Med Safety Flashcards

1
Q

what is ‘Just Culture’ in patient safety

A
  • seeks to create a system of workplace justice that fostered open reporting, while simultaneously holding people appropriately accountable for their actions
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

benefit of ‘Just Culture’ in patient safety

A
  1. creates psychological safety for staff to report errors
  2. uses common language to consistently and fairly evaluate human behavior
  3. shift focus from errors and outcomes to system designs and behavioral choices
  4. creates accountability, not punitive nor blame-free
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is side effect

A

a known effect, other than primarily intended, relating to the pharmacological properties of a medication (eg. n&v)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what is ADR

A

any response to a meds that is noxious and unintended (Eg. hypersensitivity)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what is medication error

A

any preventable event that may cause or lead to inappropriate medication use or patient harm while the medication is in the control of the healthcare professional, patient or consumer

can lead to:

  1. adverse event (pt is harmed)
  2. near miss (pt almost harmed)
  3. neither harm nor potential for harm
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what is a near miss event

A

an event or situation that could have been resulted in med error but did not (usually by chance or though timely intervention)

  • if near miss is ignored may lead to med errors reaching pt
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is an adverse drug event

A

an injury due to medication

  • may be preventable (due to medication error)
  • may not be preventable (ADR or SE of meds)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

steps involved in patient using medication

A
  1. prescribing
  2. preparation and dispensing
  3. administration (highest error rate)
  4. monitoring
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

errors in administration

A
  1. wrong patient, drug, dose, time, route
  2. omission, failure to administer
  3. inadequate documentation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

errors in monitoring

A
  1. lack of monitoring for ADR
  2. drug not ceased if not working
  3. drug ceased before complete course
  4. drug levels not measured or follow up (@ right time)
  5. communication error
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

patient at higher risk of med errors

A
  1. multiple meds or health conditions
  2. with more than 1 doctor
  3. specific conditions (renal/ hepatic impairment, preg)
  4. cannot communicate well
  5. not actively in charge of their own meds
  6. children/babies (where dose cal is required)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

errors due to medication/ tech design factors

A
  1. poor drug manufacturing/distribution practices (packaging, color)
  2. complex or poorly designed technology
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

staff/ human errors

A
  1. knowledge deficit
  2. inexperience
  3. rushing
  4. distracted/ interruptions
  5. fatigue (man mode)
  6. SOP violations
  7. poor teamwork
  8. failed communications
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

errors due to system/workplace factors

A
  1. lighting/ noise
  2. disruptions
  3. lack of safety culture
  4. lack training/ supervision
  5. inappropriate storage
  6. understaffed
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

how is swiss cheese model relevant

A

errors usually occurs as a result of a chain of events set in motion, leading to a chain effect, which is hard to detect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

latent errors or system failures

A

pose the greatest threat to safety in a complex system because they lead to operator errors.

  • built into the system and present long before the active error
  • difficult for people working in the system to see as they may be hidden in computers or layers of management
17
Q

Root cause analysis (3 question)

A
  1. what happened (key steps)
  2. what went wrong and why (identify failed processes)
  3. what to do to prevent incident recurrence and suggest risk-reduction strategies
18
Q

steps to reduce errors

A
  1. reduce reliance of (human) memory
  2. simplify
  3. standardise
  4. use forcing and constraints functions
  5. use protocols and checklist wisely
  6. improve access to information
  7. decrease reliance on vigilance
  8. reduce handoffs
  9. differentiate, eliminate look-alikes and sound alikes
  10. automate carefully
19
Q

what are high-alert meds

A

drugs that bear a heightened risk of causing significant patient harm when used in error

  • mistakes may or may not be more common
  • but consequences of an error are more devastating
20
Q

Recommended guidelines for high-alert medications management

A
  1. eliminate or reduce the possibility of error
    - remove high alert from clinical areas; limit available concentrationand volume
  2. make errors visible
    - independent double checking for infusion pump settings to catch errors
  3. minimise the consequences of errors
    - change practices to reduce the Adverse Effects of errors
    - close monitoring to improve early detection of errors
21
Q

advantages of CPOE

A
  1. elimination of handwriting discrepancies
  2. immediate error checking for dosage, frequency, ROA
  3. drug interactions and allergy checking
  4. serving DI databases
  5. tool to document administration of medications by nursing
  6. immediate transmission of orders to multiple disciplines
  7. providing data to analyse drug utilisation and workflow
  8. increase formulary adherence and compliance to prescribing guidelines
  9. allowing price comparisons
  10. intelligent prescribing
22
Q

ISMP recommendation

A
  1. use generatic names
  2. avoid including salt of chemicals
  3. differentiate generic names from brand names
  4. standardise inclusion of suffixes
  5. standardise use of mnemonics or short names
  6. standardise font (size, style and color)
23
Q

Closed Loop Medication Management system (CLMM)

A
  1. enhanced medication safety process (ensure right patient, drug, dose, time)
  2. efficiency of ward processes:
    - reduced turn around time for medication stock
    - reduced time required to administer medications to patients
24
Q

components of CLMM

A
  1. Electronic Inpatient Medication Record system- eIMR
  2. Clinical Decision Support System- CDSS
  3. inpatient Pharmacy Automated System- iPAS
  4. Electronic Medication Administration Record System- eMARS