Basics of palliative care including symptom management: pain, dyspnea, nausea and constipation; family meetings, goals-of-care, end-of-life care, and artificial nutrition.
12. 12
The Elephant In The Room
Less time and
sicker, more
complex patients
Opioid crisis /
epidemic /
apocalypse
Electronic medical
record
“Management
deferred to
primary”
Burnout
Silver tsunami
Less primary
care, more
patients
13. 13
Welcome to Healthcaria
Beware the patient doesn’t fall off!
The Healthcare
World is Flat
Nursing /
Social Work /
Therapy
Primary Care
Specialty Care
IM
FM
Peds
14. 14
Death is NOT the enemy
We die not because we lose, quit, or fail. We die because that is the natural end of life.
The Healthcare
World is Flat
Nursing /
Social Work /
Therapy
Primary Care
Specialty Care
IM
FM
Peds
16. 16
Questionable Origins
“The term palliative care was coined by
Canadian surgeon Balfour Mount in
1975. Palliative care is interdisciplinary
care that aims to relieve suffering and
improve the quality of life for patients
with critical, advanced, or terminal
illness, and their families. It is offered
simultaneously with all other
appropriate medical treatment. No
specific therapy is excluded from
consideration, including surgical
intervention. The indication for palliative
care is based on the need to achieve
quality-of-life goals, not poor prognosis.”
17. 17
Definitions
• Palliative care is an approach that improves the quality of life of patients
and their families facing the problem associated with life-threatening illness,
through the prevention and relief of suffering by means of early
identification and impeccable assessment and treatment of pain and other
problems, physical, psychosocial and spiritual.
• Palliative care, and the medical sub-specialty of palliative medicine, is
specialized medical care for people living with serious illness. It focuses on
providing relief from the symptoms and stress of a serious. Illness whatever
the diagnosis. The goal is to improve quality of life for both the patient and
the family.
• Palliative care is the relieving or soothing of symptoms of a disease or
disorder while maintaining the highest possible quality of life for patients.
WHO • CAPC • AAHPM
www.who.int/cancer/palliative/denition/en/
www.capc.org/about/palliative-care/
palliativedoctors.org/palliative/care
18. 18
Type Goal Investigations Treatments Setting
Active To improve quality of life with possible prolongation of life
by modification of underlying disease(s). Ex: Pt. who has
potentially resectable pancreatic carcinoma. May require
immediate symptom control or need guidance in setting
future goals.
Active (eg, biopsy, invasive
imaging, screenings)
Surgery, chemotherapy, radiation therapy,
aggressive antibiotic use,
Active treatment of complications
(intubation, surgery)
In-patient facilities,
including critical care units;
Active office follow-up
Comfort Symptom relief without modification of disease, usually
indicated in terminally ill patients. Ex. Pt. who has
unresectable pancreatic carcinoma, no longer a candidate
for or no longer desires chemo or radiation therapy.
Minimal (eg, chest radiograph
to rule out symptomatic
effusion, serum calcium level
to determine response to
bisphosphonate therapy)
Opioids, major tranquilizers, anxiolytics,
steroids, short- term cognitive and
behavioral therapies, spiritual support,
grief counseling, noninvasive treatment
for complications
Home or homelike
environment
Brief in-patient or respite
care admissions for
symptom relief and respite
for family
Urgent Rapid relief of overwhelming symptoms, mandatory if death
is imminent. Shortened life may occur, but is not the
intention of treatment (this must be clearly understood by
patient or proxy). Ex. Patient who has advanced pancreatic
carcinoma reporting uncontrolled pain (8 on a scale of 10),
despite opioid therapy.
Only if absolutely necessary
to guide immediate symptom
control
Pharmacotherapy for pain, delirium,
anxiety. Usually given intravenously or
subcutaneously and in doses much higher
than most physicians are accustomed to
using.
Deliberate sedation may need to be used
and may need to be continued until time
of death.
In-patient or home with
continuous professional
support and supervision
Victoria Classification of Palliative Care
J Palliat Care. 1993 Winter;9(4):26-32.
19. 19
Sufferology
• The area of medicine that deals with alleviating the
physical, mental, spiritual and familial suffering of
patients with chronic, progressive illness.
• Palliative care is concerned with three things:
• the quality of life,
• the value of life, and
• the meaning of life.
More than “there’s nothing left to do”
Doyle D, Oxford Textbook of Palliative Medicine, 3 ed.
20. 20
DIAGNOSIS $35
With 1 Hospitalization $175.
With 2 Hospitalizations 500.
With 3 Hospitalizations 1100.
With 4 Hospitalizations 1300.
With Hospice $1500.
Mortality Value $175
Hospitalizations cost $200K. each
Hospice, $0. plus (or minus) 4
hospitalizations.
If a patient owns ALL the Symptoms of any Color
Group, the opiates are Doubled on Uncontrolled
Symptoms in that group.
Mortalopoly and Morbidopoly
• Palliative care is a
philosophy of care for
seriously ill patients, it is
– NOT a place
– NOT a status
– NOT limited by curative
intent
21. 21
With, For, and To
Never say nothing
• Even when we cannot cure their
illness or prevent their death, we
can always do something:
provide the best care possible.
#with4not2
• Do as little to the patient as
possible.
• Do for the patient what they
cannot do themselves.
• Do as much with the patient as
you are able.
22. 22
Scripting
• “Palliative care works with me, your provider, to better manage
your [pain, shortness of breath or other symptom (anxiety,
fatigue, nausea)]. They are experts in looking at this holistically
and make a comprehensive plan for how best to relieve your
[symptom].
• They can answer some of the questions you may have about what
to expect in future as your [disease] worsens.
• They help me formulate a treatment plan that is based on what is
important to you and what is going on with your family.
• There is support staff at the clinic who works with the palliative
care providers to help you and your family cope with these
changes and plan for the future”
How to help other providers refer to palliative care
23. 23
Primary and Specialty Palliative Care
Primary Palliative Care
• Referrals
• Feedback
• Managing patients closer to
home
Specialty Palliative Care
• Education
• Support
• Adding value to preexisting
exemplary care
24. 24
Palliative Care and Geriatrics
Geriatrics
• Age > 65
• Foster
independence/
control over life
• Collaborative
Care Model
Palliative Care
• Any Age
• Maximize well-
being/reduce
suffering
• Interdisciplinary
Team Model
Improving
quality of
life
Nursing Facility HospitalClinic
www.dartmouth-hitchcock.org/dhmc-internet-upload/file_collection/SharedConcepts.pdf
25. 25
Palliative Care and Hospice
Clin Geriatr Med 2013; 29:1–29
www.nationalconsensusproject.org
www.nia.nih.gov/health/publication/e
nd-life-helping-comfort-and-
care/providing-comfort-end-life Palliative Care
Symptom Management of Life Limiting Illness
Curative or Palliative Treatment
Disease Management of Life Limiting Illness
Symptom burden
despite or due to
disease
modification
End of Life or
Hospice Care
Symptom Management
and Comfort Care
Untreatable disease
No longer desiring treatment
Symptom burden
increases due to
treatable disease
burden
Comfort Care is an
essential part of medical
care at the end of life. It is
care that helps or soothes
a person who is dying.
The goal is to prevent or
relieve suffering as much
as possible while
respecting the dying
person’s wishes.
26. 26
Quality and Quantity
Of the 151 patients who underwent
randomization, 27 died by 12 weeks and 107
(86% of the remaining patients) completed
assessments. Patients assigned to early
palliative care had a better quality of life than
did patients assigned to standard care (mean
score on the FACT-L scale [in which scores range
from 0 to 136, with higher scores indicating
better quality of life], 98.0 vs. 91.5; P=0.03). In
addition, fewer patients in the palliative care
group than in the standard care group had
depressive symptoms (16% vs. 38%, P=0.01).
Despite the fact that fewer patients in the
early palliative care group than in the standard
care group received aggressive end-of-life care
(33% vs. 54%, P=0.05), median survival was
longer among patients receiving early
palliative care (11.6 months vs. 8.9 months,
P=0.02).
27. 27
Carle Palliative Medicine Criteria
General Referral Criteria1
Presence of a serious illness and one or more of the following:
• New diagnosis of life-limiting illness for symptom control, patient/family
support
• Declining ability to complete activities of daily living
• Weight loss
• Progressive metastatic cancer
• Admission from long-term care facility (nursing home or assisted living)
• Two or more hospitalizations for illness within three months
• Difficult-to-control physical or emotional symptoms
• Patient, family or physician uncertainty regarding prognosis
• Patient, family or physician uncertainty regarding appropriateness of treatment
options
• Patient or family requests for futile care
• DNR order conflicts
• Conflicts or uncertainty regarding the use of non-oral feeding/hydration in
cognitively impaired, seriously ill, or dying patients
• Limited social support in setting of a serious illness (e.g., homeless, no family or
friends, chronic mental illness, overwhelmed family caregivers)
• Patient, family or physician request for information regarding hospice
appropriateness
• Patient or family psychological or spiritual/existential distress
Cancer2
• Stage IV disease
• Stage III lung or pancreatic cancer
• Stage II non-small cell lung cancer3
• Prior hospitalization within 30-days, excluding routine chemotherapy
• Hospitalization lasting longer than 7 days.
• Uncontrolled symptoms including pain, nausea/vomiting, dyspnea,
delirium, and psychological distress.
