Enhetens publikationer

Maria Ayoub, Camilla Udo, Kristofer Årestedt, Ulrika Kreicbergs, Malin Lövgren (2024). The Family Talk Intervention in Pediatric Oncology: Potential Effects Reported by Parents

Gustav Bockgård, Elisabet Mattsson, Louise von Essen, Anna Klarare (2024). Collaborative Interpretation of Researcher-Generated Photo-Elicitation Findings: Insights From Women With Lived Experience of Homelessness

Maja Holm, Tina Lundberg, Malin Lövgren, Lisa Ljungman (2024). Parenting a child with cancer and maintaining a healthy couple relationship: Findings from the Family Talk Intervention

Maja Holm, Malin Lövgren, Anette Alvariza, Rakel Eklund, Ulrika Kreicbergs (2024). Experiences of being a severely ill parent of dependent children receiving care at home: Hopes and challenges

Louise Häger Tibell, Kristofer Årestedt, Maja Holm, Viktoria Wallin, Gunnar Steineck, Peter Hudson, Ulrika Kreicbergs, Anette Alvariza (2024). Preparedness for caregiving and preparedness for death: Associations and modifiable thereafter factors among family caregivers of patients with advanced cancer in specialized home care

Andreas Karlsson Rosenblad, Anna Klarare, Penny Rapaport, Elisabet Mattsson, Sophie Nadia Gaber (2024). Health literacy and its association with mental and spiritual well-being among women experiencing homelessness

Maria Norinder, Kristofer Årestedt, Lena Axelsson, Gunn Grande, Gail Ewing, Anette Alvariza (2024). Increased preparedness for caregiving among family caregivers in specialized home care by using the Carer Support Needs Assessment Tool Intervention

Lina Oelschlägel, Anne Moen, Alfhild Dihle, Vivi L. Christensen, Kristin Heggdal, Jane Österlind, Simen A. Steindal (2024). Implementation of remote home care: Assessment guided by the RE-AIM framework

Josefine Agius, Anna Klarare, Elisabet Mattsson, Johan Vamstad, Jenny Eriksson Lundström, Sanna Vahlman (2023). Vilket stöd våldsutsatta får blir ett lotteri: Ge kommuner ett särskilt bostadsförsörjningskrav för våldsutsatta

Mehrnaz Ahmadi, Samira Beiranvand, Saeed Poormansouri, Mahsa Matbouei, Camelia Rohani (2023). Sense of coherence or self-efficacy as predictors of health-related quality of life in sickle cell disease patients

Ranaa Akkawi El Edelbi, Staffan Eksborg, Ulrika Kreicbergs, Malin Lövgren, Klara Wallén, Jennie Ekman, Synnöve Lindemalm (2023). Parents' experiences of handling oral anticancer drugs at home: 'It all falls on me …'

Renée Bergstrand, Ida Goliath, Åsa Olsson, Jane Österlind (2023). AKADEMISKT SÄBO

Nina Carlsson, Anette Alvariza, Anders Bremer, Lena Axelsson, Kristofer Årestedt (2023). Symptoms of Prolonged Grief and Self-Reported Health Among Bereaved Family Members of Persons Who Died From Sudden Cardiac Arrest

Sandra E. Doveson, Maja Holm, Per Fransson, Agneta Wennman-Larsen (2023). Identification of early symptoms and changes in QoL and functioning among men with primary localized prostate cancer who later develop metastases: A matched, prospective study

Linda Victoria Eriksson, Katarina Holmberg, Carina Lundh Hagelin, Yvonne Wengström, Karin Bergkvist, Jeanette Winterling (2023). Symptom Burden and Recovery in the First Year After Allogeneic Hematopoietic Stem Cell Transplantation

Hanna Gabrielsson, Elin Hjorth, Viktoria Wallin, Lilian Pohlkamp (2023). Övergången från att vara patient med cancer till person med erfarenhet av cancer: Civilsamhällets roll i rehabilitering

Tove Godskesen, Sara Frygner Holm, Anna T. Höglund, Stefan Eriksson (2023). YouTube as a source of information on clinical trials for paediatric cancer

Marie Granrud, Vigdis Abrahamsen Grøndahl, Ann Karin Helgesen, Carina Bååth, Cecilia Olsson, Maria Tillfors, Christina Melin-Johansson, Jane Österlind, Maria Larsson, Reidun Hov, Tuva Sandsdalen (2023). Health Care Personnel’s Perspectives on Quality of Palliative Care During the COVID-19 Pandemic: A Cross-Sectional Study

Maja Holm, Megan Weber Falk, Anette Alvariza, Josefin Sveen, Ulrika Kreicbergs (2023). How parents of dependent children reason about their partner's impending death due to cancer

Katarina Holmberg, Karin Bergkvist, Solveig Adalsteinsdóttir, Yvonne Wengström, Carina Lundh Hagelin (2023). Nursing as a balancing act in allogeneic hematopoietic cell transplantation: Nurses' experiences through participation in workshops

P L Hudson, C Gardiner, Anette Alvariza, J Nicholas Dionne-Odom, J Öhlén, E Carduff, R Harding, E Witkamp, S Payne (2023). Strategies and checklist for designing and conducting palliative care research with family carers: EAPC international expert elicitation study

Cecilia Högberg, Viktoria Wallin, Ulrika Kreicbergs, Anette Alvariza (2023). Närståendes erfarenheter av webbaserat stöd under pågående specialiserad hemsjukvård: ’Närstående.se’

Erik Landfeldt, Camilla Udo, Malin Lövgren, Thomas Sejersen, Ulrika Kreicbergs (2023). Health-related quality of life of children with spinal muscular atrophy in Sweden: A prospective cohort study in the era of disease-modifying therapy

