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Pneumonia Summary - Elaf Alshamari

The document provides a comprehensive overview of Community Acquired Pneumonia (CAP) and its complications, including definitions, etiology, evaluation, diagnostic studies, treatment, and management of pneumonia-related effusions. It details the differences between bacterial and viral pneumonia, the importance of history and physical examination, and outlines treatment protocols for both outpatient and inpatient settings. Additionally, it discusses complications, management strategies for empyema, and considerations for patients with neuromuscular diseases.

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Hashmat Mokha
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0% found this document useful (0 votes)
48 views3 pages

Pneumonia Summary - Elaf Alshamari

The document provides a comprehensive overview of Community Acquired Pneumonia (CAP) and its complications, including definitions, etiology, evaluation, diagnostic studies, treatment, and management of pneumonia-related effusions. It details the differences between bacterial and viral pneumonia, the importance of history and physical examination, and outlines treatment protocols for both outpatient and inpatient settings. Additionally, it discusses complications, management strategies for empyema, and considerations for patients with neuromuscular diseases.

Uploaded by

Hashmat Mokha
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Elaf AlShammari 2019-2020

Community Acquired Pneumonia (CAP) & Complicated Pneumonia

❖ Introduction:
▪ Definition of Pneumonia: Acute inflammation of the parenchyma of the lower respiratory tract caused by Microbial Pathogen.
▪ Definition of CAP: pneumonia in a previously healthy child caused by an infection acquired outside hospital.
▪ Definition of Empyema: Intrapleural pus or a moderate to large exudative parapneumonic effusion (stage1), which can progress to being loculated
(stage2), with further development of a fibrinous peel (stage3).
▪ Leading cause of death in children aged <5years.

❖ Etiology:

▪ Bacterial:
• Rapid onset of fever, ill appearance, Elevated WBC, lobar infiltration, rapid respond to Abx.
• Bacterial causes increase in incidence with age.

• Bacterial Etiologies:
o Streptococcus Pneumoniae:
- MCC in all age groups.
- Cases Declined after PCV7 & PCV13 vaccins.
o Staphylococcus aureus & streptococcus pyogenes (GAS).
- Increases rates of severe Pneumonia due to MRSA.
< (Influenza + S aureus): cause severe Pneumonia & high Mortality rate>
- GAS is less common but severe.
o Mycoplasma Pneumoniae.
- Epidemics occur every 3-7 years, 20% asymptomatic with only 3% resulting in pneumonia.
- PCR is a preferred test.
o Less common Bacterial Causes.
- Clamydophila pneumoniae, Non typeable Heamophilus Influenzae, Moraxella catarrhalis.

▪ Viral:
• Gradual onset of symptoms, respiratory distress, wheezing, rhinitis, interstitial infiltrate bilaterally, no response to Abx.
• Viral etiologies predominant in < 5years.
• MCC: RSV, Human Metapneumovirus (HMPV), Influenzas, Rhinovirus, Adenovirus, Parainfluenza, Coronavirus.
• Influenza can cause life threatening illness especially with co-infection or superinfection with Bacteria.

▪ Immunodeficient patients:
• In addition to typical etiologies of CAP, rare or opportunistic pathogens such as: Legionella pneumophila, Pneumocystis jiroveci, Gram negative &
fungal organisms.

❖ Evaluation:
History, physical Examination, & laboratory findings help differentiate Viral from Bacterial causes.

▪ History.
• Symptoms of pneumonia nonspecific, Acute onset of fever, cough, respiratory symptoms, difficulty breathing, poor feeding, vomiting, decrease in
activity, <Chest or Abdominal pain may be prominent features>.
• PMHx: Asthma, atopy & night symptoms.
• Immunization Hx.:
Signs of pneumonic Consolidation:
- 2,4,6 months vaccines for Pneumococcal conjugate & H influenza type B.
- Current Influenza Vaccine. ▪ Dullness on percussion.
• Family Hx.: Parents or siblings with Asthma, Atopic dermatitis or Allergic rhinitis. ▪ Increased tactile fremitus.
▪ Reduced normal vesicular
breath sounds.
▪ Vital signs. ▪ Increased bronchial breathing.

