Patient incidents Flashcards

1
Q

What does the External Reporting guidance: CQC Jan 2017 include?

A

Guidance on investigating
Guidance on when to notify
List of incident types to notify
Includes RT incidents

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2
Q

What incidents should be reported to the HSE?

A

If an exposure fails to stop and MGTI is reached

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3
Q

What do the Medical and Dental guidance notes contain?

A

Good practice on all aspects of ionising radiation protection
Chapters on RT and brachytherapy

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4
Q

What does towards safer radiotherapy contain?

A

Classification system for non-equipment errors
Allows national sharing of similar incidents
Allows national trends to be seen
Identifies most risky parts of RT process

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5
Q

When may reportable incidents not be clinically significant?

A

It is correctable by the end of treatment but 20% high for one fraction
Multiple imaging repeats due to procedural error

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6
Q

Should underdoses be reported under IRMER?

A

Technically no but it is good clinical practice

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7
Q

Are mistakes found during plan checks near misses?

A

No

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8
Q

What does the quality of the data the TSR presents dependent on?

A

How committed hospitals are to reporting ‘non-reportable’ incidents

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9
Q

What is the most common type of incident reported?

A

Treatment unit process

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10
Q

In an incident what are the first things that need to be established?

A

Description of what happened
has the patient been over-dosed?
How many fractions?
Is it correctable?
Is it an equipment fault? Should it be taken out of use?
What should happen to the patient? Stop? Continue as planned? Continue with modified dose?

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11
Q

Who should be notified of an incident locally?

A
Patient
Clinical director
RT head of service
Oncologist
Head of RT physics
Lead radiographer
Directorate manager
Physics service lead
RPA (if appropriate)
Risk department
Hospital incident database
Trust exec
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12
Q

Who reports an incident?

A

Risk office

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13
Q

What should make up the investigation?

A

Collect recollections of what happened, who was involved, who saw it?
Collect electronic logs from the computer of user actions, treatment delivery logs, equipment self monitoring logs

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14
Q

Why is it important to find the root cause of an incident?

A

A trigger may have caused long standing problems to become an incident
If procedures aren’t followed then find out why? Is it difficult to understand, is it out of date, is it ever followed?

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15
Q

What needs to be considered when deciding how to end the course of treatment?

A

Tolerance of delivery equipment
Patient condition
Trust policies
legislation and national reporting requirements

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16
Q

When should the MHRA be informed of incidents?

A

If significant harm could happen elsewhere

17
Q

When should the environment agency be informed of incidents?

A

When sources are lost

18
Q

What are standard reasons for incidents to occur?

A
Equipment failure
Inappropriate use of equipment
Failure to follow procedure
Is the procedure good enough
Misunderstanding of process
Miscommunication
Inappropriate professional judgement
Inadequate training
New staff on together?
Changes to procedures while on A/L
Noisy environment
Too many interruptions
19
Q

What mitigating circumstances can there be for incidents?

A

Condition of the patient
Workload
Uncontrollable external factors

20
Q

What actions can be taken to ensure incidents aren’t repeated?

A

Review and clarification of procedure
Training
New procedure
Disciplinary action