Patient safety Flashcards

1
Q

Discuss terminology surrounding patient safety

A

Patient safety incident: An event that could have resulted in or did result in unnecessary harm to a patient

Reportable circumstance- as situation where there was significant protentional for harm but no incident occurred

Near miss- an incident which di not reach the patient

No harm - an event reached a patient but no discernible harm resulted

Adverse event

  • also known as a harmful incident
  • an incident that results in harm to patient

Harm

  • an impairment of structure or function of the body and or any deleterious affect arising there from including disease injury suffering disability and death
  • may be physical social or psychological

Contributing factor
- a circumstance action or influence (such as poor rostering or task allocation) that contributes to the origin or development of an incident or increase the risk of an incident
#may be
-external (not under the organisations control)
-organisational
-staff related (individual cognitive or behavioural issue, poor team work, inadequate communications)
-Patient related

Adverse drug reaction
-unexpected harm from a justified treatment

Adverse effect
- a known effect that is not what is primarily intended and related to a medicine pharmacological properties

Preventable
-considered as avoidable in the particular set of circumstances

Mitigating factors
- an action or circumstance that prevents or moderates the progression of an incident towards harming a patient when the mechanism by which damage may occur is already in train, but has not led to the max possible harm

Resilience
- the degree tow which a system continuously prevent detects mitigates or ameliorates hazard or incidents

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2
Q

Discuss fatigue and performance

A

16 hours of continuous work is equivalent to a blood alcohol concentration of 0.05%
-24 hours of wakefulness is equivalent to a blood alcohol concentration of 0.1%

Adverse event rates are much lower when shorter shifts are implemented (<12 hours)

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3
Q

Discuss principles of harm minimisation

A

Error is inevitable

  • harm is not an inevitable consequence of error
  • find out what is wrong not who is wrong
  • the person who has made the error it he person
    1) least likley to make it again
    2) most likley to provide the solution
    3) most likely to prevent others from making the same error
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4
Q

Discuss saftey monitoring

A

Incident reports
-used in only 2% of adverse events

Family reports

  • in one study detected 5 x times more medical errors and 3x more AEs than the volunatary incident report system
  • increased overall error detection by 15% and AE reporting by 10%

Complaints

  • uncommon
  • often related to interpersonal issues rather than processes

Mortality/morbidity reports
-too late for that patient

Review of sentinel cases/near missed

  • more common
  • may be effective

Routine chart review
- detects only 10% of actual medical erros

General performanace measures

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5
Q

Discuss mechanism to prevent harm

A
  • Good leadership
  • situational awareness
  • open communications (team decision are generally better than individual ones)
  • Checking (never assume anything)
  • remove barriers to communications (especially hierachy effect)
  • redundancy mechanisms
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6
Q

Describe hierachy effect

A

When a subordinate does not challenge a more seniour colleague even though they know the senior colleagye to be wrong
More common when
-the subordinate is in a vulnerable position
-the organisation is very hierarchical
-there is a major difference in experience/rank
-the seniour lacks humillity

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7
Q

Discuss graded assertiveness

A

It is team member responsibility to assert a corrective action in a firm and respectful manner

  • make an opening
  • state the concern
  • suggest a solution
  • obtain agreement
  • If initial assertion is ignored make again to ensure taht it has been heard – if ignored again and outcome is still unacceptable take a stronger course of action

Graded assertiveness (pace)
Level 1: probe: “somethings not right”
Level 2: alert “maybe we should do something else”
Level 3: Challenge “why are we persisting”
Level 4: Emergency “ we are unsafe - DO something”

Levels of assertive language

  • is everything alright
  • it might be better if
  • i think we should
  • we should
  • i am still not happy
  • i think we need some help
  • i think you should call them
  • i will call them
  • if you wont i will
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8
Q

Discuss clinical handover

A

High risk procedure – associated with 25% of adverse events
-Structured approach may improve communication to improve patient safety

Bedside handover is ideal

  • introduces the patient to the next care giver
  • enable patient input into the transfer
  • updates the patient on their progress
  • provides an opportuniaty for the receiving staff member to directly asses the patient
  • may not be able to provide other features that maximise handover saftey
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9
Q

