Test:DHEA (RIA)
Other Test Request Name:
  • Dehydroepiandrosterone
  • DHA
  • Dehydro-epiandrosterone
Test Composition:

Not applicable

Intended Use:

DHEA is a weakly androgenic steroid that is useful when congenital adrenal hyperplasia is suspected. It is also useful in determining the source of androgens in hyperandrogenic conditions, such as polycystic ovarian syndrome and adrenal tumors.

DHEA is a 17-ketosteroid (17-oxosteroid) produced from 17-hydroxy-pregnenolone. It is metabolized to form delta-4-androstenedione and testosterone. In women, 50% of DHA is synthesized in the adrenal gland, 25% in the ovaries and 25% by the conversion of DHA sulfate. In patients with 3-beta-hydroxy-dehydrogenase deficiency, DHEA levels rise in a short Synacthen (adrenocortical stimulation) test. High levels are observed in the absence of stimulation in precocious puberty and in adrenal hyperplasia due to 11-beta-hydroxylase deficiency and Stein-Leventhal syndrome.

Methodology:

Radio Immuno Assay (RIA)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

No patient preparation necessary.

Collection/Sample Container:

Red or Gold tube

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

3 mL Serum

Alternative Specimen and Volume Requirement:

Not Applicable

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

3 Days

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

28 Days

Transport Temperature:

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

Rejection Criteria:

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

Running Day:

Batch Running

Cut Off Time:

Friday, 4:00 PM

TAT/Releasing of Results:

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:

DHEA-SO4; DHEA Sulfate, Dehydroepiandrosterone Sulfate

 

Test:DHEAS (CMIA)
Other Test Request Name:

• Dehydroepiandrosterone Sulfate
• DHEA-SO4
• DHEA Sulfate

Test Composition:

Not applicable

Intended Use:
  • Helps diagnose congenital adrenal hyperplasia and adult-onset adrenal hyperplasia. In women, concentrations of DHEA-S are often measured along with other hormones such as FSH, LH, prolactin, estrogen, and testosterone, to help diagnose polycystic ovarian syndrome (PCOS) and to help rule out other causes of infertility, lack of menstrual period (amenorrhea), and presence of excess facial and body hair (hirsutism).
  • DHEA-S levels may be ordered with other hormones to investigate and diagnose the cause of the development of masculine physical characteristics (virilization) in young girls and early (precocious) puberty in young boys.
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, Sodium citrate, Sodium Heparin)

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

Not specified

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

2 Months

Note:

SERUM:Avoid more than 5 freeze/thaw cycles

PLASMA:Avoid more than 2 freeze/thaw cycles

Transport Temperature:

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

Rejection Criteria:
  • Grossly hemolyzed specimen (>500 mg/dL hemoglobin)
  • Heat-inactivated
  • Markedly lipemic specimen
  • Exceeded sample stability requirement
  • Quantity not sufficient
  • Improperly labeled specimen
  • Improper collection tube used
Running Day:

Wednesday, Saturday

Cut Off Time:

Monday to Saturday:10:00 PM

Sunday:6:00PM

TAT/Releasing of Results:

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

Reference Interval/Result Interpretation:

1-6 Days: 0.70-8.20 umol/L
1-4 Weeks: 0.20-8.60 umol/L
1-12 Months: 0.90-5.80 umol/L
1Y & 1 Day – 5Y: 0.90-7.50 umol/L
5Y & 1 Day - 11Y: 0.70-5.70 umol/L
11Y & 1 Day - 15Y MALE: 0.50-6.60 umol/L
11Y & 1 Day - 15Y FEMALE: 0.20-4.60 umol/L
15Y & 1 Day - 20Y MALE: 1.20-10.40 umol/L
15Y & 1 Day - 20Y FEMALE: 1.70-13.40 umol/L
20Y & 1 Day - 25Y MALE: 6.50-14.60 umol/L
20Y & 1 Day - 25Y FEMALE: 3.60-11.10 umol/L
25Y & 1 Day - 35Y MALE: 4.60-16.10 umol/L
25Y & 1 Day - 35Y FEMALE: 2.60-13.90 umol/L
35Y & 1 Day - 45Y MALE: 3.80-13.10 umol/L
35Y & 1 Day - 45Y FEMALE: 2.00-11.10 umol/L
45Y & 1 Day - 55Y MALE: 3.70-12.10 umol/L
45Y & 1 Day - 55Y FEMALE: 1.50-7.70 umol/L
55Y & 1 Day - 65Y MALE: 1.30-9.80 umol/L
55Y & 1 Day - 65Y FEMALE: 0.80-4.90 umol/L
65Y & 1 Day - 70Y MALE: 6.20-7.70 umol/L
65Y & 1 Day - 70Y FEMALE: 0.90-2.10 umol/L

Limitations/Interferences:
  • Specimens from patients with adrenal tumors or congenital adrenal hyperplasia may exhibit elevated levels of DHEA-S.
  • Specimens from patients who have received preparations of mouse monoclonal antibodies for diagnosis or therapy may contain human anti-mouse antibodies (HAMA). Specimens containing HAMA may produce anomalous values when tested with assay kits that employ mouse monoclonal antibodies.
  • Heterophilic 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 values may be observed. Additional information may be required for diagnosis.
Frequently Asked Questions (FAQs):

