Academic literature on the topic 'Sen palliativ fas'
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Journal articles on the topic "Sen palliativ fas":
Hariprasad, Gururao, Roopa Hariprasad, Lalit Kumar, Amit Kaushik, and Alagiri Srinivasan. "Proteomics of the ascitic fluid for the differentiation of advanced ovarian cancer." Journal of Clinical Oncology 30, no. 15_suppl (May 20, 2012): e15510-e15510. http://dx.doi.org/10.1200/jco.2012.30.15_suppl.e15510.
Heery, Christopher Ryan, Ravi A. Madan, Marijo Bilusic, Joseph W. Kim, Nishith K. Singh, Myrna Rauckhorst, Clara Chen, et al. "Interim analysis of a phase II randomized clinical trial of samrium-153 (Sm-153) with or without PSA-TRICOM vaccine in metastatic castration-resistant prostate cancer after docetaxel." Journal of Clinical Oncology 30, no. 15_suppl (May 20, 2012): 2526. http://dx.doi.org/10.1200/jco.2012.30.15_suppl.2526.
Santana-Davila, R., M. Ellliott, C. Hook, S. Kaufmann, L. Letendre, R. Pruthi, A. Tefferi, D. Van Dyke, A. Wiktor, and M. R. Litzow. "Trisomy 13 in patients with hematological malignancies." Journal of Clinical Oncology 25, no. 18_suppl (June 20, 2007): 7055. http://dx.doi.org/10.1200/jco.2007.25.18_suppl.7055.
Golan, Talia, Dikla Atias, Camila Avivi, Iris Barshack, and Raanan Berger. "Ascitic derived primary pancreatic cancer cell cultures from different patients as a platform for personalized medicine." Journal of Clinical Oncology 30, no. 15_suppl (May 20, 2012): e14646-e14646. http://dx.doi.org/10.1200/jco.2012.30.15_suppl.e14646.
Yassin, Mohamed A., Firyal A. Ibrahim, Hanadi R. El-Ayoubi, Ruba Y. Taha, Ibrahim A. El-Hijji, Riham H. Negmeddine, Halima A. El-Omri, et al. "Clinico-Pathological Profile and Outcome of Acute Myeloid Leukemia: An Experience of Al-Amal Hematology/Oncology Center In Qatar." Blood 116, no. 21 (November 19, 2010): 4384. http://dx.doi.org/10.1182/blood.v116.21.4384.4384.
Sander, Annette, Martin Zimmermann, Dirk Reinhardt, Michael Dworzak, Gertjan Kaspers, and Ursula Creutzig. "Improvement of Survival after Relapse in Pediatric AML Over the Last Two Decades Is Related to a Standardized, Consistent and Intensive Relapse Treatment." Blood 112, no. 11 (November 16, 2008): 963. http://dx.doi.org/10.1182/blood.v112.11.963.963.
Luño, Elisa, Carmen Sanzo, Fermin Jonte, Jose Maria Vicente, Dolores Carrera, Francesc Sole, Pablo Chamorro, and Araceli Martinez. "Elderly Patients with De Novo Acute Myeloid Leukemia (AML): Prognostic Factors in 132 Cases." Blood 108, no. 11 (November 16, 2006): 4454. http://dx.doi.org/10.1182/blood.v108.11.4454.4454.
Santana-Davila, Rafael, Shernan G. Holtan, Rhett Ketterling, Ryan A. Knudson, David P. Steensma, Dong Chen, James Hoyer, Curtis A. Hanson, and Ayalew Tefferi. "Deletion 5q in AML: A Clinicopathological Description of 79 Cases from a Single Institution." Blood 112, no. 11 (November 16, 2008): 2523. http://dx.doi.org/10.1182/blood.v112.11.2523.2523.
Dissertations / Theses on the topic "Sen palliativ fas":
Moraga, Lynch Claudia. "Palliativ vård : Sjuksköterskors upplevelser av omvårdnad i sen palliativ fas." Thesis, Mälardalens högskola, Akademin för hälsa, vård och välfärd, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-54056.
