Islamic Teachings and Respiratory Medicine

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Questions and Answers

What is defined as pneumonia occurring 48 hours or more after hospital admission and not present at the time of admission?

  • Aspiration pneumonia
  • Ventilator-associated pneumonia
  • Community-acquired pneumonia
  • Nosocomial pneumonia (correct)

What is the rate of hospital-acquired pneumonia (HAP) occurrences per 1000 hospital admissions?

  • 11 to 15
  • 1 to 2
  • 5 to 10 (correct)
  • 3 to 4

Which of the following is a common pathogen associated with hospital-acquired pneumonia?

  • Streptococcus pneumoniae
  • Staphylococcus aureus
  • Mycoplasma pneumoniae
  • Aerobic gram-negative bacilli (correct)

Which type of pneumonia occurs more than 48 to 72 hours after tracheal intubation?

<p>Ventilator-associated pneumonia (D)</p> Signup and view all the answers

What percentage of pneumonia episodes in intensive care units occurs in patients who are intubated and mechanically ventilated?

<p>Over 90% (A)</p> Signup and view all the answers

What language does the term 'pneumonia' derive from, and what does it mean?

<p>Greek for 'lung' (A)</p> Signup and view all the answers

How is pneumonia primarily classified in the context of hospital-acquired infections?

<p>By the timing of acquisition (B)</p> Signup and view all the answers

Which of the following is NOT a recognized type of hospital-acquired pneumonia?

<p>Chronic obstructive pneumonia (B)</p> Signup and view all the answers

Flashcards

What is Nosocomial Pneumonia?

Pneumonia that develops in a patient 48 hours or more after hospital admission and was not present at the time of admission.

What is Ventilator-associated Pneumonia (VAP)?

Pneumonia that develops in a patient receiving mechanical ventilation more than 48 to 72 hours after tracheal intubation.

What is the prevalence of HAP?

It occurs at a rate of 5 to 10 per 1000 hospital admissions in Europe and the United States.

What is the prevalence of VAP in ICUs?

Over 90% of pneumonia episodes developing in ICUs occur in patients who are intubated and mechanically ventilated.

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What are some common pathogens causing HAP and VAP?

Aerobic gram-negative bacilli are often involved, including Pseudomonas aeruginosa, Acinetobacter baumannii, and Escherichia coli.

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What are some risk factors for developing HAP?

These include prolonged hospital stay, underlying health conditions, and previous antibiotic use.

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What is Pneumonia?

Inflammation of the lung parenchyma (tissue) often caused by infection.

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How does Pneumonia affect the lungs?

It can involve one or both lungs and is often caused by bacteria, but other organisms like viruses and fungi can also cause it.

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Study Notes

Islamic Teachings

  • Two phrases are easy to say but have immense value in the balance.
  • These phrases are "سبحان الله وبحمده" (Subḥān Allāh wa bihamdih) and "سبحان الله العظيم" (Subḥān Allāh al-ʿazīm).
  • These phrases are beloved by God.

Respiratory Medicine

  • Respiratory Infections: This is a broad category of diseases affecting the respiratory system.

  • Nosocomial Pneumonia: A type of pneumonia contracted in a hospital setting (often related to medical procedures), occurring 48+ hours post admission

  • Pneumonia: An infection of the lungs, causing illness ranging from minor to severe, affecting people of varying ages.

  • Causes of HAP/VAP:

    • Gram-negative bacteria (Pseudomonas, Escherichia, Klebsiella, Enterobacter, Acinetobacter)
    • Gram-positive cocci (Staphylococcus aureus, including methicillin-resistant Staphylococcus aureus, Streptococcus spp.)
    • Aerobic bacteria
  • Risk factors:

    • Prior infection with Pseudomonas spp.
    • Pseudomonas spp. colonization
    • Very severe COPD
    • Bronchiectasis
    • Tracheostomy
    • Neutropenia
    • Burns
    • Cystic fibrosis
  • Risk factors for MDR HAP/MRSA VAP/HAP/MDR Pseudomonas VAP/HAP: Prior IV antibiotic use within 90 days

  • Types of HAP: Early-onset (diagnosed 2-5 days after hospitalization) and Late-onset (diagnosed >5 days after hospitalization)

  • Pathophysiology: The processes involved in the development and progression of pneumonia include:

    • Hospital admission and presence of risk factors (e.g., prior antibiotic use)
    • Exposure to germs in the hospital environment
    • Changes in the normal oral/upper airway microbiome
    • Colonization with gram-negative Enterobacteriaceae and MRSA
    • Aspiration or inhalation of pathogens
    • Defective mucociliary and alveolar defenses
    • Macroaspiration in healthy patients or microaspiration in immunocompromised patients
    • Presence of viruses or bacteria
  • Clinical Features:

    • Clinical: Fever (≥38°C), cough with purulent sputum
    • Radiographic: New or progressive infiltrates on chest X-ray
    • Lab: Leukocytosis or leukopenia
  • Clinical Signs: Tachycardia, hypotension, tachypnea, hypoxia,r ales, wheezing, accessory respiratory muscle use, decreased/absent breath sounds, altered mental status, hypothermia

  • Diagnosis: Physical examination, chest X-rays, chest CT, and laboratory tests.

  • Differential Diagnoses: Pulmonary infarction, pulmonary/pleural tuberculosis, pulmonary edema, pulmonary eosinophilia, malignancy, cryptogenic organising pneumonia/bronchiolitis obliterans organising pneumonia

  • Investigations: Blood cultures, sputum cultures, samples of lower respiratory tract secretion (endotracheal aspirate, BAL, and protected specimen brush sample), pleural aspirate

  • Imaging techniques: Chest X-rays, Chest CT scans.

  • Criteria for ICU Admission: (Major criteria) Invasive mechanical ventilation, septic shock with need for vasopressors; (Minor criteria) Confusion/disorientation, blood urea nitrogen ≥20mg/dL, respiratory rate ≥30breaths/min, hypotension requiring aggressive fluid resuscitation, PaO2/FiO2 ratio 250, multilobar infiltrates, WBC count <4000 cells/mm, platelet count ≤100,000 cells/mm, core temperature <36°C

  • Management:
    -Monitor pulse, blood pressure, respiratory rate, temperature, oxygen saturation and mental status continually, especially important for patients with HAP or VAP.

    • Provide timely antibiotics
    • Recommend using PK/PD data for antibiotic dosing
    • Emphasize De-escalation as a principle of antimicrobial stewardship
    • Empiric antibiotics are dependent on individual risk factors
  • Treatment Options:

    • Gram-positive coverage (e.g., vancomycin, linezolid)
    • Gram-negative coverage (e.g., piperacillin/tazobactam, cefepime, levofloxacin, imipenem/meropenem, ciprofloxacin)
    • Anaerobic coverage (e.g., clindamycin)

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