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Palliative Care vs. Curative Care
CME Provider Information
Satisfactory Completion
Learners must complete an evaluation form to receive a certificate of completion. You must participate
in the entire activity as partial credit is not available. If you are seeking continuing education credit for
a specialty not listed below, it is your responsibility to contact your licensing/certification board to
determine course eligibility for your licensing/certification requirement.
Physicians
In support of improving patient care, this activity has been planned and implemented by Amedco LLC and
VITAS®
Healthcare. Amedco LLC is jointly accredited by the Accreditation Council for Continuing Medical
Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses
Credentialing Center (ANCC), to provide continuing education for the healthcare team. Credit Designation
Statement – Amedco LLC designates this live activity for a maximum of 1 AMA PRA Category 1 CreditTM.
Physicians should claim only the credit commensurate with the extent of their participation in the activity.
CE Provider Information
VITAS Healthcare programs are provided CE credits for their Nurses/Social Workers and Nursing Home Administrators through:
VITAS Healthcare Corporation of Florida, Inc./CE Broker Number: 50-2135. Approved By: Florida Board of Nursing/Florida
Board of Nursing Home Administrators/Florida Board of Clinical Social Workers, Marriage and Family Therapy & Mental
Health Counseling.
VITAS Healthcare programs in Illinois are provided CE credit for their Nursing Home Administrators and Respiratory Therapists
through: VITAS Healthcare Corporation of Illinois, Inc./8525 West 183 Street, Tinley Park, IL 60487/NHA CE Provider Number:
139000207/RT CE Provider Number: 195000028/Approved By the Illinois Division of Profession Regulation for: Licensed
Nursing Home Administrators and Illinois Respiratory Care Practitioner.
VITAS Healthcare, #1222, is approved to offer social work continuing education by the Association of Social Work Boards
(ASWB) Approved Continuing Education (ACE) program. Organizations, not individual courses, are approved as ACE
providers. State and provincial regulatory boards have the final authority to determine whether an individual course may
be accepted for continuing education credit. VITAS Healthcare maintains responsibility for this course. ACE provider
approval period: 06/06/2021 – 06/06/2024. Social workers completing this course receive 1.0 ethics continuing
education credits.
VITAS Healthcare Corporation of California, 310 Commerce, Suite 200, Irvine, CA 92602. Provider approved by the
California Board of Registered Nursing, Provider Number 10517, expiring 01/31/2025.
Exceptions to the above are as follows: AL: No NHAs, DE: No NHAs, DC: No NHAs, GA: No NHAs, KS: No NHAs, NJ:
No NHAs, OH: No NHAs, PA: No NHAs, TX: No NHAs, VA: No NHAs, WI: No NHAs and Nurses are not required –
RT only receive CE Credit in Illinois
Goal
• To appreciate the historical perspective
of curative and palliative care
• To comprehend the impact of palliative and
hospice care on patients and families,
the hospital, and the health system for
persons with advanced illness
Objectives
• Describe the history and
philosophy of the hospice and
palliative movement
• Identify the difference between
palliative and curative care
• Demonstrate the benefits
of palliative care for patients
with advanced illness
• Discuss the benefits that hospice and
palliative care can bring to hospital and
health systems
• Review how hospice as a medical
specialty fits under the palliative
care umbrella
How People Die
Emanuel, et al. (2003). The Education in Palliative and End of Life Care Curriculum
(EPEC Project). Northwestern School University Feinberg School of Medicine.
< 10% die suddenly of an unexpected event,
heart attack (MI), accident, etc.
> 90% die of a protracted, life-threatening illness
• Predictable steady decline with a relatively
short “advanced” phase (cancer)
• Slow decline punctuated by periodic crises
(advanced cardiac disease, advanced lung
disease, Alzheimer’s/dementia)
Dying Then and Now
19th Century:
• In 1900, 4% of America’s population
was > 65 years of age1
• In 1900, life expectancy was
49 years of age2
• Most people died at home
Today:
• Over 17% of the US population
is > 65 years3
• 2021 life expectancy in the US
was 76.1 years4
• Approximately 25% of Americans
die in acute-care hospitals and
25% die in nursing homes5
1
US Census Bureau (2011; US Census Briefs). The Older Population: 2010. Retrieved from https://www.census.gov/prod/cen2010/briefs/c2010br-09.pdf
2US Centers for Disease Control. (2003). National Vital Statistics Reports, Volume 54/ Retrieved from https://www.cdc.gov/nchs/data/nvsr/nvsr54/nvsr54_14.pdf
3US Census Bureau, Current Population Survey, Annual Social and Economic Supplement, 2022. Retreived from: https://www.census.gov/data/tables/2022/demo/age-and-sex/2022-older-population.html
4National Center for Health Statistic, Centers for Disease Control and Prevention (2022). Life Expectancy in the U.S. Dropped for the Second Year in a Row in 2021. Retrieved from:
https://www.cdc.gov/nchs/pressroom/nchs_press_releases/2022/20220831.htm#:~:text=Other%20findings%20documented%20in%20the,2020%20to%2073.2%20in%202021.
5
Teno, et al. (2018) “Site of death, place of care, and health care transitions among US Medicare beneficiaries, 2000-2015.” JAMA 320.3: 264-271
Hospice History
• Linguistic root words:
– Hospital
– Hospitality
– Shelter
– Respite
– Caring
• A place of refuge and solace
Hospice History (cont.)
1967
Dame Cicely
Saunders
opened
St. Christopher’s
in London
1969
Publication of
“On Death and
Dying” by
Elisabeth
Kubler-Ross
brought
death and
dying into
the mainstream
1974
New Haven
Hospice of
Connecticut
established
1978
VITAS founded
1978
National Hospice
Organization
formed National
Hospice &
Palliative Care
Organization
(NHPCO)
Mission:
“To lead and
mobilize social
change for
improved care
at the end of life”
1982
President
Ronald Reagan
signed into law the
Medicare Hospice
Benefit, which was
capitated at
conservative rates,
making hospice
one of the original
risk-assuming
health entities
Palliative Care: Definition
National Hospice and Palliative Care Organization. (2020). Explanation of Palliative Care.
Retrieved from https://www.nhpco.org/palliative-care-overview/explanation-of-palliative-care/
Palliative care is patient- and family-centered
care that optimizes quality of life by anticipating,
preventing, and treating suffering. Palliative care
throughout the continuum of illness involves
addressing physical, intellectual, emotional,
social, and spiritual needs, and facilitating patient
autonomy, access to information, and choice.
– National Consensus Project for Quality Palliative Care
Explanation of Palliative Care
National Coalition for Hospice and Palliative Care. (2018). Clinical Practice Guidelines for Quality Palliative Care, 4th Edition.
Retrieved from https://www.nationalcoalitionhpc.org/wp-content/uploads/2018/10/NCHPC-NCPGuidelines_4thED_web_FINAL.pdf
• Palliative care is:
– Appropriate at any stage
in a serious illness
– Beneficial when provided
along with curative treatments
– Provided over time to patients
based on their needs
– Offered in all care settings
– Focused on what is most
important to the patient,
family, and caregiver(s)
– Interdisciplinary to attend
to the patient's holistic
care needs
Palliative Care
• Manages pain and symptoms
• Regards dying as a
normal process
• Neither hastens nor
postpones death
• Integrates psychological and
spiritual care
• Supports patient and family
• Incorporates a team approach
• Enhances quality of life
• Is applicable early in the
course of illness
Palliative Care: Clinical Expertise
• Symptom management
in advanced illness:
–Pain
–Dyspnea
–Nausea and vomiting
–Fatigue
–Anxiety and depression
• Care transitions and
coordination of care
• Goals-of-care/end-
of-life discussions
– Timely hospice
referral and admission
How Does Hospice Differ From Palliative Care?
