Patient Safety Incident Report Template
Incident report and learning review: immediate actions, WHO ICPS classification and harm, family involvement, learning response, findings, safety actions
使い方: Use it when a patient safety incident or near miss happens. Fill the immediate actions and the factual account first, then choose a proportionate learning response. The main pitfall is blaming the last person involved instead of finding the system factors.
プレビュー
Patient Safety Incident Report and Learning Review: [Short incident title]
Report of a patient safety incident and the proportionate learning response that follows it. Incident terms and the harm scale follow the WHO Conceptual Framework for the International Classification for Patient Safety (ICPS, WHO/IER/PSP/2010.2, January 2009). The learning review section is neutral and international; dated examples show how England (NHS Patient Safety Incident Response Framework, PSIRF) and the US (patient safety work product under the Patient Safety and Quality Improvement Act of 2005) frame the same work. Replace every
[bracketed]value and every row marked Example. This is a documentation format, not legal or medical advice; check the current official texts, your organisation's policy and a qualified professional. Never put patient or staff identifiers in a report that leaves the protected reporting system.
Document control
| Field | Value |
|---|---|
| Incident ID | [INC-YYYY-NNNN] |
| Reporting system reference | [Local system ID / external system ID] |
| Date and time of incident | YYYY-MM-DD HH:MM |
| Date and time reported | YYYY-MM-DD HH:MM |
| Location | [Site, unit, area] |
| Reporter | [Role only, contact held in the reporting system] |
| Learning response lead | [Name, role] |
| Version | [0.1] |
| Status | [Reported / Under review / Learning response in progress / Closed] |
| Owner | [@patient-safety-lead] |
| Approvers/reviewers | [@clinical-director], [@patient-safety-team] |
| Last updated | YYYY-MM-DD |
| Classification | [Confidential: patient safety] |
Revision history
| Version | Date | Author | Change |
|---|---|---|---|
| 0.1 | YYYY-MM-DD | [Role] | Initial report |
| 0.2 (Example) | YYYY-MM-DD | [Role] | Learning response method agreed |
| 1.0 (Example) | YYYY-MM-DD | [Role] | Review completed, actions signed off |
Part A: Incident report
Sections 1 to 5 are completed by the reporter or the person in charge, as soon as the patient is safe.
1. Immediate actions
| Action | By (role) | Time |
|---|---|---|
| Patient assessed and treated | [Role] | HH:MM |
| Senior clinician informed | [Role] | HH:MM |
| Equipment, medicine or sample kept for review | [Yes / no / not applicable] | HH:MM |
| Patient or family told what happened | [Yes / not yet, reason] | HH:MM |
| Immediate risk to others removed | [Action] | HH:MM |
2. What happened
[Factual description in time order]
Example: At the fictional Halvermoor District Hospital, a patient admitted at 23:10 was prescribed their usual anticoagulant twice daily. The home medicine list showed once daily. The 08:00 dose was given. At 10:30 the ward pharmacist found the discrepancy during medicines reconciliation; the second dose was held and the prescriber corrected the chart.
3. Classification
| Field | Value |
|---|---|
| Incident or circumstance | [Reportable circumstance / near miss / no harm incident / harmful incident (adverse event)] |
| Incident type | [Clinical administration / clinical process or procedure / documentation / healthcare-associated infection / medication or IV fluids / blood or blood products / nutrition / oxygen, gas or vapour / medical device or equipment / behaviour / patient accident / infrastructure, building or fixtures / resources or organisational management] |
| Degree of harm (ICPS) | [None / mild / moderate / severe / death] |
| How detected | [Who or what found it] |
| Mitigating factors | [What stopped it getting worse] |
| Example | No harm incident, medication, degree of harm none, detected by pharmacist reconciliation, mitigated by holding the second dose |
ICPS terms in brief: a reportable circumstance had significant potential for harm but no incident occurred; a near miss did not reach the patient; a no harm incident reached the patient with no discernible harm; a harmful incident (adverse event) resulted in harm. Harm is graded none, mild, moderate, severe or death.
4. Patient and family involvement
| Item | Detail |
|---|---|
| Told by | [Role], YYYY-MM-DD |
| Apology given | [Yes / no] |
| Statutory openness duty applies? | [Yes / no / to be decided by the patient safety team] |
| Written follow-up sent | [Yes, date / not required] |
| Wishes about involvement in the review | [Summary] |
| Named contact for the family | [Role] |
5. Staff support
- Support offered to staff involved: [Yes, by whom / declined]
- Debrief held: [Yes, date / no]
Part B: Learning review
Sections 6 to 9 are completed by the learning response lead, who was not involved in the incident.
