J Pain Symptom Manage

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  Publication Venue For

  • Designing Psychosocial Intervention Pilot Studies: A Tutorial for Palliative Care Investigators..  63:e749-e755. 2022
  • Improving Outcomes Measurement in Palliative Care: The Lasting Impact of Randy Curtis and his Collaborators..  63:e579-e586. 2022
  • Leading from the Heart..  63:e645-e646. 2022
  • Surrogates of Patients With Severe Acute Brain Injury Experience Persistent Anxiety and Depression Over the 6 Months After ICU Admission..  63:e633-e639. 2022
  • Clinician End-of-Life Experiences With Pediatric Muslim Patients at a US Quaternary Care Center..  63:673-679. 2022
  • Clinical Decision Support for Symptom Management in Lung Cancer Patients: A Group RCT..  63:572-580. 2022
  • Opioid Prescribing and Use Among Cancer Survivors: A Mapping Review of Observational and Intervention Studies..  63:e397-e417. 2022
  • What is a Good Death? A Choice Experiment on Care Indicators for Patients at End of Life..  63:457-467. 2022
  • Use of Theoretical Frameworks in the Development and Testing of Palliative Care Interventions..  63:e271-e280. 2022
  • Communicating With Families of Children With Severe Neurological Impairment..  63:e264-e266. 2022
  • The Impact of Optimism on Cancer-Related and Postsurgical Cancer Pain: A Systematic Review..  63:e203-e211. 2022
  • Palliative Care Use for Critically Ill Patients With Brain Metastases..  62:927-935. 2021
  • Perceptions of Hematology Among Palliative Care Physicians: Results of a Nationwide Survey..  62:949-959. 2021
  • Pediatric Palliative Care for Children With Severe Neurological Impairment and Their Families..  62:662-667. 2021
  • Predictors of Response to an Evidence-Based Behavioral Cancer Pain Management Intervention: An Exploratory Analysis From a Clinical Trial..  62:391-399. 2021
  • Family Caregiver Perspectives on Suffering of Persons With Severe Dementia: A Qualitative Study..  62:20-27.e2. 2021
  • Palliative Care Specialist Access is Associated With Rankings of Hospital Quality..  62:149-152. 2021
  • Subjective Toxicity Profiles of Children in Treatment for Cancer: A New Guide to Supportive Care?.  61:1188-1195.e2. 2021
  • Yoga Practice Predicts Improvements in Day-to-Day Pain in Women With Metastatic Breast Cancer..  61:1227-1233. 2021
  • Selection Bias in Observational Studies of Palliative Care: Lessons Learned..  61:1002-1011.e2. 2021
  • Two Questions About the Design of Cluster Randomized Trials: A Tutorial..  61:858-863. 2021
  • "Pain is Subjective": A Mixed-Methods Study of Provider Attitudes and Practices Regarding Pain Management in Sickle Cell Disease Across Three Countries..  61:474-487. 2021
  • National Trends in Hospice Facility Deaths in the United States, 2003-2017..  61:350-357. 2021
  • Beyond Traditional Advance Care Planning: Tailored Preparedness for COVID-19..  60:e4-e6. 2020
  • Predictors of Intervention Session Completion in a Randomized Clinical Trial of a Behavioral Cancer Pain Intervention..  59:1268-1277. 2020
  • Prevalence and Predictors of Burnout Among Hospice and Palliative Care Clinicians in the U.S..  59:e6-e13. 2020
  • Retraction of "Prevalence and Predictors of Burnout Among Hospice and Palliative Care Professionals From 2016 Apr;51(4):690-6"..  59:965. 2020
  • Feasibility of Using Communication Coaching to Teach Palliative Care Clinicians Motivational Interviewing..  59:787-793. 2020
  • 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..  59:270-278. 2020
  • End-of-Life Care, Palliative Care Consultation, and Palliative Care Referral in the Emergency Department: A Systematic Review..  59:372-383.e1. 2020
  • Letter to the Editor Regarding "Prevalence and Predictors of Burnout Among Hospice and Palliative Care Professionals"..  59:e3-e5. 2020
  • Opportunities to Improve Utilization of Palliative Care Among Adults With Cystic Fibrosis: A Systematic Review..  58:1100-1112.e1. 2019
  • Palliative Care Opportunities Among Adults With Congenital Heart Disease-A Systematic Review..  58:891-898. 2019
  • Pilot Study to Improve Goals of Care Conversations Among Hospitalists..  58:864-870. 2019
  • Organizing Psychologists, Behavioral Scientists, and Allied Professionals: Formation of the Society of Behavioral Medicine's Palliative Care Special Interest Group..  58:e10-e11. 2019
  • Paying for Palliative Care in Medicare: Evidence From the Four Seasons/Duke CMMI Demonstration..  58:654-661.e2. 2019
  • 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
  • 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
