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General Characteristics of Antimicrobials
Invade, attach to cells, multiply, and assault tissues
Initiates an inflammatory/immune response
Adapt to survive
Inflammatory/immune response may be sufficient in some cases
Pathogens may have adapted to increase survival within the host – in these cases, antimicrobial
therapy is utilized
Bacteria
A single-celled microorganisms without nuclei that reproduce by fission or splitting
Single-celled, without nuclei
Aerobic or anaerobic
Gram-positive or gram-negative
Shape [rod, cocci…]
Treat with antibiotics
Virus
Are intracellular parasites that survive only in living tissues.
Invade and replicate inside cells
Classified according to structure or origin [e. g., adenovirus, retrovirus…]
Treat symptoms only or with antivirals
Fungi
Are plantlike microorganisms that live as parasites on living tissue or as saprophytes on decaying organic matter
Plant-like
May be treated with antifungals
Parasites
From the animal kingdom – infect other animals [e. g., protozoa, helminths, arthropods]
Colonization
Presence and growth of microorganisms on host tissues.
Does not necessarily cause injury or elicit an immune response
Normal Microbial Flora
Most parts of the body are sterile [organs and fluids]
Some parts of the body contain microorganisms that do not cause any harm or injury to the host – known as normal flora
Examples of normal flora in the human body
- Gut/Gi Tract, Mouth, Upper respiratory, Skin
Intestinal Flora synthesizes Vitamin K and Vitamin B complex
Intestinal Flora aids in digestion
Plays a role in preventing overgrowth from other pathogens
How is Normal Flora helpful to the body?
Infection
What happens if flora (microorganisms) that is normal to one tissue type enters another tissue type?
Opportunistic infection - immune suppressed
Impaired vitamin k synthesize, over growth of pathogen,
Overgrowth of pathogens, particulary yeast or C.diff
What happens if normal flora is killed by antibiotics?
Host Defense Mechanisms
Examples: skin, mucous membranes, secretions, coughing, immune system, inflammation (WBC)
Factors that increase risks of pathogenic invasion:
o Advanced age
o Break in integument (break in the skin)
o DM / other chronic diseases
o Impaired blood supply
o Malnutrition
o Neutropenia or other decrease in WBCs
o Poor personal hygiene
o Presence of tubes/catheter devices
o Suppression of normal flora
Proliferation of microbial pathogens causes harm to host, manifestations of an infectious process; infectious process
Opportunistic Infection
SERIOUS; LIFE-THREATNING
Microorganisms that do not normally cause infections in host with an intact immune system
These microorganisms are usually normal endogenous, environmental flora, and
nonpathogenic but become pathogenic in hosts whose defense mechanisms are
impaired/immunosuppressed; enters someone with compromised immune system
HIV/AIDS
Burn patinets
Chemo patients
What populations are most at risk for acquiring an opportunistic infection?
Superinfection
Emergence of a new or an additional infection that appears during the course of
treatment for a primary infection due to depletion of immune cells and/or depletion of normal flora
Difficult to treat
Serology
Identifies pathogens indirectly; a measure of antibodies (titer) in a specimen/infected host
“Measurs how many antibodies in the human that are preset for a specific pathogen”
Polymerase Chain Reaction (PCR)
Detection of antigens
Microscopic Examination
Helps with visualization
Gram Stain (dye) assists in differentiating microorganisms
Culture and Sensitivity
Process of growing microorganisms (sample) in a lab for the purpose of identifying a specific organism; 48 hrs later
“S” = susceptible
“R” = resistant
“MIC” = lowest concentration of antibiotic that prevents growth of a microorganism
ALWAYS COLLECT CULTURE & SENSITIVITY SPECIMEN FIRST
Community Acquired Infection
Infection that the host contracted outside of the hospital setting
Easier to treat
Diagnosed ≤ 48 hours of admission (first 48 hrs)
Common type: community-aquired pneumonia (inflection of lungs, does not aquired in healthcare facility, leading cause of morbidity/mortality).
