Outpatient palliative care at a tertiary cancer center: Perceptions, pathways, and pitfalls.

Authors

null

Kavitha Ramchandran

Stanford University

Kavitha Ramchandran, Sandy Trieu, Stephanie Harman, Judy Passaglia, Janet Rodriguez, Patricia Dwyer, Ryan Oden

Organizations

Stanford University

Research Funding

Other
Background: To describe an outpatient palliative care program at a quaternary cancer center- Stanford Cancer Institute. Outpatient palliative care (PC) programs are still in their nascency. Best practices are still being developed and key performance metrics are being delineated. This is a description of Stanford Cancer Institute outpatient PC program. Methods: Observational study of the first six months of encounters to the outpatient PC program. Description of potential barriers to launch and growth, as well as description of resources required for continued success. Data evaluated included program volume, referral patterns, advance care planning, symptom assessment and team structure as collected by the clinical team. Results: Initial barriers to program initiation included lack of funding and infrastructure. Additional barriers included coordination between teams, flow of care (patients late for next appointments), and cultural perceptions of palliative care as equal to end of life care. There are 32 referring practitioners to the program. Over the first six months the outpatient PC program has seen growth with volume increasing from 10 consults per month to 26 consults per month for a total of 60 patients. At the time of initial consult, 11 of the 60 patients seen had an advance directive. Only 1 patient had a physician order for life sustaining treatment (POLST). Code status was documented in 21 of the 60 patients. Conclusions: Our program had multiple barriers to launch: perceptions that palliative care equaled end of life care, lack of infrastructure and funding, and difficulty with coordination between teams. With administrative support the program secured funding, developed infrastructure with the assistance of IT, Cancer Center administration, and Care Coordination. Consults now come from a wide range of providers. Based on preliminary data indicating a very low percentage of completion of these tasks by patients on initial consult there is need for outpatient palliative care for advance care planning. Future growth will include continued penetration of the cancer center, increasing volume of consults, and additional assessments of patient satisfaction, symptom improvement, and hospital utilization.

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2012 ASCO Quality Care Symposium

Session Type

Poster Session

Session Title

General Poster Session A

Track

Involving Patients in Quality Care,Quality Measurement,Quality Improvement ,The Use of IT to Improve Quality

Sub Track

Involving Patients in Quality Care

Citation

J Clin Oncol 30, 2012 (suppl 34; abstr 28)

DOI

10.1200/jco.2013.31.31_suppl.28

Abstract #

28

Poster Bd #

C14

Abstract Disclosures

Similar Abstracts

Abstract

2023 ASCO Quality Care Symposium

Impacts of an outpatient palliative care team on the end-of-life care at a cancer center in Brazil.

First Author: Sarah Ananda Gomes

Abstract

2021 ASCO Annual Meeting

Improving end of life care with advance care planning in a rural cancer center.

First Author: Jacquelyn Barnhart

First Author: Rubina Ratnaparkhi