  • Patient-Reported Outcomes for Cancer Patients Receiving Checkpoint Inhibitors: Opportunities for Palliative Care-A Systematic Review..  58:137-156.e1. 2019
  • Helping the Demand Find the Supply: Messaging the Value of Specialty Palliative Care Directly to Those With Serious Illnesses..  57:e6-e7. 2019
  • Erratum to 'Anticholinergic Drug Burden in Noncancer Versus Cancer Patients Near the End of Life' [Journal of Pain and Symptom Management 52 (2016) 737-743]..  57:e9-e10. 2019
  • Pediatric Perioperative DNR Orders: A Case Series in a Children's Hospital..  57:971-979. 2019
  • Molding Idle Musings Into Art: What Reflective Writing Does for Me?.  57:856-860. 2019
  • Opportunities to Improve Detection and Treatment of Depression Among Patients With Breast Cancer Treated in an Integrated Delivery System..  57:587-595. 2019
  • Managing Chronic Pain in Cancer Survivors Prescribed Long-Term Opioid Therapy: A National Survey of Ambulatory Palliative Care Providers..  57:20-27. 2019
  • Themes Addressed by Couples With Advanced Cancer During a Communication Skills Training Intervention..  56:252-258. 2018
  • Evaluating the Feasibility and Acceptability of a Telehealth Program in a Rural Palliative Care Population: TapCloud for Palliative Care..  56:7-14. 2018
  • Information Framing Reduces Initial Negative Attitudes in Cancer Patients' Decisions About Hospice Care..  55:1540-1545. 2018
  • Coping Skills Practice and Symptom Change: A Secondary Analysis of a Pilot Telephone Symptom Management Intervention for Lung Cancer Patients and Their Family Caregivers..  55:1341-1349.e4. 2018
  • Developing a Path to Improve Cultural Competency in Islam Among Palliative Care Professionals..  55:e1-e3. 2018
  • Physician Decision-Making in the Setting of Advanced Illness: An Examination of Patient Disposition and Physician Religiousness..  55:906-912. 2018
  • Physicians' Opinions on Engaging Patients' Religious and Spiritual Concerns: A National Survey..  55:897-905. 2018
  • Possible Redundant Data in the Network Meta-analysis of Pharmacological Therapies for Opioid-Induced Constipation..  55:e8-e9. 2018
  • Rapid Response Events in Hospitalized Patients: Patient Symptoms and Clinician Communication..  55:946-952. 2018
  • Acute Leukemia Patients' Needs: Qualitative Findings and Opportunities for Early Palliative Care..  55:433-439. 2018
  • Utilization of Hospice Services in a Population of Patients With Huntington's Disease..  55:440-443. 2018
  • Comparing the Palliative Care Needs of Patients With Hematologic and Solid Malignancies..  55:82-88.e1. 2018
  • 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
  • Addressing Patient Emotional and Existential Needs During Serious Illness: Results of the Outlook Randomized Controlled Trial..  54:898-908. 2017
  • Quality Improvement Pearls for the Palliative Care and Hospice Professional..  54:758-765. 2017
  • The Implementation of Measuring What Matters in Research and Practice: Series Commentary..  54:772-775. 2017
  • The Quality Improvement Environment: Results of the 2016 AAHPM/HPNA Membership Needs Assessment Survey..  54:766-771. 2017
  • Current Events (With Apologies to Leonard Cohen)..  54:617. 2017
  • One Size Does Not Fit All: Disease Profiles of Serious Illness Patients Receiving Specialty Palliative Care..  54:476-483. 2017
  • State of the Science of Spirituality and Palliative Care Research Part I: Definitions, Measurement, and Outcomes..  54:428-440. 2017
  • State of the Science of Spirituality and Palliative Care Research Part II: Screening, Assessment, and Interventions..  54:441-453. 2017
  • State of the Science of Spirituality and Palliative Care Research: Research Landscape and Future Directions..  54:426-427. 2017
  • Addressing Palliative Care Clinician Burnout in Organizations: A Workforce Necessity, an Ethical Imperative..  53:1091-1096. 2017
  • Comparing the Palliative Care Needs of Those With Cancer to Those With Common Non-Cancer Serious Illness..  53:1079-1084.e1. 2017
  • "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
  • 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
  • Operationalizing the Measuring What Matters Spirituality Quality Metric in a Population of Hospitalized, Critically Ill Patients and Their Family Members..  53:650-655. 2017
  • Concordance Between Veterans' Self-Report and Documentation of Surrogate Decision Makers: Implications for Quality Measurement..  53:1-4. 2017
  • "Who Does What?" Ensuring High-Quality and Coordinated Palliative Care With Our Oncology Colleagues..  52:e1-e2. 2016
  • Adherence to Measuring What Matters Items When Caring for Patients With Hematologic Malignancies Versus Solid Tumors..  52:775-782. 2016