Tina Lundberg, Kristofer Årestedt, Mariann Olsson, Anette Alvariza, Ulla Forinder (2023). Posttraumatic Growth After Struggling With the Loss of a Parent in Young Adulthood

Elisabet Mattsson, Anna Klarare (2023). Kvinnor far illa inom ramen för samhällets institutioner

Maria Norinder (2023). A person-centred approach to support family caregivers in specialised home care: The Carer Support Needs Assessment Tool Intervention

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Maria Norinder, Lena Axelsson, Kristofer Årestedt, Gunn Grande, Gail Ewing, Anette Alvariza (2023). Family caregivers’ experiences of discussing their needs with a nurse during specialised home care utilizing the carer support needs assessment tool intervention: A qualitative study

Maria Norinder, Lena Axelsson, Kristofer Årestedt, Gunn Grande, Gail Ewing, Anette Alvariza (2023). Enabling professional and personal growth among home care nurses through using the Carer Support Needs Assessment Tool Intervention: An interpretive descriptive study

Lina Oelschlägel, Vivi L. Christensen, Anne Moen, Kristin Heggdal, Jane Österlind, Alfhild Dihle, Simen A. Steindal (2023). Patients' experiences with a welfare technology application for remote home care: A longitudinal study

Anna O'Sullivan (2023). Undocumented migrants’ access to healthcare in Sweden, and the impact of Act 2013:407

Ramona Schenell, Jane Österlind, Maria Browall, Christina Melin-Johansson, Carina Lundh Hagelin, Elin Hjorth (2023). Teaching to prepare undergraduate nursing students for palliative care: Nurse educators’ perspectives

Karoline Skedsmo, Hanne Maria Bingen, Kristin Hofsø, Simen A. Steindal, Carina Lundh Hagelin, Deborah Hilderson, Andréa Aparecida Gonçalves Nes, Dieter Smis, Hege Vistven Stenseth, Camilla Olaussen (2023). Postgraduate nursing students’ experiences with simulation-based learning in palliative care education: A qualitative study

Karoline Skedsmo, Andréa Aparecida Gonçalves Nes, Hege Vistven Stenseth, Kristin Hofsø, Marie Hamilton Larsen, Deborah Hilderson, Dieter Smis, Carina Lundh Hagelin, Camilla Olaussen, Marianne Trygg Solberg, Hanne Maria Bingen, Mia Alexandra Ølnes, Simen A. Steindal (2023). Simulation-based learning in palliative care in postgraduate nursing education: A scoping review

Simen A Steindal, Andréa Aparecida Gonçalves Nes, Tove Godskesen, Heidi Holmen, Anette Winger, Jane Österlind, Alfhild Dihle, Anna Klarare (2023). Advantages and Challenges of Using Telehealth for Home-Based Palliative Care: A Systematic Mixed Studies Review

Ingrid Thermaenius, Camilla Udo, Anette Alvariza, Malin Lövgren (2023). The Family Talk Intervention för barnfamiljer med palliativa vårdbehov: Hälso- och sjukvårdskuratorers initiala erfarenheter av hinder och möjligheter i klinisk praktik

Jane Österlind, Ann-Charlotte Östensson, Birgitta Bisholt, Susanne Pusa, Christina Melin-Johansson, Carina Lundh Hagelin (2023). 6 S-modellen för personcentrerad palliativ vård: En undersökning av personalens uppfattningar på vård-och omsorgsboende och i hemtjänst

Karin Adolfsson, Ulrika Kreicbergs, Charlotte Bratthäll, Erik Holmberg, Thomas Björk-Eriksson, Margaretha Stenmarker (2022). Referral of patients with cancer to palliative care: Attitudes, practices and work-related experiences among Swedish physicians

Anette Alvariza (2022). Att vara nära under livets sista tid: Personcentrerat stöd

Lena Axelsson, Anette Alvariza, Kristofer Årestedt (2022). Livskvalitet hos Närstående till personer i livets slut: Validering av The Quality of Life in Life-Threatening Illness - Family carer version

Cecilia Bartholdson, Ulrika Kreicbergs, Josefin Sveen, Malin Lövgren, Lilian Pohlkamp (2022). Communication about diagnosis and prognosis: A population-based survey among bereaved parents in pediatric oncology

Emily Bergersen, Maria Larsson, Malin Lövgren, Cecilia Olsson (2022). Adolescents' and young people's needs and preferences for support when living with a parent with life-threatening cancer: A grounded theory study

Fiona Cameron, Anna Klarare, Anna Janze (2022). Ett värdigt liv i rörelse nära döden: Erfarenheter av en rörelsestig på en palliativ vårdavdelning (nr 9)

Nina Carlsson, Anette Alvariza, Lena Axelsson, Anders Bremer, Kristofer Årestedt (2022). Grief reactions in relation to professional and social support among family members of persons who died from sudden cardiac arrest: A longitudinal survey study

Nina Carlsson, Anders Bremer, Anette Alvariza, Kristofer Årestedt, Lena Axelsson (2022). Losing a close person following death by sudden cardiac arrest: Bereaved family members' lived experiences

Nina Carlsson, Kristoffer Årestedt, Anette Alvariza, Lena Axelsson, Anders Bremer (2022). Det professionella och sociala stödets betydelse för symtom på förlängd sorg hos närstående till personersom avlidit till följd av hjärtstopp

Rakel Eklund, Li Jalmsell, Ulrika Kreicbergs, Anette Alvariza, Malin Lövgren (2022). Children’s experiences of the family talk intervention when a parent is cared for in palliative home care: A feasibility study

Rakel Eklund, Ulrika Kreicbergs, Anette Alvariza, Malin Lövgren (2022). Children's views are not taken into account in accordance with article 12 of the united nations convention on the rights of the child in the family talk intervention when a parent is cared for in palliative care

