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Publication Venue For
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Opportunities to Improve Utilization of Palliative Care Among Adults With Cystic Fibrosis: A Systematic Review..
58:1100-1112.e1.
2019
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Prevalence and Predictors of Burnout among Hospice and Palliative Care Clinicians in the US.
2019
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Feasibility of using communication coaching to teach palliative care clinicians Motivational Interviewing.
2019
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Palliative Care Opportunities Among Adults With Congenital Heart Disease-A Systematic Review..
58:891-898.
2019
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Pilot Study to Improve Goals of Care Conversations Among Hospitalists..
58:864-870.
2019
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End-of-Life Care, Palliative Care Consultation, and Palliative Care Referral in the Emergency Department: A Systematic Review.
2019
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Organizing Psychologists, Behavioral Scientists, and Allied Professionals: Formation of the Society of Behavioral Medicine's Palliative Care Special Interest Group..
58:e10-e11.
2019
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Coping Skills Training and Acceptance and Commitment Therapy for Symptom Management: Feasibility and Acceptability of a Brief Telephone-Delivered Protocol for Patients With Advanced Cancer.
2019
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Usability of PCforMe in Patients With Advanced Cancer Referred to Outpatient Palliative Care: Results of a Randomized, Active-Controlled Pilot Trial..
58:382-389.
2019
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Introduction to a New Special Series for the Journal of Pain and Symptom Management-Science in Action: Evidence and Opportunities for Palliative Care Across Diverse Populations and Care Settings..
58:134-136.
2019
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Patient-Reported Outcomes for Cancer Patients Receiving Checkpoint Inhibitors: Opportunities for Palliative Care-A Systematic Review..
58:137-156.e1.
2019
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Helping the Demand Find the Supply: Messaging the Value of Specialty Palliative Care Directly to Those With Serious Illnesses..
57:e6-e7.
2019
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Molding Idle Musings Into Art: What Reflective Writing Does for Me?.
57:856-860.
2019
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Managing Chronic Pain in Cancer Survivors Prescribed Long-Term Opioid Therapy: A National Survey of Ambulatory Palliative Care Providers..
57:20-27.
2019
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Themes Addressed by Couples With Advanced Cancer During a Communication Skills Training Intervention..
56:252-258.
2018
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Evaluating the Feasibility and Acceptability of a Telehealth Program in a Rural Palliative Care Population: TapCloud for Palliative Care..
56:7-14.
2018
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Information Framing Reduces Initial Negative Attitudes in Cancer Patients' Decisions About Hospice Care..
55:1540-1545.
2018
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Developing a Path to Improve Cultural Competency in Islam Among Palliative Care Professionals..
55:e1-e3.
2018
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Physician Decision-Making in the Setting of Advanced Illness: An Examination of Patient Disposition and Physician Religiousness..
55:906-912.
2018
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Physicians' Opinions on Engaging Patients' Religious and Spiritual Concerns: A National Survey..
55:897-905.
2018
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Rapid Response Events in Hospitalized Patients: Patient Symptoms and Clinician Communication..
55:946-952.
2018
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Acute Leukemia Patients' Needs: Qualitative Findings and Opportunities for Early Palliative Care..
55:433-439.
2018
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Comparing the Palliative Care Needs of Patients With Hematologic and Solid Malignancies..
55:82-88.e1.
2018
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A Survey to Evaluate Facilitators and Barriers to Quality Measurement and Improvement: Adapting Tools for Implementation Research in Palliative Care Programs..
54:806-814.
2017
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Addressing Patient Emotional and Existential Needs During Serious Illness: Results of the Outlook Randomized Controlled Trial..
54:898-908.
2017
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Quality Improvement Pearls for the Palliative Care and Hospice Professional..
54:758-765.
2017
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The Implementation of Measuring What Matters in Research and Practice: Series Commentary..
54:772-775.
2017
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The Quality Improvement Environment: Results of the 2016 AAHPM/HPNA Membership Needs Assessment Survey..
54:766-771.
