IV Drug Administration Flashcards
Reasons for IV administration
- Medicine is not available in another form
- Cannot tolerate medication by another route
- Constant or high blood level of medicine is needed
- A rapid onset of effect is needed
- Some medications are more effective via IV
- Rarely, to ensure compliance
Disadvantages of IV administration
- Increased cost and time to administer the medicine
- Requires trained staff to administer (plus location)
- Rapid onset of action
Volume of fluid needed to dilute the medicine - Can cause discomfort/pain to the patient
- Health risks (e.g. infection)
Types of intravascular devices (IVDs)
Peripheral venous catheters
Central venous catheters:
– Peripherally inserted CVCs
– Skin-tunneled CVCs (e.g. Hickman and Broviac lines)
Arterial catheters
Continuous infusion
– Stable drugs
– Short half-life
– Time dependent effects
– Needs dedicated IV site
Bolus injection
– Rapid response required
– Incompatibilities
– Unstable drugs
Intermittent infusion
– Unstable drugs
– Long half-life
– Concentration dependent effects
– Less compatibility concerns
Complications of IV drug administration
- Fear / Phobia / Pain
- Infection / Sepsis
- Thrombophlebitis
- Extravasation / Infiltration
- Emboli
- Anaphylaxis / Hypersensitivity - Overdose
Red man syndrome
Hypersensitivity reaction due to histamine release
– erythematous rash of face, neck, and upper torso
– diffuse burning, itching, generalised discomfort
– rare cases: hypotension, angioedema, chest pain, dyspnea
Vancomycin
– Treatment of MRSA
incidence of red man syndrome is reduced by
– Slowing infusion rate
– More dilute drug solution
Complications of IV drug administration - the actual solution
Insufficient mixing
Stability of medicines in solution
– Light (e.g. total parenteral nutrition [TPN]) – Temperature (e.g. insulin, TPN)
– Concentration (e.g. amiodarone)
– pH (e.g. midazolam)
Interaction of medicines with the syringe/bag
Bioavailability
Fraction of unchanged drug that reaches the systemic circulation.
IV injection gives 100% bioavailability.
Plasma drug concentrations
IF drug is infused at a constant rate AND no drug is removed from the body, then the graph of plasma concentration against time would be a straight line
For most drugs, the amount of drug eliminated per unit time is related to
the concentration of drug in the plasma (first-order kinetics):
– Higher concentrations, more drug is removed per unit of time.
– Lower concentrations, less drug is removed per unit of time.
Plasma drug concentration during IV infusion
Plasma concentration increases during infusion until rate of input equals rate of output
• “Steady state”
Clearance
defined as the volume of blood or plasma cleared of drug in a unit time – e.g. 10ml/min
In first order kinetics, whilst amount of drug eliminated per unit time varies, CL is a constant
clearance =
10ml/min
Plasma steady state conc. (Css)
the rate of the drug administered (Ko)
divided by
volume of plasma Cleared of drug per unit time (CL)
The time taken to reach Css depends on:
elimination half-life (t1/2)
t1/2 directly depends on
the volume of distribution (Vd) and inversely on the clearance (CL) of drug from the body: In2xVd divided by CL
Clinical impact
What happens if your patient’s CL is lower or
higher than expected?
– To the steady state plasma concentration?
– To the time taken to reach that steady state?
What happens if you increase or decrease the dose of a drug?
– To the steady state plasma concentration?
– To the time taken to reach that steady state?