Antibiotic Drugs Flashcards

1
Q

What are antibacterial drugs?

A

Antibacterial drugs are derived from bacteria or molds or are synthesized de novo. Technically, “antibiotic” refers only to antimicrobials derived from bacteria or molds but is often (including in THE MANUAL) used synonymously with “antibacterial drug.”

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2
Q

What are Bacteria?

A
  • Also known as prokaryotes which are single-celled organisms that lack a true nucleus and nuclear membrane
  • It has a cell wall, that determines its shape
  • Hans Christian Gram devised a method to classify bacteria using the Gram-stain method
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3
Q

How to differentiate Antiseptics and Disinfectants?

A

Antiseptic: / Disinfectants:
where it can be used: Living tissue / Nonliving objects
potency: Lower / Higher
Activity against organism: Primarily inhibits growth (Bacteriostatic) / Kills (Bactericidal)

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4
Q

How do Antibacterial drugs?

A
  • Antibacterial drugs penetrate the bacterial cell wall and have an affinity for the bacteria’s binding sites
  • The more time the drug remains bound, the longer the effect of the antibacterial action
  • MEC (Minimum Effective Concentration) – minimum amount of antibacterial drug to halt the growth of microorganisms
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5
Q

What are the 5 mechanisms of Antibacterial drugs’ action?

A

Five Mechanisms of Antibacterial Action:
1) inhibition of bacterial cell-wall synthesis;
2) alteration of membrane permeability;
3) inhibition of protein synthesis;
4) inhibition of the synthesis of bacterial RNA and DNA;
5) interference with metabolism within the cell

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6
Q

How do antibacterial drugs effects bacteria?

A
  • When bacteria is sensitive to the drug = the pathogen can be inhibited or destroyed
  • When bacteria is resistant to the drug = the pathogen will continue to grow despite administration
    • Types of Resistance:
      1) inherent – occurs without previous exposure to the drug;
      2) acquired – caused by prior exposure to the antibacterial
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7
Q

General Adverse Reactions to Antibacterial Drugs

A

Type: - Constraints
Allergy or hypersensitivity
- Allergic reactions to drugs may be mild or severe. Examples of mild reactions are rash, pruritus, and hives. An example of a severe response is anaphylactic shock, which results in vascular collapse, laryngeal edema, bronchospasm, and cardiac arrest. A severe allergic reaction generally occurs within 20 minutes, and shortness of breath is often the first symptom of anaphylaxis. Mild allergic reaction is treated with an antihistamine, whereas anaphylaxis requires treatment with epinephrine, bronchodilators, and antihistamines.
Superinfection
- Superinfection is a secondary infection that occurs when the normal microbial flora of the body is disturbed during antibiotic therapy. Superinfections can occur in the mouth, respiratory tract, intestine, genitourinary tract, and skin. Fungal infections frequently result in superinfections, although bacterial organisms (e.g., Proteus, Pseudomonas, Staphylococcus) may be the offending microorganisms. Superinfections rarely develop when the drug is administered for less than 1 week, and they occur more commonly with the use of broad-spectrum antibiotics. For fungal infection of the mouth, nystatin is frequently used.
Organ toxicity
- The liver and kidneys are involved in drug metabolism and excretion, and antibacterials may result in damage to these organs. For example, aminoglycosides can be nephrotoxic and ototoxic.

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8
Q

What are the Antibiotic Combinations?

A
  • ADDITIVE EFFECT - equal to the sum of the effects of two antibiotics
  • POTENTIATIVE EFFECT – occurs when one antibiotic increases the effectiveness of the 2nd drug
  • ANTAGONISTIC EFFECT – when two drugs are used together, the desired effect may be greatly reduced
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9
Q

How to differentiate between Narrow and broad spectrum Antibacterial drugs?

A
  • NARROW SPECTRUM
    – primarily effective against one type of organism (selective)
    – Targetted treatment for documented infections
  • BROAD SPECTRUM
    – effective against gram-positive and gram-negative organisms
    – Empiric treatment of non-documented infections
    – Rish for selection of resistance
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10
Q

What are Empiric therapy, Definitive Therapy, Subtherapeutic, and Superinfection?

A
  • EMPIRIC THERAPY – when a drug selected is known to be the best drug that can kill the MO
  • DEFINITIVE THERAPY – once the MO is identified in the lab, the antibiotic therapy is tailored by using the most narrow-spectrum, least toxic drug based on C&S results
  • SUBTHERAPEUTIC – when signs and symptoms do not improve
  • SUPERINFECTION – occurs when the antibiotics reduce or completely eliminate the normal bacterial flora
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11
Q

How would health professionals select antimicrobials?

A

Laboratory testing is performed on body fluids (blood, urine, sputum, wound drainage) to determine the MOs causing the infection:
- Gram stain – aspirate of the body fluid is examined under the microscope

 - Culture – aspirated is applied to a medium where they are grown for several days

 - Sensitivity – used for organisms where resistance is common, to test for sensitivity of the organisms to various antimicrobials
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12
Q

What are the different factors the health professionals would consider for the patient or host?

A

1.) Immune Systems
2.) Site of Injection
3.) Age
4.) Pregnancy

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13
Q

How to use prophylactic drugs?

