Test:Strongyloides Antibody
Other Test Request Name:

Strongyloidiasis Serology

Test Composition:

Not applicable

Intended Use:

A tropical infection due to the parasite Strongyloides stercoralis. Sometimes occurs in humid temperate regions. This test is usually performed when a subject who has recently visited an endemic area presents with recurrent gastrointestinal problems associated with pruritis and eosinophilia. Diagnosis relies on the identification of larvae in fresh stools. Serological results are often difficult to interpret because of the many possible cross reactions, mostly with other nematodes.

Methodology:

Enzyme Immunoassay (EIA)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

No patient preparation necessary.

Collection/Sample Container:

Red or Gold Tube

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

3 mL Serum

Alternative Specimen and Volume Requirement:

Not Applicable

Specimen Stability  
•   Room Temperature (15-25°C):

24 Hours

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

28 Days

Transport Temperature:

Transport specimen at 2 – 8 °C (with cold packs)

Rejection Criteria:
  • Hemolyzed specimen
  • Markedly lipemic specimen
  • Exceeded sample stability requirement
  • Quantity not sufficient
  • Improperly labeled specimen
  • Improper collection tube used
Running Day:

Batch Running

Cut Off Time:

Friday, 4:00 PM

TAT/Releasing of Results:

3 weeks after cut-off (excluding Saturdays, Sundays and Holidays)

Reference Interval/Result Interpretation:

Available upon request

Limitations/Interferences:

None specified.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Strongyloides stercoralis, infective filariform larva in warm, moist soil

 

Test:Sucrose (FOR HP DEL MONTE ONLY)
Other Test Request Name:

Sucrose Hemolysis Test

Test Composition:

Not Applicable

Intended Use:

The Sucrose Hemolysis Test is useful in screening for paroxysmal nocturnal hemoglobinuria (PNH). PNH describes erythrocytic destruction with the appearance of dark urine in the morning. PNH is an acquired disorder that is characterized by hemolytic anemia, large vessel thrombosis, or a deficiency of hematopoiesis.

Methodology:

Hemolysis

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:
  • Collection should be done at DEL MONTE BRANCH ONLY
  • No patient preparation necessary.
  • Inform laboratory 1 day before extraction for schedule.
  • For schedule special trip
Collection/Sample Container:

Citrated or Blue Top

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

2 pcs of 4mL Citrated whole blood

Alternative Specimen and Volume Requirement:

Not Applicable

Specimen Stability  
•   Room Temperature (15-25°C):

2 Hours

•   Refrigerated Temperature (2-8°C):

Not Applicable

•   Freezer Temperature (-20°C):

Not Applicable

Transport Temperature:

Transport specimen at 15°C ~25 °C (room temperature)

Rejection Criteria:
  • Exceeded sample stability requirement
  • Quantity not sufficient
  • Improperly labeled specimen
  • Improper collection tube used
  • Clotted Sample
  • Over-filled or Under-filled tube
Running Day:

Monday to Friday

Cut Off Time:

Monday to Friday, 7:00 AM

TAT/Releasing of Results:

3 days after running (excluding Saturdays, Sundays and Holidays)

Reference Interval/Result Interpretation:

Available upon request

Limitations/Interferences:

None Specified.

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Carbohydrate, Sugar

 

