Chapter 38: Antibiotics Part 1 pg609 Flashcards

1
Q

The patient usually manifests some

of the following classic signs and symptoms of infection:

A

fever,
chills, sweats, redness, pain and swelling, fatigue, weight loss,
increased white blood cell (WBC) count, and the formation of
pus.

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2
Q

methicillin-resistant Staphylococcus aureus

A

MRSA

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3
Q

disinfectant

A

kill organisms and is used only on nonliving objects

cidal agents

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4
Q

antiseptic

A

applied to living tissue
inhibits the growth of microorganisms
static agents

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5
Q

empiric therapy

A

The antibiotic selected is one that can
best kill the microorganisms known to be the most common
causes of the infection

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6
Q

definitive therapy

A

Once the results of culture and sensitivity
testing are available (usually in 48 to 72 hours), the antibiotic
therapy is then tailored to treat the identified organism by using
the most narrow-spectrum, least toxic drug based on sensitivity
results.

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7
Q

subtherapeutic when these signs

and symptoms do not improve. This can result from

A

use of an incorrect route of drug administration, inadequate drainage of
an abscess, poor drug penetration to the infected area, insufficient
serum levels of the drug, or bacterial resistance to the
drug.

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8
Q

Relatively minor adverse drug

reactions such as

A

nausea, vomiting, and diarrhea are quite common
with antibiotic therapy and are usually not severe enough
to require drug discontinuation

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9
Q

Superinfection can occur when antibiotics

A

reduce or completely
eliminate the normal bacterial flora, which consist of
certain bacteria and fungi that are needed to maintain normal
function in various organs

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10
Q

pseudomembranous colitis or simply C.

difficile infection. This happens because antibiotics

A

disrupt the
normal gut flora and can cause an overgrowth of Clostridium
difficile. The most common symptoms of C. difficile colitis are
watery diarrhea, abdominal pain, and fever

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11
Q

One of the more common

food-drug interactions

A

between milk or cheese and tetracycline,

which results in decreased GI absorption of tetracycline.

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12
Q

An example of a drug-drug interaction is that between

A

quinolone antibiotics and antacids or multivitamins with iron,
which leads to decreased absorption of quinolones

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13
Q

Drugs that cause development abnormalities in the fetus

are called

A

teratogens. Their use by pregnant women can result

in birth defects

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14
Q

The administration of antibiotics such as sulfonamides,

nitrofurantoin, and dapsone to a person with….

A

G6PD deficiency

may result in the hemolysis, or destruction, of red blood cells

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15
Q

Patients who are slow acetylators have a

A

physiologic makeup
that causes certain drugs to be metabolized more slowly than
usual in a chemical step known as acetylation. This can lead to
toxicity from drug accumulation

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16
Q

Antibiotics are classified into broad categories based on their
chemical structure. The common categories include

A

sulfonamides,
penicillins, cephalosporins, macrolides, quinolones,
aminoglycosides, and tetracyclines.

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17
Q

The four most common

mechanisms of antibiotic action are:

A

(1) interference with
bacterial cell wall synthesis, (2) interference with protein synthesis,
(3) interference with replication of nucleic acids (deoxyribonucleic
acid [DNA] and ribonucleic acid [RNA]), and
(4) antimetabolite action that disrupts critical metabolic reactions
inside the bacterial cell.

18
Q

Sulfonamides p616

A
antimetabolites.
bacteriostatic
antibiotics
preventing bacterial synthesis of folic acid
Photosensitivity reactions
19
Q

Sulfites are commonly used

A

as preservatives in

everything from wine to food to injectable drugs

20
Q

The use of sulfonamides is also contraindicated in…

A

pregnant women at term and in infants younger than

2 months of age

21
Q

named because of the beta-lactam ring that is part

of their chemical structure

A

includes four major subclasses: penicillins, cephalosporins,
carbapenems, and monobactams

they inhibit the synthesis of
the bacterial peptidoglycan cell wall.

22
Q

penicillins

A

bactericidal antibiotics

classified as pregnancy category B drugs

23
Q

enzymes capable of destroying penicillins

A

beta-lactamases
The enzyme can break the chemical bond
between the carbon (C) and nitrogen (N) atoms in the structure
of the beta-lactam ring

24
Q

examples of currently available combinations of a

penicillin and a beta-lactamase inhibitor

A
  • ampicillin/sulbactam (Unasyn)
  • amoxicillin/clavulanic acid (Augmentin)
  • ticarcillin/clavulanic acid (Timentin)
  • piperacillin/tazobactam (Zosyn)
25
Q

extended-spectrum penicillins are used to

A

treat many hospital-associated infections, including pneumonia,
intraabdominal infections, and sepsis.

26
Q

patients with a history of throat swelling or

hives from penicillin should not receive

A

cephalosporins

27
Q
The intravenous
(IV) formulations of some penicillins contain
A

large amounts of

sodium and/or potassium

28
Q

Cephalosporins

A

semisynthetic antibiotics
structurally and pharmacologically
related to the penicillins.
bactericidal

29
Q

Cefoxitin and cefotetan are often

referred to as cephamycins and have better coverage against

A

SECOND-GENERATION
various anaerobic bacteria such as Bacteroides fragilis, Peptostreptococcus
spp., and Clostridium spp

30
Q

Cefuroxime axetil

oral form only

A

is a prodrug. It has little antibacterial
activity until it is hydrolyzed in the liver to its active
cefuroxime form. oral form only

31
Q

cephalosporins that is indicated

for the treatment of meningitis

A

Ceftriaxone (Rocephin)
unique in that it is metabolized in the intestine after biliary
excretion

32
Q

Cefaroline (Teflaro) is the newest cephalosporin

A

only

cephalosporin that treats MRSA

33
Q

have the broadest antibacterial action of any

antibiotics to date.

A

carbapenems, bactericidal.

34
Q

Carbapenems must

be infused over 60 minutes

A

they are often reserved for complicated

body cavity and connective tissue infections

35
Q

Imipenem/cilastatin is indicated for the treatment of

A

bone,
joint, skin, and soft-tissue infections; bacterial endocarditis
caused by S. aureus; intraabdominal bacterial infections;
pneumonia; UTIs and pelvic infections; and bacterial septicemia
caused by susceptible bacterial organisms

36
Q

Aztreonam (Azactam) is the only monobactam antibiotic

A

synthetic beta-lactam antibiotic that is
primarily active against aerobic gram-negative bacteria, including
E. coli, Klebsiella spp., and Pseudomonas spp.

bacteriostatic.

37
Q

There are three macrolide antibiotics

A

azithromycin, clarithromycin, and erythromycin

38
Q

Macrolide antibiotics are bacteriostatic drugs that inhibit protein
synthesis by binding reversibly to the 50S ribosomal subunits of
susceptible microorganisms.

A

bacteriostatic; however, in

high enough concentrations they may be bactericidal

39
Q

Fidaxomicin

(Dificid) is the newest macrolide antibiotic

A

indicated
only for the treatment of Clostridium difficle–
associated diarrhea

40
Q

For drugs metabolized in the

liver, drug interactions arise from

A

competition between the different
drugs for metabolic enzymes, specifically the enzymes
known as the cytochrome P-450 complex

41
Q

Examples of some especially common drugs that compete for

hepatic metabolism with the macrolides

A

are carbamazepine,
cyclosporine, theophylline, and warfarin.
When macrolides
are given with these drugs, the results are enhanced effects and
possible toxicity of the latter drugs, and patients must be monitored