IV Drug Administration Flashcards

1
Q

Reasons for IV administration

A
  • 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
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2
Q

Disadvantages of IV administration

A
  • 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)
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3
Q

Types of intravascular devices (IVDs)

A

Peripheral venous catheters

Central venous catheters:
– Peripherally inserted CVCs
– Skin-tunneled CVCs (e.g. Hickman and Broviac lines)

Arterial catheters

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4
Q

Continuous infusion

A

– Stable drugs
– Short half-life
– Time dependent effects
– Needs dedicated IV site

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5
Q

Bolus injection

A

– Rapid response required
– Incompatibilities
– Unstable drugs

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6
Q

Intermittent infusion

A

– Unstable drugs
– Long half-life
– Concentration dependent effects
– Less compatibility concerns

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7
Q

Complications of IV drug administration

A
  • Fear / Phobia / Pain
  • Infection / Sepsis
  • Thrombophlebitis
  • Extravasation / Infiltration
  • Emboli
  • Anaphylaxis / Hypersensitivity - Overdose
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8
Q

Red man syndrome

A

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

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9
Q

Vancomycin

A

– Treatment of MRSA

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10
Q

incidence of red man syndrome is reduced by

A

– Slowing infusion rate

– More dilute drug solution

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11
Q

Complications of IV drug administration - the actual solution

A

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

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12
Q

Bioavailability

A

Fraction of unchanged drug that reaches the systemic circulation.
IV injection gives 100% bioavailability.

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13
Q

Plasma drug concentrations

A

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

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14
Q

For most drugs, the amount of drug eliminated per unit time is related to

A

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.

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15
Q

Plasma drug concentration during IV infusion

A

Plasma concentration increases during infusion until rate of input equals rate of output
• “Steady state”

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16
Q

Clearance

A

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

17
Q

clearance =

A

10ml/min

18
Q

Plasma steady state conc. (Css)

A

the rate of the drug administered (Ko)
divided by
volume of plasma Cleared of drug per unit time (CL)

19
Q

The time taken to reach Css depends on:

A

elimination half-life (t1/2)

20
Q

t1/2 directly depends on

A
the volume of distribution (Vd) and
inversely on the clearance (CL) of drug from the body:
In2xVd
divided by 
CL
21
Q

Clinical impact

A

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?