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Pharm U3 Terms
Pharmacology: Unit 3 Terms
Question | Answer |
---|---|
Bacterial resistance/”super bugs” | organisms build up resistance to drugs that have been used too frequently, infections have been treated incompletely, i.e. medication discontinued before required # of days to become fully effective |
Empiric therapy | based on probable offending organism; treatment that is initiated before test results become available b/c of seriousness of infection |
Culture and sensitivity | test of body fluids in medium with antibiotics to ascertain sensitivity or resistance to different antibiotics |
Prophylactic therapy | treatment initiated before exposure to pathogens |
Host factors that have bearing on antibiotic therapy | age of pt, allergy to anti-infective drug, impaired hepatic/renal function, pregnancy stat, site of infection, host of defenses |
Adverse reactions | allergic hypersensitivity, direct toxicity, indirect toxicity |
Allergic hypersensitivity | over-response of body to a specific substance; can be mild (rash, urticarial, fever) or severe manifested as anaphylaxis (sudden onset of dyspnea, chest constriction, shock, and collapse |
Direct toxicity | results in tissue damage, such as ototoxicity (hearing difficulty/vertigo), nephrotoxicity (kidney dysfunction), hepatotoxicity, blood dyscrasias (abnormalities in blood components), phlebitis/phototoxicity/sensitivity |
Indirect toxicity/superinfection | condition in which antibiotic decreases/completely eliminates normal bacterial flora; Manifested as new infection w/ different resistant bacteria/fungi; result of killing the normal flora in intestines/mucous membranes, esp. w/ broad spectrum antibiotics. |
Penicillins | produced from fungus; MOA bactericidal, interferes w/ cell wall synthesis. Used to treat gram+ & gram- organisms |
Penicillin classifications | natural, penicillinase resistant, aminopenicillins, extended spectrum penicillins |
Penicillin adverse/side effects | NVD, hypersensitivity reactions ranging from rash to fatal analphylaxis; superinfections; blood dyscrasias; renal/hepatic disorders; CNS effects |
Penicillin counseling tips | discontinue use & immediately report any hypersensitivity; take on time as prescribed on empty stomach one to two hours after meals w/ water; avoid alcohol & antacids; may affect birth control effectiveness; include probiotics in diet |
Cephalosporins | semisynthetic, antibiotic derivatives made by fungus; related to penicillins; some patients allergic to penicillins are also allergic to this drug (cross sensitivity); broad spectrum, active against many gram+ & gram- bacteria; vary widely in activity |
Cephalosporin MOA | bactericidal; interferes w/ bacterial cell wall synthesis (this is not penicillin) |
Cephalosporin culture and sensitivity | how would you determine which cephalosporin is appropriate for a specific condition? |
Cephalosporin side/adverse effects | NVD; hypersensitivity; cross sensitivity w/ penicillins; blood dyscrasias, respiratory distress, seizures; IM injections painful, IV admin can cause phlebitis |
Macrolides | erythromycin was first released; considered among least toxic antibiotics, so preferred for treating susceptible organisms under conditions which more toxic antibiotics might be dangerous; gram – bacilli usually resistance |
Macrolides MOA | bacteriostatic; inhibit protein synthesis |
Macrolides uses | respiratory tract infections; skin conditions i.e. acne; some STDs when patient is allergic to penicillin |
Macrolide side/adverse effects | serious adverse effects rare; mild side effects usually dose related; NVD, anorexia; GI cramping |
Macrolide counseling tips | be aware of GI side effects; take medication with full glass of water one hour before or two hours after meals, unless stomach is upset |
Aminoglycosides | not administered orally, just parenterally, IM or IV (poor absorption from GI tract) |
Aminoglycoside uses | reserved for short-term treatment of serious or life-threatening infections, particularly gram- bacteria, only when other less toxic agents are ineffective or contraindicated |
Aminoglycoside side/adverse effects | especially in older adults, dehydrated patients, or those w/ renal or hearing impairment; can include nephrotoxicity, ototoxicity, neuromuscular blocking, CNS symptoms |
Tetracyclines | first broad-spectrum antibiotics released in US; bacteriostatic, interferes w/ protein synthesis in many gram+ and gram- bacteria |
Tetracycline uses | rickettsia, chlamydia, some uncommon bacteria; some organisms are showing increasing resistance to this group, so should only be used when other antibiotics are ineffective or contraindicated |
Tetracycline side/adverse effects | NVD; superinfections such as vaginitis, stomatitis; photosensitivity; teeth discoloration in fetus/young children, so not given to kids under 8 |
Fluoroquinolones | excellent oral absorption; bactericidal, alters DNA of bacteria; possible serious side effects in children/older adults; should be reserved to treat infections nonresponsive to other antibiotics |
Fluoroquinolone uses | skin, bone, joint infections, UTIs, lower respiratory infections; gonorrhea, pneumonia, gastroenteritis; anthrax |