• Temperature: REMMBER, All of whitch may be


- High fever < may be the ONLY clinical sign>. difficult to detect in children ☺
- Occult Pneumonia. <acute onset of abdominal pain & High fever>
• RR:
Signs of an effusion:
- May be elevated due to Fever or pain.
- Serial assessment of RR over the course of the visit > provide more accurate of respiratory status. ▪ Dullness on percussion.
▪ Decreased tactile fremitus.
• Pulse Oximetry: ▪ Decreased or absent breath
- Hypoxemia “but not severe”. sounds.

▪ Physical examination.
No Single sign or symptom is pathognomonic for diagnosis of Pneumonia.
• Appearance: Ill appearing, Respiratory distress, retraction, Increase work of breathing, WITHOUT wheezing.
• Auscultation: No single findings on Auscultation increases or decrease the likelihood of pneumonia.
Elaf AlShammari 2019-2020

❖ Diagnostic studies:
▪ Differentiating viral from bacterial pneumonia on the basis of radiological or laboratory fining is difficult.
▪ Laboratory & Radiographic evaluation depends on the age, clinical scenario, severity of diseases, & wether a child requires hospitalization.
▪ Pneumonia should be considered in febrile children with elevated WBC even in the absence of respiratory symptoms.

▪ Laboratory studies:
• CBC:
- WBC >15000 Bacterial Vs <15000 Viral, However Adenovirus can cause leukocytosis >15000 ☺
• Inflammatory Markers.
- Should not be used routinely, only in sever cases.
- ESR, CRP, Procalcitonin (>7 bacterial etiology, 0.1 indicate nonbacterial).
• Chemistries.
- Useful only in critically ill or clinically dehydrated children.
- Hyponatremia (SIDAH).
• Blood Culture.
- Confirmation of Bacterial etiology is difficult because Most pts with CAP have negative blood cultures & sampling of pleural fluid or lung
tissue is performed only in complicated cases.
- Obtain blood culture ONLY in high risk patients:
(Immunocompromised, < 6months, central line, requiring hospitalization, critically ill, evidence of empyema).
- Higher likelihood of bacteremia occurs in patents with Empyema, MCC is pneumococcal.
- Blood culture should be at least 1-2ml in infants, 4-5ml in <10 years, 10-20ml >10 years.
• Sputum Culture.
- ONLY at the time of intubation of patients with Respiratory Failure. <to provide optimal Abx for specific pathogen>.
- >10 years.
• PCR.
- PCR is a preferred test for a viral etiology; However +ve result may be due to Asymptomatic infection or Viral shedding.
• Urinary S pneumoniae antigen testing.
- Not recommended due to false-positive rates.

▪ Imaging:
• Chest X-ray.
- Order it in:
highly febrile >39 & aged < 3years with ill appearing or concerning signs, Children with Leukocytosis >20000, fever with Abdominal pain,
prolonged fever without a clear source of infection, asses the extent of pneumonia & presence of pleural effusion or complication.
- Bacterial: Lobar infiltration, pleural effusions, cavitation, & Pneumatoceles.
- Viral: Interstitial infiltrates
- S pneumonia: Posteriorly located consolidation Round, <3cm.
- Radiographic resolution may take up to 4-6 weeks, repeated CXR is not recommended.

• Ultrasound.
- Operator dependent & may lead to overdiagnosis & unnecessary treatment of CAP in patients with asthma.
- Use ONLY as initial modality for Empyema demonstrated in CXR.

• Computed Tomography (CT).


- High risk of ionizing radiation, No need ☺

❖ Treatment:
• Oxygen.
- For any patient with saturation <90% or in respiratory distress with saturation <95%.
• Antipyretics.
- Acetaminophen & Ibuprofen. <will improve general appearance, decreasing HR & RR>.
- More serious causes of fever should be considered in patients without significant improvement after antipyretics administration.
• IVF.
- Assess Hydration status in all patients.
- NGT hydration not recommended for infants > impair respiratory status.

