Test:Gynecologic (Pelvic) Ultrasound
Other Test Request Name:
  • Pelvic Ultrasound
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 location of organs and structuresof the following:
  • Uterus
  • Ovaries
  • Urinary Bladder
Methodology:Not Applicable
Laboratory Section:Not Applicable
Special Instructions/Patient Preparations:

PREPARATION

  • Fasting is not required.
  • Avoid drinking colored drinks for at least 6 hours.
  • Full bladder is required prior the procedure.

SPECIAL INSTRUCTIONS

  • The staff from Imaging Department will instruct the patient as to when to start drinking water (at least 1 liter) when he/she is about to be called in queue; while taking note of the following:
  • If patient is not done with blood extraction, patient is not yet allowed to drink water.
  • If patient has not yet collected sample for urinalysis, patient is advised to drink 1 to 2 cups of water.
  • If patient's condition requires a certain amount of liquid intake.
  • 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:H. pylori (Quali)
Other Test Request Name:

• Helicobacter pylori (Rapid test)
• Helicobacter pylori antibody test (Rapid test)

Test Composition:

Not Applicable

Intended Use:

Rapid test for the qualitative detection of all H.pylori antibody isotypes (IgG, IgM, IgA, etc.). Intended as an aid in the diagnosis of H.pylori infection in patients with gastrointestinal symptoms.

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, Heparin, Na Citrate)

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

Not Specified

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

>7 Days

Transport Temperature:

Transport specimen at 2 – 10 °C (with cold packs)

Rejection Criteria:

• Contaminated and markedly lipemic serum
• Improperly labeled specimens
• Hemolyzed specimens
• Quantity not sufficient
• Specimen stored exceeded outside required stability

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:

Use of hemolytic samples, rheumatoid factors-containing samples, lipemic, icteric samples can lead to impair the test results.

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Peptic ulcer, H. pylori stool antigen test; H. pylori breath test; Urea breath test; CLO test; Rapid urease test (RUT) for H. pylori, Helicobacter pylori, Chronic Active Gastritis, type-B Gastritis

 

Test:H. pylori IgG (Quanti)
Other Test Request Name:

• Helicobacter pylori IgG
• Helicobacter pylori antibody test

Test Composition:

Not Applicable

Intended Use:

For quantitative determination of Helicobacter pylori specific IgG antibodies in human serum as an aid in diagnosing infection by H. pylori.

Methodology:

2-step indirect assay chemiluminescence immunoassay (CLIA)

Laboratory Section:

Special Test 

Special Instructions/Patient Preparations:

  No patient preparation necessary.

• Note Date and Time of collection

• Need requesting physician

• Patient Diagnosis

• License No. of Physician

Collection/Sample Container:

Red or Gold tube

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

2mL Serum

Alternative Specimen and Volume Requirement:

Not Applicable

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

24 hours

•   Refrigerated Temperature (2-8°C):

8 days

•   Freezer Temperature (-20°C):

>8 days

Transport Temperature:

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

Rejection Criteria:

• Improperly labeled specimens
• Quantity not sufficient
• Specimen stored outside the temperature range
• Hemolyzed specimens
• Markedly lipemic Sample

Running Day:
Monday-Friday

.

Cut Off Time:

 

7AM

TAT/Releasing of Results:

3 Working days (excluding saturday, sunday and holidays)

Reference Interval/Result Interpretation:Not Applicable
Limitations/Interferences:
  • Patients routinely exposed to animals, animal serum products, or other immunogenic products that may elicit heterophilic antibody production against the assay’s reagents can be prone to this interference and anomalous values may be observed.
  • The Liaison H. pylori IgG assay has not been evaluated in pediatric population.
  • Borrelia burgdorferi was not tested in the cross-reactivity study.
Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Peptic ulcer, H. pylori stool antigen test; H. pylori breath test; Urea breath test; CLO test; Rapid urease test (RUT) for H. pylori

 

Test:H. pylori Stool Antigen
Other Test Request Name:
H.Pylori Breath Test •  Urea Breath Test •  CLO Test • Rapid Urease Test for H.Pylori or RUT
Test Composition:

Not applicable

Intended Use:

• Used for the qualitative detection of Helicobacter pylori antigen in human fecal specimen.
• Aids in the diagnosis of H. pylori infection in patients with gastrointestinal symptoms

Methodology:

Immunochromatographic Assay

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 size 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):

2 Days

•   Freezer Temperature (-20°C):

Unacceptable

Transport Temperature:

•Submit specimen immediately to HPD Laboratory and transport at 2°C~8°C (with cold packs).

