Antibiotics Part 2 - Multidrug-Resistant Organisms & Specific Antibiotic Classes

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Vocabulary flashcards covering multidrug-resistant organisms, key pharmacology concepts, aminoglycosides, quinolones, and miscellaneous antibiotics from the lecture notes.

Last updated 1:37 AM on 10/5/26
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22 Terms

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Multidrug-Resistant Organisms

Organisms that are resistant to one or more classes of antimicrobial drugs.

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MRSA

Methicillin-resistant Staphylococcus aureus; a multidrug-resistant organism that can be health-care associated or community acquired, posing a threat of becoming resistant to all currently available antibiotics.

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VRE

Vancomycin-resistant enterococcus; a multidrug-resistant organism usually seen in urinary tract infections (UTIs).

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ESBL

Extended-spectrum beta-lactamase; organisms resistant to all beta-lactam antibiotics and aztreonam, usually treated with carbapenems or sometimes quinolones.

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CRE

Carbapenem-resistant Enterobacteriaceae; organisms resistant to carbapenems due to carbapenemase, requiring alternative treatments like tigecycline and colistimethate along with strict contact precautions and handwashing.

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Minimum Inhibitory Concentration (MIC)

The lowest concentration of an antimicrobial drug required to inhibit the visible growth of a microorganism.

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Peak Drug Level

The highest concentration of a drug in the patient's bloodstream, monitored during therapeutic drug monitoring to prevent toxicity.

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Trough Drug Level

The lowest concentration of a drug in the patient's bloodstream, monitored to ensure adequate renal clearance of the drug and avoid toxicity.

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Post-Antibiotic Effect

A period of continued bacterial growth suppression that persists after brief exposure to an antibiotic.

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Synergistic Effect

An enhanced therapeutic outcome produced when two antibiotics given in combination produce an effect greater than the sum of their individual effects.

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Therapeutic Drug Monitoring

The process of measuring serum peak and trough drug levels to maximize efficacy, maintain the minimum inhibitory concentration (MIC), and prevent toxicity.

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Time-Dependent Killing

A property of certain antibiotics where prolonged exposure above the minimum inhibitory concentration (MIC) is required for maximum bacterial kill.

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Aminoglycosides

A class of bactericidal antibiotics (including parenteral gentamicin and oral/rectal/topical neomycin) used against multidrug-resistant Gram-negative and some Gram-positive organisms, carrying key risks of nephrotoxicity and ototoxicity.

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Gentamicin

A prototype aminoglycoside antibiotic administered parenterally for serious multidrug-resistant bacterial infections.

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Neomycin

An aminoglycoside antibiotic administered orally, rectally, or topically; indicated for pre-op bowel preparation and hepatic encephalopathy.

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Ciprofloxacin

A prototype bactericidal quinolone/fluoroquinolone antibiotic indicated for complicated infections, sexually transmitted infections, and anthrax.

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Quinolones Black Box Warning

A major drug warning associated with quinolone antibiotics due to risks of tendonitis, ruptured tendons, and peripheral neuropathy.

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Clindamycin

A miscellaneous antibiotic indicated for chronic bone, genitourinary, intraabdominal, and other serious infections; contraindicated in patients with age<1 month\text{age} < 1\text{ month} or ulcerative colitis/enteritis, with a major adverse effect of C. difficile infection.

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Linezolid

A miscellaneous antibiotic indicated for VRE, MRSA, and healthcare-associated infections with excellent GI absorption suitable for prolonged outpatient therapy; interacts with vasopressors, SSRIs, and tyramine-containing foods.

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Metronidazole

A miscellaneous antibiotic indicated for intraabdominal, gynecologic, and protozoal infections; contraindicated during the 1st\text{1st} trimester of pregnancy and requires avoiding alcohol from 24 hr24\text{ hr} prior to 36 hr36\text{ hr} post-administration.

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Vancomycin

A bactericidal antibiotic reserved for resistant Gram-positive infections including MRSA and oral treatment for C. difficile or staph enteritis; requires serum drug level monitoring due to ototoxicity, nephrotoxicity, and Red Man Syndrome.

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Red Man Syndrome

An adverse reaction from rapid vancomycin infusion characterized by fever/chills, hives, hypotension, tachycardia, nausea/vomiting, and a red rash on the neck/chest; managed by slowing the infusion to at least 1 hour1\text{ hour}.