Relevant bibliographies by topics / Palliative help

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Palliative help'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "Palliative help"

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_, _. "Palliative Care." Journal of the National Comprehensive Cancer Network 4, no. 8 (2006): 776. http://dx.doi.org/10.6004/jnccn.2006.0068.

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Over the past 20 years, increasing attention has been paid to quality-of-life issues in oncology. As the hospice movement has grown in this country, palliative care has developed into an integral part (rather than the antithesis) of comprehensive cancer care. Palliative care must be integrated earlier into the continuum of cancer care, and palliative, symptom-modifying therapy should be provided simultaneously with disease-modifying therapy from diagnosis. The goal of the NCCN palliative care guidelines is to help assure that each patient with cancer experiences the best possible quality of li
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Meier, Diane E., and Larry Beresford. "Palliative Care Cost Research Can Help Other Palliative Care Programs Make Their Case." Journal of Palliative Medicine 12, no. 1 (2009): 15–20. http://dx.doi.org/10.1089/jpm.2009.9692.

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Fisher, John W., and David Brumley. "Palliative Care Doctors Need Help with Spiritual Wellbeing." Journal for the Study of Spirituality 2, no. 1 (2012): 49–60. http://dx.doi.org/10.1558/jss.v2i1.49.

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Samson, Kurt. "Outpatient Palliative Care Teams Help Parkinsonʼs Patients, Caregivers". Neurology Today 20, № 6 (2020): 1. http://dx.doi.org/10.1097/01.nt.0000659052.86305.e5.

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Cole, Elaine. "‘In palliative care we help children make memories’." Nursing Standard 31, no. 16-18 (2016): 38–39. http://dx.doi.org/10.7748/ns.31.16-18.38.s44.

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Blackburn, Pippa, and Caroline Bulsara. "“You either need help…you feel you don't need help…or you don't feel worthy of asking for it:” Receptivity to bereavement support." Palliative and Supportive Care 17, no. 2 (2018): 172–85. http://dx.doi.org/10.1017/s1478951517001122.

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AbstractObjectiveAlthough the needs of the bereaved have been identified widely in the literature, how these needs translate into meaningful, appropriate, and client-centered programs needs further exploration. The application of receptivity to support is a critical factor in participation by the bereaved in palliative care bereavement programs. Receptivity is a complex multifactorial phenomenon influenced by internal and external factors that ultimately influences engagement in psychosocial support in bereavement. This study explored factors that influence receptivity to bereavement support f
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Goudot, Francois-Xavier, Milena Maglio, and Sandrine Bretonniere. "How to better help cancer patients face their coming death?" Journal of Clinical Oncology 35, no. 15_suppl (2017): e21505-e21505. http://dx.doi.org/10.1200/jco.2017.35.15_suppl.e21505.

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e21505 Background: According to literature and medical experience, the doctor-patient relationship becomes strained when oncologists tell their patients that they have no more curative treatments to offer them. Patients often resist when they are told that it is in their best interest to meet with the palliative teams. Little is known about how to meet patients’ expectations at this advanced stage. Methods: We conducted a multicenter qualitative research in an oncology department, a hospital at home service and in an inpatient hospice care center. We met 47 patients (M = 21, F = 27, mean age =
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CAIN, ROY, MICHAEL MACLEAN, and SCOTT SELLICK. "Giving support and getting help: Informal caregivers' experiences with palliative care services." Palliative and Supportive Care 2, no. 3 (2004): 265–72. http://dx.doi.org/10.1017/s1478951504040350.

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Objective: Palliative care services have made significant contributions to those needing end-of-life care, but the effect of these services on informal caregivers is less clear. This article reviews the literature and examines the influences of palliative care services on caregivers of people who are dying of cancer, HIV-related illnesses, and illnesses of later life.Methods: Based on questions that we developed from the literature review, we conducted six focus groups in Toronto, Thunder Bay, and Ottawa, Canada, with informal caregivers about their experiences with caregiving and with palliat
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Geist, Marcus J. P., Jens Kessler, Susanne Frankenhauser, and Hubert J. Bardenheuer. "Bleeding Control in Palliative Care Patients With the Help of Tranexamic Acid." Journal of Palliative Care 32, no. 2 (2017): 47–48. http://dx.doi.org/10.1177/0825859717731701.

