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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 healthcare utilization and palliative care use among older adults with limited English proficiency

Journal of the American Geriatrics Society (JAGS), 2022-10, Vol.70 (10), p.2847-2857

2022

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Financial Hardship: A Qualitative Study Exploring Perspectives of Seriously Ill Patients and Their Family

Journal of pain and symptom management, 2024-08

2024

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Applying human‐centered design to adapt the Jumpstart Guide for goals‐of‐care discussions in persons living with dementia

Journal of the American Geriatrics Society (JAGS), 2024-07, Vol.72 (7), p.2111-2119

2024

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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.1171-1178

2016

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The Association between Chronic Conditions, End-of-Life Health Care Use, and Documentation of Advance Care Planning among Patients with Cancer

Journal of palliative medicine, 2020-10, Vol.23 (10), p.1335-1341

2020

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Type of Intensive Care Unit Matters: Variations in Palliative Care for Critically Ill Patients with Chronic, Life-Limiting Illness

Journal of palliative medicine, 2021-06, Vol.24 (6), p.857-864

2021

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“We’ll deal with it as it comes”: A qualitative analysis of romantic partners’ dyadic coping in cystic fibrosis

Journal of social and personal relationships, 2024-04, Vol.41 (4), p.689-705

2024

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Adults with CHD balancing motivations and concerns in pregnancy decision-making

Cardiology in the young, 2023-11, Vol.33 (11), p.1-2227

2023

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The Patient and Family Member Experience of Financial Stress Related to Critical Illness

Journal of palliative medicine, 2020-07, Vol.23 (7), p.972-976

2020

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Expanding Conceptualizations of Social Justice across All Levels of Social Work Practice: Recognition Theory and Its Contributions

The Social service review (Chicago), 2018-06, Vol.92 (2), p.143-170

2018

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The Influence of Multimorbidity on Health Care Utilization at the End of Life for Patients with Chronic Conditions

Journal of palliative medicine, 2019-10, Vol.22 (10), p.1260-1265

2019

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Addressing lung transplant with adults with cystic fibrosis: A qualitative analysis of patients' perspectives and experiences

Journal of cystic fibrosis, 2019-05, Vol.18 (3), p.416-419

2019

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Exploring Opportunities for Primary Outpatient Palliative Care for Adults with Cystic Fibrosis: A Mixed-Methods Study of Patients' Needs

Journal of palliative medicine, 2018-04, Vol.21 (4), p.513-521

2018

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Economic Feasibility of Staffing the Intensive Care Unit with a Communication Facilitator

Annals of the American Thoracic Society, 2016-12, Vol.13 (12), p.2190-2196

2016

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Predictors of Death in the Hospital for Patients with Chronic Serious Illness

Journal of palliative medicine, 2018-03, Vol.21 (3), p.307-314

2018

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It's part of who I am: The impact of congenital heart disease on adult identity and life experience

International journal of cardiology congenital heart disease, 2021-08, Vol.4, p.100146, Article 100146

2021

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Patient perspectives on clinician-patient partnerships to achieve comprehensive pregnancy care in adult congenital heart disease

International journal of cardiology congenital heart disease, 2022-03, Vol.7, p.100312, Article 100312

2022

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The Quality of Dying and Death

Chest, 2013-02, Vol.143 (2), p.289-291

2013

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Controlling for Confounding Variables: Accounting for Dataset Bias in Classifying Patient-Provider Interactions

Explainable AI in Healthcare and Medicine, 2021, p.271-282

2021

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Identifying Elements of ICU Care That Families Report as Important But Unsatisfactory

Chest, 2012-11, Vol.142 (5), p.1185-1192

2012

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Family Satisfaction in the ICU

Chest, 2007-11, Vol.132 (5), p.1425-1433

2007

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Unplanned Admission to the ICU

Chest, 2020-10, Vol.158 (4), p.1482-1489

2020

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Post-doctoral research training in palliative care: lessons learned from a T32 program

Journal of pain and symptom management, 2019-11, Vol.59 (3), p.750-760.e8

2019

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The effect of the hidden curriculum on resident burnout and cynicism

Journal of graduate medical education, 2011-12, Vol.3 (4), p.503-510

2011

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

End‐of‐life healthcare utilization and palliative care use among older adults with limited English proficiency

Financial Hardship: A Qualitative Study Exploring Perspectives of Seriously Ill Patients and Their Family

Applying human‐centered design to adapt the Jumpstart Guide for goals‐of‐care discussions in persons living with dementia

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

The Association between Chronic Conditions, End-of-Life Health Care Use, and Documentation of Advance Care Planning among Patients with Cancer

Type of Intensive Care Unit Matters: Variations in Palliative Care for Critically Ill Patients with Chronic, Life-Limiting Illness

“We’ll deal with it as it comes”: A qualitative analysis of romantic partners’ dyadic coping in cystic fibrosis

Adults with CHD balancing motivations and concerns in pregnancy decision-making

The Patient and Family Member Experience of Financial Stress Related to Critical Illness

Expanding Conceptualizations of Social Justice across All Levels of Social Work Practice: Recognition Theory and Its Contributions

The Influence of Multimorbidity on Health Care Utilization at the End of Life for Patients with Chronic Conditions

Addressing lung transplant with adults with cystic fibrosis: A qualitative analysis of patients' perspectives and experiences

Exploring Opportunities for Primary Outpatient Palliative Care for Adults with Cystic Fibrosis: A Mixed-Methods Study of Patients' Needs

Economic Feasibility of Staffing the Intensive Care Unit with a Communication Facilitator

Predictors of Death in the Hospital for Patients with Chronic Serious Illness

It's part of who I am: The impact of congenital heart disease on adult identity and life experience

Patient perspectives on clinician-patient partnerships to achieve comprehensive pregnancy care in adult congenital heart disease

The Quality of Dying and Death

Controlling for Confounding Variables: Accounting for Dataset Bias in Classifying Patient-Provider Interactions

Identifying Elements of ICU Care That Families Report as Important But Unsatisfactory

Family Satisfaction in the ICU

Unplanned Admission to the ICU

Post-doctoral research training in palliative care: lessons learned from a T32 program

The effect of the hidden curriculum on resident burnout and cynicism

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