Pneumonia: Diagnosis and Treatment Guide


Pneumonia: Diagnosis and Treatment Guide

1. Symptoms:

  • Sudden high fever, sweating or chills
  • Cough with rusty or green, purulent sputum
  • Pleuritic chest pain, difficulty breathing
  • Body aches, lung rales

2. Diagnosis:

  • Blood tests: Increased WBC, increased NEU; Increased erythrocyte sedimentation rate
  • Biochemical tests: Increased CRP, Increased procalcitonin (>0.5 ng/L)
  • Blood gas analysis: Decreased oxygen saturation
  • Imaging:
  • Chest X-ray (gold standard)
  • CT scan
  • Microbiology tests: Diagnosis of pneumonia when the number of bacteria in sputum and blood samples (2 blood cultures) reaches a certain threshold:
  • Endotracheal aspirate (EA): >10^6 CFU/ml
  • Sputum:
  • 10^5 CFU/ml (S. pneumoniae)
  • >10^6 CFU/ml (H. influenzae) or (M. catarrhalis)
  • Bronchoalveolar lavage (BAL): >10^4 CFU/ml
  • Protected specimen brush (PSB): 10^3 CFU/ml
  • PCR testing of sputum, respiratory secretions: Microbiology test
  • Criteria for microbiology testing:
  • Outpatient: Not needed
  • Inpatient:
  • Severe CAP (ICU admission, intubation)
  • Empirical treatment targeting MRSA or P. aeruginosa
  • Previous MRSA or P. aeruginosa infection
  • Hospitalization and intravenous antibiotic use within the past 90 days
  • Patients without travel to epidemic areas: Routine testing for Legionella and S. pneumoniae antigens in urine is not required.

3. Pneumonia classification:

  • According to imaging:
  • Lobar pneumonia
  • Bronchopneumonia
  • Interstitial pneumonia
  • Necrotizing pneumonia
  • According to practice:
  • Community-acquired pneumonia (CAP)
  • Hospital-acquired pneumonia (HAP)
  • Healthcare-associated pneumonia (HCAP)
  • Aspiration pneumonia

4. Community-acquired pneumonia (CAP):

  • Epidemiology: Prevalent in children under 5 years of age and individuals over 65. Average mortality rate of 5-10%. The disease is at risk of severe progression and death in elderly individuals or those with multiple underlying chronic illnesses.
  • Causative agents:
  • Bacteria:
  • Streptococcus pneumoniae
  • Staphylococcus aureus
  • Haemophilus influenzae
  • Moraxella catarrhalis
  • Legionella pneumophila
  • Chlamydia pneumoniae
  • Mycoplasma pneumoniae
  • Gram-negative bacilli (Pseudomonas aeruginosae, E. coli …)
  • Viruses:
  • Influenza A virus
  • Influenza B virus
  • SARS-coronavirus…
  • Classification by severity:
  • Mild, outpatient treatment: Atypical bacteria, Strep
  • Moderate, inpatient treatment (non-ICU): Strep, atypical bacteria, Gram-negative intestinal bacteria
  • Severe, ICU treatment: Strep, Gram-negative intestinal bacteria, S. aureus, Pseudomonas
  • CURB-65 score: Assessing CAP severity
  • C: Confusion, disorientation
  • U: Blood urea > 7 mmol/L
  • R: Respiratory rate > 30 breaths/minute
  • B: Blood pressure < 90/60 mmHg
  • 65: Age > 65
  • 0-1 point: Outpatient treatment
  • 2 points: Outpatient treatment with monitoring or consideration of short-term inpatient treatment
  • 3-5 points: Hospitalization required
  • 4-5 points: ICU admission indicated
  • ICU admission criteria:
  • At least 1 major criterion or at least 3 minor criteria.
  • Major criteria:
  • Respiratory failure requiring mechanical ventilation
  • Septic shock requiring vasopressor medication
  • Minor criteria:
  • Respiratory rate > 30 breaths/minute
  • PaO2/ FiO2< 250
  • Involvement of multiple lung lobes on chest X-ray
  • Confusion, disorientation
  • Blood urea (BUN > 20 mg/dL)
  • White blood cell count < 4000/ mm3
  • Platelet count (<100.000/ mm3)
  • Hypothermia (< 36oC)
  • Hypotension requiring aggressive fluid resuscitation.

