Dagny Renata Faksvåg Haugen's picture

Dagny Renata Faksvåg Haugen

Professor, Professor of Palliative Medicine
  • E-maildagny.haugen@uib.no
  • Visitor Address
    Haukeland Universitetssykehus Laboratoriebygget, 7. etg. Heis øst
    5009 Bergen
  • Postal Address
    Postboks 7804
    5020 Bergen

Coordinator for the international conference A Good Ending - Good for All, 6th-7th November 2019, Bergen

Academic lecture
  • Show author(s) (2003). Physiotherapy for palliative care patients in home care. Investigation from a rural coastal district of Western Norway.
  • Show author(s) (2003). Kompetansesenter i lindrende behandling Helseregion vest: Organisering og virksomhet.
  • Show author(s) (2023). Visiting restrictions during the COVID-19 pandemic and bereaved relatives’ quality of life. . Palliative Medicine. 273-274.
  • Show author(s) (2022). iLIVE Project Volunteer Study: Using a newly developed European Core Curriculum (ECC) to develop and implement end-of-life-care volunteer services within 5 hospitals across 5 countries. Palliative Medicine. 96-96.
  • Show author(s) (2022). Validation of ‘Care Of the Dying Evaluation’ (CODETM), a post-bereavement tool, within an international context. Palliative Medicine. 17-17.
  • Show author(s) (2022). Maintaining quality of palliative care in a global pandemic: experiences of health care professionals from 14 countries during the COVID-19 pandemic (the CO-LIVE study). . Palliative Medicine. 105-105.
  • Show author(s) (2022). Healthcare professionals and family caregivers’ experiences of using a medication kit for symptom management at the end of life – a literature review. . Palliative Medicine. 80-80.
  • Show author(s) (2021). Care for dying patients under the Covid-19 pandemic in Norway: a survey of bereaved relatives. Palliative Medicine. 34-34.
  • Show author(s) (2020). iLIVE project: using a delphi approach to gain international consensus on core concepts/themes to be included in a transnational hospital volunteer training programme, to support patients at the end of life and their families. Palliative Medicine. 218-218.
  • Show author(s) (2020). What do bereaved relatives want to tell us? - Free text comments of the International Care of the Dying Evaluation (i-CODE) survey: a mixed methods approach. Palliative Medicine. 97-97.
  • Show author(s) (2020). Putting international research into practice. Using bereaved relatives’ feedback to directly impact the clinical care for those dying from cancer in hospital. Palliative Medicine. 89-90.
  • Show author(s) (2020). Proof of concept: quality improvement based on results of the i-CODE survey in Argentina and Poland (Project ERAnet LAC CODE). Palliative Medicine. 96-96.
  • Show author(s) (2020). In partnership with patients and the public: conducting the international “Care Of the Dying Evaluation” (i-CODE) post-bereavement survey. Palliative Medicine. 16-16.
  • Show author(s) (2019). The international 'care of the dying evalution' (CODE) project: using bereaved relatives to assess care for dying cancer patients in Europe and South America . BMJ Supportive & Palliative Care. A2-A2.
  • Show author(s) (2019). Pilot Testing of the First Version of the European Association for Palliative Care (EAPC) Basic Dataset. Palliative Medicine. 319-320.
  • Show author(s) (2019). Healthcare professionals' views on implementation of Advance Care Planning for patients with advanced pulmonary diseases - a pilot study. Palliative Medicine. 68-69.
  • Show author(s) (2019). "Did a member of the healthcare team talk to you about what to expect when your relative was dying?" - "No." Quality of care for cancer patients dying in hospitals: first results from the international CODE (Care of the Dying Evalution) survey. . Palliative Medicine. 68-68.
  • Show author(s) (2018). The International ERANet-LAC CODE (Care Of the Dying Evaluation): Developing an international measure for quality of care for the dying. Palliative Medicine. 283-283.
  • Show author(s) (2018). Introducing advance care planning for patients with life-threatening pulmonary disease in the hospital setting – what do patients talk about? . Palliative Medicine. 278-278.
