Test:Japanese Encephalitis
Other Test Request Name:

Not applicable

Test Composition:

Not applicable

Intended Use:

Japanese encephalitis virus (JEV) is the most important cause of viral encephalitis in Asia. It is a mosquito-borne flavivirus, and belongs to the same genus as dengue, yellow fever and West Nile viruses.

Methodology:

Capture ELISA

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

No patient preparation necessary.

Collection/Sample Container:

Red Tube only (No Gel Separator)

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

3 mL Serum

Alternative Specimen and Volume Requirement:

2 mL CSF

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

14 Days

•   Refrigerated Temperature (2-8°C):

14 Days

•   Freezer Temperature (-20°C):

30 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:

Wednesday 8:00 AM

Cut Off Time:

Tuesday 4:00 PM

TAT/Releasing of Results:

After 3 days (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:

Japanese B encephalitis, mosquito-borne

 

Test:JC-Polyomavirus (PCR)
Other Test Request Name:

• JCV-PCR

• John Cunningham Virus

Test Composition:

Not applicable

Intended Use:

JC virus is the polyomavirus which causes progressive multifocal leukoencephalopathy, a fatal neurological infection which affects patients who are immunodeficient for long periods. In practice, the virus cannot be isolated but a reliable diagnosis can be based on the detection of viral DNA by PCR assay in a CSF specimen or brain biopsy material. No practical serological tests have been developed.

Methodology:

Polymerase Chain Reaction (PCR)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

Blood sample will be drawn every Wednesday-Thursday  from 8am-6pm.

Collection/Sample Container:

EDTA or Violet Tube

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

4 mL whole blood

Alternative Specimen and Volume Requirement:

• 2 ml CSF in Sterile Container
• 100 mL Random Urine

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

48 Hours

•   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
• Clotted Sample
• Over-filled or Under-filled tube

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:

Not Applicable

Limitations/Interferences:

None specified.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

John Cunningham virus, progressive multifocal leukoencephalopathy

 

Test:Kappa/Lambda Chains
Other Test Request Name:


Total Light Chain
 

Test Composition:

Kappa

Lambda

Kappa/Lambda Ratio

Intended Use:

•To help detect , diagnose and monitor plasma cell disorders (dyscrasias), including multiple myeloma and primary amyloidosis.
• To monitor effectiveness of treatment

Methodology:

Nephelometry

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):

48 Hours

•   Refrigerated Temperature (2-8°C):

8 Days

•   Freezer Temperature (-20°C):

30 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:

Monday, 12:00 PM

 

TAT/Releasing of Results:

2 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:Not Applicable

 

Test:Kappa/Lambda Chains
Other Test Request Name:

Free Light Chain

Test Composition:Not Applicable
Intended Use:

•To help detect , diagnose and monitor plasma cell disorders (dyscrasias), including multiple myeloma and primary amyloidosis.
• To monitor effectiveness of treatment

Methodology:

Electrochemiluminescence Immunoassay (ECLIA)

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):

48 Hours

•   Refrigerated Temperature (2-8°C):

21 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:

Monday 7am

Cut Off Time:

Friday 7am

TAT/Releasing of Results:

10 Working days after cut-off (excluding Saturdays, Sundays and Holidays)

Reference Interval/Result Interpretation:Not Applicable
Limitations/Interferences:Not Applicable
Frequently Asked Questions (FAQs):Not Applicable
Related Words/Test:Not Applicable

 

Test:Katocatz/Kato thick
Other Test Request Name:• Kato Thick Smear
• Kato technique
Test Composition:Not applicable
Intended Use:The Katokatz is most commonly used for detecting schistosome eggs but can also be used for the identification of other helminth eggs.
Methodology:Direct Microscopic Examination
Laboratory Section:Clinical Microscopy
Special Instructions/Patient Preparations:No patient preparation necessary.
Collection/Sample Container:Clean, leak-proof container
Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:Pea sized or size of 25 centavo coin stool
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 specimens immediately to HPD Laboratory at room temperature (15-25°C) within 2 hours.

