Test:Galectin-3
Other Test Request Name:

Not Applicable

Test Composition:

Not Applicable

Intended Use:

Galectin-3 - A galectin-3 test may be ordered for the identification of individuals with chronic heart failure at elevated risk of disease progression

Methodology:

Enzyme Linked Immunosorbent Assay (ELISA)

Laboratory Section:

Special test

Special Instructions/Patient Preparations:

 

 

 

 

1. Collect and label sample according to standard protocols.
2. Gently invert tube 5 times immediately after draw.DO NOT SHAKE.
3. Allow blood to clot for 30 minutes.
4. Centrifuge for 10 minutes.
5. Store and transport refrigerated.

Collection/Sample Container:

Gold or Red 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):

22 days

•   Refrigerated Temperature (2-8°C):

22 days

•   Freezer Temperature (-20°C):

30 days

Transport Temperature:

Transport specimen at 2ºC - 8ºC (with cold packs)

Rejection Criteria:
  • Insufficient volume
  • Improperly labeled specimens
  • Markedly lipemic sample
  • Hemolyzed sample
  • Exceeded sample stability requirement
Running Day:

Batch Running

Cut Off Time:

Monday, 12:00 PM

 

TAT/Releasing of Results:

2 weeks after cut off (excluding saturday, sunday and holidays)

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

 

Test:Gall Bladder 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 location of abnormalities such as:
  • polyps
  • porcelain gallbladder
  • perforation
Methodology:Not Applicable
Laboratory Section:Not Applicable
Special Instructions/Patient Preparations:
PREPARATION
  • No food intake for at least 6 hours.
  • Drinking of water is not prohibited.
  • 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:Gall Stone Analysis (Currently Not Accepting samples)
Other Test Request Name:

Not applicable

Test Composition:

Not applicable

Intended Use:

• A gallstone is a stone formed within the gallbladder out of bile components. 

• quantitative chemical analysis of total cholesterol bilirubin, calcium, iron and inorganic phosphate in 120 gallstones from haryana.

 

Methodology:

Colorimetric

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

Not applicable

Collection/Sample Container:

Sterile clean container

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

gall bladder

Alternative Specimen and Volume Requirement:

Not applicable

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

1 year

•   Refrigerated Temperature (2-8°C):

1 year

•   Freezer Temperature (-20°C):

1 year

Transport Temperature:

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

Rejection Criteria:

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

Running Day:

Monday to Friday

Cut Off Time:

4:00 PM

TAT/Releasing of Results:

After 3 days (excldiung Satudays,  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:Ganglioside GM-1 Ab (IgG/IgM)
Other Test Request Name:
  • GM-1 Antibody
  • Ganglioside GM-1 Antibodies (IgG/IgM)
Test Composition:
  • Ganglioside GM-1 Antibody IgG
  • Ganglioside GM-1 Antibody IgM

 

Intended Use:

Ganglioside GM-1 Antibodies (IgG, IgM), EIA - Ganglioside GM-1 Antibody IgG is associated with the Guillain-Barre syndrome, particularly the acute motor axonal neuropathy variant. Antibody IgM is associated with chronic multifocal motor neuropathy.

Methodology:

Immunoassay (IA)

 

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

8 Hours Fasting

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:

Monday, 12:00 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:

Dementia, Guillain–Barre syndrome

 

Test:Gastrin (RIA)
Other Test Request Name:

Not applicable

Test Composition:

Not Applicable

Intended Use:

Gastrin regulates the growth of the acid-producing cells of the gastric mucosa. Increased levels are seen in patients with duodenal and pyloric ulcers, and with gastrinoma (Zollinger-Ellison syndrome). The main actions of the hormone are to stimulate gastric acid secretion and contraction of the gastric musculature. Its release is stimulated by distension of the antrum, by the action of peptides at the gastric antrum, and by inadequate acid production. The latter appears to act as a negative feedback controlling gastric acid homeostasis.To determine whether you are producing too mucg gastin; to help diagnose Zollinger-Ellison Syndrome and gastrin-producing tumors (gastrinomas) or G-cell hyperplasia; to monitor for recurrence of a gastrinoma. 

