lecture 6 Flashcards

(67 cards)

1
Q

Infection

A

Most common cause of death for many people with:
- Chronic or critical illnesses
- Very young or old individuals
Major types of microorganisms include bacteria, viruses, fungi, and parasites

*There are viruses that attack and kill bacteria

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2
Q

4 types of Microorganisms

A

bacteria
viruses
fungi
parasites

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3
Q

Bacteria

A

single-celled organisms that can live INDEPENDENTLY in environment.

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4
Q

Viruses

A

tiny genetic parasites that require HOST cell to duplicate and spread.

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5
Q

Fungi

A

nonphotosynthetic creatures of single- or multi-cell structure found in environment.

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6
Q

Parasites

A

include protozoa, roundworms, flatworms, and arthropods.

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7
Q

Transmission of Infection

A

Transmission of disease requires an UNBROKEN chain of events

PATHOGENIC organism must live and reproduce in a RESERVOIR (such as a human being, an animal, or soil).

Influenza virus is an example of an organism that reproduces in a human being.

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8
Q

Transmission cycle

A

RESERVOIR (human, animal, insect, soil)

PORTAL OF EXIT (nasal mucosa, oral mucosa)

MODE OF TRANSMISSION (insect bite, nasal droplets, semen)

PORTAL OF ENTRY (nasal mucosa, oral mucosa, skin abrasion, skin puncture)

SUSCEPTIBLE VICTIM (malnourished, unimmunized, immunocompromised)

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9
Q

Controlling Infectious Disease

A

Control of infectious disease depends on breaking the chain of transmission in one or more places.

Some microorganisms have developed resistance to antibiotics

ANTIBIOTIC RESISTANCE is a major threat to the success of the management of bacterial infections.

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10
Q

Breaking Chain of Transmission

A

(you just need to break one of them)
Destroying reservoir
Blocking portal of exit
Blocking mode of transmission
Blocking portal of entry
Reducing victim’s susceptibility

(SEE IMAGE FOR EXAMPLES OF EACH)

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11
Q

Handwashing

A

Frequent handwashing with soap, friction, and warm running water is one of the most effective ways to REDUCE PATHOGENIC TRANSMISSION

  • often missed between fingers, under nails, on tops of hands (see images)

*70% alcohol also works (no more than 70% but also not too weak)

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12
Q

Antibacterial Agents

A
  • Antibiotics inhibit growth of or kill microorganisms
  • Systemic antibacterial agents can be either:

BACTERICIDAL (killing microbes)
- Penicillins, Cephalosporins, Aminoglycosides, Macrolides (high doses) and Fluroquinolones

BACTERIOSTATIC (inhibiting microbial growth)
- Penicillins, Aminoglycosides, Macrolides, Tetracyclines, and Sulfonamides

Can be dose dependent… a drug can be categorized as both

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13
Q

Antibiotics- Spectrum

A

BROAD SPECTRUM (gram +ve and gram –ve or a large variety of bacteria)
- Bacteria is not known
- There may be multiple bacteria
- Drug resistance, not responding to narrow spectrum
- Prophylaxis

*We will see mostly broad spectrum ones (narrow only kills certain types?)
*Broad Spectrum: These are antibiotics that are effective against a wide range of bacteria, both gram-positive and gram-negative. They are used when the specific bacteria causing an infection is not known or when the infection may involve multiple types of bacteria.

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14
Q

SEE ALL RED NOTES AND IMAGES IN ALL LECTURES!!!

A
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15
Q

Selecting Antibiotics

A

Factors for choosing ANTIBIOTICS:

  • Likely or specific microorganisms
  • Mechanism of action (combination therapy) - do you need more than one?
  • Bactericidal versus bacteriostatic properties - dose
  • Allergy history, age, pharmacokinetics, renal and hepatic function, pregnancy status, anatomic site of infection, defenses of host - pt history/ info
  • Antimicrobial susceptibility
  • Cost of medication
  • Adverse effects
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16
Q

Factors in antibiotic selection

A

public health
hosts
drug
pathogen
other concerns (cost)

*see image for examples of each

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17
Q

Classes of antibiotics

A

Sulfonamides
Penicillins
Cephalosporins
Macrolides
Fluoroquinolones
Aminoglycosides
Tetracyclines
Miscellaneous antibacterials

*they all kill bacteria
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18
Q

Sulfonamides

A

Primarily bacteriostatic
Broad spectrum, gram +ve and many gram –ve. Also effective on plasmodium and toxoplasma

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19
Q

Sulfonamides: Applications

A

In combination with trimethoprim, used to treat (UTIs), otitis media, sinusitis, (lower respiratory infections), inflammatory bowel disease; malaria; skin, vaginal, eye infections and rheumatic fever.

