Tests Catalogs

D DIMER QUANTITATIVE

LAB313

D-DIMER

Collect

One 2.7 mL blue top (3.2% citrate plasma).

Also acceptable: One 1.8 mL blue top tube (3.2% sodium citrate).

All blue tops collected for coagulation assays which do not have a blood culture collected first must have a discard tube collected prior to filling.Discard tube should be another blue top in which greater than 1 mL of blood is collected.

Pediatric Collection

0.5 mL platelet poor plasma.

Unacceptable Conditions

Clotted sample; tube fill volume less than 90% or greater than 110%; more than 8 hours since collection; specimen not properly identified; incorrect container; insufficient sample volume.

Storage/Transport Temperature

Internal: Deliver to lab immediately.
Offsite: Separate plasma from cells as soon as possible. Place plasma in an aliquot container and transport to lab frozen.

Stability (from collection to initiation)

Whole blood: Ambient, 8 hours.

Platelet-poor plasma aliquot: Ambient, 8 hours; Refrigerated, 8 hours; Frozen (-20 degrees C), 2 weeks; Frozen (-70 degrees C), 6 months.

Remarks

For diagnostic purposes, D-dimer levels less than 500 ng fibrinogen equivalent units (FEU) make the diagnosis of deep venous thrombosis (DVT) or pulmonary embolism (PE) unlikely.

Performed by

PCL Clinical Laboratory- Coagulation

Performed

Daily

Methodology

Immunoturbidimetric method.

Reported

Same day

Reference Interval

0-500 FEU

Interpretive Data

For diagnostic purposes, D Dimer levels less than 500 ng/mL Fibrinogen Equivalent Units (FEU) make the diagnosis of Deep Venous Thrombosis (DVT) or Pulmonary Embolism (PE) unlikely.

Performed by

PCL Clinical Laboratory- Coagulation

CPT Codes

85379

Collection

LAB313

D-DIMER

Collect

One 2.7 mL blue top (3.2% citrate plasma).

Also acceptable: One 1.8 mL blue top tube (3.2% sodium citrate).

All blue tops collected for coagulation assays which do not have a blood culture collected first must have a discard tube collected prior to filling.Discard tube should be another blue top in which greater than 1 mL of blood is collected.

Pediatric Collection

0.5 mL platelet poor plasma.

Unacceptable Conditions

Clotted sample; tube fill volume less than 90% or greater than 110%; more than 8 hours since collection; specimen not properly identified; incorrect container; insufficient sample volume.

Storage/Transport Temperature

Internal: Deliver to lab immediately.
Offsite: Separate plasma from cells as soon as possible. Place plasma in an aliquot container and transport to lab frozen.

Stability (from collection to initiation)

Whole blood: Ambient, 8 hours.

Platelet-poor plasma aliquot: Ambient, 8 hours; Refrigerated, 8 hours; Frozen (-20 degrees C), 2 weeks; Frozen (-70 degrees C), 6 months.

Remarks

For diagnostic purposes, D-dimer levels less than 500 ng fibrinogen equivalent units (FEU) make the diagnosis of deep venous thrombosis (DVT) or pulmonary embolism (PE) unlikely.

Performed by

PCL Clinical Laboratory- Coagulation

Ordering

Performed

Daily

Methodology

Immunoturbidimetric method.

Reported

Same day

Result Interpretation

Reference Interval

0-500 FEU

Interpretive Data

For diagnostic purposes, D Dimer levels less than 500 ng/mL Fibrinogen Equivalent Units (FEU) make the diagnosis of Deep Venous Thrombosis (DVT) or Pulmonary Embolism (PE) unlikely.

Performed by

PCL Clinical Laboratory- Coagulation

Administrative

CPT Codes

85379

DAT MONOSPECIFIC

Collect

One 6 mL pink top labeled with first, last name, mr#, date drawn, phleb initials. One 5 mL purple top labeled as above.

Minimum volume: 2 mL blood.

Unacceptable Conditions

Specimen not properly identified; gross hemolysis; incorrect container; uinsufficient sample volume.

Storage/Transport Temperature

Internal: Deliver to Blood Bank immediately.
Offsite: Transport at room temperature within 8 hours, or refrigerated within 24 hours.

Stability (from collection to initiation)

Ambient: 8 hours; Refrigerated: 72 hours

Remarks

Diagnosis and all medications received by patient before and during admission to the hospital should be indicated on requisition form. Indicate when a specimen is a cord blood.

