Cancer

Kanker

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Towards an open and effective dialogue on complementary medicine in oncology: protocol of patient participatory study 'COMMON'.

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VOICE Verpleegkundigen-Ouderen In ChemotherapiE

Nieuws

Europees netwerk van kankerzorgcentra beoogt gelijke toegang tot de beste kankerzorg voor alle EU-inwoners

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Quick scan of cancer infrastructures in European countries: report.

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Decision-making in screening positive participants who follow up with colonoscopy in the Dutch colorectal cancer screening programme: A mixed-method study.

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Addressing challenges in information-provision: a qualitative study among oncologists and women with advanced breast cancer.

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End-of-life communication in advanced cancer: international trends (2009–2014).

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Reduced risk of pancreatic cancer associated with asthma and nasal allergies.

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Persuasive communication in medical decision-making during consultations with patients with limited health literacy in hospital-based palliative care.

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The European multistakeholder PanCareFollowUp project: novel, person-centred survivorship care to improve care quality, effectiveness, cost-effectiveness and accessibility for cancer survivors and caregivers.

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Abdominal symptoms in general practice: frequency, cancer suspicions raised, and actions taken by GPs in six European countries. Cohort study with prospective registration of cancer.

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Abdominal symptoms and cancer in the abdomen: prospective cohort study in European primary care.

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Symptoms and signs of colorectal cancer, with differences between proximal and distal colon cancer: a prospective cohort study of diagnostic accuracy in primary care.

Peilstations 2012 e.v.: vroegdiagnostiek van buiktumoren

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Fatigue among long-term breast cancer survivors: a controlled cross-sectional study.

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Health literacy, information provision and satisfaction in advanced cancer consultations: two observational studies using level of education as a proxy.

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Diagnostic accuracy of follow-up tests for detecting colorectal cancer recurrences in primary care: a systematic review and meta-analysis.

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Development of a plain-language guide for discussing breast cancer genetic counseling and testing with patients with limited health literacy.

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Effect of a health literacy training program for surgical oncologists and specialized nurses on disparities in referral to breast cancer genetic testing.

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Communication about breast cancer genetic counseling with patients with limited health literacy or a migrant background: evaluation of a training program for healthcare professionals.

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Piloting a generic cancer consumer quality index in six European countries.

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Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based study.

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The impact of watching educational video clips on analogue patients' physiological arousal and information recall.

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Counselees’ expressed level of understanding of the risk estimate and surveillance recommendation are not associated with breast cancer surveillance adherence.

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Non-oncology physician visits after diagnosis of cancer in children.

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Health-related quality of life and health care use in cancer survivors compared with patients with chronic diseases.

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Many diseases, one model of care?

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Sharing decisions during diagnostic consultations: an observational study in pediatric oncology.

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Differences in palliative care quality between patients with cancer, patients with organ failure and frail patients: a study based on measurements with the Consumer Quality Index Palliative Care for bereaved relatives.

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Non-oncology physician visits after diagnosis of cancer in adolescents and young adults.

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An integrated process and outcome evaluation of a web-based communication tool for patients with malignant lymphoma: randomized controlled trial.

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Effect of the partner’s health and support on cancer patients’ use of general practitioner care.

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Effects of eHealth for patients and informal caregivers confronted with cancer: a meta-review.

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Palliatieve zorg voor mensen met kanker en hun naasten: Sluit het zorgaanbod in de eerste lijn aan op de behoeften?

Oncologische nazorg in de eerste lijn

‘De last van het weten’ verlichten door het verbeteren van communicatie met ernstig zieke borstkankerpatienten

Registratie gezondheidsproblemen na de (medicamenteuze) behandeling van kanker

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Talking about death with children with incurable cancer: perspectives from parents.

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Developing a digital communication training tool on information provision in oncology: uncovering learning needs and training preferences.

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Involvement of a case manager in palliative care reduces hospitalisations at the end of life in cancer patients: a mortality follow-back study in primary care.

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Incidence of isolated local breast cancer recurrence and contralateral breast cancer: a systematic review.

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Huisartsenzorg in cijfers: invloed van kanker op het zorggebruik van partners.

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Occupational exposure to endocrine disruptors and lymphoma risk in a multi-centric European study.

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Identifying patients with a history of ovarian cancer for referral for genetic counselling: non-randomised comparison of two case-finding strategies in primary care.

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Palliative care for patients with cancer: do patients receive the care they consider important? A survey study.

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How do treatment aims in the last phase of life relate to hospitalizations and hospital mortality? A mortality follow-back study of Dutch patients with five types of cancer.

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The availability and effectiveness of tools supporting shared decision making in metastatic breast cancer care: a review.

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Feasibility and acceptability of follow-up for prostate cancer in primary care: a pilot study.

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Differences in primary palliative care between people with organ failure and people with cancer: An international mortality follow-back study using quality indicators.

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Review of guidance on recurrence risk management for general practitioners in breast cancer, colorectal cancer and melanoma guidelines.

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