Rejection Criteria:

• Quantity not sufficient (QNS); or less than pea size.
• Contaminated stool (e.g. with urine or other fluids)
• Specimen submitted after 2 hours of collection if not stored and transported with ice.
• Improperly labeled specimens
• Specimen that contains preservatives and collected with transport media.

Running Day:

Daily

Cut Off Time:

Monday to Saturday
• 6:00 PM

Sunday
• 3:00 PM

TAT/Releasing of Results:

ROUTINE
• 4 hours after receipt of specimen/ arrival of messenger
STAT
• After 1½ hours from receipt of specimen/ arrival of messenger

Reference Interval/Result Interpretation:

NEGATIVE

Limitations/Interferences:

• Fecal specimens for direct test should be collected in containers that do not contain transport media, preservatives, as all of the these additives may interfere with H. Pylori Ag test kit.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Gastric biopsy for H. pylori, H. pylori IgG & IgM, H. pylori (Quali)

 

Test:H.pylori IgM (Quanti)
Other Test Request Name:

• Helicobacter pylori IgM
• Helicobacter pylori antibody test

Test Composition:

Not Applicable

Intended Use:

For quantitative determination of Helicobacter pylori specific IgM antibodies in human serum as an aid in diagnosing infection by H. pylori.

Methodology:

ELISA (Enzyme-Linked Immunosorbent Assay)

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.
:

3mL Serum

Alternative Specimen and Volume Requirement:

Not Applicable

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

Not Specified

•   Refrigerated Temperature (2-8°C):

2 Days

•   Freezer Temperature (-20°C):

>2 Days

Transport Temperature:

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

Rejection Criteria:

• Improperly labeled specimens
• Quantity not sufficient
• Specimen stored outside the temperature range
• Hemolyzed specimens
• Markedly lipemic Sample

Running Day:

Wednesday 7:00AM

Cut Off Time:

Tuesday 7:00AM

TAT/Releasing of Results:

3 working days after cut off (excluding saturday, sunday, holidays)

Reference Interval/Result Interpretation:

available upon request

Limitations/Interferences:

None identified.

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Peptic ulcer, H. pylori stool antigen test; H. pylori breath test; Urea breath test; CLO test; Rapid urease test (RUT) for H. pylori

 

Test:Hair Drug Test 17-Panel
Other Test Request Name:

None

Test Composition:
  1. Amphetamines
  2. Methamphetamines (Methamphetamine, Ecstacy (MDMA), MDA)
  3. Marijuana (THC/Carboxy THC)
  4. Cocaine (Cocaine, Benzoylecgonine, Cocaethylene, Norcocaine)
  5. Phencyclidine
  6. Opiates (Codeine, Morphine, Heroin Metabolite (6-MAM)
  7. Extended Opiates (Hydrocodone, Oxycodone, Hydromorphone, Oxymorphone)
  8.  
  9. Benzodiazepines (Alprazolam, Nordiazepam, Clonazepam, Oxazepam, Diazepam, Temazepam, Lorazepam)
  10. Ketamine/Metabolites (Ketamine, Norketamine)
  11. Tramadol
  12. Barbiturates (Phenobarbital, Secobarbital, Pentobarbital, Amobarbital, Butalbital)
  13. Fentanyl.Metabolites (Fentanyl, Norfentanyl)
  14. Buprenorphine/Metabolites (Buprenorphine, Norbuprenorphine)
  15. Methadone/Metabolites (Methadone, EDDP)
  16. Meperinidine/Metabolites (Meperidine, Normeperidine)
  17. Propoxyphene
  18. Zolpidem

 

Intended Use:

Detection of drug molecules embedded in the hair.

Use and the misuse of prescription medication. The sample is then analyzed for signs of drug use during the 90 days preceding the test.

Methodology:

Screening Method of Testing : ELISA

Gas Chromatography/Mass Spectrometry

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:
  • Available in all branches and can also be done via Home Service
  • Request DT Hair Collection Kit to Special test section atleast 2 days prior to collection
Collection/Sample Container:

DT Hair FollicleCollection Kit will be provided by HPD Special Test Section.