  • Anticholinergic Drug Burden in Noncancer Versus Cancer Patients Near the End of Life..  52:737-743.e3. 2016
  • The Symptom Experience in Rectal Cancer Survivors..  52:709-718. 2016
  • Randomized Pilot Trial of a Telephone Symptom Management Intervention for Symptomatic Lung Cancer Patients and Their Family Caregivers..  52:469-482. 2016
  • Significant Morbidity and Mortality Among Hospitalized End-Stage Liver Disease Patients in Medicare..  52:412-419.e1. 2016
  • Understanding Treatment Effect Terminology in Pain and Symptom Management Research..  52:446-452. 2016
  • Building Resilience for Palliative Care Clinicians: An Approach to Burnout Prevention Based on Individual Skills and Workplace Factors..  52:284-291. 2016
  • Measuring Burnout in Palliative Care: Authors' Reply..  52:e2. 2016
  • Assessing Emotional Suffering in Palliative Care: Use of a Structured Note Template to Improve Documentation..  52:1-7. 2016
  • Association Between Symptom Burden and Time to Hospitalization, Nursing Home Placement, and Death Among the Chronically Ill Urban Homebound..  52:73-80. 2016
  • Comparing Unmet Needs to Optimize Quality: Characterizing Inpatient and Outpatient Palliative Care Populations..  51:1033-1039.e3. 2016
  • U.S. Physicians' Opinions About Accommodating Religiously Based Requests for Continued Life-Sustaining Treatment..  51:971-978. 2016
  • An Exploratory Factor Analysis of the Scale Structure of the Patient Care Monitor Version 2.0..  51:776-783.e2. 2016
  • Are Hospice Admission Practices Associated With Hospice Enrollment for Older African Americans and Whites?.  51:697-705. 2016
  • 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
  • Prevalence and Predictors of Burnout Among Hospice and Palliative Care Clinicians in the U.S..  51:690-696. 2016
  • A Blue Ocean Strategy for Palliative Care: Focus on Family Caregivers..  51:e1-e3. 2016
  • Adherence to Measuring What Matters Measures Using Point-of-Care Data Collection Across Diverse Clinical Settings..  51:497-503. 2016
  • Characterizing the Hospice and Palliative Care Workforce in the U.S.: Clinician Demographics and Professional Responsibilities..  51:597-603. 2016
  • Feeling Heard and Understood: A Patient-Reported Quality Measure for the Inpatient Palliative Care Setting..  51:150-154. 2016
  • Methodological Research Priorities in Palliative Care and Hospice Quality Measurement..  51:155-162. 2016
  • The Burden of Polypharmacy in Patients Near the End of Life..  51:178-83.e2. 2016
  • Impact of Smoking Cessation on Subsequent Pain Intensity Among Chronically Ill Veterans Enrolled in a Smoking Cessation Trial..  50:822-829. 2015
  • Usability and Acceptability of the QDACT-PC, an Electronic Point-of-Care System for Standardized Quality Monitoring in Palliative Care..  50:615-621. 2015
  • "The Patient Is Dying, Please Call the Chaplain": The Activities of Chaplains in One Medical Center's Intensive Care Units..  50:501-506. 2015
  • A Pilot Study of a Mobile Health Pain Coping Skills Training Protocol for Patients With Persistent Cancer Pain..  50:553-558. 2015
  • 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
  • Fatigue in HIV-Infected People: A Three-Year Observational Study..  50:69-79. 2015
  • Patient and Caregiver Opinions of Motivational Interviewing Techniques In Role-Played Palliative Care Conversations: A Pilot Study..  50:91-98. 2015
  • Signposts along the journey toward high-quality palliative care: the value of measuring what matters..  49:e1-e2. 2015
  • 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
  • Comparison of seven-day and repeated 24-hour recall of symptoms in the first 100 days after hematopoietic cell transplantation..  49:513-520. 2015
  • Limits and responsibilities of physicians addressing spiritual suffering in terminally ill patients..  49:562-569. 2015
  • Re: The Sidney Project™..  49:e4-e5. 2015
  • 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
  • Quality of palliative care for patients with advanced cancer in a community consortium..  49:289-292. 2015
  • The quality imperative for palliative care..  49:243-253. 2015
  • EMPOWER: an intervention to address barriers to pain management in hospice..  49:1-12. 2015
  • Feasibility of using algorithm-based clinical decision support for symptom assessment and management in lung cancer..  49:13-26. 2015
  • Validation of a measure of family experience of patients with serious illness: the QUAL-E (Fam)..  48:1168-1181. 2014
  • Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease..  48:934-943. 2014
  • Holding back moderates the association between health symptoms and social well-being in patients undergoing hematopoietic stem cell transplantation..  48:374-384. 2014