NOTE: Do not delay transport of samples.
Rejection Criteria:• Quantity not sufficient (QNS); samples less than pea-sized stool
• Contaminated stool (e.g. with urine or other body fluids)
• Stool not delivered immediately in the laboratory within 2 hours.
Running Day:Daily
Cut Off Time:Monday to Saturday
• 6:00 PM

Sunday
• 3:00 PM
TAT/Releasing of Results:ROUTINE
• 3 hours after receipt of specimen/ arrival of messenger
STAT
• After 1½ hours from receipt of specimen/ arrival of messenger
Reference Interval/Result Interpretation:NO INTERTINAL PARASITE SEEN
Limitations/Interferences:Diarrheic or watery stool and /or stool contaminated with other fluids may affect test results..
Frequently Asked Questions (FAQs):Not applicable
Related Words/Test:Diarrhea

 

Test:Keppra
Other Test Request Name:

Levetiracetam

Test Composition:

Not applicable

Intended Use:

Kepra or Levetiracetam is an anticonvulsant used as adjunct therapy to treat adult partial seizures. As multiple anticonvulsants are administered, it is important to monitor its level to:
(1) optimize therapy
(2) assure compliance
(3) to avoid toxicity

Methodology:

Liquid Chromatography Mass Spectrometry (LCMS)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

• No patient preparation necessary.


• Note the following info:
- Dosage
- Date and Time of last dose intake
- Date and Time of extraction

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):

14 Days

•   Refrigerated Temperature (2-8°C):

28 Days

•   Freezer Temperature (-20°C):

60 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:

2 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:

Used to treat epilepsy

 

Test:Ketone (Serum)
Other Test Request Name:
  • Serum Ketones
  • Beta-hydroxybutyrate
  • Ketone Bodies
  • Beta-hydroxybutyric Acid
  • Acetoacetate
  • Acetoacetic Acid
  • Acetone
Test Composition:

Not applicable

Intended Use:

Useful in the diagnosis and monitoring of therapy for diabetic ketoacidosis

Methodology:

Nitroprusside

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):

14 Days

•   Refrigerated Temperature (2-8°C):

14 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:

Monday to Friday

Cut Off Time:

Monday to Friday, 7:00 AM

TAT/Releasing of Results:

After 3 days(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:Not Applicable

 

Test:Kidney Stone Analysis By FTIR
Other Test Request Name:

• Urinary Stone Analysis
• Renal Calculus Analysis
• Stone Analysis

Test Composition:

Not applicable

Intended Use:

Used to evaluate the composition of kidney stones to determine the cause of formation and subsequent treatment, if possible.

Methodology:

Fourier Transform Infrared Spectroscopy (FTIR)

Laboratory Section:

Clinical Microscopy

Special Instructions/Patient Preparations:

Hospital Collections:  as instructed by your physician
Using the HPD Kidney Stone Analysis Specimen Collection Kit:
1. It is very important that you filter your urine using the urinary calculi strainer during your first morning void. If your doctor has given you a diuretic to promote urination, you must start filtering your urine as soon as possible.
2. Filter your urine to catch stones that are small enough to pass out of your body on its own. Please filter each urine collection for at least 24 hours or until the stone has passed.
3. Record the time you started filtering your urine on the label provided.
4. Each time after you filter your urine, check the filter for stone particles. Stones can be as small as a grain of sand, so check carefully.
5. When stones are found on the strainer, wash stones carefully with filtered or deionized water and allow the stones to air dry. Do not use any other liquid other than water to wash the stones. Do not apply heat to dry the stones.
6. When stones are dry, transfer the stones to the specimen container.
7. Repeat steps #5 and #6 until your last urine collection or when no more stones are found.
8. Do not tape the stones to the specimen container as tape affects testing.
9.  Stones should be submitted CLEAN AND DRY as much as possible. Sample  immersed in water can be accepted but other liquid is rejected.
10. Record the time of your last filtered urine collection on the label provided.
11. Write your complete name and affix the label on the body of the specimen container.
12. Store the stones at room temperature. Do not refrigerate or freeze the stones.
13. Submit your stone specimen to any Hi-Precision Diagnostics branch for analysis.