Werner, Ellinor, and Felicia Ström. "Livskvaliteten hos patienter i sen palliativ fas : Munhälsans betydelse." Thesis, Mälardalens högskola, Akademin för hälsa, vård och välfärd, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-54235.
Hjelm, Annelie, and Patrik Svedling. "Existentiellt lidande i sen palliativ fas : En systematisk litteraturstudie utifrån vårdpersonals erfarenheter." Thesis, Mälardalens högskola, Akademin för hälsa, vård och välfärd, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-46700.
Background: Existential suffering can afflict patients in late palliative phase, regardless whether they are cared for in a ward, receive home healthcare or in a specialized palliative care unite. This may mean that health professionals need to support the patients and provide relief in their existential suffering since meeting their existential needs is important in order for the patients to receive a good quality of life. Aim: To describe health professionals' experiences of caring for patients with existential suffering in late palliative phase. Method: A qualitative approach, through a literature study with a descriptive synthesis. Results: After the analysis two themes and six subthemes emerged. The theme Meaningful caring includes Getting the patients to open up through trustful relationships and Finding ways to support the patients. The theme Challenges in caring includes Finding a work-life balance, Identifying existential suffering, Managing difficult conversations and Being limited by external conditions. Conclusion: Nursing actions such as solely sharing the silence resulting in meaningful caring are often used but time restraints and the patients’ overall health conditions limits the possibilities to identify and ease their existential suffering. Additionally, health professionals' death anxiety and experienced knowledge gaps or beliefs that death conversations increase suffering limits the possibilities to ease existential suffering.
Näsman, Emil, and Josefine Lindh. "Sjuksköterskans upplevelse av att vara verksam inom palliativ vård i den sena palliativa fasen inom hospice : En allmän litteraturöversikt." Thesis, Blekinge Tekniska Högskola, Institutionen för hälsa, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:bth-21484.
Sammer, Sarris, and Al Hakeem Nisreen. "Att vårda patienter under sen palliativ fas till vård i livets slutskede ur sjuksköterskans perspektiv." Thesis, Blekinge Tekniska Högskola, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:bth-21500.
Fischer, Lina, and Rebecka Jönsson. "Synligt- och osynligt stöd : Anhörigas upplevelser av stöd när en familjemedlem vårdas i sen palliativ fas." Thesis, Kristianstad University College, Department of Health Sciences, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:hkr:diva-4293.
When a family member is being cared for in palliative care relatives often need support to be able to support their family member. The purpose of the literature review was to illuminate the nursing staff’s support from the relatives’ perspective when a family member is being cared in a late palliative phase. The study is a literature review, there already existing research are surveyed. The findings were structured into two parts, tangible- and the intangible support. Tangible support is a one-way support; to receive information and that someone takes over. Intangible support is support within an interpersonal relation, when the nursing staff in one way or another respond to the relatives needs; that someone shows consideration, to be met with honesty, someone who gives time and to be given opportunity to feel hope. The support could make relatives feel secure and in control. Tangible- and intangible support are connected and form wholeness, but it is important to notice that there are two kinds of support and the relatives are in need of both.
Nowik, Iwona. "Sjuksköterskors erfarenhet av samtal med närstående till personer med demenssjukdom vid övergången till sen palliativ fas : en kvalitativ studie." Thesis, Sophiahemmet Högskola, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:shh:diva-2696.
Dementia is an incurable disease that leads to death. A large proportion of people living in nursing homes in Sweden have dementia. Nurses have a great responsibility for the care of people with dementia since they, among other things, carry out informative communication with the family when the resident approaches the end of life. Identification of barriers and facilitators for such communication could lead to a better understanding and development of this matter. The purpose of this study was to illuminate nurses’ experiences of conversations with families of people with dementia in the transition to end-of-life care in nursing homes.A qualitative study with semi-structured interviews was conducted, where seven nurses, working in nursing homes specialized in dementia, were included. A qualitative content analysis with an inductive approach was performed. The result consists of 8 categories: planning of care, person-centred care, information and communication, knowledge and education, transition to end-of-life care, teamwork, LCP and to die home.This study identified challenges that might hinder breakpoint communication with families of people with dementia. Some of them are families’ lack of knowledge about dementia, lack of early planning of end-of-life care and uncertainties among nurses on how to handle difficult conversations. Furthermore, improvement suggestions are presented that can increase the safety in care and improve the situation for the nurses in breakpoint communication. The two most important suggestions are the creation of a better continuity in the nursing and to organize continuous educations to increase the competence among staff.Keywords:
Nilsson, Emelie, and Anna Zlotkowska. "Att kunna förbereda sig för framtiden : En litteraturstudie om närståendes upplevelser av stöd när en familjemedlem vårdas i sen palliativ fas i hemmet." Thesis, Kristianstad University College, Department of Health Sciences, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:hkr:diva-5225.
