1month
PREVENTION
• Vaccination that prevent pneumonia are
– PCV
– Influenza vaccine
– H.influenza type b vaccine
– Pertussis vaccine
– Measles vaccine
– RSV vaccine

Childhood pneumonia

  • 1.
  • 2.
    OUTLINES • OBJECTIVES • PNEUMONIA –Ethiology, – Epidemiology, – C/Manifestation, – Pathogenesis, – Diagnosis And – Management
  • 3.
    Objectives • At theend of this lecture you should understand the etiology, epidemiology, pathogenesis, c/manifestation, diagnosis and management of pneumonia in children.
  • 4.
    Pneumonia • Is inflammationof the lung parenchyma • Etiology – Infectious – Noninfectious and aspiration – Hypersensitivity and reaction – Drugs or radiation-induced pneumonitis
  • 5.
    Bacteria • S.pnuemonia-commonest 3wk-4yr •C.pneumoniaeand M.pnuemoniae- commonest above ≥5years of age • S.aureus-commonest after influenza viruse • S.pyogenes
  • 6.
    Conti………. AGE GROUP FREQUENTPATHOGENS (IN ORDER OF FREQUENCY) Neonates (<3 wk) GBS, E.coli, other Gram-negative bacilli, S.pneumoniae, H.influenzae (type b, nontypeable) 3 wk-3 mo RSV, other respiratory viruses (rhinoviruses, parainfluenza viruses, influenza viruses, human metapneumovirus, adenovirus), S. pneumoniae, H. influenzae (type b, nontypeable); if patient is afebrile, consider C. trachomatis 4 mo-4yr RSV, other respiratory viruses (rhinoviruses, parainfluenza viruses, influenza viruses, human metapneumovirus, adenovirus), S. pneumoniae, H. influenzae (type b, nontypeable), M.pneumoniae, group A streptococcus ≥5 yr M. pneumoniae, S. pneumoniae, C.pneumoniae, H. influenzae (type b,* nontypeable), influenza viruses, adenovirus, other respiratory viruses
  • 7.
    • S. pneumoniae,H. influenzae, and S. aureus are the major causes of hospitalization and death from bacterial pneumonia. • The incidence of pneumonia caused by H. influenzae or S.pneumoniae has been significantly reduced in areas where routine immunization has been implemented.
  • 8.
    EPIDEMIOLOGY • Is theleading infectious cause of death globally • Among children younger than 5 yr, accounting for an estimated 920,000 deaths each year. • Pneumonia mortality is closely linked to poverty. • More than 99% of pneumonia deaths are in low- and middle-income countries. • The highest pneumonia mortality rate occurring in poorly developed countries.
  • 10.
    PATHOGENESIS • Defence mechanismsof respiratory tract – Mucociliary clearance – Macrophages – Secretory immunoglobulin A – Coughing refelex
  • 11.
    Viral pneumonia • Usuallyresults from spread of infection along the airways. • Then causes a direct injury of the respiratory epithelium. • Airway obstruction occurs from swelling, abnormal secretions, and cellular debris. • The small caliber of airways in young infants makes such patients particularly susceptible to severe infection. • Atelectasis, interstitial edema, and hypoxemia from ventilation–perfusion mismatch often accompany airway obstruction.
  • 12.
    • Viral infectionof the respiratory tract can also predispose to secondary bacterial infection by – Disturbing normal host defence mechanisms – Altering secretions – Through disruptions in the respiratory microbiota.
  • 13.
    Bacterial pneumonia • Mostoften occurs when respiratory tract organisms colonize the trachea and subsequently gain access to the lungs • Pneumonia may also result from direct seeding of lung tissue after bacteremia. • When bacterial infection is established in the lung parenchyma, the pathologic process varies according to the invading organism.
  • 14.
    M. pneumoniae • Attachesto the respiratory epithelium, inhibits ciliary action, and leads to cellular destruction and an inflammatory response in the submucosa. • As the infection progresses, sloughed cellular debris, inflammatory cells, and mucus cause airway obstruction, with spread of infection occurring along the bronchial tree, as is seen in viral pneumonia. S. pneumoniae • produces local edema that aids in the proliferation of organisms and their spread into adjacent portions of lung, often resulting in the characteristic focal lobar involvement.
  • 15.
    Group A streptococcus •Lower respiratory tract infection typically results in more diffuse lung involvement with interstitial pneumonia. • The pathology includes – Necrosis of tracheobronchial mucosa – Formation of large amounts of exudate – Edema and local hemorrhage, with extension into the interalveolar septa; and involvement of lymphatic vessels with frequent pleural involvement.
  • 16.
    S. aureus pneumonia •Manifests as confluent bronchopneumonia, often unilateral and characterized by – the presence of extensive areas of hemorrhagic necrosis and irregular areas of cavitation of the lung parenchyma, resulting in pneumatoceles, empyema, and bronchopulmonary fistulas.