Palliative Care
Hospice
Traditional Model
Continuum of Care - Traditional
Curative/Restorative Therapy
Presentation/
Diagnosis
Acute
Illness
Chronic
Death
End-Stage
Hospice/Palliative Care Interface
Robinson, et al. (2004). Assessment of the education for physicians on end-of-life care (EPEC™) project. Journal of Palliative Medicine, 7(5), 637-645.
Hospice
Curative/disease
modifying therapy
Time course
of illness
Last months
of life
Palliative care
Family
bereavement care
Palliative Care and Hospice Care
Eligibility
Palliative Care
• No prognosis requirements
Hospice
• 6 months or less on average,
should the advanced illness run
its normal and expected course
• Physician estimate
• Clinical determination
Reimbursement Mechanism
Palliative Care
• Fee-for-service
• Grants
• Member-based per month
(health plan contracted)
• Value-based insurance
design (VBID)
Hospice
• Medicare Part A
• Medicaid
• Private insurance
• Charity care
Location of Care
Hospice
• Patient home:
– Private residence
– Assisted living
– Long-term care
• Level of care:
– Routine home care
– Continuous care
– Inpatient care
– Respite care
Palliative Care
• Fee-for-service:
– Hospital
– Outpatient
– Skilled facilities
– Long-term care
• Member per month:
– Community-dwelling
85%
7%
5%
1%
1%
1%
Medicare Hospice Benefit
Private Insurance/Managed Care
Medicaid Hospice Benefit
Other Payment Source
Self-Pay
Charity or Uncompensated Care
Who Pays for Hospice?
National Hospice and Palliative Care Organization. (2014). 2014 NHPCO Facts and Figures. NHPCO.org
Community-Based Palliative Care Demonstration Model
• Proposed by the National
Hospice and Palliative Care
Organization (NHPCO) and
National Coalition for
Hospice and Palliative
Care (NCHPC)
• Would be implemented by
Centers for Medicare and
Medicaid Innovation (CMMI)
• Expands interdisciplinary
care access to people with
serious illness nationwide
• Eliminates 6-month
prognosis requirement
• Aims to be proactive;
anticipates and preempts
future ED usage due
to decompensation
Professional Services
Palliative Care
• Depends upon the
goals and resources
of the program
• No regulatory
requirements
Hospice
• Core services:
– Physician
– Nurse
– Social worker
– Pastoral counselor
• Non-core services:
– OT/PT/speech
– CNA/aide
– Volunteer
• Additional support:
– Respiratory therapy
– Music, massage,
pet, etc.
Other Support
Palliative Care
• No required services
Hospice
• Medications
• Equipment
• Bereavement care
• 24-hour availability
• Supplies:
– Incontinence products
– Nutritional support
– Wound care products
The Symptom Burden of Serious Illness
Seale, et al. (1994). The Year Before Death. Beatty.
Symptom Cancer
Other
Illnesses
Symptom Cancer
Other
Illnesses
Pain 84% 67% Depression 38% 36%
Trouble breathing 47% 49% Loss of appetite 71% 38%
Nausea and
vomiting
51% 27% Constipation 47% 32%
Sleeplessness 51% 36% Bedsores 28% 14%
Confusion 33% 38% Incontinence 37% 33%
Early Palliative Care in Lung Cancer
Temel, et al. (2010). Early palliative care for patients with metastatic non-small-cell lung cancer. New England Journal of Medicine, Aug 19;363(8):733-42.
0
10
20
30
40
50
HADS-D HADS-A PHQ-9
Standard Care Early Palliative Care
Concurrent Palliative Care in Metastatic Lung Cancer
Temel, et al. (2010). Early palliative care for patients with metastatic non-small-cell lung cancer. New England Journal of Medicine, Aug 19;363(8):733-42.
Patients who die on hospice live
on average 30 days longer than
those who die without it.
Lung Cancer
CHF Colon Cancer
Comparing Hospice and Non-Hospice Survival
Connor, et al. (2007). Comparing hospice and non-hospice patient survival among patients who die within a three-year window. Journal of Pain Symptom Management, 33(3):238-46.
Palliative Care Programs: Center to Advance
Palliative Care (CAPC)
Center to Advance Palliative Care. (2020). The Case for Palliative Care. Retrieved from https://www.capc.org/the-case-for-palliative-care/
• Palliative care teams working
in hospitals:
– Improve patient and family
satisfaction with care
– Reduce 30-day readmission rates
– Reduce ICU utilization
– Can save 9-25% of costs for each
inpatient stay through a mixture of
shorter length of stay and reduced
cost per day
• Palliative care teams working in
home-based programs:
– Have been shown to save ACOs, health
plans, and health systems as much as
$12,000 per person enrolled
– Reduce emergency department visits,
hospital admissions, hospital
readmissions, and hospital length of stay
• Health plans that train case managers in
skills specific to this patient population and
who provide expanded access to specialty
palliative care have seen similar savings
while maintaining high rates of satisfaction
0
200
400
600
800
1000
1200
Direct
Cost
per
Day,
$
0
200
400
600
800
1000
1200
1400
1600
1800
2000
-6 -5 -4 -3 -2 -1 0 1 2 3 4 5 6
Direct
Cost
per
Day,
$
Days Before and After Palliative Care Consultation
Cost Savings Associated With US Hospital Palliative Care
Consultation Programs
Morrison, et al. (2008). Cost savings associated with US hospital palliative care consultation programs. Archives of Internal Medicine, 168(16):1783-1790.
Mean direct costs per day for palliative care patients who were discharged alive (A) or died (B) before and after palliative care consultation.
The solid line represents the regression curve of actual costs before palliative care consultation (day 0) and estimated costs (days 1-6) assuming
that palliative care consultation had not occurred. The dashed line represents direct costs per day for usual care patients for the 6 days before and
after hospital day 6 (patients with lengths of stay of ≤ 10 days), hospital day 10 (for patients with lengths of stay of 11-20 days), or hospital day
18 (for patients with lengths of stay of > 20 days).
Before palliative care consultation
After palliative care consultation
Day of palliative care consultation
A B
Cost Savings Associated With US Hospital Palliative Care
Consultation Programs (cont.)
Morrison, et al. (2008). Cost savings associated with US hospital palliative care consultation programs. Archives of Internal Medicine, 168(16):1783-1790.
Mean direct costs per day for patients who died and who received palliative care consultation on hospital
days 7, 10, and 15 compared with mean direct costs for usual care patients matched by propensity score.
Hospital day 1 is the first full day after the day of admission.
250
500
750
1000
1250
1500
1750
2000
1 3 5 7 9 11 13 15 17 19 21 23 25
Direct
cost
per
day,
$
Usual care Palliative care consultation day 10
Palliative care consultation day 7 Palliative care consultation day 15
CAPC Cost Impact Analysis
Center to Advance Palliative Care. (2020). The Case for Palliative Care. Retrieved from https://www.capc.org/the-case-for-palliative-care/
Palliative Care Reduces Avoidable Spending and Utilization in All Settings
48%
Readmissions
28%
Cost day
50%
Admissions
35%
ED visits
43%
Hospital
ED Transfers
36%
Total Costs
INPATIENT OUTPATIENT SKILLED NURSING HOME-BASED
Routine Care vs. Inpatient Palliative Care
Gade, et al. (2008). Impact of an inpatient palliative care team: A randomized control trial. Journal of Palliative Medicine, 11(2): 180-90.