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

Head Hair: 20~30 strands of hair from five (5) small areas along the part line at the crown. Total of 90~120 strands of hair.

OR

 

Body Hair: Size of common 1” cotton ball collected from several areas of the body (including facial)

NOTE: Hair follicle drug testing can also be done on hair samples not directly harvested from the patient by collectors from HPD (for example, hair from hair brush, pillows, etc. brought in by concerned relatives), but the patient's name in the results form will only be recorded as ANONYMOUS.

Alternative Specimen and Volume Requirement:

Not applicable

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

14 Days

•   Refrigerated Temperature (2-8°C):

Not applicable

•   Freezer Temperature (-20°C):

Not applicable

Transport Temperature:

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

Send completely sealed Transport Bag containing Hair Specimen Pouch and copy 1 (white copy) of Custody and Control Form to HPD Main for daily shipment to referral lab

Rejection Criteria:
  • If head and body hair has been mixed in one collection pouch.
  • If sample was collected from just one area. Must collect from at least 5 areas.
  • Incorrect information on the Chain and Custody Form
  • More than one (1) HST per Hair Specimen Pouch
  • Artificial/ Synthetic hair
  • Incomplete details
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:

Not Applicable

Limitations/Interferences:

 • The cut-off levels used by Omega Laboratories for hair testing are based on the Federal Recommendations issued April 2004. Our interpretation of these levels is that they are designed to catch repeat usage - IE a single usage of a drug may not result in a positive hairv test.

• Since hair testing covers a much longer timeframe than urine (90 days vs. 2 - 3 days for drugs), the intent is to show more of a pattern or lifestyle choice of usage. While a negative hair test cannot necessarily be used to disprove a laboratory-confirmed positive urine test, it can still show that the donor is at least not a chronic or frequent user of the drug. 

 
Frequently Asked Questions (FAQs):

Q: What types of drug testing does Hi-Precision have ?

A: Urine and hair follicle drug testing

Q: What is Hair Follicle Drug Testing ?

A:  It measures the drug molecules embedded in the hair. Results cannot be altered by external factors such as chemicals or shampoos.

Q: What is the difference of hair follicle vs urine drug testing ?

A:  Hair follicle drug testing has a wider window of detection and test cannot be tampered.

Q: What time period does hair follicle drug testing cover?

A:  Standard of 90 days unlike urine samples which are very variable - from days to weeks only.

Q: How soon after drug use can the drug be detected in hair?

A: Approximately 7-10 days from time of drug use.

Q: Can we collect hair samples on our own without the patient’s knowledge?

A: Yes, as long as it meets standard requirement of 90-120 hair strands. The sample will be named as Anonymous.

Related Words/Test:Not Applicable

 

Test:Hair Drug Test 5-Panel
Other Test Request Name:

Drug Test

Test Composition:
  •  Amphetamines
  • Methamphetamines (Methamphetamine, Ecstacy (MDMA), MDA)
  • Marijuana (THC/Carboxy THC)
  • Cocaine (Cocaine, Benzoylecgonine, Cocaethylene, Norcocaine)
  • Phencyclidine
  • Opiates (Codeine, Morphine, Heroin Metabolite (6-MAM)
 
Intended Use:

Detection of drug molecules embedded in the hair.

Use and the misuse of prescription medication. The sample is then analyzed for signs of drug use during the 90 days preceding the test.

Methodology:
  • Screening Method of Testing : ELISA
  • Gas Chromatography/Mass Spectrometry
Laboratory Section:

Special Test

Special Instructions/Patient Preparations:
  • Available in all branches and can also be done via Home Service
  • Request DT Hair Collection Kit to Special test section atleast 2 days prior to collection
Collection/Sample Container:

DT Hair FollicleCollection Kit will be provided by HPD Special Test Section.

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

Head Hair:20~30 strands of hair from five (5) small areas along the part line at the crown. Total of 90~120 strands of hair.

OR

 

Body Hair:Size of common 1” cotton ball collected from several areas of the body (including facial)

NOTE:Hair follicle drug testing can also be done on hair samples not directly harvested from the patient by collectors from HPD (for example, hair from hair brush, pillows, etc. brought in by concerned relatives), but the patient's name in the results form will only be recorded as ANONYMOUS.