Rakel Eklund, Malin Lövgren (2022). The Family Talk Intervention in Pediatric Oncology: Ill Children’s Descriptions of Feasibility and Potential Effects

Rakel Eklund, Malin Lövgren, Anette Alvariza, Ulrika Kreicbergs, Camilla Udo (2022). Talking about death when a parent with dependent children dies of cancer: A pilot study of the Family Talk Intervention in palliative care

Seyedeh Esmat Hosseini, Mahnaz Ilkhani, Camelia Rohani, Alireza Nikbakht Nasrabadi, Raza Ghanei Gheshlagh, Ashraf Moini (2022). Prevalence of sexual dysfunction in women with cancer: A systematic review and meta-analysis

Jenny Gedda, Ida Goliath, Michael Dabrowski, Anette Alvariza (2022). We Are Co: Ett digitalt verktyg som stimulerar och inspirerar medmänniskor till en förbättradgemensam upplevelse i palliativ vård

L. Hakimi Hashjin, Camelia Rohani, M. Matbouei, M. Nasiri (2022). The effect of educational intervention based on the protective motivation theory on awareness and early detection behaviours of breast cancer in women

Leila Hashemlu, Roghayeh Esmaeili, Fatemeh Bahramnezhad, Camelia Rohani (2022). The experiences of home care team members regarding the needs of family caregivers of heart failure patients in home health care services in Iran: A qualitative study

Ingela Henoch, Jane Österlind, Bodil Holmberg, Ramona Schenell (2022). De 6 S:n: Personcentrerad palliativ vård för alla åldrar

Nastaran Heydarikhayat, Nezar Ghanbarzehi, Zarkhatoon Shahkaramzehi, Kimya Sabagh, Camelia Rohani (2022). Nurses' lived experiences of caring for patients with COVID-19: A phenomenological study

Elin Hjorth, Ulrika Kreicbergs, Thomas Sejersen, Ulla Werlauff, Jes Rahbek, Malin Lövgren (2022). Parents’ advice to other parents of children with spinal muscular atrophy: Two nationwide follow-ups

Maja Holm, Megan Weber Falk, Malin Lövgren, Ulrika Kreicbergs, Anette Alvariza, Josefin Sveen (2022). Sources of social support and its importance for cancer-bereaved spouses and their minor children: A cross-sectional study

Bodil Holmberg, Tove Godskesen (2022). Dignity in bodily care at the end of life in a nursing home: An ethnographic study

Bodil Holmberg, Tove Godskesen (2022). Barriers to and facilitators of ethical encounters at the end of life in a nursing home: An ethnographic study

Louise Häger Tibell, Anette Alvariza, Ulrika Kreicbergs, Maja Holm (2022). Webbaserat stöd för närstående inom specialiserad palliativ hemsjukvård: narstaende.se

Louise Häger Tibell, Anette Alvariza, Ulrika Kreicbergs, Viktoria Wallin, Gunnar Steineck, Maja Holm (2022). Web-based support for spouses of patients with life-threatening illness cared for in specialized home care: A feasibility study

Annika M Kisch, Karin Bergkvist, Sólveig Adalsteinsdóttir, Christel Wendt, Anette Alvariza, Jeanette Winterling (2022). A person-centred intervention remotely targeting family caregivers' support needs in the context of allogeneic hematopoietic stem cell transplantation: A feasibility study

Anna Klarare, Åsa Kneck (2022). How the selection of research methods can give women in homelessness a voice and a choice: An attempt to promote an inclusive society with gender equality, health and well-being for all

Ulrika Kreicbergs, Charlotte Castor, Frida Ekström (2022). Palliativ vård i hemmet för barn med fokus på stödjande insatser från vården

Ulrika Kreicbergs, Stefan Nilsson, Margaretha Jenholt Nolbris, Malin Lövgren (2022). Using Communication Tools to Explore Young Siblings' Experiences of Having a Brother or Sister with Pediatric Palliative Care Needs

Susanne Lind, Astrid Bengtsson, Anette Alvariza, Anna Klarare (2022). Registered nurses’ experiences of caring for patients in hospitals transitioning from curative to palliative care: A qualitative study

Tina Lundberg, Kristofer Årestedt, Ulla Forinder, Mariann Olsson, Carl Johan Fürst, Anette Alvariza (2022). Higher Self-Esteem Associated With Less Symptoms of Anxiety and Depression Among Young Adults After the Loss of a Parent to Cancer-A Longitudinal Study

Carina Lundh Hagelin, Christina Melin Johansson, Kristina Ek, Ingela Henoch, Jane Österlind, Maria Browall (2022). Undervisning om döende och död: En nationell kartläggning av palliativ vård i svenskasjuksköterskeprogram (nr 90)

Malin Lövgren (2022). Ett stödprogram till barnfamiljer drabbade av svår sjukdom: Att samtala om det som är svårt

Malin Lövgren (2022). Ett stödprogram för barnfamiljer när någon i familjen är svårt sjuk: The Family Talk Intervention

Malin Lövgren (2022). Samtal om det som är svårt

Malin Lövgren, Camilla Udo, Ulrika Kreicbergs (2022). Is the family talk intervention feasible in paediatric oncology?: An evaluation of a family-based psychosocial intervention

Nina Mogensen, Ella Saaranen, Erik Olsson, Birgitte Klug Albertsen, Päivi M Lähteenmäki, Ulrika Kreicbergs, Mats Heyman, Arja Harila-Saari (2022). Quality of life in mothers and fathers of children treated for acute lymphoblastic leukaemia in Sweden, Finland and Denmark

Azam Naderi, Abbas Abbaszadeh, Marzieh Pazokian, Camelia Rohani, Rostam Jalali (2022). The expansion of the role of nurse prescribing in intensive care units in the healthcare system of Iran: A qualitative content analysis