  • Show author(s) (2018). Clinically significant drug-drug-interactions involving medications used for symptom control in patients with advanced malignant disease. A systematic review. Palliative Medicine. 260-260.
  • Show author(s) (2017). How to design and evaluate a student-selected component in palliative medicine for medical students. European Journal of Palliative Care. 244-244.
  • Show author(s) (2017). From bed to bench and back: finding evidence to support our clinical practice. European Journal of Palliative Care. 13-13.
  • Show author(s) (2017). Evidence base for palliative drug treatment in the last days of life - a systematic review. European Journal of Palliative Care. 1070-1070.
  • Show author(s) (2016). PhD and Master education – an update. Palliative Medicine. NP6-NP6.
  • Show author(s) (2016). Does implementation of a care pathway for dying patients in nursing homes improve communication with the relatives? Palliative Medicine. NP60-NP60.
  • Show author(s) (2015). «It is difficult to talk about, but I think it can help me» - A qualitative study about Advance Care Planning for patients with life-threatening pulmonary disease. Abstract P1-158. European Journal of Palliative Care. 102-102.
  • Show author(s) (2015). Impact of the Nordic Specialist Course on the development of Palliative Medicine in the Nordic countries. A survey among 150 participants from five courses during 2003-2013.Abstract no P1-270. European Journal of Palliative Care. 124-124.
  • Show author(s) (2015). Do we need a network coordinator for Liverpool Care Pathway in Norway? Abstract P1 - 199. European Journal of Palliative Care. 110-110.
  • Show author(s) (2015). Clinically significant drug-drug interactions involving opioids in patients with cancer: a systematic review. Abstract no P1-009. European Journal of Palliative Care. 71-71.
  • Show author(s) (2014). Testing a web-based tool for registration of quality indicators in palliative care services – a qualitative analysis. Palliative Medicine. 843-843.
  • Show author(s) (2014). Obtaining an international PhD in palliative care. Part B: A biomedical research perspective from the European Palliative Care Research Centre. Palliative Medicine. 543.
  • Show author(s) (2014). Basic palliative care in a large teaching hospital - under pressure? Palliative Medicine. 684.
  • Show author(s) (2013). How is depression classified, assessed, and reported in clinical studies of palliative care cancer patients? A systematic literature review. European Journal of Palliative Care.
  • Show author(s) (2011). Quality of life in an international cohort of cancer patients with and without breakthrough cancer pain. European Journal of Palliative Care. 229-229.
  • Show author(s) (2011). Characteristics of breakthrough pain in an international cohort of cancer patients. European Journal of Palliative Care. 229-229.
  • Show author(s) (2010). Physical Exercise in Palliative Care Cancer Patients - A Phase II Randomised Clinical Trial (RCT). Palliative Medicine. S13.
  • Show author(s) (2010). Comparisons of Numerical Rating Scales (NRS), Verbal Rating Scales (VRS) and Visual Analogue Scales (VAS) for assessment of pain intensity - which is the preferred scale? Palliative Medicine. S43.
  • Show author(s) (2010). Clinical priorities, Barriers and Solutions in End-of-Life Cancer Care Research in Europe. Report from a Workshop. Palliative Medicine. S7.
  • Show author(s) (2010). Acceptability and Validity of a Computerised Body Map for Pain Assessment in Cancer Patients. Palliative Medicine. S62.
  • Show author(s) (2010). A Survey of End-of-Life Cancer Care Research in Europe. Palliative Medicine. S208-S209.

More information in national current research information system (CRIStin)

Project Coordinator, ERANet-LAC CODE project: International Care Of the Dying Evaluation (CODE): quality of care for cancer patients as perceived by bereaved relatives, European Commission FP7, 2017-2020 http://www.icode7.org/icode7/homepage.html

Partner, The I-LIVE Project. Live well, die well, Horizon 2020, 2019-2022