Intradermal Injection: Wheal Technique, TB Skin Tests & Allergy Testing
A shallow-dermis guide for nurses placing intradermal (ID) injections—from medication administration and hand hygiene through wheal verification, the 48–72 hour tuberculosis reading window, and immediate monitoring after allergy skin testing.
Contents
Quick facts
Key takeaway
Intradermal work succeeds when the dose sits in the dermis, not subcutaneous fat or muscle: verify a pale wheal after placement, schedule 48–72 hour reading for tuberculin skin tests, and treat a missing wheal or wrong depth as an invalid test that must be repeated on a new site—not charted as complete.
Quick procedure summary
| Item | Detail |
|---|---|
| Procedure | Injection administration (intradermal) |
| Also known as | ID injection, Mantoux technique, TB skin test injection, allergy testing injection |
| Category | Medication administration |
| Purpose | Deposit a small volume into the dermis to elicit a local immune response (e.g., tuberculin skin test) or deliver agent for allergy testing |
| Who performs | Registered nurses and other designated, trained clinicians per scope and local authorisation |
| Typical settings | Employee health, primary care, school health, allergy clinics, pre-admission screening, public health programmes |
Overview
Intradermal injection delivers a small volume into the dermis—the layer between epidermis and subcutaneous tissue. Nurses most often encounter it for the tuberculin skin test (TST / Mantoux), which uses purified protein derivative (PPD) to detect latent tuberculosis infection, and for allergy skin testing where wheal-and-flare responses guide interpretation.
Unlike subcutaneous or intramuscular routes, the clinical endpoint is often a visible wheal and a timed reading—not immediate systemic effect. Technique errors (too deep, wrong volume, no bleb) invalidate TST results and can delay occupational or pre-operative screening.
Placement and reading may be done by different trained providers. Your organisation should define who may place, who may read, and how missed 72-hour returns are rescheduled—consult state or local public health guidance where applicable.
Indications
| Indication category | Nursing rationale |
|---|---|
| Latent TB infection screening | TST placement when blood-based Quantiferon TB Gold testing is unavailable or not selected per protocol. |
| Baseline occupational health testing | Healthcare and congregate-setting personnel may require two-step baseline testing before periodic retesting—follow institutional policy. |
| Allergy skin testing | Intradermal dilutions after negative prick tests for selected allergens; immediate observation for systemic anaphylaxis symptoms. |
| Other ID-ordered agents | Some local anaesthetics or product-specific tests use ID technique—always follow manufacturer information for use and pharmacy guidance. |
Contraindications and when to pause
For TST, CDC guidance notes contraindication primarily after a severe prior TST reaction (e.g., necrosis, blistering, anaphylactic shock, ulcerations). Most other groups, including infants and people with HIV, are not contraindicated—but timing with live-virus vaccines and prior positive TB tests matters.
- Documented prior positive TB blood or skin test without a new clinical indication.
- History of severe reaction to previous TST unless specialist plan exists.
- Active TB treatment pathway already underway—coordinate with the TB programme.
- Recent live-virus vaccination (measles, MMR, varicella, etc.)—TST ideally same day or ≥4 weeks later per CDC timing guidance; institutional protocols may vary.
- Extensive rash, burns, or eczema at all forearm sites—seek alternate site or prescriber input.
- Patient cannot return for 48–72 h reading—reschedule rather than placing a test that will expire unread.
- Systemic allergic signs during allergy ID testing—prepare epinephrine per protocol.
- Large painful induration, blistering, or lymphangitis after placement.
- Symptoms suggestive of active TB disease—do not wait for TST reading before further work-up.
Equipment
For Mantoux TST, CDC specifies a tuberculin syringe with a short 27-gauge needle and 0.1 ml PPD solution—verify product and cold-chain storage per pharmacy policy.
Incorrect dose or depth invalidates TST. Use a fresh sterile needle and syringe for each patient; never reuse between patients. Multi-dose vial access follows your facility’s injection-safety and medication policies.
Pre-injection checks
ID vs SC vs IM: depth at the bedside
Route confusion causes absorbed medication in the wrong plane and invalid skin tests. If the order says intradermal, do not use SC or IM technique.