5. Treatment principles (CAP & HAP):

  • Eradicate the causative bacteria using appropriate antibiotics.
  • Treat clinical symptoms.
  • Reduce mortality rate, decrease disease complications, and minimize drug toxicity to organs.
  • Inpatients/hospitalized patients should be treated empirically with antibiotics shortly after diagnosis.
  • Optimize antibiotic use according to PK/PD, antibiotic penetration into the site of infection, and adjust according to renal function to reduce antibiotic resistance.
  • Microbiological samples should be collected before antibiotic administration.

6. Outpatient treatment:

  • CURB-65 (0-1 point):
  • Patients < 65 years of age:
  • No co-morbidities:
  • Amoxicillin 1g x 3 times/day
  • Doxycycline 100mg x 2 times/day
  • Azithromycin (oral) 500mg on the first day, then 250mg on subsequent days
  • Clarithromycin (oral) 500mg x 2 times/day or slow-release 1g x 1 time/day
  • Patients > 65 years of age:
  • Co-morbidities: Amoxicillin/clavulanate 500 mg/125 mg x 3 times/day
  • Immunosuppression: Amoxicillin/clavulanate 875 mg/125 mg x 2 times/day or 2,000 mg/125 mg x 2 times/day
  • Antibiotic use 3 months prior: Cefpodoxime 200 mg x 2 times/day
  • Risk of drug-resistant S.pneumoniae: Cefuroxime 500 mg x 2 times/day
  • AND:
  • Azithromycin 500 mg on the first day, then 250 mg/day
  • Clarithromycin 500mg x 2 times/day or slow-release 1g x 1 time/day
  • Doxycyclin 100 mg x 2 times/day
  • OR MONOTHERAPY:
  • Levofloxacin 750 mg/day
  • Moxifloxacin 400 mg/day
  • Gemifloxacin 320 mg/day
  • CURB-65 (2 points):
  • No risk of MRSA or P. aeruginosa infection:
  • Beta-lactam +/- betalactamase inhibitor:
  • Ampicillin + sulbactam 1.5-3 g q6h
  • Amoxicillin/clavulanate 1.2 g q8h
  • Cefotaxime 1-2 g q8h
  • Ceftriaxone 1-2 g/day
  • Ceftaroline 600 mg q12 h
  • Ertapenem 1g q24h
  • PLUS:
  • Macrolide: Azithromycin 500 mg/day, Clarithromycin 500mg x 2 times/day
  • Or quinolone: Levofloxacin 750 mg/day, Moxifloxacin 400 mg/day
  • Macrolide or quinolone allergy: Doxycyclin 100 mg x 2 times/day
  • OR monotherapy respiratory fluoroquinolone (sterile site): Levofloxacin 750 mg/day, Moxifloxacin 400 mg/day

7. Inpatient treatment:

  • CURB-65 (3-5 points):
  • Broad-spectrum beta-lactam +/- betalactamase inhibitor or carbapenem:
  • Piperacillin/tazobactam 4.5 g IV q6h
  • Cefotaxime 1-2 g q8h
  • Ceftriaxone 1-2 g/day
  • Ceftaroline 600 mg q12 h
  • Cefepim 2g q8h
  • Ertapenem 1g q24h
  • PLUS:
  • Macrolide: Azithromycin 500 mg/day, Clarithromycin 500mg x 2 times/day
  • Or quinolone: Levofloxacin 750 mg/day, Moxifloxacin 400 mg/day
  • CURB-65 (3-5 points) if suspected atypical bacterial infection:
  • Suspected Pseudomonas infection:
  • Anti-Pseudomonas β-lactam (piperacillin/tazobactam, ceftazidim, cefepime, cefoperazon, imipenem, meropenem, doripenem)
  • PLUS:
  • Ciprofloxacin or levofloxacin
  • 1 aminoglycoside and azithromycin/clarithromycin
  • Suspected MRSA infection:
  • Broad-spectrum beta-lactam +/- betalactamase inhibitor or carbapenem
  • PLUS:
  • Vancomycin or Teicoplanin, or Linezolid (preferred over patients with impaired renal function or those using nephrotoxic medications) when MIC > 1

8. Treatment monitoring:

  • Vital signs
  • If the patient does not respond, exclude other causes, consider co-infection, evaluate the appropriateness of the antibiotic used, repeat microbiological tests and antibiogram, look for TB, fungi…
  • Continue oral antibiotics after discharge for patients with pneumonia complications due to S. pneumoniae, sepsis, S. aureus, gram-negative bacteria, legionella, pneumonia complications from endocarditis, lung abscess, empyema

9. Vaccination:

  • Influenza vaccination: Annually in individuals > 50 years of age, indicated for individuals with chronic cardiopulmonary diseases, diabetes, severe renal failure, immunosuppression.
  • Pneumococcal vaccination:
  • Every 5 years when the first dose is given < 65 years of age
  • If the first dose is given > 65 years of age, then no booster is needed, indicated for individuals with chronic cardiopulmonary diseases, diabetes, alcoholism, chronic liver disease, cerebrospinal fluid leaks, splenectomy, immunosuppression.

