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Tesi sul tema "Family centred care discourse"

Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 18 febbraio 2022

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1

Sye, Jill. "A fine balance." Click here to access this resource online, 2008. http://hdl.handle.net/10292/387.

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The aim of this study is to analyse the discourses drawn upon by community paediatric nurses in relation to children’s rights to health. The philosophy of Michel Foucault has been used to underpin the analysis of the interviews and exemplars of five experienced community nurses, revealing conflicting power relationships and discourses. Rights are formalised morality and so from a children’s rights perspective, discourses reflect both the moral and ethical positions of the nurses. Children are constructed as developing human beings whose moral status gradually changes and who, through a lack of

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2

Toms, Gill. "Applications of family-centred care in clinical practice." Thesis, Bangor University, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540738.

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3

Senabye, Juliet Sejosennye. "Family centred care in an intensive care unit in Botswana : the views of families." Diss., University of Pretoria, 2018. http://hdl.handle.net/2263/65856.

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Family-centred care (FCC) is a model of care that is focused on promoting collaboration through engagement of nurses and families in information sharing and decision making. This experience is common for families with patients admitted in the intensive care unit (ICU). Disruption of the social system usually manifests in the form of depression, fear and/or anger. Families need to be supported and involved in patient care and decision making, in order to reduce complaints, improve patient outcomes, and hence promote family-centred care. AIM The aim of the study was to describe the views of fami

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4

Yuennan, Choosak. "The nature of family-centred care in Thailand : a case study." Thesis, University of East Anglia, 2015. https://ueaeprints.uea.ac.uk/59197/.

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Thalassemia is a long-term condition that is highly prevalent in children in northern Thailand and the management of this disease requires a strong input from families. Family-centred care is a key philosophy in the nursing care of children and their families, especially as parents play a key role in the health and well-being of a child. However, the concept of family-centred care is a western one and there is limited literature on its use in Thailand. The aim of this study is to explore the characteristics of family-centred care in one hospital in Thailand and the factors that influence the n

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5

Ohene, Lillian. "Family centred care for children in Ghana hospitalised through road traffic accident." Thesis, De Montfort University, 2017. http://hdl.handle.net/2086/16366.

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Road traffic accident (RTA) is one of the leading causes of injuries and hospitalisation of children in Ghana. The sudden hospitalisation of the injured child is associated with anxieties and stressful episodes for the affected families. Family Centred Care (FCC) is a concept in paediatric nursing, which forms the basis of care for sick children and their families. FCC as a product of social constructs differs in cultures and context, despite the universal principles underpinning the concept. There is a perceived lack of knowledge of the concept in childcare practice in Ghana. This study explo

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6

Pretorius, Rachele Lara. "Perceptions of stakeholders on family-centred care in the intensive care unit: an associative group analysis." Diss., University of Pretoria, 2019. http://hdl.handle.net/2263/73769.

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Introduction and background: Family-centred care in the intensive care unit has increased steadily over the past three decades, based on the premise that the illness and health of an individual family member affects the whole family unit. Although widely researched there are still inconsistencies in implementing family-centred care, which influences the ability to transfer research findings into practice. Research has shown that recognising the role of family members in the critical care environment should be considered an essential component to caring for the critically ill patient. Although

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7

Wilson, Sally B. "Family Centred Care: A Descriptive Study of the Situation in Rural Western Australia." Curtin University of Technology, School of Nursing and Midwifery, 2004. http://espace.library.curtin.edu.au:80/R/?func=dbin-jump-full&object_id=15170.

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Family centred care is a concept espoused to be fundamental to achieving excellence in paediatric nursing. Although it is recognised that family centred care includes the child's rights to self determination the focus of this study is parental participation in the decision making and care of their hospitalised child at a partnership level. This is based on negotiation and requires frequent, effective communication between parents and nurses and for each to respect the other's knowledge and appreciate the other has something to offer in the relationship which will benefit the child. The purpose

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8

Puiras, Tuija. "A family-centred case management approach in long-term health care for children, parents' perceptions of care." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape15/PQDD_0024/MQ33433.pdf.

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9

Archibong, Uduak Emmanuel. "Promoting family-centred care through primary nursing practice in Nigeria : an action research project." Thesis, University of Hull, 1995. http://hydra.hull.ac.uk/resources/hull:11269.

