PHARM: Pulmonary Antimicrobials Flashcards

1
Q

MIND ME antimicrobial creed

A
  • Microbiology-guided therapy (knowing the pathogen first)
  • Indications are evidence based
  • Narrowest spectrum possible
  • Dosage personalised to Pt
  • Minimise duration of therapy
  • Ensure oral therapy when appropriate
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2
Q

Tx for ACUTE rhinosinusitis
- what happens if it lasts >7 days?

A
  • symptomatic Tx: paracetamol, NSAIDs, degongestants (a-agonists)
  • if Sx persist for 7 days and include persistent high fever (>39˚ for >3 days), unilateral maxillary sinus tenderness or purulent nasal discharge, give antibiotic (amoxicillin OR cefuroxime/doxycycline)
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3
Q

Tx for CHRONIC rhinosinusitis

A
  • treat the CAUSE, not Sx
  • if due to inflammation = nasal or oral corticosteroid
  • if pus is seen on nasal endoscopy - antibiotic (amoxicillin, cefuroxime, doxycycline)
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4
Q

penicillin
- class
- MOA
- AEs
- indications
- is it safe for pregnant women
- what to do if inadequate response
- e.g.

A
  • B-lactams (bactericidal - gram +ve)
  • MOA: irreversibly inhibits transpeptidases which facilitate cross-linking and strengthening of peptidoglycan cell wall = cell lysis
  • AEs: generally well tolerated but GIT issues, allergies, superinfection
  • indicated for URTIs
  • safe for pregnant and breastfeeding women
  • combine with clavulanic acid if inadequate response in 2-3 days
  • e.g. amoxicillin
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5
Q

function of clavulanate

A
  • some bacteria have B-lactamase which cleaves B-lactams (penicillins)
  • clavulanate inhibits B-lactamase = increased spectrum of antibiotic
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6
Q

cephalosporins
- class
- MOA
- indication
- adverse effects
- e.g.

A
  • B-lactams (bactericidal against gram +ve and -ve)
  • MOA: irreversibly inhibits transpeptidases which facilitate cross-linking and strengthening of the cell wall, effective against B-lactamase producing bacteria
  • indicated if penicillin-sensitive
  • AEs: GIT issues (‘lex’ sounds like laxative), neurotoxicity (rare)
  • e.g. cephalexin, cefuroxime
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7
Q

tetracycline
- MOA
- indication
- AEs
- contraindications
- e.g.

A
  • MOA: reversibly binds to 30s ribosomal subunit, preventing protein synthesis
  • indication: if sensitive to penicillin
  • AEs: chelates (depletes) Ca2+, teeth discolouration, decreased bone growth in children under 8, photosensitivity, nephrotoxic, hepatotoxic
  • contraindications: children younger than 8 and pregnant women after 18 weeks
  • e.g. doxycycline
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8
Q

antibiotics for pharyngitis (if GABHS)

A
  • highly susceptible to penicillins = narrow spectrum penicillin
  • if sensitive: cephalosporin or macrolide
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9
Q

macrolides:
- MOA
- AEs
- indication
- e.g.

A
  • MOA: reversibly binds to 50s ribosomal subunit = inhibits bacterial translation
  • AEs: cardiotoxic (arrhythmias), hepatotoxic, GIT issues
  • indications: mostly gram +ve bacteria - alternative for penicillin sensitivity, indicated in URTIs and whooping cough
  • e.g. erythromycin, azithromycin
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10
Q

when do you give antibiotics for whooping cough?

A
  • ONLY in the catarrhal stage - almost no bacteria left in the paroxysmal or convalescent stage so not effective
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11
Q

factors to consider when thinking abt antibiotics for otitis media

A
  • usually works well - decreased complications e.g. contralateral infection due to vomiting etc
  • BUT in children can lead to vomiting, diarrhoea, rash
  • recommended for ATSI or immunocompromised
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12
Q

antibiotics for otitis media

A
  • treat Sx first
  • amoxicillin (1st line) or cefuroxime if sensitive
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13
Q

Tx for bronchitis

A
  • if viral: symptomatic
  • if bacterial (B. pertussis) suspected: macrolides
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14
Q

Tx for influenza

A
  • if otherwise healthy, symptomatic Tx - paracetamol
  • if high risk (e.g. healthcare worker, immunocompromised): antiviral - oseltamivir
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15
Q

oseltamivir
- MOA
- adverse effects
- indication

A
  • MOA: neuraminidase inhibitor, preventing influenza release from cell
  • need to be taken within 48 hrs of Sx and only reduce duration of disease by 1 day
  • adverse effects: GIT issues
  • indication: influenza Tx and prophylaxis
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16
Q

empirical treatment for LOW SEVERITY community-acquired pneumonia

A
  • monotherapy: amoxicillin (1st line), doxycycline or clarithromycin if sensitive OR if atypical pathogen
  • combination therapy: doxycycline + amoxicillin or cefuroxime
17
Q

empirical treatment for MODERATE and HIGH SEVERITY community-acquired pneumonia

A
  • moderate: benzylpenicillin + doxycycline OR clarithromycin
  • high: ceftriaxone + azithromycin
18
Q

tuberculosis Tx

A
  • RIPE
  • rifampicin (1st line w/ isoniazid) - inhibits RNA polymerase
  • isoniazid (1st line w/ rifampicin) - inhibits mycolic acid synthesis
  • pyrazinamide - mycolic acid
  • ethambutol - mycolic acid
19
Q

precautions + AEs when using rifampicin

A
  • significant drug interactions (CYP inducer = increased metabolism of other drugs)
  • can’t be used on its own otherwise resistance > combination therapy w/ isoniazid
  • AEs: turns secretions orange and yellow
20
Q

precautions and adverse effects when using isoniazid

A
  • can’t be used on its own otherwise resistance > combination therapy w/ rifampicin
  • AEs: allergic skin reactions, fever, hepatotoxic, haematological changes
21
Q

pyrazinamide
- optimal pH
- AEs

A
  • works at acidic pH (when bacteria are contained in macrophages)
  • AEs: increased risk of gout, GIT issues, malaise, fever, hepatotoxic
22
Q

ethambutol AE

A
  • dose-related optic neuritis