Outcome Inpatient Palliative Care Routine Care
Care experience 6.9 6.6
Doctor/nurses communication 8.3 7.5
ICU admissions on readmission 12 21
MSPB 6-months –4,855/patient –
Median hospice stay 24 days 12 days
Where Do Patients Spend Their Last Days?
National Hospice and Palliative Care Organization. (2018). 2018 NHPCO Facts and Figures. NHPCO.org
50
25
25
Without Hospice
Hospital
Home
Nursing Facility
7
48
32
11
2
With Hospice
Hospital
Home
Nursing Facility
Hospice Unit
Residential Care Facility
Hospice Days of Care
National Hospice and Palliative Care Organization. (2022). NHPCO Facts and Figures. Available at: https://www.nhpco.org/wp-content/uploads/NHPCO-Facts-Figures-2022.pdf/
≤2 Days ≤5 Days
≤17 Days
≤79 Days
≤264 Days
0
50
100
150
200
250
300
10th 25th 50th 75th 90th
Hospice
length
of
stay
among
decedents
(in
days)
Percentile
Last Place of Care Experience
Teno, et al. (2004). Family perspectives on end-of-life care at the last place of care. JAMA 291.1: 88-93.
Outcome Hospice Nursing Home Home Health Hospital
Not Enough Help
With Pain, %
18.3 31.8 42.6 19.3
Not Enough
Emotional Support, %
34.6 56.2 70 51.7
Not Always Treated
With Respect, %
3.8 31.8 15.5 20.4
Enough Information
About Dying, %
29.2 44.3 31.5 50
Quality Care Excellent, % 70.7 41.6 46.5 46.8
Hospice Decreases Acute-Care Utilization
Kelley, et al. (2013). Hospice enrollment saves money for Medicare and improves care quality across a number of different lengths-of-stay. Health Affairs, 32(3):552–561.
0.00
0.10
0.20
0.30
0.40
0.50
In-hospital deaths ICU admissions 30-day hospital readmissions
Incremental
reduction
in
various
outcomes
(proportion) 53-105 days
15-30 days
8-14 days
1-7 days
Hospice enrollment:
0
2
4
6
8
10
Hospital Days ICU days
Hospital
and
ICU
days
avoided
53-105 days
15-30 days
8-14 days
1-7 days
Hospice enrollment:
Ongoing Demonstration of Hospice Quality Advantage
to Patient, Families, and Caregivers
Aldridge M., et al. (2022). Association between hospice enrollment and total health care costs for insurers and families, 2002-2018. JAMA Health Forum. 3(2), e215104-e215104).
Harrison, et al. (2022). Hospice Improves Care Quality For Older Adults With Dementia In Their Last Month Of Life: Study examines hospice care quality for older adults with dementia
in their last month of life. Health Affairs, 41(6), 821-830.
Kleinpell, et al. (2019). Exploring the association of hospice care on patient experience and outcomes of care. BMJ Supportive & Palliative Care, 9(1), e13-e13.
Kumar, et al. (2017). Family perspectives on hospice care experiences of patients with cancer. Journal of Clinical Oncology, 35(4), 432.
Wright, et al. (2010). Place of death: correlations with quality of life of patients with cancer and predictors of bereaved caregivers' mental health. Journal of Clinical Oncology, 28(29), 4457.
*Cancer patients, when comparing death in hospital to death in hospice **Compared to death in ICU ***Compared to hospital deaths
Families remarked patients received
just the right amount of pain
medicine and help with dyspnea
Families of patients receiving >30
days of hospice reported the most
positive EOL outcomes
Families more often reported patients’
EOL wishes were followed and rated
quality of EOL care as excellent
Family
Less risk for
PTSD with home
hospice deaths**
Home hospice reduced risk
for prolonged grief disorder***
Hospice admission in last 6 months
of life correlated with increases in
patient satisfaction and better pain
control, reductions in hospital days
Less physical and
emotional distress and
better quality of life at EOL*
Caregivers
Patients
60% reduction in end-of-life transitions, allowing patients to die in location of choice
Hospice beneficiaries saw
a cost savings of $670 in
out-of-pocket expenses
during the last month
of life compared to
non-hospice users
Total Cost of Care Comparison by Disease State and
Hospice Use in Last Year of Life*
*To be eligible to elect hospice care under Medicare, an individual must be entitled to Part A of Medicare and be certified as being terminally ill. An individual is
considered to be terminally ill if the medical prognosis is that the individual’s life expectancy is 6 months or less if the illness runs its normal course. Only care
provided by (or under arrangements made by) a Medicare certified hospice is covered under the Medicare hospice benefit. The hospice admits a patient only
on the recommendation of the medical director in consultation with, or with input from, the patient's attending physician (if any).
NORC at the University of Chicago (2023). Value of Hospice in Medicare. Available at: https://www.nhpco.org/wp-content/uploads/Value_Hospice_in_Medicare.pdf
Disease
Group
No
Hospice
Hospice
< 15 Days 15 – 30 31 – 60 61 – 90 91 – 180 181 – 266 > 266
ALL $67,192 4% -5% -9% -12% -14% -10% -12%
Circulatory $66,041 7% -4% -8% -10% -11% -8% -10%
Cancer $76,625 10% -1% -6% -9% -13% -14% -20%
Neuro-
degenerative $61,004 12% -6% -9% -11% -11% -5% -4%
Respiratory $77,892 -2% -11% -14% -17% -19% -18% -22%
CKD/ESRD $82,781 1% -14% -21% -24% -24% -23% -27%
• Hospice care saved Medicare
approximately $3.5 billion for
patients in their last year of life
• Those patients with hospice
stays of ≥ 6 months* yielded
the highest percentage
of savings
– For patients whose hospice
stays were between 181-266
days, total cost of care
was almost $7K less than
non-hospice users
– Hospice patients with stays
of > 266 days spent
approximately $8K less
than non-hospice users
Spending is greater than Spending is less than
non-hospice users non-hospice users
No difference / not
statistically significant
The Medicare Hospice Benefit Is a 6-Month Benefit: Quality and
Cost Evidence Corroborate the Need for Timely Access*
*To be eligible to elect hospice care under Medicare, an individual must be entitled to Part A of Medicare and be certified as being terminally ill. An individual is considered to be
terminally ill if the medical prognosis is that the individual’s life expectancy is 6 months or less if the illness runs its normal course. Only care provided by (or under arrangements
made by) a Medicare certified hospice is covered under the Medicare hospice benefit. The hospice admits a patient only on the recommendation of the medical director in
consultation with, or with input from, the patient's attending physician (if any). under the Medicare hospice benefit. The hospice admits a patient only on the recommendation
of the medical director in consultation with, or with input from, the patient's attending physician (if any).
NORC at the University of Chicago (2023). Value of Hospice in Medicare. Available at: https://www.nhpco.org/wp-content/uploads/Value_Hospice_in_Medicare.pdf
Over the last 12 months
of life, as hospice use
increases, total spending
decreases relative to
non-hospice users.
The reduction in costs
when patients across all
disease classes, including
neurodegenerative
diseases, use hospice
can be significant.
