Community Acquired Pneumonia (CAP)
CAP refers to a pneumonia that is acquired outside hospital, commonly caused by Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, atypical bacteria (i.e. Chlamydia pneumoniae, Mycoplasma pneumoniae, Legionella species) and viral respiratory pathogens (i.e rhinovirus and influenza).
Clinical presentation
- Fever
- Cough dry or productive with/without purulent sputum,
- Dyspnea
- Pleuritic chest pain
- Decreased tactile fremitus and dullness on chest percussion
- Tachypnea
- Crepitation/Rales heard over the involved lobe or segment
- Increased tactile fremitus, bronchial breath sounds may be present if consolidation has occurred
Investigations
- Measure oxygen saturation, use pulse oximetry or Monitor
- FBC (look for increased WBC, neutrophilia)
- CRP/ESR (increased in bacterial infection)
- ABG (look for pH, bicarbonate),
- Serology for HIV test (if unknown)
- Sputum culture and sensitivity - indicated for inpatients and those with severe disease (ICU admission)
- Blood culture (are not recommended for ambulatory patients)
- CHEST X-ray-PA/LATERAL (look for one or more focal pulmonary infiltrates, consolidation, tap effusion>5cm)
- Bronchoscopy (consider if immunosuppression, critically ill, fail to respond, suspected TB or PCP or inadequate
- CT-CHEST Scan or HRCT: if patient is not improving, suspicion of fungal infection, ILD etc.
Note: Do not use CT chest to diagnose pneumonia
Non-pharmacological Treatment
- Stop smoking if previously smoking
- Vaccination when indicated, in specialized centre for patient >65yrs and below 5years
Pharmacological Treatment
First line treatment
Table 9.3: First Line Treatment of Typical Community Acquired Pneumonia
Condition
|
Treatment
|
Duration
|
Mild CAP (treated on out-patient basis)
(common organism S pneumonia and these patients have no comorbidities)
|
A: erythromycin (PO) 500mg 8hourly
OR
B: ampicillin + cloxacillin (FDC) (PO) 500–1000mg 8hourly
|
5-7 days |
Mild to Moderate CAP (failed to respond to Initial treatment)
|
A: doxycycline (PO) 100 mg 12hourly (culture guided) OR
B: azithromycin (PO) 500mg stat and then 250mg 24hourly
OR
C: clarithromycin (PO) 500mg 12hourly
|
5-7 days |
MILD CAP in patients with comorbidities (i.e. chronic heart, lung, liver, or renal disease; diabetes mellitus; alcoholism; malignancy; asplenia; immunosuppression; prior antibiotics within 90 days
|
B: amoxicillin + clavulanic acid (FDC) (PO) 500mg/125mg 8-12hourly or 875mg/125mg 12hourly OR
D: cefuroxime (PO) 500mg 12hourly
AND
A: doxycycline (PO) 100mg 24hourly
OR
C: clarithromycin (PO) 500mg 12hourly
|
5-7 days
|
Severe pneumonia/Aspiration pneumonia (in-patient)
|
D: ceftriaxone + sulbactam (FDC) (IV) 1.5g 12hourly
If suspicion of anaerobes or Aspiration pneumonia Add:
B: metronidazole (IV) 500mg 8hourly
Do culture and imaging if nonresponse, consider second line
|
7–10 days
|
Second line treatment
If no response to first line treatment further investigation is required. If patient is in respiratory distress, or no response after 3 days of first line treatment, or patient’s condition deteriorates, then investigate, start empiric treatment while waiting for culture and sensitivity
S: piperacillin + tazobactam (FDC) (IV) 4.5g 6hourly for 7days
Table 9.4: Treatment of Typical and Atypical Community Acquired Pneumonias Organism Specific
Condition
|
Treatment
|
Duration
|
Atypical pneumonias
(Bordetella pertussis, Mycoplasma pneumonia, Chlamydophila pneumonia)
|
A: erythromycin (PO) 500mg 6hourly
OR
C: clarithromycin (PO) 500mg 12hourly
|
7-10 days |
Pseudomonas pneumonia
(Risk factors structural lung disease, COPD, and bronchiectasis)
|
A: ciprofloxacin (PO) 500mg 12hourly
If culture sputum-positive or HRCT suggestive
S: piperacillin + tazobactam (FDC) (IV) 4.5g 6-8hourly
OR
S: cefepime (IV) 2g 8hourly
OR
D: ceftazidime (IV) 2g 8hourly
OR
S: meropenem (IV) 1g 8hourly
|
7-10 days
|
H. influenza |
A: amoxicillin (PO) 500mg 8hourly
OR
D: cefuroxime (PO) 250-500mg 8hourly
(culture & sensitivity should be done in order to choose alternative antibiotics)
|
7-10 days
|
Pneumocystis jirovecii Pneumonia (PJP)
(Refer to Tanzania HIV Guideline for more details)
|
A: co-trimoxazole (PO) 1920mg 8hourly AND
A: folic acid (PO) 5mg 24hourly (if cytopenic)
In sulphur allergy:
S: clindamycin (PO) 450–600mg 6hourly
|
21days
|
Staphylococcus aureus Pneumonia
|
B: ampicillin + cloxacillin (FDC) (IV) 1g 6hourly
OR
S: clindamycin (IV/PO) 600mg 6-8 hourly
|
14days
|
Klebsiella Pneumonia
(due to high mortality observe the duration of antibiotic given not < 10days)
|
B: chloramphenicol (IV) 500mg 6hourly AND/OR
A: gentamicin (IV) 4-5mg/kg 24hourly in 2 divided doses
|
10- 14 days
|
For critical ill patient and those with risk factors for MRSA (include hemoptysis, recent, influenza, neutropenia, hemodialysis, and congestive heart failure)
|
S: vancomycin (IV) 15mg/kg 12hourly |
5-7 days |
Note:
- In severe Pneumocystis jirovecii pneumonia (PCP), add 30 – 40mg prednisolone for 14days. Consider tapering down after recovery
- Patients with pneumonia should be afebrile for 48-72hours and have improved clinically before antibiotic therapy is stopped. The duration of therapy may need to be increased if the initial empirical therapy has no activity against the specific pathogen or if the pneumonia is complicated by extrapulmonary infection.
Alternative in Staphylococcal and Klebsiella Pneumonia:
D: ceftazidime (IV/IM) 2g 8hourly for 7–14days