Literature DB >> 26567328

An information model for automated assessment of concordance between advance care preferences and care delivered near the end of life.

Marianne Turley1, Susan Wang2, Di Meng3, Michael H Kanter4, Terhilda Garrido3.   

Abstract

OBJECTIVE: To develop an information model for automating evaluation of concordance between patient preferences and end-of-life care.
METHODS: We modeled and validated 15 end-of-life care preference option domains, to which we mapped preferences recorded in standardized advance care planning documents and 232 end-of-life care events defined by procedure and medication codes. Patient preferences and end-of-life care events were available in electronic health records. Data from Kaiser Permanente Southern California modeling and testing populations were evaluated for concordance between patients' preferences and the end-of-life care events they experienced.
RESULTS: The information model successfully assessed concordance between patient preferences and end-of-life care events. Among 388 expired patients in the modeling population, 4164 care events occurred, 4100 (98%) of which were preference-concordant, and 64 (2%) of which were preference-discordant. Including end-of-life care events that did not occur increased the number of observations to 6029; 99% were preference-concordant. At the level of individuals, 72% (278) of patients experienced only preference-concordant care events, 13% (50) experienced at least one preference-discordant care event, and 15% (60) experienced no preference-related care events. DISCUSSION: Model limitations pertain to assumptions that are required to match advance care planning documents with patient preference options and exclusion of preferred care that did not occur. Further research is required to apply the model to larger populations and to investigate the need for additional preference options.
CONCLUSION: An information model for automating the assessment of the concordance between patients' advance care planning preferences and the end-of-life care they received was effective in a small population and has the potential to assess population-level preference-concordance on an ongoing basis.
© The Author 2015. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  advance care planning; documentation; electronic health record; patient-centered care; population management

Mesh:

Year:  2015        PMID: 26567328      PMCID: PMC4954636          DOI: 10.1093/jamia/ocv149

Source DB:  PubMed          Journal:  J Am Med Inform Assoc        ISSN: 1067-5027            Impact factor:   4.497


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Authors:  Stephanie Johnson; Josephine Clayton; Phyllis N Butow; William Silvester; Karen Detering; Jane Hall; Belinda E Kiely; Jonathon Cebon; Stephen Clarke; Melanie L Bell; Martin Stockler; Phillip Beale; Martin H N Tattersall
Journal:  BMJ Open       Date:  2016-12-01       Impact factor: 2.692

6.  Patient Preferences in the Medical Product Life Cycle: What do Stakeholders Think? Semi-Structured Qualitative Interviews in Europe and the USA.

Authors:  Rosanne Janssens; Selena Russo; Eline van Overbeeke; Chiara Whichello; Sarah Harding; Jürgen Kübler; Juhaeri Juhaeri; Karin Schölin Bywall; Alina Comanescu; Axel Hueber; Matthias Englbrecht; Nikoletta Nikolenko; Gabriella Pravettoni; Steven Simoens; Hilde Stevens; Richard Hermann; Bennett Levitan; Irina Cleemput; Esther de Bekker-Grob; Jorien Veldwijk; Isabelle Huys
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