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Background: Persistent bleeding is a common reason for admitting patients with advanced cancer to a palliative care unit. Several reports show a successful therapeutic use of the antifibrinolytic agent tranexamic acid in palliative care patients having hemorrhages. However, it is not administered routinely in severe bleeding situations in palliative care, and general dosing recommendations are unclear. Case Presentation: We report on 3 patients who were treated with tranexamic acid due to symptomatic hemorrhage complicating different malignant processes. Case Management and Outcome: A dosing r
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Adams, James D., and Cecilia Garcia. "Palliative Care Among Chumash People." Evidence-Based Complementary and Alternative Medicine 2, no. 2 (2005): 143–47. http://dx.doi.org/10.1093/ecam/neh090.

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Chumash Healers used breathing therapy and counseling to keep patients involved in daily life and to avoid depression. Heat therapy, massage and pain medications were used to help with pain. Another primary function of the Healer was to help the patient sleep as normally as possible, possibly using mugwort or momoy. Nutrition was considered by Healers in treating their patients. The overall concern of the Healer was to help maintain the daily routine of village life during the normal process of the death of a village member.
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Dissertations / Theses on the topic "Palliative help"

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Bataitienė, Evelina. "Psichosocialinių paslaugų organizavimas slaugos ligoninėje paliatyvių ligonių artimiesiems." Master's thesis, Lithuanian Academic Libraries Network (LABT), 2008. http://vddb.library.lt/obj/LT-eLABa-0001:E.02~2008~D_20080620_134711-87713.

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Darbo tikslas – ištirti psichosocialinių paslaugų organizavimą slaugos ligoninėje paliatyvių ligonių artimiesiems. Darbo uždaviniai: 1. Ištirti paliatyvių ligonių artimųjų esamų psichosocialinių paslaugų poreikį. 2. Įvertinti psichosocialinių paslaugų poreikio tenkinimą. 3. Išsiaiškinti naujų psichosocialinių paslaugų poreikį. Tyrimo metodika: Tyrimo objektas – psichosocialinių paslaugų organizavimas slaugos ligoninėje paliatyvių ligonių artimiesiems. Tyrimo metodas – anoniminė paliatyvių ligonių artimųjų (n=67) anketinė apklausa. Duomenų analizė atlikta naudojant statistinės duomenų analizės
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Tsikai, Franciscah Ndayiziveyi. "A study to explore factors that influence family caregivers of patients receiving palliative care from Island Hospice to seek help at emergency unit in Harare, Zimbabwe." Master's thesis, University of Cape Town, 2017. http://hdl.handle.net/11427/27072.

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Background: This study investigated the factors that influence family caregivers of patients receiving palliative care from Island Hospice to seek help at emergency unit. The study was conducted at Island Hospice Service in Harare, Zimbabwe where Palliative care has been practiced in Zimbabwe since 1979 mainly using the home-based care model where patients are cared for by family caregivers with the support of the palliative care teams. Aim:To explore and understand issues that influence family caregivers at Island Hospice to seek help at emergency units for patients who are terminally ill. Me
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Carolan, Clare. "The experience of emotional distress and help-seeking for distress in families living with advanced cancer and receiving palliative care : a multi-perspective case study approach." Thesis, University of Stirling, 2018. http://hdl.handle.net/1893/28047.

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The emotional impact of serious illness in families is recognised. To enhance well-being in families living we must understand how distress is experienced within families; from this, evidenced-based systemic distress interventions can be derived. However, the success of systemic intervention programmes is reliant on whether families will seek help (or not) for distress. This PhD by publication explores emotional distress and help-seeking in families living with advanced cancer. Papers one and two used systematic review techniques. Paper one evidenced distress as a systemic construct and propos
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Klimašauskas, Donatas. "Paliatyvios pagalbos kaip alternatyvos eutanazijai teisinis reglamentavimas." Master's thesis, Lithuanian Academic Libraries Network (LABT), 2011. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20110705_133952-02991.