• Albuterol & Corticosteroids.


- Trial of Bronchodilators should be based on PMHx & FHx, and if there is no improvement discontinue it.
- Steroids should be considered in children with Wheezing that is responsive to Bronchodilators therapy even in patients with CAP.
• Viral Causes:
- If Influenza is detected > Neuraminidase inhibitors (Oseltamivir, Zanamivir).
- Other Viruses > supportive (Oxygen & Hydration).

Criteria for Hospitalization:

▪ Inadequate oral intake.


▪ Intolerance of oral therapy.
▪ Severe illness or respiratory compromise.
▪ Complicated Pneumonia.
▪ Younger than 6 months.
Elaf AlShammari 2019-2020

• Antibiotics.
- If no improvement with Abx, search for complication.

▪ Outpatients.

Empiric therapy for atypical Pneumonia


Empiric therapy for Bacterial Pneumonia
In inpatients & out patients
Amoxicillin PO 90mg/Kg/day divided BID or TID Azithromycin PO10mg/kg on Day1 followed by 5mg/Kg/day
1st line
For 7-10 days. once daily on days 2-5.
Amoxicillin/ Clavulanate PO 90mg/Kg/day divided BID or Clarithromycin or Erythromycin
Alternative
TID Children > 7years: doxycycline.
3rd Generation: Cefpodoxime, Cefdinir, Cefuroxime.
Penicillin Allergy:
Or Use Azithromycin , Clarithromycin.

▪ Inpatients.

Empiric therapy for Bacterial Pneumonia


1st line Alternative
▪ Fully Immunized with Conjugate vaccines for H
Ceftriaxone
influenzae & S pneumoniae
Ampicillin for 7-10days. For suspected Co-MRSA: add Vancomycin or
▪ Minimal penicillin resistance <25%
Clindamycin.
▪ Not Fully Immunized with Conjugate vaccines
Levofloxacin
for H influenzae & S pneumoniae.
Ceftriaxone For suspected Co-MRSA: add Vancomycin or
▪ Significant penicillin resistance >25%.
Clindamycin.
▪ Life threatening infection, including Empyema.

❖ Complication:
▪ Bacteremia, septic shock, or respiratory failure > 3ed generation cephalosporin.
▪ Empyema, Lung abscess, Pleural effusion. or necrotizing lung.

❖ Pneumonic effusion & Empyema:


▪ Initial empiric therapy: 3rd generation Cephalosporin for 2-4weeks (Ceftriaxone or Cefotaxime).
< If you considered for S aureus Add vancomycin or Clindamycin>
▪ Transition to oral Abx when drainage is completed & patient improved clinically & off O2: Amoxicillin.

▪ Size & degree of respiratory compromise are important factors in management:


- Small effusion (10mm or ¼ thorax opacified): Respond well to ABx therapy ALONE.
- Moderate effusion ( >1/4 but <1/2 thorax opacified): Drainage.
- Large effusion ( >1/2 thorax opacified): Drainage.

▪ Option for Drainage: <any pleural fluids should be sent for stain, cultures, & other labs studies>
• Chest Tube (with or w/out Fibrinolytic Therapy " tissue plasminogen activator") < CTWF is best >
• Video assisted Thoracoscopic surgery (VATS).

▪ Prognosis/ Outcome:
• Small number of patients will have minor abnormalities of both mild restrictive & mild obstructive, should follow after discharge until they have clinically
recovered & CXR returned to normal (2-3months).

❖ Patients with Neuromuscular diseases


▪ Cerebral Palsy or Muscular dystrophy often have multiple risk factors for Pneumonia.
▪ Swallowing dysfunction, GERD, muscle weakness lead to inadequate cough & clearance of oral secretion
- Consider initial Positive-Pressure ventilation prior to administering O2 .
- Empiric Abx <Ampicillin/Sulbactam, Amoxicillin/ Clavulanate> is first line or Clindamycin if allergic to Penicillin.

❖ References.
▪ Pediatric Emergency Medicine Practice April 2019.
▪ Canadian Pediatric Society Oct 2018.

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