Also used topically for burns

Clinical use has been greatly restricted as result of:
- Development of resistant bacteria
- Significant side effects
- Availability of other drugs

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20
Q

Sulfonamides: Mechanism of Action

A

(Sulfonamides interfere with folic acid synthesis) by preventing addition of PABA into the folic acid by competing for the enzyme dihydropteroate synthetase.

Efficacy is enhanced when used with trimethoprim (antibiotic that interferes with the production of tetrahydrofolic acid) - bacteriocidal

Humans do not make folic acid, we get from the diet so minimal effect.

*The antibiotic looks enough like PABA that it gets in but it doesn’t form the folic acid (folic acid is needed for bacteria to grow), but it doesn’t affect us cause we get folic acid from our diet

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21
Q

Sulfonamides: Adverse effects

A

Adverse Effects

COMMON: loss of appetite, nausea, vomiting, diarrhea, fever, stomatitis, photosensitivity, dizziness, headache, insomnia, skin rashes

SERIOUS: crystalluria (forming crystals in urine?), oliguria, anuria, hematuria, life-threatening hepatitis, thrombocytopenia (low platelet)

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22
Q

Sulfonamides: Examples

A
  • sulfadiazine
  • sulfamethoxazole
  • trimethoprim (TMP) and sulfamethoxazole (SMZ)
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23
Q

Penicillins

A

May be bactericidal or bacteriostatic
Spectrum varies with subclass - Gram +ve bacteria, some gram –ve cocci

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24
Q

Penicillin 4 classes

A

(1)natural
(2)penicillinase-resistant,
(3)aminopenicillins, and
(4)extended-spectrum

Penicillin is the most widely prescribed of all antibiotics, usually in the form of amoxicillin.

