Pneumonia Flashcards

1
Q

Define pneumonia.

A

Infection of the lung parenchyma.

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2
Q

What are causative organisms of pnuemonia in neonates?

A

Organisms from the female genital tract: Group B haemolytic streptococcus, E. coli, and gram-negative bacilli, chlamydia trachomatis.

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3
Q

What are causative organisms of pnuemonia in infants and pre-school children?

A

Viral (most common):

Parainfluenza, influenza, adenovirus and RSV.
RSV can be particularly dangerous to expreterm infants and infants with underling chronic lung disease (CLD) of prematurity.

Bacterial:

Streptococcus pneumonia (90% of bacterial pneuomonia).
Staphylococcus aureus is uncommon but causes severe infection.
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4
Q

What are causative organisms of pnuemonia in older children and adolescents?

A

As previous, but also atypical organism such as Mycoplasma pneumonia and chlamydia pneuominae.

TB should be considred at any age.

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5
Q

What are causative organisms of aspiration pneumonia?

A

Enteric gram-negative bacteria +/- Strep. Pneumonia, Staph aureus

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6
Q

What are causative organisms of pneumonia in non-immunised children?

A

Haemophilus influenza

Bordetella pertussis

Measles

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7
Q

What are causative organisms of pneumonia in immunocompromised children (acquired or inherited)?

A

Viral: CMV, VZV, HSV, measles and adenoviruses

Bacterial: Pneumpcystis carinii, TB.

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8
Q

What are risk factors for pneumonia?

A

CLD: Ex-preterm, CF, sickle cell disease

Congenital cardiac abnormality: Especially with large left to right intracardiac shunt

Chronic aspiration: Cerebral palsy, TOF, GORD

Kartagner syndrome: Ciliary dysfuntion, bhronciectasis and dextrocardia

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9
Q

What are the stages of lobar pneumonia?

A
  • Congestion with vascular engorgement, intra-alveolar bacteria
  • Red hepatisation: Alveolar spaces fill with neutrophils, fibrin and RBCs.
  • Grey hepatisation: RBC disintegrates with fibrin and suppurative inflammation.
  • Resolution: Exudate in alveolar spaces is degraded and removed by macrophages.
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10
Q

What are stages of bronchopneumonia?

A

Macro: Patchy areas of consolidation with grey/yellowish appearance.

Micro: Neutrophil inflammatory infiltrate in bronchi, bronchioles and adjacent alveoli.

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11
Q

Summarise the epidemiology of pneumonia.

A

29/10,000 children < 5 years of age. 12/10,000 children < 14 years of age.

Decreasing since the introduction of the conjugate pneumococcal vaccine in all children.

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12
Q

What are the signs and symptoms of pneumonia?

A

General: Fever, tachycardia, tachypnoea, cough, sputum (yellow, green or rusty in Strep pneuomoniae), vomiting particularly post-coughing, poor feeding, diarrhoea, preceding URTI (especially viral infections).

Signs of consolidation: Decreased breath sounds, dullness to percuss, increased tactile/vocal fremitus, bronchial breathing, coarse crepitations.

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13
Q

What are appropriate investigations for pneumonia?

A

CXR: Focal consolidation suggests a bacterial cause; diffuse consolidation bronchopneumonia suggests a viral cause.

Bloods: Increase WCC, Increase ESR/CRP, U&Es (SIADH), mycoplasma serology.

Urine: Pneumococcal antigen.

Microbiology: Blood and sputum MC&S.

Blood film: RBC agglutination by Mycoplasma (cold agglutinins; See haemolytic anaemia).

Immunofluorescence/PCR: Can detect RSV on nasopharyngeal aspirate.

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14
Q

What is the management for pneumonia?

A

Supportive treatment: Maintain oxygen saturation > 92%, IV resuscitation in dehydration or shock.

Antibiotic: Determined by presentation, i.e. viral/bacterial aetiology, severity and CXR appearance; normally oral amoxicillin or erythromycin. If severe, IV cefuroxime +/- erythromycin, metronidazole for aspiration pneumonia

Respiratory failure: CPAP/BiPAP; may require PICU transfer

Immunisation: HiB and pneumococcal (all infants), influenza (at-risk infants).

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15
Q

What are complications associated with pneumonia?

A

Pleural effusion, empyema, lung abscess, septic shock, ARDS, ARF.

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16
Q

What is the prognosis of pneumonia?

A

Most resolve within 1-3 weeks; however, children with an underlying respiratory, cardiac, immune or neurological abnormality may respond more slowly to treatment and have a higher mortality.