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Standards › Standard 1 › Standard operating procedures (SOPs)

Standard operating procedure (SOP) · ID-SOP-001 · Version 1.0 · Approved by the ASF Expert Committee

Supports: 1.1

At a glance

  • Ask the patient to say their full name and date of birth. If they cannot, check the wristband and a second identifier.
  • Compare both identifiers with the request, prescription or wristband. Every identifier must match.
  • Label each specimen at the bedside, with the patient present, using two identifiers, the date and time, and your initials.
  • If anything does not match, stop, do not label, and get help.
  • Record the check on ID-FRM-001.
  • Stop and get help straight away if: identifiers do not match, a wristband is missing and cannot be replaced, or the patient cannot confirm identity and no second identifier can be found.

1. Purpose

To make sure the right care, medicine, procedure, blood product or specimen goes to the right patient, every time [E-007]. Most misidentification errors happen at the bedside, when a label is applied away from the patient or when a bed or room is used instead of a name.

2. Scope

Applies to All staff, students and contractors who give care, medicines, blood products, or take or label specimens
Locations All wards, clinics, day care, theatres, imaging, laboratory collection points and home-visit teams at the facility
When Before every medicine, procedure, blood product, specimen collection or transfer, and at admission and discharge
Does not apply to Anonymous emergency care, where the emergency patient identification process (section 10) applies

3. Definitions

Term Meaning
Two identifiers Two separate pieces of information that identify one patient: full name, date of birth, or the hospital identification number. Bed number, room number and diagnosis are not identifiers.
Wristband The identification band with the patient’s identifiers, fitted on admission
Specimen Any sample taken from a patient: blood, urine, swab, tissue or other
Bedside labelling Applying the label while the patient is present and the specimen is in front of you

4. Background

Patients are misidentified when staff rely on the bed, the room or the order of the list rather than on two identifiers checked with the patient. The risk is highest when several patients have the same surname, when patients are sedated or confused, and when labelling is done at the desk.

This SOP is the working method for the non-negotiable criterion 1.1: every patient is verified using at least two identifiers before any medicine, procedure, blood product or specimen. The audit is in section 12.

5. Responsibilities

Role Responsibility Competence
Staff member giving care or taking a specimen Check identifiers, label at the bedside, record the check where required Trained and observed in this procedure (section 14)
Ward or department head Makes sure the procedure is followed, supports staff, reviews any event Management training in incident review
Quality lead Runs the monthly audit of the last 20 specimen labels and reports results Audit training
Laboratory director Rejects specimens that are unlabelled or wrongly labelled, and records the rejection (SOP-071) Laboratory competence

6. Materials and equipment

Item Requirement Condition
Patient wristband Hospital standard band with full name, date of birth or identification number Present, legible, correct patient, not damaged
Specimen labels Printed or handwritten label with two identifiers, date, time and initials Printed correctly, not already used on another patient
Request form or electronic order Matches the patient in front of you Name and date of birth match the wristband
Pen (for handwritten labels) Permanent ink, not erasable Working

7. Safety

8. Before you start

9. Procedure

Step 1. Ask the patient to state their full name and date of birth.

  • Say: “Please tell me your full name and date of birth.”
  • Do not say the name first, and do not nod or confirm if the patient gives a different name.
  • If the patient is sedated, confused, a young child or cannot speak, go to step 2 and the special situations in section 10.

Key point: The patient is the best source. Prompting the patient with the name increases errors.

Step 2. Check the wristband.

  • Confirm the band is on the patient, legible, and not damaged.
  • Check the full name and date of birth on the band match what the patient said.
  • If they do not match, stop and go to section 11.

Key point: A band that does not match is an error until proven otherwise.

Step 3. Compare the identifiers with the request.

  • Check the full name on the request matches the patient and the band.
  • Check the date of birth on the request matches the band.
  • If the request has no date of birth, do not proceed. Ask for the order to be corrected.

Key point: Two matching identifiers are required. A matching bed number is not enough.

Step 4. Label the specimen at the bedside.

  • Label the specimen in front of the patient, immediately after collection.
  • Write or print: full name, date of birth (or ID number), date, time and your initials.
  • Check the label against the wristband again before the specimen leaves the bedside.

Key point: Labelling away from the patient is a known cause of errors. Label at the bedside, every time.

Step 5. Before giving a medicine, blood product or procedure, repeat steps 1 to 3.

  • Do the check again at each new activity, even if it was done an hour ago.
  • If the patient has moved bed, been to another area or returned from a procedure, repeat the full check.

Key point: Identity can change through transfers. Each activity is a new check.

Step 6. Record the check where required.

  • For each specimen in the audit sample, record the identifier check on ID-FRM-001 with date, time and initials.
  • Keep the completed form in the ward or department file for the period stated in section 13.

Key point: The record is how the audit shows the check was done, not only that it should have been.

10. Decision points

11. Special situations

Situation Action
Unconscious, sedated or unable to speak Check the wristband and at least one identifier from the medical record with a second member of staff. Record who was present.
Newborns and infants Use the hospital neonatal identification process, including matched bands for the infant and the mother. Check both bands before each activity.
Patients with the same name on the ward Use both identifiers and, where possible, a second member of staff. Consider a visual flag on the record, agreed with the ward head (EC).
Emergency patients with no identity Use the hospital temporary identification number. Link it to the true identity as soon as known. Record the link in the record and on the specimen (EC).
Patients returning from theatre or procedures Repeat the full check on return, using the wristband, before handing over care.

12. Escalation

13. Monitoring

Measure Target Frequency Owner If not met
Last 20 specimen labels show two identifiers and an identifier check 100% (non-negotiable) Monthly Quality lead Immediate review of all labels in that period; retraining of staff involved; report to clinical director
Bedside labelling observed during spot checks 100% of observed samples Monthly, at least 10 observations Ward or department head Coaching and re-observation within two weeks
Incidents involving misidentification Zero harm events; every event reviewed Monthly Quality lead Root-cause review for every event

14. Records

Record Kept in Retention
ID-FRM-001 Patient Identification Check Log Ward or department file; quality lead for audit the period set by the facility’s records policy years
Incident report (INC-POL-001) Incident log the period set by the facility’s records policy years

15. Training

16. Related documents

ID Title Use
ID-FRM-001 Patient Identification Check Log Record used in step 6
REC-FRM-001 Mandatory Records List Identifiers are a mandatory record entry
INC-POL-001 Incident Reporting and Management Used when a check fails
SOP-037 Infection Prevention and Control Procedure (generic) Used before and after specimen collection
SOP-071 Specimen Rejection Procedure (generic) Laboratory rejects unlabelled specimens

17. Evidence

Reference Note
E-007 World Health Organization. Patient Safety Solutions series (2007), correct patient identification.
E-009 ASF Expert Committee consensus. Special situations and audit sample size are EC decisions.

18. Change history

Version Date What changed Approval
1.0 the date of approval Full procedure expanded from the short form; added steps, decisions, special situations and monitoring Approved by the ASF Expert Committee

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References

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