Methodology:

Radioimmunoassay (RIA)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:
  • 10 to 12 hours fasting.
  • After removing the coagulated mass, quickly centrifuge the sample to separate the serum.
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):

Not Applicable

•   Refrigerated Temperature (2-8°C):

24 Hours 

•   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, 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):

Q: Why Get Tested?

A:To determine whether you are producing too much gastrin; to help diagnose Zollinger-Ellison syndrome and gastrin-producing tumors (gastrinomas) or G-cell hyperplasia; to monitor for recurrence of a gastrinoma

Q: When To Get Tested?

A:When you have peptic ulcers and/or diarrhea and abdominal pain that your healthcare practitioner suspects is caused by excess gastrin; periodically to monitor for a gastrinoma recurrence

Q: What is being tested?

A:Gastrin is a hormone produced by "G-cells" in the part of the stomach called the antrum. It regulates the production of acid in the body of the stomach during the digestive process. This test measures the amount of gastrin in the blood to help evaluate an individual with recurrent peptic ulcers and/or other serious abdominal symptoms.

When food is eaten, the antrum of the stomach becomes distended and the presence of food stimulates the release of gastrin. Gastrin in turn stimulates parietal cells to produce gastric acid. Acidity helps to digest food and the rise in acidity eventually suppresses gastrin release. This feedback system normally results in low concentrations of gastrin in the blood, especially in the fasting state. Rare conditions such as G-cell hyperplasia and gastrinomas, including Zollinger-Ellison (ZE) syndrome, can cause an overproduction of gastrin and gastric acid. This can lead to aggressive peptic ulcers that can be difficult to treat.

Gastrinomas are gastrin-producing tumors. ZE syndrome is a condition caused by the presence of one or more gastrinomas and is characterized by high gastrin levels, greatly increased gastric acid production, and by peptic ulcers. Gastrinomas usually form in the pancreas, even though the endocrine cells of the pancreas do not normally make gastrin. More than half of them are malignant, causing cancer that can spread to other parts of the body, such as the liver. Even tiny tumors can produce large quantities of gastrin.

Q: How is it used?

A:The gastrin test is primarily used to help detect excess production of gastrin and gastric acid. It is used to help diagnose gastrin-producing tumors called gastrinomas, Zollinger-Ellison (ZE) syndrome, and hyperplasia of G-cells. G-cells are specialized cells in the stomach that produce gastrin, which in turn increases the production of gastric acid.

A gastrin test may also be used to monitor for recurrence following the surgical removal of a gastrinoma.

A gastrin stimulation test therefore may be used to provide additional information if the initial gastrin test result is moderately but not significantly elevated and the healthcare practitioner suspects that a person's symptoms are due to a gastrinoma. This procedure involves collecting a baseline gastrin sample, giving the patient a chemical (typically the hormone secretin) to stimulate gastrin production, and then collecting additional blood samples at timed intervals for gastrin testing. The other (benign) causes of elevated gastrin will not show an increase after secretin administration.

A measurement of gastric acid pH level may sometimes be ordered along with or following a gastrin test to help diagnose ZE syndrome.

Q: When it is ordered?

A:A gastrin test may be ordered when a person has diarrhea, abdominal pain, and/or recurrent peptic ulcers that do not respond to treatment and that the healthcare practitioner suspects are due to excess gastrin production. A gastrin stimulation test may be ordered when a gastrin level is moderately elevated and the healthcare practitioner suspects that a person has a gastrinoma.

When a gastrin-producing tumor has been removed, a gastrin test may be ordered periodically as a screening test to monitor for recurrence.

Q: What is Zollinger – Ellison Syndrome?

A:Zollinger-Ellison (ZE) syndrome is a rare disease of the gastrointestinal tract. It is characterized by severe recurrent peptic ulcers in the stomach, duodenum and/or the upper portion of the small intestine. The ulcers are caused by a greatly increased amount of stomach acid due to high levels of gastrin, the hormone that stimulates stomach acid production. In ZE, high gastrin levels are caused by gastrin-producing tumors called gastrinomas, which usually form in the duodenum but can be found in the pancreas and rarely in other parts of the body. More than half of them are malignant and can metastasize to other parts of the body, such as the liver. The tumors must be removed surgically, and sometimes total removal of the stomach is necessary to control the acid production. For more on this, see the Related Content section.