2017
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Current Events (With Apologies to Leonard Cohen)..
54:617.
2017
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One Size Does Not Fit All: Disease Profiles of Serious Illness Patients Receiving Specialty Palliative Care..
54:476-483.
2017
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Isolation and Suffering Related to Serious and Terminal Illness: Metaphors and Lessons From Albert Camus' Novel, The Plague..
54:400-403.
2017
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State of the Science of Spirituality and Palliative Care Research Part I: Definitions, Measurement, and Outcomes..
54:428-440.
2017
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State of the Science of Spirituality and Palliative Care Research Part II: Screening, Assessment, and Interventions..
54:441-453.
2017
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State of the Science of Spirituality and Palliative Care Research: Research Landscape and Future Directions..
54:426-427.
2017
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Addressing Palliative Care Clinician Burnout in Organizations: A Workforce Necessity, an Ethical Imperative..
53:1091-1096.
2017
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Comparing the Palliative Care Needs of Those With Cancer to Those With Common Non-Cancer Serious Illness..
53:1079-1084.e1.
2017
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"It Is Like Heart Failure. It Is Chronic … and It Will Kill You": A Qualitative Analysis of Burnout Among Hospice and Palliative Care Clinicians..
53:901-910.e1.
2017
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Cognitive Interview-Based Validation of the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events in Adolescents with Cancer..
53:759-766.
2017
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Operationalizing the Measuring What Matters Spirituality Quality Metric in a Population of Hospitalized, Critically Ill Patients and Their Family Members..
53:650-655.
2017
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Concordance Between Veterans' Self-Report and Documentation of Surrogate Decision Makers: Implications for Quality Measurement..
53:1-4.
2017
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"Who Does What?" Ensuring High-Quality and Coordinated Palliative Care With Our Oncology Colleagues..
52:e1-e2.
2016
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Adherence to Measuring What Matters Items When Caring for Patients With Hematologic Malignancies Versus Solid Tumors..
52:775-782.
2016
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Performance of Consultative Palliative Care Model in Achieving Quality Metrics in the ICU..
52:873-877.
2016
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Anticholinergic Drug Burden in Noncancer Versus Cancer Patients Near the End of Life..
52:737-743.e3.
2016
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The Symptom Experience in Rectal Cancer Survivors..
52:709-718.
2016
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Significant Morbidity and Mortality Among Hospitalized End-Stage Liver Disease Patients in Medicare..
52:412-419.e1.
2016
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Understanding Treatment Effect Terminology in Pain and Symptom Management Research..
52:446-452.
2016
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Building Resilience for Palliative Care Clinicians: An Approach to Burnout Prevention Based on Individual Skills and Workplace Factors..
52:284-291.
2016
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Assessing Emotional Suffering in Palliative Care: Use of a Structured Note Template to Improve Documentation..
52:1-7.
2016
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Comparing Unmet Needs to Optimize Quality: Characterizing Inpatient and Outpatient Palliative Care Populations..
51:1033-1039.e3.
2016
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U.S. Physicians' Opinions About Accommodating Religiously Based Requests for Continued Life-Sustaining Treatment..
51:971-978.
2016
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An Exploratory Factor Analysis of the Scale Structure of the Patient Care Monitor Version 2.0..
51:776-783.e2.
2016
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Are Hospice Admission Practices Associated With Hospice Enrollment for Older African Americans and Whites?.
51:697-705.
2016
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Concordance of Advance Care Plans With Inpatient Directives in the Electronic Medical Record for Older Patients Admitted From the Emergency Department..
51:647-651.
2016
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Prevalence and Predictors of Burnout Among Hospice and Palliative Care Clinicians in the U.S..
51:690-696.
2016
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A Blue Ocean Strategy for Palliative Care: Focus on Family Caregivers..
51:e1-e3.
2016
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Adherence to Measuring What Matters Measures Using Point-of-Care Data Collection Across Diverse Clinical Settings..
51:497-503.
2016
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Characterizing the Hospice and Palliative Care Workforce in the U.S.: Clinician Demographics and Professional Responsibilities..