Alternative Specimen and Volume Requirement:

Not applicable

Specimen Stability  
•   Room Temperature (15-25°C):Not Applicable
•   Refrigerated Temperature (2-8°C):

14 Days

•   Freezer Temperature (-20°C):

Not applicable

Transport Temperature:

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

Send completely sealed Transport Bag containing Hair Specimen Pouch and copy 1 (white copy) of Custody and Control Form to HPD Main for daily shipment to referral lab

Rejection Criteria:
  • If head and body hair has been mixed in one collection pouch.
  • If sample was collected from just one area. Must collect from at least 5 areas.
  • Incorrect information on the Chain and Custody Form
  • More than one (1) HST per Hair Specimen Pouch
  • Artificial/ Synthetic hair
  • Incomplete details
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:

Not Applicable

Limitations/Interferences:

 • The cut-off levels used by Omega Laboratories for hair testing are based on the Federal Recommendations issued April 2004. Our interpretation of these levels is that they are designed to catch repeat usage - IE a single usage of a drug may not result in a positive hairv test.

• Since hair testing covers a much longer timeframe than urine (90 days vs. 2 - 3 days for drugs), the intent is to show more of a pattern or lifestyle choice of usage. While a negative hair test cannot necessarily be used to disprove a laboratory-confirmed positive urine test, it can still show that the donor is at least not a chronic or frequent user of the drug. 

 

Frequently Asked Questions (FAQs):

Q:What types of drug testing does Hi-Precision have ?

A: Urine and hair follicle drug testing

Q:What is Hair Follicle Drug Testing ?

A:  It measures the drug molecules embedded in the hair. Results cannot be altered by external factors such as chemicals or shampoos.

Q:What is the difference of hair follicle vs urine drug testing ?

A:  Hair follicle drug testing has a wider window of detection and test cannot be tampered.

Q:What time period does hair follicle drug testing cover?

A:  Standard of 90 days unlike urine samples which are very variable - from days to weeks only.

Q:How soon after drug use can the drug be detected in hair?

A: Approximately 7-10 days from time of drug use.

Q: Can we collect hair samples on our own without the patient’s knowledge?

A: Yes, as long as it meets standard requirement of 90-120 hair strands. The sample will be named as Anonymous.

Related Words/Test:Not Applicable

 

Test:Hair Drug Test 7-Panel
Other Test Request Name:

None

Test Composition:
  1. Amphetamines
  2. Methamphetamines
  3. Marijuana (THC/Carboxy THC)
  4. Cocaine (Cocaine, Benzoylecgonine, Cocaethylene, Norcocaine)
  5. Opiates (Codeine, Morphine, Heroin Metabolite (6-MAM)
  6. Extended Opiates (Hydrocodone, Oxycodone, Hydromorphone, Oxymorphone)
  7. Benzodiazepines (Alprazolam, Nordiazepam, Clonazepam, Oxazepam, Diazepam, Temazepam, Lorazepam)
  8. Phencyclidine
Intended Use:

Detection of drug molecules embedded in the hair.

Use and the misuse of prescription medication. The sample is then analyzed for signs of drug use during the 90 days preceding the test.

Methodology:
  • Screening Method of Testing : ELISA
  • Gas Chromatography/Mass Spectrometry
Laboratory Section:

Special Test

Special Instructions/Patient Preparations:
  • Available in all branches and can also be done via Home Service
  • Request DT Hair Collection Kit to Special test section atleast 2 days prior to collection
Collection/Sample Container:

DT Hair FollicleCollection Kit will be provided by HPD Special Test Section.

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

Head Hair: 20~30 strands of hair from five (5) small areas along the part line at the crown. Total of 90~120 strands of hair.

OR

 

Body Hair: Size of common 1” cotton ball collected from several areas of the body (including facial)

NOTE: Hair follicle drug testing can also be done on hair samples not directly harvested from the patient by collectors from HPD (for example, hair from hair brush, pillows, etc. brought in by concerned relatives), but the patient's name in the results form will only be recorded as ANONYMOUS.

Alternative Specimen and Volume Requirement:

Not applicable

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

14 Days

•   Refrigerated Temperature (2-8°C):

Not applicable

•   Freezer Temperature (-20°C):

Not applicable

Transport Temperature:

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

• Send completely sealed Transport Bag containing Hair Specimen Pouch and copy 1 (white copy) of Custody and Control Form to HPD Main for daily shipment to referral lab

Rejection Criteria:
  • If head and body hair has been mixed in one collection pouch.
  • If sample was collected from just one area. Must collect from at least 5 areas.
  • Incorrect information on the Chain and Custody Form
  • More than one (1) HST per Hair Specimen Pouch
  • Artificial/ Synthetic hair
  • Incomplete details
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:

Not Applicable

Limitations/Interferences:

 • The cut-off levels used by Omega Laboratories for hair testing are based on the Federal Recommendations issued April 2004. Our interpretation of these levels is that they are designed to catch repeat usage - IE a single usage of a drug may not result in a positive hairv test.

