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FATE OF BODY MEDICINE
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RENAL
is the organ that serves to
remove urine, which are
waste products of metabolism
of the body in liquid form. Renal function is to regulate
the water balance in the body,regulating the concentration of
salt in the blood, regulate the
balance of acid - alkaline blood
and regulate the excretion of
waste material and excess salt.
When renals fail in its function,
there will be a disruption in water
balance and metabolism in the
body. Thus resulting in the buildup
of harmful substances in the
blood. (Pearce, 1995)
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Renal
excretion
Is one of the important mechanisms involved in the removal of
drugs from the workplace. Effects of a single dose of the drug will
be extended and the concentration of the saturated state (steady
state) will increase if the process decreases. In patients with renal
failure there is a decrease in renal blood flow, organ size,
glomeruler and tubular function. These changes resulted in theelimination of some drugs more slowly. Therefore, dosi drugs in the
primary excretion by the kidneys should be customized for each
individual.
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COMMON CAUSES OF
RENAL FAILURE
ALLERGENNEFRON
HypovolemiaNephrotoxic drugs / Metal-
metal
Diabetes Mellitus
HYPERTENSION
Pyelonephritis
(Shargel & Yu, 2005)
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Excretion decreased
Drug levels in the blood
increases
Toxic Effects
Bond decreasedplasma
(Sulistia , 2009:893)
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Selected drugelimination via
the liver
Avoid the use oftetracycline
group, diuretics,
aspirin and oralantidiabetic
Use lower doses
than normal,especially for
drugs primarilyeliminated
through thekidneys
GENERAL PRINCIPLES OF DRUG USE IN RENAL FAILURE
(Sulistia , 2009:893)
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Creatinine clearance can be calculated using
For Women, The results of the
above x 0.85
In patients with acute renal failure, is
considered
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Dose adjustments in renal failure is mainly done for the
maintenance dose using the equation Giusti -Hayton
G = The correction factor Giustiayton
= Fraction of drug elimination by the kidneys
= creatinine clearance in uremia= normal creatinine clearance
Furthermore, G is used to lower the dose or extend
the maintenance interval T
(Sulistia , 2009:893)
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Decrease maintenance dose with a fixed
interval T
= in uremia
= in normal
This was done for drugs with a narrow margin of safety, egdigitalis, antiarrhythmics, and anticonvulsants, to avoid large
fluctuations levels
(Sulistia , 2009:893)
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This was done for drugs that work relies on a high level,
such as aminoglycosides.
Extension of dose interval with a fixed maintenance dose
= dosing interval in uremia
= normal dose interval
(Sulistia , 2009:893)
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3. Changes in renal clearance of
the drug reflected by changes in
creatinine clearance.
2. These renal elimination is not
(especially the metabolic rate
constants) remains unchanged.
1. The elimination rate constant
decreases proportionally when
kidney function decreases.
(Shargel & Yu, 2005)
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There are several methods to estimate the appropriate
dosage regime for a patient with renal damage. The
design rules for people with uremia dose based on
pharmacokinetic changes that occur in connection with
the condition of uremia.
(Shargel & Yu, 2005)
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No dose adjustment isnecessary, if
Fraction of intact drugexcreted by the
kidneys (fr) 0:33 andinactive metabolites,
regardless LFGnya
In LFG normal value
0.67, regardless of hisfr
(Sulistia , 2009:893)
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CONCLUSION
There are two general approaches for pharmacokinetics were
dose adjustments include methods based on drug clearance and
a method based on the elimination half-life.
A dosage regime can be designed for patients with kidneyfailure by either lowering the normal dose of the drug and
keep the frequency of dosing (dosing interval) that is
constant or by decreasing the frequency of dosing
(extending the dosing interval) and maintain a constant
dose.
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