1 www.capc.org
2 www.oncologypractice.com/single-view/five-criteria-doubled-
palliative-care-cut-hospital-
readmissions/f37951d2a4828930104a3fa9b91eb013.html
3 N Engl J Med 2010; 363:733-742
28. 28
Carle Palliative Medicine Criteria
Heart Failure1
• Symptoms
• NYHA class III/IV symptoms
• Frequent heart failure readmissions
• Recurrent ICD shocks
• Refractory angina
• Anxiety or depression adversely affecting patient's
quality of life or ability to best manage illness
• Milestones
• Referral
• VAD
• Transplant
• TAVR
• Home inotropic therapy
• Caregiver distress
Kidney Disease2
• CKD Stage IIIb, IV, or V with fatigue, muscle cramps, anorexia,
nausea, insomnia, neuropathy, gout, itch, headache, or cognitive
impairment
• ESRD on dialysis with any stage V symptom as well as abdominal
pain from peritoneal dialysis or fistula problems from
hemodialysis
• Calciphylaxis
• Symptoms due to comorbid diabetes, cardiovascular disease, or
cancer
Liver Disease3
• Ascites despite maximum diuretics
• Spontaneous peritonitis
• Hepatorenal syndrome
• INR > 1.2 without anticoagulation
• Encephalopathy
• Recurrent variceal bleeding if further intervention inappropriate
1 www.acc.org/latest-in-cardiology/articles/2016/02/11/08/02/palliative-care-for-patients-with-heart-failure#sthash.ddHLsX9W.dpuf
2 Adapted from: www.nhslanarkshire.org.uk/Services/PalliativeCare/Documents/NHS%20Lanarkshire%20Palliative%20Care%20Guidelines.pdf
3 www.palliativedrugs.com/download/SpecialistPalliativeCareReferralforPatients.pdf
29. 29
Carle Palliative Medicine Criteria
Lung Disease
Chronic Obstructive Pulmonary Disease1
• Age ≥ 75
• Diabetes, cardiovascular disease, or end-stage renal
disease
• Change in 6 minute walk by 50 m
• Functional dependence and patient reported
minimal physical activity
• Poor healthcare quality-of-life
• FEV1 < 30%
• BMI < 20%
• ≥ 1 hospitalization within last year
Restrictive Lung Disease2
• TLC or FVC < 50%
Neurological Disease3
Presence of any of the General Referral Criteria
above, and/or:
• Folstein Mini Mental score < 20
• Feeding tube is being considered for any
neurological condition
• Status Epilepticus > 24 hrs
• ALS or other neuromuscular disease considering
invasive or non-invasive mechanical ventilation
• Any recurrent brain neoplasm
• Parkinson’s disease with poor functional status
or dementia
• Advanced dementia with dependence in all
activities of daily living
1 Int J Chron Obstruc Pulmon Dis. 2015; 10:1543-51
2 Based on severity obtained from review of courses.washington.edu/med610/pft/pft_primer.html#algor
3 www.capc.org
30. 30
Carle Palliative Medicine Criteria
• If you want to do everything for your patient and
they have a diagnosis which says or means failure,
they would likely benefit from a palliative care
referral.
– Symptomatic heart, lung, kidney, or liver failure
– Cancer is cellular failure.
– Stroke, dementia, and neurological degenerative
diseases (ALS) are neurological failure.
General Referral Criteria
31. 31
Choosing Wisely
Don’t delay palliative care for a patient with
serious illness who has physical,
psychological, social or spiritual distress
because they are pursuing disease-directed
treatment.
www.choosingwisely.org/doctor-patient-lists/american-academy-of-hospice-palliative-medicine/
32. 32
In-Patient Palliative Care
• Since January 2017, the in-patient service has been 7 days a week, 365 days a year during
regular business hours.
• Minimum staffing for the service is three (3) providers, one of whom is a physician,
except on weekends and holidays.
• Follow-Up Orders
– on patients we already see
– on patients that receive other care here at the main campus who would benefit from
ambulatory palliative care follow-up
If they are sick enough to be
in the hospital and need a
palliative care consult, they
need that consult in-patient.
33. 33
Ambulatory Palliative Care
• Clinic staffed Monday – Friday during regular business hours.
• To refer place order in EPIC
– Type “amb pal”
– Palliative care nurse will call patient to set-up appointment
• Embed Clinics:
– Oncology (1 day/week)
– Advanced Heart Failure (2 half-
days/week)
34. 34
Palliative Care Staff
383-6744
Anne Curtiss
Director
Jodi Murphy, RN
Nurse
Yvonne Cao
Office Coordinator
Bryan Peralta, RN
Nurse
Jenni Scott
Medical Assistant
35. 35
Specialty Palliative Care Providers
Kris Anderson, PA Mike Aref, MD, PhD
Assistant Medical Director
Andy Arwari, MD
Oncology Lead
Cathy Bond, APN Sheila Gillette, APN
Jean Holley, MD
Heart Failure Lead
Rebecca Puher, DO
Pediatric Lead
Mark Lavizzo, MD Kim Winston, APN April Yasunaga, MD
Rotation Site Director
38. 38
Central Neuropathic
• Non-dermatomal
• Direct central nervous injury
• Radiating or specific
• Burning, prickling, tingling,
electric, shock-like or lancinating
Peripheral Neuropathic
• Dermatomal
• Direct peripheral nervous injury
• Radiating or specific
• Burning, prickling, tingling,
electric, shock-like or lancinating
Visceral (,)
• C fiber activity
• Distension, ischemia and
inflammation of organs
• Diffuse, deep ache,
pressure, sickening,
squeeze, dull or sharp
Types of Pain
Psychogenic
• Pain that is caused, increased, or prolonged
by mental, emotional, or behavioral factors.
Acute < 3 months
Chronic > 3 months
Malignant pain is due
to a progressive disease
that will lead to death.
Non-malignant pain is due to a
non-threatening cause that may
persist until, but is not the cause of,
death.
1st
2nd
tramadol
oxycodone
methadone
3rd
Never
Opioid?
2nd – 3rd
Somatic (,)
• fiber activity
• Skin and deep tissue
damage
• Pinprick, stabbing or
sharp
Goldstein and Morrison, Evidenced-Based Practice of Palliative Care: Expert Consult, Ch 1, 2
Mann and Carr, Pain: Creative Approaches to Effective Management
39. 39
4-Step Model of Pain
Transduction Transmission Perception Modulation
Acute stimulation in the
form of noxious
thermal, mechanical, or
chemical stimuli is
detected by nociceptive
neurons.
Nerve impulses
transferred via axons of
afferent neurons from
the periphery to the
spinal cord, to the
medial and ventrobasal
thalamus, to the
cerebral cortex.
Cortical and limbic
structures in the brain
are involved in the
awareness and
interpretation of pain.
Pain can be inhibited or
facilitated by
mechanisms affecting
ascending as well as
descending pathways.
Wyatt SA, Adjunct Approaches to Chronic Pain Management for Individuals with Substance Abuse Disorder, July 21, 2016
40. 40
Mechanistic Classification of Pain States
Pain State Diagnostic Criteria
Nocioceptive Evidence of noxious (mechanical) insult
Symptoms: pain localized to area of stimulus/joint damage
Signs: imaging—mechanical pathology/altered joint architecture such that normal movements
will likely produce excessive forces sufficient to activate nociceptors
Inflammatory Evidence of inflammation
1. Sterile
2. Infectious
Symptoms: redness, warmth, swelling of affected area
Signs: imaging (MRI, SPECT) signs of inflammatory changes, detection of pathogens/response to antibiotics
Neuropathic Evidence of sensory nerve damage
Symptoms: burning, tingling or shock-like, spontaneous pain; paresthesias or dysthesias
Signs: decreased pinprick or vibration sense, and straight leg raise, mechanical and cold allodynia
Dysfunctional /
Centeralized
Pain in the absence of detectable pathology
No identifiable noxious stimulus, inflammation or neural damage; evidence of increased
amplification or reduced inhibition.
The Journal of Pain, Vol 17, No 9 (September), Suppl. 2, 2016: pp T50-T69
41. 41
Chronic Low Back Pain Drivers
i = inflammation; n = nocioceptive; Nep = neuropathic pain
Vardeh D et al, The Journal of Pain, Vol 17, No 9 (September), Suppl. 2, 2016: pp T50-T69
Palliative
Care
42. 42
Total Pain
Social
Psychological
Physical
•Role
•Relationships
•Occupation
•Financial cost
•Emotional response
•Comorbid mood disorder anxiety
•Adjustment to new baseline
•Cause?
•Associated symptoms
•Debility and fatigue
Superimposed on Maslow’s Hierarchy of Needs
Spiritual
•Existential coping
•Religious beliefs
•Meaning of life/illness
•Personal value
Interventional Pain Service
Other Specialties
Pharmacy
Physical Therapy
Social Work
Financial Navigator
Occupational Therapy
Chaplaincy
Art & Music Therapy
Social Work
Psychology
Psychiatry
Curr Opin Support Palliat Care. 2008; 2(2):110-3
Maslow AH, A Theory of Human Motivation, 1943
47. 47
Life-Limiting Illness Population
• It is estimated at there is 1,200 patients with life-
limiting illness for each specialty palliative care
provider.
– By comparison there are 141 cancer patients per
oncologist.
• It is estimated that 30% of hospital patients “need”
a palliative care consult:
– At Carle Foundation Hospital that would be a 120 patient
service, currently we see about 30 in-patients per day.
These numbers don’t add up either
www.capc.org/about/press-media/press-releases/2016-9-9/Hospital-Palliative-Care-Programs-Understaffed/
www.ajmc.com/journals/evidence-based-oncology/2015/april-2015/how-and-why-oncologists-should-do-palliative-careor-get-some-assistance-doing-it-
48. 48
Chronic Non-Malignant Pain Population
• 5000 opioid-dependent chronic non-malignant pain
patients in the Carle Health System.
• Opioid prescriptions are written every 28 days, or
20 working days, ≈ 250 patients per day.
• Active ambulatory palliative care physician FTEs ≈ 2.