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25
Penicillins: Applications
Penicillins are produced by the growth of various Penicillium species, or by other means Penicillin G is original penicillin; drug of choice for (gonorrhea), (syphilis), septicemia, anthrax, (meningitis), (pneumonia), (other respiratory infections), cellulitis, gangrene, tetanus, tonsillitis, strep throat, and preventing rheumatic fever The aminopenicillins are widely used for therapy of mild-to-severe urinary, respiratory, gastrointestinal tract, skin, bone and joint infections. Extended-spectrum penicillins are used to treat sepsis, skin infections, lower respiratory infection, UTIs, intra-abdominal infections, and infection caused by burns. Lots of resistance in penicillins due to frequent use
26
Penicillins: Mechanism of Action
β-Lactam antibiotics work by (inhibiting the formation of peptidoglycan cross-links in the bacterial cell wall) (An important building blocks of bacterial cell wall). The β-lactam moiety (functional group) of penicillin binds to the enzyme (DD transpeptidase) that links the peptidoglycan molecules in bacteria, which weakens the cell wall of the bacterium. *Penicillin binds with the enzyme making it ineffective (enzyme can’t join groups together, weakening bacterial wall so it can be disrupted easier to kill bacteria)
27
Penicillins: Adverse effects
Very safe with low toxicity; hypersensitivity in some patients COMMON: nausea, vomiting, diarrhea, black hairy tongue, thrush, vaginal yeast infection, rash, hives, changes in taste or smell. SERIOUS: neurotoxicity in very high doses
28
Penicillin: Contraindications
Penicillins may interfere with the effectiveness of birth control pills.
29
Penicillin Allergy
Allergic reaction to penicillin is an immediate life-threatening systemic reaction that typically occurs after exposure to penicillin injection. Observe patients closely for this reaction after injection. *rash
30
Penicillins: Examples
- penicillin G potassium - cloxacillin - amoxicillin - ticarcillin - mezlocillin
31
Cephalosporins
Closely related to penicillins Bactericidal (both gram +ve and some –ve bacteria). Broad spectrum Classified into 5 generations: - First-generation cephalosporins have highest activity against (gram-positive) bacteria and lowest activity against (gram-negative) bacteria Higher generations have expanded spectra for gram –ve and gram +ve bacteria 5th generation – Ceftaroline, Ceftolozane– works against MRSA
32
Cephalosporins: Applications
Often used to (reduce postoperative wound infections, skin, soft tissue, strep throat, sinus infections, ear infections, meningitis, gonorrhea, sepsis and UTIs.) Not usually first choice to combat infections because they are comparatively expensive. They are more resistant to penicillinase and most effective against several penicillin-resistant strains.
33
Cephalosporins: Mechanism of Action
Work similarly to penicillins. Affect bacterial cell wall synthesis.
34
Cephalosporins: Adverse Effects
Hypersensitivity in about 5 to 10% of patients (because they’re similar to penicillins) COMMON: pain, nausea, vomiting, glossitis, diarrhea, abdominal pain, yeast infection, thrush, dizziness, rash SERIOUS: anaphylaxis, neutropenia, nephritis
35
Cephalosporins: Examples
- cefaclor - cefadroxil - cefepime - cefixime
36
Aminoglycosides
Bacteriocidal Broad-spectrum antibiotics that affect gram-negative bacteria and a few gram +ve bacteria
37
Aminoglycosides - Applications
These antibiotics are poorly absorbed when taken by mouth, so they are (usually given intravenously or intramuscular) Large doses given orally before abdominal surgery to reduce number of intestinal bacteria. Sepsis, UTIs, skin infections, pneumonia, MRSA, (aminoglycosides are used to treat these) Otic and ophthalmic drops treat localized infection.
38
Aminoglycosides: Mechanism of Action
(Bind to 30S subunit and inhibit proofreading, resulting in faulty proteins. (RIBOSOMES)) Interference prevents bacterial cell reproduction !! Inhibit ribosomes (they interfere with ribosomes which help in protein synthesis!!) *Antibiotics get distributed throughout the body, they don’t just go to the site of infection?
39
Aminoglycosides – Adverse effects
Serious: (ototoxicity), nephrotoxicity and neuromuscular blockade Prolonged use: (superinfection) (occurs when chemical environment of body is altered by antibiotics; a new infection may be “superimposed” on an original infection) Careful dosing required in children and elderly patients.
40
Know these 4 things for ALL contraindications
Don’t give to pregnant women, don’t give to people who are allergic, be careful with people liver and kidney disease, it may react with other meds!!!
41
Aminoglycosides: Examples
- gentamicin - streptomycin - vancomycin
42
Macrolides
Bacteriostatic at normal doses; bactericidal at high doses. Equally effective for gram-positive and gram-negative bacteria.
43
Macrolides: Applications
Uses Alternative drugs in patients allergic to penicillin. COPD, tonsillitis, pneumonia, duodenal ulcers, rheumatic fever, Legionnaires’ disease, STIs, some skin infections, ear infections, traveller’s diarrhea Erythromycin is most commonly used (off-label) as a prokinetic to treat gastroparesis (delayed gastric emptying)
44
Macrolides: Mechanism of Action
Inhibit bacterial protein synthesis by binding to 50s subunit of the bacterial ribosome. (RIBOSOMES)
45
Macrolides: Adverse effects
COMMON: abdominal pain, (nausea), vomiting, (diarrhea), (tinnitus) (GI stuff) SERIOUS : hepatotoxicity (rare); (ototoxicity) at high doses; phlebitis (with IV administration), Long QT syndrome
46
Macrolides: Examples
- azithromycin - clarithromycin - erythromycin base
47
Fluoroquinolones
Bactericidal Broad spectrum, primarily active against gram-negative and some gram-positive organisms. The second-generation fluoroquinolone, demonstrates somewhat improved gram-positive activity.
48
4 generations of fluoroquinolones
