What is the recommended concentration for intradermal (ID) allergy skin testing?

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Recommended Concentration for Intradermal Allergy Skin Testing

For intradermal (ID) allergy skin testing, use a 1:1000 (vol/vol) or 1:10,000 (vol/vol) dilution of the maintenance concentrate, with 0.02-0.05 mL injected into the dermis. 1

Standard Testing Protocol

Volume and Technique

  • Inject 0.01-0.02 mL of allergen extract into the dermis for intradermal testing 2, 3
  • Some protocols use up to 0.05 mL for standardized testing procedures 1
  • The injection creates a visible wheal through histamine release from mast cells, with subsequent erythema from vasodilation 2, 3

Concentration Selection Based on Extract Type

For Standardized Extracts:

  • Use concentrations in the range of 10-100 BU/mL for intradermal testing 4
  • Optimal concentration is approximately 30 BU/mL for standardized grass and dust mite extracts 4
  • This provides a cutoff histamine ratio of 0.87 with 87.1% predictive value 4

For Nonstandardized Extracts:

  • Start with 1:1000 (vol/vol) dilution of the maintenance concentrate for most patients 1
  • Use 1:10,000 (vol/vol) dilution for highly sensitive patients based on history or initial prick test reactivity 1
  • Nonstandardized extracts typically come at 1:10 to 1:50 wt/vol or 20,000-100,000 PNU concentrations 1

Sequential Testing Approach

When to Perform Intradermal Testing

  • Perform ID testing after negative skin prick testing (SPT) when clinical suspicion remains high 5
  • Approximately 20.8% of negative SPT results will show positive ID tests, particularly for indoor allergens like dog (33.3%), cat (34.3%), and dust mites (39.4-39.6%) 5
  • ID testing is more sensitive but less specific than prick testing 2, 3

Dilution Series for Drug Allergy Testing

For suspected drug hypersensitivity (e.g., corticosteroids):

  • Use 10% stock concentration for skin prick tests 6
  • Progress to intradermal testing with serial dilutions: 1:1000,1:100, and 1:10 6
  • A wheal ≥3 mm greater than negative control is considered positive 6

Critical Safety Considerations

Maximum Expected Wheal Size

  • The maximum safe wheal size for 95% of the population is 26.6 mm for intradermal testing 4
  • Larger reactions may indicate excessive concentration or high sensitivity 4

Adjusting for Patient Sensitivity

  • Highly sensitive patients (based on history of severe reactions or strong prick test reactivity) require more dilute starting concentrations 1
  • The starting dilution should balance diagnostic yield against systemic reaction risk 1

Extract Variability Warning

  • Nonstandardized extracts vary widely in biologic activity regardless of weight/volume or PNU labeling and should not be considered equipotent 1
  • Standardized extracts are preferred when available (cat, dust mite, grasses, ragweed, Hymenoptera venoms) because biologic activity is more consistent 1

Common Pitfalls to Avoid

  • Do not assume equivalent potency between different manufacturers' nonstandardized extracts at the same weight/volume concentration 1
  • Do not skip prick testing and proceed directly to intradermal testing, as this increases systemic reaction risk 2, 3
  • Do not perform intradermal testing without emergency equipment immediately available, as anaphylaxis can occur 7
  • Do not confuse test doses with diagnostic skin testing—test doses (like those for iron dextran at 25 mg IV) serve a different purpose and have limited predictive value for subsequent reactions 7

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Chapter 2: Skin testing in allergy.

Allergy and asthma proceedings, 2012

Research

Skin testing in allergy.

Allergy and asthma proceedings, 2019

Research

Skin testing for immediate hypersensitivity to corticosteroids: a case series and literature review.

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, 2015

Guideline

Drug Allergy Test Dose Protocol

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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