Antibiotics Flashcards

1
Q

Beta-lactam antibiotics (properties, type of Abx, MOA)

A
  • They have a beta-lactam ring
  • It’s bactericidal antibiotics. They kill bacteria, both gram +ve and gram -ve, since all gram + and - bacteria have peptidoglycan in their cell walls
  • MOA: inhibit cell wall synthesis. They do this by binding on transpeptidase enzymes, which is needed to create linkage between the peptides and hold the cell wall together, inhibiting its action
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2
Q

Beta-lactam Abxs resistance

A
  • Altering porins in the cell walls that may change the right size and/or charge, not allowing the Abx to get into the cell (Gram -ve)
  • Beta-lactamase enzyme can change the chemical structure of the Abx by cleaving a C-N bond (Gram -ve and +ve)
  • Change in structure of the transpeptidase, not allowing Abx to bind to the enzyme (MRSA resistant to all penicillin)
  • Efflux pump that constantly pumps the Abx out of the cell and they cannot bind to transpeptidase
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3
Q

Cefuroxime (Indications, MOA, Therapeutic effects, Spectrum, Contraindication, Cautious usage, Adverse reactions/side effects)

A

Indications: treatment of respiratory tract infections, skin infections, bone and joint infections, urinary tract infections

MOA: binds to bacterial cell wall membrane, causing cell death

Therapeutic Effects: bactericidal

Spectrum: active against gram-positive and gram-negative aerobic bacteria

Contraindicated in: hypersensitivity to cephalosporins; serious hypersensitivity to penicillins

Use cautiously in: renal impairment (will need dose adjustments)

Adverse reactions/side effects: rash and Costridioides Difficile-Associated Diarrhea (CDAD)

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4
Q

Cefuroxime Pharmacokinetics (absorption, distribution, and metabolism and excretion)

A
  • Absorption: Well absorbed following IV, IM and PO administration
  • Distribution: Widely distributed. Well penetrated into CSF if IV used
  • Metabolism and excretion: Excreted primarily unchanged by the kidneys
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5
Q

Cefuroxime Nursing Implications

A
  • Assess patient for infection (vital signs, appearance of wound if they have any, sputum, urine, and stool, WBC) at beginning of and throughout therapy
  • Before initiating therapy, obtain a history to determine previous use of and reactions to penicillins or cephalosporins
  • Obtain specimens for culture and sensitivity before initiating therapy. First dose may be given before giving results
  • Observe for S+S of anaphylaxis (rash, pruritus, laryngeal edema, wheezing)
  • Monitor bowel function. Diarrhea, abdominal cramping, fever, and bloody stools
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6
Q

Cefpodoxime (Indications, MOA, Therapeutic effects, Spectrum, Contraindication, Cautious usage, Adverse reactions/side effects)

A

Indications: treatment of respiratory tract infections, skin infections, bone and joint infections, urinary tract infections

Mechanism of Action: bind to bacterial cell wall membrane, causing cell death

Therapeutic Effects: bactericidal

Spectrum: active against gram-positive and gram-negative aerobic bacteria

Contraindicated in: hypersensitivity to cephalosprins; serious hypersensitivity to penicillins

Use cautiously in: renal impairment (will need dose adjustments)

Adverse reactions/side effects: rash, Clostridioides Difficile-Associated Diarrhea (CDAD)

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7
Q

Cefpodoxime Pharmacokinetics (absorption, distribution, and metabolism and excretion)

A

-Absorption: 50% absorption in the GI tract after being converted from protype to active form

-Distribution: Widely distributed. Well penetration into CSF better than Cefuroxime

-Metabolism and excretion: 30% excreted in urine

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8
Q

Cefpodoxime Nursing Implications

A
  • Assess patient for infection (vital signs, appearance of wound if they have any, sputum, urine, and stool, WBC) at beginning of and throughout therapy
  • Before initiating therapy, obtain a history to determine previous use of and reactions to penicillins or cephalosporiins
  • Obtain specimens for culture and sensitivity before initiating therapy. First dose may be given before giving results
  • Observe for S+S of anaphylaxis (rash, pruritus, laryngeal edema, wheezing)
  • Monitor bowel function. Diarrhea, abdominal cramping, fever, and bloody stools
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9
Q

Amoxicillin-Clavulanate (Indications, MOA, Therapeutic effects, Spectrum, Contraindication, Cautious usage, Adverse reactions/side effects)

A

Indications: treatment of respiratory tract infections, skin infections, otitis media, bone and joint infections, and urinary tract infections.