Hospital Acquired Infection
Infection that originated in the hospital setting
Most difficult to treat and more costly
More likely to be drug-resistant
Diagnosed ≥ 48 hours of admission (before 48 hrs)
Antibiotic-Resistant Microorganisms
Major Public Health Issue
Microorganisms that are able to survive despite antibiotic treatment/therapy
May require lengthy hospitalizations and the administration of more toxic medications
COSTLY
EX: Penicillin-Resistant Streptococcus pneumoniae (pneumococci), vancomycin-resistant enterococci, methicillin-resistant and vancomyic intermediate/vancomycin-resistant staphylococcus species
Make sure to see if there is any improvement 24-36 hrs, if not, notify provider
Causes of Antibiotic-Resistant Microorganisms
OVERUSE OF ANTIBIOTICS – overprescribing , patients not taking antibiotic as prescribed, poor hygiene/sanitation, poor infection control in hospitals, use of antibiotics in agriculture
At risk populations: hospitalized patients, critically ill
*Patients who do not demonstrate improvement within 24-36 hours of receiving antibiotics may have an antibiotic-resistant pathogen
Drug Therapy
Purpose: Treat or prevent an infection as a result of tissue invasion by a microorganism
Goal: get rid of the invading pathogen and restore the host to a state of wellness
Role of Nurse: Monitor the patient’s response
The immune system of the host plays a role in the overall treatment/recovery
The most widely used group of medication
Broad Spectrum Antibiotics
Are effective against a wide range of bacteria (e.g., both gram-positive and gram-negative bacteria)
Narrow Spectrum Antibiotics
Are effective against a limited range or a specific type of bacteria.
Is preferred/initial choice when possible because broad-spectrum drugs are more likely to kill some normal flora, which disrupts the microbial balance.
Bactericidal
KILLS the bacteria
Bacteriostatic
INHIBITS GROWTH of the bacteria
Antibacterial Drug Therapy
Are toxic to microbes but harmless to host
Typically work by:
- Disrupting bacterial cell wall
- Blocking an enzyme unique to bacteria
- Disrupting bacterial protein synthesis
- Disrupting bacterial synthesis of RNA / DNA
Factors to choosing an Antibiotic
Identify the organism
Drug sensitivity
Host factors such as:
1. Status of health (immune system, renal/liver function…etc.
2. Site of infection
3. Allergies
4. Age
5. Pregnancy, may cross the placenta
Guidelines of Antimicrobial Drug Therapy
DO NOT USE antibacterial agents to treat viral infections
Use only if bacterial infection diagnosed or strongly suspected OR indication for prophylaxis
Narrow-spectrum is preferred over broad-spectrum and should be used initially if appropriate
Avoid antimicrobials for fever unless manifestations and/or diagnostic tests indicate infection
Practitioners should follow CDC guidelines for prevention/treatment; particularly with drug-resistant organisms
May be necessary to consult an infectious disease specialist
Obtain cultures for C&S and gram stain BEFORE administering 1st dose of antibiotics (if cultures are ordered)
Empiric Therapy
Drug therapy undertaken prior to obtaining a definite diagnosis
Beginning antimicrobial therapy while waiting for C&S results (if done)
Example of Empiric Therapy
Patient has Manifestations of Infection
Order antimicrobial
Start antimicrobial (empiric therapy)
Monitor for therapeutic response
OR
Order a C&S and antimicrobial
Collect C&S
Start antimicrobial (empiric therapy)
Review C&S results in 48-72 hours; adjust antimicrobial therapy as applicable
monitor for therapeutic response
What should a nurse do to monitor a patients response to antibiotic therapy?