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Vakarų pasaulio šalys, dažnai laikomos pasiekusiomis aukštą kultūrinį lygį ir liberalumo bei laisvės skelbėjomis, įteisino eutanaziją valstybinais įstatymais, leisdamos nužudyti žmogų dėl ligos ar senatvės. Lietuvoje kaip ir daugumoje Senojo Žemyno šalių, mažėjantis gimstamumas, senstanti visuomenė ir besikeičiantis jos požiūris į gyvybę, į senatvę, į ligą, į kančią verčia liberalią visuomenę diskutuoti apie įvairias mirties formas ir ypač eutanaziją. Gyvenimo tempams bėgant beprotišku greičiu ir dėl to žmogui patiriant daugybę įvairių traumų, kurios dažnai padaro žmogų neįgaliu; ligos, kurios
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Isaksson, Anna, and Christel Liljebäck. "I nöd och lust, tills döden skiljer oss åt : Sexualitet hos ensamstående män och kvinnor inom palliativ vård." Thesis, Ersta Sköndal högskola, Institutionen för vårdvetenskap, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:esh:diva-690.

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Held, Mareike [Verfasser], and Olivier [Akademischer Betreuer] Morin. "A new on-board imaging treatment technique for palliative and emergency treatments in radiation oncology / Mareike Held. Betreuer: Olivier Morin." Hamburg : Staats- und Universitätsbibliothek Hamburg, 2016. http://d-nb.info/1095766643/34.

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Held, Mareike Verfasser], and Olivier [Akademischer Betreuer] [Morin. "A new on-board imaging treatment technique for palliative and emergency treatments in radiation oncology / Mareike Held. Betreuer: Olivier Morin." Hamburg : Staats- und Universitätsbibliothek Hamburg, 2016. http://nbn-resolving.de/urn:nbn:de:gbv:18-78319.

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Books on the topic "Palliative help"

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Anie, Kofi. Coping with sickle cell disease & pain: A self-help manual for children. Brent Sickle Cell & Thalassaemia Centre, 1998.

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After shock: From cancer diagnosis to healing, a step-by-step guide to help you navigate your way. Roots & Wings, 2007.

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Until there's a cure: How to help Alzheimer's patients and families now : forum before the Special Committee on Aging, United States Senate, One Hundred Eleventh Congress, second session, Washington, DC, December 8, 2010. U.S. G.P.O., 2011.

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What to do before & after someone dies: A practical guide to help you through the worst possible time for making important decisions. Little Moose Press, 2005.

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Help with hospice & palliative care. Health Journeys, 2016.

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Ragsdale, Lindsay B., and Elissa G. Miller, eds. Pediatric Palliative Care. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780190051853.001.0001.

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What Do I Do Now: Pediatric Palliative Care succinctly describes the palliative care approach to children with serious illness and provides practical guidance to clinicians and trainees. This book address physical, emotional, social, cultural, and spiritual needs of ill children and their families. Many clinicians want to help children that are seriously ill but have not been taught the skills or practice guidelines to attend to their needs. This book walks a provider through a challenging clinical pediatric case and outlines how to think through clinical dilemmas and respond to the patient an
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Kaasa, Stein, and Karen Forbes. Research in palliative care. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0191.

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Research in palliative care is essential for maintaining standards and advancing knowledge and improving practice. It is challenging, sometimes daunting, often frustrating, but always exciting and rewarding when a study is successfully completed, whether the outcome is positive or negative. This chapter discusses a wide range of topics that will help those who are new to research to get started, to proceed and complete it, and contribute to improving outcomes for patients with advanced disease. Topics include, among others, collaborative and translational research, research governance, control
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Cooper, Jill, and Nina Kite. Occupational therapy in palliative care. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0046.

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Occupational therapy in palliative care aims to help patients achieve their optimum independence in activities that are important to them. The specific functional difficulties may include extreme fatigue, anxiety and shortness of breath due to advanced disease including metastatic spinal cord compression, fractures, or peripheral neuropathies. Patients may have problems with cognition and perception, body image, life role, and spiritual issues as well as physical disabilities. This chapter describes the broad range of areas in which the occupational therapist works in palliative care together
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O’Callaghan, Clare. Music therapy in palliative care. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0047.

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Music therapists are university-trained professionals who invite palliative care patients, and their significant family members and friends, to explore how creative music-based experiences in therapeutic relationships can address biopsychosocial needs and enhance spiritual well-being. The chapter illustrates how music therapists can extend music’s power to help patients across the lifespan live a quality life and support their families. Patients often choose familiar music to listen to, sing, or play that elicits people, places, emotions, and thoughts that they want to connect with. Through mu
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Fancourt, Daisy. Fact file 9: Palliative care. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780198792079.003.0022.