Performed by

PCL Clinical Laboratory - Transfusion Service (Blood Bank)

Performed

Daily

Methodology

Detect immunoproteins, IgG or complement absorbed onto red cells; detect autoimmune hemolytic anemias or other unexplained hemolysis caused by antibody and or complement components being bound to patient's red cells (including drug induced), transfusion reaction.

Reported

Same day

Performed by

PCL Clinical Laboratory - Transfusion Service (Blood Bank)

Collection

Collect

One 6 mL pink top labeled with first, last name, mr#, date drawn, phleb initials. One 5 mL purple top labeled as above.

Minimum volume: 2 mL blood.

Unacceptable Conditions

Specimen not properly identified; gross hemolysis; incorrect container; uinsufficient sample volume.

Storage/Transport Temperature

Internal: Deliver to Blood Bank immediately.
Offsite: Transport at room temperature within 8 hours, or refrigerated within 24 hours.

Stability (from collection to initiation)

Ambient: 8 hours; Refrigerated: 72 hours

Remarks

Diagnosis and all medications received by patient before and during admission to the hospital should be indicated on requisition form. Indicate when a specimen is a cord blood.

Performed by

PCL Clinical Laboratory - Transfusion Service (Blood Bank)

Ordering

Performed

Daily

Methodology

Detect immunoproteins, IgG or complement absorbed onto red cells; detect autoimmune hemolytic anemias or other unexplained hemolysis caused by antibody and or complement components being bound to patient's red cells (including drug induced), transfusion reaction.

Reported

Same day

Result Interpretation

Performed by

PCL Clinical Laboratory - Transfusion Service (Blood Bank)

Administrative

DEHYDROEPIANDROSTERONE SULFATE

LAB524

Collect

Serum separator tube or plasma separator tube. Also acceptable: Green (sodium or lithium heparin), lavender (EDTA), or pink (K2EDTA).

Specimen Preparation

Allow specimen to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Unacceptable Conditions

Hemolyzed specimens.

Storage/Transport Temperature

Frozen.

Stability (from collection to initiation)

After separation from cells: Ambient: 8 hours; Refrigerated: 48 hours; Frozen: 2 months

Performed

Sun-Sat

Methodology

Quantitative Electrochemiluminescent Immunoassay

Reported

Within 24 hours

Synonyms

  • DHEA Sulfate, Serum

Ordering Recommendations

Indicator of adrenal androgen production. Aids in the investigation of virilizing endocrinopathies in conjunction with other sex steroids. Not recommended for initial evaluation of polycystic ovarian syndrome.

Reference Interval

Age
Male
Female
0-6 days
7-30 days
1-5 months
6-35 months
3-6 years
7-9 years
10-14 years
15-19 years
20-29 years
30-39 years
40-49 years
50-59 years
60-69 years
70 years and older		108-607 µg/dL
32-431 µg/dL
3-124 µg/dL
0-33 µg/dL
0-44 µg/dL
5-115 µg/dL
22-332 µg/dL
88-483 µg/dL
280-640 µg/dL
120-520 µg/dL
95-530 µg/dL
70-310 µg/dL
42-290 µg/dL
28-175 µg/dL		108-607 µg/dL
32-431 µg/dL
3-124 µg/dL
0-29 µg/dL
0-47 µg/dL
5-94 µg/dL
22-255 µg/dL
63-373 µg/dL
65-380 µg/dL
45-270 µg/dL
32-240 µg/dL
26-200 µg/dL
13-130 µg/dL
10-90 µg/dL
Tanner Stage I
Tanner Stage II
Tanner Stage III
Tanner Stage IV & V		7-209 µg/dL
28-260 µg/dL
39-390 µg/dL
81-488 µg/dL		7-126 µg/dL
13-241 µg/dL
32-446 µg/dL
65-371 µg/dL

CPT Codes

82627
Collection

LAB524

Collect

Serum separator tube or plasma separator tube. Also acceptable: Green (sodium or lithium heparin), lavender (EDTA), or pink (K2EDTA).

Specimen Preparation

Allow specimen to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Unacceptable Conditions

Hemolyzed specimens.

Storage/Transport Temperature

Frozen.

