Living Wills Fiona Crow MD March 2009. Where to start? What do we want to achieve? When?

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“Living Wills” Fiona Crow MD March 2009

Transcript of Living Wills Fiona Crow MD March 2009. Where to start? What do we want to achieve? When?

Page 1: Living Wills Fiona Crow MD March 2009. Where to start? What do we want to achieve? When?

“Living Wills”

Fiona Crow MD

March 2009

Page 2: Living Wills Fiona Crow MD March 2009. Where to start? What do we want to achieve? When?

Where to start?

What do we want to achieve?

When?

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Where to start? The goal is to create an atmosphere with the

patient and/or appropriate other where the goals of care can be frankly, but gently, discussed. Where the “client” and significant others have enough (while not overwhelming them) information about the illness and likely outcomes to establish principles to guide ongoing care and to name a proxy.

This document is fluid because with changes in status the goals may change.

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What are the Obstacles?

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What are the Obstacles? TIME,TIME, TIME it can take a lot but.. Space and Privacy Professional’s discomfort Lack of understanding of WRHA ACP

levels and their interpretation Lack of experience/knowledge about the

legalities of Advance Care Plan, Health Care Directive, Living Wills, Proxy, POA etc

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Definitionsas pertain to Manitoba

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Health Care Directive Advance Care Plan

Often imprecise, vague, and static

Lack of consensus –then what?

Logistics (is it available when needed?)

Fit in specialty areas

Lack of understanding by health care providers

Lack of understanding by health care providers

Developed without medical input

Some physicians trump wishes (clinical evidence)

Need to be competent, must be signedSome physicians trump wishes (research based)

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Related to health care

Related to finances

Patients prior to becoming incapacitated(incompetent), appoint a person or persons to make decisions for them should they be unable to make their own decisions

Advanced directive or Living Will

= Proxy

Enduring Power of Attorney

= POA

The patient has not appointed anyone or made his or her wishes known regarding health or financial issues, but is now unable to do so. The court appoints persons to make decisions on behalf of the patient

Guardianship Trusteeship

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Manitoba Health Care Directives Act

Must be competent, aged 16 yrs old or more

A directive must be in writing and dated (witness not required unless physically incapable of signing)

“No person is required to inquire into the existence of a directive or of a revocation of a directive”

“No action lies against a person who administers or refrains from administering treatment to another person by reason only that the person

a) has acted in good faith in accordance with the wishes expressed in a directive or in accordance with a decision made by a proxy; or

b) has acted contrary to the wishes expressed in a directive if the person did not know of the existence of the directive or its contents.

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The following, in order of priority, may act as substitute decision-

makers:

1. A proxy named in a Health Care Directive/Living Will.

2. A Court-Appointed Committee appointed under section 75(2) of the

Mental Health Act, or a Substitute Decision-Maker for Personal

Care appointed under the Vulnerable Persons Living with a Mental

Disability Act. A Committee or a Substitute Decision-Maker for

Personal Care may be an individual(s) or the Public Trustee. Some

Orders of Committeeship were previously known as “Orders of

Supervision”. Existing Orders of Supervision are treated as Orders

of Committeeship under the Mental Health Act.

3. Others, including family and/or friends.

Substitute Decision Makers

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• likely to be the most common scenario.

• For ACP, must have the support of all interested and available parties.

• usually, but not necessarily, a close relative, who speaks for all.

• may, however, be a supportive friend

• Power of Attorney does not entitle its holder to make health care decisions however…

on occasion, an existing power of attorney may be most appropriate to fulfill this role, since such an individual, although limited to property decisions, has obviously been placed in a position of trust.

Family/Friends as Substitute Decision Makers

slide courtesy of Dr M Harlos

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This plan provides for all available treatment

of all conditions, and includes full CPR.

Advance Care Plan 4

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This is often referred to as palliative or comfort care. It focuses on

aggressive relief of pain and discomfort. There is no CPR

(intubation, assisted ventilation, defibrillation, chest

compressions, advanced life support medications). There are

also no life sustaining or curative treatments such as ICU, tube

feeds, transfusions, dialysis, IV’s and certain medications. All

available tests and treatments necessary for palliation are done,

including medications and transfer to hospital if necessary.

WRHA Advance Care Plan 1

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and everything in between…

ACP 1 on deeper discussion may NOT necessarily mean no lab, no treatments but rather that the focus is comfort. Depending on the burden and goals at that moment treatment, that is not aimed at cure but rather quality and time, may be considered.

ACP 4 does not mean that it is not appropriate often to discuss the

“what if ….”

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Barriers to Physician Comfort

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Barriers to Physician Comfort

Sense of failure– Reframe task , chance to connect, helping

provide a better experience for patient and family.

Patients do not want to discuss these issues.– Data does not support this, ask the patient

permission, ask what is hard for them. Do not want to take away hope.