Test:Surgical Pathology Test
Other Test Request Name:
  • Histopath
Test Composition:
  • Not applicable
Intended Use:
  • For the examination of surgical specimens or tissues removed from living patients for the purpose of diagnosis of disease and guidance in the care of patients.
  • Differentiates specimens between benign (non-cancerous) and malignant (cancerous) and identifies infectious agents in body tissues.
Methodology:
  • Routine Histopathology (Tissue Processing)
Laboratory Section:
  • Histopathology
Special Instructions/Patient Preparations:
  • Fresh tissue specimen must be immersed in adequate fixative preferably 10% Neutral Buffered Formalin
  • Fix tissue for a minimum of 6 hours to a maximum of 48 hours.
  • Container must be properly labeled with at least two identifying marker (e.g. Patient’s name, type of specimen)
  • Specimens brought to the laboratory should have its corresponding request form filled with complete patient demographics and information
Collection/Sample Container:
  • Tightly sealed, wide mouthed specimen containers
Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:
  • Volume ratio of tissue sample to fixative should be 1:10
Alternative Specimen and Volume Requirement:
  • Not applicable
Specimen Stability  
•   Room Temperature (15-25°C):
  • Indefinite if fixed with 10% neutral buffered formalin
•   Refrigerated Temperature (2-8°C):
  • Not applicable
•   Freezer Temperature (-20°C):
  • Not applicable
Transport Temperature:
  • Transport speciments at 15°C to 30°C
Rejection Criteria:
  • Improperly fixed specimen
  • Incomplete information in the Histopathology Request Form (HPD_F_258), Histopathology Service Request Form (HPD_F_259)
  • Unlabeled samples
  • NOTE: In general, anatomic pathology specimens are not rejected for testing because they are irreplaceable and/or cannot be easily recollected. Instead, any problems encountered that may affect proper diagnosis will be documented and reported.
  • Inform the attending physician, client, branch and/or pathologist at once if problems are encountered.
Running Day:
  • Daily
Cut Off Time:
  • 7:00 PM
TAT/Releasing of Results:
  • 3 to 5 days after receipt of specimen (with reading/interpretation)
  • 1 day for Metro Manila clients and 2 days for Provincial clients (processing only)
  • Note: Additional 2 days may be necessary if specimen needs further evaluation and confirmation by another Pathologist.
Reference Interval/Result Interpretation:
  • Not applicable
Limitations/Interferences:
  • Not applicable
Frequently Asked Questions (FAQs):
  • Not applicable
Related Words/Test:
  • Histopath

 

Test:Synaptophysin
Other Test Request Name:

Not applicable

Test Composition:

Not applicable

Intended Use:

It is used to differentiate carcinoid from carcinoma; merkel cell carcinoma vs. basal cell carcinoma; small cell carcinoma of lung vs. lymphoma

Methodology:

Precipitation Indirect Reaction

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

No patient preparation necessary.

Collection/Sample Container:

Slide holders or mailers for microscope slides; FFPE tissue blocks can either be wrapped in paper or placed in a box.

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

• Formalin-fixed paraffin-embedded (FFPE) tissue block
• 1 H&E stained slide representative of the submitted tissue block.
• Histopathology report for the submitted tissue block

Alternative Specimen and Volume Requirement:

Not Applicable

Specimen Stability  
•   Room Temperature (15-25°C):

Indefinite

•   Refrigerated Temperature (2-8°C):

Not applicable

•   Freezer Temperature (-20°C):

Not applicable

Transport Temperature:

• Microscope slides should be placed in slide holders or mailers and should be adequately padded before placing in a shipping/packaging container to prevent breakage.
• FFPE tissue blocks must be placed in a box and avoid direct sunlight to prevent melting and disorientation during transport or shipping.
• Transport specimen at 15°C ~25 °C (room temperature)

Rejection Criteria:

• Incomplete information in the Request Form
• Improper or insufficient labeling of tissue blocks or slides
• Inadequate tissue available on the tissue block

Running Day:

Tuesday , Thursday and Saturday

Cut Off Time:

Monday, Wednesday and Friday 3:00 P.M

TAT/Releasing of Results:

After 7 days (excluding Saturdays, Sundays and Holidays)

Reference Interval/Result Interpretation:

Not Applicable

Limitations/Interferences:

None specified.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Major synaptic vesicle protein p38

 

Test:Synovial Fluid Analysis
Other Test Request Name:

• Joint Fluid Analysis

Test Composition:

1. Macroscopic
2. Microscopic
3. Differential Count
4. Synovial Fluid Glucose
5. Synovial Fluid Protein

Intended Use:

• Cell Count and Differential Count: Cell count and identification of types of cells present are used in determining the cause of an effusion, especially when used in combination with an individual's medical history, physical examination and other tests performed.
• Body Fluid Protein and Glucose: Differentiates Transudates from Exudates. It helps identify the cause of fluid accumulation.

Methodology:

• WBC count- Fluorescent Cytometry
• RBC count- Hydrodynamic Focusing
• Differential Count- Fluorescence Cytometry/ Microscopic Examination
• Body Fluid Protein - Colorimetric (Biuret)
• Body Fluid Glucose - Enzymatic Colorimetric(Hexokinase)

Laboratory Section:

• Cell Count/Differential Count: Hematology
• Body Fluid Protein and Glucose: Chemistry

Special Instructions/Patient Preparations:

• Cell Count/Diff Count: No patient preparation necessary
• Protein and Glucose: Preferably 8 hours fasting
• Send to Laboratory within 24 hours of collection.