51:597-603.
2016
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Feeling Heard and Understood: A Patient-Reported Quality Measure for the Inpatient Palliative Care Setting..
51:150-154.
2016
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Methodological Research Priorities in Palliative Care and Hospice Quality Measurement..
51:155-162.
2016
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The Burden of Polypharmacy in Patients Near the End of Life..
51:178-83.e2.
2016
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Impact of Smoking Cessation on Subsequent Pain Intensity Among Chronically Ill Veterans Enrolled in a Smoking Cessation Trial..
50:822-829.
2015
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Usability and Acceptability of the QDACT-PC, an Electronic Point-of-Care System for Standardized Quality Monitoring in Palliative Care..
50:615-621.
2015
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"The Patient Is Dying, Please Call the Chaplain": The Activities of Chaplains in One Medical Center's Intensive Care Units..
50:501-506.
2015
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A Pilot Study of a Mobile Health Pain Coping Skills Training Protocol for Patients With Persistent Cancer Pain..
50:553-558.
2015
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Practical Dyspnea Assessment: Relationship Between the 0-10 Numerical Rating Scale and the Four-Level Categorical Verbal Descriptor Scale of Dyspnea Intensity..
50:480-487.
2015
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Fatigue in HIV-Infected People: A Three-Year Observational Study..
50:69-79.
2015
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Patient and Caregiver Opinions of Motivational Interviewing Techniques In Role-Played Palliative Care Conversations: A Pilot Study..
50:91-98.
2015
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Signposts along the journey toward high-quality palliative care: the value of measuring what matters..
49:e1-e2.
2015
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Correlation between the international consensus definition of the Cancer Anorexia-Cachexia Syndrome (CACS) and patient-centered outcomes in advanced non-small cell lung cancer..
49:680-689.
2015
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Comparison of seven-day and repeated 24-hour recall of symptoms in the first 100 days after hematopoietic cell transplantation..
49:513-520.
2015
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Limits and responsibilities of physicians addressing spiritual suffering in terminally ill patients..
49:562-569.
2015
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Re: The Sidney Project™..
49:e4-e5.
2015
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What is different about patients with hematologic malignancies? A retrospective cohort study of cancer patients referred to a hospice research network..
49:505-512.
2015
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Quality of palliative care for patients with advanced cancer in a community consortium..
49:289-292.
2015
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The quality imperative for palliative care..
49:243-253.
2015
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EMPOWER: an intervention to address barriers to pain management in hospice..
49:1-12.
2015
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Feasibility of using algorithm-based clinical decision support for symptom assessment and management in lung cancer..
49:13-26.
2015
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Validation of a measure of family experience of patients with serious illness: the QUAL-E (Fam)..
48:1168-1181.
2014
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Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease..
48:934-943.
2014
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The effectiveness of the Geritalk communication skills course: a real-time assessment of skill acquisition and deliberate practice..
48:738-44.e1-6.
2014
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Holding back moderates the association between health symptoms and social well-being in patients undergoing hematopoietic stem cell transplantation..
48:374-384.
2014
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Integrating the biopsychosocial model into quality measures in palliative care: a case for improving the hospice item set..
48:e1-e2.
2014
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Preparedness planning before mechanical circulatory support: a "how-to" guide for palliative medicine clinicians..
47:926-935.e6.
2014
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Getting to proven: evaluating quality across all of palliative care..
47:e1-e2.
2014
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Creating computable algorithms for symptom management in an outpatient thoracic oncology setting..
46:911-924.e1.
2013
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Race and residence: intercounty variation in black-white differences in hospice use..
46:681-690.
2013
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Targeted investment improves access to hospice and palliative care..
46:629-639.
2013
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Intentional sedation to unconsciousness at the end of life: findings from a national physician survey..
46:326-334.
2013
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Validity of an observation method for assessing pain behavior in individuals with multiple sclerosis..
46:413-421.
2013
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Community-based palliative care: the natural evolution for palliative care delivery in the U.S..
46:254-264.
