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The academic medical center of the future: a center for integrative study

Academic medicine, 2000-02, Vol.75 (2), p.194-196

2000

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A program of integrative humanistic study for medical students

Academic medicine, 1992-07, Vol.67 (7), p.455-6

Engelberg, J

1992

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AIDS Knowledge: Effects of Channel Involvement and Interpersonal Communication

Health communication, 1995-01, Vol.7 (2), p.73-91

1995

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Indicators of potential health-related social needs and the association with perceived health and well-being outcomes among community-dwelling medicare beneficiaries

Quality of life research, 2020-06, Vol.29 (6), p.1685-1696

2020

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The Quality of Dying and Death Questionnaire (QODD): Empirical Domains and Theoretical Perspectives

Journal of pain and symptom management, 2010-01, Vol.39 (1), p.9-22

2010

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Factors Affecting Patients’ Preferences for and Actual Discussions About End-of-Life Care

Journal of pain and symptom management, 2016-09, Vol.52 (3), p.386-394

2016

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Evaluating the Quality of Dying and Death

Journal of pain and symptom management, 2001-09, Vol.22 (3), p.717-726

2001

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Family Presence for Patients with Severe Acute Brain Injury and the Influence of the COVID-19 Pandemic

Journal of palliative medicine, 2021-05, Vol.24 (5), p.743

2021

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Heterogeneity of Treatment Effect in a Randomized Trial of a Communication Intervention

Journal of pain and symptom management, 2022-09, Vol.64 (3), p.298-303

2022

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The Influence of Race/Ethnicity and Education on Family Ratings of the Quality of Dying in the ICU

Journal of pain and symptom management, 2016-01, Vol.51 (1), p.9-16

2016

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Quality of Communication and Trust in Patients With Serious Illness: An Exploratory Study of the Relationships of Race/Ethnicity, Socioeconomic Status, and Religiosity

Journal of pain and symptom management, 2018-10, Vol.56 (4), p.530-540.e6

2018

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How Often Is End-of-Life Care in the United States Inconsistent with Patients' Goals of Care?

Journal of palliative medicine, 2017-12, Vol.20 (12), p.1400

2017

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Race/Ethnicity, Socioeconomic Status, and Healthcare Intensity at the End of Life

Journal of palliative medicine, 2018-09, Vol.21 (9), p.1308

2018

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A World of Maximalist Medicine: Physician Perspectives on Palliative Care and End-of-life for Patients With Pulmonary Arterial Hypertension

Journal of pain and symptom management, 2023-04, Vol.65 (4), p.e329-e335

2023

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Intensity of End-of-Life Care for Patients with Hematologic Malignancies and the Role of Race/Ethnicity

Journal of palliative medicine, 2018-10, Vol.21 (10), p.1466

2018

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Supporting Hope and Prognostic Information: Nurses' Perspectives on Their Role When Patients Have Life-Limiting Prognoses

Journal of pain and symptom management, 2010-06, Vol.39 (6), p.982-992

2010

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A Measure of the Quality of Dying and Death: Initial Validation Using After-Death Interviews with Family Members

Journal of pain and symptom management, 2002-07, Vol.24 (1), p.17-31

2002

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Advance Identification of Patients With Chronic Conditions and Acute Respiratory Failure at Greatest Risk for High-Intensity, Costly Care

Journal of pain and symptom management, 2022-04, Vol.63 (4), p.618-626

2022

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Shared Priorities for the End-of-Life Period

Journal of pain and symptom management, 2009-02, Vol.37 (2), p.175-188

2009

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Applying Human-Centered Design to Refinement of the Jumpstart Guide, a Clinician- and Patient-Facing Goals-of-Care Discussion Priming Tool

Journal of pain and symptom management, 2021-12, Vol.62 (6), p.1283-1288

2021

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Strategies for enhancing family participation in research in the ICU: Findings from a qualitative study

Journal of pain and symptom management, 2017-08, Vol.54 (2), p.226-230.e1

2017

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Effect of psychiatric illness on acute care utilization at end of life from serious medical illness

Journal of pain and symptom management, 2017-08, Vol.54 (2), p.176-185.e1

2017

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Patterns of Cost for Patients Dying in the Intensive Care Unit and Implications for Cost Savings of Palliative Care Interventions

Journal of palliative medicine, 2016-11, Vol.19 (11), p.1171

2016

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Did a Goals-of-Care Discussion Happen? Differences in the Occurrence of Goals-of-Care Discussions as Reported by Patients, Clinicians, and in the Electronic Health Record

Journal of pain and symptom management, 2019-02, Vol.57 (2), p.251-259

2019

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Authors' Response to: Novel Data Linkage for Quality Improvement in Palliative and End-of-Life Care

Journal of pain and symptom management, 2020-04, Vol.59 (4), p.e4-e4

2020

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The academic medical center of the future: a center for integrative study

A program of integrative humanistic study for medical students

AIDS Knowledge: Effects of Channel Involvement and Interpersonal Communication

Indicators of potential health-related social needs and the association with perceived health and well-being outcomes among community-dwelling medicare beneficiaries

The Quality of Dying and Death Questionnaire (QODD): Empirical Domains and Theoretical Perspectives

Factors Affecting Patients’ Preferences for and Actual Discussions About End-of-Life Care

Evaluating the Quality of Dying and Death

Family Presence for Patients with Severe Acute Brain Injury and the Influence of the COVID-19 Pandemic

Heterogeneity of Treatment Effect in a Randomized Trial of a Communication Intervention

The Influence of Race/Ethnicity and Education on Family Ratings of the Quality of Dying in the ICU

Quality of Communication and Trust in Patients With Serious Illness: An Exploratory Study of the Relationships of Race/Ethnicity, Socioeconomic Status, and Religiosity

How Often Is End-of-Life Care in the United States Inconsistent with Patients' Goals of Care?

Race/Ethnicity, Socioeconomic Status, and Healthcare Intensity at the End of Life

A World of Maximalist Medicine: Physician Perspectives on Palliative Care and End-of-life for Patients With Pulmonary Arterial Hypertension

Intensity of End-of-Life Care for Patients with Hematologic Malignancies and the Role of Race/Ethnicity

Supporting Hope and Prognostic Information: Nurses' Perspectives on Their Role When Patients Have Life-Limiting Prognoses

A Measure of the Quality of Dying and Death: Initial Validation Using After-Death Interviews with Family Members

Advance Identification of Patients With Chronic Conditions and Acute Respiratory Failure at Greatest Risk for High-Intensity, Costly Care

Shared Priorities for the End-of-Life Period

Applying Human-Centered Design to Refinement of the Jumpstart Guide, a Clinician- and Patient-Facing Goals-of-Care Discussion Priming Tool

Strategies for enhancing family participation in research in the ICU: Findings from a qualitative study

Effect of psychiatric illness on acute care utilization at end of life from serious medical illness

Patterns of Cost for Patients Dying in the Intensive Care Unit and Implications for Cost Savings of Palliative Care Interventions

Did a Goals-of-Care Discussion Happen? Differences in the Occurrence of Goals-of-Care Discussions as Reported by Patients, Clinicians, and in the Electronic Health Record

Authors' Response to: Novel Data Linkage for Quality Improvement in Palliative and End-of-Life Care

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