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Difficult Conversations. Learning Objectives. Learn How To:Open conversations about end of life care optionsDefine and distinguish between Hospice and Palliative CareKeep the conversation directedInteractive learning through case study and role plays. What do we mean?. Conversations about:Adva
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1. Palliative Care for Holocaust SurvivorsDifficult Conversations
2. Difficult Conversations
3. Learning Objectives Learn How To:
Open conversations about end of life care options
Define and distinguish between Hospice and Palliative Care
Keep the conversation directed
Interactive learning through case study and role plays These are difficult conversations to have with clients you’ve known for years. Holocaust Survivors are good at deflecting conversation to avoid discussions they are unwilling to have.These are difficult conversations to have with clients you’ve known for years. Holocaust Survivors are good at deflecting conversation to avoid discussions they are unwilling to have.
4. What do we mean? Conversations about:
Advance Directives
Do Not Resuscitate
Health Care Proxy
Living Will
Discussions about palliative care or hospice
5. Reasons to address end of life issues
Special needs of the Holocaust survivor make end of life discussions more important.
Informed Consent
Recent legislation – Palliative Care Information Act
6. Barriers to talking about end of life options
Worries that the patient may lose hope.
“Little hard evidence exists to support this position; in fact, it is more likely that misguided evasion or frank dishonesty may add considerably to a patient’s distress and prolong the necessary adjustment period.” (Fallowfield)
7.
“It is not clear that health care providers can either steal or instill hope. However, they can provide an empathic reflective presence that will help patients draw strength from their existing resources.” (Tulsky)
Many Holocaust Survivors, by virtue of survival, have deep faith. There is a strong belief in that G-d steers all events and leads us to important people in our lives. Physicians and caregivers are also messengers – and they can be the vehicle to help patients draw strength from their existing resources. Many Holocaust Survivors, by virtue of survival, have deep faith. There is a strong belief in that G-d steers all events and leads us to important people in our lives. Physicians and caregivers are also messengers – and they can be the vehicle to help patients draw strength from their existing resources.
8. Other barriers
Emotional vulnerability of the patient and family.
Our own feelings of attachment to the patient and family
Our feelings about our own mortality
9. “A Legacy of Silence”
Eva Metzger Brown talks about a “legacy of silence” that occurs in Holocaust Survivors and their families. This can be manifested in a heightened sensitivity to anxiety, and may be “a primary coping mechanism.” Many Survivors, as a means of coping, avoid discussions that bring pain and trigger memories that are too difficult to discuss. Some of these coping mechanisms influence behaviors of the Second Generation as well.Many Survivors, as a means of coping, avoid discussions that bring pain and trigger memories that are too difficult to discuss. Some of these coping mechanisms influence behaviors of the Second Generation as well.
10. When to initiate discussions of end of life options
Early in the disease trajectory if possible
When quality of life is compromised
When the patient is experiencing uncontrolled symptoms
After diagnosis with a life-threatening illness
Discuss ‘how’ you the professional we are speaking to would know about the illness.Discuss ‘how’ you the professional we are speaking to would know about the illness.
11. Recommendations
Ask what the patient understands about their illness, or what the doctor has told them.
Assess the patient’s emotional functioning
Allow the patient to maintain control, and let you know how much discussion they can tolerate.
12. Recommendations (continued)
Have multiple shorter conversations.
Try again if the first response is not receptive.
Maintain a patient centered approach
Respect denial as a coping mechanism
13. Advantages of receiving palliative or hospice care Hospice is a comprehensive benefit that offers a basket of services all covered by either Medicare/Medicaid
Minimize unnecessary and futile interventions and hospitalizations
Maintain quality of life for as long as possible
Expertise in pain and symptom management.
More consistent treatment team
Recent study of possible effects of receiving palliative care
Palliative care can be a “bridge” to hospice
14.
“Honest communication is surely an ethical imperative for the truly caring clinician. Patients need to plan and make decisions about the place of their death, put their affairs in order, say goodbyes or forgive old adversaries, and be protected from embarking on futile therapies.” (Fallowfield)
15.
“To continue the work requires a belief that the Holocaust survivor can face death again –with integrity, with hope, and yes, even with peace.” (Luban and Katz)
And on their own terms And on their own terms
16. Community-Based Palliative CareandHospice Services
17. Palliative Care National Consensus Definition of Palliative Care
Palliative care seeks to prevent and relieve suffering and ensure the highest possible quality of life regardless of age of the individual, stage of disease or need for other therapies.