6. Choosing the learning response
| Method | Typical use | Chosen? |
|---|---|---|
| Rapid team huddle | Soon after the event, to capture facts and fix immediate risks | [ ] |
| After action review | Structured team conversation: what was expected, what happened, why the difference, what to learn | [ ] |
| Multidisciplinary review | Several similar incidents, or one that crosses services | [ ] |
| Thematic review of reports | Look across many low-harm incidents for a pattern | [ ] |
| Full systems investigation | High learning potential or required by policy or regulation; see healthcare/root-cause-analysis | [ ] |
| No further review | Learning already known and covered by existing work | [ ] |
Decision and reason: [Method, decided by whom, date]
Dated jurisdiction examples:
| Jurisdiction | Framework | What it changes for this form |
|---|---|---|
| England (NHS) | Patient Safety Incident Response Framework (PSIRF), NHS England, first published August 2022, replaced the Serious Incident Framework. Its four aims are compassionate engagement of those affected, system-based approaches to learning, considered and proportionate responses, and supportive oversight. Learning response methods include after action review, swarm huddle, multidisciplinary team review and patient safety incident investigation (PSII) | Choose the method from the organisation's PSIRF plan; record national reporting in the national system |
| United States | Patient Safety and Quality Improvement Act of 2005 (Public Law 109-41, approved 29 July 2005); reports prepared for a listed Patient Safety Organization can be privileged patient safety work product | Ask your legal or risk team how this form is labelled and stored before you share it |
7. Findings
| ID | Factor | Category | Evidence |
|---|---|---|---|
| F-01 (Example) | Night admissions are prescribed before a full medicine history is available | Task and process | Two similar reports in six months in the reporting system |
| F-02 (Example) | Pharmacist reconciliation does not take place at night or at weekends | Organisation and resources | Rota |
| F-03 (Example) | The prescribing screen does not show the last community dispensing record | Equipment and IT | System walkthrough |
What went well: [Defences that worked, for example the pharmacist check]
8. Safety actions
| ID | Action | Addresses | Strength | Owner | Due | Measure |
|---|---|---|---|---|---|---|
| SA-01 (Example) | Add community dispensing record to the admission prescribing screen | F-03 | Stronger: system change | [IT lead] | YYYY-MM-DD | Screen live, audit of 20 admissions |
| SA-02 (Example) | Test a weekend medicine history rota with PDSA cycles | F-02 | Intermediate: process and staffing | [Pharmacy lead] | YYYY-MM-DD | Percent reconciled within 24 hours, run chart |
| SA-03 (Example) | Share this case at the medical induction | F-01 | Weaker: education | [Education lead] | YYYY-MM-DD | Delivered |
9. Sharing and closure
| Item | Detail |
|---|---|
| Findings shared with patient or family | [Yes, date / declined] |
| Learning shared with | [Unit meeting, safety bulletin, governance committee] |
| External reporting completed | [System, reference, date / not required] |
| Closed by | [Role], YYYY-MM-DD |
References
| Reference | Status | Use |
|---|---|---|
| WHO. Conceptual Framework for the International Classification for Patient Safety, version 1.1, final technical report, January 2009 (WHO/IER/PSP/2010.2), https://www.who.int/publications/i/item/WHO-IER-PSP-2010.2 | Checked 2026-10-30 (WHO page and PDF) | Incident terms, degree of harm, ten high-level classes |
| WHO. Global Patient Safety Action Plan 2021-2030 (3 August 2021), https://www.who.int/publications/i/item/9789240032705 | Checked 2026-10-30 | International policy context |
| NHS England. Patient Safety Incident Response Framework and supporting guidance, https://www.england.nhs.uk/patient-safety/patient-safety-insight/incident-response-framework/ | Official page blocked automated access; aims and methods confirmed from an NHS-funded provider policy, 2026-10-30 | England example |
| Patient Safety and Quality Improvement Act of 2005, Public Law 109-41, https://www.govinfo.gov/app/details/PLAW-109publ41 | Checked 2026-10-30 | US example |
Standard and licence note
Based on the WHO Conceptual Framework for the ICPS (January 2009) for terms and harm grades, with dated examples from NHS England PSIRF and the US Patient Safety and Quality Improvement Act of 2005. The ICPS may not be reproduced without WHO consent, so this template names its terms and classes and paraphrases them in original words. All names, organisations and events in examples are fictional. This is a documentation format, not legal or medical advice; check the current official texts and your organisation's policy. Template licence: MIT.
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