Dermis — shallow angle, visible wheal
- Small volumes (TST typically 0.1 ml per CDC)
- Bevel up, ~5–15°; needle tip just under epidermis
- Success = pale wheal; TST read at 48–72 h
Adipose — no wheal required
- Insulin, heparins, many biologics
- Often 90° or angled with skin fold
- No delayed induration reading like TST
IM injections target muscle for different absorption kinetics—see IM injection when the order is not intradermal.
Wheal verification and invalid placement
CDC states that when placed correctly, TST should produce a pale elevation (wheal) 6–10 mm in diameter. If the wheal is absent, the dose is wrong, or injection is too deep, the test is invalid.
- Report the incident per facility policy.
- Repeat on a new site at least 2 inches (5 cm) from the failed attempt when protocol allows.
- Do not document a completed TST if the wheal criteria were not met.
| Observation immediately after ID dose | Likely meaning | Action |
|---|---|---|
| Pale wheal 6–10 mm (TST) | Correct intradermal plane | Mark site lightly if policy directs; schedule 48–72 h read; teach not to cover with occlusive dressing. |
| No wheal / blood at needle hub | Too deep or subcutaneous | Invalid—repeat per policy on new site. |
| Large wheal with urticaria and systemic symptoms | Allergic reaction during allergy testing | Stop testing; emergency pathway; document and treat per protocol. |
Procedure steps (Mantoux TST focus)
Perform hand hygiene and gather supplies
Bring tuberculin syringe, PPD vial per pharmacy release, alcohol swab, sharps container, and reading appointment materials to a well-lit area.
Verify identity, indication, and contraindications
Confirm no prior positive TB test documentation; review vaccination timing and skin integrity at planned site.
Draw up 0.1 ml tuberculin
Use tuberculin syringe graduated in 0.01 ml increments; expel air carefully without wasting dose; verify concentration per product label.
Position forearm and cleanse skin
Place volar surface palm-up on a firm support; select an area 2–4 inches below the antecubital fossa free of scars; cleanse and allow to dry if policy requires.
Stretch skin and insert bevel-up
With nondominant hand, stretch skin taut. Insert needle slowly at shallow angle (about 5–15°) with bevel facing up until bevel is just visible beneath the skin surface.
Inject slowly and form wheal
Depress plunger smoothly to deliver full 0.1 ml; a pale wheal should appear. Do not aspirate for standard TST technique.
Confirm wheal diameter and that the needle did not re-enter the vial after patient contact. Engage sharps safety immediately—do not recap.
Withdraw, discard sharps, and mark site if directed
Withdraw at same angle; dispose needle/syringe in sharps bin; light ink-free mark or patient instruction card may help the reader locate the site.
Schedule reading and educate
Book 48–72 hour return; explain that induration—not redness alone—will be measured; instruct to avoid scratching and heavy occlusion at site.
Document placement
Record product, lot, site, wheal presence, time, administrator, and reading appointment in the health record.
Reading window: induration, not erythema
CDC guidance: read TST between 48 and 72 hours after placement. Measure the induration (firm swelling) in millimetres perpendicular to the long axis of the forearm—not erythema alone. Patients who miss the window need rescheduling; repeated placement can cause boosting in some persons.
Positive millimetre cut-offs depend on TB risk category (5 mm, 10 mm, or 15 mm thresholds per CDC)—interpretation is a clinical/public-health decision, not a nursing-only call in isolation.
Positive results trigger further evaluation—often including chest X-ray and clinical assessment per TB programme pathways. Report active or latent TB per local requirements.
Two-step TB baseline screening
Some employee-health programmes use two-step testing for initial baseline to detect boosted reactions in persons infected long ago. If the first TST is negative, a second test is placed 1–3 weeks later per CDC occupational guidance; a positive second test may represent boosted immunity rather than new conversion.
Coordinate with occupational health so nurses do not mislabel a boosted second test as a fresh exposure without clinical correlation.
Monitoring and complications
| Finding | Concern | Nursing action |
|---|---|---|
| Local blistering or necrosis at TST site | Severe hypersensitivity | Document; notify clinician/TB programme; avoid repeat TST without specialist plan. |
| Wheal absent at placement | Invalid technique | Repeat on new site per policy; incident report if required. |
| Urticaria + hypotension during allergy ID test | Anaphylaxis | Emergency response; discontinue further allergens; treat per protocol. |
| Patient returns after 72 h | Unreadable TST | Reschedule new placement; educate on timing importance. |
| Swelling of regional lymph nodes with fever | Possible infection or adverse reaction | Clinical review; TB programme notification if related to TST. |
Documentation
“TST (PPD) 0.1 ml intradermal left volar forearm 0900 by [name]; pale wheal 8 mm noted; patient booked TB read 0700 day after tomorrow; educated on 48–72 h window and no scratching.”
