LRI Exam 4 Flashcards

1
Q

common pathogens for CAP

A
  • Viral* (Most common)
  • Streptococcus pneumoniae* (Most common bacterial cause)
  • Haemophilus influenzae (less common than historically)
  • Moraxella catarrhalis
  • Mycoplasma pneumoniae
  • Chlamydophila pneumoniae
  • Legionella pneumophila
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2
Q

Who has a higher risk of CAP?

A

pts younger than 30 y/o

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3
Q

For CAP, if t has the following risk factors (chronic corticosteroids, severe bronchopulmonary disease, alcoholism, frequent antibiotic therapy) what are they more susceptible to?

A
  • Enterobacteriaceae

- Pseud. aeruginosa

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4
Q

common pathogens for HAP / VAP

A
  • Rarely due to viral or fungal pathogens in immunocompetent patients
  • Enterobacteriaceae
  • Pseudomonas aeruginosa
  • Acinetobacter species (VAP)
  • Stenotrophomonas maltophilia (VAP)
  • Polymicrobial infection is especially common with ARDS
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5
Q

For HAP / VAP, if pt has the following risk factors (diabetes, head trauma, ICU admission, recent Abx, tobacco use), what are they more susceptible to?

A

MSSA/MRSA

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6
Q

For infleunza, we’re worried about development of secondary bacterial infection especially for high risk patients. What are those high risk patients?

A
  • Young children
  • Elderly >= 65
  • Patients with chronic lung disease
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7
Q

What are some general risk factors for HAP / VAP?

A
  • Severe underlying disease
  • Preexisting pulmonary disease
  • Prior surgery
  • Intubation / Mechanical ventilation / Enteral feeding
  • Exposure to IV antibiotics
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8
Q

Risk factors for MDR pathogens (MRSA, Pseudomonas) to cause HAP and VAP

A

Prior IV antimicrobial therapy in preceding 90 days

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9
Q

Additional risk factors for MDR VAP

A
  • Septic shock at time of VAP
  • ARDS preceding VAP onset
  • Current hospitalization > 5 days before VAP onset
  • Acute renal replacement therapy prior to VAP onset
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10
Q

timing of CAP

A

Happens before or within 48 hours of admission

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11
Q

timing of HAP

A

Pneumonia arising > 48 hours after hospital admission

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12
Q

timing of VAP

A

Pneumonia arising > 48-72 hours after endotracheal intubation

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13
Q

Who should receive antiviral treatment?

A
  • Hospitalized patients with confirmed or suspected influenza*
  • Children < 2 years*
  • Adults >= 65 years*
  • Pregnant women or post-partum (within 2 weeks of delivery)*
  • People with chronic pulmonary (including asthma), cardiovascular (except hypertension), renal, hepatic, hematological (including sickle cell disease), neurologic, neuromuscular, or metabolic (including diabetes mellitus) disorders
  • People with immunosuppression (including medication-induced or HIV infection)
  • People < 19 years receiving long-term aspirin therapy o American Indians/Alaska Natives
  • Morbidly obese (BMI > 40)
  • Nursing home/long-term care residents
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14
Q

Who should receive antiviral prophylaxis?

A
  • young children
  • elderly > 65
  • chronic lung disease
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15
Q

candidates for influenza vaccine

A
  • > 50 years old*
  • Chronic lung disease (e.g., asthma, COPD)
  • Chronic renal, hepatic, CVD
  • Diabetes
  • Neurologic disease (e.g., spinal cord injury, seizures)
  • Immunosuppression (e.g., HIV, malignancy)
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16
Q

candidates for pneumococcal vaccine

A
  • > = 65 years old*
  • Chronic lung disease (e.g., asthma, COPD)
  • Chronic renal, hepatic, CVD
  • Diabetes
  • Immunosuppression (e.g., HIV, malignancy)
  • Asplenic (functional/anatomical)
  • Alcoholism
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17
Q

role of palliative therapies in the treatment of acute and chronic bronchitis

A
  • managing cough

- managing other symptoms

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18
Q

What can you use for cough suppression in bronchitis?

A
  • Antitussives: Dextromethorphan, benzonatate (local anesthetic)
  • Antihistamines for cough associated with allergic rhinitis; if viral infection, probably not the best choice
  • Bronchodilators
  • NSAIDS associated with improved cough control with rhinovirus infection; helps decrease severity of the cough: Highly effective in decreasing inflammation; high doses such as IBP 600-800mg TID scheduled
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19
Q

role of antibiotics in the treatment of acute and chronic bronchitis

A
  • No proven benefit in acute bronchitis

- Used in CHRONIC bronchitis (because they have trouble clearing the infection by themselves): Improves clinical outcome

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20
Q

Pneumonia Severity Index (PSI)

A
  • Class I-II: outpatient treatment
  • Class III: observation in ED; consider hospitalization
  • Class IV-V: hospitalization indicated
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21
Q

CURB-65 items

A
  • Confusion
  • Uremia (BUN >20 mg/dL)
  • RR >30
  • Low BP (SBP <90 or DBP <60)
  • Age >65
22
Q

CURB-65 interpretation

A
  • Score 0-1: outpatient treatment
  • Score >2: ospitalization
  • Score 3: ± ICU
  • Score >4: ICU
23
Q

What is the preferred method for routine testing in pneumonia?

