Literature DB >> 30632886

Understanding the Barriers to Introducing Early Palliative Care for Patients with Advanced Cancer: A Qualitative Study.

Aline Sarradon-Eck1,2, Sylvain Besle1,3, Jaïs Troian4, Géraldine Capodano5, Julien Mancini6.   

Abstract

Background: Palliative care is often underutilized or initiated late in the course of life-threatening illness. Randomized clinical Early Palliative Care (EPC) trials provide an opportunity for changing oncologists' perceptions of palliative care and their attitudes to referring patients to palliative care services. Aim: To describe French oncologists' perceptions of EPC and their effects on referral practices before a clinical EPC trial was launched. Design: A qualitative study involving semistructured face-to-face interviews. The data were analyzed using the Grounded Theory coding method. Setting/Participants: Thirteen oncologists and 19 palliative care specialists (PCSs) working at 10 hospitals all over France were interviewed. Most of them were involved in clinical EPC trials.
Results: The findings suggest that referral to PCSs shortly after the diagnosis of advanced cancer increases the terminological barriers, induces avoidance patterns, and makes early disclosure of poor prognosis harder for oncologists. This situation is attributable to the widespread idea that palliative care means terminal care. In addition, the fact that the EPC concept is poorly understood increases the confusion between EPC and supportive care.
Conclusion: Defining the EPC concept more clearly and explaining to health professionals and patients what EPC consists of and what role it is intended to play, and the potential benefits of palliative care services could help to overcome the wording barriers rooted in the traditional picture of palliative care. In addition, training French oncologists how to disclose "bad news" could help them cope with the emotional issues involved in referring patients to specialized palliative care.

Entities:  

Keywords:  France; cancer; early palliative care; medical culture; qualitative study; social representation

Year:  2019        PMID: 30632886     DOI: 10.1089/jpm.2018.0338

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  12 in total

Review 1.  Evolving Definitions of Palliative Care: Upstream Migration or Confusion?

Authors:  Suzanne Ryan; Joanne Wong; Ronald Chow; Camilla Zimmermann
Journal:  Curr Treat Options Oncol       Date:  2020-02-11

2.  An Automatic Pediatric Palliative Care Consultation for Children Supported on Extracorporeal Membrane Oxygenation: A Survey of Perceived Benefits and Barriers.

Authors:  Claudia Delgado-Corcoran; Sarah E Wawrzynski; Kelly J Mansfield; Brian Flaherty; Danielle D DeCourcey; Dominic Moore; Lawrence J Cook; Christina K Ullrich; Lenora M Olson
Journal:  J Palliat Med       Date:  2022-03-18       Impact factor: 2.947

3.  Using Quality Improvement to Increase Access to Palliative Care.

Authors:  Kate Lally; Isaac S Chua; Nancy U Lin; Jocelyn Siegel; Rachelle Bernacki
Journal:  JCO Oncol Pract       Date:  2020-11-16

4.  IDentification of patients in need of general and specialised PALLiative care (ID-PALL©): item generation, content and face validity of a new interprofessional screening instrument.

Authors:  Fabienne Teike Lüthi; Mathieu Bernard; Michel Beauverd; Claudia Gamondi; Anne-Sylvie Ramelet; Gian Domenico Borasio
Journal:  BMC Palliat Care       Date:  2020-02-12       Impact factor: 3.234

5.  Early palliative care versus standard care in haematologic cancer patients at their last active treatment: study protocol of a feasibility trial.

Authors:  Silvia Tanzi; Stefano Luminari; Silvio Cavuto; Elena Turola; Luca Ghirotto; Massimo Costantini
Journal:  BMC Palliat Care       Date:  2020-04-22       Impact factor: 3.234

6.  How views of oncologists and haematologists impacts palliative care referral: a systematic review.

Authors:  Naveen Salins; Arunangshu Ghoshal; Sean Hughes; Nancy Preston
Journal:  BMC Palliat Care       Date:  2020-11-23       Impact factor: 3.234

7.  Comparison of Palliative Care Delivery in the Last Year of Life Between Adults With Terminal Noncancer Illness or Cancer.

Authors:  Kieran L Quinn; Peter Wegier; Therese A Stukel; Anjie Huang; Chaim M Bell; Peter Tanuseputro
Journal:  JAMA Netw Open       Date:  2021-03-01

8.  "When I Heard the Word Palliative": Obscuring and Clarifying Factors Affecting the Stigma Around Palliative Care Referral in Oncology.

Authors:  Taynara Formagini; Claire Poague; Alicia O'Neal; Joanna Veazey Brooks
Journal:  JCO Oncol Pract       Date:  2021-07-26

9.  Symptom Burden and Complexity in the Last 12 Months of Life among Cancer Patients Choosing Medical Assistance in Dying (MAID) in Alberta, Canada.

Authors:  Linda Watson; Claire Link; Siwei Qi; Andrea DeIure; K Brooke Russell; Fiona Schulte; Caitlin Forbes; James Silvius; Brian Kelly; Barry D Bultz
Journal:  Curr Oncol       Date:  2022-03-03       Impact factor: 3.677

10.  Theory-Based Development of an Implementation Intervention Using Community Health Workers to Increase Palliative Care Use.

Authors:  Boateng Kubi; Zachary O Enumah; Kimberley T Lee; Karen M Freund; Thomas J Smith; Lisa A Cooper; Jill T Owczarzak; Fabian M Johnston
Journal:  J Pain Symptom Manage       Date:  2020-02-22       Impact factor: 3.612

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