Fluoroquinolone side/adverse effects | NVD; crystalluria; CNS issues; seizures, possible cartilage or tendon damage |
Fluoroquinolone counseling tips | drink liberal quantities of water, avoid strenuous exercise during and several weeks after therapy |
Lincomysins | bacteriostatic, inhibits protein synthesis; treats bone and joint, pelvic and intraabdominal, and skin and soft tissue infections; bacterial septicemia, pneumonia |
Vancomycin | structurally unrelated to other available antibiotics; bactericidal; causes cell lysis |
Vancomycin uses | IV treats potentially life-threatening that cannot be treated with less-toxic agents; drug of choice to treat MRSA, treating gram+ infections in penicillin allergic pts. Restricted to cases in which absolutely necessary due to increase in resistance. |
Vancomycin side/adverse effects | NV; “red neck” syndrome from administration too quickly; ototoxicity, nephrotoxicity |
Vancomycin-resistant enterococci (VRE) | cases of resistance have become more prevalent across the globe, leading to vancomycin used as last line of defense against staphylococcal infections; linezolid (zyvox) is latest antibiotic to target MRSA and VRE |
Metronidazole (Flagyl) | synthetic, antibacterial and antiprotozoal agent; bactericidal, trichomonacidal, and amebicidal; disrupts DNA and protein synthesis in susceptible organism; oral, parentral, topical formulations; resistance almost nonexistence |
Metronidazole (Flagyl) counseling tips | expect changes in appearance of urine; avoid alcohol |
Sulfonamides | among the most commonly used antibacterial agents in world, particularly against UTIs; bacteriostatic; inhibits bacterial enzyme to prevent synthesis of folic acid; treats UTIs, lung abscesses, burns, et al. |
Sulfonamide side/adverse effects | NVD; urticaria; photosensitivity; stomatitis; crystalluria and hematuria |
Fungi | may be unicellular (yeasts) or multicellular (hyphae), or both; some are part of the normal flora of skin, mouth, intestines, vagina; can cause allergic, toxic, and infectious disease in humans |
Antifungal drugs | used to treat specific susceptible fungi; medications are quite different in action and purpose, and are treated separately; human host cannot tolerate the high chemical concentration of the agent to treat systemic conditions |
Amphotericin B (Fungizone IV) | can be fungistatic or fungicidal depending on strength; treats severe systems, potentially fatal infections caused by fungi; can be used to treat severe fungal infections due to immunosuppressive therapy or AIDS pts |
Azole antifungals | fungistatic or fungicidal depending on dosage; inhibits synthesis of sterols, a necessary component of fungi cell membrane |
Griseofulvin products | fungistatic; administered PO in the treatment of specific fungi causing tinea infections (ringworm) of the skin and nails that do not respons to topical agents; accurate diagnosis of infection organism is essential |
Virus | tiny intracellular organism totally dependent on living host for survival and necessary material to replicate; intracellular development allows organism to bypass many of the body’s defense mechanisms |
Antiviral drugs | limiting factors; viral replication reaches peak before clinical symptoms appear, agents must be admin before disease appears; drugs designed to inhibit viral cells must also effect host cells and may be too toxic |
Neuraminidase inhibitors | indicated for treatment of uncomplicated acute illness due to influenza A and B; inhibits neuraminidase, which alters virus particle aggregation/release; i.e. Tamiflu |
Retrovirus | replicates in a unique process in which viral RNA is translated into DNA by reverse transcriptase, then integrated into the host chromosome; exists in latent state until reactiviated |
Antiretroviral drugs | used to treat HIV which has a unique way of replicating; drugs only effective when the virus is replicating; often administered as cocktail called HAART; combo of three or more agents |
HAART | highly active antiretroviral therapy |
Antiretroviral drug MOA | inhibit replication at certain sites; include antagonists and inhibitors such as CCR5-tropic antagonists, entry inhibitors, fusion inhibitors, reverse transcription inhibitors, |
Reverse transcriptase inhibitors | nucleoside analogs that look like HIV DNA and incorporate into new viral DNA as false bases to terminate synthesis |
Protease inhibitors | reversibly bind to the protease enzyme and prevent the enzyme from producing new active viral proteins |
AIDS | acquired immunodeficiency syndrome; set of defined clinical conditions that result from infection of the human immunodeficiency virus (HIV) |
HIV | human immunodeficiency virus; any of the lenteviruses and especially HIV1 that infect and destroy helper T cells of the immune system causing marked reduction in their numbers that is diagnostic of AIDS |
ELISA; enzyme linked immunosorbent assay | primary screening test of HIV/AIDS; detects antibodies produced in response to HIV infection |
Western blot | confirmatory test of AIDS/HIV; detects antibodies produced in response to the HIV infection |
PCR test | identifies HIV in blood |
HIV | infects the helper T cells and macrophages of the immune system; retrovirus that replicates DNA from RNA |