Reasons for Readmission
• Failure in discharge planning
• Insufficient outpatient and
community care
• Advanced, progressive illness
Care Transitions
Medicare Hospice Benefit
Interdisciplinary Team of
Hospice Professionals
Home Medical
Equipment
Medication Bereavement
Support
Continuous
Care
Respite Care
Inpatient Care
Routine
Home Care
These Services Are Mandated by the Medicare Hospice Benefit
1. Routine home care 98.7%
• Most common level of hospice care
• More robust and comprehensive
compared to home health
care services
• Patient’s preferred setting
• Proactive clinical approach helps
prevent ED visits/hospital readmissions
2. Intensive Comfort Care®
(continuous care) 0.2%
• Medical management in the home
for up to 24 hours per day for
acute symptom management
when medically appropriate
3. Inpatient care 1.0%
• For symptoms that cannot be
managed in the home
4. Respite 0.2%
• Provides a temporary break
for primary caregiver
• Inpatient setting
• Up to 5 days of 24-hour patient
care management when
medically appropriate
Four Levels of Hospice Care
National Hospice and Palliative Care Organization. (2022). Facts & Figures: Hospice Care in America. Available at: https://www.nhpco.org/hospice-care-overview/hospice-facts-figures/
Interdisciplinary Hospice Team
Patient and
Family
Volunteers
Physicians
Spiritual
Counselors
Social
Workers
Bereavement
Counselors
Hospice
Aides
Therapists
Nurses
Hospice: Right Care at the Right Time
Hospice Palliative Care Home Health
Eligibility Requirements
Prognosis required: ≤ 6 months
if the illness runs its usual course
Prognosis varies by program,
usually life-defining illness
Prognosis not required
Skilled need not required Skilled need not required Skilled need required
Plan of Care Quality of life and defined goals Quality of life and defined goals Restorative care
Length of Care Unlimited Variable Limited, with requirements
Homebound Not required Not required Required, with exceptions
Targeted Disease-Specific Program ✓ Variable Variable
Medications Included ✓ X X
Equipment Included ✓ X X
After-Hours Staff Availability ✓ X X
RT/PT/OT/Speech ✓ X ✓
Nurse Visit Frequency Unlimited Variable Limited, based on diagnosis
Palliative Care Physician Support ✓ Variable X
Levels of Care 4 1 1
Bereavement Support ✓ X X
Bereavement
Support groups
Bereavement specialists offer
support for a minimum of
13 months following a death
Individual grief support and
grief education resources
Memorial activities
Hospice Impact: Satisfaction
Kumar, P., et al. (2017). Family perspectives on hospice care experiences of patients with cancer. Journal of Clinical Oncology, 35(4), 432.
• Hospice care is associated
with better symptom relief,
patient goal attainment, and
quality of EOL care.
• Families of patients enrolled
in hospice more often reported
that patients received “just
the right amount” of pain
medicine and help with dyspnea.
• Families of patients enrolled
in hospice also more often
reported that patients’ EOL
wishes were followed and EOL
care was “excellent.”
• Families of patients who
received > 30 days of hospice
care reported the highest
quality EOL outcomes.
Hospice: In Conclusion
• Hospice is:
– A service, not a place
– Provided in the patient’s preferred
setting, whether
a private residence, nursing home,
assisted living facility, or inpatient
hospice setting
– Care that comforts and supports
when an advanced illness no longer
responds to curative treatments
– Making the most of the time
that remains
– Covered by the Medicare
Hospice Benefit
Summary
• Palliative care supports persons with advanced
illness and facilitates more timely hospice referral
• Hospice and palliative care support:
– Patients and families
– Clinicians
– Hospitals and health systems
• All successful palliative care programs
partner with a hospice
Partner With Hospice
“You matter because you are you.
You matter to the last moment of life, and
we will do all we can, not only to help you
die peacefully, but also to live until you die.”
—Dame Cicely Saunders
St. Christopher’s Hospice London, England
Questions?
Additional Hospice Resources
The VITAS mobile app includes helpful
tools and information:
• Interactive Palliative Performance
Scale (PPS)
• Body-Mass Index (BMI) calculator
• Opioid converter
• Disease-specific hospice
eligibility guidelines
• Hospice care discussion guides
We look forward to having you attend
some of our future webinars!
Scan now to
download the
VITAS app.
References
Aldridge M., et al. (2022). Association between hospice enrollment and total health care costs for insurers and families, 2002-2018.
JAMA Health Forum. 3(2), e215104-e215104).
Center to Advance Palliative Care. (2020). The Case for Palliative Care. Retrieved from https://www.capc.org/the-case-for-palliative-care/
Connor, et al. (2007). Comparing hospice and non-hospice patient survival among patients who die within a three-year window.
Journal of Pain Symptom Management, 33(3):238-46.
Emanuel, et al. (2003). The Education in Palliative and End of Life Care Curriculum (EPEC Project). Northwestern School University
Feinberg School of Medicine.
Gade, et al. (2008). Impact of an inpatient palliative care team: A randomized control trial. Journal of Palliative Medicine, 11.2: 180-190.
Harrison, et al. (2022). Hospice Improves Care Quality For Older Adults With Dementia In Their Last Month Of Life: Study examines
hospice care quality for older adults with dementia in their last month of life. Health Affairs, 41(6): 821-830.
Kelley, et al. (2013). Hospice enrollment saves money for Medicare and improves care quality across a number of different lengths-of-stay.
Health Affairs, 32(3): 552–561
Kleinpell, et al. (2019). Exploring the association of hospice care on patient experience and outcomes of care. BMJ Supportive &
Palliative Care, 9(1): e13-e13.
Kumar, et al. (2017). Family perspectives on hospice care experiences of patients with cancer. Journal of Clinical Oncology,
35(4): 432.
References (cont.)
MedPac March 2023 Report to the Congress: Medicare Payment Policy, Figure 10-2. Available at: https://www.medpac.gov/
document/march-2023-report-to-the-congress-medicare-payment-policy/
Morrison, et al. (2008). Cost savings associated with US hospital palliative care consultation programs. Archives of Internal
Medicine, 168(16): 1783-1790
National Center for Health Statistics, Centers for Disease Control and Prevention (2022). Life Expectancy in the U.S.
Dropped for the Second Year in a Row in 2021. Retrieved from: https://www.cdc.gov/nchs/pressroom/nchs_press_releases/
2022/20220831.htm#:~:text=Other%20findings%20documented%20in%20the,2020%20to%2073.2%20in%202021.
National Coalition for Hospice and Palliative Care. (2018). Clinical Practice Guidelines for Quality Palliative Care, 4th Edition.
Retrieved from https://www.nationalcoalitionhpc.org/wp-content/uploads/2018/10/NCHPC-NCPGuidelines_4thED_web_FINAL.pdf
National Hospice and Palliative Care Organization. (2018). 2018 NHPCO Facts and Figures. NHPCO.org
National Hospice and Palliative Care Organization. (2014). 2014 NHPCO Facts and Figures. NHPCO.org
National Hospice and Palliative Care Organization. (2020). Explanation of Palliative Care. Retrieved from https://www.nhpco.org/
palliative-care-overview/explanation-of-palliative-care/
National Hospice and Palliative Care Organization. (2022). 2022 NHPCO Facts and Figures. Retrieved from: https://www.nhpco.org/
wp-content/uploads/NHPCO-Facts-Figures-2022.pdf/
References (cont.)
Robinson, et al. (2004). Assessment of the education for physicians on end-of-life care (EPEC™) project. Journal of Palliative
Medicine, 7(5): 637-645.
Seale, et al. (1994). The Year Before Death. Beatty.
Temel, et al. (2010). Early palliative care for patients with metastatic non-small-cell lung cancer. New England Journal of Medicine,
Aug 19;363(8): 733-42.
Teno, et al. (2004). “Family perspectives on end-of-life care at the last place of care.” JAMA 291.1: 88-93.