Mechanism of Action:
-Amoxicillin: bind to bacterial cell wall membrane, causing cell death
-Clavulanate: inhibits the action of beta-lactamase – an enzyme produced by bacteria that is capable of inactivating amoxicillin

Therapeutic Effects: bactericidal

Spectrum: active against gram-positive and gram-negative aerobic bacteria

Contraindicated in: hypersensitivity to penicillins or clavulanate

Use cautiously in: renal impairment (will need dose adjustments)

Adverse reactions/side effects: rash, Clostridioides Difficile-Associated Diarrhea (CDAD)

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10
Q

Amoxicillin-Clavulanate Pharmacokinetics (absorption, distribution, and metabolism and excretion)

A
  • Absorption: Well absorbed in the GI tract
  • Distribution: Widely distributed. Does not readily enter the brain/CSF
  • Metabolism and excretion: 70% excreted unchanged in the urine; 30% metabolized in liver
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11
Q

Amoxicillin-Clavulanate Nursing Implications

A
  • Assess patient for infection (vital signs, appearance of wound if they have any, sputum, urine, and stool, WBC) at beginning of and throughout therapy
  • Before initiating therapy, obtain a history to determine previous use of and reactions to penicillins or cephalosporins
  • Obtain specimens for culture and sensitivity before initiating therapy. First dose may be given before giving results
  • Observe for S+S of anaphylaxis (rash, pruritus, laryngeal edema, wheezing)
  • Monitor bowel function. Diarrhea, abdominal cramping, fever, and bloody stools
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12
Q

General MOA of anti-ribosomal Abx

A

All cells need protein production to survive and ribosomes play a significant role in protein production through mRNA. Anti-ribosomal Abx inhibit ribosomal action, which inhibit growth and survival

NOTE: bacterial ribosomes are different form human ribosomes. It will not inhibit the function of our ribosomes

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13
Q

Azithromycin (Indications, MOA, Therapeutic effects, Spectrum, Contraindication, Cautious usage, Adverse reactions/side effects)

A

Indications:
- Upper respiratory tract infections (e.g., bacterial exacerbations of chronic bronchitis)
- Lower respiratory tract infections (e.g., bronchitis or pneumonia)

Mechanism of Action:
-Inhibits protein synthesis at the level of the 50S bacterial ribosome

Therapeutic Effects: bacteriostatic action

Spectrum: active against gram-positive and gram-negative aerobic bacteria

Contraindicated in:
- Hypersensitivity to azithromycin or other macrolide anti-infectives
- History of hepatic dysfunction with prior use of azithromycin

Use cautiously in:
- Severe hepatic impairment (may need dose adjustment)
- Severe renal impairment (CCr < 10 mL/min)

Adverse reactions/side effects:
- Torsades de points (abnormal heart rhythm that can lead to sudden cardiac arrest)
- Acute generalized exanthematous pustulosis (skin reaction – skin eruptions)
- Drug reaction with eosinophilia and systemic symptoms (DRESS) (Rash with fever, general malaise, eosinophilia [excess eosinophil formation], lymphocytosis [increase in white blood cells], multi-end organ dysfunction)
- Abdominal pain, diarrhea, nausea

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14
Q

Azithromycin Pharmacokinetics (absorption, distribution, and metabolism and excretion)

A
  • Absorption: Rapidly absorbed (40%) after oral administration
  • Distribution: Widely distributed to body tissues and fluids
  • Metabolism and excretion: Mostly excreted unchanged in bile
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15
Q

Azithromycin Nursing Implications

A
  • Assess patient for infection (vital signs, appearance of wound if they have any, sputum, urine, and stool, WBC) at beginning of and throughout therapy
  • Obtain specimens for culture and sensitivity before initiating therapy. First dose may be given before giving results
  • Observe for S+S of anaphylaxis (rash, pruritus, laryngeal edema, wheezing)
  • Assess patient for skin rash frequently during therapy. Discontinue at first sign of rash
  • May cause increases in serum bilirubin, AST, ALT, LDH, and alkaline phosphatase – liver enzymes that indicate liver dysfunction
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16
Q

Ciprofloxacin (Indications, MOA, Therapeutic effects, Spectrum, Contraindication, Cautious usage, Adverse reactions/side effects)

A

Indications: treatment of urinary tract infections, gonorrhea, infectious diarrhea

Mechanism of Action: inhibits bacterial DNA synthesis by inhibiting DNA gyrase

Therapeutic Effects: bacteriocidal

Spectrum: active against gram-positive

Contraindicated in:
- Hypersensitivity to Azithromycin, Ciprofloxacin
- History of aortic aneurysm/dissection – damages connective tissue of the heart and aorta

Use cautiously in: severe renal impairment (CCr < 10 mL/min)

Adverse reactions/side effects:
- Aortic aneurysm/dissection
- Torsades de points
- Stevens-Johnson Syndrome

17
Q

Ciprofloxacin Pharmacokinetics (absorption, distribution, and metabolism and excretion)

A
  • Absorption: 70% absorbed after PO administration
  • Distribution: Widely distributed
  • Metabolism and excretion: 15% metabolized by the liver and 40-50% excreted by the kidney
18
Q

Ciprofloxacin Nursing Implications

A
  • Assess patient for infection (vital signs, appearance of wound if they have any, sputum, urine, and stool, WBC) at beginning of and throughout therapy
  • Obtain specimens for culture and sensitivity before initiating therapy. First dose may be given before giving results
  • Observe for S+S of anaphylaxis (rash, pruritus, laryngeal edema, wheezing)
  • Assess patient for skin rash frequently during therapy. Discontinue at first sign of rash