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4. pneumonia paediatrics

Date post: 14-Apr-2017
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PNEUMONIA SITI MARIAM BINTI MOHD HAMZAH Is an infection of the lower respiratory tract that involves the airways and parenchyma with consolidation of the alveolar spaces.
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Page 1: 4. pneumonia paediatrics

PNEUMONIASITI MARIAM BINTI MOHD HAMZAH

Is an infection of the lower respiratory tract that involves the airways and parenchyma with consolidation of the

alveolar spaces.

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LOBAR PNEUMONIABRONCHOPNEUMONIAINTERSTITIAL PNEUMONIA

Pneumonia may be classified anatomically as

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The pathogens causing pneumonia may vary according to the child’s age:

Age group PathogensNewborn - Organisms from the mother’s genital tract

particularly group B streptococcus, but could be also gram –ve enterococci

Infants and young children

- Respiratory viruses (RSV are most common)- Bacterial infections include Streptococcus

pneumoniae or H. influenza, Bordetella pertussis and Chlamydia trachomatis.

- Staphylococcus aureus, infrequent but serious caused.

Children over 5 years - Mycoplasma pneumoniae, streptococcus pneumoniae and Chlamydia pneumoniae

*at all ages Mycobacterium tuberculosis should be considered.

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Bacteria invasion of lung parenchyma

Inflammatory immune response

Filling of bronchi / alveolar sacs with exudates

CONSOLIDATIONDecrease diameter airways passageWHEEZING

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CLINICAL MANIFESTATIONS

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IMPORTANT POINT TO ASSESS-RR• WHO respiratory rate thresholds for identifying children with

pneumonia :Children younger than 2 months

>= 60 breaths/min

Children aged 2-11 months

>= 50 breaths/min

Children aged 12-59 months

>= 40 breaths/min

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CLINICAL MANIFESTATIONS• Age is a determinant in the clinical manifestations of pneumonia

Neonates - Fever or hypoxia only, with subtle or absent physical examinations findings

Young infant - Apnea may be the first signsOlder infants and children

- fever, chills, tachypnea, cough, malaise, pleuritic chest pain, retractions, and nasal flaring, because of difficulty in breathing or SOB

Viral pneumonia Bacterial pneumonia- Associated more often with cough,

wheezing, or stridor- Mucosal congestion and upper airway

inflammation

- Higher fever, chills, cough, dyspnea, and auscultatory findings on lung consolidation

- Localised chest, abdominal or neck pain; feature of pleural irritation

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INVESTIGATIONS• Complete blood count & differential count

– in WBC count,• often normal or mildly elevated with predominance of lymphocytes in case of viral

pneumonias, whereas with bacterial pneumonias the WBC count is elevated >20,000 /mm3 with a predominance of neutrophils

• Mild eosinophilia is characteristics of infant C. trachomatis pneumonia.• Pulse oximetry assess oxygen saturation• Blood/ sputum culture

– Nasopharyngeal aspirate– Throat swab– Bronchoalveolar lavage– Lung aspirates

In addition- Mantoux test ( M. tuberculosis)- Serology test- Urinary antigen (Legionella

pneumophila)

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INVESTIGATIONS• Chest radiography

– To localize disease and adequately visualize retrocardiac infiltrates Bacterial pneumonia Shows lobar consolidation, or a

round pneumonia, with pleural effusion in 10% or 30% of cases

Viral pneumonia Shows diffuse, streaky infiltrates of bronchopneumonia and hyperinflation

Atypical pneumonia (M. pneumoniae and C. pneumoniae)

Shows increased interstitial markings or bronchopneumonia

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TREATMENT & MANAGEMENT• Therapy for pneumonia includes supportive and specific treatments and

depends on the degree of illness, complications, and knowledge of the infectious agent likely causing the pneumonia

• Children with hypoxemia, inability to maintain adequate hydration, or moderate to severe respiratory distress should be hospitalized

• Hospitalization should be considered in infants under 6 months with suspected bacterial pneumonia, those in whom there is a concern for a pathogen with increased virulence, or when concern exists about a family’s ability to care for the child and to assess symptom progression.

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WHO REVISED RECOMMENDATION (published on 2014)Children with fast breathing pneumonia

with no chest indrawing or general danger sign

oral amoxicillin: at least 40mg/kg/dose twice daily (80mg/kg/day) for 5 days. In areas with low HIV prevalence, give amoxicillin for 3 days.

Children with fast-breathing pneumonia who fail on first-line treatment with amoxicillin shouldhave the option of referral to a facility where there is appropriate second-line treatment.

Children age 2–59 months with chest indrawing pneumonia

oral amoxicillin: at least 40mg/kg/dose twice daily for 5 days.

Children aged 2–59 months with severe pneumonia*Not able to drink, persistent vomiting, convulsions, lethargic or unconscious, stridor in a calm child or severe malnutrition

parenteral ampicillin (or penicillin) and gentamicin as a first-line treatment.• Ampicillin: 50 mg/kg, or benzyl penicillin:

50 000 units per kg IM/IV every 6 hours for at least 5 days

• Gentamicin: 7.5 mg/kg IM/IV once a day for at least 5 days

*Ceftriaxone should be used as a second-line treatment in children with severe pneumonia havingfailed on the first-line treatment.

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for HIV-infected and -exposed infants and for children under 5 years of age with chest indrawing pneumonia or severe pneumonia

– Ampicillin (or penicillin when ampicillin is not available) plus gentamicin or ceftriaxone are recommended as a first-line antibiotic regimen

– For who do not respond to treatment with ampicillin or penicillin plus gentamicin, ceftriaxone alone is recommended for use as second-line treatment.

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• Oseltamivir or zanamivir should be used if influenza is identified or suspected, ideally within 48 hours of symptom onset.

• Oseltamivir is recommended by the CDC and American Academy of Pediatrics (AAP) for the treatment of influenza in persons aged 2 weeks and older, and for the prevention of influenza in persons aged 3 months and older.

• Zanamivir is recommended for the treatment of influenza in persons aged 7 years and older, and for the prevention of influenza in persons aged 5 years and older.

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THANK YOU


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