Stability (from collection to initiation)

After separation from cells: Ambient: 8 hours; Refrigerated: 48 hours; Frozen: 2 months
Ordering

Performed

Sun-Sat

Methodology

Quantitative Electrochemiluminescent Immunoassay

Reported

Within 24 hours

Synonyms

  • DHEA Sulfate, Serum

Ordering Recommendations

Indicator of adrenal androgen production. Aids in the investigation of virilizing endocrinopathies in conjunction with other sex steroids. Not recommended for initial evaluation of polycystic ovarian syndrome.
Result Interpretation

Reference Interval

Age
Male
Female
0-6 days
7-30 days
1-5 months
6-35 months
3-6 years
7-9 years
10-14 years
15-19 years
20-29 years
30-39 years
40-49 years
50-59 years
60-69 years
70 years and older		108-607 µg/dL
32-431 µg/dL
3-124 µg/dL
0-33 µg/dL
0-44 µg/dL
5-115 µg/dL
22-332 µg/dL
88-483 µg/dL
280-640 µg/dL
120-520 µg/dL
95-530 µg/dL
70-310 µg/dL
42-290 µg/dL
28-175 µg/dL		108-607 µg/dL
32-431 µg/dL
3-124 µg/dL
0-29 µg/dL
0-47 µg/dL
5-94 µg/dL
22-255 µg/dL
63-373 µg/dL
65-380 µg/dL
45-270 µg/dL
32-240 µg/dL
26-200 µg/dL
13-130 µg/dL
10-90 µg/dL
Tanner Stage I
Tanner Stage II
Tanner Stage III
Tanner Stage IV & V		7-209 µg/dL
28-260 µg/dL
39-390 µg/dL
81-488 µg/dL		7-126 µg/dL
13-241 µg/dL
32-446 µg/dL
65-371 µg/dL

Administrative

CPT Codes

82627

DENGUE FEVER AB - IGG

LAB3009

Collect

Serum separator tube.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.1 mL) Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Mark specimens plainly as "acute or convalescent."

Unacceptable Conditions

Contaminated, heat-inactivated, hemolyzed, or severely lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles)

Performed

Mon, Wed, Fri

Methodology

Semi-Quantitative Enzyme-Linked Immunosorbent Assay

Reported

1-4 days

Synonyms

  • LAB3009
  • DFV IGG

Ordering Recommendations

Aid in detecting past dengue infection. In endemic regions, recommend co-testing for other arthropod-born viruses including chikungunya and Zika due to overlapping symptoms.

Reference Interval

1.64 IV or less: Negative - No significant level of detectable dengue fever virus IgG antibody.
1.65-2.84 IV: Equivocal - Questionable presence of antibodies.  Repeat testing in 10-14 days may be helpful.
2.85 IV or greater: Positive - IgG antibody to dengue fever virus detected, which may indicate a current or past infection.

Interpretive Data

Patients in the early stage of dengue fever virus infection may not have detectable IgG antibodies, as the IgG response may take several weeks to develop.  In the absence of detectable IgG, testing for IgM class antibody is strongly recommended.  The best evidence for current infection is a significant change on two appropriately timed specimens, where both tests are done in the same laboratory at the same time.

CPT Codes

86790
Collection

LAB3009

Collect

Serum separator tube.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.1 mL) Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Mark specimens plainly as "acute or convalescent."

Unacceptable Conditions

Contaminated, heat-inactivated, hemolyzed, or severely lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles)
Ordering

Performed

Mon, Wed, Fri

Methodology

Semi-Quantitative Enzyme-Linked Immunosorbent Assay

Reported

1-4 days

Synonyms

  • LAB3009
  • DFV IGG

Ordering Recommendations

Aid in detecting past dengue infection. In endemic regions, recommend co-testing for other arthropod-born viruses including chikungunya and Zika due to overlapping symptoms.
Result Interpretation

Reference Interval

1.64 IV or less: Negative - No significant level of detectable dengue fever virus IgG antibody.
1.65-2.84 IV: Equivocal - Questionable presence of antibodies.  Repeat testing in 10-14 days may be helpful.
2.85 IV or greater: Positive - IgG antibody to dengue fever virus detected, which may indicate a current or past infection.

Interpretive Data

Patients in the early stage of dengue fever virus infection may not have detectable IgG antibodies, as the IgG response may take several weeks to develop.  In the absence of detectable IgG, testing for IgM class antibody is strongly recommended.  The best evidence for current infection is a significant change on two appropriately timed specimens, where both tests are done in the same laboratory at the same time.

Administrative

CPT Codes

86790

DENGUE FEVER AB - IGM

LAB3168

Collect

Serum separator tube.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.1 mL) Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Mark specimen plainly as "acute or convalescent."

