Kanker

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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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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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Oncologische nazorg in de eerste lijn

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

Registratie gezondheidsproblemen na de (medicamenteuze) behandeling van kanker

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

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

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

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

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

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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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Cancer survivors' activation to self-management and its relationship with participation in paid work and work-related problems.

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Feasibility and acceptability of follow-up for prostate cancer in primary care.

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Actively approaching women with a history of ovarian cancer for genetic counselling by GP, desirable and feasible?

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Determinants of adherence to recommendations for cancer prevention among Lynch Syndrome mutation carriers: a qualitative exploration.

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Instrumental and affective communication with patients with limited health literacy in the palliative phase of cancer or COPD.

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The Dutch LATER physical outcomes set for self-reported data in survivors of childhood cancer.

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Large variation in assessment and outcome definitions to describe the burden of long-term morbidity in childhood cancer survivors: a systematic review.

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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.

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Determinanten van niet-pluisgevoel bij kanker.

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Self-management of patients with advanced cancer: a systematic review of experiences and attitudes.

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

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Cancer screening programs should incorporate values and preferences of potential participants.

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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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Autonomy and information: do patients with advanced cancer receive what they want?

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Palliative care for patients with cancer: do patients receive the care they consider important?

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A nurse-led self-management support intervention for patients and informal caregivers facing incurable cancer: a feasibility study from the perspective of nurses.

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Huisartsenzorg bij langetermijnoverlevenden van kinderkanker.

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Motives for non-adherence to colonoscopy advice after a positive colorectal cancer screening test result: a qualitative study.

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Care provided to cancer patients in their last month of life: a retrospective study in Patients who died in Dutch university hospitals.

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