• Since hair testing covers a much longer timeframe than urine (90 days vs. 2 - 3 days for drugs), the intent is to show more of a pattern or lifestyle choice of usage. While a negative hair test cannot necessarily be used to disprove a laboratory-confirmed positive urine test, it can still show that the donor is at least not a chronic or frequent user of the drug. 

 

Frequently Asked Questions (FAQs):

Q: What types of drug testing does Hi-Precision have ?

A: Urine and hair follicle drug testing

Q: What is Hair Follicle Drug Testing ?

A:  It measures the drug molecules embedded in the hair. Results cannot be altered by external factors such as chemicals or shampoos.

Q: What is the difference of hair follicle vs urine drug testing ?

A:  Hair follicle drug testing has a wider window of detection and test cannot be tampered.

Q: What time period does hair follicle drug testing cover?

A:  Standard of 90 days unlike urine samples which are very variable - from days to weeks only.

Q: How soon after drug use can the drug be detected in hair?

A: Approximately 7-10 days from time of drug use.

Q: Can we collect hair samples on our own without the patient’s knowledge?

A: Yes, as long as it meets standard requirement of 90-120 hair strands. The sample will be named as Anonymous.

Related Words/Test:Not Applicable

 

Test:Half Sibling Test/Patient
Other Test Request Name:

Not Applicable

Test Composition:

Not Applicable

Intended Use:

DNA test to confirm relationship of 2 individuals (if they have the same 1 parent)

Methodology:

DNA Analysis

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:
  •    RTPCR negative results for BOTH PARTIES are needed 2-3 days from the date of collection.
  • Inform Special Test Section before the scheduled sample collection for the collection kit.
  • Request DNA Collection Kit to Special test section 3 days prior of swab collection.
  • Only trained doctors/RMTs are allowed to collect samples.

Sample collection/handling:

  1. Each collection kit (provided by HP Main Lab) includes 4 swabs.
  2. Collect sample using the 4 swabs for each patient (i.e. 4 swabs for Sibling 1, 4 swabs for Sibling 2)
  3. Return swabs to its sterile package and place it inside the provided envelope.
  4. Encircle whether sample came from Sibling 1 or Sibling 2.     NOTE:Sample from Sibling 1 and Sibling 2 must be placed in separate envelopes.
  5. Completely fill up the required information in the envelope.      NOTE:Signatures of patient and collector is required. For minors, legal guardian must sign on the envelope containing the Sibling's sample.
  6. Remove adhesive cover and seal the envelope with sample.
  7. Send sample immediately to HP Main Lab.

Document Requirements:

  • Birth Certificate/School I.D of Siblings actual and  2 photocopies
  • Valid I.D of guardian, actual and  2 photocopies
  • Completely filled up request form
  • Completely filled up disclaimer form

NOTE:Double check completeness and correctness of information before sending to HP Main Lab to avoid delay ing processing of sample.

Collection/Sample Container:

DNA Collection kit(provided by Special Test)

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

4 swabs each from Sibling 1 and Sibling 2

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 15°C ~25 °C (room temperature)

Rejection Criteria:
  • Incomplete details of patient
  • Unlabelled sample
  • Incorrect collection container used
  • Incomplete documents needed
Running Day:

Batch Running

Cut Off Time:

Friday, 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:

DNA

 

Test:HAMS TEST
Other Test Request Name:

Not applicable

Test Composition:

Not applicable

Intended Use:

• Maybe used as screening test for paroxysmal nocturnal hemoglobinuria (PNH) and indicates unusual sensitivity of such red cells to the action of complement.
• Evaluate patients with suspected PNH or suspected congenital dyserythropoeitic anemia,type II (HEMPAS); evaluate hemolytic anemia, especially with hemosiderinuria, pancytopenia,decreased RBC acetylcholinesterase , decreased leukocyte alkaline phosphatase, negative direct coombs test and/or apparent marrow failure.