Bakgrund: På senare tid har närståendes roll i vården fått en ökad betydelse. I Sverige insjuknar varje år 50 000 individer i cancer. När sjukdomen övergått i sen palliativ fas väljer allt fler patienter att vårdas den sista tiden av livet i hemmet. Mer ansvar läggs därigenom på närstående vilket lett till ett ökat behov av stöd åt närstående. Syfte: Syftet med litteraturstudien var att belysa närståendes upplevelse av stöd när en familjemedlem med cancer vårdas i sen palliativ fas i hemmet. Metod: Studien är en litteraturöversikt baserad på vetenskapliga artiklar från tidigare forskning. Resultat: Resultatet visade att närståendes upplevelse av stöd fanns i att klara av vardagen och att kunna förbereda sig för framtiden. Däremot framkom även att närstående upplevde avsaknad av stöd, som fanns i att känna sig otillräcklig och att känna sig övergiven. Närstående upplevde information kring familjemedlemmens sjukdom, vårdandet av den döende samt vad närstående kunde förvänta sig av framtiden framkom som ett stöd av betydelse. Närstående upplevde sig inte bli sedda av professionella vårdgivare vilket bidrog till att närstående kände sig ensamma i den svåra situation dem befann sig i. Slutsats: Då närstående befinner sig i en situation där deras behov av stöd inte alltid tillgodoses, är det av vikt att professionella vårdgivare i alla avseenden inkluderar och uppmärksammar närståendes individuella behov av stöd.
Background: The role played by next of kins in the public health care system has, of late, become increasingly important. Every year 50,000 people contract cancer in Sweden. During the final stages of life, when the illness has reached the late palliative phase, an increasing amount of patients choose to be nursed at home. Subsequently, more responsibility is placed upon relatives and their need of support increases. Purpose: The purpose with this study was to illustrate next of kin’s experiences of support when a member of the family suffering from cancer was nursed at home during the late palliative phase. Method: The study is an overview of literature based on scientific articles from previous research. Findings: The study’s findings show that next of kins experienced most support in situations associated with coping with the daily chores or when having to prepare themselves for the future. However, next of kins also experienced a lack of support and reported feeling insufficient and abandoned. Information about the family member’s illness and nursing of the same as well as a comprehension of what they, as next of kins, might expect of the future constituted a significant support. Nevertheless, they felt ignored in contacts with professional health care providers which contributed to a feeling of loneliness. Conclusion: When next of kins find themselves in a situation where their needs of support is not always fully satisfied, it is of great importance that professional health care providers notice and include the next of kins individual needs of support in all respects.
Almqvist, Sara, and Emelie Manfred. "Att som sjuksköterska möta existentiella frågor i den palliativa vårdens sena fas : en systematisk litteraturstudie." Thesis, Linnéuniversitetet, Institutionen för hälso- och vårdvetenskap (HV), 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-43862.
Johansson, Sara, and Emelia Olausson. "Att vara partner till en person med obotlig cancer i en tidig palliativ fas : -En narrativ studie med ett partnerperspektiv." Thesis, Blekinge Tekniska Högskola, Institutionen för hälsa, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:bth-17531.
Books on the topic "Sen palliativ fas":
Yennurajalingam, Sriram, and Eduardo Bruera, eds. Hospice and Palliative Medicine and Supportive Care Flashcards. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190633066.001.0001.