Laboratory：Akiruno
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- Teicoplanin
Laboratory：Akiruno
○Teicoplanin
CODE：02481 5
-
TEST NAME
SPECIMEN
REQUIREMENT
（ｍL） CONTAINER CAP COLOR STORE
TEMPERATURE
(STABILITY) TURNAROUND
TIME (DAY) METHODOLOGY REFERENCE RANGE
(UNIT) BLOOD COLLECTION TIME -
Teicoplanin
Serum
0.3
S7P
↓
A00
2-4 Latex agglutination turbidimetryTrough15-30(μg/mL) Within 30 minutes before administration (Trough concentration)LA (Latex agglutination immunoassay)
Latex agglutination turbidimetry
An antigen-antibody reaction is performed using latex particles that have adsorbed (bound) antigens or antibodies, and the turbidity of the agglutination caused by the antigen-antibody reaction is measured using light. A method of measuring from transmittance or scattering intensity of light by irradiation.
COMMENT
Targocid
Precautions regarding Blood Collection Containers: Do not use containers containing serum separators. It may affect the measurement value in drug test.
Notes on Blood Collection Time
1. It is blood collection time in TDM (therapeutic drug monitoring).
2. In continuous administration, collect blood after steady state is reached.
3. Peak concentration should also be measured at the time of poisoning.
4. This is standard time and it is desirable to collect blood according to the patient's conditions.
About Teicoplanin Test
The package insert of the drug states, ""Trough blood teicoplanin concentration should be maintained at 10 μg/mL or higher to ensure clinical efficacy in severe infectious diseases such as sepsis. However, if the trough blood concentration becomes 60 μg/mL or higher, the patient should be aware of the occurrence of side effects such as kidney failure and hearing impairment. In addition, there have been reports of transient mild elevations in the test values of liver function at trough blood concentrations of 20 μg/mL or higher. (cited from the 8th edition of the package insert of the drug, revised in January 2003.)""
CONTAINER
S7P 旧容器記号 C4 X2 X1
分離剤なし (真空採血量7mL)
貯蔵方法：室温
有効期間：製造から1年
A00 旧容器記号 X
ポリスピッツ
貯蔵方法：室温