U.S. Census Bureau, Current Population Survey, Annual Social and Economic Supplement, 2022. Retreived from:
https://www.census.gov/data/tables/2022/demo/age-and-sex/2022-older-population.html
US Census Bureau (2011; US Census Briefs). The Older Population: 2010. Retrieved from https://www.census.gov/prod/cen2010/
briefs/c2010br-09.pdf
US Centers for Disease Control. (2003). National Vital Statistics Reports, Volume 54. Retrieved from: https://www.cdc.gov/nchs/
data/nvsr/nvsr54/nvsr54_14.pdf
Wright, et al. (2010). Place of death: correlations with quality of life of patients with cancer and predictors of bereaved caregivers’
mental health. Journal of Clinical Oncology, 28(29): 4457.
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Palliative Care vs. Curative Care - December 2023

  • 1. Palliative Care vs. Curative Care
  • 2. CME Provider Information Satisfactory Completion Learners must complete an evaluation form to receive a certificate of completion. You must participate in the entire activity as partial credit is not available. If you are seeking continuing education credit for a specialty not listed below, it is your responsibility to contact your licensing/certification board to determine course eligibility for your licensing/certification requirement. Physicians In support of improving patient care, this activity has been planned and implemented by Amedco LLC and VITAS® Healthcare. Amedco LLC is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team. Credit Designation Statement – Amedco LLC designates this live activity for a maximum of 1 AMA PRA Category 1 CreditTM. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
  • 3. CE Provider Information VITAS Healthcare programs are provided CE credits for their Nurses/Social Workers and Nursing Home Administrators through: VITAS Healthcare Corporation of Florida, Inc./CE Broker Number: 50-2135. Approved By: Florida Board of Nursing/Florida Board of Nursing Home Administrators/Florida Board of Clinical Social Workers, Marriage and Family Therapy & Mental Health Counseling. VITAS Healthcare programs in Illinois are provided CE credit for their Nursing Home Administrators and Respiratory Therapists through: VITAS Healthcare Corporation of Illinois, Inc./8525 West 183 Street, Tinley Park, IL 60487/NHA CE Provider Number: 139000207/RT CE Provider Number: 195000028/Approved By the Illinois Division of Profession Regulation for: Licensed Nursing Home Administrators and Illinois Respiratory Care Practitioner. VITAS Healthcare, #1222, is approved to offer social work continuing education by the Association of Social Work Boards (ASWB) Approved Continuing Education (ACE) program. Organizations, not individual courses, are approved as ACE providers. State and provincial regulatory boards have the final authority to determine whether an individual course may be accepted for continuing education credit. VITAS Healthcare maintains responsibility for this course. ACE provider approval period: 06/06/2021 – 06/06/2024. Social workers completing this course receive 1.0 ethics continuing education credits. VITAS Healthcare Corporation of California, 310 Commerce, Suite 200, Irvine, CA 92602. Provider approved by the California Board of Registered Nursing, Provider Number 10517, expiring 01/31/2025. Exceptions to the above are as follows: AL: No NHAs, DE: No NHAs, DC: No NHAs, GA: No NHAs, KS: No NHAs, NJ: No NHAs, OH: No NHAs, PA: No NHAs, TX: No NHAs, VA: No NHAs, WI: No NHAs and Nurses are not required – RT only receive CE Credit in Illinois
  • 4. Goal • To appreciate the historical perspective of curative and palliative care • To comprehend the impact of palliative and hospice care on patients and families, the hospital, and the health system for persons with advanced illness
  • 5. Objectives • Describe the history and philosophy of the hospice and palliative movement • Identify the difference between palliative and curative care • Demonstrate the benefits of palliative care for patients with advanced illness • Discuss the benefits that hospice and palliative care can bring to hospital and health systems • Review how hospice as a medical specialty fits under the palliative care umbrella
  • 6. How People Die Emanuel, et al. (2003). The Education in Palliative and End of Life Care Curriculum (EPEC Project). Northwestern School University Feinberg School of Medicine. < 10% die suddenly of an unexpected event, heart attack (MI), accident, etc. > 90% die of a protracted, life-threatening illness • Predictable steady decline with a relatively short “advanced” phase (cancer) • Slow decline punctuated by periodic crises (advanced cardiac disease, advanced lung disease, Alzheimer’s/dementia)
  • 7. Dying Then and Now 19th Century: • In 1900, 4% of America’s population was > 65 years of age1 • In 1900, life expectancy was 49 years of age2 • Most people died at home Today: • Over 17% of the US population is > 65 years3 • 2021 life expectancy in the US was 76.1 years4 • Approximately 25% of Americans die in acute-care hospitals and 25% die in nursing homes5 1 US Census Bureau (2011; US Census Briefs). The Older Population: 2010. Retrieved from https://www.census.gov/prod/cen2010/briefs/c2010br-09.pdf 2US Centers for Disease Control. (2003). National Vital Statistics Reports, Volume 54/ Retrieved from https://www.cdc.gov/nchs/data/nvsr/nvsr54/nvsr54_14.pdf 3US Census Bureau, Current Population Survey, Annual Social and Economic Supplement, 2022. Retreived from: https://www.census.gov/data/tables/2022/demo/age-and-sex/2022-older-population.html 4National Center for Health Statistic, Centers for Disease Control and Prevention (2022). Life Expectancy in the U.S. Dropped for the Second Year in a Row in 2021. Retrieved from: https://www.cdc.gov/nchs/pressroom/nchs_press_releases/2022/20220831.htm#:~:text=Other%20findings%20documented%20in%20the,2020%20to%2073.2%20in%202021. 5 Teno, et al. (2018) “Site of death, place of care, and health care transitions among US Medicare beneficiaries, 2000-2015.” JAMA 320.3: 264-271
  • 8. Hospice History • Linguistic root words: – Hospital – Hospitality – Shelter – Respite – Caring • A place of refuge and solace
  • 9. Hospice History (cont.) 1967 Dame Cicely Saunders opened St. Christopher’s in London 1969 Publication of “On Death and Dying” by Elisabeth Kubler-Ross brought death and dying into the mainstream 1974 New Haven Hospice of Connecticut established 1978 VITAS founded 1978 National Hospice Organization formed National Hospice & Palliative Care Organization (NHPCO) Mission: “To lead and mobilize social change for improved care at the end of life” 1982 President Ronald Reagan signed into law the Medicare Hospice Benefit, which was capitated at conservative rates, making hospice one of the original risk-assuming health entities
  • 10. Palliative Care: Definition National Hospice and Palliative Care Organization. (2020). Explanation of Palliative Care. Retrieved from https://www.nhpco.org/palliative-care-overview/explanation-of-palliative-care/ Palliative care is patient- and family-centered care that optimizes quality of life by anticipating, preventing, and treating suffering. Palliative care throughout the continuum of illness involves addressing physical, intellectual, emotional, social, and spiritual needs, and facilitating patient autonomy, access to information, and choice. – National Consensus Project for Quality Palliative Care
