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Libri sul tema "Family centred care discourse"

Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 18 febbraio 2022

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1

Ainsworth, Frank. Family centred group care: Model building. Aldershot, Hants, England: Ashgate, 1997.

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2

Canada, Canada Health. Family-centred maternity and newborn care: National guidelines. Ottawa: Health Canada, 2000.

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3

Zlotnik Shaul, Randi, ed. Paediatric Patient and Family-Centred Care: Ethical and Legal Issues. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0323-8.

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4

Shaul, Randi Zlotnik. Paediatric patient and family-centred care: Ethical and legal issues. New York: Springer, 2014.

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5

Woods, Robert T. Involving families in care homes: A relationship-centred approach to dementia care. London: Jessica Kingsley Publishers, 2007.

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6

Woods, Robert T. Involving families in care homes: A relationship-centred approach to dementia care. London: Jessica Kingsley Publishers, 2007.

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7

Rush, Janet. Family centred maternity care: Scoring tool/survey : project report March 1994. Toronto, Ont: Ontario Ministry of Health, 1994.

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8

1946-, O'Neil Di, ed. Beyond child rescue: Developing family-centred practice at St Luke's. St Leonards, NSW: Allen & Unwin, 1996.

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9

Primary care diagnostics: The patient-centred approach in the new commissioning environment. 2nd ed. London: Radcliffe Publishing, 2011.

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10

Rosner, Christine. Instructor's manual and test questions to accompany Betz, Hunsberger, and Wright family-centred nursing care of children. Philadelphia: W.B.Saunders, 1994.

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11

Talking about care: Two sides to the story. Bristol, UK: Policy, 2005.

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12

Gale, Jerry Edward. Conversation analysis of therapeutic discourse: The pursuit of a therapeutic agenda. Norwood, N.J: Ablex Pub. Corp., 1991.

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13

Kunstmann, Anne-Christin. Familiale Verbundenheit und Gerechtigkeit: Fehlende Perspektiven auf die Pflege von Angehörigen : eine Diskursanalyse. Wiesbaden: VS Verlag für Sozialwissenschaften, 2010.

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14

(Editor), Lynda Smith, Maureen Bradshaw (Editor), and Valerie Coleman (Editor), eds. Family Centred Care. Palgrave Macmillan, 2001.

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15

Ainsworth, Frank. Family Centred Group Care: Model Building. Taylor & Francis Group, 2018.

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16

Ainsworth, Frank. Family Centred Group Care: Model Building. Taylor & Francis Group, 2018.

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17

Family Centred Group Care: Model Building. Taylor & Francis Group, 2018.

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18

Ainsworth, Frank. Family Centred Group Care: Model Building. Taylor & Francis Group, 2018.

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19

Ainsworth, Frank. Family Centred Group Care: Model Building. Routledge, 2018. http://dx.doi.org/10.4324/9780429460067.

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20

Lynda, Smith, Coleman Valerie, and Bradshaw Maureen, eds. Family-centred care: Concepts, theory and practice. Basingstoke: Palgrave, 2002.

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21

Chalmers, Beverley. Family-Centred Perinatal Care: Improving Pregnancy, Birth and Postpartum Care. Cambridge University Press, 2017.

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22

Webb, Janine. Counselling and the practice of family centred care. 1997.

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23

Canadian Institute of Child Health. and Canada Health Services Directorate, eds. Family-centred maternity and newborn care: National guidelines. [Ottawa?]: Published by the authority of the Minister of National Health and Welfare, 1987.

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24

Family-centred maternity and newborn care: National guidelines. Ottawa, Ont: Health Canada, 2000.

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25

Canada, Canada Health, ed. Family-centred maternity and newborn care: National guidelines. Ottawa: Health Canada, 2000.

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26

Langton, Helen. The Child with Cancer: Family-Centred Care in Practice. Bailliere Tindall, 2000.

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27

Helen, Langton, ed. The child with cancer: Family-centred care in practice. Edinburgh: Baillière Tindall, 2000.

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28

Shaul, Randi Zlotnik. Paediatric Patient and Family-Centred Care: Ethical and Legal Issues. Springer, 2016.

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29

Family Focused Grief Therapy: A Model of Family-Centred Care during Palliative Care and Bereavement (Facing Death). Open University Press, 2002.

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30

Bloch, Sidney, and David W. Kissane. Family Focused Grief Therapy: A Model of Family-Centred Care during Palliative Care and Bereavement (Facing Death). Open University Press, 2002.

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31

Williams, Brian, M. D. Dowell John, and M. D. Snadden David. Patient-Centred Prescribing: Seeking Concordance in Practice (Patient-Centered Care). Not Avail, 2007.

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32

O'Neil, Di, and Dorothy Scott. Beyond Child Rescue: Developing Family Centred Practice at st Luke's. Allen & Unwin Pty., Limited (Australia), 1998.

