Order: 1 liter or 1000 mL of D5W to infuse over 6 hours
Available: Macrodrip set: 10 gtt/mL
The IV flow rate would be ______gtt/min.
28
27
16.67
17
17
The Correct Answer is A
Given:
Volume of fluid: 1 liter = 1000 mL
Infusion time: 6 hours
Drop factor: 10 gtt/mL
Formula:
Flow rate (gtt/min) = (Volume (mL) / Time (hr)) x Drop factor (gtt/mL) / 60 min/hr
Step 1: Calculate the infusion rate in mL/hr:
Infusion rate (mL/hr) = Volume (mL) / Time (hr)
Infusion rate (mL/hr) = 1000 mL / 6 hr
Infusion rate (mL/hr) = 166.67 mL/hr
Step 2: Calculate the flow rate in gtt/min:
Flow rate (gtt/min) = (Infusion rate (mL/hr) x Drop factor (gtt/mL)) / 60 min/hr
Flow rate (gtt/min) = (166.67 mL/hr x 10 gtt/mL) / 60 min/hr
Flow rate (gtt/min) = 1666.7 gtt/hr / 60 min/hr
Flow rate (gtt/min) = 27.78 gtt/min
Step 3: Round to the nearest whole number:
Flow rate (gtt/min) ≈ 28 gtt/min
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is C
Explanation
Let's calculate the dosage using the provided information.
Information from the label:
Bumetanide concentration: 0.25 mg/mL
Available volume: 10 mL vial
Order: Bumex (bumetanide) 1 mg IV daily
Calculation:
Determine the desired dose: 1 mg
Use the formula:
Desired dose (mg) / Available concentration (mg/mL) = Volume to administer (mL)
Substitute the values:
1 mg / 0.25 mg/mL = Volume to administer (mL)
Calculate:
Volume to administer = 4 mL
Therefore, the correct answer is C. 4 mL
Correct Answer is D
Explanation
A) Distribution:. Distribution refers to the process by which a drug is transported throughout the body after it is absorbed into the bloodstream. It involves the movement of the drug to various tissues and organs, where it can exert its effects. Factors such as blood flow, tissue permeability, and protein binding affect distribution.
B) Metabolism:
Metabolism refers to the biochemical process by which the body breaks down drugs into metabolites, usually in the liver. Metabolism can transform drugs into more easily excreted forms and sometimes alters the drug’s activity. It is essential for drug clearance and can affect drug efficacy and toxicity.
C) Absorption:
Absorption is the first step in pharmacokinetics, where the drug enters the bloodstream after being administered. It occurs primarily in the gastrointestinal (GI) tract for oral medications but can also happen in other routes like subcutaneous or intramuscular injections. The rate and extent of absorption are influenced by factors such as drug formulation, route of administration, and presence of food.
D) Synthesis:
Synthesis refers to the process of creating substances, such as drugs or other compounds, typically within the body or in a laboratory setting. While drug synthesis is crucial in drug development, it is not a step involved in the movement or processing of drugs within the body (which is what pharmacokinetics describes). Pharmacokinetics focuses on how the body handles drugs, not how they are created.
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