Collection/Sample Container:

Glucose and Protein:
• Bottle #1 placed on a plain tube (Red Top with no additive)

Cell Count/Diff Count:
• Bottle #2 placed on an EDTA Tube

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

• Cell Count/Diff Count: 3-5 mL
• Glucose and Protein: 3-5 mL

Alternative Specimen and Volume Requirement:

Not applicable

Specimen Stability  
•   Room Temperature (15-25°C):

Glucose and Protein: 1 Day

Cell Count/Diff Count: 1 Day

•   Refrigerated Temperature (2-8°C):

Glucose and Protein: 6 Days

Cell Count/Diff Count: Not specified

•   Freezer Temperature (-20°C):

Unacceptable

Transport Temperature:

Transport specimen at 15–25 °C (room temperature)

Rejection Criteria:

• Quantity not sufficient
• Clotted sample (for Cell Count and Diff Count)
• Incorrect storage temperature of specimen
• Incorrect collection tube used
• Specimen stored exceeded required sample stability
• Highly viscous specimen
• Hemolyzed samples

Running Day:

Daily

Cut Off Time:

Monday to Saturday: 10:00 PM

Sunday: 6:00PM

TAT/Releasing of Results:

ROUTINE
• 4 hours after receipt of specimen/ arrival of messenger
STAT
• After 2½ hours from extraction/messenger arrival

Reference Interval/Result Interpretation:

Glucose:
Transudate: Exudate: Lower than whole blood levels

Total Protein:
Transudate: 10.00~30.00 g/L
Exudate: >30.00 g/L

Specific Gravity:
Transudate: <1.016
Exudate: >/=1.016

White Blood Cells:
Transudate: <100.00 x 10^3/uL
Exudate: >1000.00 x 10^3/uL

Limitations/Interferences:

None specified

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Uric Acid, Gram Stain, Susceptibility Testing, AFB Testing, Body Fluid Analysis, Rheumatoid Factor, Cyclic Citrullinated Peptide Antibody

 

Test:T. Calcium (COLORIMETRIC)
Other Test Request Name:

• Total Calcium
• Calcium
• Ca

Test Composition:

Not applicable

Intended Use:

• Used to screen for, diagnose, and monitor a range of conditions relating to the bones, heart, nerves, kidneys, and teeth.
• Often measured as part of a routine health screening to diagnose or monitor a variety of conditions.

Methodology:

Colorimetric

Laboratory Section:

Chemistry

Special Instructions/Patient Preparations:

• 8-12 hours fasting.
Note:
• Prolonged fasting is highly discouraged since various metabolic changes associated with starvation may begin to develop. Water intake is acceptable.
• Note in clinical info if patient drank more than 4 glasses of water during fasting period, ask patient for medical history as this is rather unusual.
• Note in clinical info in case patient overfasts and insists on proceeding test.

Collection/Sample Container:

Red or Gold tube

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

1-3 mL Serum

Alternative Specimen and Volume Requirement:

1-3 mL Plasma (Li-Heparin)

Specimen Stability  
•   Room Temperature (15-25°C):

7 Days

•   Refrigerated Temperature (2-8°C):

3 Weeks

•   Freezer Temperature (-20°C):

8 Months

Transport Temperature:

Transport specimen at 2 – 8 °C (with cold packs)

Rejection Criteria:
  • Specimens that failed serum index requirement
  • Exceeded sample stability requirement
  • Quantity not sufficient
  • Improperly labeled specimen
  • Improper collection tube used
  • EDTA Plasma
Running Day:

Daily

Cut Off Time:

Monday to Saturday:6:00 PM

Sunday: 4:00PM

TAT/Releasing of Results:

RUNNING TIME: 6:00 AM onwards

RELEASING TIME: ROUTINE
• 4 hours after receipt of specimen/ arrival of messenger
RELEASING TIME: STAT
• After 2½ hours from extraction/messenger arrival

Reference Interval/Result Interpretation:

2.10-2.55 mmol/L (8.40-10.20 mg/dL)

Limitations/Interferences:

• Blood from patients receiving Hypaque radiographic contrast agent cannot be used.
• Blood from patients on EDTA therapy cause false results.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Phosphorus, Vitamin D Tests, PTH, Magnesium, Albumin, Comprehensive Metabolic Panel, Basic Metabolic Panel, Kidney Stone Analysis, Kidney Stone Risk Panel

 

Test:T. gondii IgM (Quali) -TEMPORARILY UNAVAILABLE
Other Test Request Name:

Toxoplasma gondii Quali IgM

Test Composition:

Not Applicable

Intended Use:

Used for Qualitative detection of IgM antibodies to Toxoplasma gondii, used as screening for toxoplasmosis.

