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Patient Preference and Adherence Volume 10, 2016 - Issue
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Original Research

“My cancer is not my deepest concern”: life course disruption influencing patient pathways and health care needs among persons living with colorectal cancer

Anita Salamonsen1 National Research Center in Complementary and Alternative Medicine, Department of Community Medicine, UiT the Arctic University of Norway, Tromsø, NorwayCorrespondence[email protected]
,
Mona A Kiil2 Department of Clinical Medicine, UiT the Arctic University of Norway, Tromsø, Norway
,
Agnete Egilsdatter Kristoffersen1 National Research Center in Complementary and Alternative Medicine, Department of Community Medicine, UiT the Arctic University of Norway, Tromsø, Norway
,
Trine Stub1 National Research Center in Complementary and Alternative Medicine, Department of Community Medicine, UiT the Arctic University of Norway, Tromsø, Norway
&
Gro R Berntsen1 National Research Center in Complementary and Alternative Medicine, Department of Community Medicine, UiT the Arctic University of Norway, Tromsø, Norway;3 Norwegian Center for eHealth Research, University Hospital of Northern Norway, Tromsø, Norway
Pages 1591-1600 | Published online: 17 Aug 2016

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Read on this site (3)

Frank Hansen, Gro Rosvold Berntsen & Anita Salamonsen. (2020) Medical pluralism in the aftermath of cancer: health seeking actions and cancer patients’ shaping of trajectories to healing. Anthropology & Medicine 27:3, pages 330-346.
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Frank Hansen, Gro K. Rosvold Berntsen & Anita Salamonsen. (2019) Patient pathways as social drama: a qualitative study of cancer trajectories from the patient’s perspective. International Journal of Qualitative Studies on Health and Well-being 14:1.
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Frank Hansen, Gro K. Rosvold Berntsen & Anita Salamonsen. (2018) “What matters to you?” A longitudinal qualitative study of Norwegian patients’ perspectives on their pathways with colorectal cancer. International Journal of Qualitative Studies on Health and Well-being 13:1.
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Articles from other publishers (13)

Ellen L. Davies, Lemma N. Bulto, Alison Walsh, Danielle Pollock, Vikki M. Langton, Robert E. Laing, Amy Graham, Melissa Arnold‐Chamney & Janet Kelly. (2022) Reporting and conducting patient journey mapping research in healthcare: A scoping review. Journal of Advanced Nursing 79:1, pages 83-100.
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Cecilie Fromholt Olsen, Astrid Bergland, Asta Bye, Jonas Debesay & Anne G. Langaas. (2021) Crossing knowledge boundaries: health care providers’ perceptions and experiences of what is important to achieve more person-centered patient pathways for older people. BMC Health Services Research 21:1.
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Anne B Arreskov, Anette H Graungaard, Mads T Kristensen, Jens Søndergaard & Annette S Davidsen. (2018) Life goes on… Patient perspectives on having a cancer diagnosis and other comorbid diseases: A qualitative study. Chronic Illness 17:1, pages 17-28.
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Antonio Jorge Silva Correa Júnior, Helena Megumi Sonobe, André Aparecido da Silva Teles, Wagner Felipe dos Santos Neves & Mary Elizabeth de Santana. (2021) Experiences, dietary behavior and cultural characteristics of people with colorectal neoplasms. Revista Brasileira de Enfermagem 74:1.
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Emma Ward & Cheryl Swanson. (2020) The Impact of the Theory of Nursing for the Whole Person on the Professional Practice of Nursing School Graduates. Journal of Christian Nursing 37:2, pages 117-112.
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Sara Delilovic, Henna Hasson, Mårten Åhström & Mia von Knorring. (2019) Implementing standardized cancer patient pathways (CPPs) – a qualitative study exploring the perspectives of health care professionals. BMC Health Services Research 19:1.
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Anita Salamonsen & Solveig Wiesener. (2019) “Then I went to a hospital abroad”: acknowledging implications of stakeholders’ differing risk understandings related to use of complementary and alternative medicine in European health care contexts. BMC Complementary and Alternative Medicine 19:1.
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Manuel Finelli. (2019) Children living in families with cancer; the interplay between children's agency and family biographical disruptions. SALUTE E SOCIETÀ:3, pages 72-83.
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Clair Le Boutillier, Stephanie Archer, Claire Barry, Alex King, Louise Mansfield & Catherine Urch. (2019) Conceptual framework for living with and beyond cancer: A systematic review and narrative synthesis. Psycho-Oncology.
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Christiane Hildebrandt, Hanna Mayer & Antje Koller. (2018) Experiences of patients with colorectal cancer from diagnosis until completion of treatment: A meta‐ethnography approach. Psycho-Oncology 28:2, pages 219-227.
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Anita Salamonsen & Rolf Ahlzén. (2017) Epistemological challenges in contemporary Western healthcare systems exemplified by people’s widespread use of complementary and alternative medicine. Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine 22:4, pages 356-371.
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James W. CareyNeal CarnesAlisú Schoua-GlusbergKatherine KenwardDeborah GelaudeDamian DensonElizabeth GallLaura A. RandallPaula M. Frew. (2018) Barriers and Facilitators for Clinical Care Engagement Among HIV-Positive African American and Latino Men Who Have Sex with Men. AIDS Patient Care and STDs 32:5, pages 191-201.
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Grigorios Kotronoulas, Constantina Papadopoulou, Kathryn Burns-Cunningham, Mhairi Simpson & Roma Maguire. (2017) A systematic review of the supportive care needs of people living with and beyond cancer of the colon and/or rectum. European Journal of Oncology Nursing 29, pages 60-70.
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