Pneumonia

most common pathogens

bacterial pathogens

Streptococcus pneumoniae (pneumococcus) is the most common cause of community-acquired pneumonia. It colonizes the oropharynx of up to 25% of healthy adults. Increased predisposition is seen in people with alcoholism, chronic lung disease, renal failure, sickle cell disease, prior splenectomy, hematologic malignancy, and HIV infection. Lobar consolidation with air bronchograms is typically seen by the 2nd or 3rd day of illness. In most areas of the world, penicillin G is the treatment of choice, with cephalosporins or vancomycin indicated depending on regional sensitivity patterns.

Staphylococcus aureus accounts for 2-5% of community acquired pneumonias, 11% of hospital pneumonias, and up to 26% of pneumonias following viral infection.

Haemophilus influenzae, a gram-negative coccobacillus often present in the upper respiratory tract, is especially important in people with COPD. Even though pathologic involvement therefore depends on isolation by bronchoscopy or other methods, if seen in a sputum sample, treatment should begin with ampicillin plus a beta-lactamase inhibitor, or a 2nd- or 3rd-generation cephalosporin.

Gram-negative bacilli are increasingly important lung pathogens due to use of potent antibiotics and intensive care units. They are ubiquitious throughout hospitals, contaminating equipment and instruments, and are a major source of nosocomial pneumonia. Important pathogens include klebsiella pneumoniae, Escherichia coli, Pseudomonas spp, Legionella

Other bacteria include mycoplasmal and chlamydial pneumonias

• Francisella tularensis
• Yersinia pestis
• Rhodococcus equi

viral pathogens

Respiratory viral infection is usually limited to the upper respiratory tract, and only a small proportion of infected adults develop pneumonia. In children, viruses are the most common cause of pneumonia, with respiratory synctial virus being the most common pathogen.

Adults at increased risk of influenzal pneumonia include older adults, patients with chronic heart, lung, or kidney disease, and women in the last trimester of pregnancy.

CMV can cause severe pneumonia in immunosuppressed people. Other viral causes include varicella, measles, and hantavirus. SARS-CoV and bird flu are potential future epidemics.

Influenza-induced necrosis of epithelial cells predisposes to bacterial colonization, and S. pneumoniae, S. aureus, and H. influenzae pneumonias are the most common concomitant infections.

History

Respiratory symptoms include

• cough
• sputum
• dyspnea
• fever

absence of rhinorrhea or sore throat

past medical history

• asthma
• dementia
• immunosupression

Duration of symptoms is a critical piece of information.

• pneumococcal, mycoplasma, or virual or viral disease is usually acute, with symptoms lasting for hours or days.
• Symptoms lasting 10 days or longer are rarely caused by common bacterial pathogens and should raise suspicion of mycobacterium, fungal, or anaerobic pneumonia, and/or the presence of underlying disease.

A history of rhinitis or pharyngitis suggests respiratory virus, Mycoplasma, or Chlamydia. Abrupt onset of myalgia, arthralgia, headache, and fever are commonly seen in influenza virus infection.

Diarrhea suggests Legionella.

A persistent, hacking cough can be seen with Mycoplasma.

Abrupt onset of myalgias, arthralgia, headache, and fever suggest influenza or mycoplasma.

severe pleuritic pain and/or empyema strongly suggest bacterial infection.

Physical Exam

Most people with pneumonia have cough, fever, pleuritic chest pain, foul sputum, tachycardia, and tachypnea.

Tuberculosis can lead to high fever with few other symptoms.

FOul breath suggests anaerobes and/or lung abscess.

Confusion should immediately point to meningeal complications, or can simply represent delirium in the elderly.

The respiratory exam can show evidence of consolidation via the following:

• percussion dullness
• bronchial breath sounds
• crackles
• increased fremitus
• whispered pectoriloquy

Increasing tachypnea, cyanosis, and use of accessory muscles for respiration suggests serious illness. Foul breath suggests anaerobic infection, ie lung abscess.

If a person presents with abrupt onset of chills, cough, pleuritic chest pain, rusty or yellow sputum, and shortness of breath, and exam shows tachypnea shows even miminal signs of pulmonary inflammation, presumptive diagnosis of bacterial pneumonia should be made, sputum should be examined, and apropriate therapy should be begun.

Emperic therapy without sputum examination is often successful, but increases in antibiotic resistance and occasional misdiagnosis, leading to increased risk of morbidity and death, mean that sputum should be Gram-stained and examined immediately.

Diagnosis is made in about 20% of patients.

Lab Investigations

blood tests

• CBCD: usual elevated white cell count, with left shift
• lytes
• urea, sCR
• troponin/CK
• AST, ALT, ALP,
• bili: modest increases in conjugated bilirubin are seen in many infections
• C-reactive protein: monitoring severity of infection and treatment response

urinalysis

nasopharyngeal swab: influenza, parainfluenza, metapneumovirus, RSV, adenovirus

sputum smears

• gram stains
• Gomori's Methenamine Silver (GMS stain)
• PAS/diastase stain
• Ziehl-Neelsen stain
• viral inclusions

Sputum culture is not normally done due to contamination by oropharyngeal flora. In people with community-acquired pneumonia, it becomes important with a lack of clinical response. Both false negatives and false positives are common and should be interpreted carefully.

Blood cultures: will be positive for 20-30% of people with bacterial pneumonia.

Acid-fast or fluorescent auramine-rhodamine stains for mycobacteria should be performed unless diagnosis of acute bacterial pneumonia is clear

Mycoplasma IgM

tissue biopsy can be very helpful, but its invasiveness is an important consideration.

Diagnostic Imaging

chest X ray

Chest X-rays need to be examined in the context of clinical data to successfully lead to diagnosis. A negative chest X ray can never rule out acute pneumonia if signs and symptoms point this way.

Homogenous parenchymal consolidation involving one lobe suggests bacteria.

Mycoplasma can result in extensive infiltration on chest X-ray but scant clincial signs. Conversely, early PJP, early milliary TB, or hypersensitivity pneumonia can result in symptoms in the absence of radiographic findings.

Radiologic findings of lobar pneumonias slowly clear, suggesting 6 week interval followups.

Immediate Treatments

ABCs

Oxygen

IV access

salbutamol/Ventolin 2.5mg NEB q6h

Community-acquired

Previously healthy

No antibiotics within past three months:

• macrolide (erythromycin)
• doxycyline

antibiotics with past three months:

• fluoroquinolone
• macrolide plus amoxocillin
• macrolide plus amoxocillin-clavulante

co-morbidities (COPD, diabetes, renal failure, CHF, malignancy)

no antibiotics within past three months:

• macrolide
• fluoroquinolone

antibiotics within 3 months:

• fluoroquinolone
• macrolide plus beta-lactam

suspected aspiration (oral anaerobes)

• amoxocillin-clavulanate
• clindamycin

Nosocomial Pneumonia

Anti-pseudomonal:

• ceftazedime
• piperacillin-tazobactam

further gram -ve coverage

• ciprofloxacin
• aminoglycoside (gentamicin, tobramycin) plus fluroquinolone
• aminoglycoside (gentamicin, tobramycin) plus macrolide (azithromycin)

suspect aspiration (oral anerobe coverage)

• clindamycin
• metronidazole

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