quinolones fluoroquinolones fluoroquinolones fluoroquinolones?? (see image!!)
49
Fluoroquinolones: Applications
Since 1990, dominant class of antimicrobial agents. Prophylaxis, UTIs, prostatitis, STIs, pneumonia, infections of bones and joints, anthrax, GI and abdominal infections and eye infections. (learn the common ones here)
50
Fluoroquinolones: Mechanism of Action
(Interfere with DNA gyrase, an enzyme required by bacteria for synthesis of DNA.) Action inhibits cell reproduction. *Bacteria can’t untwist and replicate
51
Fluoroquinolones: Adverse Effects
Adverse Effects COMMON: nausea, vomiting, diarrhea, flatulence, abdominal discomfort, skin rashes, photosensitivity, dizziness, confusion. SEVERE: nephrotoxicity, neuropsychiatric effects, cardiac abnormalities (long QT), liver dysfunction, damaged cartilage or tendons (in children)
52
Fluoroquinolones: Examples
- ciprofloxacin - levofloxacin - gatifloxacin
53
Tetracyclines
Mainly bacteriostatic Broad-spectrum antibiotics; effective against gram-positive and gram-negative bacteria
54
Tetracyclines: Applications
Pulmonary infections, acne, cholera, brucellosis, tularemia, amebiasis, certain infections of skin, eye, lymphatic and intestinal system, infections that are spread by ticks, lice, mites, and infected animals. Alternative to penicillins for STIs, Lyme disease, anthrax, *see bed image**
55
Tetracyclines: Mechanism of Action
(Bind to bacterial ribosomes and prevent protein synthesis) Interferes with attachment of tRNA to mRNA-ribosome complex
56
Tetracyclines: Adverse effects and Contraindications
COMMON: heartburn, nausea, vomiting, diarrhea; superinfection (particularly CANDIDIASIS); graying in children’s developing teeth, photosensitivity SERIOUS: impaired bone growth in children, hepatoxicity with IV *milk is important??*
57
Tetracyclines: Examples
- chlortetracycline - tetracycline
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*NOTE* - contraindications
specific ones aren't in flashcards (see in notes)
59
miscellaneous abx
These kill bacteria but don’t fit into the groups above (don’t need to know as many of the details, know they are antibacterial substances??- antibacterial substances for miscellaneous!! chloramphenicol clindamycin spectinomycin vancomycin
60
Chloramphenicol (Chloromycetin)
Bacteriostatic; (inhibits microbial protein synthesis) by binding to the 50 S subunit of the 70 S ribosome and inhibiting the action of peptidyl transferase, thus preventing peptide bond formation. Used in the management and treatment of superficial eye infections such as bacterial conjunctivitis, and otitis externa. It has also been used for the treatment of typhoid and cholera. (Serious toxicity): bone-marrow injury, thrombocytopenia, granulocytopenia, aplastic anemia, gray-baby syndrome, cancer Use cautiously in patients with liver or kidney disease, elderly patients, and during pregnancy or lactation. (Rarely used now) !!Antibacterial substance
61
Clindamycin (Cleocin)- Lincosamides
Bacteriostatic; inhibits protein synthesis Strong antibiotic used for septicemia, intra-abdominal infections, lower respiratory infections, gynecological infections, bone and joint infections, and skin and skin structure infections. Marked toxicity, may cause diarrhea, nausea, vomiting, reduced urination. Do not use in newborn infants, pregnant or lactating women, or patients with impaired kidney or liver function, history of gastrointestinal disease, or asthma. !!Antibacterial substance
62
Spectinomycin (Trobicin)
Bacteriostatic; suppresses protein synthesis in Gram –ve bacteria. Penicillin-resistant, uncomplicated gonorrhea Safety during pregnancy, lactation, and children not established.
63
Vancomycin (Vancocin)
Bactericidal; suppresses cell-wall synthesis Methicillin-resistant staphylococci; serious infections such as osteomyelitis, endocarditis, and staphylococcal pneumonia Serious adverse effects: (ototoxicity), nephrotoxicity, and red-man syndrome Do not use in patients with previous hearing loss. !!Large structure, hard to put in a particular class
64
Miscellaneous Antibacterial Agents
CHLORAMPHENICOL CLINDAMYCIN SPECTINOMYCIN VANCOMYCIN **Broad-spectrum antibiotics are drugs that work against a wide range of bacteria, including both Gram-positive and Gram-negative bacteria. - Broad spectrum is more likely to develop resistance because they’re used more and they kill more things??
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ANTIBIOTIC RESISTANCE - IMPORTANT TO KNOW
3 and 3 3 ways bacteria can acquire resistance (transduction, conjugation, transformation) 3 way after it has acquired it that it can dispose of it so it doesn’t kill it Degrade it, alter it, pump it (SEE IMAGE) Acquisition of Antibiotic Resistance (left side of the image) Mechanisms to Neutralize Antibiotics (right side of the image) *Know the terms and what each one is!!!
66
3 Ways How Bacteria Acquire Antibiotic Resistance
Bacteria can gain resistance through three main mechanisms: TRANSFORMATION (purple): When a bacterium dies, it releases its genetic material (DNA) into the environment. Another bacterium can take up this free DNA, incorporating resistance genes into its own genome or plasmids. CONJUGATION (blue): A donor bacterium transfers a plasmid containing resistance genes directly to another bacterium via a pilus (a bridge-like structure). This is the most common way bacteria spread resistance. TRANSDUCTION (red): A virus (bacteriophage) can accidentally transfer resistance genes from one bacterium to another during infection.
67
3 Ways How Bacteria Defend Against Antibiotics
Once bacteria acquire resistance, they can neutralize antibiotics using three main strategies: DEGRADATION (red enzymes): The bacteria produce enzymes that break down the antibiotic molecules before they can act. ALTERATION (green enzymes): Some enzymes chemically modify the antibiotic, making it ineffective. EFFLUX PUMPS: Bacteria use specialized pumps to expel antibiotics before they reach lethal concentrations inside the cell.