Q: Is DHEA different from DHEA-S?
A: Yes, we have a different testing determination for DHEA (Test code: DHEA9), DHEA is the precursor hormone for DHEA-S

Related Words/Test:

Testosterone, ACTH, FSH, LH, Prolactin, Estrogens, SHBG, 17-Hydroxyprogesterone, Androstenedione

 

Test:Digoxin/Lanoxin (CMIA)
Other Test Request Name:

• Lanoxin
• Digitalis
• Digitalin
• Digitalis glycoside

Test Composition:

Not applicable

Intended Use:

• Used to aid in the diagnosis and treatment of digoxin overdose and in monitoring levels of digoxin to help ensure appropriate therapy.
• Digoxin is occasionally used in the treatment of various heart conditions, namely atrial fibrillation, atrial flutter and sometimes heart failure that cannot be controlled by other medication.

Methodology:

Chemiluminescent Microparticle Immunoassay (CMIA)

Laboratory Section:

Immunology

Special Instructions/Patient Preparations:

• Collect as trough specimen (generally 30 minutes before the next dose) unless specified by the requesting physician.
• Provide date and time of last Digoxin intake and sample collection. This information is important to help requesting clinicians interpret the result.
• Separate serum from red cells as soon as possible.

Collection/Sample Container:

Red tube (DO NOT USE GOLD TUBE or any other type of tube with gel separator)

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

1-3 mL Serum
 

Alternative Specimen and Volume Requirement:

1-3mL Plasma (K-EDTA, Li-Heparin, Na-heparin)

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

Not specified

•   Refrigerated Temperature (2-8°C):

48 Hours

•   Freezer Temperature (-20°C):

6 Months (3 freeze-thaw only)

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
• Serum collected in tubes with gel separator.

Running Day:

Tuesday, Friday

Cut Off Time:

Monday to Saturday:10:00 PM

Sunday:6:00PM

TAT/Releasing of Results:

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

Reference Interval/Result Interpretation:

0.80~2.00 ng/mL

Limitations/Interferences:

• Plasma samples from different anticoagulant tube types should not be used interchangeably for monitoring digoxin.
• Specimens from patients who have received preparations of mouse monoclonal antibodies for diagnosis or therapy may contain human anti-mouse antibodies (HAMA). Specimens containing HAMA may produce anomalous values when tested with assay kits that employ mouse monoclonal antibodies.
•Some immunoassays for digoxin may cross react with metabolites, which can lead to positive bias in patient results.
•Digoxin values for specimens from patients who have received DIGIBIND or DIGIFAB therapy may be impacted.
•Heterophilic antibodies in human serum can react with reagent immunoglobulins, interfering with in vitro immunoassays.

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

Cardiac drug, Therapeutic Drug Monitoring , TDM, Apo-Digoxin (CA), Digitek, Lanoxin, PMS Digoxin, Cardiac glycoside

 

Test:Dihydro Testosterone(RIA)
Other Test Request Name:
  • Dihydrotestosterone
  • 5-alpha DHT
  • Androstanolone
  • 5-alpha-Dihydrotestosterone
  • DHT -  Dihydrotestosterone -  serum
Test Composition:

Not Applicable

Intended Use:

Useful in the investigation of idiopathic hirsutism or 5-alpha-reductase deficiency (hirsutism.) In 5 alpha reductase deficiency the affected subjects show normal testosterone levels with low levels of DHT. The enzyme deficiency can best be determined by measuring testosterone and DHT after hCG stimulation.

Methodology:

Chromatography - Extraction - Radioimmunoassay

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.
:

5 mL Serum

Alternative Specimen and Volume Requirement:

Not Applicable

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

24 Hours

•   Refrigerated Temperature (2-8°C):

5 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:

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

Reference Interval/Result Interpretation:

Not Applicable

Limitations/Interferences:

None Specified

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Androgenetic alopecia (AGA; male-pattern baldness)

 

Test:Diptheria Toxin Ab (EI)
Other Test Request Name:
  • Corynebacterium diphteriae
  • Anti-Diphtheria Toxin Antibodies
  • Diphteria
  • Diphtheria Toxin - anti-antibodies
  • Diptheria - ImmunityTest - IgG Serology - Serum
Test Composition:

Not Applicable

Intended Use:

Diphtheria is caused by a toxin elaborated by a bacterium, Corynebacterium diphteriae. This test should be performed in patients with suggestive symptoms, especially if they have visited Russia or Middle Europe recently. Diagnosis is confirmed by isolation of the bacterium and proof that it is producing toxin. Assaying anti-diphtheria toxin antibodies gives a measure of the degree of protection against the disease, especially useful following immunization.

Methodology:

Enzyme Immunoassay (EIA)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

No patient preparation necessary.

Collection/Sample Container:

Red or Gold Tube

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

3 mL Serum

Alternative Specimen and Volume Requirement:

Not Applicable

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

24 Hours 

•   Refrigerated Temperature (2-8°C):

5 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:

Not Applicable

Limitations/Interferences:

None Specified

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Corynebacterium spp

 

Test:DM & BM DYSTROPHY
Other Test Request Name:

Duchenne and Becker Muscular Dystrophy

Test Composition:

Not Applicable

Intended Use:
  • Duchenne and Becker muscular dystrophies have similar signs and symptoms and are caused by different mutations in the same gene
  • In boys with Duchenne muscular dystrophy, muscle weakness tends to appear in early childhood and worsen rapidly. Affected children may have delayed motor skills, such as sitting, standing, and walking. They are usually wheelchair-dependent by adolescence.
Methodology:

Multiplex ligation-dependent probe amplification (MLPA)

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

No Patient preparation

Collection/Sample Container:

EDTA

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

1pc 5ML Whole Blood

Alternative Specimen and Volume Requirement:

Not Applicable

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

2 weeks

•   Refrigerated Temperature (2-8°C):

Not Applicable

•   Freezer Temperature (-20°C):

Not Applicable

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

-all previously conducted genetics test reports/ information.