  • 11. Explanation of Palliative Care National Coalition for Hospice and Palliative Care. (2018). Clinical Practice Guidelines for Quality Palliative Care, 4th Edition. Retrieved from https://www.nationalcoalitionhpc.org/wp-content/uploads/2018/10/NCHPC-NCPGuidelines_4thED_web_FINAL.pdf • Palliative care is: – Appropriate at any stage in a serious illness – Beneficial when provided along with curative treatments – Provided over time to patients based on their needs – Offered in all care settings – Focused on what is most important to the patient, family, and caregiver(s) – Interdisciplinary to attend to the patient's holistic care needs
  • 12. Palliative Care • Manages pain and symptoms • Regards dying as a normal process • Neither hastens nor postpones death • Integrates psychological and spiritual care • Supports patient and family • Incorporates a team approach • Enhances quality of life • Is applicable early in the course of illness
  • 13. Palliative Care: Clinical Expertise • Symptom management in advanced illness: –Pain –Dyspnea –Nausea and vomiting –Fatigue –Anxiety and depression • Care transitions and coordination of care • Goals-of-care/end- of-life discussions – Timely hospice referral and admission
  • 14. How Does Hospice Differ From Palliative Care? Palliative Care Hospice
  • 15. Traditional Model Continuum of Care - Traditional Curative/Restorative Therapy Presentation/ Diagnosis Acute Illness Chronic Death End-Stage
  • 16. Hospice/Palliative Care Interface Robinson, et al. (2004). Assessment of the education for physicians on end-of-life care (EPEC™) project. Journal of Palliative Medicine, 7(5), 637-645. Hospice Curative/disease modifying therapy Time course of illness Last months of life Palliative care Family bereavement care
  • 17. Palliative Care and Hospice Care
  • 18. Eligibility Palliative Care • No prognosis requirements Hospice • 6 months or less on average, should the advanced illness run its normal and expected course • Physician estimate • Clinical determination
  • 19. Reimbursement Mechanism Palliative Care • Fee-for-service • Grants • Member-based per month (health plan contracted) • Value-based insurance design (VBID) Hospice • Medicare Part A • Medicaid • Private insurance • Charity care
  • 20. Location of Care Hospice • Patient home: – Private residence – Assisted living – Long-term care • Level of care: – Routine home care – Continuous care – Inpatient care – Respite care Palliative Care • Fee-for-service: – Hospital – Outpatient – Skilled facilities – Long-term care • Member per month: – Community-dwelling
  • 21. 85% 7% 5% 1% 1% 1% Medicare Hospice Benefit Private Insurance/Managed Care Medicaid Hospice Benefit Other Payment Source Self-Pay Charity or Uncompensated Care Who Pays for Hospice? National Hospice and Palliative Care Organization. (2014). 2014 NHPCO Facts and Figures. NHPCO.org
  • 22. Community-Based Palliative Care Demonstration Model • Proposed by the National Hospice and Palliative Care Organization (NHPCO) and National Coalition for Hospice and Palliative Care (NCHPC) • Would be implemented by Centers for Medicare and Medicaid Innovation (CMMI) • Expands interdisciplinary care access to people with serious illness nationwide • Eliminates 6-month prognosis requirement • Aims to be proactive; anticipates and preempts future ED usage due to decompensation
  • 23. Professional Services Palliative Care • Depends upon the goals and resources of the program • No regulatory requirements Hospice • Core services: – Physician – Nurse – Social worker – Pastoral counselor • Non-core services: – OT/PT/speech – CNA/aide – Volunteer • Additional support: – Respiratory therapy – Music, massage, pet, etc.
  • 24. Other Support Palliative Care • No required services Hospice • Medications • Equipment • Bereavement care • 24-hour availability • Supplies: – Incontinence products – Nutritional support – Wound care products
  • 25. The Symptom Burden of Serious Illness Seale, et al. (1994). The Year Before Death. Beatty. Symptom Cancer Other Illnesses Symptom Cancer Other Illnesses Pain 84% 67% Depression 38% 36% Trouble breathing 47% 49% Loss of appetite 71% 38% Nausea and vomiting 51% 27% Constipation 47% 32% Sleeplessness 51% 36% Bedsores 28% 14% Confusion 33% 38% Incontinence 37% 33%
  • 26. Early Palliative Care in Lung Cancer Temel, et al. (2010). Early palliative care for patients with metastatic non-small-cell lung cancer. New England Journal of Medicine, Aug 19;363(8):733-42. 0 10 20 30 40 50 HADS-D HADS-A PHQ-9 Standard Care Early Palliative Care
  • 27. Concurrent Palliative Care in Metastatic Lung Cancer Temel, et al. (2010). Early palliative care for patients with metastatic non-small-cell lung cancer. New England Journal of Medicine, Aug 19;363(8):733-42.
  • 28. Patients who die on hospice live on average 30 days longer than those who die without it. Lung Cancer CHF Colon Cancer Comparing Hospice and Non-Hospice Survival Connor, et al. (2007). Comparing hospice and non-hospice patient survival among patients who die within a three-year window. Journal of Pain Symptom Management, 33(3):238-46.
  • 29. Palliative Care Programs: Center to Advance Palliative Care (CAPC) Center to Advance Palliative Care. (2020). The Case for Palliative Care. Retrieved from https://www.capc.org/the-case-for-palliative-care/ • Palliative care teams working in hospitals: – Improve patient and family satisfaction with care – Reduce 30-day readmission rates – Reduce ICU utilization – Can save 9-25% of costs for each inpatient stay through a mixture of shorter length of stay and reduced cost per day • Palliative care teams working in home-based programs: – Have been shown to save ACOs, health plans, and health systems as much as $12,000 per person enrolled – Reduce emergency department visits, hospital admissions, hospital readmissions, and hospital length of stay • Health plans that train case managers in skills specific to this patient population and who provide expanded access to specialty palliative care have seen similar savings while maintaining high rates of satisfaction
  • 30. 0 200 400 600 800 1000 1200 Direct Cost per Day, $ 0 200 400 600 800 1000 1200 1400 1600 1800 2000 -6 -5 -4 -3 -2 -1 0 1 2 3 4 5 6 Direct Cost per Day, $ Days Before and After Palliative Care Consultation Cost Savings Associated With US Hospital Palliative Care Consultation Programs Morrison, et al. (2008). Cost savings associated with US hospital palliative care consultation programs. Archives of Internal Medicine, 168(16):1783-1790. Mean direct costs per day for palliative care patients who were discharged alive (A) or died (B) before and after palliative care consultation. The solid line represents the regression curve of actual costs before palliative care consultation (day 0) and estimated costs (days 1-6) assuming that palliative care consultation had not occurred. The dashed line represents direct costs per day for usual care patients for the 6 days before and after hospital day 6 (patients with lengths of stay of ≤ 10 days), hospital day 10 (for patients with lengths of stay of 11-20 days), or hospital day 18 (for patients with lengths of stay of > 20 days). Before palliative care consultation After palliative care consultation Day of palliative care consultation A B
  • 31. Cost Savings Associated With US Hospital Palliative Care Consultation Programs (cont.) Morrison, et al. (2008). Cost savings associated with US hospital palliative care consultation programs. Archives of Internal Medicine, 168(16):1783-1790. Mean direct costs per day for patients who died and who received palliative care consultation on hospital days 7, 10, and 15 compared with mean direct costs for usual care patients matched by propensity score. Hospital day 1 is the first full day after the day of admission. 250 500 750 1000 1250 1500 1750 2000 1 3 5 7 9 11 13 15 17 19 21 23 25 Direct cost per day, $ Usual care Palliative care consultation day 10 Palliative care consultation day 7 Palliative care consultation day 15
