Patient safety Flashcards

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1
Q

NCCMERP med error categories

A

A - events with capacity for error
B - error occurred but did not each patient
C - error reached patient, did not result in harm
D - error reached patient, required monitoring to rule out harm
E - error reached patient, temporary harm that required intervention
F - error reached patient, temporary harm required hospitalisation
G - error reached patient, permanent harm
H - error reached patient, required intervention to sustain life
I - error, death

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2
Q

WHO medication safety definition

A
  • Freedom from unnecessary / potential harm
  • Freedom from accidental injuries during care
  • Actions undertaken to protect patients from harm
  • Reduction & mitigation of unsafe acts
  • Use of best practices for optimal outcomes
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3
Q

Medication management process

A
  1. Selection & procurement
  2. Storage & labelling
  3. Prescribing & transcribing
  4. Preparing & dispensing
  5. Administration
  6. Monitoring
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4
Q

HFACS framework

A
  1. Organisational influences
    - Organisational culture
    - Organisational process
    - Resource management
  2. Supervisory factors
    - Inadequate supervision
    - Planned inappropriate operations
    - Failure to correct known problem
    - Supervisory violation
  3. Preconditions for unsafe acts
    - Situational factors
    - Individual factors
    - Team factors
  4. Unsafe acts
    - Errors
    - Violations
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5
Q

Error reduction

A
  1. Eliminate opportunity for error
  2. Make it harder to do wrong
  3. Make it easier to do right
  4. Make errors more visible
  5. Minimise injury
  6. Policies, training, inspection
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6
Q

Roles of medication safety leaders

A
  1. Responsibility for leadership
  2. Medication safety expertise
  3. Influence practice changes
  4. Education & research
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7
Q

Categories of DRP

A
  1. Drug selection
  2. Drug regimen
  3. Drug preparation & administration
  4. Monitoring
  5. Adherence & education
  6. Operational
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8
Q

Hierarchical system for classifying DRP

A
  1. Categorisation of DRP
  2. Actions taken to address IASE
  3. Process-related causes
  4. Sub-categorisation into error / recommendations
  5. Documentation
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