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The context of the family in developing countries, especially in Nigeria, is very wide and embraces the immediate as well as the extended family members. The involvement of the family in health care can not be over-emphasised in the Nigerian society where every family member assumes the role of his/her brother's keeper. The expectations of and the role of the Nigerian extended family system in the health care of its members, the problem of incompatibility of the nursing process with the Nigerian nursing organisational pattern, which is predominantly functional nursing, and the increased call f

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10

Van, Rhyn Gabieba. "Caregivers’ experiences with implementing asthma management guidelines for children who attend a hospital in the Western Cape." University of the Western Cape, 2013. http://hdl.handle.net/11394/4832.

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>Magister Scientiae - MSc<br>Asthma education aims to reduce exacerbations by helping the patient or the caregivers to recognize early warning signs and act accordingly. However, a number of studies have indicated that childhood asthma morbidity is still rising. The goal of this research study is to explore the caregivers’ experiences of implementing the asthma education guidelines. The question to be answered by this research is: “How do caregivers experience the implementation of the guidelines for preventing an asthma attack?” Caregivers attending the asthma clinic at Red Cross War Memorial

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11

Tersing, Linda, and Mariann Lindgren. "Mödrars upplevelser av att amma det för tidigt födda barnet på en neonatalavdelning : En litteraturstudie." Thesis, Högskolan Väst, Institutionen för omvårdnad, hälsa och kultur, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:hv:diva-4809.

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Background: About five percent of the infants being born in Sweden are cared for in a neonatal unit because of their prematurity. Breastfeeding and breast milk is considered to be the best nutrition for infants in general and for premature infants in particular. The premature infant, depending on how premature, may not be able to breastfeed effectively due to their immaturity. Stress, anxiety and fatigue are factors that affect breast milk production in a negative direction and these feelings are common in the neonatal unit. Aim: To illuminate mothers’ experiences of breastfeeding the prematur

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12

Lillie, Alison Kate. "'The missing discourse' : how does the family history of cancer affect the care needs of palliative care patients?" Thesis, University of Birmingham, 2009. http://etheses.bham.ac.uk//id/eprint/293/.

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There is increasing scientific understanding and growing public awareness of the influence of genetics on the development of cancer. It is known that up to ten percent of cancers are associated with a genetic predisposition. This study asks ‘How does the family history of cancer affect the care needs of palliative care patients?’ in this context. This question is addressed using the principles of phenomenology to explore the meaning of a family history of cancer for palliative care patients and nurses. Data was collected through recorded, semi-structured interviews with purposively sampled par

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13

Bernling, Sigrid, and Nadire Kucukcelik. "Medias konstruktioner av flyktingar och hur dessa kan påverka distriktssköterskor i deras möte med flyktingar." Thesis, Högskolan Väst, Avdelningen för omvårdnad - avancerad nivå, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:hv:diva-11718.

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I den uppsatsen analyseras medias konstruktioner av flyktingar genom diskursanalys. År 2015 kom ett ökat antal flyktingar till Sverige vilket skrevs om i media. Syftet med studien var att undersöka mediers konstruktioner och diskurser av flyktingar då dessa diskurser kan komma att påverka distriktssköterskor i möten med flyktingar. Det är av vikt att diskutera hur det kan ta sig uttryck och om det hindrar ett välfungerande möte mellan distriktssköterskor och flyktingar. Att möta flyktingar bör ske utifrån ett personcentrerat synsätt där hänsyn tas till patientens subjektiva upplevelser, det

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14

Kruse, Erika, and Camilla Forsgren. "Informationens betydelse vid intensivvård : Vad påverkar och samspelar med närståendes helhetsintryck?" Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-353131.

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Bakgrund: Närstående till en person som vårdas på en intensivvårdsavdelning fyller en viktig funktion för dennas sjukdomsförlopp, utfall och rehabilitering. Närstående har själva behov under denna tid och det är viktigt att även dessa tillgodoses av sjuksköterskor. Behovet av information har i många studier påvisats vara det mest betydelsefulla för närstående. Syfte: Syftet med studien var att undersöka sambandet mellan närståendes uppfattning om information korrelerat till deras uppfattning om bemötande, förtroende, stöd och delaktighet. Vidare var syftet att belysa närståendes upplevelser

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15

Tong, Allison. "Towards consumer-centred health care and health research in nephrology understanding patient and family caregiver experiences and perspectives in chronic kidney disease /." Faculty of Medicine, 2008. http://hdl.handle.net/2123/4024.