Unacceptable Conditions

Contaminated, heat-inactivated, hemolyzed, or severely lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles)

Performed

Mon, Wed, Fri

Methodology

Semi-Quantitative Enzyme-Linked Immunosorbent Assay

Reported

1-5 days

Synonyms

  • LAB3168
  • DFV IGG

Ordering Recommendations

May be used to diagnose dengue during acute phase of disease (>5 days after symptom onset). In endemic regions, recommend co-testing for other arthropod-born viruses including chikungunya and Zika due to overlapping symptoms.

Reference Interval

1.64 IV or less: Negative - No significant level of detectable dengue fever virus IgM antibody.
1.65-2.84 IV: Equivocal - Questionable presence of antibodies.  Repeat testing in 10-14 days may be helpful.
2.85 IV or greater: Positive - IgM antibody to dengue fever virus detected, which may indicate a current or recent infection.
However, low levels of IgM antibodies may occasionally persist for more than 12 months post-infection.

Interpretive Data

The best evidence for current infection is a significant change on two appropriately timed specimens, where both tests are done in the same laboratory at the same time.

CPT Codes

86790
Collection

LAB3168

Collect

Serum separator tube.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.1 mL) Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Mark specimen plainly as "acute or convalescent."

Unacceptable Conditions

Contaminated, heat-inactivated, hemolyzed, or severely lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles)
Ordering

Performed

Mon, Wed, Fri

Methodology

Semi-Quantitative Enzyme-Linked Immunosorbent Assay

Reported

1-5 days

Synonyms

  • LAB3168
  • DFV IGG

Ordering Recommendations

May be used to diagnose dengue during acute phase of disease (>5 days after symptom onset). In endemic regions, recommend co-testing for other arthropod-born viruses including chikungunya and Zika due to overlapping symptoms.
Result Interpretation

Reference Interval

1.64 IV or less: Negative - No significant level of detectable dengue fever virus IgM antibody.
1.65-2.84 IV: Equivocal - Questionable presence of antibodies.  Repeat testing in 10-14 days may be helpful.
2.85 IV or greater: Positive - IgM antibody to dengue fever virus detected, which may indicate a current or recent infection.
However, low levels of IgM antibodies may occasionally persist for more than 12 months post-infection.

Interpretive Data

The best evidence for current infection is a significant change on two appropriately timed specimens, where both tests are done in the same laboratory at the same time.

Administrative

CPT Codes

86790

DEXAMETHASONE LEVLE BY LC/TMS

Collect

Serum separator tube, lavender (EDTA), pink (K2EDTA), or green (sodium or lithium heparin).

Patient Preparation

Specimen should be collected between 8-10 a.m.

Specimen Preparation

Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: Unacceptable; Refrigerated: 1 week; Frozen: 6 months

Performed

Wed, Sat

Methodology

Liquid Chromatography-Tandem Mass Spectrometry

Reported

1-8 days

Ordering Recommendations

Compliance assessment of dexamethasone suppression testing.

Reference Interval

Adults baseline: Less than 50 ng/dL
8:00 AM draw following 1 mg dexamethasone between 11:00 pm and 12:00 am the previous evening: 140 - 295 ng/dL
8:00 AM draw following 8 mg dexamethasone (4 x 2 mg doses) between 11:00 pm and 12:00 am the previous evening: 1600 - 2850 ng/dL

CPT Codes

80299
Collection

Collect

Serum separator tube, lavender (EDTA), pink (K2EDTA), or green (sodium or lithium heparin).

Patient Preparation

Specimen should be collected between 8-10 a.m.

Specimen Preparation

Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: Unacceptable; Refrigerated: 1 week; Frozen: 6 months
Ordering

Performed

Wed, Sat

Methodology

Liquid Chromatography-Tandem Mass Spectrometry

Reported

1-8 days

Ordering Recommendations

Compliance assessment of dexamethasone suppression testing.
Result Interpretation

Reference Interval

Adults baseline: Less than 50 ng/dL
8:00 AM draw following 1 mg dexamethasone between 11:00 pm and 12:00 am the previous evening: 140 - 295 ng/dL
8:00 AM draw following 8 mg dexamethasone (4 x 2 mg doses) between 11:00 pm and 12:00 am the previous evening: 1600 - 2850 ng/dL
Administrative

CPT Codes

80299

DHEA

LAB522

Collect

Serum separator tube or green (sodium or lithium heparin). Also acceptable: Lavender (EDTA).

Patient Preparation

Collect between 6-10 a.m.