 

Related Words/Test:

Gastric acid

 

Test:GCT- Pregnant (50grams)
Other Test Request Name:

• Oral Glucose Challenge Test
• Glucose Challenge Test
• OGCT
• Glucose Load Test
• GLT

Test Composition:

Not applicable

Intended Use:

• OGTT-Pregnant (100 gms) test is used to detect gestational diabetes.
• Usually done at 24-28 weeks of gestation.
• First step to the Two-step strategy of screening for and diagnosis of Gestational Diabetes Mellitus (GDM).

Methodology:

Hexokinase

Laboratory Section:

Chemistry

Special Instructions/Patient Preparations:

• Non-fasting
• Eat generous amounts of carbohydrate on each of the three days before the test. The carbohydrate foods that are recommended are bread, cereal, potatoes, vegetables, and fruit.
• Take your usual amounts of milk, meat, fish, eggs, cheese, butter and margarine and, as well, eat the following foods daily during each of the three days before the test in at least these amounts:
- 3 slices of bread or toast
- 1 serving of breakfast cereal or porridge, spaghetti
- 1 medium potato or one serving of rice
- 3 servings of vegetables
- 3 servings of fruit (fresh, cooked, canned or juice)
- For morning tea and afternoon tea have 2 biscuits or an extra slice of bread or toast.
***NOTE: The 3 day diet is desirable but not essential. For any patient whose doctor indicates that the diet is not required, please follow the doctor’s instructions.
• Take any medications on the same schedule prescribed by your physician, such as blood pressure or heart medication. Do not take any over-the-counter medications for 12 hours before the test, such as cough or cold preparations, vitamins, aspirin, etc.
(The test should be postponed if the patient becomes ill, even with common illnesses such as the flu or a severe cold.)

Note:
• Patient is required to consume the entire amount of the specially-formulated glucose solution within a 5-minute period.
• 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.
• Samples without preservatives (NaF) must be separated from red cells within 30 mins of blood extraction.

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:

1-3mL Plasma (Li-heparin and K2-EDTA, NaF/Na2 EDTA, KF/Na2 EDTA, NaF/K?Oxalate and NaF/citrate/Na2?EDTA)

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

Serum (no hemolysis): 8 hours
Plasma (fluoride): 3 days

•   Refrigerated Temperature (2-8°C):

72 Hours

•   Freezer Temperature (-20°C):

Not specified

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:

Daily

Cut Off Time:

Monday to Saturday:10:00 PM

Sunday:6:00PM

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:

< 7.80 mmol/L (< 140.56 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:

Diabetes, DM, Pregnancy, Gestational Diabetes

 

Test:GGT (ENZYMATIC)
Other Test Request Name:

• Gamma-Glutamyl Transferase
• Gamma-Glutamyl Transpeptidase
• GGTP
• Gamma-GT
• GTP

Test Composition:

Not applicable

Intended Use:

Used in the diagnosis and monitoring of hepatobiliary diseases. Enzymatic activity of GGT is often the only parameter with increased values when testing for such diseases, and is one of the most sensitive indicators known. GGT is also a
sensitive screening test for occult alcoholism.

Methodology:

Enzymatic colorimetric (standardized against Szasz)

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:

1-3mL Plasma (Li?heparin and K2?EDTA)

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

7 Days

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

1 Year

Transport Temperature:

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

Rejection Criteria:
  1. Specimens that failed the serum index criteria
  2. Exceeded sample stability requirement
  3. Quantity not sufficient
  4. Improperly labeled specimen
  5. Improper collection tube used
Running Day:

Daily

Cut Off Time:

Monday to Saturday: 6 PM

 

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:

MALE: 8.00-61.00 U/L
FEMALE: 5.00-36.00 U/L

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:

Liver Function, Alcoholism, AST, ALT, ALP, Bilirubin, Liver Panel, Ethanol

 

Test:Giemsa Stain
Other Test Request Name:

not applicable

Test Composition:

not applicable

Intended Use:

for Giemsa staining used in Hematology to differentiate and count differential blood cell populations in cellular preparations

Methodology:

May-Grünwald Giemsa staining

Laboratory Section:

Hematology

Special Instructions/Patient Preparations:

Blood smears should be fixed with methanol

Collection/Sample Container:

glass slides

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

Blood smearsfixed with methanol

Alternative Specimen and Volume Requirement:

not applicable

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

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.