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Doctor of Philosophy (PhD)<br>Healthcare services and health research aim to improve the physical and psychosocial well being of consumers, and to offer responsive services needed and valued by them. Research in chronic kidney disease (CKD) has predominantly focused on investigating biomedical aspects and evaluating technological or pharmacological treatment interventions to improve medical management. While research into assessing patients’ and caregivers’ quality of life, and symptom burden, is growing minimal attention has been given to gaining a broad and in-depth understanding about the

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16

Kyratsis, Ioannis. "Diffusion and adoption of complex health innovations : the case of family medicine-centred primary health care reforms in five European transition countries." Thesis, Imperial College London, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.517632.

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17

Eriksson, Rebecca, Nellie Karlsson, and Felicia Åsberg. "När minnet utmanar livet : Anhörigas upplevelser av att vårda en person med demenssjukdom." Thesis, Hälsohögskolan, Högskolan i Jönköping, HHJ, Avd. för omvårdnad, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-39866.

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Bakgrund: Demenssjukdomar är vanligt förekommande i Sverige och prevalensen beräknas öka. Många personer med demenssjukdom bor kvar i hemmet och anhöriga tar ett stort ansvar för vården av dessa personer. Att vara anhörigvårdare till en person med demenssjukdom innebär påfrestningar både fysiskt, psykiskt och socialt.Syfte: Att beskriva anhörigas upplevelser av att vårda en person med demenssjukdom. Metod: Litteraturöversikt med induktiv ansats baserad på 15 vetenskapliga artiklar med kvalitativ design, som har analyserats med Fribergs femstegsmodell. Resultat: I resultatet framkom huvudkatego

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18

Rydberg, Elin, and Velander Linda Öjkvist. "Universella och riktade hembesök inom barnhälsovården : Sjuksköterskors erfarenheter." Thesis, Hälsohögskolan, Högskolan i Jönköping, HHJ, Avd. för omvårdnad, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-44305.

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Bakgrund: Barnhälsovården (BHV) genomför universella insatser till alla barn och deras föräldrar och riktade insatser till de familjer som har särskilda behov. Hembesök är en arbetsmetod som används av BHV-sjuksköterskan och kan göras av olika orsaker. Dels som en del av de universella insatserna, dels som en riktad insats till familjer i behov av extra stöd. Syfte: Beskriva sjuksköterskors erfarenheter av att arbeta med universella och riktade hembesök inom barnhälsovården. Metod: En kvalitativ studie. Femton specialistsjuksköterskor inom BHV intervjuades. Innehållsanalys med induktiv ansat

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19

Landervik, Malin. "Sjuksköterskans upplevelser av det enskilda samtalet med den icke-födande föräldern i barnhälsovården : En kvalitativ intervjustudie." Thesis, Högskolan i Halmstad, Akademin för hälsa och välfärd, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-42304.

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Bakgrund: Barnhälsovården finns till för att främja alla barns hälsa, allsidiga utveckling och välbefinnande. Sjuksköterskans uppdrag inom barnhälsovården är att tidigt grundlägga god kontakt med båda föräldrarna till det nyfödda barnet samt främja båda föräldrarnas delaktighet i omvårdnaden av barnet. Som stöd för främjande av en jämställd vård infördes år 2018 ett enskilt samtal även med den ickefödande föräldern i det nationella barnhälsovårdsprogrammet. Syfte: Att undersöka hur sjuksköterskor inom barnhälsovården upplever det enskilda samtalet med den icke-födande föräldern. Metod: Studien

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20

Becker, Regina. "Beratung von pflegenden Angehörigen : eine queer-feministische Diskursanalyse /." Kassel : Kassel Univ. Press, 2008. http://d-nb.info/989149358/04.

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21

Rioux-Dubois, Annie. "L'intégration et la négociation du rôle de l'infirmière praticienne en soins de santé primaires en contexte de collaboration interprofessionnelle." Thesis, Université d'Ottawa / University of Ottawa, 2019. http://hdl.handle.net/10393/38717.

