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OVERVIEW
PALLIATIVE CARE IN HOSPITAL

Ika Syamsul Huda MZ

Tim Perawatan Paliatif
RSUP Dr. Kariadi – Semarang
2014

Tim Perawatan Paliatif, 2014
KEPUTUSAN MENTERI KESEHATAN REPUBLIK INDONESIA
NOMOR : 812/Menkes/SK/VII/2007
TENTANG

KEBIJAKAN PERAWATAN PALIATIF

LATAR BELAKANG:
Meningkatnya jumlah pasien dengan penyakit yang belum dapat
disembuhkan baik pada dewasa dan anak seperti penyakit kanker,
penyakit degeneratif, penyakit paru obstruktif kronis, cystic
fibrosis, stroke, Parkinson, gagal jantung/heart failure, penyakit
genetika dan penyakit infeksi seperti HIV/AIDS yang memerlukan
perawatan paliatif, disamping kegiatan promotif, preventif,
kuratif, dan rehabilitatif.

Incurable

Promotive
Preventive
Rehabilitative

Tim Perawatan Paliatif, 2014

Curative

Palliative
Masyarakat menganggap perawatan paliatif hanya untuk
pasien dalam kondisi terminal yang akan
segera meninggal.
Namun konsep baru perawatan paliatif menekankan
pentingnya integrasi perawatan paliatif lebih dini agar
masalah fisik, psikososial dan spiritual
dapat diatasi dengan baik.
Rumah sakit yang mampu
memberikan pelayanan
perawatan paliatif di Indonesia
masih terbatas di 5 (lima) ibu
kota propinsi yaitu Jakarta,
Yogyakarta, Surabaya, Denpasar
dan Makassar.
KMK, No: 812/Menkes/SK/VII/2007

Tim Perawatan Paliatif, 2014
WHO Definition of Palliative Care
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.

(WHO, 2010)
http://www.who.int/cancer/palliative/definition/en/
Tim Perawatan Paliatif, 2014
Palliative care:
•
•
•
•
•
•
•
•

provides relief from pain and other distressing symptoms;
affirms life and regards dying as a normal process;
intends neither to hasten or postpone death;
integrates the psychological and spiritual aspects of patient
care;
offers a support system to help patients live as actively as
possible until death;
offers a support system to help the family cope during the
patients illness and in their own bereavement;
uses a team approach to address the needs of patients and
their families, including bereavement counseling, if indicated;
will enhance quality of life, and may also positively influence
the course of illness;
http://www.who.int/cancer/palliative/en/

Tim Perawatan Paliatif, 2014
Palliative care should be initiated
when the patient becomes
symptomatic of their active,
progressive, far-advanced disease
and should never be withheld until
such time as all treatment
alternatives for the underlying
disease have been exhausted.
The IAHPC Manual of Palliative Care

3rd Edition

Tim Perawatan Paliatif, 2014
Many health care workers believe
that palliative care is the "soft
option“ adopted when "active"
therapy stops!

Palliative care, addressing all
the patient’s physical and
psychosocial problems, is
active therapy
The IAHPC Manual of Palliative Care

3rd Edition

Tim Perawatan Paliatif, 2014
Death

Treatment

Old Concept

Curative care

Palliative
care
Time 

Death

Treatment

Better Concept
Diseases modifying or
Potentially curative
Supportive and
Palliative care

Time 
Bereavement care

Tim Perawatan Paliatif, 2014

Murray SA, Kendall M, Boyd K, Sheikh A.
Illness trajectories and palliative care.
BMJ. 2005; 330:1007-1011.
BARRIERS to PALLIATIVE CARE
Relatives
Physician

Society and Culture
Patient

Tim Perawatan Paliatif, 2014
Barriers related to the physician
• poor prognostication: does not recognise how advanced the patient’s
illness is
• may not recognise how much the patient is suffering
• lacks communication skills to address end-of-life issues
• believe they are already providing good palliative care and need no
assistance
• misunderstands what a palliative care service does or has to offer
• does not want to hand over the patient’s care: loss of control, loss of
income
• opiophobia: worries the patient may become addicted to opioids or
suffer severe side effects
• does not believe in palliative care
• does not know of the palliative care service
The IAHPC Manual of Palliative Care

