Meier, Diane E.
Diane E. Meier American geriatrician
Diane E. Meier
VIAF ID: 39612646 (Personal)
Permalink: http://viaf.org/viaf/39612646
Preferred Forms
- 100 0 _ ‡a Diane E. Meier
- 100 0 _ ‡a Diane E. Meier ‡c American geriatrician
- 200 _ | ‡a Meier ‡b Diane E.
- 100 1 _ ‡a Meier, Diane E.
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- 100 1 _ ‡a Meier, Diane E.
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4xx's: Alternate Name Forms (5)
Works
Title | Sources |
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Accountability for Community-Based Programs for the Seriously Ill. | |
Advance Care Planning Documentation in Electronic Health Records: Current Challenges and Recommendations for Change | |
Advancing Alzheimer's disease diagnosis, treatment, and care: recommendations from the Ware Invitational Summit | |
American Society of Clinical Oncology provisional clinical opinion: the integration of palliative care into standard oncology care. | |
America's care of serious illness: a state-by-state report card on access to palliative care in our nation's hospitals | |
Assessing the outcome of a palliative care educational initiative. | |
Association Between Hospice Use and Depressive Symptoms in Surviving Spouses. | |
Characteristics of Hospitalized Cancer Patients Referred for Inpatient Palliative Care Consultation. | |
Characteristics of patients requesting and receiving physician-assisted death | |
Does palliative care improve quality? A survey of bereaved family members | |
Drivers of care costs and quality in the last 3 months of life among older people receiving palliative care: A multinational mortality follow-back survey across England, Ireland and the United States | |
Education, implementation, and policy barriers to greater integration of palliative care: A literature review | |
Educational Offerings and Technology. | |
End-of-life care, c2001: | |
Evidence for new standard of care in non-small cell lung cancer patients | |
Geriatric palliative care | |
The growth of palliative care programs in United States hospitals | |
High rates of advance care planning in New York City's elderly population | |
Hospice Care for Patients With Dementia in the United States: A Longitudinal Cohort Study | |
Hospital mortality rates: how is palliative care taken into account? | |
How empowering is hospital care for older people with advanced disease? Barriers and facilitators from a cross-national ethnography in England, Ireland and the USA. | |
Identifying Patients in Need of a Palliative Care Assessment in the Hospital SettingA Consensus Report from the Center to Advance Palliative Care | |
Improving the management of pain in hospitalized adults | |
It's All a Matter of Perspective | |
Meeting the needs of older adults with serious illness : challenges and opportunities in the age of health care reform | |
Methods for constructing and assessing propensity scores | |
The National Agenda for Quality Palliative Care: The National Consensus Project and the National Quality Forum | |
The National Palliative Care Research Center: Ten Years of Promoting and Developing Research in Palliative Care | |
Operational features for hospital palliative care programs: consensus recommendations | |
Outcomes that Define Successful Advance Care Planning: A Delphi Panel Consensus | |
Palliative care academic career awards : a public-private partnership to improve care for the most vulnerable | |
The Palliative Care Challenge: Analysis of Barriers and Opportunities to Integrate Palliative Care in Europe in the View of National Associations | |
Palliative care consultation teams cut hospital costs for Medicaid beneficiaries. | |
Palliative Care Leadership Centers Are Key To The Diffusion Of Palliative Care Innovation. | |
Palliative Care Team Perceptions of Standardized Palliative Care Referral Criteria Implementation in Hospital Settings | |
Palliative Care Teams' Cost-Saving Effect Is Larger For Cancer Patients With Higher Numbers Of Comorbidities. | |
A Person-Centered, Registry-Based Learning Health System for Palliative Care: A Path to Coproducing Better Outcomes, Experience, Value, and Science | |
Prospective Cohort Study of Hospitalized Adults With Advanced Cancer: Associations Between Complications, Comorbidity, and Utilization. | |
Quality Measurement of Serious Illness Communication: Recommendations for Health Systems Based on Findings from a Symposium of National Experts | |
Response to Bharadwaj et al., Challenges of Promoting Uniformity in Programs Within a Health Care System (DOI: 10.1089/jpm.2019.0404) | |
Social and clinical determinants of preferences and their achievement at the end of life: prospective cohort study of older adults receiving palliative care in three countries | |
Switching Between Medicare Advantage And Traditional Medicare Before And After The Onset Of Functional Disability | |
Training Clinicians with Communication Skills Needed to Match Medical Treatments to Patient Values | |
Training of palliative medicine fellows: a report from the field | |
The Use of a Brief 5-Item Measure of Family Satisfaction as a Critical Quality Indicator in Advanced Cancer Care: A Multisite Comparison | |
Use of an Item Bank to Develop Two Short-Form FAMCARE Scales to Measure Family Satisfaction With Care in the Setting of Serious Illness | |
Use of an Online Palliative Care Clinical Curriculum to Train U.S. Hospital Staff: 2015-2019 | |
When critical illness becomes chronic: informational needs of patients and families |