Drug Therapy with Beta-Lactam Antibacterial Agents
Includes: penicillin, cephalosporins, carbapenems & monobactams
This class of drugs binds to proteins on the cell membrane of bacteria and inhibits the synthesis of the bacterial cell wall
- These types of drugs have a chemical structure called a “beta-lactam ring”
- This “ring' must stay together in order for antibacterial effects
- Some microorganisms produce enzymes [beta-lactamase] that break down this ring, thus making the drug ineffective; contributes to resistance to this class of med – therefore a chemical called clavulanic acid [beta-lactamase inhibitor] is added to some in this class to inhibit these enzymes
- Generally safe with children
- Safe with older adults except with renal impairment
Penicillins
“cillin”
Examples: PCN G, PCN V, ampicillin (P), oxacillin, nafcillin, amoxicillin, piperacillin,
Extensively used; originates from mold and semisynthetic substances
All forms of PCN are available for IM route; Pharmacokinetics:
- Widely distributed
- Excreted by kidneys
Mechanism of Action [MOA]: binds to protein on cell wall of bacterial, weakens cell wall, inhibits cell wall synthesis, then causes cell to rupture (bactericidal); Does not damage/injure host cells
Indications: bacterial infections – skin/soft tissue, pulmonary, GI, GU, endocarditis
Contraindications: hypersensitivity/allergy to ANY PCN
Adverse Effects of Penicillin
Hypersensitivity; 1-10% experience allergic response
GI: N/V/D, gastritis, abdominal pain
Superinfection
Nephropathy
CNS: confusion, lethargy, dysphagia, seizures, coma
BBW: DO NOT ADMINISTER IV PCN G
Nursing Implications for Penicillin
Generally safe for use in children and older adults
Should be taken on an empty stomach to increase absorption – take with a full glass of H2O
If patient experiences GI upset – may take with food but be aware that absorption will be impaired–
Renal Excretion
Hepatic Impairment:
1st dose – ALWAYS monitor for at least 30 minutes
If given IM give deep in large muscle (painful/tissue irritation)
Monitor for adverse effects and therapeutic response
QSEN: Be aware that PCN beta-lactamase inhibitor combinations contain PCN + clavulanate (clavulanic acid). Amoxicillin + clavulanate [Augmentin] is commonly used and each tablet contains a specified amount of amoxicillin and 125 mg of clavulanate. Therefore, a 500 mg tablet of Augmentin is NOT equal to two 250mg tablets
Cephalosporins
“cef” “ceph”
Originate from a fungus; related to PCN; Broad-spectrum, bactericidal
MOA: similar to PCN; Most effective against cells undergoing division
Indications: surgical prophylaxis, infections of the respiratory tract, skin/soft tissues, bones, joints, GU, brain/spinal cord, & sepsis
Contraindications: hypersensitivity or previous anaphylactic reaction to PCN [chemically similar to PCN
Adverse Effects of Cephalosporins
Hypersensitivity
GI: Abd pain, diarrhea, gastritis, N/V
Superinfection
Types of Cephalosporins
NOTE: as the generations of cephalosporins progress, they have
↑ high ability against gram–bacteria and anaerobic bacteria
↑ high ability to resist destruction by beta-lactam enzymes
↑ high capacity to get to CSF
1st Generation Cephalosporins
EX: Cefazolin (Ancef), Cephalexin (Keflex)
Indications: Surgical prophylaxis; Rarely used
2nd Generation Cephalosporins
EX: Cefaclor (Ceclor), cefprozil (Cefzil)
Indications: Surgical prophylaxis (colorectal/gynecologic)
3rd Generation Cephalosporins
Cefdinir (Omnicef), Ceftriaxone (Rocephin)
Indications: Able to penetrate meninges and enter CSF; good choice for
meningeal infections. Pseudomonas infections when used in combination with