10. Treatment duration:

  • CAP:
  • Until the patient reaches a stable state, no fever for 48-72 hours, no unstable clinical factors.
  • If outpatient treatment, not less than 5 days.
  • HAP:
  • Antibiotic discontinuation should only occur when clinical response is achieved for at least 72 hours.
  • Typically 14-21 days.
  • 7 days: In patients without clinical symptoms and the cause is not Pseudomonas.

11. Comparison of CAP and HAP:

  • HAP has a higher mortality rate than CAP, possibly due to age, exposure to infection sources…
  • HAP is less likely to have typical symptoms (fever, chills…) but occurs along with confusion and altered consciousness.

12. Risk factors for exposure to multi-drug resistant bacteria:

  • Hospitalization for multiple days in a healthcare facility within the past 90 days.
  • Exposure to antibiotics, chemotherapy, wound care within the past 30 days.
  • Residence in a nursing home or long-term care facility.
  • Hemodialysis at a hospital/clinic.
  • Nursing care (infusion, wound care…)
  • Contact with family members/personnel infected with multi-drug resistant bacteria.

13. Hospital-acquired pneumonia (HAP):

  • Pneumonia acquired after hospitalization > 48 hours.
  • Includes early-onset pneumonia (<5 days after hospitalization) and late-onset pneumonia (>5 days after hospitalization).
  • Characterized by an increased risk of exposure to multi-drug resistant bacteria.

14. Causative agents of HAP:

  • Gram-negative bacilli:
  • E.coli
  • Klebsiella pneumoniae
  • Enterobacter spp.
  • Pseudomonas aeruginosa (late)
  • Acinetobacter spp. (late)
  • Haemophillus influenzae (early)
  • Moraxella catarrhalis
  • Gram-positive cocci:
  • S.aureus: MSSA (early) and MRSA (late)
  • Streptococcus pneumoniae (early)

15. High risk factors for exposure to multi-drug resistant HAP bacteria:

  • Late-onset hospital-acquired pneumonia.
  • Intravenous antibiotic use within the past 90 days.
  • Recent hospitalization (> 5 days).
  • Underlying conditions (Immunodeficiency, Respiratory conditions such as cystic fibrosis, bronchiectasis, COPD, diabetes…)
  • Frequent use of glucocorticoids.
  • Alcoholism.
  • Prior infection with multi-drug resistant bacteria.
  • Epidemiology with a high prevalence of MRSA, gram-negative bacilli dominance.

16. Ventilator-associated pneumonia (VAP):

  • A form of hospital-acquired pneumonia.
  • Pneumonia develops after endotracheal intubation for at least 48 hours.

17. Diagnosis of pneumonia causative agents based on experience:

  • Need to consider:
  • Pneumonia classification: HAP (early/late onset), CAP, HCAP, VAP
  • Severity: Outpatient treatment, inpatient treatment in respiratory ward, inpatient treatment in ICU
  • Patient background: Age, lifestyle habits, co-morbidities (pulmonary/systemic)

18. Pneumonia prevention measures:

  • Influenza and pneumococcal vaccination.
  • Environmental hygiene.
  • Hand washing, wearing masks when sick.
  • Smoking cessation.
  • Treatment of underlying conditions that damage lung structure/reduce immunity.

19. Principles of antibiotic use in HAP:

  • Early antibiotic use, within 24 hours or earlier after diagnosis.
  • Selection of antibiotics different from those previously administered to the patient.

