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Policy · CAN-POL-001 · Version 1.0 · Approved by the ASF Expert Committee

Supports: B2.14

At a glance

  • When a patient is harmed by their care, the facility tells the patient, and where appropriate their family, promptly.
  • The disclosure explains what happened, what is known so far, what will be done, and includes a clear apology.
  • The disclosure is recorded, and a written summary follows within the timescale set by the governing body.
  • Staff involved in the harm are supported, and disclosure is never delayed to protect the facility.
  • Stop and get help straight away if: a patient harmed by care is not told, or a disclosure is made with no apology and no account of what happens next.

1. Purpose

To make sure patients and their families are told openly and promptly when they are harmed by care, and receive an apology and a clear account of what will happen next (B2.14).

2. Scope

Applies to Clinical and support staff in the hospital
Locations All wards, clinics and departments of the facility
When Whenever the activity described is carried out
Does not apply to Activities covered by another document listed in section 15

3. Definitions

Term Meaning
Harm Any unintended or unexpected injury or harm to a patient caused by their care, that results in or may result in a need for further treatment, extra time in care, or lasting effect.
Disclosure The conversation in which the facility tells a patient or family what happened, and what it will do.
Apology A clear statement that the facility is sorry that the harm happened. It is not an admission of legal liability and is not withheld for that reason.
Responsible clinician The clinician with the most direct knowledge of the care, who leads the disclosure with the support of a manager.

4. Background

To make sure patients and their families are told openly and promptly when they are harmed by care, and receive an apology and a clear account of what will happen next (B2.14).

5. Responsibilities

Role Responsibility Competence
Clinical director Makes sure the policy is followed, reviews every disclosure each quarter, and reports to the governing body Governing body
Responsible clinician Leads the disclosure conversation, apologises, and writes the summary Clinical director
Ward or department manager Supports the clinician, arranges the meeting, and records the disclosure Clinical director
Quality lead Keeps the disclosure register and checks timescales Clinical director

6. Materials and equipment

Item Requirement Condition
Records and forms named in this document Current version Checked before use

7. Safety

8. Before you start

9. Procedure

Step 1. Identify.

  • Within the incident review, classify each incident that caused harm to a patient.
  • Tell the clinical director the same day for any serious harm.

Key point: Harm identified.

Step 2. Plan.

  • Name the responsible clinician and the manager who will support them.
  • Arrange a private meeting at a time the patient and family can attend, with an interpreter where needed.

Key point: Meeting planned.

Step 3. Disclose.

  • Explain what happened, what is known so far, and what the facility will do next.
  • Give a clear, sincere apology, and invite questions.
  • Record the date, the people present, what was said and the questions asked.

Key point: Disclosure made and recorded.

Step 4. Write and follow up.

  • Send a written summary to the patient within the timescale set by the governing body, and in any case within 10 working days.
  • Record the summary date in the disclosure register (CAN-REG-001). Review what was learned at the next quality meeting.

Key point: Summary sent and follow-up recorded.

10. Decision points

11. Special situations

Situation Action
Out of hours Follow the same steps. Use the on-call contact on the wall of the area.

12. Escalation

13. Monitoring

Measure Target Frequency Owner If not met
Harm incidents with a disclosure record 100% Quarterly Clinical director Escalate to the governing body
Disclosures made within the set timescale 90% or more Quarterly Quality lead Review the process with the managers involved
Disclosures with an apology and an account of next steps 100% Quarterly Clinical director Retrain the clinicians involved

14. Records

Record Kept in Retention
Record named in this document Patient record or the area file the period set by the facility’s records policy years

15. Training

16. Related documents

ID Title Use
CAN-REG-001 Harm disclosure register (existing) Register
TRM-SOP-001 Disclosure of evidence to patients (existing) SOP
HH-POL-001 Hand Hygiene Policy (existing) Policy

17. Evidence

Reference Note
E-006 ASF Policy Framework v1.2. Adapted.
E-009 ASF Expert Committee consensus.

18. Change history

Version Date What changed Approval
1.0 the date of approval First version set Expert Committee approval

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