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RESEARCH PRODUCT
Reflections on communication of disease prognosis and life expectancy by patients with colorectal cancer undergoing palliative care: a qualitative study.
Ulrika SöderhamnIngvild VistadGudrun Rohdesubject
Research designAdultMalemedicine.medical_specialtyPalliative careColorectal cancer1720vulnerabilitycompassionDiseasepalliative care informationInterviews as Topic03 medical and health sciences0302 clinical medicineLife ExpectancyDrug TherapymedicineHumans030212 general & internal medicine1506Disease prognosisQualitative ResearchAgedPhysician-Patient Relationsbusiness.industryNorwayCommunicationResearchPalliative CareGeneral MedicineMiddle Agedlife-worldmedicine.diseasePrognosisPeer reviewVDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Onkologi: 762Family medicineLife expectancyFemalebusinessColorectal Neoplasms030217 neurology & neurosurgeryQualitative researchdescription
ObjectivesPatients with colorectal cancer undergoing palliative treatment receive extensive treatment-related information throughout their disease trajectory. We aimed to explore the experiences of patients with incurable colorectal cancer while in palliative care and their reflections on the information provided by physicians and nurses. Our main focus was the patients’ thoughts about how information about disease status and life expectancy was communicated, from the first time that they were informed about the incurable nature of their disease through to postsurgery palliative treatment.SettingsPatients with colorectal cancer receiving palliative chemotherapy.Research designWe used a qualitative approach, and the data were analysed by qualitative content analysis.Participants20 patients (34–75 years of age) were included in the study; 12 received first-line chemotherapy and 8 received second-line chemotherapy. Eleven patients were treated by oncologists, and nine were treated by junior physicians.ResultsData-driven empirical analysis identified three themes: (1) inadequate information during the initial phase of the disease trajectory; (2) hope and information further into the disease trajectory and (3) personal, professional and organisational factors that influenced information and communication throughout the disease trajectory.ConclusionThe participants’ experience of being told for the first time that they had an incurable disease was perceived as inadequate, while postsurgery palliative chemotherapy, physicians and nurses offered hope. The participants preferred customised information about their treatment and likely future prospects and physicians and nurses who took a holistic and compassionate approach focusing on their lifeworld. To be a sensitive, holistic and compassionate physician or nurse requires knowledge and confidence. To achieve this requires training and guidance at universities and in hospitals.
year | journal | country | edition | language |
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2019-03-10 | BMJ open |