Methodology:

Immunochromatography

Laboratory Section:

Serology

Special Instructions/Patient Preparations:

No patient preparation necessary.

Collection/Sample Container:

Red or Gold tube

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

1-2mL Serum

Alternative Specimen and Volume Requirement:

1-2mL Plasma (EDTA)

Specimen Stability  
•   Room Temperature (15-25°C):

Not Specified

•   Refrigerated Temperature (2-8°C):

3 Days

•   Freezer Temperature (-20°C):

>3 Days

Transport Temperature:

Transport specimen at 2 – 8 °C (with cold packs)

Rejection Criteria:

• Improperly labeled specimens
• Hemolyzed specimens
• Lipemic specimens
• Quantity not sufficient
• Specimen storage and transport exceeded required temperature

Running Day:

Daily

Cut Off Time:

Monday to Saturday
• 8:00 PM

Sunday
• 3:00 PM

TAT/Releasing of Results:

ROUTINE
• 3 hours after receipt of specimen/ arrival of messenger
STAT
• 1½ hours from extraction/messenger arrival

Reference Interval/Result Interpretation:

NEGATIVE

Limitations/Interferences:

None identified.

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Newborn Infection, Toxoplasmosis, Toxoplasma gondii Antibodies, IgG, IgM; Toxoplasma gondii Molecular Detection by PCR

 

Test:T. Protein (COLORIMETRIC)
Other Test Request Name:

• TP
• Total Protein

Test Composition:

Not applicable

Intended Use:

• May be used for evaluation of nutritional status and protein altering diseases like kidney disease or liver disease

Methodology:

Colorimetric

Laboratory Section:

Chemistry

Special Instructions/Patient Preparations:

• No patient preparation necessary.

Collection/Sample Container:

Red or Gold tube

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

1-3 mL Serum

Alternative Specimen and Volume Requirement:

1-3 mL Plasma (Li- or Na-Heparin)

Specimen Stability  
•   Room Temperature (15-25°C):

1 Week

•   Refrigerated Temperature (2-8°C):

34 Days

•   Freezer Temperature (-20°C):

2 Months

Transport Temperature:

Transport specimen at 2 – 8 °C (with cold packs)

Rejection Criteria:
  1. Failed serum index samples
  2. Specimen stored/transported outside the temperature range
  3. Quantity not sufficient
  4. Improperly labeled specimen
  5. Improper collection tube used
  6. EDTA plasma
Running Day:

Daily

Cut Off Time:

Monday to Saturday:  6:00 PM

Sunday: 4:00PM

TAT/Releasing of Results:

RUNNING TIME: 6:00 AM onwards

RELEASING TIME: ROUTINE
• 4 hours after receipt of specimen/ arrival of messenger
RELEASING TIME: STAT
• After 2½ hours from extraction/messenger arrival

Reference Interval/Result Interpretation:

0-3Y: 59.00-70.00 g/L (5.90-7.00 g/dL)
3Y & 1 Day - 6Y: 59.00-78.00 g/L (5.90-7.80 g/dL)
6Y & 1 Day - 9Y: 62.00-81.00 g/L (6.20-8.10 g/dL)
9Y & 1 Day - 11Y : 63.00-86.00 g/L (6.30-8.60 g/dL)
11Y & 1 Day - 999Y: 64.00-87.00 g/L (6.40-8.70 g/dL)

Limitations/Interferences:

Interferences from medications or endogenous substances may affect results.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Albumin, Liver Panel, Protein Electrophoresis, Comprehensive Metabolic Panel, BUN, Creatinine, Urine Protein, Body Fluid Analysis

 

Test:T3 (ECLIA)
Other Test Request Name:

• Triiodothyronine
• Total T3

Test Composition:

Not applicable

Intended Use:

The determination of T3 is utilized in the diagnosis of T3-hyperthyoridism , the detection of early stages of hyperthyroidism and for indicating a diagnosis of thyrotoxicosis factitia.