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Palliative care is support for seriously ill patients and their families. The aim of palliative care is to minimize pain and discomfort as much as possible and provide psychological, social, and spiritual support. An important part of palliative care is end-of-life care, which aims to improve quality of life as much as possible while patients are alive and then help them to die with dignity....
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Book chapters on the topic "Palliative help"

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Galchutt, Paul, and Judy Connolly. "Palliative Chaplain Spiritual Assessment Progress Notes." In Charting Spiritual Care. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-47070-8_11.

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Abstract Research question “What is helpful as well as missing from palliative chaplain spiritual assessment progress notes?” arose from the context of seeking to know how palliative chaplain spiritual assessment progress notes can best be relevant and make a difference for a patient’s care. Seven focus groups, two of which were in a children’s hospital context, were hosted with 42 non-chaplain palliative team participants. The major results revealed four important considerations for palliative care chaplains. First, palliative interprofessional team members want more help and information regarding a patient’s decision-making, especially related to a patient’s religion and/or spirituality. Second, and in line with palliative care principles, the participants discussed their desire for relevant notation on a patient’s sense of suffering and coping. Third, a request was made for the chaplain to consistently document his/her perception of emotion emerging from the patient and/or family. The last major result to emerge was that the progress notes should have a summary content section at the top of the note with the most important information contained there.
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Keles, Sukru. "Palliative Care Ethics: Medicine’s Duty to Help." In Palliative Care. IntechOpen, 2019. http://dx.doi.org/10.5772/intechopen.85160.

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Dunning, Trisha, and Peter Martin. "Diabetes and Palliative Care: A Framework to Help Clinicians Proactively Plan for Personalized care." In Palliative Care. IntechOpen, 2019. http://dx.doi.org/10.5772/intechopen.83534.

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Wittenberg, Elaine, Joy V. Goldsmith, Sandra L. Ragan, and Terri Ann Parnell. "Palliative Care." In Caring for the Family Caregiver. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780190055233.003.0003.

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Whether they are thrust into the caregiving role or volunteer for it, most caregivers want to know what to do, how to do it, and how to prepare for what is ahead. For some caregivers, information is empowering, and for other caregivers, it is overwhelming. Regardless, examine any study on family caregiving or talk to any family caregiver, and the conclusion will be the same: Family caregivers need information, education, and support. Few caregivers are able to fully understand and use available health information when advocating and caring for chronically ill patients, and this seriously complicates their ability to contribute to patient self-management and support at home. To help caregivers understand their role and get them the help they need, they have to be included in the healthcare system and in the patient care process. In recognizing that caregivers are current and future patients who need care too, this chapter (a) introduces palliative care to illustrate how the patient and family’s illness journey is powerfully influenced by their understanding of the disease and its treatment and (b) outlines the health literate care model to identify important reasons to integrate caregivers. Both foci of this chapter are radically impacted by the pre-existing structure and function of the family. Narrative features of caregiving are used to describe three illness journeys that caregivers traverse.
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Regnard, Claud, and Margaret Kindlen. "How can I help a breathless patient?" In Supportive and Palliative Care in Cancer. CRC Press, 2018. http://dx.doi.org/10.1201/9781315378596-29.

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Regnard, Claud, and Margaret Kindlen. "How can I help an angry person?" In Supportive and Palliative Care in Cancer. CRC Press, 2018. http://dx.doi.org/10.1201/9781315378596-39.

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Regnard, Claud, and Margaret Kindlen. "How can I help a withdrawn patient?" In Supportive and Palliative Care in Cancer. CRC Press, 2018. http://dx.doi.org/10.1201/9781315378596-40.

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Regnard, Claud, and Margaret Kindlen. "How can I help a confused patient?" In Supportive and Palliative Care in Cancer. CRC Press, 2018. http://dx.doi.org/10.1201/9781315378596-41.

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Ragsdale, Lindsay B. "How Do We Go Back to Work Now?" In Pediatric Palliative Care, edited by Lindsay B. Ragsdale and Elissa G. Miller. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780190051853.003.0013.

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Patient care can have a significant impact on health care professionals both professionally and personally. Understanding and responding to these emotionally charged situations can help providers work through their emotions and build resiliency over time. Many institutions use debriefings to help providers unpack these situations and learn how to cope together. Debriefing after a significant patient event can help provide a time for medical staff to discuss the event, talk about their emotions, enhance teamwork, and improve the feeling of being supported by peers. Creating a space for these difficult conversations can help providers recover and get back to patient care.
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Mejías-Estévez, Manuel, Rocio Dominguez Álvarez, and Ignacio Jauregi Lobera. "Psychosomatic Medicine and Palliative Care." In Psychosomatic Medicine. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.93154.