other antibacterials [to prevent drug resistance]
4th Generation Cephalosporins
EX: cefepime (Maxipime)
Indication: Broader spectrum, May be used with strains that have developed resistance to 3rd generation
5th Generation Cephalosporins
EX: Ceftaroline (Teflaro)
Community-acquired pneumonia, MRSA, VRSA, skin infections
Nursing Implications for Cephalosporins
Generally safe with children; cautious with neonates
May need to decrease dose in older adults
May impair Vitamin K synthesis in the intestinal tract which is pertinent for patients taking a specific type of anticoagulant [Anticoagulants will be covered in cardiac lecture]
PO – take with food / milk
QSEN: If used for surgical prophylaxis, give 60 minutes before first incision so that the drug has time to reach therapeutic serum and tissue concentrations
Carbapenems
Broad-spectrum, bactericidal, beta-lactam antimicrobials
Imipenem-cilastatin (Primaxin) – parenteral
Ertapenem (Invanz) – parenteral
Monobactam
Bactericidal
Aztreonam (Azactam) - parenteral
Aminoglycosides
“micin, mycin”
Examples: gentamicin (P), amikacin (Amikin), streptomycin
Potent; Poorly absorbed from GI tract
Widely distributed with parenteral administration
MOA: Bactericidal – enters cell walls – attaches to specific ribosome and impairs ability of bacteria to synthesize proteins that are required for cellular function and reproduction
Indications: serious systemic infections (septicemia); gram negative aerobic (aerobic-needs O2 to cross cell wall) pathogens (e.g. tuberculosis, osteomyelitis) in conjunction with other antibacterials for synergistic effect
Adverse Effects of Aminoglycosides
BBW: NEPHROTOXICITY & OTOTOXICITY (EARS & KIDNEYS)
Nephrotoxic
Ototoxic such as vertigo, tinnitus
Peripheral neuropathy
Use cautiously with myasthenia gravis
Contradtications: Hypersensitivity
Nursing Implications of Aminoglycosides
Cautious use with neonates, children, and older adults
Dosing
(a) Conventional Dosing: multiple doses throughout the day
(b) **Once daily dosing (ODA): once a day with higher doses
Loading dose vs Maintenance dose
Id patients at high risk for nephrotoxicity [renal impairment]
Hydration [2-3L per day]
Monitor therapeutic serum levels
(a) Creatinine clearance (CrCl)
(b) Peak and Trough serum laboratory values
Peak
Highest serum level of drug
Time: 0.5-1 hour after administration
Trough
Lowest serum level of drug
Immediately before the next schedules dose
Gentamicin 400 mg IV daily. The nurse will administer the ordered Gentamicin at 0830 over 1
hour. A peak and trough have been ordered?
What time will the nurse draw the serum trough level?
What time will the nurse draw the serum peak level?
Fluoroquinolones
“floxacin”
Examples: ciprofloxacin (P)(Cipro), levofloxacin (Levaquin), moxifloxacin (Avelox)
MOA: interferes with bacterial DNA replication; bactericidal; Cells/DNA of host are not affected;
Indications: gram-negative aerobic pathogens; lower respiratory tract, bone/joint, GU, GI, skin/soft tissue, ciprofloxacin 1st line for anthrax
Adverse Effects of Fluoroquinolones
Usually well tolerated, N/V, abd discomfort, photosensitivity
BBW: tendinitis and tendon rupture, peripheral neuropathy, CNS/CV effects
BBW: Myasthenia gravis – may exacerbate muscle weakness
GI, HA, photosensitivity reactions
Contradications: Hypersensitivity
Nursing Implcations of Fluoroquinolones
Not routinely used in children except with complicated UTI, pyelonephritis, anthrax exposure
Once a day dosing increases compliance
Avoid taking with dairy products
2-3 L fluid each day if not contraindicated
Cautious with severe liver disease
May prolong QT interval
Assess for therapeutic effects/adverse effects