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La prestation coordonnée de soins de santé primaires (SSP) a été éprouvée comme améliorant la qualité et l’accès des soins prodigués aux Canadiens. Plusieurs études ont notamment confirmé les avantages des infirmières praticiennes (IP) et des modèles interprofessionnels en SSP pour le système de santé. Les écrits suggèrent toutefois que l’intégration des IP en SSP est jalonnée de tensions et restructurations en raison d’une confusion supposée de leur rôle. À ce jour, les recherches ont principalement ciblé les barrières et facilitateurs de l’intégration du rôle des IP. Une analyse critique des

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22

Achiampong, Julie. "A literature review of research into what family caregivers do in support of their loved one with Dementia, and research examining links between perceptions of continuity and the levels of person-centred care people give to their spouse with Dementia." Thesis, University of Birmingham, 2011. http://etheses.bham.ac.uk//id/eprint/3162/.

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The following work has been completed as part of the Birmingham University Clinical Psychology Doctorate. Volume One contains three research papers: a literature review on work exploring care-giving approaches in family carers of people with dementia; an empirical paper exploring the link between perceptions of continuity in spouses caring for someone with dementia and person-centred care; and an executive summary of the empirical paper. Volume Two contains the following clinical practice reports (CPR) completed whilst on placements within the NHS. The models CPR describes the assessment, Cogn

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23

Ndlovu, Mathoto Sinnah. "Parent's views of family centred care in a South African academic Hospital in Gauteng." Thesis, 2017. https://hdl.handle.net/10539/24655.

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Introduction Admission of a child in hospital is a stressful situation for the child, parents and family. According to the American National Centre for Family/Professional Development (2009) Family Centred Care is important as this can improve patient and family outcomes, improve the patient’s and family’s experience, increase patient and family satisfaction, build on child and family strengths, increase professional satisfaction, decrease health care costs, and lead to more effective use of health care resources. Hence, there is a need for Family Centred Care and this should be st

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24

Brown, Devon. "The lived experience of family-centred care by primary caregivers of critically ill children in the pediatric intensive care unit." 2012. http://hdl.handle.net/1993/5111.

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The unexpected admission of a child to the pediatric intensive care unit (PICU) creates feelings of uncertainty, distress, and fear and is a devastating experience for primary caregivers. Health care providers must address primary caregivers` concerns to enhance primary caregivers’ coping abilities. While a family-centred approach to care can assist in diminishing uneasy feelings experienced by primary caregivers, this philosophy of care is not consistently used in everyday practice. The PICU is a unique area of care that focuses on restoring the health of critically ill children with the use

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Dimitris, MICHELLE. "PREDICTORS OF UP-TO-DATE COLORECTAL CANCER SCREENING AND PATIENT-CENTRED CARE IN FAMILY HEALTH TEAM PRIMARY CARE PRACTICES." Thesis, 2012. http://hdl.handle.net/1974/7550.

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Introduction: The Family Health Team (FHT) is an Ontario-based initiative that aims to provide primary care through multidisciplinary teams of healthcare professionals. Little is known about variability between and within teams, and whether certain organizational characteristics are associated with quality of patient care. Objectives: (1) To describe FHT-level organizational characteristics for seven FHTs in Southeastern Ontario. (2) To examine the role of physician-level organizational characteristics in predicting: (a) Up-to-date colorectal cancer screening and (b) episodic patient-centred

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Tatterton, Michael J., and C. Walker. "The prevalence of nonprescription cannabinoid-based medicines in British children's hospices: results of a national survey." 2019. http://hdl.handle.net/10454/18243.

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No<br>Background: Almost 50,000 children and young people are affected by life-limiting conditions in the United Kingdom, around a third of which use children's hospices. Anecdotal evidence suggests that cannabinoid-based medicines (CBMs), specifically cannabis oil (CO), are being used by families with increasing frequency to manage distressing symptoms. The use of most nonprescription CBMs in the United Kingdom remains illegal. Objective: The objective of the study was to identify the prevalence of CO use by families who use children's hospices in the United Kingdom, and the approaches taken

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Tatterton, Michael J., A. Honour, J. Lyon, L. Kirkby, M. Newbegin, and J. Webster. "Sources of emotional challenge for practitioners delivering family centred care after the death of child: an inductive thematic analysis." 2021. http://hdl.handle.net/10454/18496.