Maria Norinder, Anette Alvariza, Kristofer Årestedt, Susanne Lind (2022). Ett personcentrerat förhållningssätt för att stödja närstående i den specialiserade palliativa hemsjukvården: CSNAT interventionen (CSNAT-I)

Maria Norinder, Anette Alvariza, Kristofer Årestedt, Susanne Lind (2022). Närstående med ej tillgodosedda behov av stöd har sämre livskvalitet: En studie inom specialiserad palliativhemsjukvård (nr 48)

Lena Palmryd, Tove Godskesen, Åsa Rejnö (2022). Integritet vid vård i livets slutskede inom intensivvård: En kvalitativ studie från sjuksköterskors perspektiv (nr 26)

Lilian Pohlkamp (2022). Att möta människor i komplicerad sorg

Camelia Rohani (2022). Early and Integrated Palliative Care as Valuable Support in Patients With Metastatic Breast Cancer

Camelia Rohani, Hasanali Jafarpoor, Yousef Mortazavi, Behnam Esbakian, Hemmat Gholinia (2022). Mortality in patients with myocardial infarction and potential risk factors: A five-year data analysis

Linda Rönnberg, Ulrica Nilsson, Ove Hellzén, Christina Melin-Johansson (2022). Beyond the monitors: Anaesthesiologists' experiences of the process of extubation

Ulrika Rönningås, Maja Holm, Sandra Doveson, Per Fransson, Lars Beckman, Agneta Wennman-Larsen (2022). Signs and symptoms in relation to progression, experiences of an uncertain illness situation in men with metastatic castration-resistant prostate cancer: A qualitative study

Susanne Schultz, Charlotte Weiner, Helena Bergius, Malin Lövgren (2022). Pediatrisk palliativ vård på akutsjukhus: Strategier för att tillgodose barns behov av palliativ vård (nr 15)

Johan Sundelöf, Christina Melin Johansson, Bodil Holmberg, David Thurfjäll, Valerie DeMarinis (2022). H.O.P.E: Ett frågeformulär på svenska för att identifiera religiösa, andliga och existentiella behov (nr 69)

Julia Wager, Larissa Alice Kubek, Maria Brenner, Sara Calmanti, Carmel Doyle, Malin Lövgren, Ulrika Kreicbergs, Leontien Kremer, Philippe Le Moine, Guillaume Robert, Meggi Schuiling-Otten, Peter Schröder-Bäck, Eduard Verhagen, Boris Zernikow (2022). Expert survey on coverage and characteristics of pediatric palliative care in Europe: A focus on home care

Viktoria Wallin (2022). Mealtimes in palliative care contexts: Perspectives of patients, partners, and registered nurses

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Viktoria Wallin, Elisabet Mattsson, Pernilla Omerov, Anna Klarare (2022). Caring for patients with eating deficiencies in palliative care—Registered nurses' experiences: A qualitative study

Viktoria Wallin, Pernilla Omerov, Elisabet Mattsson, Anna Klarare (2022). Patienters erfarenheter av mat och måltider vid kronisk livsbegränsande sjukdom: En litteraturöversikt med mixade metoder

Megan Weber Falk, Anette Alvariza, Ulrika Kreicbergs, Josefin Sveen (2022). End-of-Life-Related Factors Associated with Posttraumatic Stress and Prolonged Grief in Parentally Bereaved Adolescents

Megan Weber Falk, Rakel Eklund, Ulrika Kreicbergs, Anette Alvariza, Malin Lövgren (2022). Breaking the silence about illness and death: Potential effects of a pilot study of the family talk intervention when a parent with dependent children receives specialized palliative home care

Megan Weber Falk, Alison Salloum, Anette Alvariza, Ulrika Kreicbergs, Josefin Sveen (2022). Outcomes of the grief and communication family support intervention on parent and child psychological health and communication

Megan Weber, Anette Alvariza, Ulrika Kreicbergs, Josefin Sveen (2022). The Grief and Communication Family Support Intervention: Intervention Fidelity, Participant Experiences, and Potential Outcomes

Anna Wikman, Emma Hovén, Anette Alvariza, Malin Lövgren, Ulrika Kreicbergs, Charlotte Skoglund, Emma Fransson, Gustaf Ljungman, Rickard Ljung, Lisa Ljungman (2022). Psychotropic medication use in parents of survivors of adolescent cancer: A register-based cohort study

Jeanette Winterling, Annika Kisch, Anette Alvariza, Kristofer Årestedt, Karin Bergkvist (2022). Preparedness for family caregiving prior to allogeneic hematopoietic stem cell transplantation

H Yaghoobi, A Shirinabadi Farahani, Camelia Rohani (2022). The role of the mothers' sense of coherence in predicting dental caries risk in children

Jane Österlind, Ingela Henoch, Britt-Marie Ternestedt, Bodil Holmberg, Ramona Schenell, Birgitta Andershed (2022). De 6 S:n: en modell för personcentrerad palliativ vård

Zahra Alizadeh, Camelia Rohani, Maryam Rassouli, Mahnaz Ilkhani, Maryam Hazrati (2021). Transitional Cancer Care Program from Hospital to Home in the Health Care System of Iran

Anette Alvariza, Li Jalmsell, Rakel Eklund, Malin Lövgren, Ulrika Kreicbergs (2021). The Family Talk Intervention in palliative home care when a parent with dependent children has a life-threatening illness: A feasibility study from parents' perspectives

Charlotte Angelhoff, Josefin Sveen, Anette Alvariza, Megan Weber Falk, Ulrika Kreicbergs (2021). Communication, self-esteem and prolonged grief in parent-adolescent dyads, 1-4 years following the death of a parent to cancer

Maria Browall, Amir H. Pakpour, Christina Melin-Johansson, Carina Lundh Hagelin, Jane Österlind, Ingela Henoch (2021). Development and Psychometric Evaluation of a New Short Version of the Swedish Frommelt Attitudes Toward Care of the Dying Scale

Tove Bylund-Grenklo, Dröfn Birgisdóttir, Kim Beernaert, Tommy Nyberg, Viktor Skokic, Jimmie Kristensson, Gunnar Steineck, Carl Johan Fürst, Ulrika Kreicbergs (2021). Correction to: Acute and long-term grief reactions and experiences in parentally cancer-bereaved teenagers.