A
  • Indications:
    1. Prevention of infection for clients with GIT, Cardio, Orthopedic or Gynecologic surgeries
    2. Prevention of STI’s following sexual exposure
  • Limit prophylactic use to patients with;
    1. Prosthetic heart valves
    2. Recurring urinary tract infections
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14
Q

What could be some preventive measures for the nurse to do to protect the patient and the nurse?

A
  1. Perform hand hygiene before and after client contact
  2. Recognize invasive procedures that increase the chance of infection
  3. Encourage health measures by maintaining up-to-date immunization status
  4. Use infection control procedures to prevent transmission
  5. Evaluate the effectiveness of the treatment
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15
Q

What are some drugs used for affecting Bacterial cell walls?

A

1.Penicillin
2.Cephalosporins
3.Other Inhibitors

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16
Q

What are beta-lactam Antibiotics?

A
  • The drugs contain beta-lactam rings in their structures that include: penicillin, cephalosporins, carbapenems and monobactams that inhibit the synthesis of bacterial peptidoglycan cell wall
  • Some bacterial strains produce an enzyme, BETALACTAMASE which provides resistance by destroying the beta-lactam ring in the drugs
  • Thus beta-lactam drugs need an additional drug called, BETA-LACTAMASE INHIBITOR to make the drug more powerful than those MOs
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17
Q

facts about Penicillin

A
  • Drug of choice for gram-positive cocci such as Streptococcus pneumoniae, viridans, and pyogenes
  • Drug of choice for meningitis caused by gram-negative cocci, Neisseria meningitides
  • Drug of choice for syphilis caused by Spirochete treponema pallidum
  • Extended Spectrum is effective against Pseudomonas, Enterobacter, proteus, Bacteroides, klebsiella
  • Prophylaxis against bacterial endocarditis prior to dental and other procedures
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18
Q

What are some complications with using Penicillin? What are your nursing interventions?

A
  1. Allergies/anaphylaxis
    - Interview clients for prior allergies.
    - Advise clients to wear an allergy identification bracelet.
    - Observe clients for 30 min following the administration of parenteral penicillin.
  2. Renal Impairment
    - Monitor kidney function.
    - Monitor I&O.
  3. Hyperkalemia/dysrhythmias (high doses of penicillin G potassium) and Hypernatremia (IV ticarcillin)
    - Monitor the cardiac status and electrolyte levels.
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19
Q

what are some contraindications and precautions before using Penicillin

A
  • Penicillins are contraindicated for clients who have a severe history of allergies
  • Use cautiously in clients who have or are at risk for kidney dysfunction
  • Penicillin Skin Test is done before administration
  • Pregnancy Category B
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20
Q

What to expect when administering penicillin?

A

= Most as excreted via the kidneys thus assessment of BUN and Creatinine for the renal function is important
= Common adverse reaction includes: hypersensitivity and superinfection (occurrence of secondary infection when the flora of the body are disturbed); GI Distress (anorexia, N&V, diarrhea)
= W/O for interactions with potassium supplements and use of aminoglycosides
= W/O Clostridium difficile- associated diarrhea (superinfection)
= Teach patients to take the entire prescribed penicillin product to prevent drug resistance

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21
Q

What are Cephalosporins and what are the different generations of cephalosporins?

A

From a fungus discovered in seawater, its molecules are chemically altered and semi-synthetic medications are produced

Generation and Activity
First - Effective mostly against gram-positive bacteria (streptococci and most staphylococci) and some gram-negative bacteria (Escherichia coli and species of Klebsiella, Proteus, Salmonella, and Shigella)
Second - Same effectiveness as the first generation but with a broader spectrum against other gram-negative bacteria such as Haemophilus influenza, Neisseria gonorrhoeae and N. meningitides, Enterobacter species, and several anaerobic organisms
Third - Same effectiveness as first and second generations and also effective against gram-negative bacteria (Pseudomonas aeruginosa and Serratia and Acinetobacter species) but with increased resistance to destruction by beta-lactamases
Fourth - Similar to third-generation drugs and highly resistant to most beta-lactamase bacteria with broad-spectrum antibacterial activity and good penetration to cerebrospinal fluid; effective against E. coli, P. aeruginosa, and Klebsiella, Proteus, and Streptococcus species, and certain staphylococci
Fifth - Similar characteristics of third and fourth generations, also broad spectrum, and the only cephalosporins effective against methicillin-resistant Staphylococcus aureus (MRSA)

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22
Q

The different drugs based on the generation of cephalosporins

A

First generation:
IV: Cefazolin, Cephradine
PO: Cefadroxil, Cephalexin, Cephradine

Second generation:
IV: Cefoxitin, Cefuroxime, Cefotetan, Locacarbel
PO: Cefactor, Cefuroxime Axetil, cefprozil

Third generation:
IV: Cefotaxime, Ceftizoxime, Ceftriaxone, Ceftazidime
PO: Cefpodoxime, Ceftibuten, Cefdinir

Fourth generation:
IV: Cefepime

Fifth generation:
IV: Ceftaroline

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23
Q

Cephalosporins drug interactions with other drugs

A
  1. Ethanol (alcohol)
    Mechanism: Accumulation of acetaldehyde metabolite of ethanol
    Result: Acute alcohol intolerance (disulfiram-like reaction) after drinking alcoholic
    beverages within 72 hr of taking cefotetan. Symptoms include stomach cramps, nausea, vomiting, diaphoresis, pruritus, headache, and hypotension.
  2. Antacids, iron
    Mechanism: Decreased absorption of certain oral cephalosporins (cefdinir, cefditoren)
    Result: Decreased effectiveness of the drug
  3. probenecid
    Mechanism: Decreased renal excretion
    Result: Increased cephalosporin levels
  4. Oral contraceptives (OCs)
    Mechanism: Enhanced OC metabolism
    Result: Increased risk for unintended pregnancy
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23
Q

What are some complications with using Cephalosporins? What are your nursing interventions?