Methodology:

Acidified Serum Lysis

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

• No patient preparation necessary.
• Freshly collected (whole blood do not separate)
• Inform laboratory 1 day before extraction for schedule
• Send sample immediately to laboratory

Collection/Sample Container:

Red top tube and EDTA (Violet top tube)

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

5 mL Serum from Red Top and 5 mL EDTA whole blood

Alternative Specimen and Volume Requirement:

Not Applicable

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

Not applicable

•   Refrigerated Temperature (2-8°C):

1 hour upon extraction 

•   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 specimen

Running Day:

Monday to Friday

Cut Off Time:

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:

Paroxysmal nocturnal hemoglobinuria (PNH)

 

Test:Haptoglobin
Other Test Request Name:

• HPT
• Hemoglobin-binding Protein
• Hp

Test Composition:

Not applicable

Intended Use:

Used as an acute-phase marker of red blood cell (RBC) destruction. Its value decreases and may even be absent when RBCs are destroyed at twice the normal rate. Levels can also become elevated in infection and inflammation.

Methodology:

Immunoturbidimetric

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-,NH4-,Na-Heparin or Na2-K2-,K3-EDTA)

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

3 Months

•   Refrigerated Temperature (2-8°C):

8 Months

•   Freezer Temperature (-20°C):

Not specified

Transport Temperature:

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

Rejection Criteria:

• Improper collection tube used
• Specimen stored/transported outside the temperature range
• Quantity not sufficient
• Hemolyzed specimen
• Lipemic specimen
• Improperly labeled specimen

Running Day:

Wednesday and Saturday

Cut Off Time:

Monday to Saturday:6:00 PM

Sunday:4:00PM

TAT/Releasing of Results:

RUNNING TIME: 11AM onwards (on running days)

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

Reference Interval/Result Interpretation:

0.30-2.00 g/L (30.00-200.00 mg/dL)

Limitations/Interferences:

• In very rare cases, gammopathy, in particular type IgM (Waldenstrom’s macroglobulinemia), may cause unreliable results.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Complete Blood Count, Reticulocyte Count, Blood Smear, Hemoglobin, Hematocrit, Bilirubin, LD, Direct Antiglobulin Test, G6PD

 

Test:HBeAg (CMIA)
Other Test Request Name:

Hepatitis B envelope Antigen

Test Composition:

Not applicable

Intended Use:

• HBeAg determinations can be used to monitor the progress of hepatitis B viral infection.
• Often used as a marker of ability to spread the virus to other people (infectivity)

Methodology:

Chemiluminescent Microparticle Immunoassay (CMIA)

Laboratory Section:

Immunology

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 (K-EDTA, Na-citrate, ACD-B, CPDA-1, CPD, and Na-Heparin, Potassium oxalate)

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

24 Hours

•   Refrigerated Temperature (2-8°C):

3 Days

•   Freezer Temperature (-20°C):

6 Freeze-Thaw cycles

Transport Temperature:

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

Rejection Criteria:

• Hemolyzed specimen
• Markedly lipemic specimen
• Specimen stored/transported outside the temperature range
• Quantity not sufficient
• Improperly labeled specimens

Running Day:

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

Reference Interval/Result Interpretation:

NON-REACTIVE: C.O.V. 0.000~0.900
GRAYZONE: C.O.V. 0.910~5.000
REACTIVE: C.O.V. GREATER THAN (>) 5.000

Limitations/Interferences:

•Specimens from patients who have received preparations of mouse monoclonal antibodies for diagnosis of therapy may contain human anti-mouse antibodies (HAMA). Specimens containing HAMA may produce anomalous values when tested with this assay.
•Hemophilic antibodies in human serum can react with reagent immunoglobulins, interfering with in vitro immunoassays. Patients routinely exposed to animals or to animal serum products can be prone to this interference and anomalous results may be observed. Additional information may be required for diagnosis.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Hepatitis B, HBV, HBV Tests; Hep B; anti-HBs; Hepatitis B Surface Antibody; HBsAg; Hepatitis B Surface Antigen; HBeAg; Hepatitis B e Antigen; anti-HBc; Hepatitis B Core Antibody; anti-HBc, IgM; anti-HBe; Hepatitis B e Antibody; HBV DNA, Hepatitis B Virus

 

Test:HBsAg II Quantification
Other Test Request Name:
  • Hepatitis B Surface Antigen Quantitative Determination
  • HBsAg Quantitative
Test Composition:

Not Applicable

Intended Use:

Quantitative determination of HbsAg in confirmed HbsAg positive samples to monitor pegylated interferon alpha therapy.