3rd Edition

Tim Perawatan Paliatif, 2014
Barriers related to the relatives
• they may never have heard of palliative care or a local service
• they may not know whom to ask about it
• they may worry if they can afford it
• they may fear what relatives and neighbours will say about home care
• they may not want many professionals visiting the home
• there may be patient-family disagreement about treatment options
• they may feel unskilled and unable to care for their loved one at home
• they may want the patient to stay at home or the hospital ward they
are currently in
• they may fear unexpected emergencies at home and not know if the
• palliative care service can cope with them
• they may fear it may mean telling the patient they are dying (which
may have been previously resisted)
• they may think it is euthanasia by another name
The IAHPC Manual of Palliative Care

3rd Edition

Tim Perawatan Paliatif, 2014
Barriers related to the patient
• they may have unrealistic expectations about their disease
and prognosis
• there may have been no advance care planning/discussions
• they may not have heard of hospice or palliative care
• they may suspect that it is dismal, gloomy and frightening
with people dying all around you and everyone talking about
death
• they may suspect that people die as a result of euthanasia
• they may worry about opioid addiction
• they may not want to leave home or the unit they are
currently in
• they may not want to have to develop relationships with new
professionals
The IAHPC Manual of Palliative Care

3rd Edition

Tim Perawatan Paliatif, 2014
Barriers related to society and culture
• Ethnic minorities
• Language barriers
• Poor or underprivileged
• Rural communities
• Dying and death still remain, to a large extent,
taboo subjects
• There is still a deeply held view that maintaining
life—whatever its quality—is a prime responsibility of health care
professionals and services.
• Opiophobia

The IAHPC Manual of Palliative Care

3rd Edition

Tim Perawatan Paliatif, 2014
Tim Perawatan Paliatif, 2014
Well-being
Emotional
Social
Physical
Disease
Disability
Disorder

In general, quality of life (QoL or QOL) is the
perceived quality of an individual's daily life,
that is, an assessment of their well-being or
lack thereof. This includes all emotional,
social, and physical aspects of the individual's
life.
In health care, health-related quality of life
(HRQoL) is an assessment of how the
individual's well-being may be affected over
time by a disease, disability, or disorder.
(Wikipedia)
http://en.wikipedia.org/wiki/Quality_of_life_%28healthcare%29

Tim Perawatan Paliatif, 2014
Dimensi Kualitas Hidup
yang diinginkan pasien paliatif :
1.
2.
3.
4.
5.
6.

7.
8.
9.
10.

Penanganan permasalahan fisik (luka, nyeri, mual,
muntah, sesak nafas, dan lain-lain)
Kemampuan fungsional dalam beraktifitas
Kesejahteraan keluarga
Kesejahteraan emosional
Kemampuan melakukan aktifitas spiritual
Kemampuan melakukan fungsi sosial
Kepuasan pada layanan terapi
Orientasi masa depan (rencana dan harapan)
Kehidupan seksual, termasuk gambaran terhadap diri
sendiri
Kemampuan / fungsi dalam bekerja
KMK, No: 812/Menkes/SK/VII/2007
Jennifer J. Clinch, Deborah Dudgeeon dan Harvey Schipper (2000)

Tim Perawatan Paliatif, 2014
Without research,
palliative care is an art,
not a science.
http://www.npcrc.org/

Tim Perawatan Paliatif, 2014
Tim Perawatan Paliatif, 2014
Chrisye

Tim Perawatan Paliatif, 2014

Nira Stania

dr. Abdul Mun'im Idries, SpF
Dying is a 4D activity
Physical

Psychological

Social

Spiritual
Scott A Murray (2010)
Concept of trajectories at the end of life: physical and other dimensions.