A

A.) Allergic/hypersensitivity/anaphylaxis
› If indications of allergy appear (urticaria, rash, hypotension, and/or dyspnea) stop cephalosporin immediately, and notify the provider.
A.2.)Possible cross-sensitivity to penicillin
› Question the client carefully regarding past history of allergy to penicillin or another cephalosporin, and notify the provider if present.
B.) Bleeding tendencies with the use of cefotetan and ceftriaxone
› Avoid use in clients who have bleeding disorders and those taking anticoagulants.
› Observe clients for signs of bleeding.
› Monitor prothrombin time and bleeding time. Abnormal levels can require discontinuation of the medication.
› Administer parenteral vitamin K.
C.) Thrombophlebitis with IV infusion
› Rotate injection sites.
› Administer as a diluted intermittent infusion or, if a bolus dose is prescribed, administer slowly over 3 to 5 min and in a dilute solution.
D.) Pain with IM injection
› Administer IM injection deep in large muscle mass.
E.)Antibiotic-associated pseudomembranous colitis
› Observe clients for diarrhea and notify the provider.
› Medication should be discontinued.

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24
Q

Drug Interactions of Cephalosporins and nursing interventions and nursing administration

A

A.) Disulfiram reaction (intolerance to alcohol) occurs with the combined use of cefotetan, cefazolin, cefoperazone, and alcohol
= Instruct clients not to consume alcohol while taking these cephalosporins
B.) Probenecid delays renal excretion
= Monitor I&O

Nursing administration:
* Instruct clients to complete the prescribed course of therapy, even though symptoms can resolve before the full course of antimicrobial treatment is completed.
* Advise clients to take oral cephalosporins with food.
* Instruct clients to store oral cephalosporin suspensions in a refrigerator.

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25
Q

What is Carbapenemss?

A
  • Have the broadest antibacterial actions of any antibiotics; Bactericidal and inhibit cell wall synthesis and are often reserved for complicated body cavity and connective tissue infections
  • W/O for drug-induced seizure activity
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26
Q

the complications and interactions of Carbapenems

A

A.) Allergy/hypersensitivity - Possible cross-sensitivity to penicillin or cephalosporins
> Monitor clients for indications of allergic reactions, such as rashes or pruritus.
> Question clients carefully regarding past history of allergy to penicillin or other cephalosporin and notify the provider if present.

B.) Gastrointestinal symptoms (nausea, vomiting, diarrhea)
> Observe clients for manifestations and notify the provider if they occur.
> Monitor I&O.

C.) Suprainfection
> Monitor for indications of colitis (diarrhea, oral thrush, and/or vaginal yeast infection).

Interactions
MEDICATION/FOOD INTERACTIONS
> Imipenem-cilastatin can reduce blood levels of valproic acid (Depakote). Breakthrough seizures are possible.
NURSING INTERVENTIONS/CLIENT EDUCATION
> Avoid using together. If concurrent use is unavoidable, monitor for increased seizure activity.

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27
Q

ANTIBIOTICS AFFECTING PROTEIN SYNTHESIS

A
  1. Tetracyclines
  2. Macrolides
  3. Aminoglycosides
28
Q

About Tetracyclines:

A
  • Binds to 30s ribosomal unit of the MOs
  • Binds to Ca, Mg, and Al metallic ions to form complexes which reduces the absorption of the drug when administered together with milk, antacids, and iron salts
  • Not given to children below 8 years old, pregnant and lactating mothers d/t significant tooth discoloration of the child
  • Drug of choice for Rickettsia, Chlamydia, and Mycoplasma, spirochetes such as syphilis and Lyme
  • CI: pregnancy category D, use cautiously for patients with liver and renal disease
  • Should be taken on an empty stomach with a full glass of water
  • Advise patients not to take tetracyclines before lying down d/t to the increased risk of esophageal ulceration
29
Q

Drug interactions of Tetracyclines with other medication or food and Nursing intervention:

A

Medication/food interaction - Nursing Intervention
A.) Interaction with milk products, calcium or iron supplements, laxatives containing magnesium such as magnesium hydroxide (Milk of Magnesia), and antacids causes the formation of nonabsorbable chelates, thus reducing the absorption of tetracycline.
* Tetracycline should be taken on an empty stomach with a full glass of water.
* Minocycline may be taken with meals.
* Administer tetracyclines at least 1 hr before and 2 hr after taking food and supplements containing calcium and magnesium.

B.) Tetracycline decreases the efficacy of oral contraceptives.
* Advise the client to use an alternative form of birth control.