  • Integrating the biopsychosocial model into quality measures in palliative care: a case for improving the hospice item set..  48:e1-e2. 2014
  • Preparedness planning before mechanical circulatory support: a "how-to" guide for palliative medicine clinicians..  47:926-935.e6. 2014
  • Getting to proven: evaluating quality across all of palliative care..  47:e1-e2. 2014
  • Creating computable algorithms for symptom management in an outpatient thoracic oncology setting..  46:911-924.e1. 2013
  • Race and residence: intercounty variation in black-white differences in hospice use..  46:681-690. 2013
  • Targeted investment improves access to hospice and palliative care..  46:629-639. 2013
  • Intentional sedation to unconsciousness at the end of life: findings from a national physician survey..  46:326-334. 2013
  • Validity of an observation method for assessing pain behavior in individuals with multiple sclerosis..  46:413-421. 2013
  • Community-based palliative care: the natural evolution for palliative care delivery in the U.S..  46:254-264. 2013
  • Authors' reply to Dirksen et al..  45:e2-e3. 2013
  • 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
  • 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
  • Enrollment and events of hospice patients with heart failure vs. cancer..  45:552-560. 2013
  • Demonstration of a sustainable community-based model of care across the palliative care continuum..  44:797-809. 2012
  • Religiosity, spirituality, and end-of-life planning: a single-site survey of medical inpatients..  44:843-851. 2012
  • Assessment of the psychometric properties of an English version of the cancer dyspnea scale in people with advanced lung cancer..  44:741-749. 2012
  • 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
  • Burden and well-being among a diverse sample of cancer, congestive heart failure, and chronic obstructive pulmonary disease caregivers..  44:410-420. 2012
  • Dignity in end-of-life care: results of a national survey of U.S. physicians..  44:331-339. 2012
  • Parent perceptions of child vulnerability are associated with functioning and health care use in children with chronic pain..  43:953-960. 2012
  • Refining a checklist for reporting patient populations and service characteristics in hospice and palliative care research..  43:902-910. 2012
  • Self-compassion in patients with persistent musculoskeletal pain: relationship of self-compassion to adjustment to persistent pain..  43:759-770. 2012
  • Development of a prognostic model for six-month mortality in older adults with declining health..  43:527-539. 2012
  • 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
  • Collecting data on quality is feasible in community-based palliative care..  42:663-667. 2011
  • Comparing three life-limiting diseases: does diagnosis matter or is sick, sick?.  42:331-341. 2011
  • Caregiver-assisted coping skills training for lung cancer: results of a randomized clinical trial..  41:1-13. 2011
  • Validation of the Patient Care Monitor (Version 2.0): a review of system assessment instrument for cancer patients..  40:545-558. 2010
  • Hope in the context of lung cancer: relationships of hope to symptoms and psychological distress..  40:174-182. 2010
  • ASCPRO recommendations for the assessment of fatigue as an outcome in clinical trials..  39:1086-1099. 2010
  • A comparison of two spirituality instruments and their relationship with depression and quality of life in chronic heart failure..  39:515-526. 2010
  • 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
  • Genetic and nongenetic covariates of pain severity in patients with adenocarcinoma of the pancreas: assessing the influence of cytokine genes..  38:894-902. 2009
  • Mucositis-related morbidity and resource utilization in head and neck cancer patients receiving radiation therapy with or without chemotherapy..  38:522-532. 2009
  • Indwelling catheters for the management of refractory malignant ascites: a systematic literature overview and retrospective chart review..  38:341-349. 2009
  • 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
  • Pain catastrophizing and pain-related fear in osteoarthritis patients: relationships to pain and disability..  37:863-872. 2009
  • Pain behavior in rheumatoid arthritis patients: identification of pain behavior subgroups..  36:69-78. 2008
  • Perceived Resources and Barriers to Pediatric Palliative Care Among HealthCare Practitioners Attending the V Latin American Palliative Care Association (ALCP) Meeting (755). 2011
  • Race and residence: county-level variation in black-white disparities in hospice use (312-B). 2011