Patient-clinician relationship/communication | Service-related/organizational factors |
---|---|
Giving an objective overview of options Establishing a trusting relationship Verifying patients prior knowledge together with their desire for information Working to an individualized approach (more ‘counseling’ rather than ‘education’, with regard to time and content, e.g. discussing impact on the daily life) Encouraging patients to participate in the decision (increasing confidence) Training health care staff in emotional support (e.g. leaving room for fear/doubt of patients) Improving skills in bringing bad news Engaging relatives, and learning how to deal with informing relatives Making patients and their relatives reflect (listing pros and cons) Using straight-forward language Summarizing regularly, checking for understanding, and clearly identifying the next steps | Improving clinical expertise for all health care providers, ensuring that informal in-hospital conversations are not biased Creating pre-dialysis opportunities to talk to patients already on dialysis Fine-tuning decision support tools Ensuring private space and taking time for each patient, though considering an accurate workflow Improving cultural and spiritual understanding and support Reflecting in group about ethical dilemmas Routinely establishing prognosis through prediction instruments Providing consecutive appointments, also once patients have started (some patients may think about switching from modality) Offering advanced care planning early in the disease Assisting patients to complete advance care directives Training in palliative support, avoiding therapeutic persistence Obtaining greater institutional engagement Focusing on multidisciplinary cooperation and discussion meetings |