C.) Both minocycline and doxycycline increase the risk of digoxin toxicity.
* Monitor digoxin level carefully if taking concurrently.

30
Q

What is Macrolides?

A
  • Bacteriostatic but with high enough concentrations may be bactericidal via binding with 50s ribosomes of MOs
  • Most common macrolides are:
    1) Azithromycin,
    2) Clarithromycin,
    3) Erythromycin
  • Erythromycin is not given IM usually
    > DOC for LEGIONNAIRES CAMP on My Border (Legionella, Campylobacter, Mycoplasma, Bordetella )
    > Prescribed when patients are allergic to penicillins
    > S/E: & A/E GI Distress, tinnitus, superinfection, ototoxicity, and hepatotoxicity
  • Drug Interactions:
    > compete with drugs in hepatic metabolism (cyclosporine, theophylline, warfarin)
    > Reduce. Efficacy of oral contraceptives
    > Concurrent use with simvastatin or lovastatin d/t cytochrome P-450 complex (enzyme in the liver)

Macrolides drug:
Azithromycin:
> Administer oral preparation on an empty stomach (1hr before or 2 hrs after) with a full glass of water unless with GI distress
> Azithromycin may be administered with food
> Monitor PT/INR of clients who take warfarin and liver function for patients\ taking the medication for more than 2 weeks

31
Q

Complications with Macrolides and nursing interventions for it

A

A.) GI discomfort (nausea, vomiting, epigastric pain)
> Administer erythromycin with meals.
> Observe for GI symptoms and notify the provider.

B.) Prolonged OT interval causing dysrhythmias and possible sudden cardiac death
> Use in clients who have prolonged QT intervals is not recommended
> Avoid concurrent use with medications that affect hepatic drug-metabolizing enzymes.

C.) Ototoxicity with high-dose therapy
> Monitor for hearing loss, vertigo, and ringing in the ear. Notify the provider if these occur.

32
Q

What is Aminoglycosides?

A
  • Bactericidal and potent thus DOC for virulent infections through binding with the 30S ribosome
  • Have a post-antibiotic effect – continued bacterial growth suppression after antibiotic exposure
  • Not given orally d/t poor absorption (except neomycin)
  • Most common aminoglycosides are:
    1) amikacin,
    2) gentamicin,
    3) tobramycin
  • High nephrotoxicity and ototoxicity risk so maintained on TDM
33
Q

Complications of Aminoglycosides and nursing interventions for those situations

A

A.) Ototoxicity — cochlear damage (hearing loss) and vestibular damage (loss of balance)
- Monitor clients for tinnitus (ringing in the ears), headache, hearing loss, nausea, dizziness, and vertigo.
- Instruct clients to notify the provider if tinnitus, hearing loss, or headaches occur.
- Stop aminoglycoside if manifestations occur. Do baseline audiometric studies (hearing test).

B.) Nephrotoxicity related to high total cumulative dose resulting in acute tubular necrosis (proteinuria, casts in the urine, dilute urine, elevated BUN, creatinine levels)
- Monitor I&O, BUN, and creatinine levels.
- Report hematuria and/or cloudy urine

C.) Intensified neuromuscular blockade resulting in respiratory depression or muscle weakness
- Closely monitor use in clients who have myasthenia gravis, clients taking skeletal muscle relaxants, and clients receiving general anesthetics.

D.) Hypersensitivity (rash, pruritus, paresthesia of hands and feet, and urticaria)
- Monitor clients for allergic effects.

34
Q

Precautions with Aminoglycosides

A
  • Use cautiously in clients with kidney impairment, premature and full-term neonates
  • Pregnancy Category C-D- with several case reports of total irreversible bilateral congenital deafness
  • Duration of therapy is as short as possible
  • Concurrent use with loop diuretics and other antibiotics may increase the risk of ototoxicity, may reduce vitamin K in the gut
35
Q

Drugs for Urinary tract Infections

A
  1. SULFONAMIDES
  2. TRIMETHOPRIM
  3. FLUOROQUINOLONES
  4. ANTISEPTICS
36
Q

About Quinolones and some drugs of QUinolones

A
  • Destroy bacteria by altering their DNA, does not affect human DNA
  • Very potent bactericidal broad-spectrum antibiotics
  • Suitable for treating complicated UTIs, but can be given to patients with respiratory, skin, GIT, and, bone infections
  • DOC for prevention of anthrax
  • Cardiac effect – prolongs QT interval leading to dangerous arrhythmias
  • Avoid concurrent use with amiodarone, disopyramide, antacids, calcium, magnesium, zinc, dairy products and nitrofurantoin
  • Use in caution for patients younger than 18y/o d/t achilles tendon rupture (except Ciprofloxacin)

GENERIC NAME (TRADE NAME, YEAR OF FDA APPROVAL) /ANTIBACTERIAL SPECTRUM / COMMON INDICATIONS
1. norfloxacin (Noroxin, 1986) /
Extensive gram-negative and selected gram-positive coverage
/ Urinary tract infections, prostatitis, STIs