Tim Perawatan Paliatif, 2014
Tim Perawatan Paliatif, 2014
Tim Perawatan Paliatif, 2014
“To cure sometimes, to relieve often, and to comfort always,"
Oxford Textbook of Palliative Medicine
Second Edition

Tim Perawatan Paliatif, 2014

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Workshop - Palliative Care in Hospital - 13 januari 2014

  • 1. OVERVIEW PALLIATIVE CARE IN HOSPITAL Ika Syamsul Huda MZ Tim Perawatan Paliatif RSUP Dr. Kariadi – Semarang 2014 Tim Perawatan Paliatif, 2014
  • 2. KEPUTUSAN MENTERI KESEHATAN REPUBLIK INDONESIA NOMOR : 812/Menkes/SK/VII/2007 TENTANG KEBIJAKAN PERAWATAN PALIATIF LATAR BELAKANG: Meningkatnya jumlah pasien dengan penyakit yang belum dapat disembuhkan baik pada dewasa dan anak seperti penyakit kanker, penyakit degeneratif, penyakit paru obstruktif kronis, cystic fibrosis, stroke, Parkinson, gagal jantung/heart failure, penyakit genetika dan penyakit infeksi seperti HIV/AIDS yang memerlukan perawatan paliatif, disamping kegiatan promotif, preventif, kuratif, dan rehabilitatif. Incurable Promotive Preventive Rehabilitative Tim Perawatan Paliatif, 2014 Curative Palliative
  • 3. Masyarakat menganggap perawatan paliatif hanya untuk pasien dalam kondisi terminal yang akan segera meninggal. Namun konsep baru perawatan paliatif menekankan pentingnya integrasi perawatan paliatif lebih dini agar masalah fisik, psikososial dan spiritual dapat diatasi dengan baik. Rumah sakit yang mampu memberikan pelayanan perawatan paliatif di Indonesia masih terbatas di 5 (lima) ibu kota propinsi yaitu Jakarta, Yogyakarta, Surabaya, Denpasar dan Makassar. KMK, No: 812/Menkes/SK/VII/2007 Tim Perawatan Paliatif, 2014
  • 4. WHO Definition of Palliative Care 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. (WHO, 2010) http://www.who.int/cancer/palliative/definition/en/ Tim Perawatan Paliatif, 2014
  • 5. Palliative care: • • • • • • • • provides relief from pain and other distressing symptoms; affirms life and regards dying as a normal process; intends neither to hasten or postpone death; integrates the psychological and spiritual aspects of patient care; offers a support system to help patients live as actively as possible until death; offers a support system to help the family cope during the patients illness and in their own bereavement; uses a team approach to address the needs of patients and their families, including bereavement counseling, if indicated; will enhance quality of life, and may also positively influence the course of illness; http://www.who.int/cancer/palliative/en/ Tim Perawatan Paliatif, 2014
  • 6. Palliative care should be initiated when the patient becomes symptomatic of their active, progressive, far-advanced disease and should never be withheld until such time as all treatment alternatives for the underlying disease have been exhausted. The IAHPC Manual of Palliative Care 3rd Edition Tim Perawatan Paliatif, 2014
  • 7. Many health care workers believe that palliative care is the "soft option“ adopted when "active" therapy stops! Palliative care, addressing all the patient’s physical and psychosocial problems, is active therapy The IAHPC Manual of Palliative Care 3rd Edition Tim Perawatan Paliatif, 2014
  • 8. Death Treatment Old Concept Curative care Palliative care Time  Death Treatment Better Concept Diseases modifying or Potentially curative Supportive and Palliative care Time  Bereavement care Tim Perawatan Paliatif, 2014 Murray SA, Kendall M, Boyd K, Sheikh A. Illness trajectories and palliative care. BMJ. 2005; 330:1007-1011.
  • 9. BARRIERS to PALLIATIVE CARE Relatives Physician Society and Culture Patient Tim Perawatan Paliatif, 2014
  • 10. Barriers related to the physician • poor prognostication: does not recognise how advanced the patient’s illness is • may not recognise how much the patient is suffering • lacks communication skills to address end-of-life issues • believe they are already providing good palliative care and need no assistance • misunderstands what a palliative care service does or has to offer • does not want to hand over the patient’s care: loss of control, loss of income • opiophobia: worries the patient may become addicted to opioids or suffer severe side effects • does not believe in palliative care • does not know of the palliative care service The IAHPC Manual of Palliative Care 3rd Edition Tim Perawatan Paliatif, 2014