2013
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Authors' reply to Dirksen et al..
45:e2-e3.
2013
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A pilot cluster-randomized trial of a 20-week Tai Chi program in elders with cognitive impairment and osteoarthritic knee: effects on pain and other health outcomes..
45:660-669.
2013
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Delivery strategies to optimize resource utilization and performance status for patients with advanced life-limiting illness: results from the "palliative care trial" [ISRCTN 81117481]..
45:488-505.
2013
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Enrollment and events of hospice patients with heart failure vs. cancer..
45:552-560.
2013
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Direct observation of prognosis communication in palliative care: a descriptive study..
45:202-212.
2013
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Demonstration of a sustainable community-based model of care across the palliative care continuum..
44:797-809.
2012
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Religiosity, spirituality, and end-of-life planning: a single-site survey of medical inpatients..
44:843-851.
2012
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Assessment of the psychometric properties of an English version of the cancer dyspnea scale in people with advanced lung cancer..
44:741-749.
2012
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Analyzing phase III studies in hospice/palliative care. a solution that sits between intention-to-treat and per protocol analyses: the palliative-modified ITT analysis..
44:595-603.
2012
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Burden and well-being among a diverse sample of cancer, congestive heart failure, and chronic obstructive pulmonary disease caregivers..
44:410-420.
2012
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Dignity in end-of-life care: results of a national survey of U.S. physicians..
44:331-339.
2012
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Parent perceptions of child vulnerability are associated with functioning and health care use in children with chronic pain..
43:953-960.
2012
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Refining a checklist for reporting patient populations and service characteristics in hospice and palliative care research..
43:902-910.
2012
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Self-compassion in patients with persistent musculoskeletal pain: relationship of self-compassion to adjustment to persistent pain..
43:759-770.
2012
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Development of a prognostic model for six-month mortality in older adults with declining health..
43:527-539.
2012
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Does health-related quality of life improve for advanced pancreatic cancer patients who respond to gemcitabine? Analysis of a randomized phase III trial of the cancer and leukemia group B (CALGB 80303)..
43:205-217.
2012
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Collecting data on quality is feasible in community-based palliative care..
42:663-667.
2011
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Comparing three life-limiting diseases: does diagnosis matter or is sick, sick?.
42:331-341.
2011
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Caregiver-assisted coping skills training for lung cancer: results of a randomized clinical trial..
41:1-13.
2011
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Validation of the Patient Care Monitor (Version 2.0): a review of system assessment instrument for cancer patients..
40:545-558.
2010
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Hope in the context of lung cancer: relationships of hope to symptoms and psychological distress..
40:174-182.
2010
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A comparison of two spirituality instruments and their relationship with depression and quality of life in chronic heart failure..
39:515-526.
2010
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Parent pain responses as predictors of daily activities and mood in children with juvenile idiopathic arthritis: the utility of electronic diaries..
39:579-590.
2010
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Genetic and nongenetic covariates of pain severity in patients with adenocarcinoma of the pancreas: assessing the influence of cytokine genes..
38:894-902.
2009
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Mucositis-related morbidity and resource utilization in head and neck cancer patients receiving radiation therapy with or without chemotherapy..
38:522-532.
2009
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Indwelling catheters for the management of refractory malignant ascites: a systematic literature overview and retrospective chart review..
38:341-349.
2009
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Feasibility and acceptability to patients of a longitudinal system for evaluating cancer-related symptoms and quality of life: pilot study of an e/Tablet data-collection system in academic oncology..
37:1027-1038.
2009
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Pain catastrophizing and pain-related fear in osteoarthritis patients: relationships to pain and disability..
37:863-872.
2009
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Pain behavior in rheumatoid arthritis patients: identification of pain behavior subgroups..
36:69-78.
2008
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Perceived Resources and Barriers to Pediatric Palliative Care Among HealthCare Practitioners Attending the V Latin American Palliative Care Association (ALCP) Meeting (755).
2011
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Race and residence: county-level variation in black-white disparities in hospice use (312-B).
2011