Discuss handover tools

A

Non proven to be superior
#ISBAR
-Identity of patient (Name, age, UR,)
-Situation (symptoms/problem, pateint stability and level of concern)
-Background ( History of presentation, date of admission and diagnosis, relevant pmhx)
-Assessment and action ( what is the diagnosis/impression, what have you done so far)
-Response/rationale (what you want done, treatment IX underway or taht need monitoring, review: by whom and for waht, plan)

-5 Ps

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10
Q

Discuss techniques to maximise saftey at handover

A

Reduce number of handovers

  • decrease LOS
  • shift overlap
  • encourage staff to finish off problems

Limit disruption and interruptions during handover
Provide concise overview
-highlight outstanding tasks
-anticipate changes
-have a clear plan
-make information readily available for direct review
-encourage questioning and discussion of assessment
-account for all patients
-specify when transition of care occurs

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11
Q

Discuss individual factors that can contributed to adverse incidents

A

Usually multifactorial and involves deficits at multiple levels of the organisation

  • Staff seniority
  • staff training or prior experience
  • decision making
  • procedural skills
  • exceeding limits of position
  • communications/documentaiton
  • pateitn specific factors ie: language difficulty
  • hazardous attitudes
  • —Impulsive or resigned
  • —Invincible or fearful
  • —Anti-authority or unquestioning
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12
Q

Discuss system factors that can contribute to adverse incidents

A
  • Staff supervision
  • education and training
  • staff operating outside their role delineation (if so why)
  • Confusion about responsibilites between teams
  • supports - absence/ failure of
  • Work load
  • Work conditions e.g night shift
  • multi tasking - e.g responsible for two areas at once
  • consultations process e.g telephone advice from inpatient reg
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13
Q

Discuss management of patient saftey incident

A

Should be by senior staff
must address both clinical and non clinical issues
must manage patient, family and staff
invovles immediate response and follow-up action

Clinical issues

  • provide immediate medical attention
  • manage any complications
  • involve appropriate senior staff
  • arrange appropriate disposition and ongoing care
  • notify staff providing ongoing care of the circumstances
  • if identity error involved ensure taht a second patient is not harmed as well

Non clinical

  • explain situation to patient and carers
  • reassure where possible
  • manage staff memebers
  • document (event, management, notification)
  • complete appropriate saftey system notification

Notifications for an ED incident

  • senior ED staff
  • receiving medical unit senior staff
  • hospital administration
  • clinical risk team
  • medical defence
  • other as required

Investigation consideration

  • establish facts as soon as possible after the event
  • individual vs system factos
  • RCA
  • hospital clinical risk unit investigation
  • coronial investigation
  • QI

Good communications with the patient and family following an adverse event strongly influences the actions of the patients (e.g complaint, litigation, no action)

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14
Q

Discuss open disclosure

A

Encouraged in all jurisdications in Australia – not currently a legal requirement

Benefits
-limited evidence that disclosure reduces the likelihood of litigation
-most health professionals feel a moral obligation to disclose
-meets ethical expectation for health professional in their practice
-allows patients to make autonomous decisions about thier care
0 meets the expectation of patients and thier families for disclosure after adverse events
-may lead to an improvement in the quality of services
-may ameliorate the -ve psychological consequence of the event for the patient

AIms

  • reduce psychological harm to the patient
  • help re-esatblish the patients trust in the service
  • – it is crucial that you are open honest and can seen thigns from their perspective
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15
Q

Discuss an approach to open disclosure (12)

A

1) Inform the patient as soon as possible of the adverse event
- senior as possible staff member should do this

2) briefly establish the facts surrounding the event
- do not interrogate the patient at this time
- establish the facts in more detail later in the conversation or get someone else to do this if your actions may have led to the adverse incident

3) reply promptly to a letter of complaint

4) express sincere regret and concern for the patients welfare ( i am sorry this has happened to you)
- express regret on behalf of other involved
- do not admit liability prior to comprehensive investigation
- further analysis may lead to the conclusion there was no liability
- avoid drawing premature conclusion before investigation