- The family genetic history

- The clinical information/prescription details.

- The patient's and doctor consent

 

Rejection Criteria:

Not applicable

Running Day:

Batch Running

Cut Off Time:

Every friday 4 pm

TAT/Releasing of Results:

30 working days except saturday's, sunday's and holiday

Reference Interval/Result Interpretation:

Not Applicable

Limitations/Interferences:

Not Applicable

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Not Applicable

 

Test:DRVVT
Other Test Request Name:

Dilute Russel Viper Venom Test

Test Composition:

Not applicable

Intended Use:

•For autoimmune disorder that is associated with pregnancy
•Used to help in the diagnosis and/or assess a person with an autoimmune disease associated with Systemic Lupus Erythematosus (SLE).

Methodology:
multi-wavelength transmitted light detection method
Laboratory Section:

Hematology

Special Instructions/Patient Preparations:
  • No patient preparation necessary.
  • DO NOT use glass collection and transport tube
Collection/Sample Container:

Citrated Blue top

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

At least1 mL citrated plasma

Alternative Specimen and Volume Requirement:

Not applicable

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

4 Hours

•   Refrigerated Temperature (2-8°C):

Not applicable

•   Freezer Temperature (-20°C):

7 Days

Transport Temperature:

• Sample must be sent to laboratory immediately after collection at 15-25°c
• Samples that cannot be sent to HPD laboratory within 4 hours should be stored at -20°C and should be transported with dry ice.

Rejection Criteria:

• Improper use of anticoagulant
• Insufficient volume of blood to anticoagulant
• Improperly labeled specimens
• Hemolyzed specimens
• Specimen stored and transported outside the temperature requirement

Running Day:

Wednesday and Saturday

Cut Off Time:

Wednesday and Saturday 2PM

TAT/Releasing of Results:

Thursday and Sunday 9AM

Reference Interval/Result Interpretation:

0.80-1.20 

Limitations/Interferences:

• Dysfibrinogenemia
• Heparin intake
• Intrinsic pathway deficiencies
• Presence of factor inhibitors
• Hepatic disorders
• Treatments with vitamin K antagonists
• Treatment with thrombin inhibitors
• DIC

Frequently Asked Questions (FAQs):

Not applicable

Related Words/Test:

LA, LAC, Lupus Anticoagulant Panel, Lupus Inhibitor, LA Sensitive PTT, PTT-LA, Lupus Anticoagulant

 

Test:Du Typing
Other Test Request Name:

Rh Confirmatory

Test Composition:

Not Applicable

Intended Use:

For confirmation of Rh negative blood type

Methodology:

Du Typing Agglutination

Laboratory Section:

Serology

Special Instructions/Patient Preparations:

No patient preparation necessary.

Collection/Sample Container:

EDTA (purple top)

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

1.5-2mL EDTA whole blood

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):

Unacceptable

Transport Temperature:

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

Rejection Criteria:

• Improperly labeled specimen
• Insufficient volume of specimen
• Clotted specimen
• Exceeded sample stability requirement

Running Day:

Daily

Cut Off Time:

Monday to Saturday
• 8:00 PM

Sunday
• 3:00 PM

TAT/Releasing of Results:

• 6 hours after receipt of specimen/ arrival of messenger

No STAT Requests

Reference Interval/Result Interpretation:

Not applicable

Limitations/Interferences:

None identified.

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Blood & Rh Typing

 

Test:e-GFR (<19 y/o)
Other Test Request Name:
  • Estimated Glomerular Filtration Rate
  • eGFR
Test Composition:
  1. Serum Creatinine
  2. Height (cm)
  3. Estimated GFR (CKD-EPI)
Intended Use:
  • The estimated glomerular filtration rate (eGFR) is used to screen for and detect early kidney damage, to help diagnose chronic kidney disease (CKD), and to monitor kidney status. It is a calculation based on the results of a blood creatinine  test along with other variables such as age and sex.
  • This equation should only be used for patients less than 19 years old.
Methodology:
  • Creatinine:Enzymatic
  • Estimated GFR (CKD-EPI):  Calculated based on CREATININE-BASED “BEDSIDE SCHWARTZ” EQUATION (2009)
Laboratory Section:

Chemistry

Special Instructions/Patient Preparations:
  • Provide Height (cm) of patient.
  • Refrain from eating a high meat diet and doing strenuous physical activity 8-12 hours before blood extraction.
  • Refrain from taking medicines such as Acetaminophen (Paracetamol), N-acetyl-p-benzoquinone imine (NAPQI) metabolites, N-Acteylcysteine (NAC), Metamizole (Novaminsulfone, Dipyrone), 4-aminoantipyrine (4-AAP) and 4-Methylamino-antipyrine (4-MAP) metabolites 8-12 hrs before sample collection.