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33

Lethborg, Carrie, and David W. Kissane. The family perspective. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0176.

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Abstract (sommario):

In considering cancer as an illness that affects not only the patient but their entire family, this chapter offers a model of family-centred care to encourage an understanding of the impact of illness on the family, the family in the caregiver role, and the needs of family-based caregivers. From a clinical perspective, the authors offer a guide for assessing these families for interventions, including the use of open communication and information provision, the recognition of past patterns of relating, the encouragement of acceptance of support, discussions with the family as a whole, and supp

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34

Charlotte, Ikels, ed. Filial piety: Practice and discourse in contemporary East Asia. Stanford, Calif: Stanford University Press, 2004.

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35

Kissane, David W. Psychosocial care of families in palliative care. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198806677.003.0007.

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Abstract (sommario):

The families of patients in the palliative care setting have a range of educational and care needs that form part of the basic responsibility of the hospice service. Routine family meetings are an important way to address these needs. Additionally, up to one third of families have some level of dysfunction in their relationships, which prove predictive of morbid bereavement outcomes—prolonged grief and major depressive disorders. These families who carry risk of poorer outcomes need additional care, optimally commenced during palliative care, and continued into bereavement to provide continuit

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36

Sampson, Elizabeth, and Karen Harrison Dening. Palliative care and end of life care. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199644957.003.0028.

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Abstract (sommario):

Our ageing population and changes in cause of death, mean that increasing number of people will die in old age. Older people have, in many countries, had poor access to good quality end of life care. Many will develop multiple co-morbidities associated with age; dementia, mental health problems and general frailty. Palliative care is an approach which aims to relieve suffering and take account of a person’s physical, psychosocial and spiritual needs as they near the end of life. Advanced dementia is now being perceived as a “terminal illness”. Interventions such as antibiotics and enteral tube

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37

Sorin-Peters, Riva. The development and evaluation of a learner-centred training program for spouses of adults with chronic aphasia. 2002.

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38

Makarychev, Andrey, and Alexandra Yatsyk. Sovereignty and Russian national identity-making: The biopolitical dimension. Edinburgh University Press, 2018. http://dx.doi.org/10.3366/edinburgh/9781474433853.003.0005.

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The chapter addresses Russian national identity by applying the concept of biopolitics. This approach constitutes a departure from dominant schools of thought, which view contemporary Russian political and social concepts through traditional lenses: institutional change, state–society relations, centre–periphery controversies, etc. Biopolitics offers a specific way of anchoring the uncertain Russian identity in a set of consensually understood nodal points that encapsulate bodily practices of corporeal discipline and control. The chapter argues that Putin’s regime utilises such a biopolitical

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39

LeBlanc, Thomas W., and James A. Tulsky. Communication with the patient and family. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0061.

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Abstract (sommario):

High-quality palliative medicine depends upon communication that is patient-centred, clear, and attends to the central role of emotion in the medical encounter. Good communication leads to a number of improved outcomes including greater adherence to therapy, higher patient satisfaction, decreased anxiety and depression, and care that is more consistent with patients’ goals. Unfortunately, in practice, communication frequently does not meet these standards and opportunities are lost to meet patients’ most basic needs. That said, good communication can be deconstructed and conceptualized as a se

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40

Hain, Richard, Ann Goldman, Adam Rapoport, and Michelle Meiring, eds. Oxford Textbook of Palliative Care for Children. 3rd ed. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780198821311.001.0001.

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Abstract (sommario):

The importance of palliative care for children facing life-threatening illness and their families is now widely acknowledged as an essential part of care, which should be available to all children and families, throughout the child’s illness and at the end of life. The new edition of the Oxford Textbook of Palliative Care for Children brings together the most up to date information, current knowledge, evidence, and developments of clinical practice in the field. The main principles underlying this edition remain child and family-centred care, flexible and individualized care, evidence based an

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41

Zaider, Talia, Shira Hichenberg, and Lauren Latella. Advancing family communication skills in oncology nursing. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198736134.003.0028.

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Abstract (sommario):

This chapter presents a new communication skills training initiative designed to advance family-centred care in the inpatient oncology setting. Because of their consistent contact with families, oncology nurses are well-positioned to initiate and model supportive care to the family. Two formats of training are presented: (i) a single-session module for acute care nurses focuses on responding to challenging family interactions at the bedside; (ii) a comprehensive, six-month curriculum for advanced practice nurses focuses on conceptualization and intervention skills, as applied to a range of com

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42

Cullum, Sarah. Management of dementia. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199644957.003.0039.

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Abstract (sommario):

The management of dementia discusses the needs of people in both the early and later stages of dementia, focusing on social and environmental aspects as well as physical and psychological. The main management tasks in early dementia are helping the person with dementia and their family come to terms with the diagnosis, optimising quality of life in the present, and planning for the future. In later dementia we deal with maintaining person-hood, the emergence of behavioural and psychological symptoms of dementia, making decisions for a person who no longer has capacity to do so for themselves,

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43

Scheunemann, Leslie P., and Robert M. Arnold. Communication with patients and families in the ICU. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0011.