Tetracyclines
Examples: tetracycline (P), doxycycline (Vibramycin)
MOA: Inhibit protein synthesis, thereby suppressing bacterial cell growth (bacteriostatic
Indications: Lyme disease, select animal bites, some sexually transmitted infections (STI’s), acne, H pylori bronchitis
Doxycycline is approved by FDA to treat anthrax after exposure
Contraindications: hypersensitivity, renal failure, pregnant women, < 8 yrs age
Should not be used in children less than 8 years of age or during pregnancy; deposits in bone- forming tissue
- < 8 years of age: may cause permanent discoloration to the teeth (yellow, gray, brown)
- Pregnancy: hepatotoxic to pregnant females; may interfere with fetal bone and skeletal development
Adverse Effects of Tetracyclines
N/V, photosensitivity, GI symptoms, CNS, hepatotoxicity, renal toxicity, superinfections
QSEN: Avoid taking expired tetracyclines; severe reactions including renal damage may occur due to alteration in the chemical structure after expiration
Nursing Implications of Tetracyclines
Take on empty stomach
Take with 8 oz H2O to reduce GI irritation
Avoid milk products, Fe, and antacids within 2 hours of administration
Avoid prolonged exposure to sunlight, tanning beds
If on oral contraceptives – use another form of birth control
Sulfonamides (Sulfa Drugs)
Examples: trimethoprim (TMP)/sulfamethoxazole (SMZ) (P) (Bactrim, Septra), silversulfadiazine (silvadene); “sulfa”
MOA: inhibits synthesis of folic acid [necessary component for RNA/DNA synthesis], bacteriostatic; halt
Do not harm host synthesis of folic acid
Highly resistant – used less often
Indications: UTI’s, burns (topical Silvadene), chronic bronchitis
Contraindication: renal failure, hypersensitivity to this class or other sulfa based drugs, late pregnancy
Adverse Effects of Sulfonamides
N/V/D, photosensitivity, kernicterus (newborn), renal damage, blood dyscrasias such
as aplastic anemia, thrombocytopenia, leukopenia
*Steven-Johnson Syndrome: rare hypersensitivity reaction; high mortality rate
Nursing Implications of Sulfonamides
Drink at least 2 liters of fluid daily to avoid crystallization in urine
May monitor pH of the urine alkaline urine better
Give with glass of H2O
Oral contraceptive effectiveness is decreased with TMP-SMZ
Avoid prolonged exposure to sunlight, tanning beds
Nitrofurantoin (Macrobid Macrodantin): An anti-infective agent used to treat and prevent UTI’s
SULF
S = sunlight (photosensitivity)
U = urine crystalization
L = Liquid (2-3 L/day)
F = Another Form of birth control
Macrolides
(macro – “big molecules”)
Examples: erythromycin (P), clarithromycin (Biaxin), azithromycin (Zithromax)
MOA: interferes with bacterial protein synthesis
May be bactericidal or bacteriostatic, depending on concentration of drug
Erythromycin is administered as an ophthalmic ointment to newborns
to prevent rheumatic fever, gonorrhea, syphilis, pertussis, and
chlamydial conjunctivitis
Contraindications: Hypersensitivity
Adverse Effects of Macrolides
GI, (N/V/D, cramping, anorexia, hepatotoxicity, pseudomembranous colitis); use
cautiously with liver disease (hepatic metabolism and excretion), CNS (reversible hearing loss), confusion, emotional lability
Miscellaneous Anti-Infective Agents
Chloramphenicol, Clindamycin (Cleocin), Dalbavacin (Dalvance), Daptomycin (Cubicin), Linezolid (Zyvox), Metronidazole (Flagyl), Oritavancin (Kimyra), Quinupristin-Dalopristin (Synercid), Rfiaximin (Xifazan), Tedizolid (Sivextro), Televancin (Vibativ), Tigecycline (Tygacil) “thromycin” “ceph”
Vancomycin
Rising incidence of Vancomycin Resistance Enterococcus (VRE), limited use is recommended, used for serious infections
