Allergen, Fungi/Mold, P. notatum

LAB4060

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • ImmunoCAP m1
  • Penicillium chrysogenum
  • LAB4060
  • PENICIL

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

CPT Codes

86003
Collection

LAB4060

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
Ordering

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • ImmunoCAP m1
  • Penicillium chrysogenum
  • LAB4060
  • PENICIL
Result Interpretation

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

Administrative

CPT Codes

86003

Allergen, Grass, Bent Grass/Redtop Grass

LAB4060

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • ImmunoCAP m1
  • Penicillium chrysogenum
  • LAB4060
  • PENICIL

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

CPT Codes

86003
Collection

LAB4060

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
Ordering

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • ImmunoCAP m1
  • Penicillium chrysogenum
  • LAB4060
  • PENICIL
Result Interpretation

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

Administrative

CPT Codes

86003

Allergen, Grass, Bermuda Grass

LAB4024

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Bahama Grass
  • Cynodon dactylon
  • Devil Grass
  • ImmunoCAP g2
  • Panicum dactylon
  • Scutch Grass
  • Star Grass
  • Wire Grass
  • LAB4024
  • BERMUNDA

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

CPT Codes

86003
Collection

LAB4024

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
Ordering

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Bahama Grass
  • Cynodon dactylon
  • Devil Grass
  • ImmunoCAP g2
  • Panicum dactylon
  • Scutch Grass
  • Star Grass
  • Wire Grass
  • LAB4024
  • BERMUNDA
Result Interpretation

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

Administrative

CPT Codes

86003

Allergen, Grass, Meadow Fescue

LAB4053

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • English Bluegrass
  • Festuca arundinacea
  • Festuca elatior
  • Festuca pratensis
  • ImmunoCAP g4
  • Tall Fescue
  • LAB4053
  • MEADOW
  • MEADOW GRASS

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

CPT Codes

86003
Collection

LAB4053

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
Ordering

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • English Bluegrass
  • Festuca arundinacea
  • Festuca elatior
  • Festuca pratensis
  • ImmunoCAP g4
  • Tall Fescue
  • LAB4053
  • MEADOW
  • MEADOW GRASS
Result Interpretation

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

Administrative

CPT Codes

86003

Allergen, Grass, Timothy Grass

LAB4074

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Cat's Tail
  • Herd's Grass
  • ImmunoCAP g6
  • Phleum nodosum
  • Phleum parnassicum
  • Phleum pratense
  • Phleum pratense var. nodosum
  • Phleum pratense var. pratense
  • LAB4074
  • TIM

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

CPT Codes

86003
Collection

LAB4074

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
Ordering

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Cat's Tail
  • Herd's Grass
  • ImmunoCAP g6
  • Phleum nodosum
  • Phleum parnassicum
  • Phleum pratense
  • Phleum pratense var. nodosum
  • Phleum pratense var. pratense
  • LAB4074
  • TIM
Result Interpretation

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

Administrative

CPT Codes

86003

Allergen, Insect, Cockroach, German

LAB4034

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Blatella germanica
  • ImmunoCAP i6
  • LAB4034
  • COCKROACH

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

CPT Codes

86003
Collection

LAB4034

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
Ordering

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Blatella germanica
  • ImmunoCAP i6
  • LAB4034
  • COCKROACH
Result Interpretation

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

Administrative

CPT Codes

86003

Allergen, Insect, White-faced Hornet

LAB1705

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Notes

Due to the rise and fall of circulating specific IgE antibodies to insect venom, blood samples for allergen testing should be collected no sooner than 2-3 weeks and no later than 6 months after an insect sting.

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • LAB1705
  • HORNET WF
  • Dolichovespula maculata
  • ImmunoCAP i2

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

CPT Codes

86003
Collection

LAB1705

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Notes

Due to the rise and fall of circulating specific IgE antibodies to insect venom, blood samples for allergen testing should be collected no sooner than 2-3 weeks and no later than 6 months after an insect sting.
Ordering

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • LAB1705
  • HORNET WF
  • Dolichovespula maculata
  • ImmunoCAP i2
Result Interpretation

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

Administrative

CPT Codes

86003

Allergen, Mites, D. farinae

LAB4038

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Dermatophagoides farinae
  • ImmunoCAP d2
  • LAB4038
  • DFARI

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00v4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

CPT Codes

86003
Collection

LAB4038

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
Ordering

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Dermatophagoides farinae
  • ImmunoCAP d2
  • LAB4038
  • DFARI
Result Interpretation

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00v4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

Administrative

CPT Codes

86003

Allergen, Mites, D. pteronyssinus

LAB4040

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Dermatophagoides pteronyssinus
  • ImmunoCAP d1
  • LAB4040
  • DPTERONIGE

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

CPT Codes

86003
Collection

LAB4040

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
Ordering

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Dermatophagoides pteronyssinus
  • ImmunoCAP d1
  • LAB4040
  • DPTERONIGE
Result Interpretation

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

Administrative

CPT Codes

86003

Allergen, Occupational, Latex IgE Enh.

LAB4050

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Notes

Latex-specific IgE antibodies may show cross-reactivity with ragweed and certain food allergens such as banana, avocado, kiwi and chestnut.

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Hevea brasiliensis (Allergen, Occupational, Latex IgE, Enhanced)
  • ImmunoCAP k82 (Allergen, Occupational, Latex IgE, Enhanced)
  • LAB4050
  • LATEX

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

CPT Codes

86003
Collection

LAB4050

Collect

Serum separator tube. Multiple specimen tubes should be avoided.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.25 mL serum plus 0.1 mL for each additional allergen ordered to an ARUP Standard Transport Tube. (Min: 0.25 mL plus 0.04 mL for each allergen ordered)

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Notes

Latex-specific IgE antibodies may show cross-reactivity with ragweed and certain food allergens such as banana, avocado, kiwi and chestnut.
Ordering

Performed

Sun-Sat

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Reported

1-2 days

Synonyms

  • Hevea brasiliensis (Allergen, Occupational, Latex IgE, Enhanced)
  • ImmunoCAP k82 (Allergen, Occupational, Latex IgE, Enhanced)
  • LAB4050
  • LATEX
Result Interpretation

Reference Interval

Effective 02/18/2014
Reporting Range
(reported in kU/L)
Probability of IgE Mediated
Clinical Reaction
Class Scoring
Less than 0.10No significant level detected0
0.10 - 0.34Clinical relevance undetermined0/1
0.35 - 0.70Low1
0.71 - 3.50Moderate2
3.51 - 17.50High3
17.51 - 50.00Very high4
50.01 - 100.00Very high5
Greater than 100.00Very high6

Interpretive Data

Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.

Administrative

CPT Codes

86003

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