Note:If recommended preparation is not followed, you may accept but NOTE in clinical info.

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):

3 Months

Transport Temperature:

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

Rejection Criteria:
  • Specimens that failed serum index (hemolyzed and lipemic)
  • Exceeded sample stability requirement
  • Quantity not sufficient
  • Improperly labeled specimen
  • Improper collection tube used
Running Day:

Daily

Cut Off Time:

Monday to Saturday:6:00 PM


 

TAT/Releasing of Results:
  • ROUTINE (on running day only): 4 hours after receipt of specimen/ arrival of messenger
  • STAT (on running day only): 2.5 hours after receipt of specimen/ arrival of messenger
Reference Interval/Result Interpretation:

CREATININE:

  • 0~2 Months: 27.00-77.00 umol/L (0.31-0.87 mg/dL)
  • 2M & 1 Day - 1Y: 14.00-34.00 umol/L (0.16-0.38 mg/dL)
  • 1Y & 1 Day - 3Y: 15.00-31.00 umol/L (0.17-0.35 mg/dL)
  • 3Y & 1 Day - 5Y: 23.00-37.00 umol/L (0.26-0.42 mg/dL)
  • 5Y & 1 Day - 7Y: 25.00-42.00 umol/L (0.28-0.47 mg/dL)
  • 7Y & 1 Day - 9Y: 30.00-47.00 umol/L (0.34-0.53 mg/dL)
  • 9Y & 1 Day - 11Y: 29.00-56.00 umol/L (0.33-0.63 mg/dL)
  • 11Y & 1 Day - 13Y: 39.00-60.00 umol/L (0.44-0.68 mg/dL)
  • 13Y & 1 Day - 15Y: 40.00-68.00 umol/L (0.45-0.77 mg/dL)
  • 15Y & 1 Day - 999Y MALE: 59.00-104.00 umol/L (0.67-1.18 mg/dL)
  • 15Y & 1 Day - 999Y FEMALE: 45.00-84.00 umol/L (0.51-0.95 mg/dL)

eGFR: >60 mL/min/1.73m^2

Limitations/Interferences:
  • Creatinine-based estimating equations are not recommended for use with:
  1. Individuals with unstable creatinine concentrations. This includes pregnant women; patients with serious co-morbid conditions; and hospitalized patients, particularly those with acute renal failure. Creatinine-based estimating equations should be used only for patients with stable creatinine concentrations.
  2. Persons with extremes in muscle mass and diet. This includes, but is not limited to, individuals who are amputees, paraplegics, bodybuilders, or obese; patients who have a muscle-wasting disease or a neuromuscular disorder; and those suffering from malnutrition, eating a vegetarian or low-meat diet, or taking creatine dietary supplements.
  • Rifampicin, Levodopa and Calcium dobesilate (e.g. Dexium) cause artificially low creatinine results. Dicynone (Etamsylate) at therapeutic concentrations may lead to falsely low results.
  • N-ethylglycine at therapeutic concentrations and DL-proline at concentrations ≥ 1 mmol/L (≥ 115 mg/L) give falsely high results.
  • 2-Phenyl-1,3-indandion (Phenindion) at therapeutic concentrations interferes with the assay.
  • In very rare cases, gammopathy, in particular type IgM (Waldenstrom’s macroglobulinemia), may cause unreliable results.
  • Acetaminophen intoxications are frequently treated with N-Acetylcysteine. N-Acetylcysteine at a plasma concentration above 333 mg/L and the Acetaminophen metabolite N-acetyl-p-benzoquinone imine (NAPQI) independently may cause falsely low results.
  • Venipuncture should be performed prior to the administration of Metamizole. Venipuncture immediately after or during the administration of Metamizole may lead to falsely low results. A significant interference may occur at any plasma Metamizole concentration.
Frequently Asked Questions (FAQs):

Q: How is it used?

A: The estimated glomerular filtration rate (eGFR) is used to screen for and detect early kidney damage, to help diagnose chronic kidney disease (CKD), and to monitor kidney status. It is a calculation based on the results of a blood creatinine test along with other variables such as age, sex, and race (e.g., African-American, non-African American), depending on the equation used.

Q: When is it ordered?

A creatinine test and eGFR may be ordered when a healthcare practitioner wants to evaluate a person's kidney function as part of a health checkup or if kidney disease is suspected.

Related Words/Test:

BUN, Creatinine Clearance, Comprehensive Metabolic Panel, Basic Metabolic Panel, Urinalysis, Urine Protein to Creatinine Ratio, Urine Albumin and Urine Albumin/Creatinine Ratio, Renal Panel, Beta-2 Microglobulin

 

Test:e-GFR (>/=19 y/o)
Other Test Request Name:
  • Estimated Glomerular Filtration Rate
  • eGFR
Test Composition:

1. Creatinine
2. Estimated GFR (CKD-EPI)

Intended Use:
  • The estimated glomerular filtration rate (eGFR) is used to screen for and detect early kidney damage, to help diagnose chronic kidney disease (CKD), and to monitor kidney status. It is a calculation based on the results of a blood creatinine test along with other variables such as age and sex.
  • This equation should only be used for patients 19 years old and older.
Methodology:
  • Creatinine:Enzymatic
  • Estimated GFR (CKD-EPI):  Calculated based on  CKD-EPI CREATININE EQUATION (2009)
Laboratory Section:

Chemistry

Special Instructions/Patient Preparations:
  • Refrain from eating a high meat diet and doing strenuous physical activity 8-12 hours before blood extraction.
  • Refrain from taking medicines such as Acetaminophen (Paracetamol), N-acetyl-p-benzoquinone imine (NAPQI) metabolites, N-Acteylcysteine (NAC), Metamizole (Novaminsulfone, Dipyrone), 4-aminoantipyrine (4-AAP) and 4-Methylamino-antipyrine (4-MAP) metabolites 8-12 hrs before sample collection.

