Journal of Pain and Symptom Management

Applying the Multiphase Optimization Strategy for the Development of Optimized Interventions in Palliative Care.  62:174-182. 2021

Relationships Between Advanced Cancer Patients' Worry About Dying and Illness Understanding, Treatment Preferences, and Advance Care Planning.  61:723-731.e1. 2021

Launching the Next Steps to Improve Hospice and Palliative Medicine Fellow Performance Assessment: A Look Back to the Initial Toolkit of Assessment Methods.  61:613-627. 2021

Examining Adherence and Dose Effect of an Early Palliative Care Intervention for Advanced Heart Failure Patients 2021

To Disclose or Not to Disclose: A Case Highlighting the Challenge of Conflicts in Pediatric Disclosure.  61:211-215. 2021

Witnesses and Victims Both: Healthcare Workers and Grief in the Time of COVID-19 2021

Healing the Hearts of Bereaved Parents: Impact of Legacy Artwork on Grief in Pediatric Oncology.  60:790-800. 2020

Heightened Tamoxifen Activation Masquerading as a Venlafaxine-Associated Adverse Event After Rotation From Duloxetine.  60:e104-e106. 2020

Development of Subspecialty-Specific Reporting Milestones for Hospice and Palliative Medicine Fellowship Training in the U.S..  60:151-157. 2020

Hospital or Home? Where Should Children Die and How Do We Make That a Reality?.  60:106-115. 2020

One Size Does Not Fit All: Exploring Dose Effect of an Early Palliative Care Intervention for Advanced Heart Failure Patients (GP800).  60:304-305. 2020

The Family Caregiving Crisis Meets an Actual Pandemic.  60:e66-e69. 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” (Journal of Pain and Symptom Management (2016) 51(4) (690–696), (S0885392415006144), (10.1016/j.jpainsymman.2015.10.020)).  59:965. 2020

Letter to the Editor Regarding “Prevalence and Predictors of Burnout Among Hospice and Palliative Care Professionals”.  59:e3-e5. 2020

Reliability and Validity of the Turkish Version of the FACIT-PAL Quality of Life Instrument.  58:297-305.e4. 2019

Disparities in Hospice Utilization for Older Cancer Patients Living in the Deep South.  58:86-91. 2019

Toward a Conceptual Model of Affective Predictions in Palliative Care.  57:1151-1165. 2019

Development of Curricular Milestones for Hospice and Palliative Medicine Fellowship Training in the U.S..  57:1009-1017.e6. 2019

Exploring the Role of Religion and Spirituality in Provider-Patient Communication Among African-Americans with Advanced Heart Failure and Their Family Caregivers (FR421B).  57:411-412. 2019

Effects of Shared Decision Making on Distress and Health Care Utilization Among Patients With Lung Cancer: A Systematic Review.  56:975-987.e5. 2018

Adapting an Early Palliative Care Intervention to Family Caregivers of Persons With Advanced Cancer in the Rural Deep South: A Qualitative Formative Evaluation.  55:1519-1530. 2018

Culture and Palliative Care: Preferences, Communication, Meaning, and Mutual Decision Making.  55:1408-1419. 2018

Our Differences Make Us Stronger.  55:1398-1399. 2018

Challenges to Safe and Effective Pain Management in Patients With Super Obesity: Case Report and Literature Review.  55:1047-1052. 2018

California's End of Life Option Act: What Can We Learn from One Year of Legalization? (TH312).  55:565-565. 2018

The Implementation of Measuring What Matters in Research and Practice: Series Commentary.  54:772-775. 2017

Development of Entrustable Professional Activities for Hospice and Palliative Medicine Fellowship Training in the United States.  54:609-616.e1. 2017

Palliative Care Clinicians Caring for Patients Before and After Continuous Flow-Left Ventricular Assist Device.  54:601-608. 2017

Palliative Medicine and Preparedness Planning for Patients Receiving Left Ventricular Assist Device as Destination Therapy—Challenges to Measuring Impact and Change in Institutional Culture.  54:231-236. 2017

Gait Speed and Survival in Patients With Brain Metastases.  54:105-109. 2017

I Never Thought “That Person” Could Be Me ….  54:e3-e5. 2017

Addressing Palliative Care Clinician Burnout in Organizations: A Workforce Necessity, an Ethical Imperative.  53:1091-1096. 2017