Collection/Sample Container:

Specimen collection kit provided by HPD or any clean container

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

20 mg, or at least the size equivalent of 2-3 small grains of rice

Alternative Specimen and Volume Requirement:

Not applicable

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

1 Year

•   Refrigerated Temperature (2-8°C):

Unacceptable

•   Freezer Temperature (-20°C):

Unacceptable

Transport Temperature:

Transport specimen at 15 °C – 25 °C (Room Temperature)

Rejection Criteria:

• Stones immersed in any other liquid other than water
• Stones with tape or any type of adhesive
• Stone specimens with non-stone particulates
• Exceeded sample storage and transport temperature requirement
• Improperly labeled specimens
• Insufficient sample quantity

Running Day:

Daily except Sundays and Holidays

samples received on Sundays will be processed the next day.

Cut Off Time:

1:00 PM

samples received after cut off time will be processed the next day.

TAT/Releasing of Results:

1 day  from receipt of specimen / messenger arrival

Reference Interval/Result Interpretation:

Not applicable

Limitations/Interferences:

Presence of water or moisture in sample will cause interference in the spectrum

Frequently Asked Questions (FAQs):

Q: How is the test being used?

A: A kidney stone analysis is performed to determine the chemical composition of a stone when it is filtered out of the urine or removed from the urinary tract. A laboratory will typically document the physical characteristics of a stone – its size, shape, weight, color, and texture. One or more tests will then be performed to determine the stone's composition.

 

Related Words/Test:

Urolithiasis, Nephrolithiasis, Urinalysis, Uric Acid, Calcium, Phosphorus, Creatinine, Oxalate, Citrate, Cystine

 

Test:Kidneys / Renal Ultrasound
Other Test Request Name:

-

Test Composition:Not Applicable
Intended Use:

Ultrasound imaging or sonography is considered to be a non-invasive procedure and does not involve ionizing radiation which is usual in X-rays. An ultrasound scan is not only useful in assessing the structure of organs and different internal structures but can also show the movement of organs in real time.

It may be used to assess the size and structures of the following:

  • Right Kidney
  • Left Kidney
Methodology:Not Applicable
Laboratory Section:Not Applicable
Special Instructions/Patient Preparations:

PREPARATION

  • No special preparation.
  • Full bladder is not required.
  • Bring previous ultrasound result for comparison.
Collection/Sample Container:Not Applicable
Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:Not Applicable
Alternative Specimen and Volume Requirement:Not Applicable
Specimen Stability  
•   Room Temperature (15-25°C):Not Applicable
•   Refrigerated Temperature (2-8°C):Not Applicable
•   Freezer Temperature (-20°C):Not Applicable
Transport Temperature:Not Applicable
Rejection Criteria:Not Applicable
Running Day:Not Applicable
Cut Off Time:Not Applicable
TAT/Releasing of Results:

-

Reference Interval/Result Interpretation:

-

Limitations/Interferences:Not Applicable
Frequently Asked Questions (FAQs):

-

Related Words/Test:Not Applicable

 

Test:KIF6 Genotype
Other Test Request Name:

Not applicable

Test Composition:

Not applicable

Intended Use:

This test detects a gene variant associated with increased coronary heart disease (CHD) risk and such CHD event can be reduced from atorvastatin and pravastatin therapy.

Methodology:

Real-Time Polymerase Chain Reaction (RT-PCR)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

No patient preparation necessary.

Collection/Sample Container:

EDTA or Violet Tube

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

2 pcs of 4 mL EDTA whole blood

Alternative Specimen and Volume Requirement:

Not Applicable

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

8 Days

•   Refrigerated Temperature (2-8°C):

8 Days

•   Freezer Temperature (-20°C):

30 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
• Clotted Sample

Running Day:

Batch Running

Cut Off Time:

Monday, 12:00 PM

 

TAT/Releasing of Results:

2 weeks 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:

Coronary Heart Disease (CHD)

 

Test:KOH
Other Test Request Name:

• KOH prep
• Potassium Hydroxide Preparation
• Fungal smear

Test Composition:

Not applicable

Intended Use:

• It is used for detecting fungal elements.
• Potassium Hydroxide (KOH) solution is a strong base which can dissolve tissue cells and keratinized material making fungal elements more visible.