18. Palliative Care Therapeutic Model Palliative Care is intended to:
Reduce the burden of illness
Maintain quality of life
Minimize suffering
Ensure that care is guided by goals consistent with:
Medical realities
Values and preferences of the patient
19. MJHS Palliative Care Consultation Services Comprehensive, Specialist Palliative Care Assessments
Collaboration with other agencies
Pain and symptom treatment plans
Goals of care
Family meetings
Prescriptive writing
Compatible with CHHA and Long Term Care Programs
20. Eligibility for Palliative Care Services Advanced life-limiting illness
One or more of the following:
Symptoms that are difficult to control. Examples:
Pain
Nausea
Dyspnea
Depression
Fatigue
Multiple recent hospitalizations
Multiple Physicians and need for “Goals of Care” discussion
Weight loss of more than 10% in past year
21. Screening for Palliative Care Inclusion Criteria
Life-limiting illness with evidence of distressing symptoms
Patient’s medical provider acceptance
Patient/family consent to care
Exclusion Criteria
Management of persistent pain in absence of life-limiting illness
Counseling needs in absence of life-limiting illness
Lack of active symptoms
Psychiatric issues in the absence of life-limiting illness
22. Palliative Care Consultation Options One-time Consultations
Comprehensive assessment by Palliative Care Physician or NP
Recommendations to patient’s PCP and patient/family
May include assessment to determine hospice eligibility
Ongoing Palliative Care Consultation Visits
Initial Consultation with follow-up visits for up to a 60-day period
Evaluation for recertification into a 2nd 60-day period if reason for consult remains unresolved
Visits and case coordination by members of interdisciplinary team
Development of patient/family’s goals of care
Treatment of patient’s symptoms (including prescriptive writing)
Psychosocial counseling
Assistance with obtaining additional social services
23. Hospice Program
The continuous feedback from our National Hospice and Palliative Care Organization (NHPCO) Family Satisfaction Survey is
“I wish we had known about Hospice earlier”
24. When Hospice Should Be Introduced
25. When is Hospice Indicated? Prognostication may be difficult, depending on the patient and the disease. A very good indicator for physicians would be the answer to the following question.
Would you be surprised if your patient died within the year? If your answer to the question is “no,” then a referral for Hospice is indicated.
It is an approximate 6 months prognosis should the patient’s disease run its normal course.
Patient is not informed of the 6-month prognosis criteria unless the patient asks.
The 2nd eligibility criterion is that the patient would no longer be seeking curative interventions.
* Clinical Guidelines are included in presentation folders.
26. General Indicators of End of Life Disease Frequent UTI or respiratory infections
Multiple hospital or emergency room visits
Unexplained weight loss > 10%
Loss of appetite; withdrawal from environment
Unhealing decubiti
Hgb<10; Albumin<2.5
Unexplained or refractory temps
Multi-organ system failure
27. Cancer/Malignancy
Patient no longer receiving curative treatment
Evidence of end stage or metastatic disease
Recent lab/diagnostic studies support evidence of disease
Confirmed diagnosis by pathology or radiology
End Stage Pulmonary Disease
Severe dyspnea at rest
Oxygen dependent
FEV less than 30% of predicted
Significant decline in the last three months
Hypoxemia: p02<55mmHg/02Sat<88% or Hypercapnia: pCO2 greater than 50mmHg
28. End Stage Cerebrovascular Disease (CVA)
Poor nutritional status
Chair or bed bound
Chronic: post stroke dementia; Acute: persistent vegetative state
End Stage Alzheimer’s
Ability to speak six word or less
Cannot eat, walk or sit up without assistance
Marked decrease in intake
Urinary and bowel incontinence
#7 on the FAST Scale
Explain FAST scaleExplain FAST scale
29. End Stage Renal Failure
No dialysis related to the Hospice diagnosis.
BUN>100; Creatnine>8.0mg/dl; and Creatnine Clearance<10cc/min
End Stage AIDS
CD4 Count<25; viral load>100,000
History of successive opportunistic infections
Wasting (loss of 33% body mass)
30. End Stage Cardiac Disease
Two categories: CHF or Cardiomyopathy Ischemic Heart Disease – ASHD/CAD
Dyspnea with minimal exertion needing 02
Optimal tx’ed with diuretics and vasodilators
Ejection Fraction of 40% or less.
CHF: Fluid overload despite meds
CAD: history of angina, arrhythmia, MI
Angina syndrome present – even at rest
31. End Stage Liver Disease
INR>1.5; PT>5 sec. over control
Ascites, recurrent or refractory to tx
Hepatorenal Syndrome or Hepatic Encephalopathy
End Stage ALS
Dyspnea; 02 at rest; No mechanical vent
Severe loss ambulation and normal speech
Dysphagia with no tube feed; loss of ADLs
32. What Services MJHS Hospice Offers Hospice Medical Directors RN for case management Medical Social Workers for case management, discharge planning, supportive counseling Music Therapists Pastoral Care Coordinators for spiritual support and counseling Bereavement Services including Art and Soul program Home Health Aides for personalized one on one care Volunteers PT, OT and Speech Therapists Registered Dietician for consultation related to nutrition at end of life Staff that are trained in Jewish Cultural Competency and Holocaust Sensitivity