  1. ciprofloxacin (Cipro. 1987) /
    Comparable to that of norfloxacin /
    Anthrax (inhalational, post-exposure); respiratory, skin, urinary tract, prostate, intraabdominal, GI, bone, and joint infections; typhoid fever; selected nosocomial pneumonia
  2. levofloxacin (Levaquin, 19961 /
    Comparable to that of ciprofloxacin with better gram-positive coverage /
    Respiratory and urinary tract infections; prophylaxis in various transrectal and transurethral prostate surgical procedures
  3. moxifloxacin (Avelox, 1999) /
    Comparable to that of levofloxacin plus anaerobic coverage /
    Respiratory and skin infections; CAP caused by PRSP; anaerobic infections
  4. gemifloxacin (Factive, 2004) /
    Comparable to ciprofloxacin /
    CAP, exacerbation of COPD
37
Q

Complications of Quinolones and nursing interventions for those situations

A

A.) GI discomfort (nausea, vomiting, diarrhea)
- Administer medications accordingly.

B.) Achilles tendon rupture
- Instruct the client to observe for clinical manifestations of pain, swelling, and redness at the Achilles tendon site, and to notify the provider if they occur.
- Ciprofloxacin should be discontinued. The client should not exercise until the inflammation subsides.

C.) Suprainfection (thrush, vaginal yeast infection)
- Instruct the client to observe for clinical manifestations of yeast infection (cottage cheese/curd-like lesions on the mouth and genital area) and to notify the provider if they occur.

D.) Phototoxicity (severe sunburn) when exposed to direct and indirect sunlight, and sunlamps even when sunscreen is applied
- Instruct the client to avoid sun exposure and to wear protective clothing and sunscreen at all times.
- Discontinue immediately (ciprofloxacin and other fluoroquinolones) if phototoxicity occurs.

38
Q

SULFONAMIDES AND TRIMETHOPRIM

A
  • E.g: Sulfamethoxazole-Trimethoprim (SMZ-TMP)
  • Inhibit bacterial growth by preventing the synthesis of folic acid
  • Treatment of UTI caused by: E. Coli, Klebsiella, Enterobacter, Neisseria
  • C/I: folic acid deficiency, with renal dysfunction, older than 65y/o taking ACEi and ARBs for risk of hyperkalemia
  • Take on an empty stomach with a full glass of water
38
Q

The adverse effect of Sulfonamides and Trimethoprim and nursing interventions in those events

A

A.) Hypersensitivity, including Stevens-Johnson syndrome
> Do not administer Sulfamethoxazole-Trimethoprim(SMZ-TMP) to a client who has allergies
o Sulfonamides (sulfa)
o Thiazide diuretics (hydrochlorothiazide [Microzide])
o Sulfonylurea-type oral hypoglycemia (tolbutamide [Orinasel)
o Loop diuretics (furosemide [Lasix])

  • Stop Sulfamethoxazole-Trimethoprim(SMZ-TMP) at the first indication of hypersensitivity, such as rash.

B.) Blood dyscrasias (hemolytic anemia, agranulocytosis, leukopenia, thrombocytopenia, aplastic anemia)
* Draw the client’s baseline and periodic CBC levels to detect any hematologic disorders.
* Observe for bleeding episodes, sore throat, or pallor.
* If the above symptoms occur, instruct the client to notify the provider.

C.) Crystalluria (crystalline aggregates in the kidneys, ureters, and bladder causing irritation and obstruction that leads to acute kidney injury)
* Maintain adequate oral fluid intake.
* Instruct the client to drink for 2 to 3 L/day.
* Monitor urine output of at least 1,200 mL each day.

D.) Kernicterus (jaundice, increased bilirubin levels, which is neurotoxic to infants)
* Avoid administering SMZ-TMP to women who are pregnant near term or breastfeeding, and infants younger than 2 months (risk of kernicterus).
* Avoid administering SMZ-TMP during the first trimester to prevent birth defects in the fetus.

E.) Photosensitivity
* Advise the client to avoid prolonged exposure to sunlight, use sunscreen, and wear appropriate protective clothing.

F.) Sulfonamides can increase the effects of warfarin (Coumadin), phenytoin (Dilantin), sulfonylurea oral hypoglycemics, and tolbutamide (Orinase).
* Reduced dosages of these medications may be required during SMZ-TMP therapy. * Monitor laboratory levels (prothrombin time and INR, phenytoin levels, and blood glucose levels).

39
Q

Drugs for Antiseptics, the procedure before administration, and the nursing process:

A
  • E.g. Nitrofurantoin, nitrofurantoin microcrystals, methenamine
  • Broad spectrum antiseptic through damaging MO’s DNA
  • Indicated for acute UTI and prophylaxis of recurrent UTI
  • Contraindicated for patients with renal dysfunction = increased toxicity
  • Urine may have brownish discoloration, which may cause tooth staining

> ASSESSMENT BEFORE ADM:
* History of hypersensitivity to medications
* Determine age, weight, V/S
* Examine Labs such as BUN, Creatinine, AST and ALT, cardiac function, CBC, platelet, and clotting
* Monitor I&O (NV: 30mL/hr or 600mL/day)

Nursing Process:
> Nursing Diagnoses:

  1. Noncompliance with the treatment regimen related to lack of information and/or inability to pay for and obtain the necessary medication
  2. Deficient knowledge related to lack of information about the disease process and the medication regimen
  3. Risk for infection related to the patient’s possible development of a compromised immune status (due to using of sulfonamides)

> Nursing Planning

  1. Patient remains compliant with the antibiotic therapy regimen for the full duration of treatment.
  2. Patient demonstrates an increase in knowledge and information about the disease process and related drug therapy.
  3. Patient maintains homeostasis and a healthy immune system and is free from risk for infection.