Specimen Preparation

Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.3 mL)

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 24 hours; Refrigerated: 1 week; Frozen: 6 months

Performed

Sun-Sat

Methodology

Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry

Reported

1-4 days

Synonyms

  • DHEA, Serum
  • LAB522

Ordering Recommendations

Adjunct test for the investigation of hyperandrogenic and adrenal disorders. Not recommended for initial evaluation of polycystic ovarian syndrome.

Reference Interval

Effective August 19, 2013
AgeFemaleMale
PrematureLess than 40 ng/mLLess than 40 ng/mL
0-1 dayLess than 11 ng/mLLess than 11 ng/mL
2-6 daysLess than 8.7 ng/mLLess than 8.7 ng/mL
7 days-1 monthLess than 5.8 ng/mLLess than 5.8 ng/mL
1-5 monthsLess than 2.9 ng/mLLess than 2.9 ng/mL
6-24 monthsLess than 1.9 9 ng/mLLess than 2.5 ng/mL
2-3 yearsLess than 0.85 ng/mLLess than 0.63 ng/mL
4-5 yearsLess than 1.03 ng/mLLess than 0.95 ng/mL
6-7 yearsLess than 1.79 ng/mL0.06-1.93 ng/mL
8-9 years0.14-2.35 ng/mL0.10-2.08 ng/mL
10-11 years0.43-3.78 ng/mL0.32-3.08 ng/mL
12-13 years0.89-6.21 ng/mL0.57-4.10 ng/mL
14-15 years1.22-7.01 ng/mL0.93-6.04 ng/mL
16-17 years1.42-9.00 ng/mL1.17-6.52 ng/mL
18-39 years1.33-7.78 ng/mL1.33-7.78 ng/mL
40 years and older0.63-4.70 ng/mL0.63-4.70 ng/mL
Postmenopausal0.60-5.73 ng/mLDoes Not Apply
Tanner Stage I0.14-2.76 ng/mL0.11-2.37 ng/mL
Tanner Stage II0.83-4.87 ng/mL0.37-3.66 ng/mL
Tanner Stage III1.08-7.56 ng/mL0.75-5.24 ng/mL
Tanner Stage IV-V1.24-7.88 ng/mL1.22-6.73 ng/mL

CPT Codes

82626
Collection

LAB522

Collect

Serum separator tube or green (sodium or lithium heparin). Also acceptable: Lavender (EDTA).

Patient Preparation

Collect between 6-10 a.m.

Specimen Preparation

Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.3 mL)

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 24 hours; Refrigerated: 1 week; Frozen: 6 months
Ordering

Performed

Sun-Sat

Methodology

Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry

Reported

1-4 days

Synonyms

  • DHEA, Serum
  • LAB522

Ordering Recommendations

Adjunct test for the investigation of hyperandrogenic and adrenal disorders. Not recommended for initial evaluation of polycystic ovarian syndrome.
Result Interpretation

Reference Interval

Effective August 19, 2013
AgeFemaleMale
PrematureLess than 40 ng/mLLess than 40 ng/mL
0-1 dayLess than 11 ng/mLLess than 11 ng/mL
2-6 daysLess than 8.7 ng/mLLess than 8.7 ng/mL
7 days-1 monthLess than 5.8 ng/mLLess than 5.8 ng/mL
1-5 monthsLess than 2.9 ng/mLLess than 2.9 ng/mL
6-24 monthsLess than 1.9 9 ng/mLLess than 2.5 ng/mL
2-3 yearsLess than 0.85 ng/mLLess than 0.63 ng/mL
4-5 yearsLess than 1.03 ng/mLLess than 0.95 ng/mL
6-7 yearsLess than 1.79 ng/mL0.06-1.93 ng/mL
8-9 years0.14-2.35 ng/mL0.10-2.08 ng/mL
10-11 years0.43-3.78 ng/mL0.32-3.08 ng/mL
12-13 years0.89-6.21 ng/mL0.57-4.10 ng/mL
14-15 years1.22-7.01 ng/mL0.93-6.04 ng/mL
16-17 years1.42-9.00 ng/mL1.17-6.52 ng/mL
18-39 years1.33-7.78 ng/mL1.33-7.78 ng/mL
40 years and older0.63-4.70 ng/mL0.63-4.70 ng/mL
Postmenopausal0.60-5.73 ng/mLDoes Not Apply
Tanner Stage I0.14-2.76 ng/mL0.11-2.37 ng/mL
Tanner Stage II0.83-4.87 ng/mL0.37-3.66 ng/mL
Tanner Stage III1.08-7.56 ng/mL0.75-5.24 ng/mL
Tanner Stage IV-V1.24-7.88 ng/mL1.22-6.73 ng/mL

Administrative

CPT Codes

82626

DIALYSIS PANEL HD/CAPD MONTHLY (RESTRICTED TEST)

LAB3660

Collect

One 4.5 mL Green top with gel (PST), lithium heparin plasma.