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Abstract (sommario):

Regular, consistent communication with families of intensive care unit (ICU) patients is important for family satisfaction, patient-centred decision-making, and reducing the emotional burden of the ICU stay on family members. In fact, the family meeting can appropriately be considered a core procedure of intensive care practice. Good communication requirements include the appropriate clinicians and family members, providing a quiet and undisturbed setting, and choosing appropriate goals for each meeting. Clinicians should strive to develop skills for listening, observing family dynamics, and r

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44

Raveesh, B. N., Swaran P. Singh, and Soumitra Pathare. Coercion and mental health services in the Indian subcontinent and the Middle East. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198788065.003.0016.

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Abstract (sommario):

Mental health law in the Indian subcontinent and the Middle East has been evolving over the past few decades. There have been rapid socio-economic, cultural, and psychosocial changes in the traditional, rural and family-centred societies. People with mental disorders are amongst the most vulnerable in these societies but there is meagre literature on the issue about coercion, coercive practice, standard measures on coercion, and restraint in this region. There are problems of limited resources and training and inadequate service provision. Anecdotal evidence suggests that coercion, is common,

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45

Muriel, Anna C., and Paula K. Rauch. Talking with families and children about the death of a parent. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0161.

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Abstract (sommario):

The untimely death of a parent is one of the most challenging events for families and the clinicians who care for them. This chapter discusses how a basic knowledge of child development and the ways that children understand illness and death can provide a template from which to engage families about how to help their children during this time and into bereavement. It addresses such topics as how children understand death at different ages, timing of discussions with children, decisions about the setting for end-of-life care in a family context, visits between ill parents and children, legacy l

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46

Emanuel, Linda L., and Rebecca Johnson. Truth telling and consent. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0104.

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Abstract (sommario):

Truth telling and informed consent are relatively recently established legal and ethical norms in end-of-life health care. This chapter provides an exploratory guide to the evolution of both norms, highlighting some of the benefits, problems, and issues associated with both terms. It also presents a selection of the stepwise protocols and practices which Western medicine has developed in order to deliver patient-centred palliative care which comforts and relieves. In addition, the chapter discusses the impact that constant adjustment to loss can have on patient psychology and decision-making i

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47

Mathers, Nigel, and Craig Sinclair. Planning ahead in all areas. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198802136.003.0026.

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Abstract (sommario):

Advance care planning (ACP) has traditionally been identified as a means by which patients can give anticipatory directions for future medical treatment. However the narrow focus on medical treatments has been criticized by those who argue that ACP should commence early in a life-limiting illness, be an ongoing process, and encompass goals and values in a broad range of domains (e.g. cultural, spiritual, lifestyle, and/or financial). Benefits would include reduced focus on end-of-life care, alignment with person-centred care principles, and greater capacity for incorporating ‘future planning’

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48

Wein, Simon, and Limor Amit. Adjustment disorders and anxiety. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0174.

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Abstract (sommario):

Adjustment disorders and anxiety are two of the more common responses to stressors in palliative care. At one end of the spectrum, adjustment and anxiety are normal defences. However, when coping mechanisms fail these responses can become pathological. Judging when a response is pathological is based on two principles: the severity of symptoms and the extent of disruption of normal functioning or homeostatic adaptation. The intimate two-way relationship between physical and psychological symptoms in palliative care means that physical symptoms have to be well controlled and that psychological

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49

Tasker, Robert C., Carlo L. Acerini, Edward Holloway, Asma Shah, and Pete Lilitos, eds. Oxford Handbook of Paediatrics 3e. 3rd ed. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198789888.001.0001.

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Abstract (sommario):

This new edition of the Oxford Handbook of Paediatrics is a compact, pocket-sized compendium of clinical problems and treatment options from a team of specialist contributors and editors with years of clinical experience. Taking a child-centred approach, the practical advice and know-how contained within this handbook will be invaluable to all those involved in the care of the younger patient. Fully revised and updated, this third edition of the handbook provides vital information on areas such as neonatology, surgery, genetics and congenital malformations, and child protection in a user-frien

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50

Goddard, Shannon L., and Brian H. Cuthbertson. ICU Follow-Up Clinics. Oxford University Press, 2014. http://dx.doi.org/10.1093/med/9780199653461.003.0053.

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Abstract (sommario):

ICU follow-up clinics have been proposed and, in some cases, adopted in an effort to improve post-ICU care. Clinics are heterogeneous in staffing and organization and may provide a range of services, from drug reconciliation to mental health referrals. Some clinics integrate support services for family members and caregivers. In other cases, the clinics exist largely as a research environment where they may help to better understand long-term outcomes of survivors of critical illness. Thus far, clinical trials have not shown these clinics to improve patient-centred outcomes or to be cost-effec

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