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Psychosomatic medicine (MP) and palliative care are disciplines with history and both are based in the scientific world. Although the psychosomatic diagnosis is exclusionary, it can help palliative care to be more effective. The influence of the psychosomatic in the palliative exists. According to all the bibliography available in the electronic databases, psychosomatic medicine is a biopsychosocial model related to both physical and psychosocial factors, which helps improve the care of patients with advanced cancer in palliative care (improved survival, quality of life, reduces the burden on caregivers). It helps analyze and address psychiatric disorders, as well as in the control of complex symptoms such as life-threatening anxiety, depression or delirium. Therefore, both medical disciplines are related from the beginning and help to the quality of life of terminally ill patients.
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Conference papers on the topic "Palliative help"

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Barnes-Harris, Matilda, Miriam Johnson, Flavia Swan, et al. "8 Battery-operated fan and chronic breathlessness: does it help?" In Marie Curie Palliative Care Research Conference. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/spcare-2019-mariecuriepalliativecare.8.

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Bailey, Alison. "P-132 Dry mouth in palliative care, how essential oil mouthwash can help." In Dying for change: evolution and revolution in palliative care, Hospice UK 2019 National Conference, 20–22 November 2019, Liverpool. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjspcare-2019-huknc.155.

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Thompson, Anthony. "P-75 Development of a palliative care d.r.e.a.m. aide memoire to help in complex decision-making and assessments in the palliative care arena." In People, Partnerships and Potential, 16 – 18 November 2016, Liverpool. British Medical Journal Publishing Group, 2016. http://dx.doi.org/10.1136/bmjspcare-2016-001245.99.

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Hodges, Emma, and Sue Read. "P-232 How can institutional theory help hospices plan for the future?" In Transforming Palliative Care, Hospice UK 2018 National Conference, 27–28 November 2018, Telford. British Medical Journal Publishing Group, 2018. http://dx.doi.org/10.1136/bmjspcare-2018-hospiceabs.257.

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Hewitt, Abbie, and Lucy Hines. "P-226 Reducing hospital admissions in patients with cancer: can joint palliative care clinics help?" In Dying for change: evolution and revolution in palliative care, Hospice UK 2019 National Conference, 20–22 November 2019, Liverpool. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjspcare-2019-huknc.248.

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Griffith, Sue. "P-248 Prepared to care? how a concept analysis can help prepare the nursing workforce." In Transforming Palliative Care, Hospice UK 2018 National Conference, 27–28 November 2018, Telford. British Medical Journal Publishing Group, 2018. http://dx.doi.org/10.1136/bmjspcare-2018-hospiceabs.273.

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Sheehy-Skeffington, Barbara. "O-2 Dying as a homeless person – how can we help?" In Dying for change: evolution and revolution in palliative care, Hospice UK 2019 National Conference, 20–22 November 2019, Liverpool. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjspcare-2019-huknc.2.

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Hayes, Jennifer. "35 Does australian-modified karnofsky performance status (akps) help predict outcome for patients admitted to a hospice inpatient unit?" In The APM’s Annual Supportive and Palliative Care Conference, In association with the Palliative Care Congress, “Towards evidence based compassionate care”, Bournemouth International Centre, 15–16 March 2018. British Medical Journal Publishing Group, 2018. http://dx.doi.org/10.1136/bmjspcare-2018-aspabstracts.62.

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Pike, Lawrence, Louise Price, and Kirsty Boyd. "P-56 Spict-4all – a tool to help everyone identify people who may need palliative and supportive care." In Leading, Learning and Innovating, Hospice UK 2017 National Conference, 22–24 November 2017, Liverpool. British Medical Journal Publishing Group, 2017. http://dx.doi.org/10.1136/bmjspcare-2017-hospice.83.

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Smith, Susan, and Kathryn Hamling. "P-27 Innovative partnership working to help support the needs of diverse communities." In Dying for change: evolution and revolution in palliative care, Hospice UK 2019 National Conference, 20–22 November 2019, Liverpool. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjspcare-2019-huknc.51.

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