Back

Needle-Stick Injury



Needle-Stick Injury: Risk Stratification & Management

Contents

  1. Overview
  2. Learning objectives
  3. What counts as a needle-stick or sharps injury?
  4. Risk stratification
  5. Immediate management
  6. Post-exposure prophylaxis (PEP)
  7. Follow-up
  8. Prevention
  9. Case example
  10. References & further reading
  11. Disclaimer

Overview

Needle-stick and other sharps injuries risk exposure to blood-borne viruses (BBVs) including HIV, Hepatitis B (HBV), and Hepatitis C (HCV). They occur most frequently in healthcare but also arise in community settings (e.g., discarded needles). Timely first aid, structured risk assessment, and evidence-based management reduce transmission risk.

Transmission risk (approximate after percutaneous exposure):

  • HIV: ~0.3%
  • HBV (if unvaccinated): ~6–30%
  • HCV: ~1–3%

High-risk features:

  • Deep percutaneous injury
  • Hollow-bore needle, visible blood, large volume
  • Source patient known/suspected BBV positive

Learning objectives

  1. Define needle-stick/sharps injuries and when they are clinically significant.
  2. Apply a structured, UK-aligned risk stratification to exposures.
  3. Outline immediate management steps including first aid and baseline testing.
  4. Determine when and how to start PEP for HIV and manage HBV/HCV exposures.
  5. Implement prevention strategies and reporting pathways.

What counts as a needle-stick or sharps injury?

Any percutaneous injury with a used or potentially contaminated sharp (e.g., hypodermic needle, suture needle, scalpel, broken glass) or mucosal/broken-skin splash with potentially infectious fluid.

Remember: Hollow-bore needles and deep injuries carry higher risk than solid sharps or superficial scratches.

Risk stratification

Use these factors to categorise exposure (minimal/low / high) and guide investigations and PEP.

Exposure factorHigher-risk indicators
RouteDeep percutaneous injury; mucosal exposure to blood/body fluids; broken skin contact
DeviceHollow-bore needle > suture needle/scalpel
Blood/volumeVisible blood on device; large volume; device used in vein/artery
Source patientKnown HIV/HBV/HCV positive; high-risk factors; unknown source in high-prevalence context
Time since useImmediate post-use injury > found needle of uncertain timing (still assess)
Host factorsHBV non-immune; pregnancy (discuss risks/benefits of PEP); immunosuppression

Source testing (with consent): HIV Ag/Ab, HBsAg, HCV Ab (and RNA if indicated).

Immediate management

First aid

  • Wash area gently with soap and running water.
  • Do not scrub or suck; do not use harsh chemicals.
  • Encourage slight bleeding; irrigate mucous exposures with water or saline.

Report & document

  • Notify supervisor and Occupational Health / attend ED promptly.
  • Record time, device, depth, visible blood, source details if known.
  • Complete incident reporting per local policy.

Baseline actions

  • Check tetanus status and HBV immunisation history.
  • Baseline bloods (exposed person): HIV, HBsAg/anti-HBs (if needed), HCV Ab ± RNA per local pathway.
  • Seek senior/ID advice for complex cases (e.g., pregnancy, renal disease, drug interactions).

Time-critical: If HIV PEP is indicated, aim to start as soon as possible (ideally < 1 hour, up to 72 hours).

Post-exposure prophylaxis (PEP)

HIV PEP

  • Indicated when the source is known or strongly suspected to be HIV-positive and exposure is significant.
  • Start urgently (ideally < 1 hour; do not exceed 72 hours).
  • UK regimen (per BHIVA era):
  • Tenofovir disoproxil + Emtricitabine plus an integrase inhibitor (e.g., Raltegravir or Dolutegravir) for 28 days. Follow local formulary.
  • Arrange follow-up HIV testing at baseline, ~6 weeks, ~12 weeks, and ~6 months (per local protocol/4th-gen assays).

Hepatitis B

Exposed person statusRecommended action
Fully vaccinated, known responder (anti-HBs ≥10 mIU/mL)No further action typically required; consider booster if titres unknown and high-risk exposure.
Partially vaccinated / response unknownGive booster and check anti-HBs according to local policy.
UnvaccinatedStart HBV vaccine series. Consider HBIG if source is HBsAg-positive or high risk.

Hepatitis C

  • No proven post-exposure prophylaxis.
  • Baseline and follow-up testing (HCV Ab and/or RNA). Early referral if seroconversion occurs.

Follow-up

  • Book an Occupational Health or GP review within 48–72 hours.
  • Schedule repeat serology per local/UK pathways:
    • HIV: typically at ~6 and ~12 weeks, and ~6 months.
    • HBV: per vaccination/antibody response schedule.
    • HCV: consider HCV RNA at ~3 months; antibody/RNA at ~6 months.
  • Provide psychological support and counselling; discuss work adjustments if needed.
  • Ensure documentation, incident learning, and sharps safety review.

Prevention

Safe sharps practices

  • Avoid recapping. Activate safety devices immediately after use.
  • Dispose of sharps promptly into approved containers at the point of care.
  • Use safety-engineered devices where available.

Systems & training

  • Maintain HBV immunisation for all relevant staff.
  • Ensure easy access to PEP and clear out-of-hours pathways.
  • Foster a report-without-blame culture; audit incidents and provide feedback learning.

Case example

Scenario: A junior doctor sustains a hollow-bore needle-stick from a used cannula in a patient with known HIV infection.

  1. Immediate first aid (wash; do not scrub; encourage bleeding).
  2. Notify senior and Occupational Health; document the incident.
  3. Urgently initiate HIV PEP (within 1 hour) after risk assessment.
  4. Baseline and source bloods: HIV Ag/Ab, HBsAg, HCV Ab (± RNA per policy).
  5. Arrange follow-up testing and counselling; check HBV immunity.

References & further reading

Always follow your trust and local microbiology advice; drug choices and testing intervals may vary with updates and availability.

Disclaimer

This webpage is for educational purposes only and does not constitute medical advice.

Dr Mehdi Hassan Teeli
Clinical Director & Consultant in Emergency Medicine
(University Teaching Hospitals of East Lancashire NHS Trust)
Honorary Senior Lecturer of the University of Central Lancashire
CESR Lead Emergency Department 
C0-Chair portfolio pathway(CESR) at The Royal College of Emergency Medicine.