Tove Bylund-Grenklo, Dröfn Birgisdóttir, Kim Beernaert, Tommy Nyberg, Viktor Skokic, Jimmie Kristensson, Gunnar Steineck, Carl Johan Fürst, Ulrika Kreicbergs (2021). Acute and long-term grief reactions and experiences in parentally cancer-bereaved teenagers

Fiona Cameron, Anna Janze, Anna Klarare (2021). Homecoming—Dignity Through Movement at the End of Life: A Qualitative Interview Study With Healthcare Professionals

Iréne Ericsson, Anne W. Ekdahl, Ingrid Hellström (2021). "To be seen": older adults and their relatives' care experiences given by a geriatric mobile team (GerMoT)

Sofi Fristedt, Annika Grynne, Christina Melin-Johansson, Ingela Henoch, Carina Lundh Hagelin, Maria Browall (2021). Registered nurses and undergraduate nursing students' attitudes to performing end-of-life care

Monica Hermann, Nina Carstens, Lars Kvinge, Astrid Fjell, Marianne Wennersberg, Kjersti Follesø, Knut Skaug, Ake Seiger, Berit Seiger Cronfalk, Anne-Marie Boström (2021). Polypharmacy and Potential Drug-Drug Interactions in Home-Dwelling Older People: A Cross-Sectional Study

Elin Hjorth, Hanna Gabrielsson, Lilian Pohlkamp, Viktoria Wallin (2021). Patientorganisationer som företräder riskgrupper under covid-19-pandemin: förändringar i organisation och relation till andra aktörer

Elin Hjorth, Malin Lovgren, Ulrika Kreicbergs, Thomas Sejersen, Eric Asaba (2021). "Suddenly we have hope that there is a future": Two families’ narratives when a child with spinal muscular atrophy receives a new effective drug

Bodil Holmberg (2021). Self-determination when the body fails: Views on assisted bodily care at the end of life in a nursing home

Kerstin Ivéus, Rakel Eklund, Ulrika Kreicbergs, Malin Lövgren (2021). Family bonding as a result of the family talk intervention in pediatric oncology: Siblings’ experiences

Elsa Karlsson, Anna Klarare, Elisabet Mattsson (2021). Låt våra hemlösa få bo på de tomma hotellen

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Hanna Karlsson, Anna Klarare, Elisabet Mattsson, Johan Vamstad (2021). Låt berörda vara del i forskning

Caritha Klasson, Maria Helde Frankling, Carina Lundh Hagelin, Linda Björkhem-Bergman (2021). Fatigue in Cancer Patients in Palliative Care: A Review on Pharmacological Interventions

Caritha Klasson, Maria Helde-Frankling, Carina Sandberg, Marie Nordström, Carina Lundh Hagelin, Linda Björkhem-Bergman (2021). Vitamin D and Fatigue in Palliative Cancer: A Cross-Sectional Study of Sex Difference in Baseline Data from the Palliative D Cohort

Ulrika Kreicbergs (2021). Paediatric palliative care: A personal perspective

Ulrika Kreicbergs, Lilian Pohlkamp, Josefin Sveen (2021). No impact of previous evidence advocating openness to talk to children about their imminent death

Fatemeh Lashani, Camelia Rohani, Fatemeh Estebsari, Malihe Nasiri (2021). Exploring the relationship between sexual function, sense of coherence, and well-being in a sample of Iranian breast cancer survivors

Reena Lasrado, Therese Bielsten, Mark Hann, James Schumm, Siobhan Theresa Reilly, Linda Davies, Caroline Swarbrick, Robyn Dowlen, John Keady, Ingrid Hellström (2021). Developing a Management Guide (the DemPower App) for Couples Where One Partner Has Dementia: Nonrandomized Feasibility Study

Emma Lundin, Tove Godskesen (2021). End-of-life care for people with advanced dementia and pain: a qualitative study in Swedish nursing homes

Seyedreza Mirsoleymani, Mahsa Matbouei, Parvaneh Vasli, Milad Ahmadi Marzaleh, Camelia Rohani (2021). The Role of Family Caregiver's Sense of Coherence and Family Adaptation Determinants in Predicting Distress and Caregiver Burden in Families of Cancer Patients

Stefan Nilsson, Annie Eriksson, Anna Sörman, Ulrika Kreicbergs, Malin Lövgren, Margaretha Jenholt Nolbris (2021). Children's and adolescents' experiences of living with cancer

Maria Norinder, Kristofer Årestedt, Susanne Lind, Lena Axelsson, Gunn Grande, Gail Ewing, Maja Holm, Joakim Öhlén, Inger Benkel, Anette Alvariza (2021). Higher levels of unmet support needs in spouses are associated with poorer quality of life: A descriptive cross-sectional study in the context of palliative home care

Lina Oelschlägel, Alfhild Dihle, Vivi L. Christensen, Kristin Heggdal, Anne Moen, Jane Österlind, Simen A. Steindal (2021). Implementing welfare technology in palliative homecare for patients with cancer: a qualitative study of health-care professionals' experiences

Marie Olsen, Camilla Udo, Anne-Marie Boström, Lena Marmstål Hammar (2021). Important aspects of home care service: An interview study of persons with dementia.

