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Books on the topic 'Palliative care. Comfort. Patient'

Author: Grafiati

Published: 5 June 2025

Last updated: 24 June 2025

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1

L, Ragan Sandra, ed. Communication as comfort: Multiple voices in palliative care. Routledge, 2008.

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2

L, Ragan Sandra, ed. Communication as comfort: Multiple voices in palliative care. Routledge/Taylor and Francis Group, 2008.

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3

Dunn, Hank. Hard choices for loving people: CPR, artificial feeding, comfort measures only, and the elderly patient. 3rd ed. A & A Pub.,Inc., 1993.

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4

N, Di Lima Sara, Eutsey Dwayne E, and Aspen Reference Group (Aspen Publishers), eds. Palliative care patient and family counseling manual. Aspen Publishers, 1996.

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5

Jean, Lugton, and McIntyre Rosemary Ph D, eds. Palliative care: The nursing role. 2nd ed. Elsevier/Churchill Livingstone, 2005.

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6

Australian Institute of Health and Welfare., ed. Admitted patient palliative care in Australia 1999-00. Australian Institute of Health and Welfare, 2003.

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7

W, Sweetenham J., and Williams C. J, eds. Supportive care of the cancer patient. Arnold, 1997.

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8

Mari, Lloyd-Williams, ed. Psychosocial issues in palliative care. Oxford University Press, 2003.

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9

Steel, R. Knight, and John N. Morris. interRAI palliative care clinical assessment protocols (PC CAPs): For use with the palliative care assessment instrument. 9th ed. interRAI, 2013.

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10

Consortium, Midwest Bioethics Center Ethics Committee. Pathways to patient-centered palliative care: A community initiative. Midwest Bioethics Center, 1997.

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11

H, Lewko John, Hein Carol, Rose Julia, and Laurentian University. Centre for Research in Human Development., eds. Patient and family members perceptions of palliative care services. Centre for Research in Human Development, Laurentian University, 1989.

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12

W, Norman Richard, and Currow David, eds. Supportive care for the urology patient. Oxford University Press, 2005.

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13

Sveṭlanah, Ts'aḥmir, Mekhon Bruḳdail le-geronṭologyah ṿe-hitpatḥut adam ṿe-ḥevrah be-Yiśraʼel, American Jewish Joint Distribution Committee та Merkaz le-ḥeḳer ha-ziḳnah, ред. תכנית ארצית להכשרה פליאטיבית בישראל: Meḥḳar haʻarakhah. Mayers : G'oinṭ : Mekhon Bruḳdail, 2007.

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14

Barbara, Monroe, and Oliviere David, eds. Patient participation in palliative care: A voice for the voiceless. Oxford University Press, 2003.

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15

Natalie, Moryl, ed. Dx/Rx: Palliative cancer care. Jones and Bartlett Publishers, 2006.

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16

1934-, Goldberg Ivan K., Kutscher Austin H, and Malitz Sidney 1923-, eds. Pain, anxiety, and grief: Pharmacotherapeutic care of the dying patient and the bereaved. Columbia University Press, 1986.

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17

E, Quill Timothy, and Battin M. Pabst, eds. Physician-assisted dying: The case for palliative care and patient choice. Johns Hopkins University Press, 2004.

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18

Smith, Trevor Frise. interRAI palliative care (PC) assessment form and user's manual. 9th ed. interRAI, 2010.

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19

Philip, Jevon, ed. Care of the dying and dead patient. Blackwell Pub., 2010.

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20

Ragan, Sandra L., Joy Goldsmith, Elaine M. Wittenberg-Lyles, and Sandra Sanchez Reilly. Communication As Comfort: Multiple Voices in Palliative Care. Taylor & Francis Group, 2008.

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21

Ragan, Sandra L., Joy Goldsmith, Elaine M. Wittenberg-Lyles, and Sandra Sanchez Reilly. Communication As Comfort: Multiple Voices in Palliative Care. Taylor & Francis Group, 2008.

