about
Communicating uncertainty can lead to less decision satisfaction: a necessary cost of involving patients in shared decision making?The urban underserved: attitudes towards gaining full access to electronic medical recordsEstablishing local priorities for a health research agendaPatient and family involvement in adult critical and intensive care settings: a scoping reviewThe effect of qualitative vs. quantitative presentation of probability estimates on patient decision-making: a randomized trialHealthcare in a land called PeoplePower: nothing about me without meConvergences and divergences of diabetic patients' and healthcare professionals' opinions of care: a qualitative studyYoung adults' experiences of seeking online information about diabetes and mental health in the age of social mediaThe PRIME project: developing a patient evidence-baseCommunication practices that encourage and constrain shared decision making in health-care encounters: Systematic review of conversation analytic researchDecision influences and aftermath: parents, stillbirth and autopsyEffect on cardiovascular disease risk factors of interventions to alter consultations between practitioners and patients with type 2 diabetes: A systematic review and meta-analysis of trials in primary care.Patient expectations for management of chronic non-cancer pain: A systematic review.Towards generic online multicriteria decision support in patient-centred health carePatient experience with, and use of, an electronic monitoring system to assess vaccination responses.Who prefers the 'cost-effectiveness ratio' prioritization approach in health-care decisions? Results of an empirical analysis.Patient-centred improvements in health-care built environments: perspectives and design indicatorsExpect the unexpected: patients' and families' expectations and experiences of new clinical procedures.A questionnaire to measure health practitioners' attitudes to partnership in medicine taking: LATCon II.Patient participation as dialogue: setting research agendas.Lessons from local engagement in Latin American health systems.Involving patients in health technology funding decisions: stakeholder perspectives on processes used in AustraliaPandemic influenza communication: views from a deliberative forum.A devolved model for public involvement in the field of mental health research: case study learning.Empowerment, patient centred care and self-managementLay people's interpretation of ethical values related to mass vaccination; the case of A(H1N1) vaccination campaign in the province of Quebec (French Canada)'No one wants to be the face of Herpes London': a qualitative study of the challenges of engaging patients and the public in sexual and reproductive health and HIV/AIDS services.Hearing the voices of service user researchers in collaborative qualitative data analysis: the case for multiple codingGiving tape recordings or written summaries of consultations to people with cancer: a systematic review.Public preferences for communicating personal genomic risk information: a focus group studyImproving communication between health professionals and women in maternity care: a structured review.'She believed in me'. What patients with depression value in their relationship with practitioners. A secondary analysis of multiple qualitative data setsFeedback from community pharmacy users on the contribution of community pharmacy to improving the public's health: a systematic review of the peer reviewed and non-peer reviewed literature 1990-2002.Patient participation in clinical encounters: a systematic review to identify self-report measures.HELP - the Health Education Library for People, India's first Consumer Health Education Resource Centre.Opinions of women with high inherited breast cancer risk about prophylactic mastectomy: an initial evaluation from a screening trial including magnetic resonance imaging and ductal lavage.Depressed patients' perceptions of depression treatment decision-making.Meeting information needs to facilitate decision making: report cards for people with disabilities.Understanding why patients with immune thrombocytopenia are deeply divided on splenectomy.Literacy disparities in patient access and health-related use of Internet and mobile technologies.
P1433
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P1433
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journal
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revista científica
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rivista scientifica
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vědecký časopis
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wetenschappelijk tijdschrift van Wiley-Blackwell
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wissenschaftliche Fachzeitschrift
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مجلة
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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Health Expectations
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P31
P3181
P1055
P1058
P1156
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P1277
P1476
Health Expectations
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