• We don’t manage chronic non-malignant pain any
better than you would.
The numbers don’t add up
55. 55
Chronic Nocioceptive Pain
1st Line
•Topical agents:
capsaicin 0.025% - 0.075%
topically TID
lidocaine 5% topically TID
2nd Line
•Acetaminophen
acetaminophen 1000 mg
TID
3rd Line
•NSAID + PPI
see tables previous
•Selective COX-2 Inhibitors
celecoxib 200 mg daily or
100 mg every 12 hours
4th Line
•Serotonin-norepinephrine
reuptake inhibitors
(SNRIs):
duloxetine 60-120 mg PO
daily
venlafaxine 75-112 mg PO
BID
•Tricyclic antidepressants
(TCAs):
amitriptyline 25-150 mg PO
QHS
nortriptyline 25-150 mg PO
QHS
5th Line
•Strong Opiates < 90 mg
MEDD
Pharmacological Management
Up-To-Date
If signs/symptoms of muscle
spasm:
• cyclobenzaprine 5 mg PO TID
• tizanidine 2 mg PO TID
• baclofen 5 mg PO TID
61. 61
Start Smart
• What type of pain are we managing?
• Stress functional improvement and pain
management rather than “pain free”.
• Opiates are neuro-hormonal-psychiatric
scaffolding they are not cure for pain
nor the cornerstone of good pain
management.
• Opiate dichotomy: Judged due to social
stigma, shocked by abuse, but desire to
provide pain relief.
• What is your patient’s goal?
• What is the plan and is everyone in
agreement?
Proc (Bayl Univ Med Cent). 2000 Jul; 13(3): 236–239.
62. 62
Procedural Interventions
• Patient controlled analgesia pump
• Neurolysis
• Spinal stimulator
• Intrathecal pump
• Neurosurgery
Methadone PO
Fentanyl IV (0.05 mg = 50 mcg)
Hydromorphone IV (0.8 mg)
Hydromorphone PO (4 mg)
Oxycodone PO (10 mg)
Morphine PO (15 mg) Morphine IV (5 mg)
Hydrocodone PO (15 mg)
Tramadol PO (100 mg)
Codeine PO (100 mg)
Ibuprofen PO (1100 mg)
Acetaminophen PO (3610 mg)
Salicylate (choline magnesium
trisalicylate)
Ascending WHO Analgesic Ladder
Adjuncts
• Anticonvulsants
• Neuropathic pain + muscle spasm = gabapentin
• Neuropathic pain + anxiety - depression = pregabalin
• Post-operative pain + anxiety - depression = pregabalin
• Antidepressants (SNRI, TCA)
• Muscle spasm + anxiety = diazepam
• Depression anxiety + neuropathic pain = duloxetine
• Baclofen
• Cyclobenzaprine (muscle relaxant, fibromyalgia)
• Corticosteroids
• Ketamine
Interventions
• Transcutaneous electrical nerve stimulation
• Acupuncture
• Art / Music Therapy
• Massage
• Physical Therapy
• Psychological Treatment
Procedures
• Nerve blocks
Canadian Family Physician 2010; 56(6):514-517
Opioid tablet images WebMD
Chronic pain
Non-malignant pain
Malignant pain
Morphine IV comes in 4 and 6 mg
Actually 120 mg of codeine
Sedation
36-72 hours
Nausea / Vomiting
Pruritus
7-10 days
Constipation
Flushing / Sweating
Never
70. 70
Scheduled Dosing
• Calculate opiate dosage used in the past 24 hours
and set scheduled dose to be 75-100% this total.
• PRN dosing is 10% every hour to three hours as
needed.
Theory
72. 72
Scheduled or as needed for pain every 4 hours (Q4H) with as needed for
breakthrough pain every 1 hour (Q1H)
IV PCAmorphine(mg)
hydromorphone
(mg)
fentanyl(mcg)
morphine(mg)
hydromorphone
(mg)
fentanyl(mcg)
Q4H Q4H Q4H Q10MIN 4-hour LO Q10MIN 4-hour LO Q10MIN 4-hour LO
4 0.5 50 0.5 12 0.1 1.7 6.25 150
8 1 100 1 24 0.2 3.4 12.5 300
12 1.5 150 1.5 36 0.2 5.1 20 450
16 2 200 2 48 0.3 6.2 25 600
20 2.5 250 3 68 0.4 8.5 35 850
73. 73
Descending WHO Analgesic Ladder
0
100
200
300
400
500
0 3 6 9 12 15 18 21 24 27 30 33 36 39 42 45 48 51
10% wean per week
10% wean per month
90 mg OME
50 mg OME
Chronic Pain – Short Acting Opiates
Hydromorphone 1 mg IV every hour
Oxycodone-APAP 10-325 mg PO every 2 hours
Hydrocodone-APAP 10-300 mg PO every 2 hours
Morphine 30 mg PO every 3 hours
Weeks
MorphineEquivalentDailyDose(MEDD)(mg)
Slow wean, if:
• Tachycardia
• Diaphoresis, lacrimation, salivation
• Diarrhea
74. 74
Descending WHO Analgesic Ladder
0 5 10 15 20 25 30 35 40 45 50 55
0
100
200
300
400
500
25% wean every 7 days
20% wean every 3 days
10% wean everyday
20% wean everyday to 90 mg OME
Chronic Pain – Short Acting Opiates
AAPM 2005
paincommunity.org/blog/wp-content/uploads/Safely_Tapering_Opioids.pdf
Hydromorphone 1 mg IV every hour
Oxycodone-APAP 10-325 mg PO every 2 hours
Hydrocodone-APAP 10-300 mg PO every 2 hours
Morphine 30 mg PO every 3 hours
Slow wean, if:
• Tachycardia
• Diaphoresis, lacrimation, salivation
• Diarrhea
Decrease frequency of doses
90 mg OME
50 mg OME
MorphineEquivalentDailyDose(MEDD)(mg)
75. 75
Case
• A 57-year-old male is on a fentanyl patch 50 mcg/hr and has oxycodone 10 mg
Q3H PRN pain. He indicates that he is having a skin reaction from the fentanyl
patch. He would like to switch to an oral pain medication but wants to minimize
his pill intake.
• What is his total morphine equivalent daily dose (MEDD)?
76. 76
Case
What is his total morphine equivalent daily
dose (MEDD)?
• It depends…
– His MEDD from fentanyl patch is between
135 and 224 mg daily.
– His oxycodone dose means that he could be
taking between 0 and 120 mg daily
– Thus his total MEDD is somewhere between
135 and 344 mg daily.
77. 77
Case
• A 57-year-old male is on a fentanyl patch 50 mcg/hr and has oxycodone 10 mg
Q3H PRN pain. He indicates that he is having a skin reaction from the fentanyl
patch. He would like to switch to an oral pain medication but wants to minimize
his pill intake. He tells you that he is taking his oxycodone six times daily. Labs
today show that his kidney and liver function are within normal limits.
• What could we prescribe?
78. 78
Case
What could we prescribe?
• His MEDD from fentanyl patch is between
210 (135 + 75) and 299 (224 + 75) mg daily.
• Since we are class switching we want to
decrease the dose by between 25% and
33%, e.g. he should get a prescription for
140 to 225 mg. Given variable absorption
with fentanyl patch would err on the lower
side but make sure PRNs are available
often.
• Thus, options for scheduled
medications:
– MSSR 45 mg PO Q8H
– Oxycodone ER 40 mg PO Q12H
– Hydromorphone ER 32 mg PO Q24H
– Hydrocodone ER 60 mg PO Q12H
79. 79
Case
• Ideally the PRN dose is 10% of scheduled dose. Thus, options for PRN
medications:
– MSIR 15 mg PO Q3H PRN
– Oxycodone IR 10 mg PO Q3H PRN
– Hydromorphone 2-4 mg PO Q3H PRN
– Hydrocodone-APAP 5-325 to 7.5-325 mg PO Q3H PRN
What PRN dose should we prescribe?
80. 80
Case
• A 57-year-old male is on a fentanyl patch 50 mcg/hr and has oxycodone 10 mg
Q3H PRN pain. He takes his oxycodone IR 1-2 times per day. Review of the IL-
PMP reveals adherence with a single prescriber and regular refills approximately
every 30 days. Prior to this visit you obtained a urine “quicktox” which was
positive for oxycodone and negative for everything else including opiates.
• Would you refill this patient’s prescriptions?
• If his “quicktox” was positive for oxycodone and opiates, would this change your
management?
81. 81
All Opioids
Codeine, hydrocodone, hydromorphone, and morphine are opiates
(+)ve oxycodone (+)ve opiates
Fentanyl
Does NOT
show up on
Quicktox
82. 82
Quicktox
(+)ve oxycodone and (-)ve opiates
• Probably taking oxycodone (or
substance that causes false
positive for oxycodone) but likely
NOT using opiates
– In this case, more likely adherent
(+)ve oxycodone and (+)ve opiates
• Probably taking oxycodone AND
opiates (or substance that causes
false positives for oxycodone and
opiates)
– In this case, more likely non-
adherent and using
illicit/unprescribed opiates
Quicktox is a SCREENING test, i.e. used to RULE OUT, thus:
a NEGATIVE result is more likely to be TRUE and
a POSITIVE results needs confirmatory testing (e.g. Aegis)
86. 86
Case
• 23-year-old female with chronic abdominal pain, nausea, and food aversion
secondary to multiple surgeries for hereditary pancreatitis and complications
thereof.
• Non-malignant abdominal pain managed with progressive increases in opiates,
now on high-dose opiates, 200 mcg/hr fentanyl patch with 4-8 mg of
hydromorphone as needed every 2-3 hours.
• Mother strong advocate for patient.