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22

Ragan, Sandra L., Joy Goldsmith, Elaine M. Wittenberg-Lyles, and Sandra Sanchez Reilly. Communication As Comfort: Multiple Voices in Palliative Care. Taylor & Francis Group, 2008.

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23

Communication as Comfort: Multiple Voices in Palliative Care. Routledge, 2008.

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24

Ragan, Sandra L., Joy Goldsmith, Elaine M. Wittenberg-Lyles, and Sandra Sanchez Reilly. Communication As Comfort: Multiple Voices in Palliative Care. Taylor & Francis Group, 2008.

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25

Sanchez-Reilly, Sandra. Communication As Comfort. Routledge, 2008.

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26

Strada, E. Alessandra. The Seventh Domain of Palliative Care. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199798551.003.0008.

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This chapter describes palliative psychology competencies in the seventh domain of palliative care, which addresses palliative care for the patient approaching end of life and the patient’s family. The medical context of dying is reviewed by discussing the interplay of psychological and medical factors related to approaching death and the dying process. The physiological and psychological changes expected in advanced illness and during the dying process are also discussed. The chapter presents a role for the palliative psychologist at different junctures during advanced illness and the dying process. Complications that may arise during the dying process, including hemorrhage and agitated delirium, are discussed and psychological interventions that can promote safety and comfort for the patient and the family are described.

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27

Wittenberg, Elaine, Joy V. Goldsmith, Sandra L. Ragan, and Terri Ann Parnell. Communication in Palliative Nursing. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780190061326.001.0001.

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Communication in Palliative Nursing presents the COMFORT Model, a theoretically-grounded and empirically-based model of palliative care communication. Built on over a decade of communication research with patients, families, and interdisciplinary providers, and reworked based on feedback from hundreds of nurses nationwide, the chapters outline a revised COMFORT curriculum: Connect, Options, Making Meaning, Family caregivers, Openings, Relating, and Team communication. Based on a narrative approach to communication, which addresses communication skill development, this volume teaches nurses to consider a universal model of communication that aligns with the holistic nature of palliative care. This work moves beyond the traditional and singular view of the nurse as patient and family educator, to embrace highly complex communication challenges present in palliative care—namely, providing care and comfort through communication at a time when patients, families, and nurses themselves are suffering. In light of the vast changes in the palliative care landscape and the increasingly pivotal role of nurses in advancing those changes, this second edition provides an evidence-based approach to the practice of palliative nursing. This book integrates communication theory and health literacy constructs throughout, and provides clinical tools and teaching resources to help nurses enhance their own communication and create comfort for themselves, as well as for patients and their families.

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28

Hard choices for loving people: CPR, artificial feeding, comfort measures only, and the elderly patient. 5th ed. A & A Pub.,Inc., 2009.

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29

Dunn, Hank. Hard Choices for Loving People: CPR, Artificial Feeding, Comfort Measures Only and the Elderly Patient. A & A Publishers, Inc., 1999.

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30

Hard Choices for Loving People: CPR, Feeding Tubes, Palliative Care, Comfort Measures, and the Patient with a Serious Illness, 6th Ed. Quality of Life Publishing Co., 2016.

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31

Hard Choices for Loving People : CPR, Artificial Feeding, Comfort Care and the Patient with a Life-Threatening Illness. Not Avail, 2001.

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32

Hard Choices for Loving People: CPR, Artificial Feeding, Comfort Care, and the Patient with a Life-Threatening Illness. A & A Publishers, Incorporated, 2013.

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33

Hard Choices for Loving People: CPR, Artificial Feeding, Comfort Care, and the Patient with a Life-Threatening Illness. A & A Publishers, Incorporated, 2013.

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34

Schrijvers, Dirk. Disease-modifying therapies in advanced cancer. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0122.

