Literature DB >> 33675919

Measuring Goal-Concordant Care in Palliative Care Research.

Natalie C Ernecoff1, Kathryn L Wessell2, Antonia V Bennett3, Laura C Hanson4.   

Abstract

>Goal-concordant care is a priority outcome for palliative care research, yet the field lacks consensus on optimal methods for measurement. We sought to 1) categorize methods used to measure goal-concordant care, and 2) discuss strengths and limitations of each method using empirical examples from palliative care research. We categorized measurement methods for goal-concordant care. We identified empirical examples of each method to illustrate the strengths, limitations, and applicability of each method to relevant study designs. We defined four methods used to measure goal-concordant care: 1) Patient- or Caregiver-Reported, 2) Caregiver-Reported After Death, 3) Concordance in Longitudinal Data, and 4) Population-Level Indicators. Patient or caregiver-reported goal-concordant care draws on strengths of patient-reported outcomes, and can be captured for multiple aspects of treatment; these methods are subject to recall bias or family-proxy bias. Concordance in longitudinal data is optimal when a treatment preference can be specifically and temporally linked to actual treatment; the method is limited to common life-sustaining treatment choices and validity may be affected by temporal variation between preference and treatment. Population-level indicators allow pragmatic research to include large populations; its primary limitation is the assumption that preferences held by a majority of persons should correspond to patterns of actual treatment in similar populations. Methods used to measure goal-concordant care have distinct strengths and limitations, and methods should be selected based on research question and study design. Existing methods could be improved, yet a future gold standard is unlikely to suit all research designs.
Copyright © 2021 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Goal-concordant; goals; palliative care

Mesh:

Year:  2021        PMID: 33675919      PMCID: PMC9082654          DOI: 10.1016/j.jpainsymman.2021.02.030

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   5.576


  49 in total

1.  Racial and ethnic differences in preferences for end-of-life treatment.

Authors:  Amber E Barnato; Denise L Anthony; Jonathan Skinner; Patricia M Gallagher; Elliott S Fisher
Journal:  J Gen Intern Med       Date:  2009-04-23       Impact factor: 5.128

2.  Using Electronic Health Records for Quality Measurement and Accountability in Care of the Seriously Ill: Opportunities and Challenges.

Authors:  J Randall Curtis; Seelwan Sathitratanacheewin; Helene Starks; Robert Y Lee; Erin K Kross; Lois Downey; James Sibley; William Lober; Elizabeth T Loggers; James A Fausto; Charlotta Lindvall; Ruth A Engelberg
Journal:  J Palliat Med       Date:  2017-11-28       Impact factor: 2.947

3.  Safety and Effectiveness of Palliative Drug Treatment in the Last Days of Life-A Systematic Literature Review.

Authors:  Kristian Jansen; Dagny F Haugen; Lisa Pont; Sabine Ruths
Journal:  J Pain Symptom Manage       Date:  2017-08-10       Impact factor: 3.612

Review 4.  Stability of end-of-life preferences: a systematic review of the evidence.

Authors:  Catherine L Auriemma; Christina A Nguyen; Rachel Bronheim; Saida Kent; Shrivatsa Nadiger; Dustin Pardo; Scott D Halpern
Journal:  JAMA Intern Med       Date:  2014-07       Impact factor: 21.873

5.  Validation of a decisional conflict scale.

Authors:  A M O'Connor
Journal:  Med Decis Making       Date:  1995 Jan-Mar       Impact factor: 2.583

6.  Determining Consistency of Surrogate Decisions and End-of-Life Care Received with Patient Goals-of-Care Preferences.

Authors:  Mi-Kyung Song; Sandra E Ward; Laura C Hanson; Maureen Metzger; SuHyun Kim
Journal:  J Palliat Med       Date:  2016-03-16       Impact factor: 2.947

7.  Outcomes That Define Successful Advance Care Planning: A Delphi Panel Consensus.

Authors:  Rebecca L Sudore; Daren K Heyland; Hillary D Lum; Judith A C Rietjens; Ida J Korfage; Christine S Ritchie; Laura C Hanson; Diane E Meier; Steven Z Pantilat; Karl Lorenz; Michelle Howard; Michael J Green; Jessica E Simon; Mariko A Feuz; John J You
Journal:  J Pain Symptom Manage       Date:  2017-09-01       Impact factor: 3.612

8.  Change in end-of-life care for Medicare beneficiaries: site of death, place of care, and health care transitions in 2000, 2005, and 2009.

Authors:  Joan M Teno; Pedro L Gozalo; Julie P W Bynum; Natalie E Leland; Susan C Miller; Nancy E Morden; Thomas Scupp; David C Goodman; Vincent Mor
Journal:  JAMA       Date:  2013-02-06       Impact factor: 56.272

9.  A comparison of the quality of care provided to cancer patients in the UK in the last three months of life in in-patient hospices compared with hospitals, from the perspective of bereaved relatives: results from a survey using the VOICES questionnaire.

Authors:  J M Addington-Hall; A C O'Callaghan
Journal:  Palliat Med       Date:  2009-02-27       Impact factor: 4.762

10.  Which outcome domains are important in palliative care and when? An international expert consensus workshop, using the nominal group technique.

Authors:  Susanne de Wolf-Linder; Marsha Dawkins; Francesca Wicks; Sophie Pask; Kathy Eagar; Catherine J Evans; Irene J Higginson; Fliss E M Murtagh
Journal:  Palliat Med       Date:  2019-06-12       Impact factor: 4.762

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  4 in total

1.  Deficits in Identification of Goals and Goal-Concordant Care After Sepsis Hospitalization.

Authors:  Stephanie Parks Taylor; Marc A Kowalkowski; Katherine R Courtright; Henry L Burke; Sangnya Patel; Samantha Hicks; Cristina Hurley; Stephen Mitchell; Scott D Halpern
Journal:  J Hosp Med       Date:  2021-11       Impact factor: 2.960

2.  Trends in advance care planning and end-of-life care among persons living with dementia requiring surrogate decision-making.

Authors:  Hiroshi Gotanda; Anne M Walling; David B Reuben; Marie Lauzon; Yusuke Tsugawa
Journal:  J Am Geriatr Soc       Date:  2022-02-04       Impact factor: 7.538

3.  Mapping and characterising electronic palliative care coordination systems and their intended impact: A national survey of end-of-life care commissioners.

Authors:  Jacqueline Birtwistle; Pablo Millares-Martin; Catherine J Evans; Robbie Foy; Samuel Relton; Suzanne Richards; Katherine E Sleeman; Maureen Twiddy; Michael I Bennett; Matthew J Allsop
Journal:  PLoS One       Date:  2022-10-14       Impact factor: 3.752

4.  Hospital-Free Days: A Pragmatic and Patient-centered Outcome for Trials among Critically and Seriously Ill Patients.

Authors:  Catherine L Auriemma; Stephanie P Taylor; Michael O Harhay; Katherine R Courtright; Scott D Halpern
Journal:  Am J Respir Crit Care Med       Date:  2021-10-15       Impact factor: 30.528

  4 in total

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