Management of respiratory tract infections Flashcards

(25 cards)

1
Q

What is a mnemonic letter to remember the key symptoms and management approach of Acute Bacterial Rhino-Sinusitis (ABRS)?
A: “F”

A

Facial pain
• Fatigue
• Fever
• Fullness in ear
• Foul drainage (nasal/postnasal)
• Function loss of smell (Hyposmia/Anosmia)
• Failed culture (→ Empiric treatment)

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2
Q

What are the common bacterial pathogens and their prevalence rates in Acute Bacterial Rhinosinusitis (ABRS)?
A:

A

• Streptococcus pneumoniae: 20–43%
• Haemophilus influenzae: 22–36%
• Moraxella catarrhalis: 2–16%
• Staphylococcus aureus: 10–13%
• Streptococcus pyogenes: 3%

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3
Q

What is the first-line treatment for ABRS and how is it adjusted in patients with risk factors for resistance?
A:

A

• First-line: Amoxicillin or Amoxicillin/Clavulanate.
• If risk factors for resistance:
• Use high-dose oral Amoxicillin
• Or high-dose Amoxicillin/Clavulanate

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4
Q

Why is clavulanate added to amoxicillin in ABRS treatment, and in whom is its use better supported?
A:

A

• Clavulanate improves coverage against ampicillin-resistant H. influenzae and M. catarrhalis.
• Its use is better supported in children than in adults.

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5
Q

Why are macrolides (azithromycin/clarithromycin) and trimethoprim-sulfamethoxazole not recommended in ABRS?

A

A: Because of high resistance rates of Streptococcus pneumoniae to these antibiotics.

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6
Q

What are treatment options for patients with penicillin allergy in ABRS?
A:

A

• Oral doxycycline
• 3rd generation oral cephalosporin (e.g., cefixime) ± clindamycin

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7
Q

Why are respiratory fluoroquinolones (levofloxacin, moxifloxacin) reserved for ABRS patients with no alternative treatment options?

A

A: Because they carry a risk of serious adverse effects such as

Tendonitis and tendon rupture, neuropathies, and gait disturbance.

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8
Q

What are the risk factors for pneumococcal resistance?
A:

A

• Regions with >10% penicillin-non-susceptible S. pneumoniae
• Age ≥ 65 years
• Hospitalization in last 5 days
• Antibiotics use in previous month
• Immunocompromise
• Multiple comorbidities (DM, liver, kidney, heart diseases)
• Severe infection

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9
Q

In what percentage of Community Acquired Pneumonia (CAP) cases is the definitive microbiologic cause identified?

A

A: Less than 50% of CAP cases have a definitive microbiologic etiology identified.

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10
Q

What are the typical pathogens in Community Acquired Pneumonia (CAP) and their special considerations?

A:

A

• Streptococcus pneumoniae: most common pathogen
• Haemophilus influenzae
• Moraxella catarrhalis
• Staphylococcus aureus: unlikely cause, mainly post-influenza infection
• Pseudomonas & Klebsiella: seen in alcoholism, bronchiectasis, and diabetes mellitus patients

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11
Q

What is the key principle in the treatment plan of Community Acquired Pneumonia (CAP)?

A:

A

• Start rapid empiric antibiotics promptly
• Ensure adequate coverage for Streptococcus pneumoniae and atypical pathogens

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12
Q

What is the outpatient treatment for CAP in patients with no comorbidities?

A

A: Amoxicillin, Macrolide, or Doxycycline.

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13
Q

What is the outpatient treatment for CAP in patients with comorbidities?

A

 (Beta-lactam: amoxicillin/clavulanate or cefuroxime) + macrolide
or doxycycline
 Respiratory fluorquinolones: levofloxacin or moxifloxacin

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14
Q

What are the risk factors for Pseudomonas infection in CAP?

A

A: Structural lung disease, COPD, and bronchiectasis.

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15
Q

What is the treatment if Pseudomonas is suspected in CAP?

A

Use anti-pneumococcal and anti-pseudomonal beta-lactams such as Piperacillin/tazobactam, Cefepime, Meropenem, or Imipenem.

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16
Q

What antibiotic is used in CAP patients with severe penicillin allergy?

A

A: Aztreonam.

17
Q

What is the recommended duration of therapy for CAP?
A:

A

• Uncomplicated CAP: 5 days
• CAP with suspected/proven Pseudomonas or MRSA: 7 days

18
Q

What are the common causative organisms of Hospital-Acquired Pneumonia (HAP)?
A:

A

• Pseudomonas aeruginosa
• Staphylococcus aureus (including MSSA & MRSA)
• Klebsiella pneumoniae
• Escherichia coli (E. coli)
• Acinetobacter species
• Serratia marcescens
• Stenotrophomonas maltophilia

19
Q

What are the common causative organisms of Ventilator-Associated Pneumonia (VAP)?
A:

A

• Pseudomonas aeruginosa
• Staphylococcus aureus (MSSA & MRSA)
• Stenotrophomonas maltophilia
• Acinetobacter species
• Enterobacteriaceae (less commonly seen in VAP)

20
Q

How is suspected Ventilator-Associated Pneumonia (VAP) managed empirically?
A:

A

• Empiric therapy should cover S. aureus, Pseudomonas, and other gram-negative bacilli (GNB)
• The causative organism is usually unknown, so empiric treatment is essential
• Use Vancomycin or Linezolid to cover MRSA, guided by the local antibiogram
• Recommended duration of therapy: 7 days

21
Q

What antibiotics are used for empiric and confirmed MSSA coverage?
A:

A

• Empiric MSSA coverage:
• Piperacillin-tazobactam
• Cefepime
• Levofloxacin
• Imipenem
• Meropenem
• Confirmed MSSA infection:
• Oxacillin
• Nafcillin
• Cefazolin

22
Q

What are the risk factors for MDR pathogens in HAP/VAP? (1–3)
A:

A
  1. IV antibiotic use within the preceding 90 days
    1. Septic shock at the time of VAP
    2. Acute respiratory distress syndrome (ARDS) before VAP
23
Q

What are the risk factors for MDR pathogens in HAP/VAP? (4–6)
A:

A
  1. ≥5 days of hospitalization before VAP onset
  2. Acute renal replacement therapy before VAP
  3. ICU location with >10% resistance among Gram-negative isolates or lacking local antibiogram data
24
Q

What is the recommended treatment approach for HAP/VAP in patients with risk factors for multi-drug resistant (MDR) pathogens?

A

 Double drug coverage of P.aeruginosa, should combine agents with a
high degree of anti-pseudomonal activity and low resistance potential

25
What are key points about Acinetobacter baumannii in HAP/VAP? A:
• Many isolates show carbapenem resistance • MDR Acinetobacter baumannii has high mortality • Polymyxins show strongest in-vitro activity • Colistin (IV and inhaled) is the most commonly used treatment