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Yes<br>Care after the death of a child and support of their bereaved family is an important element of the services offered by children’s hospices in the United Kingdom. The study aims to explore the emotional challenges of those delivering care to families of children in hospice cool rooms. An internet-based questionnaire was sent to all practitioners to explore their perspectives of providing care to bereaved families whilst the child’s body was in the hospice, as well as caring for a child’s body after death. In total, 94.9% (n=56) of staff responded. Two key themes were identified that

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Romaniuk, Daria K. "The parent-nurse relationship in family-centred care of the hospitalized child with cancer : the parents' perspective." 1994. http://hdl.handle.net/1993/18426.

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Chalifour, Emma E. ""Can I see my Daddy?": child and adult family members as visitors in the adult intensive care unit." Thesis, 2020. http://hdl.handle.net/1828/12534.

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The purpose of this qualitative study was to supply preliminary insights into improving the support of visiting families with children who are minors during the intensive care unit stay (ICU) of an adult family member. Hospitals often restrict children from visiting in ICUs; however, a review of the literature revealed that despite the prevalence of this policy, there has been little research into whether visiting is harmful or supportive (Liu et al., 2013; Manici & Ghillani, 2018). Although family-centred care (FCC) is considered beneficial for adult family members (Davidson et al., 2012; Egg

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Tatterton, Michael J., and C. Walshe. "Understanding the bereavement experience of grandparents following the death of a grandchild from a life-limiting condition: A meta-ethnography." 2018. http://hdl.handle.net/10454/18237.

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yes<br>To increase understanding of grandparental grief following the death of a grandchild from a life-limiting condition. Meta-ethnography. Academic Search Complete CINHAL, Embase, psycINFO, PubMed and Web of Science, supplemented by manual search strategies (in 2015, updated 2018). Studies were appraised and synthesized using the principles of meta-ethnography. Three superordinate themes were identified: 'influence of the relationship with their grandchild', 'influence of the relationship with the grandchild's family' and 'pain'. The simultaneous, multigenerational position of grandpare

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Yun, Tae-Young. "Family Members, Not Workers." Doctoral thesis, 2012. http://hdl.handle.net/11858/00-1735-0000-002E-E5CA-8.

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Tatterton, Michael J., and J. A. Lyon. "‘I no longer feel alone’: meeting the needs of bereaved grandparents through a children’s hospice support group." 2020. http://hdl.handle.net/10454/18216.

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yes<br>Background: Children’s hospices provide a range of family-centred care services, including bereavement support. Not all hospices provide specific services for grandparents. Aim: To explore how a hospice-based bereavement support group supported grandparents in their grief following the death of a grandchild. Methods: Grandparents attending a group were invited to complete an anonymous questionnaire. Questionnaires from eight groups, run between 2015 and 2019 were collated and interpreted to identify themes. Findings: 121 grandparents attended the groups; 113 returned the questionnai

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MacLeod, Suzanne. "From the "rising tide" to solidarity: disrupting dominant crisis discourses in dementia social policy in neoliberal times." Thesis, 2014. http://hdl.handle.net/1828/5213.

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As a social worker practising in long-term residential care for people living with dementia, I am alarmed by discourses in the media and health policy that construct persons living with dementia and their health care needs as a threatening “rising tide” or crisis. I am particularly concerned about the material effects such dominant discourses, and the values they uphold, might have on the collective provision of care and support for our elderly citizens in the present neoliberal economic and political context of health care. To better understand how dominant discourses about dementia work at t

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Archibong, Uduak E. "Evaluating the Impact of Primary Nursing Practice on the Quality of Nursing Care: A Nigerian Study." 1999. http://hdl.handle.net/10454/3230.

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No<br>This paper is abstracted from an action research project on promoting family-centred care in Nigeria through the practice of Nigerian Primary Nursing (NMPN). This article will present results of comparative evaluation of the impact of primary nursing on the quality of care received by patients in a 37-bedded acute medical-surgical, mixed sex ward in a specialist hospital in eastern Nigeria. A total of 44 nurses' interactions with 10 patients in the pre-NMPN period and 58 nurses' interactions with eight patients in the post-NMPN period were assessed using QUALPACS (Quality Patient Care Sc

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Phillips-Beck, Wanda. "Development of a framework of improved childbirth care for First Nation women in Manitoba: A First Nation family centred approach." 2010. http://hdl.handle.net/1993/3985.

