2. Pneumonia
• Very common (1-10/1000), significant mortality
• Severity assessment, aided by score, is a key
management step
• Caused by a variety of different pathogens
• Antibiotic treatment initially nearly always
empirical, local guidelines and microbial
resistance rates may support it
10. Clinical classification
• Community-acquired, CAP
• Nosocomial, hospital-acquired, HAP, VAP
• Aspiration and anaerobic
• Pneumonia in the immuncompromised host
• AIDS-related
• Reccurent
• Pneumonias peculiar to specific geographical
areas
12. Pathogenesis
• Inhalation of infected droplets
• Aspiration /residents from nasopharynx/
• Spread through bloodstream
• Direct spread (concomittant)
13. Risk factors
• Prolonged supine position
• Antibiotics, antacids
• Patient contact
• Decreased defense mechanisms
• Infected health care materials
19. Radiological features
• Lobar or segmental opacification
• Patchy shadows
• Small pleural effusions
• Cavitation (infrequent, Staphylococcus,
Pneumococcus serotype 3)
• Spread to more than one lobe (Legionella.
Mycoplasma)
• Clearance of shadow may last for months
21. CURB65 score (1-1point)
C Mental confusion
U UN > 7 mM/L
R Respiratory rate > 30/min
B RR<90/60 mmHg
65 Age > 65 years
Mild: 0-1point, 1.5% mortality
Moderate: 2point, 9% mortalility
Severe: 3-5 point, 22% mortalitty
22. “Ten commandments” of CAP treatment
• Only a few pathogens are
involved
• Always cover
Pneumococcus
• Consider epidemiology,
age and health status
• Mycoplasma during
epidemics, Staph.aur. in flu
• Do not delay starting
antibiotics
• Assess prognostic factors
and severity early
• Establish etiology quickly
• Adequate oxygen,
hydration and nutrition
• Careful monitoring –
transfer early to ICU
• Initial antibiotics must
cover all the likely
pathogens
All Severe
23. Treatment of CAP
1) <65 year, no comorbidity, home:
macrolide, doxycyclin,
amoxycillin/clavulanic acid, 2. gen.
cephalosporin
2) >65 year, comorbidity, home:
amoxycillin/clavulanic acid, 2-3 gen.
cephalosporin +- macrolide, respiratory
fluoroquinolon (levofloxacin,
moxifloxacin)
24. Treatment of CAP
3) hospital: amoxycillin/clavulanic acid,
2-3 gen. cephalosporin + macrolide,
resp.fluoroquinolon
4) ICU: ceftriaxon/cefotaxim, cefepim,
carbapenemes (imipenem, meropenem),
piperacillin/tazobactam +
macrolides, resp. fluoroquinolon
26. Pathogens and treatment of non-severe HAP
‘Core’ pathogens ‘Core’ antibiotics
Gram-neg.
Enterobacteriaceae:
E. coli, Klebsiella spp.,
Proteus spp,
Serratia marcescens,
Enterobacter spp.
‘Usual’ community pa-
thogens:Pneumococcus,
H.influenzae,Staph.aureus
2nd
- or 3 rd- gen
cephalosporins,
beta-lactam/lactamase
inhibitor,
fluoroquinolones
27. Pathogens and treatment of non-severe HAP with
additional risk factors
‘Core’ path.
plus
Risk factor ‘Core’ ant. plus
Anaerobes Surgery, impaired swal-
loing, aspiration, dental
sepsis
clindamycin,beta-
lactam + inhibitor,
moxifloxacin
Staph.aureus Diabetes,renal failure, coma,
head trauma, neurosurgery
add vancomycin if
MRSA susp.
Legionella
spp
High dose steroid, endemic
in hospital
macrolides +-fluo-
roquinolones+- rifam.
Pseuodomonas
aeruginosa
prior ant., high dose ster.
ICU, CF,bronchiectasia
ciprofloxacin,amino-
glycoside,3rd
gen ceph.
with antipseud. act.
28. Pathogens and treatment of severe HAP
‘Core’ pathogens plus ‘Core’ antibiotics
Pseudomonas aeruginosa,
Acinetobacter spp,
MRSA
ciprofloxacin or
aminoglycoside,
plus one of:
antipseudomonal beta-lactam,
meropenem,
vancomycin
40. Lung abscess
• many other cavitating lesions than abscess
• careful review of chest x-ray to distinguish from
empyema
• most are secondary to aspiration of oropharyngeal
secretions
• exclude malignancy or other cause, bronchoscopy!
• a single microbe is unusual unless abscesses developed
after bacterial pneumonia.
• More commonly, there is a mixed growth, including
anaerobes