MOA: inhibits cell wall synthesis; bactericidal; gram positive only
Poor GI absorption, mostly given intravenously
Contrainfications: Hypersensitivity
Indications of Vancomycin
Intravenous (IV) for MRSA, bacterial endocarditis, other serious systemic infections
Oral is only used for pseudomembranous colitis caused by C. dificile and staphylococcal
enterocolitis; oral administration does not absorbed from the GI tract, works directly within the bowel lumen
Adverse Effects of Vancomycin
Nephrotoxicity (reversible)
Vancomycin Infusion Reaction (aka Redman Syndrome): hypotension, flushing, skin rash related to histamine release
Nursing Implications of Vancomycin
IV administration slowly, over 1-2 hours to decrease risk of vancomycin infusion reaction
Monitor renal function (renal excretion)
- [nasal administration of bactroban for prevention of staph sternal incision]
Review for Drugs for Tuberculosis
Refer to the CDC for the most current evidence-based treatment for TB
Mycobacterium tuberculosis
Review pathology of TB independently to include C&S takes 4-6 weeks
- Latent versus active TB
- Manifestations of active TB
Drugs for Tuberculosis
Drug resistance (secondary to mutations) is a major barrier to successful drug therapy for TB
Multidrug-resistance tuberculosis (MDR-TB) is a public health issue because it is a type of TB that is resistant to at least one first-line antitubercular medication
Multidrug therapy: ALWAYS TREAT TB WITH 2 OR MORE MEDICATIONS
- Latent TB = 3 drugs approved over 3-9 months
- Active TB = 10 drugs approved over 6-9 months
- Second-line antimicrobials may be used in combination with antitubercular medications when
there is drug resistance to one or more of the first-line antitubercular medications
[Ex: aminoglycosides, some fluoroquinolones]
Isoniazid (INH)
Rifampin (Rifadin)
What 2 antitubercular medications are used with latent TB?
Isoniazid (INH)
Bactericidal
Most commonly used; Affordable
MOA: Inhibits cell wall synthesis
Indications:
- Latent TB: may be used alone or in combination with other antitubercular medications
- Active TB: must be used in combination with other antitubercular medication
Adverse Effects of Isoniazid
BBW: HEPATOTOXIC
INH-induced peripheral neuropathy
Prevention of INH-induced peripheral neuropathy: Pyridoxine, (B6) 25-50 mg daily
Nursing Implications of Isoniazid
Monitor liver function tests (LFT); may need to discontinue if hepatotoxicity occurs
Avoid ETOH
Teaching to ensure compliance
Home care nurse may use Direct Observation Therapy (DOT)
Treatment of latent TB can be delayed until after delivery
Several drug-drug interactions
Take on an empty stomach with a full glass of water
Rifampin: Rifamycins (Rifadin)
Bactericidal
MOA: inhibits synthesis of RNA
Synergistic effect with INH
Enzyme inducer – interacts with many other drugs, including some antiretroviral agents
Indications:
- Latent TB: may be used alone or in combination with other antitubercular medications
- Active TB: must be used in combination with other antitubercular medication
- Staphylococcus infections
Adverse Effects of Rifampin
GI, rash, liver dysfunction/hepatotoxicity, acute kidney injury
Reddish-orange discoloration (harmless) to urine, saliva, tears, sputum, sweat
Nursing Implications for Rifampin
Monitor LFT
Avoid ETOH
Take on an empty stomach
If on oral contraceptives – use another form of birth control
NOTE: Ethambutol is indicated for active TB and has an adverse effect of optic neuritis (inflammation of the optic nerve). Patients on this medication should be taught to notify the provider immediately of any visual changes. If visual changes arise, the medication should be discontinued.
