Antimicrobial Agents Study Guide: Spectrum, Classifications, and Uses, Exams of Microbiology

This comprehensive study guide covers various aspects of antimicrobial agents, including their differences as bacteriostatic and bactericidal, the concepts of broad and narrow spectrum, and classifications by mechanism of action (moa) and organism. It also discusses empiric antibiotic use, therapeutic use, and diagnostic methods like gram staining and polymerase chain reaction (pcr) tests.

Typology: Exams

2023/2024

Available from 03/31/2024

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NURS 5334 Antimicrobials Study Guide
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NURS 5334 Antimicrobials Study Guide

▪ Differentiate Bacteriostatic and Bacterialcidal.

  • bactericidal – directly lethal to bacteria at clinically achievable concentrations
  • bacteriostatic – slow bacterial growth but do not cause cell death ▪ What is the difference between broad spectrum and narrow spectrum?
  • Narrow – active against only a few species of microorganisms
  • Broad – active against a wide variety of microbes ▪ Which is preferred?
  • Narrow-spectrum ▪ antibiotic classifications by MOA?
  • Drugs that inhibit bacterial cell wall synthesis o Penicillins, cephalosporins
  • Drugs that increase cell membrane permeability o Amphotericin B
  • Drugs that cause lethal inhibition of bacterial protein synthesis o Aminoglycosides
  • Drugs that cause nonlethal inhibition of protein synthesis o Tetracyclines
  • Drugs that inhibit bacterial synthesis of DNA and RNA o Rifampin, metronidazole, ciprofloxacin
  • Antimetabolites o Trimethoprim, sulfonamides
  • Drugs that suppress viral replication ▪ antibiotic classifications by organism?
  • Narrow Spectrum o Gram positive cocci and gram positive bacilli ➢ Penicillin ➢ Vancomycin ➢ Erythromycin ➢ clindamycin o Gram negative aerobes ➢ Aminoglycosides – gentamicin ➢ cephalosporins o TB ➢ Isoniazid ➢ Rifampin ➢ Ethambutol ➢ pyrazinamide
  • Broad Spectrum o Gram positive cocci and gram negative bacilli ➢ Ampicillin

➢ Carbapenems ➢ Sulfonamides ➢ Fluoroquinolones - ciprofloxacin

  • Antivirals o HIV ➢ Reverse transcriptase inhibitors – zidovudine ➢ Protease inhibitors – ritonavir ➢ Fusion inhibitors – enfuvirtide ➢ Integrase inhibitors – raltegravir ➢ CCR5 antagonists - maraviroc o Influenza ➢ Adamantanes – amantadine ➢ Neuraminidase inhibitors - oseltamivir o Others ➢ Acyclovir ➢ Ribavirin ➢ Interferon alfa
  • Antifungals o Polyene antibiotics – amphotericin o Azoles – itraconazole o Echinocandins – caspofungin ▪ Bacteriostatic: ECSTaTiC
  • E rythromycin
  • C lindamycin
  • S ulfamethoxazole
  • T rimethoprim
  • a
  • T etracycline
  • i
  • C hloramphenicol ▪ Bacterialcidal: Very Finely Proficient At Cell Murder
  • V ancomycin
  • F luoroquinolones
  • P enicillin
  • A minoglycosides
  • C ephalosporins
  • M etronidazole ▪ What is empiric antibiotic use?
  • When the patient has a severe infection, we may have to initiate treatment before test results are available.
  • Under these conditions, drug selection must be based on clinical evaluation and knowledge of which microbes are most likely to cause infection at a particular site.
  • If necessary, a broad-spectrum agent can be used for initial treatment.
  • After the identity and drug sensitivity of the infecting organism have been determined, we can switch to a more selective antibiotic.
  • When conditions demand that we start therapy in the absence of laboratory data, it is essential that samples of exudates and body fluids be obtained for culture before initiation of treatment; if antibiotics are present at the time of sampling, they can suppress microbial growth in culture and can thereby confound identification. ▪ Therapeutic use?
  • The first rule of antimicrobial therapy is to match the drug with the bug. Hence, whenever possible, the infecting organism should be identified before starting treatment.
  • If treatment is begun in the absence of a definitive diagnosis, positive identification should be established as soon as possible so as to permit adjustment of the regimen to better conform with the drug sensitivity of the infecting organism.
  • The quickest, simplest, and most versatile technique for identifying microorganisms is microscopic examination of a Gram-stained preparation.
  • Samples for examination can be obtained from exudate, sputum, urine, blood, and other body fluids. The most useful samples are direct aspirates from the site of infection.
  • In some cases, only a small number of infecting organisms will be present. Under these conditions, positive identification may require that the microbes be grown out in culture.
  • As stressed previously, material for culture should be obtained before initiating treatment. the samples should not be exposed to low temperature, antiseptics, or oxygen.
  • A relatively new method, known as the polymerase chain reaction (PCR) test or nucleic acid amplification test, can detect very low titers of bacteria and viruses.
  • Testing is done by using an enzyme— either DNA polymerase or RNA polymerase— to generate thousands of copies of DNA or RNA unique to the infecting microbe.
  • As a result of this nucleic acid amplification, there is enough material for detection.
  • Microbes that we can identify with a PCR test include important bacterial pathogens (e.g., C. difficile, S. aureus, Mycobacterium tuberculosis, Neisseria gonorrhoeae, Chlamydia trachomatis, Helicobacter pylori) and important viral pathogens (e.g., HIV,

