chapter 9 part 3
Quiz yourself by thinking what should be in
each of the black spaces below before clicking
on it to display the answer.
Help!
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| the iv admixture services in most hospitals share | iv antibiotics, thrombolytics, nutrition, & cancer chemotherapy
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| the iv admixture services are staffed by | specially trained pharmacists/techs
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| the iv admixture services are centralized pharm] services that | prepares iv & tpn solution in a sterile, germ-free work environment
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| total parenteral nutrition service are in | many hospitals
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| a tpn is | a total parenteral nutrition service
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| tpn services have trained/certified | techs, pharmacists, nurses, nutritionists & physicians
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| the tpn service is for | patients who can't eat
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| the tpn is a special formulated | parenteral solution with nutrients
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| in the tpn & iv admixtures, large hospitals | use automation
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| the automation for tpn & iv admixtures allows pharm ] to efficiently | operate, minimizes med errors, & reduces inventory
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| tech errors must be watched eventhough | automation reduces errors
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| a med. administration record is | the MAR
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| MAR's record any | med. administration
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| MAR's are patient specific & includes | med. orders, drug names, doses, administration routes & times, start & stop dates, and special instruction
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| the MAR is a form in the | patient med. chart used by nurses
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| MAR's cam be electronic which is | eMAR
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| med. orders are input in | hand held computer & sent to pharm]s
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| patient info. is scanned from | barcode on wristband
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| to units, pharm]s | check, fills, & sends meds
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| eMAR documents patients administer drugs using | barcode technology
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| many committees support | functions of hospitals
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| pharm] hospital functions include | pharm] & therapeutics, infection control, & institutional review board
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| a tech represents a department on | the committees
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| the pharm] & the therapeutic committee reviews, approves, & revises | hospital formularies & keeps drug use policies in hospital
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| the pharm] & therapeutic committee has | medical staff , administrators, pharm] director, & drug info. pharmacist
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| a medical staff can apply to a P&T committee to have | a new drug added to the formulary
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| the new drug is compared with the existing formulary in terms of | costs, advantages, and advantages
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| the application is considered by the | full committee
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| the institutional review board is a committee ensuring protection is provided to patients using | investigational drugs; otherwise known as human use committee
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| the IRB is the | institutional review board
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| the IRB is charged with ensuring patient safety interns of | investigational drugs, procedures, or other clinical research studies
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| the IRB has consumer representatives & members of | medicine, pharm], nursing, & hospital administration
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| investigational drugs are drugs used in | clinical trials not yet approved by FDA for general use
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| the investigator/researcher submits an application to | the IRB outlining study of number, age, & type of subjects & informed consent forms to be used
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| the IRB protects patients by assuming knowledge of | risks & confidentiality of the medical information collected
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| informed consent is written permission by a patient to participate in an | IRB approved research study to understand the lay public
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