Note:If recommended preparation is not followed, you may accept but NOTE in clinical info.

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):

3 Months

Transport Temperature:

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

Rejection Criteria:
  • Specimens that failed serum index (hemolyzed and lipemic)
  • Exceeded sample stability requirement
  • Quantity not sufficient
  • Improperly labeled specimen
  • Improper collection tube used
Running Day:

Daily

Cut Off Time:

Monday to Saturday:6:00 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:

CREATININE:
0-2 Months: 27.00-77.00 umol/L (0.31-0.87 mg/dL)
2M & 1 Day - 1Y: 14.00-34.00 umol/L (0.16-0.38 mg/dL)
1Y & 1 Day - 3Y: 15.00-31.00 umol/L (0.17-0.35 mg/dL)
3Y & 1 Day - 5Y: 23.00-37.00 umol/L (0.26-0.42 mg/dL)
5Y & 1 Day - 7Y: 25.00-42.00 umol/L (0.28-0.47 mg/dL)
7Y & 1 Day - 9Y: 30.00-47.00 umol/L (0.34-0.53 mg/dL)
9Y & 1 Day - 11Y: 29.00-56.00 umol/L (0.33-0.63 mg/dL)
11Y & 1 Day - 13Y: 39.00-60.00 umol/L (0.44-0.68 mg/dL)
13Y & 1 Day - 15Y: 40.00-68.00 umol/L (0.45-0.77 mg/dL)
15Y & 1 Day - 999Y MALE: 59.00-104.00 umol/L (0.67-1.18 mg/dL)
15Y & 1 Day - 999Y FEMALE: 45.00-84.00 umol/L (0.51-0.95 mg/dL)

Estimated GFR: >60 mL/min/1.73m^2

Limitations/Interferences:

- Creatinine-based estimating equations are not recommended for use with:

  1. Individuals with unstable creatinine concentrations. This includes pregnant women; patients with serious co-morbid conditions; and hospitalized patients, particularly those with acute renal failure. Creatinine-based estimating equations should be used only for patients with stable creatinine concentrations.
  2. Persons with extremes in muscle mass and diet. This includes, but is not limited to, individuals who are amputees, paraplegics, bodybuilders, or obese; patients who have a muscle-wasting disease or a neuromuscular disorder; and those suffering from malnutrition, eating a vegetarian or low-meat diet, or taking creatine dietary supplements.

- Rifampicin, Levodopa and Calcium dobesilate (e.g. Dexium) cause artificially low creatinine results. Dicynone (Etamsylate) at therapeutic concentrations may lead to falsely low results.

- N-ethylglycine at therapeutic concentrations and DL-proline at concentrations ≥ 1 mmol/L (≥ 115 mg/L) give falsely high results.

- 2-Phenyl-1,3-indandion (Phenindion) at therapeutic concentrations interferes with the assay.

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

- Acetaminophen intoxications are frequently treated with N?Acetylcysteine. N-Acetylcysteine at a plasma concentration above 333 mg/L and the Acetaminophen metabolite N-acetyl-p-benzoquinone imine (NAPQI) independently may cause falsely low results.

- Venipuncture should be performed prior to the administration of Metamizole. Venipuncture immediately after or during the administration of Metamizole may lead to falsely low results. A significant interference may occur at any plasma Metamizole concentration.

Frequently Asked Questions (FAQs):

Q:How is it used?

A: The estimated glomerular filtration rate (eGFR) is used to screen for and detect early kidney damage, to help diagnose chronic klidney disease, and to monitor kidney status. It is a calculation based on the results of a blood creatinine test along with other variables such as age, sex, and race (e.g., African-American, non-African American), depending on the equation used.

Q:When is it ordered?

A creatinine test and eGFR may be ordered when a healthcare practitioner wants to evaluate a person's kidney function as part of a health checkup or if kidney disease is suspected.

Q:Why are results being reported as >60 and not an actual value?

A: Because the calculation works best for estimating reduced kidney function, actual numbers are only reported once values are less than 60 mL/min/1.73m2

Related Words/Test:

BUN, Creatinine Clearance, Comprehensive Metabolic Panel, Basic Metabolic Panel, Urinalysis, Urine Protein to Creatinine Ratio, Urine Albumin and Urine Albumin/Creatinine Ratio, Renal Panel, Beta-2 Microglobulin

 