Methodology:

Electrochemiluminescence Immunoassay (ECLIA)

Laboratory Section:

Immunology

Special Instructions/Patient Preparations:

Samples should not be taken from patients receiving therapy with high biotin doses (i.e. > 5 mg/day) until at least 8 hours following the last biotin administration.

Collection/Sample Container:

Red or Gold tube

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

1-3 mL Serum

Alternative Specimen and Volume Requirement:

1-3 mL Plasma (Li-, Na-, NH4 -heparin, K3-EDTA, Sodium Citrate, Sodium Fluoride, Potassium Oxalate)

Specimen Stability  
•   Room Temperature (15-25°C):

Not specified

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

1 Month (Freeze only once)

Transport Temperature:

Transport specimen at 2°C – 8 °C (with cold packs)

Rejection Criteria:

• Hemolyzed specimen
• Markedly lipemic sample
• Exceeded sample stability requirement
• Quantity not sufficient
• Improperly labeled specimen
• Improper collection tube used

Running Day:

Monday, Tuesday, Wednesday, Thursday, Friday, Saturday

Cut Off Time:

Monday to Saturday:10:00 PM

Sunday:6:00PM

TAT/Releasing of Results:

ROUTINE (on running days)
• 4 hours after receipt of specimen/ arrival of messenger
STAT (on running days only)
• 2½ hours from extraction/messenger arrival

Reference Interval/Result Interpretation:

1.30-3.10 nmol/L

Limitations/Interferences:

• Samples should not be taken from patients receiving therapy with high biotin doses (i.e. > 5 mg/day) until at least 8 hours following the last biotin administration.
• In rare cases, interference due to extremely high titers of antibodies to analyte-specific antibodies, streptavidin or ruthenium can occur.
• Therapy with amiodarone can lead to depressed T3 values.
• Phenytoin, phenylbutazone, and salicylates cause release of T3 from the binding proteins, thus leading to a reduction in the total T3 hormone level at normal fT3 levels.
• Autoantibodies to thyroid hormones can interfere with the assay.
• Binding protein anomalies seen with FDH (familial dysalbuminemic hyperthyroxinemia), for example, may cause values which, while characteristic of the condition, deviate from the expected results.
• Pathological concentrations of binding proteins (TBG, albumin) can lead to total T3 values outside the normal range being found despite a euthyroid metabolic state (e.g. in NTI-patients, pregnancy, use of oral contraceptives). In such cases an fT3 or fT4 determination is indicated.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Thyroid Function Test, TSH; Free T4; Thyroid Panel; Thyroid Antibodies

 

Test:T3 Reverse (RIA)
Other Test Request Name:
  • Reverse T3
  • Reverse triiodothyronine
  • rT3
Test Composition:

Not applicable

Intended Use:

The assay may be useful in the diagnosis of nonthyroidal illness (NTI). Patients with NTI have low T3 concentrations and increased concentrations of rT3. RT3 may be useful in neonates to distinguish euthyroid sick syndrome from central hypothyroidism.

Mainly produced by the deiodination of thyroxine (T4) in peripheral tissue.

Methodology:

Radioimmunoassay (RIA)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

No patient preparation necessary.

Collection/Sample Container:

Red or Gold Tube

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

3 mL Serum

Alternative Specimen and Volume Requirement:

Not Applicable

Specimen Stability  
•   Room Temperature (15-25°C):

24 Hours

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

28 Days

Transport Temperature:

Transport specimen at 2 – 8 °C (with cold packs)

Rejection Criteria:
  • Hemolyzed specimen
  • Markedly lipemic specimen
  • Exceeded sample stability requirement
  • Quantity not sufficient
  • Improperly labeled specimen
  • Improper collection tube used
Running Day:

Batch Running

Cut Off Time:

Friday, 4:00 PM

TAT/Releasing of Results:

3 months after cut-off (excluding Saturdays, Sundays and Holidays)

Reference Interval/Result Interpretation:

Available upon request

Limitations/Interferences:

None specified.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Isomer of triiodothyronine

 

Test:T4 (ECLIA)
Other Test Request Name:

• Thyroxine
• Total T4

Test Composition:

Not applicable

Intended Use:

The determination of T4 can be utilized for the detection of primary and secondary hypothyroidism and for monitoring of TSH-supression therapy.