Feasibility of a Telehealth Educational Program on Self-Management of Pain and Fatigue in Adult Cancer Patients.  53:1071-1078. 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

Implementation and Impact of Patient Lay Navigator-Led Advance Care Planning Conversations.  53:682-692. 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

Looking Back, Moving Forward: A Retrospective Review of Care Trends in an Academic Palliative and Supportive Care Program from 2004-2015 (S744).  53:434-434. 2017

Concordance Between Veterans' Self-Report and Documentation of Surrogate Decision Makers: Implications for Quality Measurement.  53:1-4. 2017

Adherence to Measuring What Matters Items When Caring for Patients With Hematologic Malignancies Versus Solid Tumors.  52:775-782. 2016

Family Caregiver Depressive Symptom and Grief Outcomes From the ENABLE III Randomized Controlled Trial.  52:378-385. 2016

Assessing Emotional Suffering in Palliative Care: Use of a Structured Note Template to Improve Documentation.  52:1-7. 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

A Quantitative Study of Triggered Palliative Care Consultation for Hospitalized Patients with Advanced Cancer the results of Cohorts 1 and 2 were presented at the 2014 Annual Assembly of the American Academy of Hospice and Palliative Medicine (AAHPM) and the Hospice and Palliative Nurses Association (HPNA)..  50:462-469. 2015

Hospice and palliative medicine clinician views of deactivation of ventricular assist devices at the end of life.  50:e6-e8. 2015

A study to improve communication between clinicians and patients with advanced heart failure: Methods and challenges behind the working to improve discussions about defibrillator management trial.  48:1236-1246. 2014

A novel website to prepare diverse older adults for decision making and advance care planning: A pilot study.  47:674-686. 2014

Advance directives, advance care planning, and shared decision making: Promoting synergy over exclusivity in contemporary context.  47. 2014

Can senior volunteers deliver reminiscence and creative activity interventions? results of the legacy intervention family enactment randomized controlled trial.  48:590-601. 2014

Preparedness planning before mechanical circulatory support: A "how-to" guide for palliative medicine clinicians.  47. 2014

Symptom burden predicts nursing home admissions among older adults.  46:591-597. 2013

Management of end-of-life care and of difficult behaviors associated with borderline personality disorder.  45:934-938. 2013

Advance care planning beyond advance directives: Perspectives from patients and surrogates.  46:355-365. 2013

Opioid pain medication orders and administration in the last days of life.  44:681-691. 2012

An assessment of the screening performance of a single-item measure of depression from the edmonton symptom assessment scale among chronically ill hospitalized patients.  43:866-873. 2012

Preliminary assessment of a neuropathic pain treatment and referral algorithm for patients with cancer.  42:822-838. 2011

Hospice use in Alabama, 2002-2005.  41:374-382. 2011

Symptom Cluster and Quality of Life in Multiple Sclerosis.  39:1025-1032. 2010

Trends and Racial Differences in the Use of Androgen Deprivation Therapy for Metastatic Prostate Cancer.  39:872-881. 2010

Mucositis-Related Morbidity and Resource Utilization in Head and Neck Cancer Patients Receiving Radiation Therapy With or Without Chemotherapy.  38:522-532. 2009

Symptom Cluster as a Predictor of Physical Activity in Multiple Sclerosis: Preliminary Evidence.  38:270-280. 2009

Reliability and Validity of the Functional Assessment of Chronic Illness Therapy-Palliative Care (FACIT-Pal) Scale.  37:23-32. 2009

Physical Activity Behaviors in Individuals with Multiple Sclerosis: Roles of Overall and Specific Symptoms, and Self-Efficacy.  36:46-53. 2008

The nature of suffering and the goals of nursing: A long time coming but worth the wait. 2008

Palliative care program effectiveness research: Developing rigor in sampling design, conduct, and reporting.  31:270-284. 2006

Clinical applications for change-point analysis of herpes zoster pain.  23:510-516. 2002

A mixed model for factors predictive of pain in AIDS patients with herpes zoster.  17:410-417. 1999

Knowledge and attitudes of health care providers towards cancer pain management: A comparison of physicians, nurses, and pharmacists in the state of new hampshire 1998