Test:e-GFR Panel (>/=19 y/o)
Other Test Request Name:
  • Estimated Glomerular Filtration Rate
  • eGFR
Test Composition:
  1. Cystatin
  2. Serum Creatinine
  3. Estimated GFR (CKD-EPI)
Intended Use:
  • The estimated glomerular filtration rate (eGFR) is used to screen for and detect early kidney damage, to help diagnose chronic kidney disease (CKD), and to monitor kidney status.
  • May provide more accurate estimates of kidney function in patients with differences in diet, extremes of muscle mass (such as body builders or patients with muscle wasting)
  • May also prove useful in estimating change in eGFR over time in people with changing muscle mass or diet.
  • May have a role in identifying persons with CKD who have the highest risk for complications.
  • This equation is used for patients 18 years old and older.
Methodology:
  • Creatinine:Enzymatic
  • Cystatin C:Particle-Enhanced Turbidimetric Immunoassay (PETIA)
  • Estimated GFR (CKD-EPI):  Calculated based on  CKD-EPI CREATININE-CYSTATIN EQUATION (2012)
Laboratory Section:

Chemistry

Special Instructions/Patient Preparations:
  • Refrain from eating a high meat diet and doing strenuous physical activity 8-12 hours before blood extraction.
  • Refrain from taking medicines such as Acetaminophen (Paracetamol), N-acetyl-p-benzoquinone imine (NAPQI) metabolites, N-Acteylcysteine (NAC), Metamizole (Novaminsulfone, Dipyrone), 4-aminoantipyrine (4-AAP) and 4-Methylamino-antipyrine (4-MAP) metabolites 8-12 hrs before sample collection.

Note:If recommended preparation is not followed, you may accept but NOTE in clinical info.

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)

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

2 Days

•   Refrigerated Temperature (2-8°C):

7 Days

•   Freezer Temperature (-20°C):

1 Month

Transport Temperature:

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

Rejection Criteria:
  • Specimens that failed serum index (hemolyzed and lipemic)
  • Exceeded sample stability requirement
  • Quantity not sufficient
  • Improperly labeled specimen
  • Improper collection tube used
Running Day:

Tuesday and Friday

Cut Off Time:

Monday to Saturday:6:00 PM

TAT/Releasing of Results:

RUNNING TIME:6:00 AM onwards

RELEASING TIME:

ROUTINE: 4 hours after receipt of specimen/ arrival of messenger

STAT: After 2½ hours from extraction/messenger arrival

Reference Interval/Result Interpretation:

CREATININE:
0-2 Months: 27.00-77.00 umol/L (0.31-0.87 mg/dL)
2M & 1 Day - 1Y: 14.00-34.00 umol/L (0.16-0.38 mg/dL)
1Y & 1 Day - 3Y: 15.00-31.00 umol/L (0.17-0.35 mg/dL)
3Y & 1 Day - 5Y: 23.00-37.00 umol/L (0.26-0.42 mg/dL)
5Y & 1 Day - 7Y: 25.00-42.00 umol/L (0.28-0.47 mg/dL)
7Y & 1 Day - 9Y: 30.00-47.00 umol/L (0.34-0.53 mg/dL)
9Y & 1 Day - 11Y: 29.00-56.00 umol/L (0.33-0.63 mg/dL)
11Y & 1 Day - 13Y: 39.00-60.00 umol/L (0.44-0.68 mg/dL)
13Y & 1 Day - 15Y: 40.00-68.00 umol/L (0.45-0.77 mg/dL)
15Y & 1 Day - 999Y MALE: 59.00-104.00 umol/L (0.67-1.18 mg/dL)
15Y & 1 Day - 999Y FEMALE: 45.00-84.00 umol/L (0.51-0.95 mg/dL)
 

Cystatin C:

  • 0~49 Y/O Male: 0.31~0.79 mg/L
  • 0~49 Y/O Female: 0.40~0.99 mg/L
  • 50~999Y/O  Male: 0.41~0.99 mg/L
  • 50~999Y/O  Female: 0.40~0.99 mg/L

Estimated GFR:>60 mL/min/1.73m^2

Limitations/Interferences:

-Creatinine-based estimating equations are not recommended for use with:

  1. Individuals with unstable creatinine concentrations. This includes pregnant women; patients with serious co-morbid conditions; and hospitalized patients, particularly those with acute renal failure. Creatinine-based estimating equations should be used only for patients with stable creatinine concentrations.
  2. Persons with extremes in muscle mass and diet. This includes, but is not limited to, individuals who are amputees, paraplegics, bodybuilders, or obese; patients who have a muscle-wasting disease or a neuromuscular disorder; and those suffering from malnutrition, eating a vegetarian or low-meat diet, or taking creatine dietary supplements.

- Rifampicin, Levodopa and Calcium dobesilate (e.g. Dexium) cause artificially low creatinine results. Dicynone (Etamsylate) at therapeutic concentrations may lead to falsely low results.

- N-ethylglycine at therapeutic concentrations and DL-proline at concentrations ≥ 1 mmol/L (≥ 115 mg/L) give falsely high results.

- 2-Phenyl-1,3-indandion (Phenindion) at therapeutic concentrations interferes with the assay.

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

- Acetaminophen intoxications are frequently treated with N-Acetylcysteine. N-Acetylcysteine at a plasma concentration above 333 mg/L and the Acetaminophen metabolite N-acetyl-p-benzoquinone imine (NAPQI) independently may cause falsely low results.

- Venipuncture should be performed prior to the administration of Metamizole. Venipuncture immediately after or during the administration of Metamizole may lead to falsely low

- Bilirubin, conjugated: 66 mg/dL(1128.6 umol/L)

- Bilirubin, unconjugated: 60 mg/dL (1026 umol/L)

- Hemoglobin: 1000 mg/dL (10 g/L)

- Intralipid: 1000 mg/dL (10 g/L)

- Rheumatoid factor: 500 IU/mL (300 kU/L)

Frequently Asked Questions (FAQs):

Q:How is it used?