5) acknowledge impact on patient

6) provide information about what actually happened
- only speak about what you know
- do now speculate about a cause a the time
- do not make excuses
- explain that multiple factors often contribute to advers event

7) explain the potential consequences of the event on them
8) explain the steps being taken to mininmise harm from the event

9) advise that
- a full investigation will occur to identify the reasons for the event
- the investigation will be independent of the people involved
- they will be advised of the outcome

10) explain the process of the investigation, key people and time frame
- formal reporting of the incident using the orgnisations saftey mangement system
- patient liason officer
- saftey and quality unit
- involvement of the ED director
- incident review panel(for more serious incidents)

11) validate the patients right to fell how they do
12) if a patient perception of the facts and your differ do not try to show taht you are right

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16
Q

List specific emergency department factors that may compromise patient saftey

A

Staff factors
-Staffing profile

Clinical factors

  • inherent high severity of illness placing them at greater risk of serious adverse sequaelae if an error occurs
  • undifferentiated nature of illness and injuries care for
  • incomplete clinical information

Physical

  • noisey, busy
  • Intrusions from alarms, pages, calls and personal consultations

Linkage to other care system
-poor linage or referral from or to other care providers

Overcrowding
-little control over patient attendance and increasingly suffer overcrowding

17
Q

List common safety problems

A

1) Patient identification errors
2) hospital acquired infection
3) incorrect interpretation or failure to follow-up pending imaging or lab ix
4) Medication errors
5) communications error s
6) physical care errors
7) triage errors

18
Q

List techniques to improve saftey in the ED

A

1) Understand the environment
- initially it is essential that the specific environment of emergency care including the characteristics of EDs and emergency patients that impair safety and the types of errors encountered in ED are fully understood

2) identify specific risks
- risk identification is usually undertaken with the aid of clinical incident reporting systems that encourage the structured reporting of clinical incidents. THese reports are usually collated at both the ED and organization level

3) Near misses
- For every 1000 prevented or no harm incident tghere may be 100 of the same type that cause minor, 10 that cause major and 1 that causes death. Therefore it is important to learn from prevented or no-harm incidents

4) analyse and evaluate the risks
- risk analysis should be undertaken using an accepted methodology with the support of staff trained in its use. Two common forms are root cause analysis and failure modes and effect analysis
- Root cause is conducted after the event and aims to identify what happened, why and what can be done to prevent it in the future by attempting to identify system problems that contributed to the event.
- Failure modes and effect analysis can be conducted in the absence of a specific clinical event. It uses a proactive systematic approach to evaluate clinical processes and workflows in order to identify how they might fail and to assess the relative impact of different failures - this is particularly useful in evaluating a new process prior to implementation and in assessing the impact of a proposed change to an existing process

5) Treat the risks
- 80% of erros may be attributed to poorly designed care systems, workflows and processes that fail to account for human fallibility.
- unfortunately the mere publication of a new clinical guideline rarely results in sustained change in practice.
- Unreliable and dangerous processes or systems replaced with standardized and sustainable processes that make errors more difficult and the right thing to do easier and aid in the detection of errors e.g replacement of vials of similar appearing drugs with well labelled prefilled syringes on a resus trolley

6) monitor and review
- the improvement of patient saftey is a continuous process andinforation concerning saftey should be collated systemically and routinely and evaluated at scheduled intervals

7) Communicatte and consult
- an open and fair culture rahter than a blame culture must be cultivated to yield a beneficial reporting system.

19
Q

Describe an approach to investigation of significant Error

A

1) Address legalities and obtain aurhtorisation from executirve and legal departments
2) Ensure family are aware, ensure they are aware of formal review, ensure that they will be kept up to date
3) Establish multidisciplinary indepdendent team with members from appropriate stake holders
4) arrange calender of meeting with teams as well as establish liason team with family/parents of child to keep them informed
5) gather relevant date and establish timeline of events
- personnel factors
- department factors/environement
- patient factors and disease factors
- depratment processes such as resus protocols, access to speciality input , staffing levels and experience at night
6) list conclusions and develop recommendations
7) detalied confidential report
8) feedback to relevant partiers including relevant stakeholders and staff invovled + family
9) M&M process and educational progrems
10) monitor implementation and recommendations