  • 17.
    Recurrent pneumonia • Isdefined as 2 or more episodes in a single year or 3 or more episodes ever, with radiographic clearing between occurrences. • An underlying disorder should be considered if a child experiences recurrent pneumonia. • Differential diagnosis of recurrent pneumonia are the following
  • 18.
    HEREDITARY DISORDERS – Cysticfibrosis – Sickle cell disease DISORDERS OF IMMUNITY – HIV/AIDS – Primary immunodeficiencies
  • 19.
    DISORDERS OF CILIA –Primary ciliary dyskinesia – Kartagener syndrome ANATOMIC DISORDERS – Pulmonary sequestration – Lobar emphysema – Congenital cystic adenomatoid malformation – Gastroesophageal reflux – Foreign body aspiration – Tracheoesophageal fistula (H type) – Bronchiectasis – Aspiration (oropharyngeal incoordination) – Aberrant bronchus
  • 20.
    CLASSIFICATION Criteria used forclassification • Etiologic • Anatomic • severity
  • 21.
    Anatomic • Lobar • Bronchial •interstitial Severity • Sever pneumonia • Pneumonia • No pneumonia Ethiology • Viral • Bacterial • Fungal
  • 22.
    COMPLICATIONS LOCAL COMPLICATIONS • Pleuraleffusion, • empyema, abscess, • Bronchopleural fistula, • Necrotizing pneumonia, acute • Acute respiratory distress syndrome • Respiratory failure DISTANT COMPLICATIONS • Meningitis • Arthritis • Pericarditis • Osteomyelitis • Endocarditis • Haemolytic uremic syndrome • Sepsis
  • 23.
    Clinical Manifestations • Frequentlypreceded by several day symptoms of URTI • Cough: chief symptom • Increased respiratory rate: – > 60/minute infants younger than 2 months old – >50/minute infants 2-12 months old – > 40/minute children 1-5 years old • Grunting (keeps narrow airways open) • Sign of severe distress and impending respiratory failure • Nasal flaring (air hunger)
  • 24.
    • In infants –vomiting, anorexia, diarrhea, and abdominal distention secondary to a paralytic ileus. – may have a prodrome of URTI and poor feeding, leading to the abrupt onset of fever, restlessness, apprehension, and respiratory distress. • In older children sudden onset high fever, cough, and chest pain may presentation.
  • 25.
    • Retractions: intercostal,supraclavicular, subcostal • Increased effort to breathe, decreased lung compliance • Hypoxemia: normal >95% • Fever
  • 26.
    Diagnosis • Chet x-ray •Chest U/S • CBC • ESR/CRP • PCR • Blood culture (fail to improve, have clinical deterioration, complicated pneumonia, or require hospitalization) • ASO and anti-DNase B titers
  • 27.
    MANAGEMENT • INDICATION FORADMISSION – Age <6 mo – Immunocompromised state – Toxic appearance – Moderate to severe respiratory distress – Hypoxemia (oxygen saturation <90% breathing room air, sea level) – Complicated pneumonia – Sickle cell anemia with acute chest syndrome – Vomiting or inability to tolerate oral fluids or medications – Severe dehydration – No response to appropriate oral antibiotic therapy – Social factors (e.g., inability of caregivers to administer medications at home or follow-up appropriately)
  • 28.
    1. Oxygen Therapy:IN o2, CPAP, MV 2. Fluid Therapy: MF, dehydration mgt. 3. Antipyretics: paracetamol 4. Antibiotics 5. Oral Zinc for 7days
  • 29.
    ANTIBIOTICS • Empiric antibioticchoice for hospitalised suspected pneumonia patient depends on – local epidemiology, – the immunization status of the child, and – the clinical manifestations at the time of presentation
  • 30.
    Ampicillin or penicillinG for inpatient GIVEN – without substantial high-level penicillin resistance for s.pneumoniae – Fully immunized for H.influenzae type b and s.pneumoniae – Not severely ill child – Ceftriaxone or cefotaxime can be given for those that don’t fulfil the above criteria. – Total duration continued upto 10days
  • 31.
    • Outpatient – Highdose amoxacillin – Macrolides for pencillin allegy and suspected antipical bacteria – Total duration 5-7days if azithromycin for 5days
  • 32.
    PROGNOSIS • Tachycardia andhypotension- Within two days • Fever, tachypnea, chest and arterial oxygenation (PaO2)- Within three days • Cough and fatigue- ≥14 days • Radiographic improvement up to 1month
  • 33.
    PREVENTION • Vaccination thatprevent pneumonia are – PCV – Influenza vaccine – H.influenza type b vaccine – Pertussis vaccine – Measles vaccine – RSV vaccine