•   Refrigerated Temperature (2-8°C):

not applicable

•   Freezer Temperature (-20°C):

not applicable

Transport Temperature:

15-25°C

Rejection Criteria:

blood smears not fixed with methanol

Running Day:

daily

Cut Off Time:

6:00pm

TAT/Releasing of Results:

not applicable

Reference Interval/Result Interpretation:

not applicable

Limitations/Interferences:

not applicable

Frequently Asked Questions (FAQs):

not applicable

Related Words/Test:

PBS, blood smears, smear, CBC, complete blood count, stain, staining

 

Test:Glomerular Membrane Antibody (IFF)
Other Test Request Name:
  • Anti-GBM antibodies
  • Goodpasture's syndrome
  • Glomerular basement membrane - anti-antibodies
  • Anti tubular basement membrane antibodies
  • GBM - anti-antibodies
Test Composition:

Not Applicable

Intended Use:

A marker for Goodpasture's syndrome (severe glomerulonephritis associated with pulmonary infiltration and hemoptysis). The level of these antibodies reflects the extent of the involvement. The efficacy of treatment can be monitored by following the rate of negativation of this marker.

Methodology:

Flow Immunofluorimetry

 

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, 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:GLUCAGON (RIA) - Temporarily Unavailable (currently not accepting samples)
Other Test Request Name:

Pancreatic Hypercalcemic Factor

Test Composition:

Not applicable

Intended Use:

Glucagon measurement is useful primarily when considering a glucagon-secreting tumor of the pancreas. Glucagon is also used to diagnose glucagon deficiency in patients with hypoglycemia.

Methodology:

Radio Immuno Assay (RIA)

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.
:

4 mL of Plasma

Alternative Specimen and Volume Requirement:

Not Applicable

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

24 Hours

•   Refrigerated Temperature (2-8°C):

24 Hours

•   Freezer Temperature (-20°C):

30 Days

Transport Temperature:

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

Rejection Criteria:

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

Hypoglycemia

 

Test:GlycoMark (1,5 AG)
Other Test Request Name:

• 1,5-anhydroglucitol
• 1,5-AG

Test Composition:

Not applicable

Intended Use:

GlycoMark test provides quantitative measurement of 1,5-anhydroglucitol (1,5-AG); it is used for intermediate-term monitoring of glycemic control in people with diabetes. GlycoMark test reflect changes in glycemia (glucose in blood) over a 1 to 2-week time period.

Methodology:

Enzymatic

Laboratory Section:

Chemistry

Special Instructions/Patient Preparations:

• Refrain from taking nutraceuticals and Chinese medicines( such as Polygala, Tenuifolia, and Senega Syrup), and anti-diabetic drugs like Invokana, and alpha-glucosidase inhibitors, such as Acarbose, 8-12 hours before sample collection.
• Avoid intravenous hyperalimentation (artificial supply of nutrients) 8-12 hours before sample collection.

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:

1-3mL Plasma (EDTA)

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

Not Specified

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

Up to 6 freeze-thaw cycles

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:

Daily

Cut Off Time:

Monday to Saturday: 6:00 PM

 

TAT/Releasing of Results:

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

Reference Interval/Result Interpretation:

MALE: 10.70~32.00 ug/mL
FEMALE: 6.80~29.30 ug/mL

Limitations/Interferences:

• Persistently positive urinary glucose levels, or oxyhyperglycemia after gastrectomy, may result in a low 1,5-AG value. Low values have also been observed in pregnancy, terminal stage renal failure, dialysis patients, advanced cirrhosis, and prolonged incapability of oral ingestion of food.
Abnormal values have also been noted in individuals with abnormal glomerular filtration rates.
• For some patients with severe hyperglycemia, the internal pool of 1,5-AG may tend to remain depleted as a result of persistent glucosurea. In these cases, measurements of 1,5-AG may be less indicative of initial recovery following initiation of anti-diabetic treatment.
• 1,5-AG values may be increased when some Chinese medicines, such as Polygala Tenuifolia and Senega syrup, are administered.
• Values may also be increased during intravenous hyperalimentation.
• 1,5-AG values may be lower in patients undergoing therapy with steroids.
• 1,5-AG blood levels are falsely lowered by the diabetes drug INVOKANA which prevents reabsorption of 1,5-AG in the kidneys. INVOKANA is part of a new class of diabetes medications known as sodium-glucose co-transporter 2 (SGLT2) inhibitors, which block reabsorption of glucose in the kidneys, and other SGLT2 inhibitors may have the same effect.
• Some alpha-glucosidase inhibitors, such as Acarbose, may potentially reduce 1,5-AG levels due to interference with intestinal absorption of 1,5-AG.

