Laboratory Test Preparation

| 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. |
| 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 | : |
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| Running Day | : | Batch Running |
| Cut Off Time | : | Monday, 12:00 PM
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| 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:
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| Methodology | : | Not Applicable |
| Laboratory Section | : | Not Applicable |
| Special Instructions/Patient Preparations | : | PREPARATION
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| 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.
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| 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 |
| 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 | : |
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| Test Composition | : |
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| 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)
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| 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 | : |
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| Running Day | : | Batch Running |
| Cut Off Time | : | Monday, 12:00 PM
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| 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 | : |
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| 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 | : |
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| 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.
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| Related Words/Test | : | Gastric acid |
| Test | : | GCT- Pregnant (50grams) |
| Other Test Request Name | : | • Oral Glucose Challenge Test |
| Test Composition | : | Not applicable |
| Intended Use | : | • OGTT-Pregnant (100 gms) test is used to detect gestational diabetes. |
| Methodology | : | Hexokinase |
| Laboratory Section | : | Chemistry |
| Special Instructions/Patient Preparations | : | • Non-fasting |
| 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 |
| • 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 |
| 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
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| 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 |
| 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 |
| Methodology | : | Enzymatic colorimetric (standardized against Szasz) |
| Laboratory Section | : | Chemistry |
| Special Instructions/Patient Preparations | : | 8-12 hours fasting. |
| 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 | : |
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| Running Day | : | Daily |
| Cut Off Time | : | Monday to Saturday: 6 PM
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| TAT/Releasing of Results | : | RUNNING TIME: 6:00 AM onwards RELEASING TIME: ROUTINE |
| Reference Interval/Result Interpretation | : | MALE: 8.00-61.00 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 | : |
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| 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
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| 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 | : |
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| 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 |
| 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 |
| 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. |
| 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 |
| Running Day | : | Daily |
| Cut Off Time | : | Monday to Saturday: 6:00 PM
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| TAT/Releasing of Results | : | ROUTINE (on running day/s) |
| Reference Interval/Result Interpretation | : | MALE: 10.70~32.00 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. |
| Frequently Asked Questions (FAQs) | : | Q: How do I correlate my FBS and HbA1c results with GlycoMark? |
| Related Words/Test | : | DM, Diabetes, Diabetes mellitus |
| Test | : | Glycosylated Hb |
| Other Test Request Name | : | • HbA1c |
| 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 |
| 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 |
| Running Day | : | Daily |
| Cut Off Time | : | Monday to Saturday |
| TAT/Releasing of Results | : | ROUTINE |
| Reference Interval/Result Interpretation | : | Normal : <5.70% |
| Limitations/Interferences | : | • Cold agglutinins |
| 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 | : |
Sample collection/handling:
Document Requirements:
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 | : |
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| 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 | : |
|
| 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 | : |
|
| 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 | : |
|
| 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 | : |
|
| 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 |