Anne M Walling
Datos Biográficos
| ID | 1246696 |
|---|---|
| NOMBRE | Anne M Walling |
| NOMBRES | Anne M |
| APELLIDO | Walling |
| FIRMA | WALLING A M |
| AFILIACIONES | University of California, Los Angeles |
| ORCID | 0000-0001-6026-3249 |
| VERIFICADO | Sí |
| TOTAL DE OBRAS | 7 |
| TOTAL DE CITAS | 1 |
| TOTAL COMO AUTOR | 7 |
| TOTAL COMO EDITOR | 0 |
| PRIMER AÑO DE PUBLICACIÓN | 2022 |
| AÑO MÁS RECIENTE DE PUBLICACIÓN | 2026 |
| ÍNDICE H | 1 |
The Family Perspectives Project
While guidelines recommend that families of critically ill patients receive emotional support from intensive care unit (ICU) clinicians, few receive it. To address this gap, we designed the Family Perspectives Project, an intervention that utilizes hospital chaplains to enhance the emotional support that ICU teams provide to families. This study's objective was to refine and preliminarily test the feasibility and acceptability of the intervention…
End-of-Life Care for Older Adults With Dementia by Race and Ethnicity and Physicians’ Role
Findings from this cohort study suggest that non-Hispanic Black and Hispanic decedents with dementia received more intensive end-of-life care despite higher rates of billed advance care planning and palliative care counseling than non-Hispanic White decedents. Observed racial and ethnic variations were not explained by differences in the physicians treating them
End-of-Life Care and Health Care Spending for Medicare Beneficiaries With Dementia in Accountable Care Organizations
Using nationally representative data on beneficiaries with dementia at EOL, this quasi-experimental study found no evidence that EOL care processes, outcomes, or spending changed with ACO entry for Medicare fee-for-service beneficiaries vs non-ACO beneficiaries. Alternative payment models to ACOs may be needed to coordinate high-quality care with lower spending for beneficiaries with dementia at the EOL
Implementing Patient-Centered Outcomes Research Institute Stakeholder Engagement Principles in Models of Palliative Care Delivery and Advance Care Planning Research
BACKGROUND: Given the many challenges of conducting research that addresses the palliative and end-of-life care needs of patients with serious illnesses, stakeholder engagement starting from the moment of study conceptualization and design is critical to ensure successful participant recruitment, data collection, intervention delivery, data analysis, and dissemination. METHODS: Guided by a conceptual model published by the Patient-Centered Outcom…
Assessing Representativeness of Seriously Ill Patient Survey Responders in a Pragmatic Clinical Trial
A tailored survey and recruitment strategy yielded a representative sample of seriously ill, largely older, primary care respondents in the context of a pragmatic clinical trial
Integrating Patient and Expert Perspectives to Conceptualize High-Quality Palliative Cancer Care for Symptoms in the US Veterans Health Administration
Quality measurement is typically the domain of clinical experts and health system leaders; patient/caregiver perspectives are rarely solicited. We aimed to describe and integrate clinician and patient/caregiver conceptualizations of high-quality palliative symptom care for patients receiving care for advanced cancer within the US Veterans Health Administration in the context of existing quality measures. We conducted a secondary qualitative analy…
The chosen and the unchosen
The chosen and the unchosen
Assessing Representativeness of Seriously Ill Patient Survey Responders in a Pragmatic Clinical Trial
A tailored survey and recruitment strategy yielded a representative sample of seriously ill, largely older, primary care respondents in the context of a pragmatic clinical trial
Integrating Patient and Expert Perspectives to Conceptualize High-Quality Palliative Cancer Care for Symptoms in the US Veterans Health Administration
Quality measurement is typically the domain of clinical experts and health system leaders; patient/caregiver perspectives are rarely solicited. We aimed to describe and integrate clinician and patient/caregiver conceptualizations of high-quality palliative symptom care for patients receiving care for advanced cancer within the US Veterans Health Administration in the context of existing quality measures. We conducted a secondary qualitative analy…
Implementing Patient-Centered Outcomes Research Institute Stakeholder Engagement Principles in Models of Palliative Care Delivery and Advance Care Planning Research
BACKGROUND: Given the many challenges of conducting research that addresses the palliative and end-of-life care needs of patients with serious illnesses, stakeholder engagement starting from the moment of study conceptualization and design is critical to ensure successful participant recruitment, data collection, intervention delivery, data analysis, and dissemination. METHODS: Guided by a conceptual model published by the Patient-Centered Outcom…
End-of-Life Care for Older Adults With Dementia by Race and Ethnicity and Physicians’ Role
Findings from this cohort study suggest that non-Hispanic Black and Hispanic decedents with dementia received more intensive end-of-life care despite higher rates of billed advance care planning and palliative care counseling than non-Hispanic White decedents. Observed racial and ethnic variations were not explained by differences in the physicians treating them
End-of-Life Care and Health Care Spending for Medicare Beneficiaries With Dementia in Accountable Care Organizations
Using nationally representative data on beneficiaries with dementia at EOL, this quasi-experimental study found no evidence that EOL care processes, outcomes, or spending changed with ACO entry for Medicare fee-for-service beneficiaries vs non-ACO beneficiaries. Alternative payment models to ACOs may be needed to coordinate high-quality care with lower spending for beneficiaries with dementia at the EOL
The Family Perspectives Project
While guidelines recommend that families of critically ill patients receive emotional support from intensive care unit (ICU) clinicians, few receive it. To address this gap, we designed the Family Perspectives Project, an intervention that utilizes hospital chaplains to enhance the emotional support that ICU teams provide to families. This study's objective was to refine and preliminarily test the feasibility and acceptability of the intervention…
Health care (5 obras) · Medicine (5 obras) · Palliative Care and End-of-Life Issues (5 obras) · Palliative care (4 obras) · Nursing (3 obras) · Psychology (3 obras) · Advance care planning (2 obras) · Context (archaeology (2 obras) · Dementia (2 obras) · Disease (2 obras)