> IMPLEMENTATION

  1. Give oral medications within the recommended time frames and fluids as indicated
  2. All medicated are to be taken as ordered and in full to maintain effective blood levels
  3. Doses are not doubled up or omitted
  4. Not given at the same time as antacids, calcium, iron, laxatives, and some anti-lipemic medications
  5. Herbal products may be used only if there are no interactions
  6. Continue checking for hypersensitivity until 72h
  7. withhold medications immediately when signs of hypersensitivity is observed
40
Q

MYCOBACTERIAL, FUNGAL AND PARASITIC AGENTS

A
  1. Antimycobacterial
  2. Antiprotozoal
  3. Antifungal
40
Q

ANTITUBERCULOSIS MEDICATIONS/ ANTI MYCOBACTERIUM

A
  • Drugs used to treat infections caused by Mycobacterium bacterial species
  • TUBERCULOSIS – characterized by granulomas in the lungs from the accumulation of inflammatory cells with a cheesy caseated consistency

Types:
> Mycobacterium tuberculosis – most common, present as a pulmonary disease
> Mycobacterium leprae – causing leprosy, observed symptoms on the skin and neurological system
>Mycobacterium Avium Complex (M. avium-intracellulare) – often with GI symptoms

  • MULTI-DRUG RESISTANT TB – tuberculosis that demonstrates
    resistance to two or more drugs
41
Q

Classification based on drug susceptibility testing

A

a.) Monoresistant-TB - Resistance to one first-line anti-TB drug only.
b.) Polydrug-resistant TB - Resistance to more than one first-line anti-TB drug (other than both Isoniazid and Rifampicin).
c.) Multidrug-resistant TB (MDR-TB) - Resistance to at least both Isoniazid and Rifampicin.
d.) Extensively drug-resistant TB (XDR-TB) - Resistance to any fluoroquinolone and to at least one of three second-line injectable drugs (Capreomycin, Kanamycin, and Amikacin), in addition to multidrug resistance.
e.) Rifampicin-resistant TB (RR-TB) - Resistance to Rifampicin detected using phenotypic or genotypic methods, with or without resistance to other anti-TB drugs. It includes any resistance to Rifampicin, whether monoresistance, multidrug resistance, polydrug resistance, or extensive drug resistance.

42
Q

What is RIPES and what Multidrug-resistant TB (MDR TB) Medication?

A

R - RIFAMPICIN
I - ISONIAZID
P - PYRAZINAMIDE
E - ETHAMBUTOL
S - STREPTOMYCIN

MDR-TB medication:
1. KANAMYCIN
2. LEVOFLOXACIN
3. PROTHIONAMIDE
4. CYCLOSERINE

43
Q

Fungal Infections

A

Mycosis- a term used to describe a fungal infection
> Four types include
1. Systemic
2. Cutaneous
3. Subcutaneous
4. Superficial

  • Fungi that cause integumentary infections are called dermatophytes
  • Commonly, patients with weaker immune systems such as organ transplant recipients, taking immunosuppressive therapy, cancer, and AIDS patients are at risk for mycosis
  • Topical Antifungal drugs are commonly used and often administered without prescription for oral and vaginal mycoses
  • Polyenes (Amphotericin B, Nystatin) – binds to sterols in the cell membranes of the fungi
  • Imidazoles (Ketoconazole) & Triazoles ( Fluconazole, Itraconazole, Voriconazole, Posaconazole) – combat rapidly growing fungi and inhibits fungal cell P450 enzymes
  • Echinocandins (Caspofungin, Micafungin, Anidulafungin) - prevent the synthesis of glucans which are found in fungal cell walls
  • Anti-metabolite (Flucytosine) - disrupts cellular metabolic pathways of the fungi
44
Q

Complications with Antifungal medication and nursing intervention in those events

A

Complications
> Infusion reactions (fever, chills, rigors, and headache) 1 to 3 hr after initiation

  • A test dose of 1 mg amphotericin B, infused slowly IV, may be prescribed to assess the client’s reaction.
  • Pretreat with diphenhydramine (Benadryl) and acetaminophen.
  • Meperidine (Demerol), dantrolene, or hydrocortisone may be given for rigors.

> Thrombophlebitis

  • Observe infusion sites for signs of erythema, swelling, and pain.
  • Rotate injection sites.
  • Administer in a large vein and administer heparin before infusing amphotericin B.

> Nephrotoxicity

  • Obtain baseline kidney function (BUN and creatinine) and do weekly kidney function tests.
  • Monitor I&O.
  • Infuse 1 L saline on the day of amphotericin B infusion.

> Hypokalemia

  • Monitor electrolyte levels, especially potassium.
  • Administer potassium supplements accordingly.

> Bone marrow suppression

  • Obtain baseline CBC and hematocrit, and monitor weekly.