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This paper reports on a qualitative exploratory study focusing on the childbirth experiences of women and their families from a northern isolated community in Manitoba - who had to leave or were about to leave home to give birth. Perspectives from critical medical anthropology, cultural relativism and human ecological theory provided the theoretical foundation for this study. This study utilized ethnographic approaches to explore the perspectives of the women, their families and “significant others” and how they have been affected by policies, practices and structures at all levels of their

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Knutson, Shannon. "The Missing Link: Explorations of Wellness when a Family Member Resides in Long-Term Care." Thesis, 2012. http://hdl.handle.net/10012/6754.

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With the aging of our population and the higher risk of chronic illness and disability with age, more and more family members may be faced with the experience of having a relative transition into a long-term care (LTC) home. This reality necessitates greater understanding of family care partner needs to ensure wellness throughout their caring career. Using participatory action research, notions of wellness were explored for family partners in care with relatives residing in LTC homes. Using two LTC homes from a privately owned company called Specialty Care, ten family members were interviewed

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Jamal, Sherin. "Needs, preferences and decision-making regarding long-term residential care: South Asian older adults' and family caregivers' perspectives." Thesis, 2021. http://hdl.handle.net/1828/12862.

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The aging Canadian population is becoming increasingly ethno-culturally diverse primarily due to immigration. This, together with research indicating increased likelihood of long-term residential care (LTRC) use at older ages and challenges in providing these services, prompt important questions about whether LTRC services are prepared to provide culturally responsive and competent care to immigrant and ethno-cultural minority older adults (EMOA). This ethnographic study, informed by a critical theoretical perspective, explored these questions from the perspectives of South Asian older adults

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MULAČOVÁ, Romana. "Integrace rodičů do péče o kriticky nemocné dítě." Master's thesis, 2011. http://www.nusl.cz/ntk/nusl-110118.

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Abstract (sommario):

Nowadays the parental presence in the pediatric intensive care units (PICU) is quite common. Building a fellowship between parents and health care staff and high quality parents' integration into the care is a very demanding process. First of all, the success of this process largely depends upon the nurse. It is the very nurse who leads, educates, supports and also professionally integrates parents into their child's care. In addition, critically ill child's care in cooperation with parents is complicated by a high parental stress level, child's serious condition and high professional and tech

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Inoue, Chiho Sunakawa. "Virtual "ie" household : transnational family interactions in Japan and the United States." Thesis, 2012. http://hdl.handle.net/2152/ETD-UT-2012-05-5158.

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This dissertation explores the impact of technology on social life. Focusing on webcam-mediated audio-visual conversations between Japanese families in the United States and their extended family members in Japan, I examine how technology participates in creating an interactional space for the families to manage intra- and intergenerational relationships. Combining ethnography with turn-by-turn analyses of naturally occurring webcam interactions, I specifically investigate how cultural, discursive, and family practices are transformed in innovative ways and how families adapt to the emerging m

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Brander, ROSEMARY. "Collaborative care relations: Examining perspectives for application and change within a Canadian hospital." Thesis, 2012. http://hdl.handle.net/1974/7288.

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Abstract (sommario):

Collaborative care is a philosophy which guides the work of interdisciplinary teams and patients and their families internationally. It has been demonstrated to improve quality of care, safety, and patient and staff satisfaction, yet applying this philosophy still requires much investigation. This thesis describes processes of change directed towards a vision to enhance collaborative care relationships with patients and families within one hospital site of a non-acute academic health science centre in Ontario, Canada. By building focused conversations around existing patient and family centred

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41

Smythe, A., P. Bentham, C. Jenkins, and Jan R. Oyebode. "The experiences of staff in a specialist mental health service in relation to development of skills for the provision of person centred care for people with dementia." 2013. http://hdl.handle.net/10454/9272.

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Abstract (sommario):

No<br>It is estimated that 820,000 people in the UK have dementia. Dementia costs the UK 17 billion a year and in the next 30 years this will treble to over pound50 billion a year. There is a need to raise competence of staff delivering care to people living with dementia across health, social and voluntary sector provision. Effective education and training will build capacity and improve staff knowledge. However, at present not enough is known about the experiences of staff involved in gaining the skills, knowledge and attitudes required to support provision of high quality care for people wi

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Phiri, Lesego Margaret. "Assessment of the needs of critically ill / injured patients' famalies in an accident and emergency unit." Diss., 2010. http://hdl.handle.net/2263/26551.

