safety Flashcards

1
Q

Types of error

A
  1. Dose omission
    a. The failure to administer an ordered dose to a patient before the next scheduled dose, it any. This excludes patients who refuse to take a medication or a decision not to administer.
  2. Improper dose
    a. Resulting in overdose/underdose/extra dose
  3. Wrong strength/concentration
  4. Wrong drug
  5. Wrong dosage form
  6. Wrong technique
    a. Includes inappropriate crushign of tablets.
  7. Wrong route of administration
  8. Wrong rate
    a. Too fast/slow
  9. Wrong duration
  10. Wrong time
    a. Administration outside a predefined time interval from its scheduled administration time, as defined by each health care facility
  11. Wrong patient
  12. Monitoring error
    a. Contraindication
    b. DDI-2
    c. DFI
    d. Documented allergy
    e. Clinical (eg glucose, prothrombin, BP)
  13. Deteriorated Drug error
    a. Dispensing drug that has expired
  14. Others
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2
Q

Types of patient outcomes

A

A. No error, but circumstances/events that have the capacity to cause error
B. Error caught before med reached patient
C. Error reached patient; no harm
D. Increased monitoring, no harm
E. Temporary harm requiring intervention
F. Temporary harm requiring hospitalization
G. Permanent harm
H. Near death
I. Death

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3
Q

medication use process

A

prescribing –> prep & dispensing –> adminstration –> monitoring –> repeat

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4
Q

how can prescribing go wrong

A

inadequate knowledge about drug indication and contraindication

individual factors (allergy, comorbid etc)

wrong

  • pt
  • dose
  • frequency
  • drug
  • route
  • time

inadequate communication (written/verbal)

dosumentation (illegeible, incomplete, ambiguous

math error

incorrect data entry

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5
Q

how can dispensing go wrong

A

poor inventory control (exp drug)

labelling / packaging mixed up

transcription error

failure to check DDI, pt factor etc

documentation (illegeible, incomplete, ambiguous)

math error

miscommunication

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6
Q

how can drug administration go wrong

A

wrong

  • drug
  • route
  • time
  • dose
  • patient

forget give
documentaion error

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7
Q

how can monitoring go wrong

A

lack of monitoring adr
drug not ceased when not working or course completed

drug ceased before course completed

drug level not measure / followed up

communication failure

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8
Q

Why do errors occur?

A

1) Patient factors
- Multi Ds / communication prob / age
2) Medication/technology design factors
- Poor drug manufacturing/distribution practices (marketing stuff, eg name and packaging)
- Complex or poorly design technology
3) Staff/human factors
- Communication/knowledge/fatigue/distraction/violation of SOPs
4) System / workplace factors
- IT/environment/training /manpower

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9
Q

latent errors or system failure pose the greatest threat to safety in a complex system because they lead to operator errors
.
they are failure built into the system and present long before the active error

latent errors are difficult for the people working in the system to see since they may be hidden in computers or layers of management and people become accustomed to working around the problem

A

latent errors or system failure pose the greatest threat to safety in a complex system because they lead to operator errors
.
they are failure built into the system and present long before the active error

latent errors are difficult for the people working in the system to see since they may be hidden in computers or layers of management and people become accustomed to working around the problem

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10
Q

Root cause analysis is a systematic approach to understanding the causes of an adverse event and identifying system flaws (ie. latent error) that can be corrected to prevent the error from happening again

focusing on these causes and vulnerabilities is a much more effective way to improve quality and safety than simply blaming the individual who made a mistake

focusing on system causes, rather than blame is the central feature of root cause analysis. this is called a systems approach to error

focusing on systems causes means analyzing all the factors that contributed to the error not just the error itself.

A

Root cause analysis is a systematic approach to understanding the causes of an adverse event and identifying system flaws (ie. latent error) that can be corrected to prevent the error from happening again

focusing on these causes and vulnerabilities is a much more effective way to improve quality and safety than simply blaming the individual who made a mistake

focusing on system causes, rather than blame is the central feature of root cause analysis. this is called a systems approach to error

focusing on systems causes means analyzing all the factors that contributed to the error not just the error itself.

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11
Q

RCA is usually conducted by _____ people.

the team shuld be _______ and should include individuals at all level of the organisation who are close to and have fundamental knowledge of the issues and processes involved in the indident.

A

RCA is usually conducted by _4-6____ people.

the team shuld be __interprofessional_____ and should include individuals at all level of the organisation who are close to and have fundamental knowledge of the issues and processes involved in the indident.

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12
Q

simplified RCA 3 questions

A

1) what happened? Describe the key steps
2) what went wrong and why? identify the failed processes
3) what to do to prevent incident recurrence? suggest risk reduction strategies and their implementation

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13
Q

steps to reduce error

A

1) Reduce Reliance on memory
2) Simplify
3) Standardise
4) Use forcing and constraints function
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

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14
Q

high alert medication

soecial safe guard

A

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

mistakes may or may not be more common

consequences of an error are clearly more devastating

safeguard:

  • improve access to information about these drugs
  • limit access to high alert medication
  • use auxiliary labels and automated alerts
  • standardize ordering, storage, preparation and administration
  • employ automated or independent double checks when necessary,
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15
Q

ISMP key recommendtion for safe electroniccomunication of medication order`

A

use generic name

avoid including salt of chemical

differentiate generic name from brand name

standardise inclusion of suffixes

sstandardise use of mnemonic or short names

standardise fonts and colours

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16
Q

advantage of CPOE

A

eliminate handwritting discrepency

immediate error checking

DDI and allergy check

serve as drug information if tied to formularies, policy and external data sources.

a tool to document administration of medication by nursing

immediate transmission of order to multiple disciplines

providng data to analyse drug utilisation and workflow

increase formulary adherencce and compliance to prescribing guidelines

allowing price comparisons

link to other databases (lab data) providing complete patient information

intelligent prescribing (allowing use of automatic dose calculators)