A: A cystatin C test may be used as an alternative to creatinine and creatinine clearance to screen for and monitor kidney dysfunction in those with known or suspected kidney disease. It is most useful in special cases where creatinine measurement could be misleading. Examples are patients with liver cirrhosis, are very obese, are malnourished, practice a vegetarian diet, have amputated limbs, or have reduced muscle mass (elderly and children). Cystatin C is not affected by body mass or diet, and hence is a more reliable marker of kidney function than creatinine. Measuring cystatin C may also be useful in the early detection of kidney disease when other test results (eGFR, creatinine or urine albumin) may still be normal or borderline and an affected person may have few, if any, symptoms. In this case, the healthcare practitioner may want to confirm if chronic kidney disease is present by measuring cystatin c.

Q:What does the result mean?

A: A high level of cystatin C in the blood corresponds to a decreased glomerular filtration rate (GFR) and hence to kidney dysfunction. Since cystatin C is produced throughout the body at a constant rate and removed and broken down by the kidneys, it should remain at a steady level in the blood if the kidneys are working efficiently and the GFR is normal. Recent studies suggest that increased levels of cystatin C may also indicate an increased risk of heart disease, heart failure, and mortality.

Q:What are the limitations of Cystatin Test?

A: Although cystatin C is less variable and less affected by age, body mass, and diet than creatinine in some individuals, it is not a perfect test and can be affected by a number of drugs and other medical conditions. Some studies have reported increased cystatin C levels associated with higher levels of C-reactive protein (CRP) or body mass index (BMI), hyperthyroidism, steroid use, malignant diseases, HIV/AIDS, rheumatic diseases, and certain metabolic conditions such as hyperhomocysteinemia (increased homocysteine). In addition, other studies suggest that cystatin C can be cleared by non-kidney pathways, such as in the gut, and that its levels tend to fluctuate among patients with kidney transplants.

Q: Can Cystatin C be measured in urine samples?

A: No. Unlike creatinine, cystatin C is reabsorbed from the glomerular filtrate and then metabolized in the kidneys. Under normal conditions, cystatin C is not found at detectable levels in the urine.

Related Words/Test:

BUN, Creatinine Clearance, Comprehensive Metabolic Panel, Basic Metabolic Panel, Urinalysis, Urine Protein to Creatinine Ratio, Urine Albumin and Urine Albumin/Creatinine Ratio, Renal Panel, Beta-2 Microglobulin

 

Test:E. Histolytica (ELISA) (FOR HP DEL MONTE ONLY)
Other Test Request Name:
  • Amoeba Elisa Test
  • Entamoeba histolytica ELISA Test

 

Test Composition:

Not Applicable

Intended Use:

Help in establishing the diagnosis of amoebiasis.

Serologic testing for amebiasis is the best single test to distinguish between the two major type of liver abscesses : Amebic and Pyogenic.

Methodology:

Enzyme Linked Immunosorbent Immunoassay (ELISA)

Laboratory Section:

Special Test

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

Sterile leak proof container/wide mouth

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

Pea size of Stool/Feces (Freshly Collected)

Alternative Specimen and Volume Requirement:

Not Applicable

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

Not Applicable

•   Refrigerated Temperature (2-8°C):

1 Hour

•   Freezer Temperature (-20°C):

Not Applicable

Transport Temperature:

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

Rejection Criteria:
  •  Quantity not sufficient or less than pea size
  • Contaminated stool (e.g) with urine or other fluids
  • Improperly labeled samples 
  • Sample that contains formalin and other preservatives and collected with transport media.
  • Exceeded sample stability requirement 
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:

None Specified.

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

O&P, Parasitic Examination, stool, intestinal protozoa including: E. coli, E. hartmanni, E. gingivalis, Endolimax nana, and Iodamoeba buetschlii (the nonpathogenic amebae); Dientamoeba fragilis (which is a flagellate not an ameba); and the possibly pathogenic Entamoeba polecki.

 

Test:EBER Test
Other Test Request Name:

Not applicable

Test Composition:
  • RNA Positive
  • RNA Negative
  • EBER Test
Intended Use:

Not applicable

Methodology:

Immunohistochem

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

No Patient preparation

Collection/Sample Container:

Slides and Blocks

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

Not Applicable

Alternative Specimen and Volume Requirement:

Not Applicable

Specimen Stability 

Not Applicable

•   Room Temperature (15-25°C):

Indefinite

•   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:

not properly labeled specimen

Running Day:

Batch running

Cut Off Time:

Friday 4PM

TAT/Releasing of Results:

15 working days except saturdays, sundays and Holidays

Reference Interval/Result Interpretation:

Not Applicable

Limitations/Interferences:

Not Applicable

Frequently Asked Questions (FAQs):

Not Applicable

Related Words/Test:

Not Applicable

 

Test:EBV DNA (QUANTITATIVE)
Other Test Request Name:
  • EBV
  • IMN
  • Infectious Mononucleosis
  • Epstein-Bar Virus EBV
  • EBV Antibodies
  • EBV Viral Capsid Antigen Antibody
  • EBV Nuclear Antigen Antibody
  • Epstein-Barr Virus Antibodies
  • EBV DNA QT, PCR
Test Composition:

Not applicable

Intended Use:

Epstein-Barr Virus DNA, Quantitative, Real-Time PCR - Monitoring EBV DNA levels by quantitative PCR in patients at risk of EBV-associated lymphoproliferative disorders may allow timely recognition of virus reactivation and permit installment of antiviral treatment. This is a quantitative molecular test, with a linear range of 200-2,000,000 copies/mL.