Pediatric Collection

Minimum volume: 0.2 mL plasma/serum

Unacceptable Conditions

Sample not properly identified; incorrect container; insufficient sample volume.

Stability (from collection to initiation)

Plasma/Serum: 

Ambient, 4 hours; Refrigerated, 48 hours; Frozen (-20 degrees C), 1 month.

Performed by

PCL Clinical Laboratory - Core Chemistry

Notes

Includes: BUN, CREAT, NA, K, CO2, CA, MG, PHOS, PROT TOT, ALB.

THIS IS A RESTRICTED TEST - For dialysis use only.

Methodology

See individual tests

Synonyms

  • LAB3660
  • HDAM

Reference Interval

See individual tests.

Interpretive Data

See individual tests.

Performed by

PCL Clinical Laboratory - Core Chemistry

CPT Codes

See individual tests.

Collection

LAB3660

Collect

One 4.5 mL Green top with gel (PST), lithium heparin plasma.

Pediatric Collection

Minimum volume: 0.2 mL plasma/serum

Unacceptable Conditions

Sample not properly identified; incorrect container; insufficient sample volume.

Stability (from collection to initiation)

Plasma/Serum: 

Ambient, 4 hours; Refrigerated, 48 hours; Frozen (-20 degrees C), 1 month.

Performed by

PCL Clinical Laboratory - Core Chemistry

Notes

Includes: BUN, CREAT, NA, K, CO2, CA, MG, PHOS, PROT TOT, ALB.

THIS IS A RESTRICTED TEST - For dialysis use only.

Ordering

Methodology

See individual tests

Synonyms

  • LAB3660
  • HDAM
Result Interpretation

Reference Interval

See individual tests.

Interpretive Data

See individual tests.

Performed by

PCL Clinical Laboratory - Core Chemistry

Administrative

CPT Codes

See individual tests.

DIALYSIS PANEL HD/CCPD MONTHLY (RESTRICTED TEST)

LAB3589

Collect

One 4.5 mL Green top with gel (PST), plasma (lithium heparin).

Pediatric Collection

Minimum volume = 0.2 mL plasma

Unacceptable Conditions

Sample not properly identified; incorrect container; insufficient sample volume.

Storage/Transport Temperature

Internal: Deliver to lab immediately.

Offsite: Centrifuge within 30 minutes of collection. Transport to laboratory at ambient temperature.

Stability (from collection to initiation)

Plasma: Ambient, 4 hours; Refrigerated, 2 days; Frozen (-20 degrees C), 1 month.

Performed by

PCL Clinical Laboratory - Core

Notes

Includes: CA, K, CL, CO2, PHOS, PROT TOT, ALB BCG.

THIS IS A RESTRICTED TEST - For dialysis use only

Performed

Daily

Methodology

See individual tests

Reported

Same day

Synonyms

  • LAB3589
  • HDCM

Reference Interval

See individual tests.

Interpretive Data

See individual tests.

Performed by

PCL Clinical Laboratory - Core

CPT Codes

See individual tests.

Collection

LAB3589

Collect

One 4.5 mL Green top with gel (PST), plasma (lithium heparin).

Pediatric Collection

Minimum volume = 0.2 mL plasma

Unacceptable Conditions

Sample not properly identified; incorrect container; insufficient sample volume.

Storage/Transport Temperature

Internal: Deliver to lab immediately.

Offsite: Centrifuge within 30 minutes of collection. Transport to laboratory at ambient temperature.

Stability (from collection to initiation)

Plasma: Ambient, 4 hours; Refrigerated, 2 days; Frozen (-20 degrees C), 1 month.

Performed by

PCL Clinical Laboratory - Core

Notes

Includes: CA, K, CL, CO2, PHOS, PROT TOT, ALB BCG.

THIS IS A RESTRICTED TEST - For dialysis use only

Ordering

Performed

Daily

Methodology

See individual tests

Reported

Same day

Synonyms

  • LAB3589
  • HDCM
Result Interpretation

Reference Interval

See individual tests.

Interpretive Data

See individual tests.

Performed by

PCL Clinical Laboratory - Core

Administrative

CPT Codes

See individual tests.

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