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Abstract (sommario):

The critical illness/injury of a family member warranting an admission to an A&E unit can predispose a family to psychological and physiological needs. The patient-centred-care approach rendered in an A&E unit focuses on the patient as a priority, resulting in the family’s needs being neglected during a crisis situation. Based on the Family Resilience Framework, the aim of this study was to assess the needs of the families of the critically ill/injured patients in an A&E unit. Based on the identified needs, recommendations were made with regard to a family-centred-care approach as a relevant r

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Královec, Jiří. "Charta práv dětí v nemocnici ("EACH Charter") jako nástroj posilování a ochrany etických aspektů pediatrické hospitalizace." Master's thesis, 2020. http://www.nusl.cz/ntk/nusl-448716.

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Abstract (sommario):

The Charter of rights of children in hospital (the EACH Charter) is an international document authored by the European Association for Children in Hospital (EACH) in the eighties of the twentieth century. The Charter can be perceived as a response to the fact that a child's stay in hospital - and paediatric hospital as an institution - is strongly influenced and formed by economical, technological and administrative aspects prevailing over the ethical ones. The Charter highlights specific situations where the health care profession - by neglecting children's needs and ignoring and/or toleratin

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Dahan, Sonia. "Parents ressources en néonatologie : évaluations d'expériences locales et perspectives de développement de pratiques partenariales innovantes." Thèse, 2019. http://hdl.handle.net/1866/22803.

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Botha, Carolina Stephanusina. "Reconstructing rainbows in a remarried family : narratives of a diverse group of female adolescents 'doing family' after divorce." Thesis, 2003. http://hdl.handle.net/10500/986.

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Abstract (sommario):

This research journey investigated the ways in which (1) the lives of adolescents have been influenced by parental divorce and subsequent remarriage, (2) exploring the relationships participants have with biological, nonresidential fathers and (3) to collaboratively present ways of doing family in alternative. Four adolescent girls took part in group conversations where they could were empowered to have their voices heard in a society where they are usually marginalized and silenced. As a result of these conversations a family game, FunFam, was developed that aimed to assist families in ex

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Chibamba, Fortune Michelo. "The role of community-based organisations in response to the HIV/AIDS in Botswana : the case of Gabane Community Home Based Care Organisation." Diss., 2011. http://hdl.handle.net/10500/4796.

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Abstract (sommario):

This study examines the role of Community Based-Organisations (CBOs) in the response to HIV/AIDS as a development challenge drawing examples from the Gabane Community Home-Based Care CBO in Botswana. The study adopted qualitative methods of research and used group discussions, relative unstructured interviews, direct observation and literature review as methods of data collection. The study found out that HIV/AIDS is indeed a development problem and that it can be dealt with using some existing development approaches such as the sustainable livelihoods approaches. The study further identified

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Van, Pevenage Isabelle. "De l'aide au lien : des enfants adultes nous parlent de leurs parents âgés." Thèse, 2011. http://hdl.handle.net/1866/5905.

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Abstract (sommario):

Cette thèse s’intéresse aux parents âgés et à l’implication de leurs enfants adultes lorsque le besoin d’aide se fait sentir. Plus précisément, il s’agit ici de comprendre la signification que les enfants adultes attribuent à ce qu’ils considèrent comme un besoin d’aide de la part de leur parent âgé. Elle s’inscrit à la croisée de trois champs sociologiques : le vieillissement, les relations et solidarités familiales, les aides aux personnes âgées dépendantes. La démarche a consisté, d’une part, à repérer dans le récit que nous livrent des enfants adultes à propos de leurs parents, les signif

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Moola, Sabihah. "Communication dynamics in producing effective patient care : a case study at Stanger Hospital’s diabetes clinic in Kwazulu-Natal, South Africa." Thesis, 2015. http://hdl.handle.net/10500/20679.

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Abstract (sommario):

Text in English<br>Interactive health communication between the health-care professional (HCP) and patient relationship for diabetes health-care positively contributes to patient-centred care. Hence individual patient concerns are addressed and catered for in the medical system. The purpose of this study was to analyse in-depth how HCP-patient relationships and HCP-HCP teamwork dynamics positively contribute to effective diabetes patient care and treatment adherence. Different health communication models and theories were reviewed and a conceptual framework was developed from the literature. A

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