  • 32. CAPC Cost Impact Analysis Center to Advance Palliative Care. (2020). The Case for Palliative Care. Retrieved from https://www.capc.org/the-case-for-palliative-care/ Palliative Care Reduces Avoidable Spending and Utilization in All Settings 48% Readmissions 28% Cost day 50% Admissions 35% ED visits 43% Hospital ED Transfers 36% Total Costs INPATIENT OUTPATIENT SKILLED NURSING HOME-BASED
  • 33. Routine Care vs. Inpatient Palliative Care Gade, et al. (2008). Impact of an inpatient palliative care team: A randomized control trial. Journal of Palliative Medicine, 11(2): 180-90. Outcome Inpatient Palliative Care Routine Care Care experience 6.9 6.6 Doctor/nurses communication 8.3 7.5 ICU admissions on readmission 12 21 MSPB 6-months –4,855/patient – Median hospice stay 24 days 12 days
  • 34. Where Do Patients Spend Their Last Days? National Hospice and Palliative Care Organization. (2018). 2018 NHPCO Facts and Figures. NHPCO.org 50 25 25 Without Hospice Hospital Home Nursing Facility 7 48 32 11 2 With Hospice Hospital Home Nursing Facility Hospice Unit Residential Care Facility
  • 35. Hospice Days of Care National Hospice and Palliative Care Organization. (2022). NHPCO Facts and Figures. Available at: https://www.nhpco.org/wp-content/uploads/NHPCO-Facts-Figures-2022.pdf/ ≤2 Days ≤5 Days ≤17 Days ≤79 Days ≤264 Days 0 50 100 150 200 250 300 10th 25th 50th 75th 90th Hospice length of stay among decedents (in days) Percentile
  • 36. Last Place of Care Experience Teno, et al. (2004). Family perspectives on end-of-life care at the last place of care. JAMA 291.1: 88-93. Outcome Hospice Nursing Home Home Health Hospital Not Enough Help With Pain, % 18.3 31.8 42.6 19.3 Not Enough Emotional Support, % 34.6 56.2 70 51.7 Not Always Treated With Respect, % 3.8 31.8 15.5 20.4 Enough Information About Dying, % 29.2 44.3 31.5 50 Quality Care Excellent, % 70.7 41.6 46.5 46.8
  • 37. Hospice Decreases Acute-Care Utilization Kelley, et al. (2013). Hospice enrollment saves money for Medicare and improves care quality across a number of different lengths-of-stay. Health Affairs, 32(3):552–561. 0.00 0.10 0.20 0.30 0.40 0.50 In-hospital deaths ICU admissions 30-day hospital readmissions Incremental reduction in various outcomes (proportion) 53-105 days 15-30 days 8-14 days 1-7 days Hospice enrollment: 0 2 4 6 8 10 Hospital Days ICU days Hospital and ICU days avoided 53-105 days 15-30 days 8-14 days 1-7 days Hospice enrollment:
  • 38. Ongoing Demonstration of Hospice Quality Advantage to Patient, Families, and Caregivers Aldridge M., et al. (2022). Association between hospice enrollment and total health care costs for insurers and families, 2002-2018. JAMA Health Forum. 3(2), e215104-e215104). Harrison, et al. (2022). Hospice Improves Care Quality For Older Adults With Dementia In Their Last Month Of Life: Study examines hospice care quality for older adults with dementia in their last month of life. Health Affairs, 41(6), 821-830. Kleinpell, et al. (2019). Exploring the association of hospice care on patient experience and outcomes of care. BMJ Supportive & Palliative Care, 9(1), e13-e13. Kumar, et al. (2017). Family perspectives on hospice care experiences of patients with cancer. Journal of Clinical Oncology, 35(4), 432. Wright, et al. (2010). Place of death: correlations with quality of life of patients with cancer and predictors of bereaved caregivers' mental health. Journal of Clinical Oncology, 28(29), 4457. *Cancer patients, when comparing death in hospital to death in hospice **Compared to death in ICU ***Compared to hospital deaths Families remarked patients received just the right amount of pain medicine and help with dyspnea Families of patients receiving >30 days of hospice reported the most positive EOL outcomes Families more often reported patients’ EOL wishes were followed and rated quality of EOL care as excellent Family Less risk for PTSD with home hospice deaths** Home hospice reduced risk for prolonged grief disorder*** Hospice admission in last 6 months of life correlated with increases in patient satisfaction and better pain control, reductions in hospital days Less physical and emotional distress and better quality of life at EOL* Caregivers Patients 60% reduction in end-of-life transitions, allowing patients to die in location of choice Hospice beneficiaries saw a cost savings of $670 in out-of-pocket expenses during the last month of life compared to non-hospice users
  • 39. Total Cost of Care Comparison by Disease State and Hospice Use in Last Year of Life* *To be eligible to elect hospice care under Medicare, an individual must be entitled to Part A of Medicare and be certified as being terminally ill. An individual is considered to be terminally ill if the medical prognosis is that the individual’s life expectancy is 6 months or less if the illness runs its normal course. Only care provided by (or under arrangements made by) a Medicare certified hospice is covered under the Medicare hospice benefit. The hospice admits a patient only on the recommendation of the medical director in consultation with, or with input from, the patient's attending physician (if any). NORC at the University of Chicago (2023). Value of Hospice in Medicare. Available at: https://www.nhpco.org/wp-content/uploads/Value_Hospice_in_Medicare.pdf Disease Group No Hospice Hospice < 15 Days 15 – 30 31 – 60 61 – 90 91 – 180 181 – 266 > 266 ALL $67,192 4% -5% -9% -12% -14% -10% -12% Circulatory $66,041 7% -4% -8% -10% -11% -8% -10% Cancer $76,625 10% -1% -6% -9% -13% -14% -20% Neuro- degenerative $61,004 12% -6% -9% -11% -11% -5% -4% Respiratory $77,892 -2% -11% -14% -17% -19% -18% -22% CKD/ESRD $82,781 1% -14% -21% -24% -24% -23% -27% • Hospice care saved Medicare approximately $3.5 billion for patients in their last year of life • Those patients with hospice stays of ≥ 6 months* yielded the highest percentage of savings – For patients whose hospice stays were between 181-266 days, total cost of care was almost $7K less than non-hospice users – Hospice patients with stays of > 266 days spent approximately $8K less than non-hospice users Spending is greater than Spending is less than non-hospice users non-hospice users No difference / not statistically significant
  • 40. The Medicare Hospice Benefit Is a 6-Month Benefit: Quality and Cost Evidence Corroborate the Need for Timely Access* *To be eligible to elect hospice care under Medicare, an individual must be entitled to Part A of Medicare and be certified as being terminally ill. An individual is considered to be terminally ill if the medical prognosis is that the individual’s life expectancy is 6 months or less if the illness runs its normal course. Only care provided by (or under arrangements made by) a Medicare certified hospice is covered under the Medicare hospice benefit. The hospice admits a patient only on the recommendation of the medical director in consultation with, or with input from, the patient's attending physician (if any). under the Medicare hospice benefit. The hospice admits a patient only on the recommendation of the medical director in consultation with, or with input from, the patient's attending physician (if any). NORC at the University of Chicago (2023). Value of Hospice in Medicare. Available at: https://www.nhpco.org/wp-content/uploads/Value_Hospice_in_Medicare.pdf Over the last 12 months of life, as hospice use increases, total spending decreases relative to non-hospice users. The reduction in costs when patients across all disease classes, including neurodegenerative diseases, use hospice can be significant.
