scholarly journals Corrigendum to Advance Care Planning Discussions in a Substance Use Disorder Recovery Program [Journal of Pain and Symptom Management 58 (2019) e3–e6]

2020 ◽  
Vol 59 (2) ◽  
pp. e6
2020 ◽  
Vol 37 (11) ◽  
pp. 985-987
Author(s):  
Benjamin Roberts ◽  
Scott M. Wright ◽  
Colleen Christmas ◽  
Mariah Robertson ◽  
David Shih Wu

Context: The coronavirus disease 2019 (COVID-19) pandemic laid bare the immediate need for primary palliative care education for many clinicians. Primary care clinicians in our health system reported an urgent need for support in advance care planning and end-of-life symptom management for their vulnerable patients. This article describes the design and dissemination of palliative care education for primary care clinicians using an established curriculum development method. Objectives: To develop a succinct and practical palliative care toolkit for use by primary care clinicians during the COVID-19 pandemic, focused on 2 key elements: (i) advance care planning communication skills based on the narrative 3-Act Model and (ii) comfort care symptom management at the end of life. Results: The toolkit was finalized through an iterative process involving a team of end-users and experts in palliative care and primary care, including social work, pharmacy, nursing, and medicine. The modules were formatted into an easily navigable, smartphone-friendly document to be used at point of care. The toolkit was disseminated to our institution’s primary care network with practices spanning our state. Early feedback has been positive. Conclusion: While we had been focused primarily on the inpatient setting, our palliative care team at Johns Hopkins Bayview Medical Center pivoted existing infrastructure and curriculum development expertise to meet the expressed needs of our primary care colleagues during the COVID-19 pandemic. Through collaboration with an interprofessional team including end-users, we designed and disseminated a concise palliative care toolkit within 6 weeks.


2013 ◽  
Vol 3 (2) ◽  
pp. 282.2-283
Author(s):  
N Kubokawa ◽  
M Nishikawa ◽  
Y Yokoe ◽  
K Fukuda ◽  
H Hattori ◽  
...  

Author(s):  
Michelle Koh ◽  
Finella Craig ◽  
Joanne Wolfe

This chapter on palliative care for children with advanced cancer addresses the challenges of decision making and the care of the child and family. It explores decision making with regards to ongoing treatment, advance-care planning, and the importance of establishing goals of care. The nature and management of common physical and psychological symptoms are examined, in particular pain and the use of opioids and neuropathic adjuvants. Cancer-directed therapies, specific symptom management, and steroids are discussed. The chapter also includes specific issues around the care of the child and family at the end of life, such as feeding, spiritual distress, and ongoing bereavement care. This chapter is aimed at professionals in the multidisciplinary team caring for children in this context.


2019 ◽  
Vol 34 (11) ◽  
pp. 2630-2633 ◽  
Author(s):  
Michelle J. Fleshner ◽  
Amy J. Kennedy ◽  
Peter J. Veldkamp ◽  
Julie W. Childers

2014 ◽  
Vol 10 (2) ◽  
pp. 104-104 ◽  
Author(s):  
Gordon Kuntz ◽  
Jane Tozer ◽  
Jeff Snegosky ◽  
John Fox ◽  
Kurt Neumann

Purpose: The Michigan Oncology Medical Home Demonstration Project (MOMHDP) is an innovative multipractice oncology medical home model, supported by payment reform. Sponsored by Priority Health, Physician Resource Management, and ION Solutions, MOMHDP includes four oncology practices and 29 physicians. Methods: Oncology practices used existing technologies, with MOMHDP providing evidence-based treatment guideline selection and compliance tracking, automated physician order entry, a patient portal, symptom management/standardized nurse triage, and advance care planning. To support changes in care and administrative models and to focus on quality, MOMHDP modifies provider payments. The program replaces the average sales price payment methodology with a drug acquisition reimbursement plus a care management fee, calculated to increase total drug reimbursement. Additionally, it reimburses for chemotherapy and treatment planning and advance care planning consultation. There is also a shared savings opportunity. MOMHDP will be enhanced in its second year to include a survivorship program, patient distress screening, imaging guidelines, and standardized patient satisfaction surveys. Priority Health patients receiving chemotherapy for a cancer diagnosis were recruited to the program. Results for this group were compared with a control group of patients from a prior period. Results: In addition to the financial results, the project also accomplished the following: (1) adherence to practice-selected guidelines, (2) institution of advance care planning, (3) effective and standardized symptom management; and (4) payment reform. Conclusion: We have identified a number of critical success factors: strong payer/provider collaboration built on trust through transparent use and cost data; timing of clinical standardization must come from the practices, so they can effectively absorb new approaches; having comprehensive, written program documentation and consistently applied training facilitate practice understanding; existing, off-the-shelf technologies help control costs; independent clinical, administrative, and technical coordination improves provider/payer collaboration; everything takes longer than anticipated, including practice commitment, contracting, and technology implementation. Practices are willing to take on clinical standardization with payment reform. Neither practice size nor technology platform variation was a barrier to participation or success in the project. These results represent preliminary reporting from the first multipractice oncology medical home in the United States, to our knowledge, with payer support that includes payment reform. The results are promising, and the concept warrants further study, review, and reporting. [Table: see text]


Author(s):  
Michael W. Rabow ◽  
Judith Redwing Keyssar ◽  
Judith Long ◽  
Maki Aoki ◽  
Gayle Kojimoto

In the setting of the COVID-19 pandemic as well as the recognition of systemic racism in our institutions, the symptom management, emotional/psychological support and advance care planning at the core of palliative care—once considered “an extra layer of support” —have been revealed as instrumental to individuals, families, communities, and countries facing the threat of the global pandemic. In this article, we outline the primary palliative care education efforts of one palliative care education center (The MERI Center at UCSF/Mt Zion campus) and detail the critical adjustments necessary and opportunities found in the COVID crisis.


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