Test Code

RA266

Ordering Code

2552

Questions?

Please call Clinical Labs of Hawaii at 808.677.7998 (Option 1) with questions about this test.

Synonyms

  • O. quadripetalus
  • Oxycocus palustris
  • Rf341
  • V. hagerupii
  • Vaccinium oxycoccus
  • O. intermedius
  • O. oxycoccus

Patient Preparation

Multiple patient encounters should be avoided.

Collect

Serum separator tube.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.5 mL serum to an ARUP Standard Transport Tube. (Min: 0.25 mL). For multiple allergen orders refer to "Allergen Specimen Collection Instructions" at www.aruplab.com/testing/resources/specimen.

Stability (from collection to initiation)

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

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Additional Technical Information

Performed

Sun-Sat

Reported

1-3 days

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Test Site

ARUP (98874)

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.

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

CPT Codes

86003

LOINC

  • 7262-9

Collect

Serum separator tube.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.5 mL serum to an ARUP Standard Transport Tube. (Min: 0.25 mL). For multiple allergen orders refer to "Allergen Specimen Collection Instructions" at www.aruplab.com/testing/resources/specimen.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

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

Additional Technical Information

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.

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

LOINC

  • 7262-9

Synonyms

  • O. quadripetalus
  • Oxycocus palustris
  • Rf341
  • V. hagerupii
  • Vaccinium oxycoccus
  • O. intermedius
  • O. oxycoccus

CPT Codes

86003

Test Code

RA266

Ordering Code

2552

ARUP Test

Performed

Sun-Sat

Reported

1-3 days

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

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

Test Site

ARUP (98874)
Summary

Test Code

RA266

Ordering Code

2552

Questions?

Please call Clinical Labs of Hawaii at 808.677.7998 (Option 1) with questions about this test.

Synonyms

  • O. quadripetalus
  • Oxycocus palustris
  • Rf341
  • V. hagerupii
  • Vaccinium oxycoccus
  • O. intermedius
  • O. oxycoccus

Patient Preparation

Multiple patient encounters should be avoided.

Collect

Serum separator tube.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.5 mL serum to an ARUP Standard Transport Tube. (Min: 0.25 mL). For multiple allergen orders refer to "Allergen Specimen Collection Instructions" at www.aruplab.com/testing/resources/specimen.

Stability (from collection to initiation)

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

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Additional Technical Information

Performed

Sun-Sat

Reported

1-3 days

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

Test Site

ARUP (98874)

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.

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

CPT Codes

86003

LOINC

  • 7262-9
Collection

Collect

Serum separator tube.

Patient Preparation

Multiple patient encounters should be avoided.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.5 mL serum to an ARUP Standard Transport Tube. (Min: 0.25 mL). For multiple allergen orders refer to "Allergen Specimen Collection Instructions" at www.aruplab.com/testing/resources/specimen.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

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

Additional Technical Information

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.

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

Unacceptable Conditions

Hemolyzed, icteric, or lipemic specimens.
Administrative

LOINC

  • 7262-9

Synonyms

  • O. quadripetalus
  • Oxycocus palustris
  • Rf341
  • V. hagerupii
  • Vaccinium oxycoccus
  • O. intermedius
  • O. oxycoccus

CPT Codes

86003
Ordering

Test Code

RA266

Ordering Code

2552

ARUP Test

Result Interpretation

Performed

Sun-Sat

Reported

1-3 days

Methodology

Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay

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

Test Site

ARUP (98874)

ARUP Consult®

Disease Topics