▪ Which antibiotics work by weakening the cell wall?

  • Penicillins
  • Cephalosporins
  • Carbapenems
  • Aztreonam ▪ Beta Lactam?
  • Beta-lactam ring in their structure o Penicillins o Cephalosporins o Carbapenems o Aztreonam ▪ What are the medications that react with PCN?
  • Bacteriostatic antibiotics (tetracycline)
  • Penicillin only works on bacteria that are active and growing ▪ What organisms are susceptible to PCN?
  • Gram positive bacteria
  • Gram negative cocci
  • Anaerobic bacteria
  • spirochetes ▪ What are the first generation, second generation and 3 rd^ generation cephalosporins?
  • 1 st^ – cephalexin o Highly active against gram-positive bacteria
  • 2 nd^ – cefoxitin o Enhanced activity against gram-negative bacteria
  • 3 rd^ – cefotaxime o Broad spectrum w/ increased resistance to beta-lactamases o More active against gram-negative aerobes
  • 4 th^ – cefepime o Very broad spectrum
  • 5 th^ – ceftaroline o Broad spectrum o Only cephalosporin against MRSA ▪ Why is there a cross reaction with PCN and cephalosporins?
  • cephalosporins should not be given to patients with a history of severe reactions to penicillins.
  • Because of structural similarities between penicillins and cephalosporins, ▪ What are the beta lactam antibiotics?
  • Penicillin
  • Cephalosporins
  • Acute diphtheria – Corynebacterium diptheriae
  • Pneumonia caused by M. pneumoniae ▪ How do they work?
  • Inhibits protein synthesis
  • Binds to 50S ribosomal subunit
  • Thereby blocks addition of new amino acids to the growing peptide chain ▪ Side effects?
  • GI effects
  • QT prolongation and sudden cardiac death – torsades de pointes
  • Superinfection of the bowel Linezolid ▪ What organisms are susceptible to Linezolid?
  • Has activity against VRE and MRSA
  • Bacteriostatic inhibitor of protein synthesis Telithromycin ▪ What are side effects of?
  • Injury to liver
  • Check liver enzymes regularly ▪ BB Warning?
  • In patients with myasthenia gravis, it can make muscle weakness much worse
  • Some have died from respiratory failure Dalfopristin? ▪ What bugs are susceptible? o Vancomycin resistant E. Faecium o MRA o Methicillin resistant S. epidermidis o Drug resistant S. pneumoniae ▪ BB Warning? o Should be reserved for infections that have not responded to vancoymcin ▪ What is BB warning for chloramphenicol?
  • Produces aplastic anemia o Characterized by pancytopenia and bone marrow aplasia o Reaction is usually fatal ▪ What are retapamulin and mupirocin used for?
  • Indicated for impetigo
  • Also used for clearing nostrils of MRSA