– Reframe hope and opportunities

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Discomfort with lack of certainty – Help patients ask for and get the info they

need to make decisions. Getting close to the patient will interfere with

my ability to care for them.– With time you will take lessons from your

patient and grow because of the experience. Discomfort with silence.

– Practice it will feel okay, think about what the silence is saying.

Barriers to Physician Comfort…cont’d

Weiner, J.S.et al 2004

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Essentials Of Discussion

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Essentials Of Discussion

Willing? Capable? Where? With whom? Confirm diagnosis and expected outcome. What options are there for treatment?

– What is reversible and what is not. Be as clear as possible

Leave space for hope, address fear of abandonment.

Uniqueness of their situation.– Prognosis is an estimate

– Possibility of unexpected events for good and bad

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Essentials Of Discussion

Is there an advance directive already. Address sense of unfairness, of being a

burden. Make eye contact and appropriate

physical contact. Finally ask for some sense of

understanding of discussion.

cont’d..

Pentz,R.D. et al 2002

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How to open the discussion when not a response to an enquiry.

Family Conference

Proxy

Bedside

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“Family Conference”

1. Introductions.

2. Ask them for quick background of their understanding of illness.

3. Ask them for a sense of the trajectory over the last while.

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Help for substitute decision makers:

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Help for substitute decision makers: Remind them of their role.

– Speak from loved one’s head and not their heart

Have there been recent comments reflecting a probable approach?– “I’ve had enough… I wish this would end soon”

Consider the difference between prolonging living and making someone take longer to die.– A concept that depends on interpretation of the quality of

life… need input from patient / family.

Values exhibited/ discussed with decisions in the past

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Treatment / Intervention Considerations

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Treatment / Intervention Considerations

What are the goals of the treatment?

Whose goals are they, and are they consistent with those of the patient?

Is it possible to achieve the goals?

What are the:

Positive effects vs. Side effects (clinical assessment by health care team)

Benefits vs. Burdens (experiential interpretation by patient / family)

Is there enough reserve to tolerate the treatment?

slide courtesy of Dr M Harlos

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Bedside with patient

Do they want to talk about their illness and its implications??

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Values What do you value about your life?

– Pleasurable activity, cognition, dignity, relationships, surroundings.

How do you feel about death and dying.– Fears of process and / or afterlife.

Do you believe life should always be preserved as long as possible, if not what situations might lead you to feel otherwise? Can you imagine scenarios where this would be tolerable temporarily?

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Values, cont’d

What is fair to tolerate in the face of various prognoses.

Do you hold any religious or moral views that influence your treatment choices.

Have you heard of or witnessed end of life scenes that influence your answers and feelings.

Lynn.J, & Harrold,J.1999

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Example:

In case of a serious illness or injury, there are a number of medical procedures called interventions, which can prolong life and delay the moment of death. These include ventilation, tube feeding, intravenous fluids, etc. It is important to think about and choose what you want from the following:

 

Fraser Health

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• Have full life support with medical interventions.

• Have a trial period of life support with medical interventions and, if unsuccessful, allow natural death to occur. The trial period could last several days or weeks and would be the result of a discussion between your substitute decision maker and your healthcare providers.

• Limit the use of life support with medical interventions and allow natural death to occur.

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Patient / family resources WRHA advance Care Planning booklet ( available on line at

the WRHA site). ERIK booklet .Winnipeg Fire and Ambulance. Let me Decide .

http://www.newgrangepress.com/let_me_decide_series_books_videos.html

Government of Manitoba

(www.gov.mb.ca/health/livingwill.html) ▪ Manitoba Ministry of Healthy Living:

http://www.gov.mb.ca/health/legislation/statutes.html ▪ Health Care Directives Act, C.C.S.M. 1992, c. H27:

http://web2.gov.mb.ca/laws/statutes/ccsm/h027e.php Fraser Health

http://www.fraserhealth.ca/Services/HomeandCommunityCare/AdvanceCarePlanning/Pages/Workbook.aspx

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References

Knopps, K.M. et al. 2005. Patient desires: A model for assessment of patient preferences for severe or terminal illness. Palliative and Supportive Care. 3: 289-299.

Weiner, J.S. et al. 2004. Acare, a communication training program for shared decision making along a life limiting illness. Palliative and Supportive Care 2: 231-241

Pentz R.D. et al. 2002 Discussion of the Do Not Resuscitate order: A pilot study… Support Care Cancer 10: 573-578

Lynn, J and Harrold, J. Handbook for Mortals. Guidance for people facing serious illness. 1999, Oxford University Press. p 122

WRHA presentation on ACP Pallium

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Facilitating Advance Care Planning: An Interprofessional Educational Program. Curriculum Materials. Educating Future Physicians in Palliative and

End of Life Care (EFPPEC)