Medication safety and errors Flashcards

1
Q

what is a medication error?

A

Any preventable event that may cause or lead to inappropriate mediation use or patient harm, when it is in the control of the professional, patient or consumer

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2
Q

Why do we need medication safety?

A

Reduce errors, reduce hospital admission (and ADRs) and reduce errors in administration.
We also must take care with high risk medications e.g NSAIDS, anti-coagulants, anti-platelets, anti-hypertensives, diuretics

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3
Q

what is the duty of candour?

A

legal duty of all trusts to inform, apologise to patients if mistakes have been made in their care that have resulted in significant harm.
Also - speaking up when other things go wrong.
Help patients receive accurate and truthful information, contributing to the transparent culture in the health provision - openesss in error and harm

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4
Q

what are all bodies registered with?

A

The care quality commission in which they must all comply with the statutory duty of candour

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5
Q

what strategies can we take to reduce medication errors? (5)

A
clinical decision support systems
utilisation of clinical pharmacists
double checking medication orders
education and training
incident reporting
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6
Q

what are the RPS standards for incident reporting? (6)

A
1- open and honest
2- report
3- learn
4- share
5- act
6- review
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7
Q

what are the reasons why people don’t report incidents?

A

Time and workload pressure

lack of knowledge - how to report, to who, and what to report, or don’t know of support networks

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8
Q

how can we encourage people to report?

A

Design and improve reporting, learning an shearing systems so they are easy and quick to use e.g mobile apps, online (technology)
Raise awareness of the local processes of incident reporting, and tools to help with this. Encourage individual reflection and CPD as an incident can be an indication of a learning need
Make aware the patient safety networks across the UK e.g freedom to speak guardians - use leadership to help staff

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9
Q

importance of medication error reporting to the MHRA?

A

via the yellow card - report side effects.
Some people may experience side effects that aren’t in the PIL, so if we report we can increase awareness
reports are analysed and warnings may be added to packaging to benefit patients
it makes medicines safer and leads to better prescribing

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10
Q

what changes can be done to practice in pharmacy to reduce errors?

A

changing packaging to avoid mix ups
change connecters on intrathecal injections
tabarts for drug rounds
greater control in monitoring warfarin

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11
Q

what are Never events?

A

Serious incident that meets the requirements:
wholly preventable
potential to cause serious harm/death
evidence that it has occurred in the past through reports to the NRLS and risk of recurrence remains
easily recognised and clearly defined as a never event

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12
Q

Examples of never events

A

Wrong route of drug administration
mis selection of the wrong potassium chloride solution
falls from poorly restricted windows
blood transfusion incompatibility

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13
Q

How can we report at Local level?

A
Near miss error log - 
Date/time
Drug name
type of near miss
learning points/consideration points
possible causes
action taken
potential adverse event discussion
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14
Q

what is the human factors approach to reducing medication errors?

A

It is about accepting that majority of people come to work to do a good job. Mistakes are usually caused by ineffective systems.
Systems should be in place to make it easy to do the right thing
create a culture where human error is seen as a source of learning
taking responsibility for safety

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