Ketoconazole
> Hepatotoxicity (anorexia, nausea, vomiting, jaundice, dark urine, and clay-colored stools)

  • Obtain baseline liver function studies, and monitor liver function monthly.
  • If manifestations occur, notify the provider and discontinue the medication.

> Effects on sex hormones
» In males, gynecomastia (enlargement of the breast), decreased libido, erectile dysfunction
» In females, irregular menstrual flow

  • Advise clients to observe these effects and notify the provider.
45
Q

What is Malaria?

A

> Most significant protozoal disease due to high morbidity and mortality
Transmitted through the bite of an infected female anopheles mosquito which is endemic in the Philippines
It can also be transmitted through blood transfusions, mother-to-child, or through the use of contaminated needles
Antimalarial drugs cannot affect the parasite during its sexual cycle (inside the mosquito) but during its asexual stage (inside the human body)

46
Q

ANTIMALARIAL DRUGS

A

> Chloroquine and hydroxychloroquine; Mefloquine and Quinine - work by inhibiting DNA and RNA polymerase and raising the pH within the parasite which interferes with the parasite’s ability to metabolize and use erythrocyte’s hemoglobin

> Primaquine – binds and alters parasitic DNA

> Pyrimethamine – inhibit dihydrofolate reductase, the enzyme needed for the production of vital substances

> Used to kill Plasmodium organisms and work during the phases of the
parasite’s growth inside humans.

> Drugs such as chloroquine, pyrimethamine, quinine, and mefloquine cannot prevent infection as they are only effective during the erythrocytic phase of the organisms

> The most effective antimalarial drug for eradicating the parasite during the exoerythrocytic phase is PRIMAQUINE

> QUININE is indicated for chloroquine-resistant P. falciparum

> Contraindication: drug allergy, tinnitus, pregnancy, severe renal and hepatic impairment

47
Q

Antimalarial Drugs side effects and drug-to-drug interactions

A

Side Effects:
> GI distress, vision changes, dizziness
> Confusion, delirium, seizures
> Eighth cranial nerve involvement, tinnitus
> Renal impairment, blood dyscrasias
> Cardiovascular

Drug-Drug Interactions:
> With antifolate drugs (methotrexate, sulfonamides) + Pyrimethamine equates with the Increased risk of bone marrow suppression

48
Q

Nursing Management for Antimalarial drugs

A
  1. Monitor kidney and liver function
  2. Take a complete course.
  3. Take drugs with meals to prevent GI distress
  4. Report vision changes
  5. Avoid alcohol
  6. Advise individuals traveling to endemic countries to take prophylactic drug
  7. Avoid pregnant women
49
Q

List of medications for the treatment of Malaria in the DOH manual book

A

FOR UNCOMPLICATED INFECTION
1. Artemeter-Lumifantrine (AL)
2. Primaquine

FOR SEVERE MALARIA
1. Artesunate IV
2. Primaquine
3. Quinine
* Dosage calculated by weight in kg

50
Q

Non-Malarial Antiprotozoals (Metronidazole)

A

Contraindication:
> Allergy
> Used in caution on patients with CNS, hepatic diseases, and lactating women

Side Effects:
> Headache
> dizziness
> confusion
> fatigue
> peripheral neuropathy
> blurred vision
>dysuria
> rash
> neutropenia

51
Q

ANTI-HELMINTHIC DRUGS

A

> Helminths are large and complex multicellular structures
anti-helminthic drugs are very specific with the worms they can kill, thus accurate identification of
causative organisms prior to treatment is necessary

52
Q

Different types of parasites, Larval migration, Gastrointestinal parasitism, and General Features

A

A.) Ascaris Lumbricoides
Larval mitigation: Pneumonitis
Gastrointestinal parasitism: Lactose Intolerance, Vitamin A Malabsorption, Intestinal obstruction, acute Appendicitis, hepatobiliary, and Pancreatic complications

B.) Trichuris Trichiura
Larval mitigation: None
Gastrointestinal parasitism: Colitis, Trichuris dysentery syndrome, Rectal Prolapsed

C. Hookworm
Larval mitigation: Ground itch, Cough, and Pneumonitis
Gastrointestinal parasitism: Intestinal Blood Loss, Iron-deficiency anemia, pneumonitis Protein malnutrition

(FOR A, B, and C) General Appearance
Impaired physical growth
impaired cognitive growth
poor school performance

53
Q

HELMINTHS

A

> Platyhelminths for (flatworms)
Cestodes for (tapeworms)
Trematodes for (flukes)
Nematodes for (roundworms

54
Q

ANTIHELMINTHICS DRUGS

A

> Albendazole – destroys the worm’s cytoplasm which immobilizes and kills the worm
Praziquantel – increases the permeability of the cell membrane of the worm which causes dislodgement on the site of residence where they are then killed by the host
Thiabendazole – inhibits the helminth-specific enzyme
Ivermectin – potentiates CNS of the nematode leading to paralysis
Pyrantel – blocks ACh which results in paralysis of the worm