Anna O'Sullivan (2021). Bereaved family members’ VOICES of support and care during the last three months of life for people with advanced illness

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Anna O'Sullivan, Anette Alvariza, Joakim Öhlén, Cecilia Larsdotter (2021). Support Received by Family Members Before, at and After an Ill Person’s Death

Anna O'Sullivan, Anette Alvariza, Joakim Öhlén, Cecilia Larsdotter ex. Håkanson (2021). The influence of care place and diagnosis on care communication at the end of life: bereaved family members' perspective

Lena Palmryd, Åsa Rejnö, Tove Godskesen (2021). Integrity at end of life in the intensive care unit: a qualitative study of nurses' views

Lilian Pohlkamp, Josefin Sveen, Ulrika Kreicbergs, Malin Lövgren (2021). Parents’ views on what facilitated or complicated their grief after losing a child to cancer

Lilian Pohlkamp, Viktoria Wallin, Elin Hjorth, Hanna Gabrielsson (2021). Ömsesidiga hjälporganisationer i Sverige uppvisar resiliens under covid-19-pandemin

Susanna Pusa, Susanne Lind, Marie Häggström (2021). Social processes in academic-community partnership in health care: A grounded theory study

Eva Randell, Camilla Udo, Maria Warne (2021). A sense of health and coherence in young rural schoolchildren in Sweden

Faezeh Rastgoo, Parvaneh Vasli, Camelia Rohani, Aminreza Amini (2021). Predictors of osteoporosis preventive behaviors among adolescent: A cross-sectional study

E. Saaranen, N. Mogensen, P. Lahteenmaki, B. Klug Albertsen, Ulrika Kreicbergs, M. Heyman, E. Olsson, A. Harila-Saari (2021). Quality of Life in Mothers and Fathers of Children with Acute Lymphoblastic Leukemia in Sweden, Finland and Denmark

Simen A Steindal, Andréa Aparecida Goncalves Nes, Tove E. Godskesen, Susanne Lind, Alfhild Dihle, Anette Winger, Jane Österlind, Fredrik Solvang Pettersen, Heidi Holmen, Anna Klarare (2021). Advantages and Challenges in Using Telehealth for Home-Based Palliative Care: Protocol for a Systematic Mixed Studies Review

Josefin Sveen, Susanna Jernelöv, Lilian Pohlkamp, Ulrika Kreicbergs, Viktor Kaldo (2021). Feasibility and preliminary efficacy of guided internet-delivered cognitive behavioral therapy for insomnia after the loss of a child to cancer: Randomized controlled trial

Megan Weber Falk, Charlotte Angelhoff, Anette Alvariza, Ulrika Kreicbergs, Josefin Sveen (2021). Psychological symptoms in widowed parents with minor children, 2-4 years after the loss of a partner to cancer

Megan Weber, Anette Alvariza, Ulrika Kreicbergs, Josefin Sveen (2021). Family Communication and Psychological Health in Children and Adolescents Following a Parent's Death From Cancer.

Kristofer Årestedt, Margareta Brännström, Lorraine S. Evangelista, Anna Strömberg, Anette Alvariza (2021). Palliative key aspects are of importance for symptom relief during the last week of life in patients with heart failure

Jane Österlind, Ingela Henoch (2021). The 6S-model for person-centred palliative care: A theoretical framework

Anette Alvariza (2020). Hur är det att vara forskare inom palliativ vård?

Anette Alvariza, Bertil Axelsson, Birgit Rasmussen, Britt-Marie Ternestedt, Carl Johan Fürst (2020). Ny definition av palliativ vård med fokus på lidande

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Anette Alvariza, Maria Mjörnberg, Ida Goliath (2020). Palliative care nurses' strategies when working in private homes: A photo-elicitation study

Birgitta Andershed, Britt-Marie Ternestedt (2020). Palliativ vård: begrepp och perspektiv i teori och praktik

Charlotte Angelhoff, Peter Johansson, Erland Svensson, Anna Lena Sundell (2020). Swedish translation and validation of the Pediatric Insomnia Severity Index

Charlotte Angelhoff, Peter Johansson, Erland Svensson, Anna Lena Sundell (2020). Correction to: Swedish translation and validation of the Pediatric Insomnia Severity Index

Lena Axelsson, Anette Alvariza, Nina Carlsson, S. Robin Cohen, Richard Sawatzky, Kristofer Årestedt (2020). Measuring quality of life in life-threatening illness: Content validity and response processes of MQOL-E and QOLLTI-F in Swedish patients and family carers

Lena Axelsson, Anette Alvariza, Maja Holm, Kristofer Årestedt (2020). Intensity of Predeath Grief and Postdeath Grief of Family Caregivers in Palliative Care in Relation to Preparedness for Caregiving, Caregiver Burden, and Social Support

Tommy Carlsson, Anna Klarare, Elisabet Mattsson (2020). Peer support among parents of children with congenital heart defects: A qualitative analysis of written responses submitted via an online survey

Sahar Dabaghi, Fatemeh Esmaielzadeh, Camelia Rohani (2020). Application of Rasch Analysis for Development and Psychometric Properties of Adolescents' Quality of Life Instruments: A Systematic Review

Sandra Doveson, Maja Holm, Lena Axelsson, Per Fransson, Agneta Wennman-Larsen (2020). Facing life-prolonging treatment: The perspectives of men with advanced metastatic prostate cancer - An interview study

Alexandra Eilegård Wallin, Camilla Udo, Ulrika Kreicbergs, Malin Lövgren (2020). Cancer-bereaved siblings’ advice to peers: A nationwide follow-up survey

Rakel Eklund (2020). Barns erfarenheter av ”the Family Talk Intervention”: Att leva med en svårt sjuk förälder som vårdas inom specialiserad palliativ hemsjukvård

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Rakel Eklund, Anette Alvariza, Ulrika Kreicbergs, Li Jalmsell, Malin Lövgren (2020). The family talk intervention for families when a parent is cared for in palliative care: Potential effects from minor children’s perspectives

Rakel Eklund, Ulrika Kreicbergs, Anette Alvariza, Malin Lövgren (2020). Children’s Self-Reports About Illness-Related Information and Family Communication When a Parent Has a Life-Threatening Illness

Ingrid Hellström (2020). Hur kan framtidens vård för äldre utvecklas?