87. 87
Question
A. Addiction / “drug seeking” behavior
B. Narcotic bowel syndrome
C. Undertreated non-malignant pain
D. Complex abdominal and pelvic pain syndrome
(CAPPS)
What is the most likely diagnosis?
88. 88
Question
A. Addiction / “drug seeking” behavior
B. Narcotic bowel syndrome
C. Undertreated non-malignant pain
D. Complex abdominal and pelvic pain syndrome
(CAPPS)
What is the most likely diagnosis?
89. 89
Narcotic Bowel Syndrome
• The pain worsens or incompletely resolves with continued or escalating dosages
of narcotics.
• There is marked worsening of pain when the narcotic dose wanes and
improvement when narcotics are reinstituted (“Soar and Crash”).
• There is a progression of the frequency, duration and intensity of pain episodes.
• The nature and intensity of the pain is not explained by a current or previous
gastrointestinal diagnosis:
– A patient may have a structural diagnosis (e.g., inflammatory bowel disease,
chronic pancreatitis) but the character or activity of the disease process is
not sufficient to explain the pain.
Chronic or frequently recurring abdominal pain that is treated with acute high dose or chronic
narcotics and all of the following:
Clin Gastroenterol Hepatol. Oct 2007; 5(10): 1126–1122.
90. 90
Case
• 72-year-old male with metastatic pancreatic cancer,
admitted for pain control.
• Patient has been on rapidly escalating doses of
morphine. He is delirious. The weight of his sheets
appear to be painful, in his lucid moments he weeps. In
the past 24 hours he developed intermittent jerking of
his limbs.
91. 91
Question
A. Terminal agitation / delirium
B. Undertreated terminal malignant pain
C. Opiate-induced hyperalgesia
D. Status epilepticus
What is happening to the patient?
92. 92
Answer
A. Terminal agitation / delirium
B. Undertreated terminal malignant pain
C. Opiate-induced hyperalgesia
D. Status epilepticus
What is happening to the patient?
93. 93
Opiate-Induced Hyperalgesia
• Increasing sensitivity to pain stimuli (hyperalgesia). Pain
elicited from ordinarily non-painful stimuli, such as stroking
skin with cotton (allodynia).
• Worsening pain despite increasing doses of opioids.
• Pain that becomes more diffuse, extending beyond the
distribution of pre-existing pain.
• Presence of other opioid hyperexcitability effects: myoclonus,
delirium or seizures.
• Can occur at any dose of opioid, but more commonly with
high parenteral doses of morphine or hydromorphone most
often in the setting of renal failure.
www.mypcnow.org/blank-h5muh
95. 95
Dyspnea and Hypoxia
Dyspnea
• Subjective feeling of difficulty or
distress in breathing.
• Patients who feel dyspnea may
not appear dyspneic.
Hypoxia
• Objective finding of lower-than-
normal concentration of oxygen
in arterial blood. Occurs with any
interruption of normal
respiration.
• Hypoxia and dyspnea are
independent of one another.
If a patient’s breathing pattern is noticeable as you approach them it is abnormal.
97. 97
Total Dyspnea
•Role
•Relationship
•Occupation
•Financial Cost
•Existential coping
•Religious beliefs
•Meaning of life/illness
•Personal value
•Emotional Response
•Anxiety
•Exacerbation of
comorbid mood disorder
•Adjustment to new
baseline
•Cause?
•At rest or with exertion?
•Assoc. Sx?
•Drowsiness or Fatigue?
Physical Psychological
SocialSpiritual
Physical • Psychological • Social • Spiritual
Dyspnea
Curr Opin Support Palliat Care. 2008; 2(2):110-3
98. 98
Management of Physical Symptoms of Dyspnea
Non-Pharmacological
• Education in purse-lipped breathing.
• Referral to pulmonary rehabilitation in
COPD and some other pulmonary
diseases.
• Obtaining a fan at bedside (these must
be purchased by the patient or family
and are not provided).
• Use of supplemental oxygen 2-6 L/min.
• In some cases NIPPV improves dyspnea
Pharmacological
• Opiates
• Benzodiazepines if comorbid
anxiety is worsening dyspnea
Carle Palliative Medicine, Palliative Care: Guide to Symptom Management
101. 101
Constipation Prevention and Management Options
Non-pharmacological ways to prevent and treat
constipation
1. Optimize oral hydration
2. Physical activity
3. Scheduled visits to the
commode
4. Privacy when using the
commode
Yakima Valley Anti-Constipation Fruit Paste
1 lb pitted prunes
4 oz senna tea leaves (at health foods store)
1 lb raisins
1 lb figs
1 cup lemon juice
1. Prepare tea; use about 2 1/2 cups boiled water, add to tea leaves
and steep for 5 minutes.
2. Strain tea and remove tea leaves.
3. Place 2 cups of tea, or amount left, in large pot.
4. Add all of the fruit to the tea.
5. Boil fruit and tea for 15 - 20 minutes, until soft.
6. Remove from heat and add lemon juice. Allow to cool.
7. Use hand mixer/blender or food processor to turn fruit and tea
mix into a paste.
8. Place in glass jars or Tupperware and place in freezer (paste will
not freeze but will keep forever in freezer also very long in
fridge).
DOSAGE: 1 - 2 Tablespoons per day
102. 102
Bowel movement frequency
normal for you without needing
other as needed medications
Bowel movement frequency
normal for you without needing
other medications
Bowel movement frequency
normal for you without other
medications
Bowel movement frequency
normal for you without needing
other medications
All opiates cause constipation and
unlike other side effects this does
not improve with time!
Start senna 1 tablet
twice daily plus as
needed adjunct*
Increase senna to 2
tablets twice daily plus
as needed adjunct*
Increase senna to 4
tablets twice daily plus
as needed adjunct*
Continue senna 4
tablets twice daily and
add MiraLax daily plus
as needed adjunct*
Contact your provider
for other
pharmacological
options for managing
your constipation
No changes
No changes
No changes
No changes
Yes
Yes
Yes
Yes
No
No
No
No
*Adjunct medications should be
used if there is no bowel
movement in the last 48 hours,
firstly:
• MiraLax 17g 1-2 times daily
If no relief or unable to tolerate
MiraLax consider:
• Bisacodyl suppository 10 mg
daily
• Glycerin suppository daily
• Soaps suds or tap water
enema daily
103. 103
Advanced Constipation Prevention and
Management Options
• Lubiprostone (Amitiza)
– Acts on gut chloride channels (CIC-2) increasing intestinal secretions and causes accelerated
intestinal transit.
– Indications: Chronic idiopathic and opiate-induced constipation.
– 24 mcg PO BID
• Naloxegol (Movantik)
– Peripheral acting µ-opioid receptor antagonist (PAMORAs) that do not cross the blood-brain
barrier which prevents effects of constipation but does not significantly impair analgesia.
– Indications: Opiate-induced constipation.
– 25 mg PO QAM
• Methylnaltrexone (Relistor)
– Another PAMORA that is given subcutaneously and has a shorter time of onset and is slightly
more effective than naloxegol.
– Indications: Opiate-induced constipation.
– Dosing is weight based and it is given every other day
Typically need to have failed 4 other laxatives for insurance to cover.
107. 107
Case
• 57-year-old female with stage IV ovarian cancer with
carcinomatosis peritonei notes nausea, bloating, and
abdominal discomfort. This has led to associated anorexia and
insomnia. She is having flatus but no bowel movements for 72
hours. No fever and no urinary symptoms.
• She takes MSSR 15 mg PO TID at home and has been at this
dose with regular bowel movements daily using senna and
MiraLax.
• Vital signs are stable. Elevated BUN and creatinine on labs.
KUB is shows non-specific bowel gas pattern and no
significant stool burden. UA is negative for infection.
108. 108
Question
A. Cancer pain crisis
B. Ileus
C. Opiate-induced constipation
D. Partial malignant bowel obstruction
What is happening to the patient?
109. 109
Answer
A. Cancer pain crisis
B. Ileus
C. Opiate-induced constipation
D. Partial malignant bowel obstruction
What is happening to the patient?
110. 110
Malignant Bowel Obstruction
• Prevalence 5-25% in ovarian carcinoma or
colorectal cancer, in advanced ovarian cancer
frequency up to 42%.
• Imaging of choice: CT abdomen and pelvis with
contrast (ACR Appropriateness Criteria Rating 9)
followed by without contrast (ACR 7). X-ray
abdomen and pelvis is ACR 5.
Partial or Complete
www.cancer.gov/resources-for/hp/education/epeco/self-study/module-3/module-3e.pdf
acsearch.acr.org/docs/69476/Narrative/
111. 111
Management
• Venting gastrostomy is definitive management.
• Dexamethasone 6-16 mg IV may bring about resolution
of bowel obstruction.
• Dexamethasone + ranitidine = octreotide
• Dexamethasone + octreotide + metoclopramide
– Malignant Bowel Obstruction (MBO): Pain and nausea
improved within 24 hours, PO intake within 48 hours
– Malignant Bowel Dysfunction (MBD): 84% of patients had
improved pain and nausea within 24 hours, PO intake within
1-4 days
Inoperable
Support Care Cancer. 2009 Dec;17(12):1463-8
Am J Hosp Palliat Care. 2016 May;33(4):407-10
Support Care Cancer. 2009 Dec;17(12):1463-8
Am J Hosp Palliat Care. 2016 May;33(4):407-10
117. 117
Three-Phase Model of Goals of Care
Curative or restorative phase (“beating
it”)
Comfort phase (“living with disease,
anticipating death”)
Terminal phase (“dying very soon”)
Definition
The default position for all patients —
all appropriate life-prolonging
treatment will be deployed as
indicated.
The disease is deemed to be incurable
and progressive.