Methodology:

Electrochemiluminescence Immunoassay (ECLIA)

Laboratory Section:

Immunology

Special Instructions/Patient Preparations:

• Samples should not be taken from patients receiving therapy with high biotin doses (i.e. > 5 mg/day) until at least 8 hours following the last biotin administration.
• Patients treated with lipid-lowering agents (D-T4) should be discontinued 4-6 weeks of therapy prior to collection (please consult your doctor before following this preparation).

Collection/Sample Container:

Red or Gold tube

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

1-3 mL Serum

Alternative Specimen and Volume Requirement:

1-3 mL Plasma (Li-, Na?heparin and  K3?EDTA)

Specimen Stability  
•   Room Temperature (15-25°C):

Not specified

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

1 Month (Freeze only once)

Transport Temperature:

Transport specimen at 2°C – 8 °C (with cold packs)

Rejection Criteria:

• Hemolyzed specimen
• Markedly lipemic sample
• Exceeded sample stability requirement
• Quantity not sufficient
• Improperly labeled specimen
• Improper collection tube used

Running Day:

Monday, Tuesday, Wednesday, Thursday, Friday, Saturday

Cut Off Time:

Monday to Saturday:10:00 PM

Sunday:6:00PM

TAT/Releasing of Results:

ROUTINE (on running days)
• 4 hours after receipt of specimen/ arrival of messenger
STAT (on running days only)
• 2½ hours from extraction/messenger arrival

Reference Interval/Result Interpretation:

66.00-181.00 nmol/L

Limitations/Interferences:

• Samples should not be taken from patients receiving therapy with high biotin doses (i.e. > 5 mg/day) until at least 8 hours following the last biotin administration.
• In rare cases, interference due to extremely high titers of antibodies to analyte?specific antibodies, streptavidin or ruthenium can occur.
• The test cannot be used in patients receiving treatment with lipid-lowering agents containing D?T4. If the thyroid function is to be checked in such patients, the therapy should first be discontinued for 4?6 weeks to allow the physiological state to become re-established.
• Autoantibodies to thyroid hormones can interfere with the assay.
• Binding protein anomalies seen with FDH (familial dysalbuminemic hyperthyroxinemia), for example, may cause values which, while characteristic of the condition, deviate from the expected results.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Thyroid Function Test, TSH, Free T3 or Total T3, Thyroid Panel, Thyroid Antibodies, Calcitonin, Free T4

 

Test:Tacrolimus (ECLIA)
Other Test Request Name:
  • Tacro
  • FK506
  • Fujimycin
  • Prograf
Test Composition:

Not applicable

Intended Use:

To monitor the adequacy of drug dosage levels in management of immunosuppression for organ transplant recipients.

Methodology:

Electrochemiluminescence Immunoassay (ECLIA)

Laboratory Section:

Immunology

Special Instructions/Patient Preparations:
  • Collect as 12-hour trough specimen (12 hours after last intake of Tacrolimus medication)
  • Provide date and time of last Tacrolimus intake, dosage and date and time of sample collection. This information is important to help requesting clinicians interpret the result.
  • An interaction with Itraconazole (INN international nonproprietary name) was found. Samples from patients under Itraconazole treatment cannot be tested.
  • Sample should not be taken from patients receiving therapy with high biotin doses (i.e >5 mg/day) until at least 8 hours following the last biotin administration.
Collection/Sample Container:

EDTA

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

2mL EDTA whole blood (K2- or K3- EDTA only)

Alternative Specimen and Volume Requirement:

Not Applicable

Specimen Stability  
•   Room Temperature (15-25°C):

5 Days

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

6 Months

Transport Temperature:

Transport specimen at 2°C – 8 °C (with cold packs)

Rejection Criteria:
  • Markedly lipemic specimen
  • Exceeded sample stability requirement
  • Quantity not sufficient
  • Improperly labeled specimen
  • Improper collection tube used
  • Clotted sample
  • Over-filled or Under-filled tube
Running Day:

Monday to Saturday: 12:00 PM

Cut Off Time:

Monday to Saturday: 6:00 PM

 

TAT/Releasing of Results:

ROUTINE (on running days)

  • 4 hours after receipt of specimen/ arrival of messenger

STAT (on running days only)

  • 2 1/2 hours from extraction or messenger arrival

 

Reference Interval/Result Interpretation:

5.00~20.00 ng/mL

NOTE: No firm therapeutic range exists for tacrolimus in whole blood. The complexity of the clinical state, individual differences in sensitivity to immunosuppressive and nephrotoxic effects of tacrolimus, coadministration of other immunosuppressants, type of transplant, time post-transplant, and a number of other factors contribute to different requirements for optimal blood levels of tacrolimus. Individual tacrolimus values cannot be used as the sole indicator for making changes in the treatment regimen. Each patient should be thoroughly evaluated clinically before treatment adjustments are made, and each assay user must establish his or her ranges based on clinical experience.