Frequently Asked Questions (FAQs):

Q: How do I correlate my FBS and HbA1c results with GlycoMark?
A: The GlycoMark test measures the presence of the “good” glucose-like sugar 1,5-AG in your blood. The higher your blood glucose peaks, the lower the amount of 1,5-AG in your blood. And the lower your GlycoMark test value. With A1C, your score increases when your blood glucose increases. Your GlycoMark result actually decreases when your blood glucose spikes.

Related Words/Test:

DM, Diabetes, Diabetes mellitus

 

Test:Glycosylated Hb
Other Test Request Name:

• HbA1c
• Glycated Hemoglobin                                                                                                     •A1c                                                                                                            •Glycohemoglobin                                                                                                     •Glycosylated Hemoglobin

Test Composition:

Not applicable

Intended Use:

Used for monitoring long-term control of diabetes mellitus and evaluates the effectiveness of diabetes therapy.

Methodology:

High Performance Liquid Chromatography (HPLC)

Laboratory Section:

Hematology

Special Instructions/Patient Preparations:

No patient preparation necessary.

Collection/Sample Container:

EDTA (purple top)

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

• 2mL EDTA whole blood
Note: 0.250- 0.500 mL EDTA whole blood if microtainer is used

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):

Not applicable

Transport Temperature:

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

Rejection Criteria:

• Improperly labeled specimen
• Clotted specimen
• Quantity not sufficient
• Insufficient volume of blood to anticoagulant
• Exceed sample stability requirement

Running Day:

Daily

Cut Off Time:

Monday to Saturday
• 6:00 PM

 

TAT/Releasing of Results:

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

Reference Interval/Result Interpretation:

Normal : <5.70%
Pre-Diabetes: 5.70% ~ 6.40%
Diabetes : >/= 6.50%
Note: This is in accordance with the American Diabetes Association’s(ADA) recommendation

Limitations/Interferences:

• Cold agglutinins
• Hemoglobin variants

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Diabetes, Glucose, Glucose monitoring, GlycoMark, Fructosamine, Urine Albumin and Albumin to Creatinine Ratio.

 

Test:Grandparents Testing
Other Test Request Name:

Not applicable

Test Composition:

Not Applicable

Intended Use:

Determines if biological relationship exists between the alleged grandparent and child.

Methodology:

DNA Analysis

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:
  • Hard copy of 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 grandparent, 4 swabs for child)
  3. Return swabs to its sterile package and place it inside the provided envelope.
  4. Encircle whether sample came from father or child.                  NOTE: Sample from father and child 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 child'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 child, actual and  2 photocopies
  • Valid I.D of grandparent, actual and  2 photocopies
  • Completely filled up request form
  • Completely filled up disclaimer form
  • Mother's consent; Valid ID of mother, actual and 2 photocopies
  • Valid ID of requesting party (if not the alleged grandparent), actual and 2 photocopies

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 Swab Collection Kit - 4 swabs each

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

4 swabs each from grandparent  and child

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:Group B Streptococcus Ag
Other Test Request Name:Streptococcus agalactiae
Test Composition:Not applicable
Intended Use:For qualitative presumptive detection of Group B Streptococcal (Streptococcus agalactiae) antigen in female vaginal swab.
Methodology:Immunochromatographic Assay
Laboratory Section:Bacteriology
Special Instructions/Patient Preparations:Instructions to Send-in Clients:
• Indicate patient’s diagnosis, medical history and sample type on request forms.
• Use only Dacron or Rayon tipped sterile swabs with plastic shafts.
• It is recommended to use the swab supplied by the kits manufacturer.
• Swabs with cotton tips or wooden shafts are not recommended.
• Request for the sterile swabs from HP Main Lab prior to sample collection.