A

respiratory culture semiquantitative method

24
Q

biomarkers (PCT, sTREM, CRP) in pneumonia

A

biomarkers are not sensitive or specific; there is not current use for them in treatment guidelines at the moment

25
Q

CPIS in pneumonia

A
  • Developed to assist with diagnosis of VAP

- does not reliably discriminate between patients with or without VAP

26
Q

Out-pt treatment for CAP: Previously healthy/ No recent antibiotics

A
  • Macrolide (azithromycin, clarithromycin, erythromycin)

- Doxycycline

27
Q

Out-pt treatment for CAP: Recent Antibioticsa or Comorbidities

A
  • Respiratory fluoroquinoloneb

- β-lactamc plus a macrolide

28
Q

Out-pt treatment for CAP: Regions with High Rates (>25%) of MacrolideResistant Pneumococci (MIC >16 µg/mL)

A

β-lactam PLUS doxycycline

29
Q

In-pt treatment for CAP: Medical ward

A
  • Respiratory fluoroquinolone

- β-lactam plus a macrolide

30
Q

In-pt ICU treatment for CAP: No concern for Pseudomonas

A
  • β-lactam plus azithromycin

- β-lactam plus respiratory fluoroquinolone

31
Q

In-pt ICU treatment for CAP: No concern for Pseudomonas, but β-lactam allergy

A

Aztreonam plus respiratory fluoroquinolone

32
Q

In-pt ICU treatment for CAP: Concern for Pseudomonas

A
  • Antipseudomonal β-lactam plus ciprofloxacin or levofloxacin (750 mg)
  • Antipseudomonal β-lactam plus an aminoglycosidek plus azithromycin
  • Antipseudomonal β-lactam plus an aminoglycosidek fluoroquinolone
33
Q

In-pt ICU treatment for CAP: Concern for Pseudomonas, but β-lactam allergy

A

Aztreonam plus an aminoglycoside plus respiratory fluoroquinolone

34
Q

In-pt ICU treatment for CAP: Concern for CA-MRSA

A

Add vancomycin or linezolid

35
Q

What are the appropriate respiratory fluoroquinolones?

A
  • Moxifloxacin
  • levofloxacin (750 mg)
  • gemifloxacin
36
Q

What are antipseudomonal β-lactam?

A
  • Piperacillin-tazobactam
  • imipenem
  • meropenem
  • cefepime
  • aztreonam (PCN-allergy)
37
Q

β-lactam therapy for CAP out-pt

A
  • High-dose amoxicillin (1 gm po TID)
  • high-dose amoxicillin-clavulanate (2 gm po BID) preferred
  • alternatives include ceftriaxone (if IV access available), cefpodoxime, or cefuroxime
38
Q

β-lactam therapy for CAP in-pt

A

Cefotaxime, ceftriaxone, ampicillin-sulbactam, or ertapenem preferred

39
Q

In which population should AMG be avoided in?

A

elderly

40
Q

Examples of comorbidities

A
  • Chronic obstructive pulmonary disease
  • malignancy
  • diabetes
  • renal failure
  • congestive heart failure
41
Q

In-pt ICU treatment for HAP / VAP: low risk for mortality or MDR pathogens, no MRSA risk

A
  • Penicillin (Piperacillin-Tazobactam)
  • Cephalosporin (Cefepime)
  • Fluoroquinolone (Levofloxacin)
  • Carbapenem (Imipenem / Meropenem)
42
Q

In-pt ICU treatment for HAP / VAP: low risk for mortality or MDR pathogens, MRSA risk

A
  • Penicillin (Piperacillin-Tazobactam)
  • Cephalosporin (Cefepime)
  • Fluoroquinolone (Levofloxacin)
  • Carbapenem (Imipenem / Meropenem)
  • Monobactam (Aztreonam)
  • WITH Linezolid or Vancomycin
43
Q

In-pt ICU treatment for HAP / VAP: high risk for mortality or MDR pathogens

A
  • Linezolid or Vancomycin
  • WITH Zosyn or Cefepime / Ceftazidime or Imipenem / Meropenem or Aztreonam
  • WITH Ciprofloxacin / Levofloxacin or Amikacin / Gentamicin / Tobramycin or Polymixin (colistin; VAP ONLY)
44
Q

What is the vanc trough target for HAP / VAP?

A

15-20 µg/mL

45
Q

Use of Amantadine for influenza virus

A

Not recommended due to high rates of resistance among Type A isolates (>99%)

46
Q

Use of Rimantadine for influenza virus

A

Not recommended due to high rates of resistance among Type A isolates (>99%)

47
Q

Use of Oseltamivir (Tamiflu®) for influenza virus

A
  • used for both treatment and prophylaxis
  • treatment at any age for both A and B
  • prophylaxis not to be used in younger than 3 months
  • ADE: Nausea/vomiting, neuropsychiatric effects
48
Q

Use of Zanamivir (Relenza®) for influenza virus

A
  • used for both treatment and prophylaxis
  • NOT to be used if pt also has asthma / COPD, milk allergy
  • treatment for >= 7 y/o
  • prophylaxis for >= 5 y/o
  • ADE: Allergic rxns, diarrhea, nausea, respiratory infections
49
Q

Organism-Specific Therapy for Chronic Bacterial Bronchitis: Atypicals (Mycoplasma. pneumoniae, Chlamydophila pneumoniae)

A
  • Macrolide (azithromycin, clarithromycin, erythromycin)
  • Doxycycline
  • Respiratory fluoroquinolone
50
Q

Organism-Specific Therapy for Chronic Bacterial Bronchitis: Streptococcus pneumoniae

A
  • High-dose amoxicillin
  • Doxycycline
  • Respiratory fluoroquinolone
  • Not first line: Macrolide (azithromycin, clarithromycin, erythromycin)
  • Not first line: 3rd Gen. Cephalosporin + Clindamycin
51
Q

Organism-Specific Therapy for Chronic Bacterial Bronchitis: Haemophilus influenzae, Moraxella catarrhalis

A
  • Amoxicillin / clavulanate
  • Respiratory fluoroquinolone
  • Not first line: 3rd Gen. Cephalosporin
  • Not first line: Trimethoprim / sulfamethoxazole