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Diterbitkan olehRifqy Rachman Telah diubah "9 tahun yang lalu
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Bagian Farmakologi & Terapi Fakultas Kedokteran Universitas Andalas
FARMAKOLOGI KLINIK Rahmatini Bagian Farmakologi & Terapi Fakultas Kedokteran Universitas Andalas
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DEFINISI WHO ( 1988) Disiplin dalam bidang kedokteran berdasarkan prinsip ilmiah, menyatukan keahlian farmakologi & keahlian klinik dengan tujuan meningkatkan manfaat & keamanan obat
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Terapi Efektif, Aman , Rasional
TUJUAN FARMAKOLOGI KLINIK Terapi Efektif, Aman , Rasional
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RATIONAL DRUG USE Benefit – Risk - Cost Ratio F.Kinetika F Dinamika
F Ekonomi
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PHARMACOLOGICAL ASPECTS IN CLINICAL PRACTICE
Pharmacokinetic Pharmacodynamic How drugs act The dynamics of drug conc. in the body * Absorption / bioavailability * Distribution * Biotransformation * Excretion
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THERAPEUTIC DRUG MONITORING (TDM)
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Measuring the plasma drug conc.
Provide useful information about the adequacy of the dosage regimen or the likehood toxicity
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Measuring/ interpreting plasma drug conc.
Therapeutic Drug Monitoring (TDM) Ph dynamic Ph kinetic Drug-interaction Measuring/ interpreting plasma drug conc. Therapeutic response Side effects Toxic effects
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Time-drug conc. relationship
40 30 Drug toxicity 20 Drug conc. (mg/l) Therapeutic level 10 m.e.c Low therapy 1 2 3 4 Time (hour)
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Therapeutic Drug Monitoring (TDM)
1. Narrow margin of safety drugs 2. Drugs for prevention/ therapy of life threatening diseases or life saving drugs 3. Difficulty in ditinguishing between the effects of a disease and the toxic effects of a drug 4. Potent drugs drug amount is very small 5. Drugs that show variability of drug conc. in plasma
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Factors that modify drug plasma concentration for a given dose
Drug formulation Drug interaction Environmental factors Genetic variation Renal and hepatic function
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Reasons for monitoring 2. To assess drug toxicity
drug treatment To see whether there is therapeutic response 2. To assess drug toxicity 3. To assess compliance
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DRUG THERAPEUTIC TOXIC DIGOXIN 0,0010-0,0022 µg/ml > 0,0025 DIPHENYLHI DANTOIN 10- 20 > 25 LIDOCAIN 1,5-5 > 9 PHENOBARBITAL 15-30 > 40 THEOPHYLINE 10-20 > 20
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the toxic effects of a drug Nausea / anorexia / arrythmias
Examples of difficulty in ditinguishing between the effects of a disease and the toxic effects of a drug 1. Digoxin toxicity Congest.Heart Failure Nausea / anorexia / arrythmias 2. Gentamycin toxicity Gram (–) septicaemia Renal damage
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Pharmacokinetic parameters
Cmax (peak) Drugs- plasma conc. Half life AUC 24 Cmin (trough) Time
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Visualisation of half-life
First order elimination of a drug (t ½ : 2 hours) The plasma conc. falls by half each half-life 20 Drug conc. (mg/l) t ½ 10 t ½ 5 t ½ 2.5 2 4 6 Hours
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Clinical application of half life (t½) * Designing drug dosage regimen
* Determining time to reach steady state drug level which show clinical effect * Determining time to reach the drug level which have no clinical effect anymore
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RATIONAL & GOOD CLINICAL THERAPY
CONSIDERATION Ph’kinetic Ph’dynamic Ph’economic RATIONAL & GOOD CLINICAL THERAPY
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SESUNGGUHNYA BAGIMU, ADA MALAIKAT- MALAIKAT YANG SELALU
MENGAWASI PEKERJAANMU QS 82 :10
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