Elin Hjorth (2020). Experiences of care and everyday life in a time of change for families in which a child has spinal muscular atrophy

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Maja Holm, Anette Alvariza (2020). Stödinterventioner till närstående under pågående vård

Bodil Holmberg (2020). När kroppen inte räcker till: Assisterad kroppslig omvårdnad i livets slut på vård- och omsorgsboende

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Bodil Holmberg, Ingrid Hellström, Jane Österlind (2020). Elements of assisted bodily care: Ethical aspects

Annika M. Kisch, Karin Bergkvist, Anette Alvariza, Kristofer Årestedt, Jeanette Winterling (2020). Family caregivers' support needs during allo-HSCT: a longitudinal study

Anna Klarare, Susanne Lind, Johan Hansson, Bjöörn Fossum, Carl Johan Fürst, Carina Lundh Hagelin (2020). Leadership in specialist palliative home care teams: A qualitative study

Ulrika Kreicbergs (2020). När barn får livshotande sjukdom: familjers erfarenheter

Tina Lundberg, Ulla Forinder, Mariann Olsson, Carl Johan Fürst, Kristofer Årestedt, Anette Alvariza (2020). Poor Psychosocial Well-Being in the First Year-and-a-Half After Losing a Parent to Cancer: A Longitudinal Study Among Young Adults Participating in Support Groups

Carina Lundh Hagelin, Carol Tishelman, Birgit H. Rasmussen, Olav Lindqvist (2020). Den komplexa vården under livets sista dagar: Det räcker inte med fyra hörnstenar

Malin Lövgren, Camilla Udo, Anette Alvariza, Ulrika Kreicbergs (2020). Much is left unspoken: Self-reports from families in pediatric oncology

Astrid Norberg (2020). Tröst

Astrid Norberg (2020). Livet med avancerad demenssjukdom

Astrid Norberg, Britt-Marie Ternestedt (2020). Jämlikhet inför döden

Ulrika Olsson Möller, Christa Pranter, Carina Lundh Hagelin, Ingela Beck, Marlene Malmström, Carl Johan Fürst, Birgit H. Rasmussen (2020). Using Cards to Facilitate Conversations About Wishes and Priorities of Patients in Palliative Care

Lilian Pohlkamp (2020). Factors During a Child's Illness Are Associated With Levels of Prolonged Grief Symptoms in Bereaved Mothers and Fathers

Lilian Pohlkamp (2020). Bereaved mothers and fathers: Grief and psychological health 1 to 5 years after losing a child to cancer

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Åsa Rejnö, Britt-Marie Ternestedt, Lennart Nordenfelt, Gunilla Silfverberg, Tove E. Godskesen (2020). Dignity at stake: Caring for persons with impaired autonomy

Simen A. Steindal, Andréa Aparecida Gonçalves Nes, Tove Godskesen, Alfhild Dihle, Susanne Lind, Anette Winger, Anna Klarare (2020). Patients’ Experiences of Telehealth in Palliative Home Care: Scoping Review

Josefin Sveen, Kristina Bondjers, Julia Heinsoo, Filip K Arnberg (2020). Psychometric Evaluation of the Swedish Version of the Prolonged Grief Disorder-13 (PG-13) in a Bereaved Mixed Trauma Sample

Britt-Marie Ternestedt (2020). Döden i samhället

Britt-Marie Ternestedt, Birgitta Andershed (2020). Den palliativa vårdens utveckling

Britt-Marie Ternestedt, Astrid Norberg (2020). Identitet

Megan Weber Falk (2020). Development and Evaluation of the Grief and Communication Family Support Intervention for Parentally Bereaved Families in Sweden

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Cecilia Widberg, Birgitta Wiklund, Anna Klarare (2020). Patients’ experiences of eHealth in palliative care: an integrative review

Jane Österlind, Ingela Henoch (2020). De 6 S:n: en modell för personcentrerad palliativ vård

Anette Alvariza, Maja Holm (2019). Palliativ vård i hemmet

Anette Alvariza, Olav Lindqvist, Joakim Öhlén, Birgit Holritz Rasmussen (2019). Omvårdnad vid livets slut

Rebecka Andersen, Anna O'Sullivan (2019). De som samhället inte vill se

Kim Beernaert, Malin Lövgren, Jørgen Jeppesen, Ulla Werlauff, Jes Rahbek, Thomas Sejersen, Ulrika Kreicbergs (2019). Parents' Experiences of Information and Decision Making in the Care of Their Child With Severe Spinal Muscular Atrophy: A Population Survey

Elisabeth Bergdahl, Britt-Marie Ternestedt, Carina Berterö, Birgitta Andershed (2019). The theory of a co-creative process in advanced palliative home care nursing encounters: A qualitative deductive approach over time.

Dröfn Birgisdóttir, Tove Bylund Grenklo, Tommy Nyberg, Ulrika Kreicbergs, Gunnar Steineck, Carl J Fürst (2019). Losing a parent to cancer as a teenager: Family cohesion in childhood, teenage, and young adulthood as perceived by bereaved and non-bereaved youths.

Elin Frögli, Anna Rudman, Malin Lövgren, Petter Gustavsson (2019). Problems with task mastery, social acceptance, and role clarity explain nurses’ symptoms of burnout during the first professional years: A longitudinal study

Ragnhild Hedman, Astrid Norberg, Ingrid Hellström (2019). Agency and communion in people with Alzheimer's disease, as described by themselves and their spousal carers.