Death is believed to be imminent (i.e.,
within a few days) — implementation of
a terminal care pathway.
Aim
GoC are directed towards cure,
prolonged disease remission and/or
restoration to the pre-episode health
status for those with chronic diseases,
especially in the aged care context.
GoC are modified in favor of comfort,
quality of life and dignity; period of
survival is no longer the sole
determinant of treatment choice; life
prolongation is a secondary objective of
medical treatment.
Comfort, quality of life and dignity are
the only considerations.
Definitions and Aims
Med J Aust 2014; 201 (8): 452-455
118. 118
Three-Phase Model of Goals of Care
Curative or restorative phase (“beating
it”)
Comfort phase (“living with disease,
anticipating death”)
Terminal phase (“dying very soon”)
Prognosis
Life expectancy is probably the same as
the population mean because the
present health episode is unlikely to
affect longevity; a key question could be
“is there a reasonable chance of the
patient leaving hospital and living the
same life span as might have been
expected before the episode?”; a key
question in aged care and chronic
disease settings (where the goals might
be restorative) could be “is there a
reasonable chance of the patient
leaving hospital and/or returning to his
or her previous level of functioning?”
Life expectancy is usually months, but
sometimes years; a key question could
be “would I/we be surprised if this
patient died in the next 12 months?”
Life expectancy is hours or days; a key
question could be “would I/we be
surprised if this patient died this
week?”
Prognosis
BMJ 2010; 341: c4863
Med J Aust 2014; 201 (8): 452-455
119. 119
Three-Phase Model of Goals of Care
Curative or restorative phase (“beating
it”)
Comfort phase (“living with disease,
anticipating death”)
Terminal phase (“dying very soon”)
Level of adverse effects
A high level of adverse effects and even
a significant chance of treatment-
related mortality might be accepted for
curative treatment (e.g., brain
aneurysm surgery, bone marrow
transplant); while pain and symptom
control should always be addressed,
comfort may be a secondary
consideration if it conflicts with curative
treatment.
Active treatment of the underlying
disease may be undertaken for specific
symptoms (e.g., radiotherapy or
chemotherapy for palliative end point in
cancer treatment) and/or short-term
life expectancy gains; treatment-related
adverse effects should be proportionate
to the goals and acceptable to the
patient.
Active treatment of the underlying
disease should stop; no treatment-
related toxicity is acceptable (this
applies to all medical, nursing and allied
health interventions e.g., turns in bed if
these are distressing).
Level of Adverse Effects
BMJ 2004; 329: 909-912
Med J Aust 2014; 201 (8): 452-455
120. 120
Three-Phase Model of Goals of Care
Curative or restorative phase (“beating
it”)
Palliative phase (“living with disease,
anticipating death”)
Terminal phase (“dying very soon”)
Life-sustaining treatments
Given as needed. Life-sustaining treatments for other
chronic medical conditions are usually
continued (e.g., treatment with insulin
or anticonvulsants) in cases where
cessation would result in premature
death or preventable unpleasant
symptoms such as hyperglycemia and
seizures (i.e., symptoms unrelated to
the main disease that is anticipated to
cause death) or where quality of life
would be adversely affected.
Life-sustaining treatments for other
chronic medical conditions are usually
stopped (e.g., treatment with steroids,
insulin or anticonvulsants), unless doing
so would cause suffering.
Life-Sustaining Treatments
Med J Aust 2014; 201 (8): 452-455
121. 121
Three-Phase Model of Goals of Care
Curative or restorative phase (“beating
it”)
Palliative phase (“living with disease,
anticipating death”)
Terminal phase (“dying very soon”)
Artificial nutrition and hydration
Given as needed. Given if indicated and desired (e.g.,
percutaneous endoscopic gastrostomy
feeding for head and neck cancer
patients with obstructed swallowing).
Usually ceased and replaced with
careful hand feeding and rigorous
mouth care.
Cardiopulmonary resuscitation
Given as needed. Usually not recommended but should
be discussed with the patient, if
competent, or their representative.
Contraindicated.
Artificial Nutrition and Hydration and Cardiopulmonary Resuscitation
Intern Med J 2013; 43: 77-83
Med J Aust 2014; 201 (8): 452-455
122. 122
DNAR is a (Small) Part of Goals of Care
Birth
Actively
Dying (B)
Death (A)
(C)
www.polstil.org
Diagnosis
Treatment
New
Problem
123. 123
POLST
A. “If you had no heart beat and
are not breathing, that is you
are dead, what do you think
would be the best thing to
do? Try to bring you back,
which is a Full code, or
knowing that you have a
number of progressive
health conditions feel that a
natural death is right at that
time, which is Do Not
Attempt Resuscitation?”
124. 124
POLST Continued
B. If they choose Full Code in A, then the only
appropriate selection in B is “Full
Treatment”
If they chose DNAR, “If you are dying, that
is your lungs and heart cannot get oxygen
to your organs, what would like us to do,
take you to the hospital and try to correct
the situation, even using life support (Full
Treatment) or using everything short of
that (Selective Treatment), or try to keep
you comfortable at home and only moving
you to keep you comfortable (Comfort-
Focused Care). No matter what you chose
if you are feeling ill you can always elect to
see your physician or come to the
hospital.”
125. 125
POLST Continued
C. If they elected Comfort Care in B
the only appropriate selection is No
medically administered nutrition.
If they elected Selective Treatment
in B then any option is appropriate.
If they elected Full Treatment only
Long-term or Trial period of
medical nutrition is appropriate.
“Would you want artificial
nutrition, that is a tube in the nose
or in the belly that supplies
nutrition?”
126. 126
POLST Continued
D. Make sure the patient or
surrogate and witness sign
it.
E. Make sure that you sign
the POLST to complete it.
I make a copy to be
scanned in and return the
original to the patient. I
tell them to place it on
their fridge.
127. 127
Advance Care Planning
• CPT Code 99497
– Advance care planning including the explanation and
discussion of advance directives such as standard forms (with
completion of such forms, when performed), by the physician
or other qualified health care professional; first 30 minutes,
face-to-face with the patient, family member(s), and/or
surrogate
• CPT Code 99498
– each additional 30 minutes (List separately in addition to code
for primary procedure)
Billing
Frequently Asked Questions about Billing the Physician Fee Schedule for Advance Care Planning Services , www.cms.gov, July 14, 2016
128. 128
Speaking and Translating Caring
Goals of Care
• Identify what is important to and
priorities for the patient.
• Identify what they hope to
achieve by receiving care.
• Identify what they fear will
happen because of the disease.
• Life review and legacy building
are separate, equal, but not
independent parts of care.
Plan of Care
• Representation of the goals of care in the form
of
– Documentation
• Advanced Directive
• Living Will
• HCPOA
– Orders
• POLST
• Code Status
– Medications
• Starting and stopping
– Services
• Social Work
• Chaplaincy
• Hospice
• Home Health
National Committee for Quality Assurance: Goals to Care
129. 129
S.M.A.R.T. Goal
• Specific
– What does the patient mean to accomplish with this goal?
• Measurable
– What observable shows we are meeting the stated goal?
• Agreed Upon
– Are the patient, family, and provider all on the same page?
• Realistic
– Is this possible – physiologically, clinically, financially, humanly, etc.?
• Time-Bound
– When will this be observable?
General goals cannot be translated into a plan of care
Management Review. AMA FORUM. 70 (11): 35–36
National Committee for Quality Assurance: Goals to Care
130. 130
Unclear Goals = Unplannable Caring
Goals of Care
• “I’m going to beat this [disease]!”
• “My family won’t let me go to a
nursing home.”
• “We’re going to fight this!”
• “I’m going to get my miracle.”
Plan of Care
• These are general, usually not agreed
upon, often unrealistic, and do not
meet a timeline consistent with life
expectancy.
• The plan of care in these case is to
explore:
– “Tell me what this means to you.”
– “Help me understand more about this
by telling me how you feel about…”
And get a family meeting with all the key
partners in the patient’s care both family
and providers.
vitaltalk.org
131. 131
Clear Goals Lead to a Care Plan
Goals of Care
• “I want to be able to enjoy the
holidays with my family,
particularly my grandchildren.”
Plan of Care
• This is specific, measurable, can be
agreed upon, may be realistic, and
has a set time frame.
• Perhaps a chemotherapy “holiday”
or stopping hemodialysis after the
holidays. Certainly documenting
code status and likely involving
some sort of home nursing care, be
it private duty, home health, or
hospice.
133. 133
High-Quality End-of-Life Care
• Begin goals-of-care
conversations NOW…Years
Months
• …to provide high-quality end-of-life
care LATER!Weeks
Days
Life Expectancy
J Pain Symptom Manage. 2014 Jan; 47(1): 77–89.
134. 134
Definition of High-Quality Family Meeting
↑ Satisfaction
↑ Symptom
Control
Plan of Care
↓ PTSD
↑ Satisfaction
↓ Burnout
Goals
Established
↓ $$$
↓ LOS
↓ Readmissions
↓ Mortality
↓ Resource
Requirements
Standardized
EMR
Documentation
↑ Efficiency
Plan Consensus
Among
Treatment
Team
↑ Listening
↑ Understanding
Process Outcome
Patient/Family
Provider
Institution
135. 135
Communication Components Associated with Increased Quality of Care, Decrease
Family Psychological Symptoms, and Improved Family Ratings of Communication
• Conduct family conference within 72 hours of ICU admission.
• Identify a private place for communication with family members.
• Provide consistent communication from different team members.
• Increase proportion of time spent listening to family rather than talking.
• Empathetic statements.
• Identify commonly missed opportunities.
• Affirm non-abandonment of the patient and family.
• Assure family that the patient will not suffer.