- Product, lot, dose, route ID, time, administrator
- Site (left/right forearm) and wheal presence/size at placement
- Reading appointment and who will read
- At reading visit: induration mm, erythema noted separately, interpreter of result
- Adverse events and TB programme notifications
Patient education
Clinical pearls
- Stretch the skin taut before insertion—loose skin invites subcutaneous deposition.
- If you see a drop of blood but no wheal, assume invalid and repeat rather than hoping the read will suffice.
- BCG history complicates interpretation but is not a contraindication to placement—risk-based follow-up still applies.
- Allergy intradermal tests need resuscitation readiness; TST rarely causes anaphylaxis but severe local reactions occur—document objectively.
NCLEX practice questions
NCLEX-style clinical judgment practice — A wheal that spreads or blanches wrong can hide anaphylaxis—rehearse site selection, angle, and observation timing for intradermal injection, including a priority action, select-all-that-apply cue recognition, trend interpretation after intervention, and matrix escalation matching (recognise cues → analyse → prioritise → act → evaluate outcomes).
Unfolding case — employee health clinic. Ms. Rivera, 28, a new healthcare assistant, needs baseline TB screening before ward placement. She had BCG as an infant, denies TB symptoms, and can return Friday for a read (placement is Wednesday morning). Supplies: PPD vial from pharmacy, tuberculin syringe with 27 G needle, and Mantoux training checklist per policy.
Answer key & rationale
Frequently asked questions
What angle is used for intradermal injection?
For tuberculin skin tests, insert at a shallow angle—often about 5–15 degrees with the bevel up—so the solution forms a wheal in the dermis. Exact technique should match your training materials and CDC Mantoux guidance.
How soon must a TB skin test be read?
CDC recommends reading between 48 and 72 hours after placement. Results read outside that window are not reliable; the test usually needs to be repeated.
Should nurses aspirate before intradermal injection?
Standard Mantoux TST technique does not include aspiration. Allergy intradermal protocols may differ—follow the specific test kit and institutional policy.
What if no wheal forms after injection?
An absent wheal or incorrect volume typically invalidates the test. Report per policy and repeat on a new site at least 2 inches from the first attempt when allowed.
Can intradermal injections cause anaphylaxis?
TST anaphylaxis is rare; allergy intradermal testing carries higher systemic risk. Observe per protocol and escalate immediately for airway or circulation changes.
Is BCG vaccination a contraindication to TST?
No—but BCG can cause false-positive TST reactions. Interpret results using risk stratification; blood-based IGRA tests may be preferred in BCG-vaccinated persons per CDC guidance.
References
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Centers for Disease Control and Prevention. Clinical testing guidance for tuberculosis: tuberculin skin test.https://www.cdc.gov/tb/hcp/testing-diagnosis/tuberculin-skin-test.html
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Centers for Disease Control and Prevention. Mantoux tuberculin skin test toolkit.https://www.cdc.gov/tb/hcp/mantoux/index.html
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Centers for Disease Control and Prevention. Safe injection practices and your health.https://www.cdc.gov/injection-safety/index.html
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Centers for Disease Control and Prevention. Core infection prevention and control practices for safe healthcare delivery.https://www.cdc.gov/infection-control/hcp/core-practices/index.html
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Royal Marsden Manual of Clinical Nursing Procedures — Procedures (RMM Online).https://www.rmmonline.co.uk/contents/procedures
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World Health Organization. Tuberculosis (health topic).https://www.who.int/health-topics/tuberculosis
Editorial standards & medical review
About the author: Sid A. Abdala Balal, RN, writes evidence-based nursing education focused on practical bedside skills, patient safety, and clinical decision support for nurses.
Medical review: This guide is reviewed by Dr. Adam Sayedi, MD, for clinical accuracy, clarity, and alignment with current nursing standards for intradermal injection and tuberculin skin test placement.
Policies: Medical Review Process · Editorial Policy · Correction Policy
