Literature DB >> 34468826

Oncology team perspectives on distress screening: a multisite study of a well-established use of patient-reported outcomes for clinical assessment.

Tenbroeck G Smith1, Asher E Beckwitt2, Lonneke V van de Poll-Franse3,4,5, Jeuneviette E Bontemps-Jones6, Ted A James7,8, Ryan M McCabe9, Amanda B Francescatti9, Neil K Aaronson3.   

Abstract

PURPOSE: Cancer care team attitudes towards distress screening are key to its success and sustainability. Previous qualitative research has interviewed staff mostly around the startup phase. We evaluate oncology teams' perspectives on psychosocial distress screening, including perceived strengths and challenges, in settings where it has been operational for years.
METHODS: We conducted, transcribed, and analyzed semi-structured interviews with 71 cancer care team members (e.g., MDs, RNs, MSWs) at 18 Commission on Cancer-accredited cancer programs including those serving underrepresented populations.
RESULTS: Strengths of distress screening identified by participants included identifying patient needs and testing provider assumptions. Staff indicated it improved patient-provider communication and other aspects of care. Challenges to distress screening included patient barriers (e.g., respondent burden) and lack of electronic system interoperability. Participants expressed the strengths of distress screening (n = 291) more than challenges (n = 86). Suggested improvements included use of technology to collect data, report results, and make referrals; complete screenings prior to appointments; longitudinal assessment; additional staff training; and improve resources to address patient needs.
CONCLUSION: Cancer care team members' perspectives on well-established distress screening programs largely replicate findings of previous studies focusing on the startup phase, but there are important differences: team members expressed more strengths than challenges, suggesting a positive attitude. While our sample described many challenges described previously, they did not indicate challenges with scoring and interpreting the distress screening questionnaire. The differences in attitudes expressed in response to mature versus startup implementations provide important insights to inform efforts to sustain and optimize distress screening.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Cancer; Patient-reported outcome measures; Psychosocial distress; Support care; Symptoms

Mesh:

Year:  2021        PMID: 34468826     DOI: 10.1007/s00520-021-06458-5

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  14 in total

1.  Barriers and facilitators to implementing the commission on cancer's distress screening program standard.

Authors:  Andrea K Knies; Devika R Jutagir; Elizabeth Ercolano; Nicholas Pasacreta; Mark Lazenby; Ruth McCorkle
Journal:  Palliat Support Care       Date:  2018-06-08

Review 2.  The experiences of professionals with using information from patient-reported outcome measures to improve the quality of healthcare: a systematic review of qualitative research.

Authors:  Maria B Boyce; John P Browne; Joanne Greenhalgh
Journal:  BMJ Qual Saf       Date:  2014-02-06       Impact factor: 7.035

3.  Incident Cases Captured in the National Cancer Database Compared with Those in U.S. Population Based Central Cancer Registries in 2012-2014.

Authors:  Katherine Mallin; Amanda Browner; Bryan Palis; Greer Gay; Ryan McCabe; Leticia Nogueira; Robin Yabroff; Lawrence Shulman; Matthew Facktor; David P Winchester; Heidi Nelson
Journal:  Ann Surg Oncol       Date:  2019-02-08       Impact factor: 5.344

Review 4.  Screening for distress and unmet needs in patients with cancer: review and recommendations.

Authors:  Linda E Carlson; Amy Waller; Alex J Mitchell
Journal:  J Clin Oncol       Date:  2012-03-12       Impact factor: 44.544

Review 5.  Patient-reported outcomes in routine cancer clinical practice: a scoping review of use, impact on health outcomes, and implementation factors.

Authors:  D Howell; S Molloy; K Wilkinson; E Green; K Orchard; K Wang; J Liberty
Journal:  Ann Oncol       Date:  2015-04-17       Impact factor: 32.976

6.  Psychosocial distress among oncology patients in the safety net.

Authors:  Theora Cimino; Kiana Said; Leslie Safier; Heather Harris; Anne Kinderman
Journal:  Psychooncology       Date:  2020-09-28       Impact factor: 3.894

7.  Use of Patient-Reported Outcome Measures in Quality Oncology Practice Initiative-Registered Practices: Results of a National Survey.

Authors:  Biqi Zhang; Whit Lloyd; Mohammad Jahanzeb; Michael J Hassett
Journal:  J Oncol Pract       Date:  2018-09-12       Impact factor: 3.840

Review 8.  Exploring the implementation of patient-reported outcome measures in cancer care: need for more real-world evidence results in the peer reviewed literature.

Authors:  Milena Anatchkova; Sarah M Donelson; Anne M Skalicky; Colleen A McHorney; Dayo Jagun; Jennifer Whiteley
Journal:  J Patient Rep Outcomes       Date:  2018-12-27

Review 9.  A systematic review of the impact of routine collection of patient reported outcome measures on patients, providers and health organisations in an oncologic setting.

Authors:  Jack Chen; Lixin Ou; Stephanie J Hollis
Journal:  BMC Health Serv Res       Date:  2013-06-11       Impact factor: 2.655

10.  The dynamic sustainability framework: addressing the paradox of sustainment amid ongoing change.

Authors:  David A Chambers; Russell E Glasgow; Kurt C Stange
Journal:  Implement Sci       Date:  2013-10-02       Impact factor: 7.327

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