• Provide explicit support for decisions made by the family.
Crit Care Med. 2001;29:1893–1897.
Am J Respir Crit Care Med. 2005;171:844–849.
Am J Med. 2000;109:469–475.
Crit Care Med. 2004;32:1484–1488.
Crit Care Med. 2006;43:1679–1685.
J Gen Intern Med. 2008;23:1311–1317.
J Palliat Med. 2005;8:797–807.
136. 136
Family Meeting Formats
Format Roadmap Supportive Urgent Discharge Planning
Timing < 72 hours < 72 hours < 24 hours of clinical
change
> 24 hours prior to
discharge
Information
Flow
Patient Provider Patient Provider Patient Provider Patient Provider
Clinical
Participants
Primary Service
Specialist(s)
Primary Service
+ Social Work
+ Chaplain
Specialist(s)
Primary Service
Specialist(s)
Social Work
Chaplain
Primary Service
+ Case Management
Specialist(s)
Objective Possible treatment
courses of disease,
hoped for and worst
case scenarios
Hopes and fears of
patient and family,
identify educational and
resource deficits
Change in treatment
goals, code status, limits
on intensity of treatment
POLST form, follow-up,
out-patient support and
resources, negotiated
criteria for discharge
137. 137
V.A.L.U.E.
• Value family statements
• Acknowledge family emotions
• Listen to the family
• Understand the patient as a person
• Elicit family questions
Chest. 2008 Oct; 134(4): 835–843
138. 138
Family Meeting Talking Map
Step What you can say
Gather for a pre-meeting “Let’s decide who will talk about what.”
“Could I propose a way to structure the meeting?”
“When the meeting ends, what would be a constructive outcome?”
Introduce everyone and the agenda “Let’s start with introductions. My name is [x], and my role is [y].”
“The purpose of this meeting is to talk about [z].”
“Is there anything that you would like to cover in addition?”
Explain what’s happening “Tell me what you took away from our last conversation.”
“Could I hear from everybody?”
“Here is the most important piece of news.”
Empathize with each person “I can see you are concerned about [a].”
“I am impressed that you have been here to support [patient’s name].”
Highlight the patient’s voice “If [patient’s name] could speak, what do you think she would say?”
“How would she talk about what is important to her?”
Plan the next steps together “Based on what we’ve talked about, could I make a recommendation?”
“I’d like to hear everyone’s thoughts about the plan.”
Reflect post-meeting “What did we learn?”
vitaltalk.org
139. 139
Pre-Meeting
• If you do this right, someone is going to need a tissue.
• Where is the meeting taking place and is the patient
participating?
• Is the meeting place clear of distractions and can everyone
sit down?
• What are the desired outcomes?
• Who is going to moderate the meeting?
• What is each person’s clinical communication
responsibility?
140. 140
Sitting in the Right Setting
Actual and patient perceived time of provider at
bedside
1.04 1.28
5.14
3.44
0
1
2
3
4
5
6
Sit Stand
Actual
Time (min)
Perceived
Time (min)
Percentage of positive and negative comments by
provider posture
95%
61%
5%
39%
0%
20%
40%
60%
80%
100%
Sit (n = 20) Stand (n = 18)
K.J. Swayden et al./ Patient Education and Counseling 86 (2012) 166–171
141. 141
Impact of Physician Sitting Versus Standing
• 69 patient randomized to watch one of two videos
in which physician was standing then sitting or
sitting than standing:
– 51% preferred the sitting physician
– 23% standing
– 26% no difference
J of Pain and Symp Management 2005; Vol 29 (5). 489-497
142. 142
An AIDET Application
• Acknowledge
– “Nice to meet you.”
– “Great to see you again.”
– Not: “You look great” (the patient might not feel great!)
• Introduce
– “Let’s go around the room so everyone knows who is who. My
name is [x], and my role is [y].
• Duration
– “We have about 30 minutes to talk today as a group. I would be
happy to spend more time with you afterward if needed.”
• Explanation
– “The purpose of this meeting is to talk about [z].”
• Thank You
– “Thank you all for taking the time to meet today.”
www.studergroup.com/aidet
Goldman W, The Princess Bride, 1973
143. 143
Agenda Setting
Step What you say
Ask about your patient’s
main concerns for the visit
“What are the important questions you wanted answered today?”
“Is there anything you wanted to ask your physicians about?”
“Do you have anything to put on our agenda?”
“Anything else?” (often the most important issue is not first)
Explain your agenda “There are two things I wanted to make sure we talked about…”
Propose an agenda that
combines the patient’s and
your concerns
“How about if we talk about your question first, then cover my two things?”
or
“Given these things, what is most important for you to cover?”
Be prepared to negotiate.
“Ok, I understand that the most important issue for you today is ___.”
“I hear that you have a number of questions. Could we prioritize them so that we cover
the most important ones if we don’t have time to get through all of them?”
Ask for feedback “Do you feel like we’ve covered the agenda? How did we do?”
Fortin AH, Dwamena FC, Frankel RM, Smith RC. Smith’s Patient Centered Interviewing: An Evidence-Based Method 3rd Ed. McGraw-Hill Lange
vitaltalk.org
144. 144
Explain What’s Happening
Cure •“Fix it”, healed
•Treatment = cure
Delay
•Slow it down,
“palliative
treatment”
•Treatment = not
dying
Die
•There’s “nothing”
left to do
•No treatment =
quitting
“Tell me what you took away from our last conversation.” “Could I hear from everybody?” “Here is
the most important piece of news.”
Where they
are
mentally
Where they
are clinically
145. 145
Teach-Back
A Priori A Posteriori
• Patient has seen a specialist or
been referred from another
physician.
• Minimum: Review documentation.
Ideally speak with other physician.
• “To make sure I provide you with
the best care, it helps me to
understand if you can tell me, in
your own words, what Dr. X, the
[specialty] doctor, explained to
you.”
• You are finishing your visit and
want to assess that the patient has
increased understanding of the
clinic situation.
• “We talked about a lot today and
sometimes I can get a little
technical. For my benefit, if you
were to explain the most important
points of today’s visit to your
family, what would you tell them?”
JBI Database System Rev Implement Rep. 2016 Jan;14(1):210-47
146. 146
E.M.P.A.T.H.Y
• Eye contact
• Muscle of facial expression
• Posture
• Affect
• Tone of voice
• Hearing the whole patient
• Your response
Academic Medicine 2014;vol 89 (8): 1108-1112
147. 147
Articulating Empathy
Tool Example Notes
Naming (1) “It sounds/looks like you are scared / sad /
frustrated”
Naming the emotion will usually decrease the
intensity of emotion
Understanding (<5) “This helps me understand what you are
thinking”
Use to convey acknowledgement while avoiding
implications that you understand “everything”
Respecting (1-2) “I can see you have really been trying to follow
our instructions”
Give the patient/family credit for what they have
done, praise is a motivator
Supporting (1-2) “I will do my best to make sure you have what
you need”
Commit 100% of what you can commit to without
committing to things beyond your control
Exploring (∞) “Could you say more about what you mean
when you say that…”
Open-beginning statement with a focused end
www.vitaltalk.org/sites/default/files/quick-guides/NURSEforVitaltalkV1.0.pdf
148. 148
Naming the Four Basic Human Emotions
Happy
Sad
Scared Angry
J Exp Psychol Gen. 2016 Jun;145(6):708-30
149. 149
Silence
Type of Silence Clinician Intent
Awkward Often without clear intention (uncertainty), but also may reflect distractedness
or hostility, often masked by the clinician.
Invitational Wanting to give the patient a moment (or longer) to think about or feel what is
happening, often after an empathic response. The clinician deliberately creates
a silence meant to convey empathy, allow a patient time to think or feel, or to
invite the patient into the conversation in some way.
Compassionate Recognizing a spontaneous moment (or longer) of silence that has emerged in
the conversation, often when the clinician and patient share a feeling or the
clinician is actively generating a sense of compassion for the patient. The
clinician must:
• Give attention
• Maintain stable focus
• Have clarity of perception
J Palliat Med. 2009 Dec;12(12):1113-7.
150. 150
Three-step Approach to Patient- and Family-
Centered Decision Making
Assess prognosis
and certainty of
prognosis
Assess family
preference for
role in decision-
making
Adapt
communication
strategy based
in patient and
family factors
and reassess
regularly
SharedDecisionMaking
Chest. 2008 Oct; 134(4): 835–843
151. 151
Plan Medical Treatments that Match Patient Values
Parentalism
“Doctor Decides”
“Would it be helpful if I made
a recommendation?”
Autonomy
“Patient/Family Decides”
“Would it be helpful to have
some time to talk with your
family about this?”
“Here’s what I can do now that will help you do those important things. What do you think about it?”
152. 152
Align With the Patient’s Values
Decisional Patient
• Acknowledge and address patient
and family emotions (empathy).
• Explore and focus on patient values
and treatment preferences:
– “As I listen to you, it sounds the most
important things are [x,y,z].”
Non-Decisional Patient
• Acknowledge and address family
emotions (empathy).
• Explore family’s understanding of
patient values and focus patient’s
values on treatment preferences.
• Explain the principle of surrogate
decision making to the family – the
goal of surrogate decision making is
to determine what the patient would
want if the patient were able to
participate.
Chest. 2008 Oct; 134(4): 835–843
153. 153
Plan the Next Steps Together
“Based on what we’ve talked about, could I make a recommendation?” “I’d like to hear everyone’s
thoughts about the plan.”