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In many situations, anti-cancer therapies may be critical components of a palliative care plan to optimize patient comfort, function, quality of life, and duration of survival. Optimal care often requires the integration of oncological and palliative care and it is important for palliative care clinicians to be familiar with oncological approaches to improve patient well-being, and also the limitations of such approaches. This integrative role requires that palliative care clinicians have a basic literacy regarding anti-cancer therapies and that they be familiar with information resources to update them on new and developing therapeutic options which may be of benefit to their patients.

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35

Palliative Care: Bringing Comfort and Hope. Bailliere Tindall, 2001.

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36

Mitchell, Geoff. Palliative Care: A Patient-Centered Approach. Taylor & Francis Group, 2018.

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37

Thompson, Genevieve, Carla Ens, and Harvey Chochinov. Patient-centred supportive and palliative care. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199550173.003.0014.

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Chapter 14 expands on the role of palliative care within the framework of cancer control. In addition, the public health approach outlined by the WHO, including appropriate policy, adequate drug availability, education, and palliative care delivery at all levels of health care, will be discussed. Finally, the challenges in adapting these principles into high and low resource settings will be described.

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38

Whitehead, Phyllis B. Palliative Care of the Geriatric Patient. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190204709.003.0015.

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More than 50% of all deaths occur in medical and surgical units where the focus is on active, curative treatment, not on managing symptoms and establishing realistic goals of care. Many of these patients are older adults and are vulnerable to many condition. Often they develop end-stage renal disease dementia, hip fractures, and pulmonary conditions and their associated sequelae. Seriously ill, hospitalized patients represent a specialized patient population that greatly benefits from the expanded skills and knowledge of palliative advanced practice registered nurses (APRNs). This chapter reviews renal failure, dementia, pulmonary conditions, and hip fractures and their management for the geriatric patient.

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39

Mitchell, Geoff. Palliative Care: A Patient-Centered Approach. Taylor & Francis Group, 2018.

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40

Mitchell, Geoff. Palliative Care: A Patient-Centered Approach. Taylor & Francis Group, 2018.

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41

Mitchell, Geoff. Palliative Care: A Patient-Centered Approach. Taylor & Francis Group, 2018.

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42

Morris, Jane, Diane Meier, Emily Chai, and Suzanne Goldhirsch. Geriatric Palliative Care. Oxford University Press, Incorporated, 2013.

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43

Geriatric Palliative Care. Oxford University Press, Incorporated, 2013.

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44

Geriatric Palliative Care. Oxford University Press, Incorporated, 2014.

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45

Franklin, Deborah Julie, and Andrea L. Cheville. Medical rehabilitation and the palliative care patient. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0415.

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Maintaining function, specifically independent function, is a key determinant of quality of life for patients receiving palliative care and their caregivers. Techniques, interventions, and strategies from the field of rehabilitation can be adapted to meet the needs of patients with advanced disease. This chapter explores aspects of rehabilitation medicine that are of greatest value for patients requiring palliative care. The first section describes pertinent rehabilitation services available in hospitals, outpatient settings, as well as home-based programmes. The next section reviews the timing of rehabilitation interventions with an emphasis on distinctive features of rehabilitation goal setting for palliative care patients. Some in-depth examples of specific rehabilitation interventions are given that can improve function for patients with advanced disease processes, including the important areas of caregiver training and support. The final section examines current barriers to the effective use of rehabilitation strategies in palliative care medicine and outlines some emerging approaches for improving outcomes.

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46

Ellis, Mary, Robin Hull, and Vicki Sargent. Teamwork in Palliative Care. Radcliffe Publishing Ltd, 1989.

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47

Intensive Care Of The Cancer Patient. W.B. Saunders Company, 2009.

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48

Latestage Dementia Promoting Comfort Compassion And Care. iUniverse.com, 2011.

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49

Regnard, Claud. Helping The Patient With Advanced Disease (Current Learning in Pallative Care). Radcliffe Medical Press, 2004.

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50

Traille, Joy Myra. PALLIATIVE CARE FOR THE TERMINALLY ILL CANCER PATIENT. 1991.

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