  • 11. Barriers related to the relatives • they may never have heard of palliative care or a local service • they may not know whom to ask about it • they may worry if they can afford it • they may fear what relatives and neighbours will say about home care • they may not want many professionals visiting the home • there may be patient-family disagreement about treatment options • they may feel unskilled and unable to care for their loved one at home • they may want the patient to stay at home or the hospital ward they are currently in • they may fear unexpected emergencies at home and not know if the • palliative care service can cope with them • they may fear it may mean telling the patient they are dying (which may have been previously resisted) • they may think it is euthanasia by another name The IAHPC Manual of Palliative Care 3rd Edition Tim Perawatan Paliatif, 2014
  • 12. Barriers related to the patient • they may have unrealistic expectations about their disease and prognosis • there may have been no advance care planning/discussions • they may not have heard of hospice or palliative care • they may suspect that it is dismal, gloomy and frightening with people dying all around you and everyone talking about death • they may suspect that people die as a result of euthanasia • they may worry about opioid addiction • they may not want to leave home or the unit they are currently in • they may not want to have to develop relationships with new professionals The IAHPC Manual of Palliative Care 3rd Edition Tim Perawatan Paliatif, 2014
  • 13. Barriers related to society and culture • Ethnic minorities • Language barriers • Poor or underprivileged • Rural communities • Dying and death still remain, to a large extent, taboo subjects • There is still a deeply held view that maintaining life—whatever its quality—is a prime responsibility of health care professionals and services. • Opiophobia The IAHPC Manual of Palliative Care 3rd Edition Tim Perawatan Paliatif, 2014
  • 15. Well-being Emotional Social Physical Disease Disability Disorder In general, quality of life (QoL or QOL) is the perceived quality of an individual's daily life, that is, an assessment of their well-being or lack thereof. This includes all emotional, social, and physical aspects of the individual's life. In health care, health-related quality of life (HRQoL) is an assessment of how the individual's well-being may be affected over time by a disease, disability, or disorder. (Wikipedia) http://en.wikipedia.org/wiki/Quality_of_life_%28healthcare%29 Tim Perawatan Paliatif, 2014
  • 16. Dimensi Kualitas Hidup yang diinginkan pasien paliatif : 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. Penanganan permasalahan fisik (luka, nyeri, mual, muntah, sesak nafas, dan lain-lain) Kemampuan fungsional dalam beraktifitas Kesejahteraan keluarga Kesejahteraan emosional Kemampuan melakukan aktifitas spiritual Kemampuan melakukan fungsi sosial Kepuasan pada layanan terapi Orientasi masa depan (rencana dan harapan) Kehidupan seksual, termasuk gambaran terhadap diri sendiri Kemampuan / fungsi dalam bekerja KMK, No: 812/Menkes/SK/VII/2007 Jennifer J. Clinch, Deborah Dudgeeon dan Harvey Schipper (2000) Tim Perawatan Paliatif, 2014
  • 17. Without research, palliative care is an art, not a science. http://www.npcrc.org/ Tim Perawatan Paliatif, 2014
  • 19. Chrisye Tim Perawatan Paliatif, 2014 Nira Stania dr. Abdul Mun'im Idries, SpF
  • 20. Dying is a 4D activity Physical Psychological Social Spiritual Scott A Murray (2010) Concept of trajectories at the end of life: physical and other dimensions. Tim Perawatan Paliatif, 2014
  • 23. “To cure sometimes, to relieve often, and to comfort always," Oxford Textbook of Palliative Medicine Second Edition Tim Perawatan Paliatif, 2014

Notas del editor

  1. they may never have heard of palliative care or a local servicethey may not know whom to ask about itthey may worry if they can afford itthey may fear what relatives and neigh bours will say about home carethey may not want many professionals visiting the homethere may be patient-family disagreement about treatment optionsthey may feel unskilled and unable to care for their loved one at homethey may want the patient to stay at home or the hospital ward they are currently inthey may fear unexpected emergencies at home and not know if thepalliative care service can cope with themthey may fear it may mean telling the patient they are dying (which may have been previously resisted)they may think it is euthanasia by another name