Care to
Cure
•Probabilities
•Side effects
•Disease > Patient
Care to Slow
Progression
•Time
•Side effects
•Disease > Patient
Care to
Allow Death
•Reframing
concept of disease
care
•Patient > Disease
154. 154
Expect Questions About More Curative Treatment
•Testing
•DocTx •Testing
•DocTx •Testing
•DocTx
No Tx
No Testing
No Doc
Death
“Here are the pros and cons of what you are asking about. Overall, my experience tells me that more [x] would do more harm than good
at this point. It’s hard to say that though." “The treatment has become worse than the disease.”
155. 155
Plan Medical Treatments that Match Patient Values
Patient Values
• Identify what is important to and priorities for
the patient.
• Identify what they hope to achieve by receiving
care.
• Identify what they fear will happen because of
the disease.
Plan Medical Treatments
• Representation of the goals of care in the form
of
– Documentation
• Advance Directive
• Living Will
• HCPOA
– Orders
• POLST
• Code Status
– Medications
• Starting and stopping
– Services
• Social Work
• Chaplaincy
• Hospice
• Home Health
National Committee for Quality Assurance: Goals to Care
156. 156
Talk About Services that Would Help Before Introducing Hospice
• “We’ve talked about wanting to
conserve your energy for important
things. One thing that can help us is
having a nurse come to your house to
can help us adjust your medicines so
you don’t have to come in to clinic so
often. The best way I have to do that
is to call hospice, because they can
provide this service for us, and
more.”
It's a service not a sentence (it's
hospice not house arrest).
Hospice is a program, not a place.
Patient's with an estimated life-span
of less than six months who are no
longer candidates for curative
therapy are eligible for services.
Patient's requiring active symptom
management, who are too tenuous
to move, or are actively dying may
be eligible for in-patient hospice. In
these patients death is expected
within 5 days.
157. 157
Post-Meeting Reflection
• What worked well?
• What could have been better?
• What changes to the plan of care need to be taken
care of?
• What are the next steps?
158. 158
Homework
• CAPC Central
– Home ► Training Curriculum ► Symptom Management
Curriculum ►Communication Skills Curriculum
• VitalTalk
– Review videos
160. 160
Nutrition Dependent Disease And Disease Independent of Nutrition
Malnutrition
• Malnutrition or malnourishment
is a condition that results from
eating a diet in which nutrients
are either not enough or are too
much such that the diet causes
health problems.
Cachexia
• Cachexia or wasting syndrome is
loss of weight, muscle atrophy,
fatigue, weakness, and significant
loss of appetite in someone who
is not actively trying to lose
weight.
161. 161
Benefits of Artificial Nutrition and Hydration
• Physiological support for temporary inability to swallow or
to use their gastrointestinal tract due to otherwise
reversible conditions.
• Artificial nutrition and hydration (ANH) may prolong life
and allow a more accurate assessment of the patient's
chance of recovery.
• For patients with chronic disabilities who are unable to take
in adequate nutrition by mouth and who enjoy the life they
lead, ANH is physiologically and qualitatively useful.
Nutr Clin Pract. 2006 ;21:118-125
162. 162
Supportive NOT Curative
• ANH alone, while sometimes supportive, does not
cure or reverse any terminal or irreversible disease
or injury.
• Multiple studies have consistently failed to show
meaningful clinical benefit from ANH in terminally
ill patients.
Nutr Clin Pract. 2006 ;21:118-125
Nutr Clin Pract.1994;9:91– 100
163. 163
System Shut Down
• Terminal illness is a biochemical and metabolic
process = slowing of bodily function.
– Loss of appetite and thirst.
– Difficulty swallowing.
– Simultaneous inability to utilize nutrients.
• Few symptoms from dehydration or lack of
nutrition.
ANH is “counterpalliative”
Palliat Support Care. 2006;4:135–43.
NEJM. 2004;350:2582–90.
Medsurg Nurs. 2000;9:233–44.
164. 164
Little Quantity-of-Life, Less Quality-of-Life
• ANH support by either the enteral or parenteral route
to terminally ill patients suggests increased suffering
without improved outcome.
• ANH, whether provided by “feeding tube” or vein, is
often associated with significant complications,
including bleeding, infection, physical restraints such as
tying the patient down, and in some cases a more
rapid death.
• TPN does not alleviate hunger.
JAMA.1999 ;282:1365– 1370
J Gerontol.1998 ;53:M207– M213
Lancet.1997 ;349:496– 498
Appetite. 1989;13(2):129-41
165. 165
Artificial Nutrition and Hydration
• Amyotrophic lateral sclerosis
– Improves quality of life in patients with the bulbar form of
amyotrophic lateral sclerosis.
• Cancer
– A review of 70 published, prospective, randomized trials of ANH
among cancer patients failed to demonstrate the clinical efficacy of
nutrition support for such patients.
• Dementia
– Tube feeding does not increase life expectancy and worsens quality
of life in end-stage dementia, i.e. when dysphagia develops due to
dementia.
End-of-Life Indications and Contraindications
Clin Nutr. 2006 Apr;25(2):330-60
Nutr Clin Pract. 2006 ;21:118-125
167. 167
Emotional Perspective
• Family members
– Unwillingness to accept terminal prognosis.
– Belief in cruelty of dying process if ANH not
administered.
– Need to demand interventions to avoid guilt.
– Would not ask for themselves, but do ask for
family members.
• Physicians
– Lack of familiarity with palliative care
techniques and evidence.
– Length of time required to educate families
on true facts of ANH.
– Reimbursement for insertion of PEG tube, etc.
– Desire to avoid controversial discussions.
– Fears of litigation.
• Administrators
– Reimbursement for tube feedings, etc.
– Fear of regulatory sanctions if ANH not
administered (nursing homes).
– Extra time and staff needed to assist with oral
feedings in weakened or demented patients.
– Fears of litigation.
• Withholding ≠ Withdrawal
Clin Nutr. 2016 Jun;35(3):545-56
J Gen Intern Med. 2011 Sep;26(9):1053-8
J Am Med Dir Assoc. 2007;8:224–28.
168. 168
Ethical Perspective
• Prerequisites of artificial nutrition and hydration
are:
1. an indication for a medical treatment, and
2. the definition of a therapeutic goal to be achieved, and
3. the will of the patient and his or her informed consent.
In all cases however the treating physician has to take the
final decision and responsibility.
• Withholding = Withdrawal
Clin Nutr. 2016 Jun;35(3):545-56
J Gen Intern Med. 2011 Sep;26(9):1053-8
J Am Med Dir Assoc. 2007;8:224–28.
169. 169
C for Critical or Comfort
Critical Care
• Mechanical Ventilation
• Vasopressors
• Artificial Nutrition and Hydration
– D5 or D10 is not nutritional
support
Comfort Care
• Supplemental oxygen for comfort
• Symptom management
• Pleasure feeding
171. 171
Talk Early. Talk Often.
• Anticipate trajectory of disease so that you can
have continuing conversations about goals-of-care
and advance directives.
• Making decisions empowers patients and
decreases burden on family because these
conversations have already occurred.
172. 172
REMAP (ET) Artificial Nutrition and Hydration
Step What you say or do
Reframe why the artificial nutrition
and hydration aren’t appropriate.
You may need to discuss dysphagia or why artificial nutrition and hydration will not be helpful “Given this news, it
seems like a good time to talk about what to do now.”
Expect emotion and empathize.
“It’s hard to deal with all this.” “I can see you are really concerned about [x].” “Tell me more about that—what are
you worried about?” “Is it OK for us to talk about what this means?” “It is human nature to worry about feeding our
loved ones.”
Map the future.
“Given this situation, what’s most important for you?” “When you think about the future, are there things you want
to do?” “As you think towards the future, what concerns you?”
Align with the patient’s values. “As I listen to you, it sounds the most important things are [x,y,z]."
Plan medical treatments that match
patient values.
“Here’s what I can do now that will help you do those important things. What do you think about it?“ “Trying to
force calories down a tube won’t make you feel any better or live any longer. What do you think about talking about
things that we can do that will help you going forward?”
Expect questions about more
artificial nutrition and hydration
“Here are the pros and cons of what you are asking about. Overall, the studies of artificial nutrition and hydration in
advanced illness tells me that trying it would do more harm than good at this point.“ “’Pleasure feeding’ or ‘careful
hand feeding’ focuses on the humanness of enjoying the taste of favorite foods in the company of those we most
enjoy. If calories won’t fix their disease trying to push them will likely do more harm than good.”
Talk about continuing to provide
aggressive care but now focused on
comfort rather than cure.
“We can help your [x] have as much good time as they can going forward. We’ll focus on the joy of being able to
taste food and be around family. Does that sound like a good plan?”
vitaltalk.org
174. 174
Voluntary Stopping Eating and Drinking (VSED)
• Why?
– To preserve patient autonomy.
– To retain control.
– To hasten death because of unacceptable suffering without
infringing on fundamental ethical principles of Western
society.
– “Being tired of life” or “having it done”.
– Viewing themselves as a burden to their family members.
175. 175
Voluntary Stopping Eating and Drinking (VSED)
• Variant of stopping life-sustaining treatment.
• Not physician assisted suicide (PSA):
– Provider must assess decision making capacity.
– Provider need only agree not to interfere.
– Provider should be prepared to address symptom
burden.
• VSED usually leads to death in 1-3 weeks.
“The desire for a hastened death regularly occurs, but such thoughts are frequently kept secret by
patients unless clinicians specifically inquire.”
BMC Palliat Care. 2014 Jan 8;13(1)
Ann Intern Med. 2000 Mar 21;132(6):488-93
Widener Law Rev. 2011, 17: 351-361
177. 177
Admission and Increased Mortality
Cohort Number %
Died in ED 205 / 76,060 0.27
Died within 30 days of discharge from ED 111 / 59,366 0.19
Died within 30 days of being admitted from ED 876 / 16,489 4.6
Emerg Med J. Aug 2006; 23(8): 601–603
178. 178
Death Does NOT Respect Age
www.medicine.ox.ac.uk/bandolier/booth/Risk/dyingage.html
181. 181
End-of-Life Concepts
Years
• Terminally Ill / End-of-
Life Care (< 6 months)Months
• Imminent Death (< 2 weeks)
Weeks
• Actively Dying (< 3 days)
Days
Life Expectancy
J Pain Symptom Manage. 2014 Jan; 47(1): 77–89.
