Incident Reporting Flashcards

1
Q

What is a Patient safety incident

A

Patient Safety Incident (PSI) is:
an event or circumstance that could have resulted, or did result in unnecessary harm to a patient

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2
Q

PSI can be classified as?

A

• harmful (adverse events)
• near misses and
• no harm incidents

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3
Q

6 Management principles of PSI include?

A

• Just Culture
• Confidential
• Timely
• Responsive
• Openness about failures
• Emphasis on learning

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4
Q

WHO’s Minimum Information Model (MIM) for PSI

A
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5
Q

Objectives of minimum information model

A

Classification according to:
• Incident identification (Patient information, time, location and agents involved)
• Incident type
• Incident outcomes
• Resulting actions
• Reporter

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6
Q

What are the 9 Steps to follow for the management of PSI?

A

Steps to follow for the management of PSI:
Step 1: Identifying PSIs
Step 2: Immediate action taken
Step 3: Prioritisations
Step 4: Notification
Step 5: Investigation
Step 6: Classification
Step 7: Analysis
Step 8: Implementation of recommendations
Step 9: Learning

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7
Q

Step 1

A

Step 1: Identifying PSIs
○ PSI prevention and or management can only happen if PSIs are detected in time.
○ Although there are different mechanisms that may be used to detect PSIs, most managers get to know about PSIs in their own health establishments from tip-offs, media publications and law-suits or from complaints by patients and members of the public.
○ There are various ways that are used to detect PSIs without the need for additional costs.
○ All PSIs should be reported in one central Patient Safety Incident Management Systems irrespective of the manner in which it was detected/ identified.
○The following are some of the well-known PSI detection methods:
• Patient safety incident reporting by health professionals
• Medical record/retrospective patient record review
• Focus teams
• External sourcesReview of record on follow-up of patients
• Surveys on patients’ experience of careSafety walk rounds
• Use data to identify and guide management of patient safety incidents
• Research studies and findings

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8
Q

Ways in which PSI can be identified

A

Patient safety incident reporting by health professionals
• Inpatient medical record review / retrospective patient
record review
• Focus teams
• External sources
• Review of record on follow-up of patients
• Surveys on patients’ experience of care
• Safety walk rounds
• Use data to identify and guide management of patient
safety incidents
• Research studies and findings

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9
Q

Step 2

A

Actions may include:
• providing immediate care to individuals (patient, staff or visitors) to prevent the harm from becoming worse
• making the situation/scene safe
• gathering basic information from staff while the details are still fresh
• notify South African Police Service (SAP), health establishment’s security or other institution where applicable

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10
Q

severity assessment codes (SAC)

A

3 classes in the Severity Assessment Code
(Annexure E)
• SAC 1 - includes incidents where serious harm or death occurred.
• SAC 2 - includes incidents that caused moderate harm
• SAC 3 - includes incidents that caused minor harm

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11
Q

Definition of SAC 1

A

Serious harm or death that is/could be specifically caused by healthcare rather than the patient’s underlying condition or illness

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12
Q

Type of event/incident

A

incident
 Wrong patient or body part resulting in death or
major permanent loss of function
 Retained instruments/other material after surgery
 Wrong surgical procedure
 Surgical site infections that lead to death or
morbidity
 Suicide of a patient in an inpatient unit
 Death or serious morbidity due to assault or injury
 Nosocomial infections resulting in death or
neurological damage
 Blood transfusion that caused serious harm or
death
 Medication error resulting in death of a patient
 Adverse drug reaction (ADR)that results in death
or is life-threatening
 Maternal death or serious morbidity
 Neonatal death or serious morbidity
 Missing/swopped/abscond patient and assisted or
involuntary mental healthcare user/mental ill
prisoner/State patient
 Any other clinical incident which results in serious
harm or death of a patient

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13
Q

SAC 2

A

Moderate harm that is/could be specifically caused by healthcare rather than the patient’s underlying condition or illness

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14
Q

Type of event/incident SAC 2

A

Incidents include but are not limited to Moderate harm resulting in:
• Increased length of stay (More than 72 hours to seven days)
• Additional investigations performed
• Referral to another clinician
• Surgical intervention
• Medical intervention
• ADR that resulted in moderate harm
• Blood transfusion reaction