Manifestations of hepatotoxicity
Antiviral Drugs
Viruses reproduce inside the cell
Viral infections induce the host to create antibodies (review antibody response of the immune system)
Individuals with impaired/weak immune response are at greater risk with viral infections
Most viral infections are self-limiting
Several vaccines are available against viruses
MOA: penetrate cell and inhibit viral DNA replication
Because viruses replicate inside host tissues and utilize host cells for metabolic processes, most antiviral meds are likely to cause some harm to host
Drugs for COVID-19
Remdesivir; administered in a healthcare facility
Nirmatrelvir + Ritonavir (Paxlovid); outpatient management
“vir”
Drugs for Herpes (simplex & zoster)
Acyclovir (Zovirax) (P) – PO, topical, IV
Famciclovir (Famvir) - PO
Valacyclovir (Valtrex) – PO
Docosanol (Abreva) – OTC
Monitor for liver and renal impairments; “vir”
Drugs for Cytomegalovirus (CMV)
Ganciclovir (P) – PO, IV
- Monitor for bone marrow suppression – thrombocytopenia/ granulocytopenia. Do not
administer with neutropenia/thrombocytopenia
Foscarnet - IV
Cidofovir – IV
“vir”
Drugs for Respiratory Syncytial Virus (RSV)
Antiviral: Ribavirin (Virazole) (P)
- BBW: Teratogenic
Monoclonal antibodies such as
- Palivizumab (Synagis)
- Nirsevimab-alip (Beyfortus) [FDA approved July 2023
Drugs for Influenza
Amantadine (Symmetrel) (P)
Oseltamivir (Tamiflu)
Peramivir (Rapivab)
Drugs for HIV / AIDS
**Refer to the CDC for the most current evidence-based treatment for HIV
Remember – NO CURE
MOA: prevents or inhibits viral reverse transcriptase (synthesis of DNA); inhibits protease enzyme
Individuals with HIV should begin treatment as soon as possible.
Antiretroviral Therapy (ART)
GOAL: Reduce the viral load (amount of HIV), preserve the immune system, prevent illness
Classifications:
- Nucleoside Reverse Transcriptase Inhibitors (NRTI’s)
- Non-Nucleoside Reverse Transcriptase Inhibitors (NNTRI’s)
- Protease Inhibitors
- Fusion Inhibitors
- CCR5 Antagonist
- *Combination Therapy is A MUST*
Zidovudine (AZT) (P) a NRTI, is the drug of choice for pregnant women who are HIV positive to prevent maternal-fetal HIV transmission during labor; administered at the onset of labor or before a C-section
AZT = A Zero Transmission
Combination HIV Therapies
Dovato:
Integrase inhibitor
Reverse transcriptase inhibitor
Nucleoside
Preferred for pregnant women who are HIV + as long as viral load is controlled
Truvada
Nucleoside reserve transcriptive Inhibitors
Nucleotide reserve transcriptive Inhibitors
General Nursing Implications for Antiretroviral Drugs
Prevention such as handwashing, vaccinations, sexual precautions, clean needles if IV drug abuser
Take as prescribed
Stress Reduction
Observe for therapeutic effects
Monitor CD4 count, viral load, CBC
Adverse Effects: anorexia, N/V/D, fever, HA, bone marrow depression, renal impairment
HIV Pre-Exposure and Post-Exposure Prophylaxis
Antifugal Drugs
Molds and yeasts
Fungal cells are very much like human cells; therefore, antifungal drugs may induce serious adverse effects to host
Fungal infections are more severe, serious in individuals who are immunocompromised
Used for local and systemic fungal infections (vaginal, oral, skin, candida)
Amphotericin B (Fungizone)
Given for serious systemic fungal infections
IV infusion, with IV pump, use an in-line filter
Nephrotoxic
Monitor liver function
Pre-medicate with antipyretic, antiemetic, and antihistamine to reduce side effects of chills, hypotension, tachycardia, malaise, muscle pain, joint pain
BBW: should only be used for potentially fatal fungal infections due to adverse effects and risk of toxicity
Azoles
Fluconazole (Diflucan) (P), ketoconazole; “azole”
Indicated for local and systemic fungal infections such as candida
Nursing Implications
- Avoid exposure, especially if an impaired immune system
- Monitor liver and renal function
Antiparasitics
Living organisms that survives at the expense of the host
Examples of medications used for various parasitic infestations
- Metronidazole (Flagyl) (P), used for intestinal parasites
- Tetracycline/doxycycline – intestinal parasites
- Chloroquine (Aralen) – antimalarial
- Mebendazole (Vermox) – hookworms, pinworms, roundworms, whipworms, tapeworms
- Permethrin (Nix) - pediculosis scabies
- Malathion (RID) – lice