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Pharmacotherapeutics

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Processes of drug absorption. Absorption is dependent on ... Phase 2 conjugation. Hepatic first pass phenomena. Enterohepatic cycling. Extrahepatic phenomena ... – PowerPoint PPT presentation

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Title: Pharmacotherapeutics


1
Lecture 4
  • Pharmacotherapeutics
  • Pharmacokinetics
  • Pharmacodynamics

2
Pharmacotherapeutics / Indications
  • Purposes of giving a drug
  • Prevent illness
  • Diagnose illness
  • Relieve symptoms
  • Treat and cure illness

3
Effective concentration is influenced by
  • Pharmaceutical phase
  • Pharmacokinetic phase
  • Pharmacodynamic phase

4
Pharmaceutic Disintegration and dissolution
Rate limiting
5
Pharmaco kinetics
  • How the body processes the drug
  • Absorption
  • Metabolism
  • Distribution
  • elimination

6
Pharmacokinetics
  • Absorption
  • Processes of drug absorption

7
Absorption is dependent on -Route of
administration
  • Enteral route length of time in the stomach,
    consumption of alcohol, solubility of the drug,
    stability in gastric ph, interactions with other
    food/ drugs, circulation in the GIT, surface area
    for absorption
  • Parenteral route solubility, surface area for
    absorption and circulation

8
Metabolism / biotransformation
  • Occurs in two phases
  • Phase 1 drug breakdown
  • Phase 2 conjugation
  • Hepatic first pass phenomena
  • Enterohepatic cycling
  • Extrahepatic phenomena

9
BIOAVAILABILITY
  • Bioavailability
  • fraction of administered drug that reaches the
    systemic system
  • Factors which affect it
  • Factors which affect the absorption
  • Route of administration
  • Changes in liver metabolism

10
BIOAVAILABILITY
11
Distribution process by which drug is carried
in the blood and delivered to the tissues and
cells
  • Protein binding
  • Lipid solubility
  • Tissue affinity
  • Amount of drug present in the tissues
  • Cardiac output and blood supply
  • Density of blood vessels in the tissues
  • Placenta and blood brain barrier

12
Distribution (contd)
13
Distribution (contd)
14
Elimination
  • Via the kidneys ( primarily), liver , GIT tract,
    lungs , sweat glands, skin and breast milk

15
Half life (t ½)
  • Half life
  • time for plasma concentration of drug to be
    eliminated by 50
  • Affected by
  • Metabolism
  • Elimination

16
Pharmacodynamics
  • Dose-response and maximal efficacy
  • Onset, peak, and duration of action

17
Pharmacodynamics (contd)
  • Receptor theory

18
Pharmacodynamcis
  • Drug receptor activity
  • Drug Receptor -gt Drug Receptor Complex -gt
    Response
  • Drug receptor affinity affects potency.
  • An agonist is a drug capable of combining with
    receptors to initiate a drug response.
  • An antagonist is a drug that opposes or prevents
    receptor response.

19
Agonists and Antagonists
20
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21
Pharmacodynamics (contd)
  • Nonspecific drug effect

22
Pharmacodynamics (contd)
  • Nonselective drug effect

23
Pharmacodynamics (contd)
  • Categories of drug action
  • Stimulation or depression
  • Replacement
  • Inhibition or killing of organisms
  • Irritation

24
  • Therapeutic index
  • the ratio of effective dose to lethal dose. A
    wide TI means the drug is relatively safe.

25
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26
Therapeutic Index
27
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28
Therapeutic Index (contd)
  • Therapeutic range (therapeutic window)
  • Peak and trough levels, see Table 1-4
  • Loading dose
  • Side effects, adverse reactions, and toxic effect
  • Pharmacogenetics
  • Tachyphylaxis
  • Placebo effect

29
Drug Effects
  • To achieve therapeutic effect the drug must be
    in appropriate concentration

30
Effects of Dosing on Pharmacokinetic Processes
  • Steady state
  • even distribution of drug concentration
  • administration rate rate of clearance
  • dependent on half-life

31
  • Loading maintenance doses
  • higher than usual dose needed to sustain
    therapeutic effect
  • faster therapeutic effect than can be achieved
    with steady state
  • Volume of distribution
  • hypothetical volume of fat, blood, and total body
    water in which drug appears distributed.
  • Highly water soluble drugs have a low Vd and
    reach high serum levels. Drugs with high Vd are
    more widely distributed in tissues. Figure is
    used to help determine drug dose.

32
  • Clearance
  • rate of removal of drug from the body
  • Tolerance
  • successively larger doses of a drug are required
    to maintain the same level of effect.

Tacyphlaxis when drug tolerance occurs
33
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34
Implications for Nursing Management
  • Maximizing therapeutic effect
  • understand principles of drug action
  • assess core patient variables to see if drug
    action is typical
  • assess appropriateness of therapeutic regime
  • assess appropriateness of administration site,
    route, probable effects
  • assess drug to be given and time of
    administration

35
Nursing Management cont.
  • Minimize Adverse Effects
  • make appropriate modifications to promote
    effective action
  • monitor drug level
  • assess for early signs of adverse effects

36
Summary
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