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Randomized Trial of Communication Facilitators to Reduce Family Distress and Intensity of End-of-Life Care

American journal of respiratory and critical care medicine, 2016-01, Vol.193 (2), p.154-162

2016

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The Influence of Race/Ethnicity and Socioeconomic Status on End-of-Life Care in the ICU

Chest, 2011-05, Vol.139 (5), p.1025-1033

2011

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Italian cross-cultural adaptation of the Quality of Communication questionnaire and the 4-item advance care planning engagement questionnaire

PloS one, 2023-03, Vol.18 (3), p.e0282960-e0282960

2023

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Comparing Quality of Dying and Death Perceived by Family Members and Nurses for Patients Dying in US and Dutch ICUs

Chest, 2017-02, Vol.151 (2), p.298-307

2017

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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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ICU Care Associated With Symptoms of Depression and Posttraumatic Stress Disorder Among Family Members of Patients Who Die in the ICU

Chest, 2011-04, Vol.139 (4), p.795-801

2011

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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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A Randomized Trial to Improve Communication About End-of-Life Care Among Patients With COPD

Chest, 2012-03, Vol.141 (3), p.726-735

2012

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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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Satisfaction with quality of ICU care for patients and families: the euroQ2 project

Critical care (London, England), 2017-09, Vol.21 (1), p.239-239, Article 239

2017

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Missed Opportunities during Family Conferences about End-of-Life Care in the Intensive Care Unit

American journal of respiratory and critical care medicine, 2005-04, Vol.171 (8), p.844-849

2005

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Differences in End-of-Life Care in the ICU Across Patients Cared for by Medicine, Surgery, Neurology, and Neurosurgery Physicians

Chest, 2014-02, Vol.145 (2), p.313-321

2014

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Family Member Satisfaction With End-of-Life Decision Making in the ICU

Chest, 2008-03, Vol.133 (3), p.704-712

2008

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Barriers and Facilitators to End-of-Life Care Communication for Patients with COPD

Chest, 2005-06, Vol.127 (6), p.2188-2196

2005

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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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Life-Sustaining Treatment Preferences: Matches and Mismatches Between Patients' Preferences and Clinicians' Perceptions

Journal of pain and symptom management, 2013-07, Vol.46 (1), p.9-19

2013

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Measuring Depression-Severity in Critically Ill Patients' Families with the Patient Health Questionnaire (PHQ): Tests for Unidimensionality and Longitudinal Measurement Invariance, with Implications for CONSORT

Journal of pain and symptom management, 2016-05, Vol.51 (5), p.938-946

2016

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Understanding Response Rates to Surveys about Family Members’ Psychological Symptoms after Patients’ Critical Illness

Journal of pain and symptom management, 2017-07, Vol.54 (1), p.96-104

2017

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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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Definitions of resilience and resilience resource use as described by adults with congenital heart disease

International journal of cardiology congenital heart disease, 2023-06, Vol.12, p.100447, Article 100447

2023

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End-of-Life Expenditure in the ICU and Perceived Quality of Dying

Chest, 2014-12, Vol.146 (6), p.1594-1603

2014

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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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Alterations During Medical Interpretation of ICU Family Conferences That Interfere With or Enhance Communication

Chest, 2008-07, Vol.134 (1), p.109-116

2008

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Potential for Response Bias in Family Surveys About End-of-Life Care in the ICU

Chest, 2009-12, Vol.136 (6), p.1496-1502

2009

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Randomized Trial of Communication Facilitators to Reduce Family Distress and Intensity of End-of-Life Care

The Influence of Race/Ethnicity and Socioeconomic Status on End-of-Life Care in the ICU

Italian cross-cultural adaptation of the Quality of Communication questionnaire and the 4-item advance care planning engagement questionnaire

Comparing Quality of Dying and Death Perceived by Family Members and Nurses for Patients Dying in US and Dutch ICUs

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

ICU Care Associated With Symptoms of Depression and Posttraumatic Stress Disorder Among Family Members of Patients Who Die in the ICU

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

A Randomized Trial to Improve Communication About End-of-Life Care Among Patients With COPD

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

Satisfaction with quality of ICU care for patients and families: the euroQ2 project

Missed Opportunities during Family Conferences about End-of-Life Care in the Intensive Care Unit

Differences in End-of-Life Care in the ICU Across Patients Cared for by Medicine, Surgery, Neurology, and Neurosurgery Physicians

Family Member Satisfaction With End-of-Life Decision Making in the ICU

Barriers and Facilitators to End-of-Life Care Communication for Patients with COPD

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

Life-Sustaining Treatment Preferences: Matches and Mismatches Between Patients' Preferences and Clinicians' Perceptions

Measuring Depression-Severity in Critically Ill Patients' Families with the Patient Health Questionnaire (PHQ): Tests for Unidimensionality and Longitudinal Measurement Invariance, with Implications for CONSORT

Understanding Response Rates to Surveys about Family Members’ Psychological Symptoms after Patients’ Critical Illness

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

Definitions of resilience and resilience resource use as described by adults with congenital heart disease

End-of-Life Expenditure in the ICU and Perceived Quality of Dying

Shared Priorities for the End-of-Life Period

Alterations During Medical Interpretation of ICU Family Conferences That Interfere With or Enhance Communication

Potential for Response Bias in Family Surveys About End-of-Life Care in the ICU

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