  • 41. Reasons for Readmission • Failure in discharge planning • Insufficient outpatient and community care • Advanced, progressive illness
  • 43. Medicare Hospice Benefit Interdisciplinary Team of Hospice Professionals Home Medical Equipment Medication Bereavement Support Continuous Care Respite Care Inpatient Care Routine Home Care These Services Are Mandated by the Medicare Hospice Benefit
  • 44. 1. Routine home care 98.7% • Most common level of hospice care • More robust and comprehensive compared to home health care services • Patient’s preferred setting • Proactive clinical approach helps prevent ED visits/hospital readmissions 2. Intensive Comfort Care® (continuous care) 0.2% • Medical management in the home for up to 24 hours per day for acute symptom management when medically appropriate 3. Inpatient care 1.0% • For symptoms that cannot be managed in the home 4. Respite 0.2% • Provides a temporary break for primary caregiver • Inpatient setting • Up to 5 days of 24-hour patient care management when medically appropriate Four Levels of Hospice Care National Hospice and Palliative Care Organization. (2022). Facts & Figures: Hospice Care in America. Available at: https://www.nhpco.org/hospice-care-overview/hospice-facts-figures/
  • 45. Interdisciplinary Hospice Team Patient and Family Volunteers Physicians Spiritual Counselors Social Workers Bereavement Counselors Hospice Aides Therapists Nurses
  • 46. Hospice: Right Care at the Right Time Hospice Palliative Care Home Health Eligibility Requirements Prognosis required: ≤ 6 months if the illness runs its usual course Prognosis varies by program, usually life-defining illness Prognosis not required Skilled need not required Skilled need not required Skilled need required Plan of Care Quality of life and defined goals Quality of life and defined goals Restorative care Length of Care Unlimited Variable Limited, with requirements Homebound Not required Not required Required, with exceptions Targeted Disease-Specific Program ✓ Variable Variable Medications Included ✓ X X Equipment Included ✓ X X After-Hours Staff Availability ✓ X X RT/PT/OT/Speech ✓ X ✓ Nurse Visit Frequency Unlimited Variable Limited, based on diagnosis Palliative Care Physician Support ✓ Variable X Levels of Care 4 1 1 Bereavement Support ✓ X X
  • 47. Bereavement Support groups Bereavement specialists offer support for a minimum of 13 months following a death Individual grief support and grief education resources Memorial activities
  • 48. Hospice Impact: Satisfaction Kumar, P., et al. (2017). Family perspectives on hospice care experiences of patients with cancer. Journal of Clinical Oncology, 35(4), 432. • Hospice care is associated with better symptom relief, patient goal attainment, and quality of EOL care. • Families of patients enrolled in hospice more often reported that patients received “just the right amount” of pain medicine and help with dyspnea. • Families of patients enrolled in hospice also more often reported that patients’ EOL wishes were followed and EOL care was “excellent.” • Families of patients who received > 30 days of hospice care reported the highest quality EOL outcomes.
  • 49. Hospice: In Conclusion • Hospice is: – A service, not a place – Provided in the patient’s preferred setting, whether a private residence, nursing home, assisted living facility, or inpatient hospice setting – Care that comforts and supports when an advanced illness no longer responds to curative treatments – Making the most of the time that remains – Covered by the Medicare Hospice Benefit
  • 50. Summary • Palliative care supports persons with advanced illness and facilitates more timely hospice referral • Hospice and palliative care support: – Patients and families – Clinicians – Hospitals and health systems • All successful palliative care programs partner with a hospice
  • 51. Partner With Hospice “You matter because you are you. You matter to the last moment of life, and we will do all we can, not only to help you die peacefully, but also to live until you die.” —Dame Cicely Saunders St. Christopher’s Hospice London, England
  • 53. Additional Hospice Resources The VITAS mobile app includes helpful tools and information: • Interactive Palliative Performance Scale (PPS) • Body-Mass Index (BMI) calculator • Opioid converter • Disease-specific hospice eligibility guidelines • Hospice care discussion guides We look forward to having you attend some of our future webinars! Scan now to download the VITAS app.
  • 54. References Aldridge M., et al. (2022). Association between hospice enrollment and total health care costs for insurers and families, 2002-2018. JAMA Health Forum. 3(2), e215104-e215104). Center to Advance Palliative Care. (2020). The Case for Palliative Care. Retrieved from https://www.capc.org/the-case-for-palliative-care/ Connor, et al. (2007). Comparing hospice and non-hospice patient survival among patients who die within a three-year window. Journal of Pain Symptom Management, 33(3):238-46. Emanuel, et al. (2003). The Education in Palliative and End of Life Care Curriculum (EPEC Project). Northwestern School University Feinberg School of Medicine. Gade, et al. (2008). Impact of an inpatient palliative care team: A randomized control trial. Journal of Palliative Medicine, 11.2: 180-190. Harrison, et al. (2022). Hospice Improves Care Quality For Older Adults With Dementia In Their Last Month Of Life: Study examines hospice care quality for older adults with dementia in their last month of life. Health Affairs, 41(6): 821-830. Kelley, et al. (2013). Hospice enrollment saves money for Medicare and improves care quality across a number of different lengths-of-stay. Health Affairs, 32(3): 552–561 Kleinpell, et al. (2019). Exploring the association of hospice care on patient experience and outcomes of care. BMJ Supportive & Palliative Care, 9(1): e13-e13. Kumar, et al. (2017). Family perspectives on hospice care experiences of patients with cancer. Journal of Clinical Oncology, 35(4): 432.
  • 55. References (cont.) MedPac March 2023 Report to the Congress: Medicare Payment Policy, Figure 10-2. Available at: https://www.medpac.gov/ document/march-2023-report-to-the-congress-medicare-payment-policy/ Morrison, et al. (2008). Cost savings associated with US hospital palliative care consultation programs. Archives of Internal Medicine, 168(16): 1783-1790 National Center for Health Statistics, Centers for Disease Control and Prevention (2022). Life Expectancy in the U.S. Dropped for the Second Year in a Row in 2021. Retrieved from: https://www.cdc.gov/nchs/pressroom/nchs_press_releases/ 2022/20220831.htm#:~:text=Other%20findings%20documented%20in%20the,2020%20to%2073.2%20in%202021. National Coalition for Hospice and Palliative Care. (2018). Clinical Practice Guidelines for Quality Palliative Care, 4th Edition. Retrieved from https://www.nationalcoalitionhpc.org/wp-content/uploads/2018/10/NCHPC-NCPGuidelines_4thED_web_FINAL.pdf National Hospice and Palliative Care Organization. (2018). 2018 NHPCO Facts and Figures. NHPCO.org National Hospice and Palliative Care Organization. (2014). 2014 NHPCO Facts and Figures. NHPCO.org National Hospice and Palliative Care Organization. (2020). Explanation of Palliative Care. Retrieved from https://www.nhpco.org/ palliative-care-overview/explanation-of-palliative-care/ National Hospice and Palliative Care Organization. (2022). 2022 NHPCO Facts and Figures. Retrieved from: https://www.nhpco.org/ wp-content/uploads/NHPCO-Facts-Figures-2022.pdf/
  • 56. References (cont.) Robinson, et al. (2004). Assessment of the education for physicians on end-of-life care (EPEC™) project. Journal of Palliative Medicine, 7(5): 637-645. Seale, et al. (1994). The Year Before Death. Beatty. Temel, et al. (2010). Early palliative care for patients with metastatic non-small-cell lung cancer. New England Journal of Medicine, Aug 19;363(8): 733-42. Teno, et al. (2004). “Family perspectives on end-of-life care at the last place of care.” JAMA 291.1: 88-93. U.S. Census Bureau, Current Population Survey, Annual Social and Economic Supplement, 2022. Retreived from: https://www.census.gov/data/tables/2022/demo/age-and-sex/2022-older-population.html US Census Bureau (2011; US Census Briefs). The Older Population: 2010. Retrieved from https://www.census.gov/prod/cen2010/ briefs/c2010br-09.pdf US Centers for Disease Control. (2003). National Vital Statistics Reports, Volume 54. Retrieved from: https://www.cdc.gov/nchs/ data/nvsr/nvsr54/nvsr54_14.pdf Wright, et al. (2010). Place of death: correlations with quality of life of patients with cancer and predictors of bereaved caregivers’ mental health. Journal of Clinical Oncology, 28(29): 4457.
  • 57. Palliative Care vs. Curative Care