Parenteral Medications - NAPLEX
- What does the term "vesicant" mean for an IV medication if extravasation occurs?
- Can cause tissue necrosis and severe local injury. Vesicants damage tissues upon extravasation due to their irritant properties, leading to blistering and potential long-term injury.
- What is the USP <797> definition of a "single-dose container" for parenteral products?
- Container intended for one-time use for a single patient/procedure. USP <797> specifies single-dose containers to prevent microbial growth by limiting use to one entry, ensuring sterility for individual patient needs.
- Which filter size is standard for most aqueous IV solutions: or ?
- . The size effectively removes bacteria and small particles from aqueous solutions without impeding flow.
- What is the formula to calculate an IV infusion rate in mL/hr from volume (mL) and time (hr)?
- . The formula derives the rate by dividing total volume by infusion time for consistent delivery.
- Which filter size is commonly used for lipid-containing parenteral nutrition admixtures: or ?
- . Lipids require larger pores like to pass through without being trapped, unlike smaller filters for aqueous solutions.
- What does the USP <797> term "immediate-use CSP" mean in terms of preparation and administration timing?
- A CSP prepared for immediate administration with minimal delay. USP <797> defines immediate-use CSPs as those prepared aseptically outside controlled environments for administration starting within 4 hours to reduce microbial contamination risk.
- What is the key clinical reason bacteriostatic water for injection is generally avoided in neonates?
- Risk of benzyl alcohol toxicity (gasping syndrome). Benzyl alcohol in bacteriostatic water can cause metabolic acidosis and respiratory distress in neonates due to immature liver function.
- What is the clinical meaning of an IV medication labeled "for IV use only" regarding route of administration?
- It must not be given IM, SC, intrathecal, or epidural. The label restricts administration to IV to prevent adverse effects like tissue irritation or inefficacy associated with other routes.
- What is the beyond-use date (BUD) after first puncture for a multiple-dose vial unless otherwise specified?
- 28 days after initial entry (unless manufacturer states otherwise). The 28-day BUD balances preservative efficacy against contamination risk, aligning with USP <797> guidelines unless shorter stability is indicated by the manufacturer.
- What is the maximum recommended osmolarity for routine peripheral parenteral nutrition (PPN) to reduce phlebitis risk?
- Approximately (institution-specific limits may vary). Osmolarity limits for PPN prevent vein irritation and phlebitis, with ~900 mOsm/L as a common threshold based on institutional protocols.
- Which diluent is preferred to reconstitute most IV antibiotics when both are acceptable: sterile water or bacteriostatic water?
- Sterile water for injection (SWFI). SWFI lacks preservatives like benzyl alcohol, reducing toxicity risks in vulnerable patients compared to bacteriostatic water.
- What is the primary purpose of using an in-line filter for certain parenteral infusions?
- To remove particulates (and sometimes air/microprecipitates) from the infusion. In-line filters capture contaminants to ensure infusion safety, particularly for solutions prone to particle formation.
- Calculate mL/hr for an infusion ordered at using a bag concentration of .
- . Dividing dose rate by concentration ensures the infusion delivers the ordered amount per hour.
- Calculate the infusion rate in mL/hr for to infuse over .
- . Dividing volume by time yields the rate, ensuring accurate delivery over the specified period.
- Which IV access is generally preferred for continuous vesicant infusions: peripheral IV or central venous access?
- Central venous access. Central access reduces extravasation risk by diluting vesicants in larger blood volumes, unlike peripheral veins.
- What is the USP <797> definition of a "multiple-dose container" for parenteral products?
- Container that allows repeated entries and usually contains a preservative. USP <797> allows multiple-dose containers for repeated access due to preservatives that inhibit microbial growth, extending usability beyond single entry.
- What is the formula to calculate IV infusion rate in mL/hr from dose rate (mg/hr) and concentration (mg/mL)?
- . The formula determines volume rate by dividing desired dose rate by solution concentration for therapeutic accuracy.
- What is the preferred diluent for reconstituting or diluting medications for intrathecal administration?
- Preservative-free 0.9% sodium chloride (or preservative-free SWFI if specified). Preservatives can cause neurotoxicity in the CSF, so preservative-free diluents ensure safety for intrathecal routes.
- What is the formula for IV drip rate in gtt/min using drop factor (gtt/mL), volume (mL), and time (min)?
- . The formula accounts for drop factor to convert volume over time into countable drops per minute.
- What is the standard concentration of dextrose in D5W expressed as grams per 100 mL?
- 5 g per 100 mL. D5W provides 5% dextrose by weight, equating to 5 grams per 100 mL for caloric support in parenteral nutrition.
- Which parenteral solution is isotonic and commonly used for IV dilution: 0.9% sodium chloride or 0.45% sodium chloride?
- 0.9% sodium chloride (normal saline). 0.9% sodium chloride matches plasma osmolarity at approximately 308 mOsm/L, minimizing cellular damage during infusion unlike hypotonic 0.45%.
- Calculate gtt/min for over with a set.
- . Multiplying volume by drop factor and dividing by minutes provides the precise manual adjustment rate.
- Identify the correct route for an oil-based depot injection: IV, IM, or intrathecal?
- IM. IM route allows slow absorption of oil-based formulations, providing sustained release unlike rapid IV dispersion.
- Calculate final concentration in mg/mL when is diluted to a total volume of .
- . Dividing total drug amount by final volume gives concentration for dosing calculations.
- What is the major safety concern if a medication intended for epidural use contains preservatives?
- Neurotoxicity; neuraxial products should be preservative-free. Preservatives in neuraxial medications can irritate neural tissues, leading to inflammation or damage in the spinal area.