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15
Q

SAC 3 type of incident

A

Incidents include but are not limited to the following:
 Minor harm resulting in increased length of stay of up to 72 hours
 No harm
 Only first aid treatment required
 Near miss that could have resulted in minor harm
 ADR that resulted in minor or no harm
 Blood transfusion reaction that resulted in minor or no harm

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16
Q

SAC 3

A

Minor or no harm that is/could be specifically caused by healthcare
rather than the patient’s underlying condition or illness

17
Q

Step 4

A

Record keeping
o Patient Safety Incident Reporting Form
o Patient Safety Incident Register
• Incident notification to management – SAC1
Report to next line of management within 24 hours
• Incident notification to patient

18
Q

Step 5

A

An investigative report should include:
• detailed chronology of circumstances
• summary of the interviews conducted
• root cause analysis that includes the actions to be taken
• conclusions by Patient Safety committee
• recommendations arising from the investigation
Conclude investigation within 60 working days

19
Q

Step 6

A

A uniform classification system according to the Minimal Information Model as described in section 5.6 ensures accurate data analysis. All PSIs should be classified according to the following classes:
• agents (contributing factors), see annexure A
• incident type, see annexure B
• incident outcome, see annexure C

20
Q

step 6 classification of incident outcome

A

Patient Organisation
None Property damage
Mild Increase in required resource allocation for
patient
Moderate Media attention
Severe Formal complaint
Death Damaged reputation
Legal ramifications
Othe

21
Q

Step 7

A

Analysis
Reduce the occurrence of PSIs by analysing the data
o make recommendations
o implement recommendations for change
• Analyse statistical data on (reporting templates):
o data on classifications of agents involved, see
annexure H
o data on classifications of incident type, see annexure I
o data on classifications of incident outcome, see
annexure J
o indicators for PSIs, see annexure K

22
Q

Step 7 indicators

A
23
Q

Step 7 actions

A

• Implimantation of recommendations
• Recommendations from the investigations and reviews to be implemented to ensure the development of better systems to ensure improved practices
• The Root Cause Analysis indicates the time frames as well as the staff responsible for implementation – see PSI form

24
Q

Step 9

A

Learning
Purpose of PSI reporting systems is to
enhance patient safety by learning from
failures of the health-care system
• Reporting can lead to learning and improved
safety through:
o the generation of alerts regarding significant
new hazards,
o feedback and
o analysing reports

25
Q

Step 9

A

To make an error is human,
to cover up is unforgivable,
but to fail to learn is
inexcusable

26
Q
A
27
Q

Classify medical error according to severity

A

Medical error:
 Serious: potential life threatening harm
 Minor: does not cause harm nor have potential to cause harm
 “Near miss”:

28
Q

2 types of medical error

A

Preventable
None Preventable

29
Q

Define preventable adverse event

A

Preventable adverse event: error from error or systems failure

30
Q

Classification of preventable medical error/adverse event

A

 Type 1: error caused by attending physician
 Type 2: error caused by anyone else in theatre team
 Type 3: systems failure not attributable to an individual

31
Q

Define unpreventable medical error

A

Unpreventable adverse event: injury or complication not due to error or systems failure, not usually preventable

32
Q

Classify unpreventable error

A

 Type 1: well known risks associated with high risk therapies
 Type 2: rare but known risks associated with normal treatments. Patient may be unaware of problem

33
Q

Breaking bad news
 4 essential steps:

A

 Tell the family what happened. Do not speculate.
 Take responsibility for event. Do not assume culpability
 Apologise
 Explain what will be done to prevent future events
 Support of (patient and) family: psychological, social, +- financial
 Do not make personal commitment for financial support (cf Mx)
 Follow-up care. Communication about developments

34
Q

Long-term consequences of adverse even on anaesthetic provider

A

Defensive, emotionally detached, irritable,
withdrawn.
 Accident prone
 Desensitization: dissociation, disconnect:
burnout
 Substance abuse: alcohol, medication:
addiction
 Suicide

35
Q

Short term consequences of adverse even on anaesthetic provider

A

Re-living the event: flash backs, nightmares, day dreams
common
 Feeling shock: numb, tired, exhausted, cold.
 Restless, would up: insomnia, irritability, tearfulness
 Doom and gloom: “Everyone hates me, no-one loves me”.
Give up anaesthetics
 Anger and rage: projecting blame
 Guilt and fear: most common and long lasting.
 Withdrawal: ANS imbalance