Methodology:

Immunometric Immunoassay

Laboratory Section:

Special Test

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.
:

4 mL Serum

Alternative Specimen and Volume Requirement:

Not Applicable

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

7 Days

•   Refrigerated Temperature (2-8°C):

14 Days

•   Freezer Temperature (-20°C):

30 Days

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:

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:

Not Applicable

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

HBV DNA Viral Load, Hepatitis B Full Panel (HBsAg, Anti HBs, Anti HBe, HBeAg, Anti HBc Total, Anti HBc IgM), Liver Function tests

 

Test:HbsAg with TITER (CMIA)
Other Test Request Name:

• Hepatitis B surface Antigen
• Australia antigen

Test Composition:

Not applicable

Intended Use:

HBsAg assays are used to identify persons infected with HBV and to prevent transmission of the virus by blood and blood products as well as to monitor the status of infected individuals in combination with other hepatitis B serological markers.

Methodology:

Chemiluminescent Microparticle Immunoassay (CMIA)

Laboratory Section:

Immunology

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, K2- or K3-EDTA, CPD, CPDA-1, Na-citrate, ACD, Potassium oxalate, or NaF)

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

24 Hours

•   Refrigerated Temperature (2-8°C):

6 Days

•   Freezer Temperature (-20°C):

3 Freeze-Thaw cycles

Transport Temperature:

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

Rejection Criteria:

• Hemolyzed specimen
• Markedly lipemic specimen
• Specimen stored/transported outside the temperature range
• Quantity not sufficient
• Improperly labeled specimens

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

Reference Interval/Result Interpretation:

• NON-REACTIVE: C.O.V. 0.000~0.800
• GRAYZONE: C.O.V. 0.810~1.20
• REACTIVE, LOW TITER: C.O.V. 1.210~20.000
• REACTIVE: C.O.V. GREATER THAN (>) 20.000

Limitations/Interferences:

•Specimens from patients who have received preparations of mouse monoclonal antibodies for diagnosis of therapy may contain human anti-mouse antibodies (HAMA). Specimens containing HAMA may produce anomalous values when tested with this assay.
•Hemophilic antibodies in human serum can react with reagent immunoglobulins, interfering with in vitro immunoassays. Patients routinely exposed to animals or to animal serum products can be prone to this interference and anomalous results may be observed. Additional information may be required for diagnosis.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Hepatitis B, HBV, HBV Tests; Hep B; anti-HBs; Hepatitis B Surface Antibody; HBsAg; Hepatitis B Surface Antigen; HBeAg; Hepatitis B e Antigen; anti-HBc; Hepatitis B Core Antibody; anti-HBc, IgM; anti-HBe; Hepatitis B e Antibody; HBV DNA, Hepatitis B Virus

 

Test:HBsAg(RAPID)Screening
Other Test Request Name:

•Hepatitis B (RAPID)Screening
•Hepa B (RAPID)Screening

•Hepatitis B Surface Antigen (RAPID)Screening
•Hepatitis B Virus Testing (RAPID)Screening

•HBSAG Rapid Qualitatvive

Test Composition:

Not Applicable

Intended Use:

Aid to detect Hepatitis B surface Antigen from infected individuals. Used for diagnosis of acute, recent or chronic Hepatitis B infection.

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, Heparin, Na Citrate)

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

Not Specified

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

>2 Weeks

Transport Temperature:

Transport specimen at 2 – 10 °C (with cold packs)

Rejection Criteria:

• Contaminated and markedly lipemic serum
• Improperly labeled specimens
• Hemolyzed specimens
• Quantity not sufficient
• Specimen stored exceeded outside required stability

Running Day:

Daily

Cut Off Time:

Monday to Saturday
• 10:00 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:

NONREACTIVE

Limitations/Interferences:

None identified.

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Liver function, HBV Tests; Hep B; anti-HBs; Hepatitis B Surface Antibody; HBeAg; Hepatitis B e Antigen; anti-HBc; Hepatitis B Core Antibody; anti-HBc, IgM; anti-HBe; Hepatitis B e Antibody; HBV DNA, Hepatitis B Virus Testing