Health Expectations: Vol 21, No 1

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Health Expectations: Volume 21, Issue 1

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EDITORIAL BRIEFING

Challenges to measuring and achieving shared decision-making in practice

REVIEW ARTICLES

Black and minority ethnic group involvement in health and social care research: A systematic review

“This illness diminishes me. What it does is like theft”: A qualitative meta-synthesis of people's experiences of living with asthma

Impact and experiences of delayed discharge: A mixed-studies systematic review

Patient value: Perspectives from the advocacy community

ORIGINAL RESEARCH PAPERS

Views of general practice staff about the use of a patient-oriented treatment decision aid in shared decision making for patients with type 2 diabetes: A mixed-methods study

Extent, quality and impact of patient and public involvement in antimicrobial drug development research: A systematic review

Using CollaboRATE, a brief patient-reported measure of shared decision making: Results from three clinical settings in the United States

Assessing the public acceptability of proposed policy interventions to reduce the misuse of antibiotics in Australia: A report on two community juries

Improving the quality of prison research: A qualitative study of ex-offender service user involvement in prison suicide prevention research

Getting on the same page: Communication, patient involvement and shared understanding of “decisions” in oncology

A qualitative study exploring the difficulties influencing decision making at the end of life for people with dementia

Decision making in NICE single technological appraisals: How does NICE incorporate patient perspectives?

Improving adherence to multiple medications in older people in primary care: Selecting intervention components to address patient-reported barriers and facilitators

Citizen's Charter in a primary health-care setting of Nepal: An accountability tool or a “mere wall poster”?

Material practices for meaningful engagement: An analysis of participatory learning and action research techniques for data generation and analysis in a health research partnership

Comparison of preferences of healthcare professionals and MS patients for attributes of disease-modifying drugs: A best-worst scaling

Understanding leisure-time physical activity: Voices of people with MS who have moderate-to-severe disability and their family caregivers

Involved, inputting or informing: “Shared” decision making in adult mental health care

The role of experiential knowledge within attitudes towards genetic carrier screening: A comparison of people with and without experience of spinal muscular atrophy

Factors associated with shared decision making among primary care physicians: Findings from a multicentre cross-sectional study

Involving citizens in priority setting for public health research: Implementation in infection research

A coproduced patient and public event: An approach to developing and prioritizing ambulance performance measures

Multiple influences on participating in physical activity in older age: Developing a social ecological approach

Prioritizing novel and existing ambulance performance measures through expert and lay consensus: A three-stage multimethod consensus study

Tensions in perspectives on suicide prevention between men who have attempted suicide and their support networks: Secondary analysis of qualitative data

Willingness to pay for antiretroviral drugs among HIV and AIDS clients in south-east Nigeria

Decision aid use during post-biopsy consultations for localized prostate cancer

Measuring recall of medical information in non-English-speaking people with cancer: A methodology

Patient-centred care is a way of doing things: How healthcare employees conceptualize patient-centred care

Carers' involvement in decision making about antipsychotic medication: A qualitative study

Quantity over quality—Findings from a systematic review and environmental scan of patient decision aids on early abortion methods

Optimizing patient and public involvement (PPI): Identifying its “essential” and “desirable” principles using a systematic review and modified Delphi methodology

How do people with long-term mental health problems negotiate relationships with network members at times of crisis?

The midwife–woman relationship in a South Wales community: Experiences of midwives and migrant Pakistani women in early pregnancy

“Telling” and assent: Parents’ attitudes towards children's participation in a birth cohort study

Regenerative medicine: Stroke survivor and carer views and motivations towards a proposed stem cell clinical trial using placebo neurosurgery

Patient family advisors’ perspectives on engagement in health-care quality improvement initiatives: Power and partnership

Talking to the people that really matter about their participation in pandemic clinical research: A qualitative study in four European countries

An empirically based conceptual framework for fostering meaningful patient engagement in research

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