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>Joan M. Teno - Publications

Joan M. Teno — Publications

Association of Hospice Profit Status With Family Caregivers' Reported Care Experiences 2023
Evaluation of Phase II of the Medicare Advantage Value-Based Insurance Design Model Test: First Three Years of Implementation (2020–2022) 2023
Hospice Care Experiences Among Medicare Decedents With and Without COVID-19, 2020–2021 2023
Patient-Reported Quality Measures for Palliative Care: The Time Is Now 2023
Adjusting for Patient Characteristics to Compare Quality of Care Provided by Serious Illness Programs 2022
Hospice Care Experiences Among Cancer Patients and Their Caregivers 2021
"If We Turned Our Backs, They Would Ignore Our Wishes": Bereaved Family Perceptions of Concordance of Care at the End of Life 2021
Reliable and Valid Survey-Based Measures to Assess Quality of Care in Home-Based Serious Illness Programs 2021
Association Between Receipt of Emotional Support and Caregivers' Overall Hospice Rating 2020
Bereaved Family More Likely to Report "Too Little" Care Than "Too Much" Care at the End of Life 2020
Characteristics of Hospices Providing High-Quality Care 2020
Differences in Caregiver Reports of the Quality of Hospice Care Across Settings 2020
Racial Differences in End-of-Life Care Quality Between Asian Americans and Non-Hispanic Whites in San Francisco Bay Area 2020
Black and Hispanic Patients Receive Hospice Care Similar to That of White Patients When in the Same Hospices 2017
Challenges Of Measuring Quality Of Community-Based Programs For Seriously Ill Individuals And Their Families 2017
Factors Associated with Family Reports of Pain, Dyspnea, and Depression in the Last Year of Life 2016
Measuring Experience with End-of-Life Care: A Systematic Literature Review 2015
Symptom Trends in the Last Year of Life from 1998 to 2010: A Cohort Study 2015
Hospice Experience of Care Survey: Development and Field Test 2014
Discussions with Physicians About Hospice Among Patients with Metastatic Lung Cancer 2009
Cost Effectiveness of Aggressive Care for Patients with Nontraumatic Coma 2002
Are Aggressive Treatment Strategies Less Cost-Effective for Older Patients? The Case of Ventilator Support and Aggressive Care for Patients with Acute Respiratory Failure 2001
Age-related Differences in Care Preferences, Treatment Decisions, and Clinical Outcomes of Seriously Ill Hospitalized Adults: Lessons from SUPPORT 2000
Communication and Decision-Making in Seriously Ill Patients: Findings of the SUPPORT Project 2000
Decision-Making and Outcomes of Prolonged ICU Stays in Seriously Ill Patients 2000
Family Satisfaction with End-of-Life Care in Seriously Ill Hospitalized Adults 2000
Patients Who Want Their Family and Physician to Make Resuscitation Decisions for Them: Observations from SUPPORT and HELP 2000
Physician Understanding of Patient Resuscitation Preferences: Insights and Clinical Implications 2000
Predicting Functional Status Outcomes in Hospitalized Patients Aged 80 Years and Older 2000
Prediction of Survival for Older Hospitalized Patients: The HELP Survival Model 2000
A Prospective Study of Patient-Physician Communication About Resuscitation 2000
Withholding Versus Withdrawing Life-Sustaining Treatment: Patient Factors and Documentation Associated with Dialysis Decisions 2000
Patient Age and Decisions to Withhold Life-Sustaining Treatments from Seriously Ill, Hospitalized Adults 1999
Influence of Patient Preferences and Local Health System Characteristics on the Place of Death 1998
Resuscitation Preferences Among Patients with Severe Congestive Heart Failure: Results from the SUPPORT Project 1998
Role of Written Advance Directives in Decision Making: Insights from Qualitative and Quantitative Data 1998
Do Advance Directives Provide Instructions That Direct Care? 1997
Outcomes and Cost-Effectiveness of Initiating Dialysis and Continuing Aggressive Care in Seriously Ill Hospitalized Adults 1997
Patient Preferences for Communication with Physicians About End-of-Life Decisions 1997
Patients with DNR Orders in the Operating Room: Surgery, Resuscitation, and Outcomes 1997
Perceptions by Family Members of the Dying Experience of Older and Seriously Ill Patients 1997
Relationship of Body Mass Index to Subsequent Mortality Among Seriously Ill Hospitalized Patients 1997
Surrogate and Physician Understanding of Patients* Preferences for Living Permanently in a Nursing Home 1997
Choices of Seriously Ill Patients About Cardiopulmonary Resuscitation: Correlates and Outcomes 1996
Factors Associated with Do-Not-Resuscitate Orders: Patients' Preferences, Prognoses, and Physicians' Judgments 1996
Is Economic Hardship on the Families of the Seriously Ill Associated with Patient and Surrogate Care Preferences? 1996
Race, Resource Use, and Survival in Seriously Ill Hospitalized Adults 1996
Seriously Ill Hospitalized Adults: Do We Spend Less on Older Patients? 1996
The Stability of DNR Orders on Hospital Readmission 1996
Accurate Prognostications of Death: Opportunities and Challenges for Clinicians 1995
Identification of Comatose Patients at High Risk for Death or Severe Disability 1995
Predicting Future Functional Status for Seriously Ill Hospitalized Adults: The SUPPORT Prognostic Model 1995
Preferences for Cardiopulmonary Resuscitation: Physician-Patient Agreement and Hospital Resource Use 1995
Do Formal Advance Directives Affect Resuscitation Decisions and the Use of Resources for Seriously Ill Patients? 1994
The Impact of Serious Illness on Patients' Families 1994
Prognosis-based Futility Guidelines: Does Anyone Win? 1994

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