SPECIMEN COLLECTION:
1. Insert the swab into the vagina and rotate for 20 secs. Pull the swab out gently.
2. Do not place the swab in any transport medium since the media interferes with the assay and viability of the organisms is not required for the assay.
3. Put the swab to the extraction tube, if the test may be run immediately.
4. If immediate testing is not possible, the patient sample should be placed in a dry transport tube for storage or transport.
5. Do not use 0.9% Sodium Chloride to treat swabs before collecting specimens.
Collection/Sample Container:Sterile swab provided by kit manufacturer
Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:Vaginal Swab
Alternative Specimen and Volume Requirement:Not applicable
Specimen Stability  
•   Room Temperature (15-25°C):24 Hours
•   Refrigerated Temperature (2-8°C):1 Week
•   Freezer Temperature (-20°C):6 Months
Transport Temperature:Swabs should be placed in a dry sterile tube / container and transported at room temp. (15°C-30°C)

NOTE: Do not delay transport of samples.
Rejection Criteria:• Improperly labeled specimen
• Specimen collected using unsterile cotton swab
• Specimen held longer than 24 hours before delivery to the laboratory
• Specimen stored beyond room temperature (15°C to 30°C.)
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:
• 1½ hours from extraction/messenger arrival
Reference Interval/Result Interpretation:A positive result indicates that the patient is positive for Group B Streptococcus when consistent with clinical signs and symptoms.
Limitations/Interferences:• Detection of Group B Streptococcus is dependent on the number of organisms present in the specimen. This may be affected by specimen collection methods and patient factors such as age, history of STD, presence of symptoms, etc. The minimun detection level of this test may vary according to serovar.
• Like with all diagnostic tests, a confirmed diagnosis should only be made by a physcian after all clinical and laboratory findings have been evaluated.
Frequently Asked Questions (FAQs):Q: What is the rapid Strep B Test for?
A: It is a screening test for the detection of Group B Streptococcus (Streptococcus agalactiae) that can cause complications in pregnancy both for the mother and the newborn.

Q: Why is it important to test for Group B Streptococcus (GBS)?
A: The primary concern with GBS is the risk to the baby. If you are a carrier, you may likely pass it to your newborn that can cause serious illness or worse, even miscarriage and stillbirth. This is also a routine part of prenatal care.

Q: How does someone get in contact with Group B Streptococcus bacteria?
A: The bacterium is a normal flora (non-pathogenic) of gastrointestinal tract. It normally lives in the intestine, vagina and in rectal areas. However, this causes a threat when there is a pregnancy involved.

Q: How is GBS screening done?
A: The doctor will take a swab from the vagina during pregnancy similar to the procedure in taking a pap smear. This swab will then be submitted to the laboratory for testing.

Q: What if I get tested positive for GBS, what should I do?
A: If you are tested positive for Group B Streptococcus bacteria, it does not mean that you are ill or that your baby will be affected automatically. It is best to consult your doctor for disease prevention and management for both the mother and the baby. Your physician may recommend prophylactic antibiotics to decrease the chances of infecting your baby.
Related Words/Test:Strep B

 

Test:Growth Hormone (ECLIA)
Other Test Request Name:
  • GH
  • HGH
  • Somatotropin
  • Human Growth Hormone
Test Composition:

Not applicable

Intended Use:

Used in the diagnosis and treatment of various forms of inappropriate growth hormone secretion.

Methodology:

Electrochemiluminescence Immunoassay (ECLIA)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:
  • 8 Hours fasting
  • Limit physical activity (Must be rested for at least 30 minutes)
  • Samples cannot be taken from pregnant women
  • 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.
:

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°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 to Friday

Cut Off Time:

Monday to Friday, 7:00 AM

TAT/Releasing of Results:

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

Reference Interval/Result Interpretation:

Available upon request

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 assay is affected by pegvisomant (a highly selective GH receptor antagonist) and is therefore not suitable for patients under pegvisomant treatment. There is no interference with Octreotide (somatostatin analogue) or Cabergoline (dopamine agonist).
  • The assay is not suitable for the determination of hGH in samples from pregnant women. This is due to a cross-reactivity to placental hGH. Placental hGH is a variant of pituitary hGH36 and its serum levels increase during the course of pregnancy.
Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

IGF-1, Growth Hormone Releasing Hormone, Cortisol, ACTH, Free T4, TSH, Glucose Tests, Prolactin, IGF BP-3