Methodology:

Real-Time Polymerase Chain Reaction

Laboratory Section:

Special Test

Special Instructions/Patient Preparations:

Avoid repeated freezing and thawing.

Collection/Sample Container:

Red or Gold Top

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

3 mL Serum

 

 

Alternative Specimen and Volume Requirement:

2 mL CSF in sterile leakproof container

 

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:
  • Thawed specimen
  • Quantity Not sufficient
  • Improperly labeled specimen
  • Improperly container used
Running Day:

Batch running

Cut Off Time:

Monday, 12:00 PM

 

TAT/Releasing of Results:

2 weeks after cut-off (expect saturday, sunday & holiday)

Reference Interval/Result Interpretation:

Available upon request

Limitations/Interferences:

None specified

Frequently Asked Questions (FAQs):

Q: Why get tested?

A:To help diagnose infectious mononucleosis (mono); to distinguish between an Epstein-Barr virus (EBV) infection and another illness with similar symptoms; to help evaluate susceptibility to EBV

Q: When to get tested?

A:When you have symptoms of mono but a negative mono test; when a pregnant woman has flu-like symptoms; occasionally when an asymptomatic person has been exposed to someone with mono; or possibly as a means to check immune system function

Q: When is it ordered?

A:EBV antibody tests may be ordered when someone has symptoms suggesting mono but a negative mono test  and when a pregnant woman has flu-like symptoms and her healthcare provider wants to determine whether the symptoms are due to EBV or another microbe. Some signs and symptoms  associated with mono include:

  • Extreme weakness or fatigue
  • Fever
  • Headache
  • Sore throat
  • Swollen lymph glands in the neck and/or armpits
  • Enlarged spleen and/or liver (sometimes)

Testing may be ordered when a healthcare practitioner wants to establish previous exposure to EBV. Testing may occasionally be repeated when the healthcare provider wants to track antibody concentrations (titers)  and/or when the first test was negative but the healthcare practitioner still suspects that the person's symptoms are due to EBV.

Q: How is Epstein-Bar Virus (EBV) infection or infectious mononucleosis (mono) treated?

A:Care is largely supportive and typically includes plenty of rest and fluids as well as treatment of the symptoms. Avoiding any contact sports or heavy lifting for several weeks to months may be recommended to avoid spleen rupture. There are no anti-viral medications available to speed healing; however, anti-virals and steroids can be used to treat symptoms in severe cases. At present, there is no vaccine for EBV, but clinical trials are underway.

Related Words/Test:

EBV Antibodies; EBV VCA-IgM Ab; EBV VCA-IgG Ab; EBNA-IgG Ab; EA-D IgG Ab, Epstein-Barr Virus Antibody to Viral Capsid Antigen, IgM, IgG; Epstein-Barr Virus Antibody to Nuclear Antigen, IgG; Epstein-Barr Virus Antibody to Early D Antigen, IgG; Heterophile Antibodies, Mononucleosis (Mono) Test, Complete Blood Count, White Blood Coun, Blood Smear, CMV Tess, Toxoplasmosis Testing

 

Test:Ecstacy
Other Test Request Name:• XTC
• Adam
• Essence
• E
• Herbals
• MDMA
Test Composition:Not applicable
Intended Use:Used as a screening test for qualitative detection of ecstasy in urine.
Methodology:Lateral Flow Immunochromatography (Competitive Binding)
Laboratory Section:Drug Test
Special Instructions/Patient Preparations:No patient preparation necessary
Collection/Sample Container:60-mL clean, screw cap, polyethylene container
Specimen and Volume Requirement
Note:Follow tube manufacturer recommendation.
:60 mL urine
Alternative Specimen and Volume Requirement:Not applicable
Specimen Stability  
•   Room Temperature (15-25°C):Not specified
•   Refrigerated Temperature (2-8°C):48 Hours
•   Freezer Temperature (-20°C):Not specified
Transport Temperature:Not applicable
Rejection Criteria:• Incompatibility of the ID number on the specimen received by the laboratory with the number on the CCF.
• Absence of ID number on the specimen
• No printed Authorized Specimen Collector’s name and signature on the CCF.
• Broken or tampered seal on the specimen container
• Insufficient quantity of specimen, below 60 mL for single collection; below 30 mL for spilt collection
Running Day:Daily
Cut Off Time:Monday to Saturday
• 6:00 PM

Sunday
• 3:00 PM
TAT/Releasing of Results:ROUTINE
• 3 hours after receipt of specimen/ arrival of messenger
STAT
• After 1½ hours from receipt of specimen/ arrival of messenger
Reference Interval/Result Interpretation:Not applicable
Limitations/Interferences:• Other drugs with the same structure with the abused drugs
• Cross-reactant chemicals
• Bleach or alum
Frequently Asked Questions (FAQs):Not applicable
Related Words/Test:Psychoactive drug