Methodology:

Direct Microscopic Examination

Laboratory Section:

Bacteriology

Special Instructions/Patient Preparations:

Instructions to Send-in Clients:
• Indicate patient’s diagnosis, medical history and sample type on request forms.

Instructions to Phlebotomists: Sample Collection & Preparation Procedures
A. SKIN / SCALP SCRAPINGS
1. Using a sterile scalpel or edge of a glass slide, gently scrape skin scales from the infected area.
2. Scrapings may be collected in a black paper or directly on to a glass slide.
3. Add at least 2-3 drops of 10% KOH to the scrapings, put a cover slip and place the slide in a moist container to prevent it from drying. (Samples with KOH solution can be stored in a petri dish with moist tissue paper).
4. Label samples properly with patient name, sample type and site of collection.
5. Sample must be transported to Laboratory/Bacteriology section within 24 hours.

B. NAIL CLIPPINGS
1. Using a clean nail cutter, cut off a portion of affected nail. It is important to cut the nails as thin as possible.
2. Nail clippings may be collected in a black paper and transferred to a sterile container.
3. Label samples properly with patient name and source of tissue scraping.

C. HAIR
1. Using clean tweezer, remove hair shafts with follicles from the infected site.
2. Hair samples may be directly placed on to a glass slide.
3. Add at least 2-3 drops of 20% KOH to the hair samples, put a coverslip and place the slide in a moist container. (Samples with KOH solution can be stored in a petri dish with moist tissue paper to prevent it from drying).
4. Label samples properly with patient name and source of tissue scraping.
5. Sample must be transported to Laboratory/Bacteriology section within 24 hours.
6. In case sample needs to be sent to HPD Main lab, place hair strands in sterile container.

NOTE: For fungal culture with KOH requests (skin scraping, nail clippings, hair), follow the collection procedures listed above except that samples must be placed in a sterile container without KOH solution.

Collection/Sample Container:

Clean dry sterile container, plain tube or any tightly closed container

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

With visible materials of the following:

  • Skin scrapings
  • Hair
  • Nail clippings

Fluids: 1-3 mL

Alternative Specimen and Volume Requirement:

Not applicable

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

24 Hours

•   Refrigerated Temperature (2-8°C):

Not applicable

•   Freezer Temperature (-20°C):

Not applicable

Transport Temperature:

Transport specimen immediately at room temperature (15°C -25°C).

NOTE: Do not delay transport of samples.

Rejection Criteria:

• Dried up prepared slides
• Improperly labeled specimens
• Exceeded sample stability requirement
• Specimen transported outside the temperature requirement

Running Day:

Daily

Cut Off Time:

Monday to Saturday
• 6:00 PM

Sunday
• 3:00 PM

TAT/Releasing of Results:

4 hours after receipt of sample in the laboratory

Reference Interval/Result Interpretation:

NEGATIVE RESULT:

  • No Fungal Elements Seen

 

POSITIVE RESULT:

  • Positive for yeast cells or budding yeast cells or budding yeast cells with hyphae
Limitations/Interferences:
  • Sensitivity is 20-75%
  • False positive results may occur if the specimen is contaminated with cotton fibers, cellulose fibers, or cholesterol deposits, which may be mistaken for hyphae.
  • If specimen is from mucous membrane, bronchial aspirate or sputum, Gram Stain may be more sensitive
Frequently Asked Questions (FAQs):

Q: What are the causes of positive KOH result but negative in Fungal Culture?

A: Inoculated fungi are nonviable; Fungi may have dried during sample processing; Inoculated sample was not enough to include causative fungi; sample chosen/collected from non-optimal site.