182. 182
Years – Months – Weeks – Days
Birth
Actively
Dying
Death
J Pain Symptom Manage. 2014 Jan; 47(1): 77–89.
Diagnosis
Treatment
New
Problem
183. 183
Case
• 46-year old male patient with stage IV colon cancer on
hospice. He is bed bound and receives all his care from
his wife, sister, and teenage son. He has minimal intake
and is sleeping more. When awake he remains at his
cognitive baseline. He states that he is comfortable.
• Vital signs are stable on exam. He is cachectic. No
pressure ulcers. He has drooping of the nasolabial folds
bilaterally. Abdomen is distended but non-tender.
186. 186
Palliative Performance Scale (PPS)
PPS Level Ambulation Activity & Evidence of Disease Self-Care Intake Conscious Level Life Expectancy
100% Full
Normal activity & work No
evidence of disease
Full Normal Full
90% Full
Normal activity & work Some
evidence of disease
Full Normal Full
80% Full
Normal activity with Effort
Some evidence of disease
Full Normal or reduced Full
70% Reduced
Unable Normal Job/Work
Significant disease
Full Normal or reduced Full Months
60% Reduced
Unable hobby/house work
Significant disease
Occasional assistance
necessary
Normal or reduced Full or Confusion
Weeks-
Months
50% Mainly Sit/Lie
Unable to do any work Extensive
disease
Considerable
assistance required
Normal or reduced Full or Confusion Weeks
40% Mainly in Bed
Unable to do most activity
Extensive disease
Mainly assistance Normal or reduced
Full or Drowsy +/-
Confusion
Weeks
30% Totally Bed Bound
Unable to do any activity
Extensive disease
Total Care Normal or reduced
Full or Drowsy +/-
Confusion
Days-Weeks
20% Totally Bed Bound
Unable to do any activity
Extensive disease
Total Care Minimal to sips
Full or Drowsy +/-
Confusion
Days
10% Totally Bed Bound
Unable to do any activity
Extensive disease
Total Care Mouth care only
Drowsy or Coma +/-
Confusion
Days
0% Death - - -
Victoria Hospice Society
188. 188
Syndrome of Imminent Death
• Early Stage
– Bed bound
– Loss of interest and/or ability to drink/eat
– Cognitive changes: increasing time spend sleeping and/or delirium
• Middle
– Further decline in mental status to obtundation
• Late
– “Death rattle”
– Coma
– Fever
– Altered respiratory pattern
– Mottled extremities
24 hours to 14 days
www.mypcnow.org/blank-iwkmp
189. 189
Identifying the Actively Dying Patient
Profound progressive weakness
Bed-bound state
Sleeping much of the time
Indifference to food and fluids
Difficulty swallowing
Disorientation to time, with increasingly short attention span
Low or lower blood pressure not related to hypovolemia
Urinary incontinence or retention caused by weakness
Oliguria (positive LR 15.2, 95% CI 13.4-17.1)
Drooping of the nasolabial fold (positive LR 8.3, 95% CI 7.7-8.9)
Loss of ability to close eyes (positive LR 13.6, 95% CI 11.7-15.5)
Nonreactive pupils (positive LR 16.7, 95% CI 14.9-18.6)
Hallucinations involving previously deceased important individuals
References to going home or similar themes
Changes in respiratory rate and pattern
Respiration with mandibular movement (positive LR 10, 95% CI 9.1-
10.9)
Cheyne-Stoke breathing (positive LR 12.4, 95% CI 10.8-13.9)
Apnea
Hyperextension of the neck (postive LR 7.3, 95% CI 6.7-8)
Grunting of the vocal cords (positive LR 11.8, 95% CI 10.3-13.4)
Noisy breathing, pooling of airway secretions — “death rattle” (positive
LR 9, 95% CI 8.1-9.8)
Mottling and cooling of the skin due to vasomotor instability with venous
pooling, particularly tibial
Dropping blood pressure with rising, weak pulse
Pulselessness of the radial artery (positive LR 15.6, 95% CI 13.7-17.4)
Mental status changes (terminal delirium, terminal restlessness,
agitation, coma)
Decreased response to verbal stimuli (positive LR 8.3, 95% CI 7.7-9)
Decreased response to visual stimuli (positive LR 6.7, 95% CI 6.3-7.1)
Bicanovsky L. Comfort Care: Symptom Control in the Dying. In: Palliative Medicine, Walsh D, Caraceni AT, Fainsinger R, et al (Eds), Saunders, Philadelphia 2009.
Oncologist. 2014;19(6):681
Cancer. 2015;121(6):960.
193. 193
Guidelines for Physicians Providing Comfort Care for Hospitalized Patients Who Are Near the End of Life
Blinderman CD, Billings JA. N Engl J Med 2015;373:2549-2561
194. 194
Case
• 83-year old female patient with end-stage COPD is on
comfort-only measures. She is nonverbal but appears
agitated, with her neck extended at the head, tachypnea,
use of accessory muscles, and tachypnea. She is on 4
L/min NC and is opiate naïve. The patient is being cared
for by a nurse who just graduated and is paging you for
orders as the patient just lost IV access.
195. 195
Question
A. Morphine 1 mg intramuscular Q6H PRN dyspnea
B. Lorazepam 1 mg sublingually Q1H PRN agitation
C. Oxycodone concentrate 10 mg sublingually Q1H
PRN dyspnea
D. Intubation and mechanical ventilation
What is the most appropriate course?
196. 196
Answer
A. Morphine 1 mg intramuscular Q6H PRN dyspnea
B. Lorazepam 1 mg sublingually Q1H PRN agitation
C. Oxycodone concentrate 10 mg sublingually Q1H
PRN dyspnea
D. Intubation and mechanical ventilation
What is the most appropriate course?
197. 197
National Cancer Institute: Last Days of Life (PDQ®)
• “Many patients fear uncontrolled pain during the final hours of
life, while others (including family members and some health
care professionals) express concern that opioid use may hasten
death. Experience suggests that most patients can obtain pain
relief during the final hours of life and that very high doses of
opioids are rarely indicated. Several studies refute the fear of
hastened death associated with opioid use. In several surveys of
high-dose opioid use in hospice and palliative care settings, no
relationship between opioid dose and survival was found.”
• The goal is to provide symptom management, specifically of
pain and dyspnea, not to cause death.
www.cancer.gov/cancertopics/pdq/supportivecare/lasthours/healthprofessional/page2
198. 198
Basics: Pain and Dyspnea
• First line for alleviation of pain and dyspnea is
opiates:
– Morphine IV 4-8 mg Q15MIN PRN
– Hydromorphone IV 0.6-1 mg Q15MIN PRN
– Fentanyl IV 50-100 mcg Q10MIN PRN
• Second line for alleviation of anxiety due to total
pain:
– Lorazepam 0.5-2 mg IV Q2H PRN
• Delirium should be managed with haloperidol 0.5
mg IV Q30MIN PRN
199. 199
Continuous Opioid Infusions
• If the patient has been receiving opiates calculate
rate based on total dosage in the past 24 hours.
• Titrate a continuous infusion rate every 8 hours by
the dosage of PRN pushes given in the past 8
hours, divided by 8.
200. 200
Case
• 64-year-old female with end-stage COPD and HFrEF was admitted
with acute respiratory failure. She had already completed a POLST
and was explicit that she is DNAR and did not wish to be placed on
invasive positive pressure ventilation. She has elected comfort
measures.
• On admission kidney and liver function were normal. She is on nasal
cannula 4 L/min. She has been given sublingual doses of morphine
for dyspnea and is still taking her home dose of scheduled
clonazepam.
• In the last 12 hours she has been observed speaking and seeing her
deceased parents and brother. She appears comforted and happy
regarding her perception of their presence.
203. 203
End-of-Life Dreams and Visions (ELDV)
• Most common dreams/visions include deceased
friends/relatives and living friends/relatives.
• Dreams/visions featuring the deceased were
significantly more comforting than those of the
living, living and deceased combined, and other
people and experiences.
• As death approaches, comforting dreams/visions of
the deceased became more prevalent.
Carefully distinguish between terminal agitation and ELDV
J Palliat Med. 2014 Mar;17(3):296-303
204. 204
Case
• 89-year-old male with HFpEF and chronic kidney disease
stage V is at home on hospice. He has gradually been less
active, more dependent for activities of daily living,
sleeping more, speaking and eating less. You are the
covering hospice physician when you get a telephone call
that the patient is awake, alert, showing more energy
and conversing more than he has in weeks.
205. 205
Question
A. Continue hospice and educate them about end-of-
life burst of energy.
B. Continue hospice and treat the patient for
terminal agitation.
C. Discharge from hospice as the patient is
improving.
D. Discharge from hospice and admit to the hospital
for work-up.
What should you tell the family?
206. 206
Answer
A. Continue hospice and educate them about end-
of-life burst of energy.
B. Continue hospice and treat the patient for
terminal agitation.
C. Discharge from hospice as the patient is
improving.
D. Discharge from hospice and admit to the hospital
for work-up.
What should you tell the family?
207. 207
End-of-Life Burst of Energy
• Some patients will have a sudden burst of energy
approximately 48 hours before death. This is not a
sign of improvement but may actually be a marker
of active dying.
www.niagarahospice.org/documents/final_journey.pdf