HIV routes of transmission | unprotected sexual contact, IV drug use, mother to child transmission during pregnancy, delivery, breast feeding. |
Stages of HIV infection | infection, asymptomatic state, symptomatic disease official diagnosis made when T-4 count drops below 200, endstage disease (immune system collapse) |
Start of treatment for HIV/AIDS | universal agreement to start with T-4 count at 350 cells/mL and below |
Tuberculosis (TB) | chronic granulamotous infection caused by mycobacterium; single biggest infectious killer in world. Most commonly affects lungs, but other body areas can also be infected; transmitted by airborne droplets |
Anti-TB treatment | treated even if asymptomatic (due to exposure) or due to positive skin test; if even one dose is missed of the six to twelve month long treatment, treatment must be started over from the beginning |
Specific anti-TB drug MOA | inhibit cell wall synthesis or protein synthesis; drug regimen must be strictly followed |
Anti-TB drug side/adverse effects of rifampin/INH | usually more pronounced in first weeks of therapy; can be treated symptomatically; NVD, hepatotoxicity; red orange excretions seen in sweat, saliva, tears, etc. |
Malaria | caused by plasmodium and insect vector mosquito; symptoms appear in erythrocytic phase |
Anti-malarial drug MOA | interrupt the multiplication of parasites within the erythrocyte by interfereing with protein synthesis and by inhibiting DNA and RNA production |
Prophylactic drugs | taken as prevention and require continuous administration to reduce risk of infection |
Therapy drugs | taken once a person is already infected to treat and cure the disease |
Amebiasis | infection of large intestine produced by protozoan parasite entamoeba hisolytica; transmitted via ingestion of cysts (fecal oral route) from food/water or person to person contact |
Toxoplasmosis | infestation by intracellular parasite, toxoplasma gondii. Contracted by ingesting cysts in inadequately cooked raw meat or by ingesting cat feces |
Trichomoniasis | disease of the vagina caused by trichomonas vaginalis; symptoms include wet, inflamed vagina, strawberry cervix, thin yellow malodorous discharge |
Helminthiasis | infestation of helminthes; agents for treatment are specifici to the type of worms they kill; meds generally given orally |
Hansens’s disease/leprosy | caused by mycobacterium lepra in humans; mode of transmission is unknown; symptoms include peripheral trunk involvement leading to loss of fingers and toes and portions of hands and feet |
Community-acquired infections | usually in healthy individuals; often benign and responsive to treatment |
Nosocromial infections | infections acquired in a hospital at least 72 hours after hospitalization and most frequently are due to gram-negative infections; UTI most common |
Medical asepsis | absence of pathogenic organisms |
Surgical asepsis | absence of all microorganisms |
Sterilization | process that destroys all forms of life on an instrument or utensil, in a liquid, or within a substance. |
Antiseptics | chemicals typically applied only to living tissue; bacteriostatic or bactericidal |
Disinfectants | chemicals only used on non-living objects; are toxic to living tissue; bacteristatic or bactericidal; mainly bactericidal |
Natural immunity | body’s innate and inherited ability to resist antigens |
Acquired immunity | both natural and artificial antigen resistance against antigens |
Naturally passively acquired immunity | antibodies obtained by transfer via placenta or breast milk |
Actively passively acquired immunity | protection obtained by actually contracting the disease |
Artificially passively acquired immunity | temporary prophylactic immunity is acquired by direct injection of antibodies (immune serums) |
Artificially actively acquired immunity | protection acquired by immunization of vaccines or toxoids |
Vaccines | suspension of live attenuated or dead organisms; greatest prevention success story of modern medicine so far |
Toxoids | toxins produced by organisms that stimulate antibody production |
Immunosuppressants | decrease or prevent an immune response; act at several sites in the immune response; used to prevent rejection of organ transplants |
Biologic response modifiers (BRMs) | activate the body’s immune defenses or modify a biologic response to an unwanted stimulus; i.e. interferons |
Interferon MOA | enhance activity of macrophages and natural killer cells; used as antiviral, immunomodulating, and antineoplastic |
Interleukins (lymphokines) | stimulate killer T cell production, natural killer cells and to a certain extent B cell production; used as immunomodulaters and immunorestorers. |
Immunomodulators | increase T cells, synthesis of cytokines, increase B cells, increase natural killer cells |
Immunorestorers | enhance killer T cell activity, amplifies effects of cytokines, enhances cytotoxic actions of natural killer cells. |
Interleukin side/adverse effect | capillary leak syndrome resulting in massive fluid retention of 20 to 30 pounds; fever, chills, rash, fatigue |
Colony stimulating factors | bind to receptors on surface of cells and in bone marrow; responsible for production of RBCs, WBCs, platelets, etc. Increase # of RBCs, granulocytes, macrophages |