55
Q

Nursing Management for Antihelminthics Drugs

A
  1. Obtain thorough medication history and head-toe PA, measure V/S, note health conditions such as G6PD
  2. Perform skin and hearing assessments for anti-malarial drugs. Ensure that oral doses are taken with a full glass of water. Photosensitivity precautions should be put in place such as sun protection
  3. Perform baseline blood count and electrolyte values for anti-protozoal drugs. Administration of medications with food. IV doses are infused 30-60mins and not given as a bolus. Report
    changes in neurological status
  4. Thorough diet history for patients taking anti-helminthic drugs. Obtain stool specimen as
    indicated. Inform clients that primaquine may cause dark discoloration in urine.
56
Q

VIRAL INFECTIONS, HIV/AIDS

A
  1. ANTIVIRALS
  2. ANTIRETROVIRALS
57
Q

What is Viruses

A

> Small microorganisms and replicate only inside the cells of their host = obligate intracellular parasites
Virion – mature virus particle

58
Q

ANTIVIRAL DRUGS

A

> Chemicals that kill or suppress viruses by either destroying virions or inhibiting their ability to replicate
Even the best medications never fully eradicate a virus from its host, but the body’s immune system has a better chance of controlling the viral infection
Antivirals are all synthetic compounds that work by inhibiting viral replication
Viral illnesses are difficult to eradicate
1) replicate inside host cells
2) virus has replicated itself thousands/millions of times before symptoms appear

59
Q

NON-HIV ANTIVIRALS

A
  • Used to treat influenza, HSV, VZV, and CMV
  • May also be used to treat Hepatitis A, B, and C
  • Blocks polymerase enzyme that stimulates the synthesis of new viral genomes which results to low viral concentration enabling the host’s defenses to eliminate the virus
60
Q

Contraindications and Nursing Management For Antivirals of Non-HIV drugs

A

> Antiviral (non-HIV) drugs are usually well-tolerated
* Contraindications – in general, severe allergy
- Amantadine – lactating women, children below 12y/o, eczematous rash
- Cidofovir – renal toxicity and those receiving nephrotoxic drugs
- Ribavirin – high teratogenic potential

Nursing Management:
> Ensure good hydration.
> Instruct to take the complete course.
>Wear protective gloves when applying meds topically.
> Warn patient that GI upset, N/V can occur.

61
Q

What is HIV infection and AID? and the stages of the infection

A

¡ HIV is a retrovirus that attaches to a host cell in order to replicate
¡ RNA change to DNA using enzyme reverse transcriptase
¡ Antitretrovirals do not treat HIV infection but do not decrease the risk of passing HIV to others

Stages of HIV infection:
> The most recent WHO model lists four stages as follows:
* Stage 1: asymptomatic infection (A few weeks to months after exposure)
* Stage 2: early, general symptoms of disease (lymphadenopathy with fever, rash, sore throat, night sweats, candidiasis. The patient is termed HIV positive. May still be able to seroconvert.CD4 cells begin to drop
* Stage 3: moderate symptoms – infection progresses, and opportunistic infection begins
* Stage 4: severe symptoms, often leading to death – increasing destruction of helper T cells and decline in immune function. When CD4 drops to 200 cells/mm3 below, severe opportunistic infections and other system symptoms appear.
* Death is most likely when CD4 falls below 50 cells/mm3

62
Q

ANTI-RETROVIRALS

A

MECHANISM OF ACTION:
> FUSION/ENTRY INHIBITORS and CCR5 Antagonists - act by preventing the virus from entering the cells
> Nucleoside Reverse Transcriptase Inhibitor (NRTI), Non-nucleoside reverse transcriptase inhibitors (NNRTIs), Protease Inhibitor (PI), and Integrase strand transfer inhibitors (INSTIs) enzymes needed for HIV replication
> Treatment usually involves 3-4 HIV medications in combination to reduce resistance, Adverse Effects, and decreased dosages

63
Q

What is high-active antiretroviral therapy (HAART?

A
  • Aggressive treatment method using three or more different medications to reduce the amount of virus and increase CD4 counts
  • Skipping doses or taking decreased dosages may cause medication resistance and possible treatment failure
64
Q

What is the goal of high-active antiretroviral therapy(HAART)

A
  1. Decrease viral load to undetectable levels
  2. Preserve and increase the number of CD4+ T cells
  3. Prevent resistance
  4. Have the client in good clinical condition
  5. Prevent secondary infections and cancers
65
Q

About Anti-Retroviral and Nursing interventions for medication administration

A

Indications: when CD4 cells decrease below 350 cells/mm3 (NV: 800-1200 cells/mm3)

> Zidovudine may be safely used during pregnancy

Contraindications: severe drug allergy or toxicity

Side Effects:
> Protease Inhibitor – lipodystrophy or redistribution of fat stores under the skin, dyslipidemia, insulin resistance
> Bone demineralization and osteodystrophy
> Lactic Acidosis, peripheral neuropathy, myopathy, and pancreatitis

Nursing interventions:
1. Perform a thorough head-to-toe assessment with medical history
2. Document is known allergies and assess nutritional status
3. For localized reaction, rotate injection sites and monitor for swelling
4. For fever, chills, rash, or hypotension, discontinue meds and notify the provider
5. For CNS effects, advise the client to move carefully from different positions
6. For NRTIs – monitor CBC as it can suppress bone marrow
7. Take with food if it causes gastric irritation
8. Monitor for hypotension and changes in vision