Ingela Henoch, Jane Österlind (2019). Development of the 6S Dialogue Tool to facilitate person-centred palliative care.

Elin Hjorth, Ulrika Kreicbergs, Thomas Sejersen, Jørgen Jeppesen, Ulla Werlauff, Jes Rahbek, Malin Lövgren (2019). Bereaved Parents More Satisfied With the Care Given to Their Child With Severe Spinal Muscular Atrophy Than Nonbereaved

Bodil Holmberg, Ingrid Hellström, Astrid Norberg, Jane Österlind (2019). Assenting to exposedness: meanings of receiving assisted bodily care in a nursing home as narrated by older persons.

Bodil Holmberg, Ingrid Hellström, Astrid Norberg, Jane Österlind (2019). Assenting to exposedness: meanings of receiving assisted bodily care (RABC) in a nursing home as narrated by older persons

Bodil Holmberg, Ingrid Hellström, Jane Österlind (2019). End-of-life care in a nursing home: Assistant nurses' perspectives

Bodil Holmberg, Ingrid Hellström, Jane Österlind (2019). Being a spectator in ambiguity: Family members' perceptions of assisted bodily care in a nursing home

Cecilia Högberg, Anette Alvariza, Ingela Beck (2019). Patients' experiences of using the Integrated Palliative care Outcome Scale for a person-centered care: A qualitative study in the specialized palliative home-care context

Linda Høgsnes, Karl-Gustaf Norbergh, Christina Melin-Johansson (2019). “Being in Between”: Nurses' Experiences When Caring for Individuals With Dementia and Encountering Family Caregivers' Existential Life Situations

Anna Klarare (2019). Kommunikation i palliativ vård

Anna Klarare, Johan Hansson, Bjöörn Fossum, Carl Johan Fürst, Carina Lundh Hagelin (2019). Team type, team maturity and team effectiveness in specialized palliative home care: an exploratory questionnaire study

Susanne Lind, Lars Wallin, Carl Johan Fürst, Ingela Beck (2019). The integrated palliative care outcome scale for patients with palliative care needs: Factors related to and experiences of the use in acute care settings.

Tina Lundberg, Ulla Forinder, Mariann Olsson, Carl Johan Fürst, Kristofer Årestedt, Anette Alvariza (2019). Corrigendum to "Bereavement stressors and psychosocial well-being of young adults following the loss of a parent - A cross-sectional survey" [Eur. J. Oncol. Nurs. 35 (2018) 33-38].

Malin Lövgren, Ulrika Kreicbergs, Camilla Udo (2019). Family talk intervention in paediatric oncology: A pilot study protocol

Malin Lövgren, Christina Melin-Johansson, Camilla Udo, Josefin Sveen (2019). Telling the truth to dying children: End‐of‐life communication with families

Malin Lövgren, Josefin Sveen, Gunnar Steineck, Alexandra Eilegård Wallin, Mary-Elizabeth B Eilertsen, Ulrika Kreicbergs (2019). Spirituality and religious coping are related to cancer-bereaved siblings' long-term grief

Titti Melin-Johansson (2019). Egna val och frihetens baksidor

Astrid Norberg (2019). Sense of Self among Persons with Advanced Dementia

Anneli Ozanne, Richard Sawatzky, Cecilia Håkanson, Anette Alvariza, Carl Johan Fürst, Kristofer Årestedt, Joakim Öhlén (2019). Symptom relief during last week of life in neurological diseases.

Lilian Pohlkamp, Ulrika Kreicbergs, Josefin Sveen (2019). Bereaved mothers' and fathers' prolonged grief and psychological health 1 to 5 years after loss-A nationwide study.

Lilian Pohlkamp, Ulrika Kreicbergs, Josefin Sveen (2019). Prolonged Grief is Associated with Different Factors During the Child’s Illness for Mothers and Fathers

Linda Rönnberg, Ulrica Nilsson, Ove Hellzén, Christina Melin-Johansson (2019). The Art Is to Extubate, Not to Intubate: Swedish Registered Nurse Anesthetists' Experiences of the Process of Extubation After General Anesthesia

Josefin Sveen, Susanna Jernelöv, Lilian Pohlkamp, Ulrika Kreicbergs, Viktor Kaldo (2019). Guided internet cognitive behavioral therapy for insomnia after the loss of a child: randomized controlled trial

Josefin Sveen, Lilian Pohlkamp, Ulrika Kreicbergs, Maarten C Eisma (2019). Rumination in bereaved parents: Psychometric evaluation of the Swedish version of the Utrecht Grief Rumination Scale (UGRS).

I Svenningsson, E-L Petersson, Camilla Udo, J. Westman, C Björkelund, L Wallin (2019). Process evaluation of a cluster randomised intervention in Swedish primary care: Using care managers in collaborative care to improve care quality for patients with depression.

Camilla Udo, Ulrika Kreicbergs, Bertil Axelsson, Olle Björk, Malin Lövgren (2019). Physicians working in oncology identified challenges and factors that facilitated communication with families when children could not be cured

Camilla Udo, Malin Lövgren, Josefin Sveen, Tove Bylund-Grenklo, Anette Alvariza, Ulrika Kreicbergs (2019). A Nationwide Study of Young Adults' Perspectives on Participation in Bereavement Research

Megan Weber, Anette Alvariza, Ulrika Kreicbergs, Josefin Sveen (2019). Communication in families with minor children following the loss of a parent to cancer.

Megan Weber, Anette Alvariza, Ulrika Kreicbergs, Josefin Sveen (2019). Adaptation of a Grief and Communication Family Support Intervention for Parentally Bereaved Families in Sweden

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Följ oss på sociala medier