Article
Inpatient Pediatric Palliative Care Consult Requests and Recommendations

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Introduction

Little is known about the requests for and recommendations from inpatient pediatric palliative care (PPC) consults and whether they differ by patient location (ward vs. intensive care unit) or patient type (new vs. established with PPC).

Methods

Single-center, retrospective cohort study comparing PPC consult requests and recommendations for children who received a PPC consult between January 1, 2018 and June 30, 2019. Comparisons were made by patient location and patient type using bivariate statistics.

Results

Three hundred twenty-seven PPC encounters were evaluated. Symptoms were more likely to be addressed in consults for ward patients than for intensive care unit patients. Compared with established patients, consults for new patients occurred significantly later in the hospital course and were more likely to be for psychosocial support or goals of care.

Discussion

We found variability in PPC consult requests and recommendations that may inform future work and targeted education for primary providers.

Section snippets

INTRODUCTION

Pediatric palliative care (PPC), as described by the World Health Organization (2018), is the comprehensive care of a child facing a life-threatening illness, which includes caring for the child's body, mind, and spirit while also offering support to the child's family. The American Academy of Pediatrics (American Academy of Pediatrics Committee on Bioethics and Committee on Hospital Care, 2000) recommends that palliative care be introduced at diagnosis and continue throughout the child's

Setting

We conducted a retrospective cohort study deemed exempt from human subjects research by our institutional review board. Our institution is a free-standing, quaternary care, > 400-bed children's hospital with a 48-bed pediatric ICU, 24-bed cardiac ICU, and 83-bed neonatal ICU. Inpatient ward teams that consult PPC include hospital medicine, pulmonology, gastroenterology/hepatology, hematology/oncology, and nephrology. Consults are requested at the discretion of the primary teams, and the PPC

RESULTS

Of the 500 reviewed encounters, 327 encounters from 260 unique patients were eligible for inclusion (Figure). Demographic and clinical information for unique patients is presented in Table 1. Patients were a median age of 1 year (interquartile range, 0.0–11.0), 53.1% male, 70.9% White, and over 80% had public insurance. Seventy-eight percent of patients had four or more CCCs. Technology dependence, cardiovascular conditions, gastrointestinal conditions, and neurological/neuromuscular conditions

DISCUSSION

Our study demonstrates that patients in our system who received PPC consults were likely to be (1) highly complex with a wide variety of CCCs, (2) reliant on medical technology, and (3) covered by public insurance. Most PPC consults, especially those for new patients, were conducted for patients on ICU teams. Key differences were noted between ward and ICU consults in symptoms addressed and recommendations provided by the PPC team. Furthermore, differences between consults for new and

Kristin Carter, Pediatric Hospice and Palliative Medicine Fellow, Northwestern University Feinberg School of Medicine, Department of Pediatrics, Division of Palliative Care, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL.

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Cited by (0)

Kristin Carter, Pediatric Hospice and Palliative Medicine Fellow, Northwestern University Feinberg School of Medicine, Department of Pediatrics, Division of Palliative Care, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL.

Jennifer L. Raybin, Pediatric Palliative Care Program Leader, University of Colorado School of Medicine, Department of Pediatrics, Section of Palliative Care, Children's Hospital Colorado, Aurora, CO.

Lilliam Ambroggio, Associate Professor, Director of Research (Hospital Medicine), Associate Director of Research (Emergency Medicine), University of Colorado School of Medicine, Department of Pediatrics, Sections of Emergency Medicine and Hospital Medicine, Children's Hospital Colorado, Aurora, CO.

Mitchell Frydenlund, Medical Student, University of Colorado School of Medicine, Aurora, CO.

Jacob Thomas, Data Analyst, Adult and Child Consortium for Health Outcomes Research and Delivery Science, Aurora, CO.

Kathryn Squiers, Clinical Associate, University of Chicago, Department of Pediatrics, Section of Pediatric Hospital Medicine, Comer Children's Hospital, Chicago, IL.

Mark Brittan, Associate Professor, Pediatric Hospital Medicine Fellowship Director, Associate Director of Research, University of Colorado School of Medicine, Department of Pediatrics, Section of Hospital Medicine, Children's Hospital Colorado, Adult and Child Consortium for Health Outcomes Research and Delivery Science, Aurora, CO.

This work was supported by the National Institutes of Health/National Center for Advancing Translational Sciences and the Colorado Clinical and Translational Sciences Institute (grant no. UL1 TR002535). Contents are the authors’ sole responsibility and do not necessarily represent official National Institutes of Health views. The funding agency did not have any involvement in the study design, in the collection, analysis, and interpretation of data, in the writing of the report, or in the decision to submit the article for publication.

Conflicts of interest: None to report.

Kristin Carter has full access to the data and will provide access to the data on which the manuscript is based for examination by the editors or their assignees if requested.

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