Limitations/Interferences:
  • Sample should not be taken from patients receiving therapy with high biotin doses (i.e >5 mg/day) until at least 8 hours following the last biotin administration.
  • An interaction with Itraconazole (INN international nonproprietary name) was found. Do not use samples from patients under Itraconazole treatment.
  • In rare cases, interference due to extremely high titers of antibodies to analyte-specific antibodies, streptavidin or ruthenium can occur.
Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Organ Transplant, Immuno suppressant, Immuno suppressant agent

 

Test:Tamoxifen and Metabolites
Other Test Request Name:• Tamoxifen
• Endoxifen
• N-Desmethyl Tamoxifen
• 4-Hydroxy Tamoxifen
• N-Desmethyl-4'-Hydroxy Tam
• 4'-Hydroxy Tamoxifen)
Test Composition:Not applicable
Intended Use:Tamoxifen is a prodrug and undergoes biotransformation into a series of metabolites. N-desmethyl tamoxifen is the most abundant metabolite. 4-Hydroxy tamoxifen and N-desmethyl-4-hydroxy tamoxifen (endoxifen) are the most potent metabolites. Studies have shown that genetic variations in the CYP2D6 enzymes influence endoxifen levels. Due to this variability, monitoring endoxifen levels and phase one metabolite rather than CYP2D6 genotype testing is suggested to be a better approach for monitoring tamoxifen therapy.
Methodology:Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS)
Laboratory Section:Special Test
Special Instructions/Patient Preparations:No patient preparation necessary.
Collection/Sample Container:Red tube (DO NOT USE GOLD TUBE or any other type of tube with gel separator)
Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:3 mL Serum
Alternative Specimen and Volume Requirement:Not Applicable
Specimen Stability  
•   Room Temperature (15-25°C):7 Days
•   Refrigerated Temperature (2-8°C):7 Days
•   Freezer Temperature (-20°C):Not applicable
Transport Temperature:Transport specimen at 2 – 8 °C (with cold packs)
Rejection Criteria:• Hemolyzed specimen
• Markedly lipemic specimen
• Exceeded sample stability requirement
• Quantity not sufficient
• Improperly labeled specimen
• Improper collection tube used
Running Day:Batch Running
Cut Off Time:Friday 4:00 PM
TAT/Releasing of Results:14 days after cut-off (excluding Saturdays, Sundays and Holidays)
Reference Interval/Result Interpretation:Available upon request
Limitations/Interferences:None specified.
Frequently Asked Questions (FAQs):Not applicable
Related Words/Test:Nolvadex, medication that is used to prevent breast cancer in women

 

Test:TB C/S
Other Test Request Name:
  • Mycobacterium Tuberculosis
  • MTB c/s
Test Composition:

Not Applicable

Intended Use:

Tuberculosis is a chronic, granulomatous disease caused by M. tuberculosis. Identification, and, if appropriate, antibiotic sensitivity, is required to initiate necessary therapy.

TB is an infectious bacterial disease caused by mycobacterium tuberculosis, which most commonly affects the lungs.

Methodology:

Bactec MGIT

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

 

Note:

  • Indicate Diagnosis and Medications
  • Culture and Sensitivity of Sputum samples (expectorated/induced)
  • Sample should be sputum not saliva. In case sample submitted does not fit the criteria of a sputum specimen, a repeat collection will be requested.
  • Sample must be properly packed (trtiple packaging)
  • For Sputum Samplemust be at Laboratory, Monday to Friday before 7:00 AM., sample must be collected Monday to Thursday, on or before 3:00 PM and need to be send to MAIN branch within that day.


