Useful revision guide Instant Clinical Pharmacology E.J. Begg Useful information on individual drugs...
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Transcript of Useful revision guide Instant Clinical Pharmacology E.J. Begg Useful information on individual drugs...
![Page 1: Useful revision guide Instant Clinical Pharmacology E.J. Begg Useful information on individual drugs (although a bit old now) Basic Clinical Pharmacokinetics.](https://reader034.fdocuments.us/reader034/viewer/2022051613/5515e27055034638038b4ca8/html5/thumbnails/1.jpg)
Useful revision guide
Instant Clinical PharmacologyE.J. Begg
Useful information on individual drugs(although a bit old now)
Basic Clinical Pharmacokinetics (2nd Edition)M.E. Winter
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Drug dosing
Important factors• concentration of drug in plasma
• rate of drug elimination
• rate of drug absorption
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Toxic level
Minimumtherapeutic levelCp
time
Therapeutic window
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Revision of pharmacokinetic terms
1st order eliminationrate of elimination depends on plasma concentration
C = C0e-kt (k= rate constant of elimination)
Half life (t1/2)time for plasma concentration to fall by 50%
Zero order elimination (pseudo zero order)rate of elimination is constant and independent of plasma concentration
PlasmaConcn(Cp)
time
1st
zero
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PlasmaConcn(Cp)
time
Zero order elimination
Half life varies with concentration
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Volume of distribution (Vd)
Vd = doseC0
Volume of water in which a drug would have to be distributed to give its plasma concentration at time zero.Can be larger than total body volume
frusemide 7 litresaspirin 14 litrespropranolol 273 litresdigitoxin 38 liters 4 ml min-1
digoxin 640 litres 130ml min -1
Plasma clearance (ClP)volume of blood cleared of its drug content in unit time
CP= ClM + ClR + ClB + …….
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Bioavailability (F)
measure of the amount of drug absorbed into the general circulation
Area under the curve (AUC)
obtained from the plasma concentration v time plot
gives a measure of the amount of drug absorbed
Foral = AUCoral
AUCiv
Clearance = F. doseAUC
iv
oral
Cp
time
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Same drug, same dose different formulation• different amounts absorbed• different peak concentration• different AUCs
Cp
time
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Toxic level
Minimumtherapeutic level
Same drug, same route, different doses
Cp
time
Therapeutic window
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Different rates of absorption (different routes of administration)
Assume the bioavailability is the same (i.e. 1 for all routes)
Slower the rate of absorption• time to peak longer• amplitude of peak is less• longer drug in body
iv
sc
oral
Cp
time
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Two compartment model
plasma tissues
elimination
PlasmaConcn(Cp)
time
Redistribution + elimination
elimination
e.g. thiopentone
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At steady staterate of infusion = rate of elimination
= Css.Clearance
Css (plateau)
Time to 90 % of Css = 4 t1/2
Intravenous infusion
Cp
time
C = Css(1- e-kt)
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Lignocaine 2 8 hours
Valproate 6 24 hours
Digoxin 32 6 days
Digitoxin 161 28 days
Half life hours steady state
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X mg min-1
2X mg min-1
Rising phase of the infusion curve is governed by the rate of elimination
Height of plateau is governed by the rate of infusion
Cp
time
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Dosing interval
MTLCp
time
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Cavss
At Steady State amount administered = amount eliminated between doses
Multiple dosing
time
CpRising phase of the curve is stillgoverned by the rate of elimination
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Loading dose(s)
time
Cp
Loading dose = Cpeak . Volume of distribution
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Tetracycline t1/2 = 8 hours
500mg loading dose followed by 250mg every 8 hours
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Cavss = F . Dose Clearance. T
Cavss
Reducing the dose AND reducing the intervalCavss remains the same but fluctuation in Cp is less
T = dosing interval
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Drug plasma concentration monitoring is helpful for drugs
•that have a low therapeutic index •that are not metabolized to active metabolites
•whose concentration is not predictable from the dose •whose concentration relates well to either the therapeutic effect or the toxic effect, and preferably both
•that are often taken in overdose
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For which specific drugs is drug concentration monitoring helpful?
The important drugs are: • aminoglycoside antibiotics (plasma or serum)• ciclosporin (whole blood)• digoxin and digitoxin (plasma or serum)• lithium (serum)• phenytoin (plasma or serum)• theophylline (plasma or serum)• paracetamol and salicylate (overdose) (plasma or serum).
Other drugs are sometimes measured:• anticonvulsants other than phenytoin (eg carbamazepine, valproate)• tricyclic antidepressants (especially nortriptyline) • anti-arrhythmic drugs (eg amiodarone).
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The uses of monitoring are
• to assess adherence to therapy
• to individualize therapy
• to diagnose toxicity
• to guide withdrawal of therapy
• to determine whether a patient is already taking a drug before starting therapy (eg theophylline in an unconscious patient with asthma)
• in research (eg to monitor for drug interactions in post-marketing surveillance using population pharmacokinetics).
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Altered pharmacokinetic profile
• liver metabolismDiseasePharmacogenetics (cytochrome P450 polymorphisms)
• renal impairmentDiseaseElderly