exp date isn't null, but text field is
Management of injuries from needles discarded in the community, e.g in the park or street.
November 2023: This guidance is currently under review as it has gone beyond the standard review date. It reflects best practice at the time of authorship / last review and remains safe for use. If there are any concerns regarding the content then please consult with senior clinical staff to confirm.
The risk of bloodborne virus transmission from a needle found discarded in the community is very low. To date, there have been no published reports in the UK of HIV or Hepatitis C infection being acquired following injury with such needles. Estimates of the risk of BBV transmission following needlestick with a used needle from an injecting drug user are given in appendix 1.
Following such an injury, basic first aid should be carried out (see appendix 2) and, after an initial assessment to confirm that a significant injury has ocurred, the patient should be referred to the Emergency Department for further management as follows:
The risk of BBV transmission following a percutaneous injury involving a used needle from an IDU is dependent on the risk that the source is HIV, HCV or HBV positive, and the time that has elapsed since the needle was used. Estimates of the risks associated with such injuries in Scotland are given in the table below.
Infections | Probability of infection in the IDU population in Scotland | Risk of transmission if exposedi | Estimated risk following exposure to needle |
||
Very short interval after useii (seconds/minutes) | Intermediate interval after useiii (minutes/hours) | Long interval after useiii (hours/days) | |||
HIV | 1/100 | 1/33 | 1/30,000 | 1/3,000,000 | 1/30,000,000 |
HBV | 1/33 | 1/3 (eAg+ve) - 1/17 (eAg-ve) | 1/100-1/560 | 1/1,000-1/5,600 | 1/10,000-1/56,000 |
HCV | 1/3 | 1/50 | 1/150 | 1/15,000 | 1/150,000 |
i The risk of transmission following percutaneous injury from an infected source
ii Probability of infection in the IDU population in Scotland x Risk of transmission if exposed
iii Adjusted by an estimated factor of 1/10 (HIV and HCV) for an intermediate interval scenario and of 1/100 (HBV) and 1,1000 (HIV and HCV) for a long interval scenario to account for the reduced viability of the particular virus outside the body and how recently the needle has been used.
Make sure proper First Aid has been carried out:
HBV Status of person exposed | HBsAg positive source | Unknown source | HBsAg negative source |
Known responder to HB vaccine (anti-HBs≥10 mIU/ml) | Give booster dose of HB vaccine | No treatment required | No treatment required |
≥ 2 Doses of HB vaccine given, or course completed but response unknown. |
Give one dose of HB vaccine followed by second dose one month later. | Give one dose of HB vaccine. | Finish course of HB vaccine. |
Unvaccinated or only 1 dose of HB vaccine given. | Accelerated course of HB vaccine†. HBIG X 1 in other arm. |
Accelerated course of HB vaccine†. | Initiate or complete course of HB vaccine. |
Non responder to vaccine (anti-HBs <10mIU/ml) | Give booster dose of HB vaccine. Give HBIG X 1 in other arm. Repeat HBIG in 30 days. |
Give booster dose of HB vaccine. Give HBIG X 1 in other arm. Repeat HBIG in 30 days. |
No treatment required. |
Table is based on guidance from the Joint Committee on Vaccination and Immunisation1 and the Center for Disease Control and Prevention2
†An accelerated course of vaccine consists of doses spaced at zero, one and two months. A fourth dose should be given at 12 months. A very rapid course consisting of the first three doses given at 0, 7 and 21 days, with a fourth dose at 12 months.
Dose of Energix B in children under 16 = 10 micrograms (IM)
PLEASE REMEMBER TO SEND LETTER TO GP TO GIVE REST OF COURSE
Last reviewed: 24 August 2017
Next review: 30 April 2024