A. Sputum Collection
The most productive sputum can be collected in the morning.

1. Expectorated Sputum

  • Rinse the mouth and gargle with water. Do not brush teeth prior to collection.
  • Take a deep breath and make a deep cough. Good quality sputum should not contain saliva. Specimen should be collected in a sterile leak-proof container and delivered to the laboratory without delay.
  •  Properly close and wipe dry the container. Label sample container with patient's complete name, with date and time of collection.


2. Induced Sputum

  • Rinse the mouth and gargle with water. Do not brush teeth prior to collection.
  • Take a deep breath and make a deep cough. Collect the induced sputum into a sterile leak-proof container and deliver to the laboratory without delay.
  • Properly close and wipe the container dry. Label sample container with patient's complete name, with date and time of collection.


B. Endotracheal Aspirate Collection

  • Aspirate the specimen into a sterile Luken trap and aseptically transfer sample to a sterile screw-cap container.
  • Label the sterile container or the catheter cover properly and submit to the laboratory.

C. Pleural Effusion

  • Aspirate the specimen into a sterile Luken trap and aseptically transfer sample to a sterile screw-cap container.
  • Label the sterile container and cover properly, always indicate the site of collection If RIGHT or LEFT LUNG, then submit to the laboratory.

D. Urine

  • Indicate patient’s diagnosis, medical history and sample type on request forms.
  • Clean-voided midstream urine collection
  • Before starting the procedure, wash hands thoroughly with soap and water.
  • Cleanse the genital area before collection.


 

Collection/Sample Container:

Plastic leak proof sterile container (screw cap) 

NOTE:Sample must be properly packed (trtiple packaging)

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:
  • 2 mL Sputum/ETA/Pleural Fluid
  • 100 mL Urine
Alternative Specimen and Volume Requirement:

Not Applicable

Specimen Stability  
•   Room Temperature (15-25°C):

24 Hours

•   Refrigerated Temperature (2-8°C):

SPUTUM- 24 Hours

URINE- 24 Hours

OTHER BODY FLUIDS- 7 Days

•   Freezer Temperature (-20°C):

Not applicable

Transport Temperature:

Transport specimen at 2°C - 8°C (with cold packs)

Rejection Criteria:
  • Quantity Not sufficient
  • Improperly labeled specimen
  • Specimen stored and transported outside the required temperature
  • Wrong container
Running Day:

Monday to Friday

Cut Off Time:

Monday to Friday, 7:00 AM

 

For Sputum Samplemust be at Laboratory, Monday to Friday before 7:00 AM., sample must be collected Monday to Thursday, on or before 3:00 PM and need to be send to MAIN branch within that day.

TAT/Releasing of Results:

3 months after cut-off (excluding Saturdays, Sundays and Holidays)

Reference Interval/Result Interpretation:

Not Applicable

Limitations/Interferences:

None specified.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Bacteria or fungi that are causing an infection of the lungs

 

Test:TB PCR (BY APPOINTMENT)
Other Test Request Name:

Not applicable

Test Composition:

Not applicable

Intended Use:

Used to aid the physician in the rapid diagnosis and treatment of a possible tuberculosis infection.

Methodology:

Polymerase Chain Reaction (PCR)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:
  • No patient preparation necessary.
  • Call Special Test Section (By Appointment/Schedule).
  • Sample must be properly packed (trtiple packaging)

NOTE: Do not collect specimen without approval of Special Test Section

 

Collection/Sample Container:

Plastic leak proof sterile container (screw cap) 

NOTE: Sample must be properly packed (trtiple packaging)

 

Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:

Atleast 2 mL Sputum

Alternative Specimen and Volume Requirement:

Atleast 2 mL Any body fluids or 60 mL Random Urine

Specimen Stability  
•   Room Temperature (15-25°C):

24 Hours

•   Refrigerated Temperature (2-8°C):

5 Days

•   Freezer Temperature (-20°C):

Not applicable

Transport Temperature:

Transport specimen at 2°C - 8°C (with cold packs)

Rejection Criteria:
  • Quantity Not sufficient
  • Improperly labeled specimen
  • Specimen stored and transported outside the required temperature
  • Improper collection container
Running Day:

Wednesday

Cut Off Time:

Tuesday, 7:00 AM

TAT/Releasing of Results:

3 days after running day (excluding Saturdays, Sundays and Holidays)

Reference Interval/Result Interpretation:

Not Applicable

Limitations/Interferences:

None specified.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Confirm an infection of Tuberculosis