Joan M. Teno — Publications
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Evaluation of the Medicare Advantage Value-Based Insurance Design Model Test: 2020 to 2023
2025
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Psychometric Properties of Patient-Reported Quality Measures for Community-Based Serious Illness Care
2025
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Serious Illness Survey for Community-Based Care
2025
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Changes in Hospice Care Experiences During the COVID-19 Pandemic
2024
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Effects of a Web-Mail Mode on Response Rates and Responses to a Care Experience Survey: Results of a Randomized Experiment
2024
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Association of Hospice Profit Status With Family Caregivers' Reported Care Experiences
2023
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Evaluation of Phase II of the Medicare Advantage Value-Based Insurance Design Model Test: First Three Years of Implementation (2020–2022)
2023
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Hospice Care Experiences Among Medicare Decedents With and Without COVID-19, 2020–2021
2023
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Patient-Reported Quality Measures for Palliative Care: The Time Is Now
2023
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Adding Telephone Follow-Up Can Improve Representativeness of Surveys of Seriously Ill People
2022
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Adjusting for Patient Characteristics to Compare Quality of Care Provided by Serious Illness Programs
2022
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Hospice Care Experiences Among Cancer Patients and Their Caregivers
2021
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"If We Turned Our Backs, They Would Ignore Our Wishes": Bereaved Family Perceptions of Concordance of Care at the End of Life
2021
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Reliable and Valid Survey-Based Measures to Assess Quality of Care in Home-Based Serious Illness Programs
2021
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Association Between Receipt of Emotional Support and Caregivers' Overall Hospice Rating
2020
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Bereaved Family More Likely to Report "Too Little" Care Than "Too Much" Care at the End of Life
2020
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Characteristics of Hospices Providing High-Quality Care
2020
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Differences in Caregiver Reports of the Quality of Hospice Care Across Settings
2020
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Racial Differences in End-of-Life Care Quality Between Asian Americans and Non-Hispanic Whites in San Francisco Bay Area
2020
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Black and Hispanic Patients Receive Hospice Care Similar to That of White Patients When in the Same Hospices
2017
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Challenges Of Measuring Quality Of Community-Based Programs For Seriously Ill Individuals And Their Families
2017
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Factors Associated with Family Reports of Pain, Dyspnea, and Depression in the Last Year of Life
2016
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Measuring Experience with End-of-Life Care: A Systematic Literature Review
2015
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Symptom Trends in the Last Year of Life from 1998 to 2010: A Cohort Study
2015
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Hospice Experience of Care Survey: Development and Field Test
2014
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Discussions with Physicians About Hospice Among Patients with Metastatic Lung Cancer
2009
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Cost Effectiveness of Aggressive Care for Patients with Nontraumatic Coma
2002
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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
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Age-related Differences in Care Preferences, Treatment Decisions, and Clinical Outcomes of Seriously Ill Hospitalized Adults: Lessons from SUPPORT
2000
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Communication and Decision-Making in Seriously Ill Patients: Findings of the SUPPORT Project
2000
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Decision-Making and Outcomes of Prolonged ICU Stays in Seriously Ill Patients
2000
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Family Satisfaction with End-of-Life Care in Seriously Ill Hospitalized Adults
2000
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Patients Who Want Their Family and Physician to Make Resuscitation Decisions for Them: Observations from SUPPORT and HELP
2000
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Physician Understanding of Patient Resuscitation Preferences: Insights and Clinical Implications
2000
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Predicting Functional Status Outcomes in Hospitalized Patients Aged 80 Years and Older
2000
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Prediction of Survival for Older Hospitalized Patients: The HELP Survival Model
2000
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A Prospective Study of Patient-Physician Communication About Resuscitation
2000
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Withholding Versus Withdrawing Life-Sustaining Treatment: Patient Factors and Documentation Associated with Dialysis Decisions
2000
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Patient Age and Decisions to Withhold Life-Sustaining Treatments from Seriously Ill, Hospitalized Adults
1999
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Influence of Patient Preferences and Local Health System Characteristics on the Place of Death
1998
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Resuscitation Preferences Among Patients with Severe Congestive Heart Failure: Results from the SUPPORT Project
1998
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Role of Written Advance Directives in Decision Making: Insights from Qualitative and Quantitative Data
1998
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Do Advance Directives Provide Instructions That Direct Care?
1997
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Outcomes and Cost-Effectiveness of Initiating Dialysis and Continuing Aggressive Care in Seriously Ill Hospitalized Adults
1997
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Patient Preferences for Communication with Physicians About End-of-Life Decisions
1997
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Patients with DNR Orders in the Operating Room: Surgery, Resuscitation, and Outcomes
1997
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Perceptions by Family Members of the Dying Experience of Older and Seriously Ill Patients
1997
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Relationship of Body Mass Index to Subsequent Mortality Among Seriously Ill Hospitalized Patients
1997
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Surrogate and Physician Understanding of Patients* Preferences for Living Permanently in a Nursing Home
1997
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Choices of Seriously Ill Patients About Cardiopulmonary Resuscitation: Correlates and Outcomes
1996
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Factors Associated with Do-Not-Resuscitate Orders: Patients' Preferences, Prognoses, and Physicians' Judgments
1996
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Is Economic Hardship on the Families of the Seriously Ill Associated with Patient and Surrogate Care Preferences?
1996
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Race, Resource Use, and Survival in Seriously Ill Hospitalized Adults
1996
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Seriously Ill Hospitalized Adults: Do We Spend Less on Older Patients?
1996
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The Stability of DNR Orders on Hospital Readmission
1996
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Accurate Prognostications of Death: Opportunities and Challenges for Clinicians
1995
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Identification of Comatose Patients at High Risk for Death or Severe Disability
1995
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Predicting Future Functional Status for Seriously Ill Hospitalized Adults: The SUPPORT Prognostic Model
1995
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Preferences for Cardiopulmonary Resuscitation: Physician-Patient Agreement and Hospital Resource Use
1995
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Do Formal Advance Directives Affect Resuscitation Decisions and the Use of Resources for Seriously Ill Patients?
1994
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The Impact of Serious Illness on Patients' Families
1994
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Prognosis-based Futility Guidelines: Does Anyone Win?
1994