20. HAP treatment:

  • Early-onset HAP AND no suspicion of multi-drug resistant bacteria infection:
  • Ampicillin + sulbactam 1.5-3 g q6h
  • Amoxicillin/clavulanate 1.2 g q8h
  • Ertapenem 1g q24h
  • Ceftriaxone 1-2g q24h or Cefotaxime 1-2g q6h
  • Levofloxacin 750mg IV q24h or Ciprofloxacin 400mg IV q8h-12h or Moxifloxacin 400mg q24h (if atypical bacteria are suspected)
  • HAP with risk of multi-drug resistant bacteria infection (No high mortality risk + No MRSA infection risk):
  • Piperacillin-tazobactam 4.5 g IV q6h
  • Cefepime 2 g IV q8h
  • Levofloxacin 750 mg IV q24
  • Imipenem/cilastatin 500 mg IV q6h
  • Meropenem d 1 g IV q8h
  • HAP with risk of multi-drug resistant bacteria infection (No high mortality risk + MRSA infection risk):
  • Piperacillin-tazobactam 4.5 g IV q6h
  • Cefepime 2 g IV q8h
  • Levofloxacin 750 mg IV q24/Ciprofloxacin 400mg q8h
  • Imipenem/cilastatin 500 mg IV q6h
  • Meropenem 1 g IV q8h
  • Aztreonam 2g q8g
  • PLUS:
  • Vancomycin 15 mg/kg IV q8-12h (monitor antibiotic levels during treatment)
  • Linezolid 600 mg IV q12h
  • Teicoplanin: Initial dose: 400mg q12h x 3, Maintenance: 400mg (6mg/kg) q24h.
  • HAP with risk of multi-drug resistant bacteria infection (High mortality risk + IV antibiotic use within the past 90 days):
  • Combine 2 of the following antibiotics, avoid using 2 beta-lactams:
  • Piperacillin-tazobactam 4.5 g IV q6h
  • Cefepime 2 g IV q8h/ ceftazidime 2g IV q8h
  • Imipenem_cilastatin 500 mg IV q6h / Meropenem d 1 g IV q8h
  • Levofloxacin 750 mg IV q24/Ciprofloxacin 400mg q8h
  • Amikacin 15-20 mg/kg IV q24h/ Gentamicin 5-7 mg/kg IV q24h/ Tobramycin 5-7mg/kg IV q24h
  • PLUS:
  • Vancomycin 15 mg/kg IV q8-12h (monitor antibiotic levels during treatment)
  • Linezolid 600 mg IV q12h
  • Teicoplanin: Initial dose: 400mg q12h x 3, Maintenance: 400mg (6mg/kg) q24h.

21. Side effects of some antibiotics:

  • Vancomycin:
  • Nephrotoxicity (especially when combined with piperacillin/tazobactam, aminoglycosides)
  • Hearing loss (especially when combined with aminoglycosides)
  • Rapid infusion causes “red man” syndrome
  • Leukopenia (rare) when used for 2-3 weeks
  • Penicillin:
  • Allergy (urticaria, angioedema, anaphylactic shock)
  • Nausea, vomiting, and diarrhea
  • Drug fever, rash, interstitial nephritis, neurotoxicity, and hematologic abnormalities
  • Cephalosporin:
  • Allergy (rare), cross-allergy with penicillin is low (5%)
  • Leukopenia, thrombocytosis, hemolysis, diarrhea, and elevated liver enzymes (rare)
  • Decreased prothrombin time and disulfiram-like reaction with alcohol (cefotetan and cefoperazon)
  • Cetriaxone: High doses can cause bile duct obstruction (excreted through bile)
  • Carbapenem:
  • Nausea, vomiting, diarrhea, rash, and drug fever
  • Seizures (high risk in patients with CNS disorders and renal failure)
  • Fluoroquinolone:
  • Tendinitis, Achilles tendon rupture (watch out for patients complaining of leg pain, swelling without mechanical cause)
  • Prolonged QT interval
  • TDP in the CNS such as headache, dizziness
  • Avoid use in patients with a history of myasthenia gravis (can cause relapse of myasthenia gravis)
  • TDP in the gastrointestinal tract is the most common
  • Clostridium difficile-associated diarrhea
  • Aminoglycoside:
  • Nephrotoxicity, recovery after discontinuation
  • Ototoxicity: Hearing loss (irreversible) and vestibular toxicity (causes loss of balance)
  • Linezolid:
  • Diarrhea, nausea, vomiting
  • Headache
  • Anemia, thrombocytopenia, leukopenia
  • Clindamycin:
  • Clostridium difficle-associated pseudomembranous colitis
  • Diarrhea, rash

Note: This information is for reference only and cannot replace medical advice. Please consult a doctor for timely diagnosis and treatment.



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