Related Words/Test:

Fungal test

 

Test:KRAS Mutation
Other Test Request Name:

Not applicable

Test Composition:

Not applicable

Intended Use:

Activating Ras mutations can be found in human malignancies with overall frequency of 15-20%. A high incidence of Ras gene mutations has been reported in 80-90% malignant tumors of the pancreas, 30-60% in colon rectal carcinomas, and in 18-30% of hematopoietic neoplasia of myeloid origin. Ras proteins were shown to influence proliferation, differentiation, transformation, and apoptosis by relaying mitogenic and growth signals into the cytoplasma and the nucleolus. Mutations leading to an amino acid substitution at positions 12,13 and 61 are the most common in naturally occurring neoplasms and are frequent in adenocarcinomas of the pancreas, colon, and certain types of hematological malignancies.

Methodology:

Polymerase Chain Reaction (PCR)

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:

Batch Running

Cut Off Time:

Monday to Friday, 12:00 PM

 

TAT/Releasing of Results:

14 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:

Oncogenes, Normal cells to cancerous cells

 

Test:Lactic Acid
Other Test Request Name:

Lactate

Test Composition:

Not applicable

Intended Use:

An intermediate in the glycolytic pathway. Measuring its level can be helpful in evaluating lactic acidosis observed during intense muscular activity, shock and a variety of different conditions including diabetic ketoacidosis, renal or hepatic insufficiency, drug overdosage and certain genetic diseases.

Methodology:

Spectrophotometry

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:
  • Avoid any hand or arm exercises before and during the blood extraction
  • Blood extraction is done when the patient is at rest and without the use of the tourniquet.NOTE:Do not use tourniquet.
  • Extracted blood is cooled in ice and must be immediately forwarded to the laboratory
  • No patient preparation necessary.

Note the following info:

  • Dosage
  • Date and Time of last dose intake
  • Date and Time of extraction
Collection/Sample Container:

Gray Tube

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

3 mL Plasma

Alternative Specimen and Volume Requirement:

Not Applicable

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

Not Applicable

•   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:

Monday to Friday

Cut Off Time:

Monday to Friday, 7:00 AM

TAT/Releasing of Results:

After 3 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:

Lactic Acid, L-Lactate, CSF Lactate, Lactate

 

Test:Lamotrigine
Other Test Request Name:

Lamictal

Test Composition:

Not applicable

Intended Use:

An antiepileptic drug which can induce allergic reactions, especially when taken at the same time as sodium valproate.

Methodology:

LCMS/MS

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

• No patient preparation necessary.


• Note the following info:

  • Dosage
  • Date and Time of last dose intake
  • Date and Time of extraction
  • Diagnosis

NOTE: The therapeutic drug monitoring code suggests that the sample should be carried out at the residual rate (just before taking medication).

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):

3 Days

•   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:

Anti-epileptic medication

 

Test:LAP - Temporarily Unavailable (currently not accepting samples)
Other Test Request Name:

Leukocyte alkaline phosphatase

Test Composition:

Not applicable

Intended Use:

Aid in the differential diagnosis of chronic myelogenous leukemia (CML) versus leukemoid reaction

Aid in the evaluation of polycythemia and myelofibrosis

Methodology:

HPLC/UV Detection

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

Note the following requirements:

  • Need requesting physician
  • Patient Diagnosis
  • License No. of Physician
Collection/Sample Container:

Slide holders or mailers for microscope slides

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

10 pcs of Peripheral Blood Smear (Wedge-type) -UNSTAINED

Alternative Specimen and Volume Requirement:

Not Applicable

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

7 Days

•   Refrigerated Temperature (2-8°C):

Not applicable

•   Freezer Temperature (-20°C):

Not applicable

Transport Temperature:

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

Rejection Criteria:
 
  • Improper or insufficient labeling of slides
  • No requesting physician
  • No Patient Diagnosis
  • No  License No. of Physician
Running Day:

Batch Running

Cut Off Time:

Monday to Friday, 7:00 AM

TAT/Releasing of Results:

1 Month 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:

Chronic myeloid leukemia