Literature DB >> 23652842

Recommendations for managing missing data, attrition and response shift in palliative and end-of-life care research: part of the MORECare research method guidance on statistical issues.

Nancy J Preston1, Peter Fayers, Stephen J Walters, Mark Pilling, Gunn E Grande, Vicky Short, Eleanor Owen-Jones, Catherine J Evans, Hamid Benalia, Irene J Higginson, Chris J Todd.   

Abstract

BACKGROUND: Statistical analysis in palliative and end-of-life care research can be problematic due to high levels of missing data, attrition and response shift as disease progresses. AIM: To develop recommendations about managing missing data, attrition and response shift in palliative and end-of-life care research data.
DESIGN: We used the MORECare Transparent Expert Consultation approach to conduct a consultation workshop with experts in statistical methods in palliative and end-of-life care research. Following presentations and discussion, nominal group techniques were used to produce recommendations about attrition, missing data and response shift. These were rated online by experts and analysed using descriptive statistics for consensus and importance.
RESULTS: In total, 20 participants attended the workshop and 19 recommendations were subsequently ranked. There was broad agreement across recommendations. The top five recommendations were as follows: A taxonomy should be devised to define types of attrition. Types and amount of missing data should be reported with details of imputation methods. The pattern of missing data should be investigated to inform the imputation approach. A statistical analysis plan should be pre-specified in the protocol. High rates of attrition should be assumed when planning studies and specifying analyses. The leading recommendation for response shift was for more research.
CONCLUSIONS: When designing studies in palliative and end-of-life care, it is recommended that high rates of attrition should not be seen as indicative of poor design and that a clear statistical analysis plan is in place to account for missing data and attrition.

Entities:  

Keywords:  Statistics; consensus; palliative care; research design

Mesh:

Year:  2013        PMID: 23652842     DOI: 10.1177/0269216313486952

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  30 in total

1.  Advancing palliative care by learning.

Authors:  Irene Higginson
Journal:  J Palliat Med       Date:  2013-10       Impact factor: 2.947

2.  Factors Associated With Attrition in a Multicenter Longitudinal Observational Study of Patients With Advanced Cancer.

Authors:  Pedro E Perez-Cruz; Omar Shamieh; Carlos Eduardo Paiva; Jung Hye Kwon; Mary Ann Muckaden; Eduardo Bruera; David Hui
Journal:  J Pain Symptom Manage       Date:  2017-11-16       Impact factor: 3.612

3.  A group intervention to improve quality of life for people with advanced dementia living in care homes: the Namaste feasibility cluster RCT.

Authors:  Katherine Froggatt; Ashley Best; Frances Bunn; Girvan Burnside; Joanna Coast; Lesley Dunleavy; Claire Goodman; Ben Hardwick; Clare Jackson; Julie Kinley; Anne Davidson Lund; Jennifer Lynch; Paul Mitchell; Gareth Myring; Shakil Patel; Guillermo Perez Algorta; Nancy Preston; David Scott; Kate Silvera; Catherine Walshe
Journal:  Health Technol Assess       Date:  2020-01       Impact factor: 4.014

4.  The selection and use of outcome measures in palliative and end-of-life care research: the MORECare International Consensus Workshop.

Authors:  Catherine J Evans; Hamid Benalia; Nancy J Preston; Gunn Grande; Marjolein Gysels; Vicky Short; Barbara A Daveson; Claudia Bausewein; Chris Todd; Irene J Higginson
Journal:  J Pain Symptom Manage       Date:  2013-04-28       Impact factor: 3.612

5.  Experiences of patients, family and professional caregivers with Integrated Palliative Care in Europe: protocol for an international, multicenter, prospective, mixed method study.

Authors:  Marlieke van der Eerden; Agnes Csikos; Csilla Busa; Sean Hughes; Lukas Radbruch; Johan Menten; Jeroen Hasselaar; Marieke Groot
Journal:  BMC Palliat Care       Date:  2014-11-21       Impact factor: 3.234

6.  Results of a transparent expert consultation on patient and public involvement in palliative care research.

Authors:  Barbara A Daveson; Susanne de Wolf-Linder; Jana Witt; Kirstie Newson; Carolyn Morris; Irene J Higginson; Catherine J Evans
Journal:  Palliat Med       Date:  2015-04-30       Impact factor: 4.762

7.  Re-evaluating randomized clinical trials of psychological interventions: Impact of response shift on the interpretation of trial results.

Authors:  M G E Verdam; W van Ballegooijen; C J M Holtmaat; H Knoop; J Lancee; F J Oort; H Riper; A van Straten; I M Verdonck-de Leeuw; M de Wit; T van der Zweerde; M A G Sprangers
Journal:  PLoS One       Date:  2021-05-25       Impact factor: 3.240

8.  Brief Engagement and Acceptance Coaching for Hospice Settings (the BEACHeS study): results from a Phase I study of acceptability and initial effectiveness in people with non-curative cancer.

Authors:  Nicholas J Hulbert-Williams; Sabrina F Norwood; David Gillanders; Anne M Finucane; Juliet Spiller; Jenny Strachan; Susan Millington; Joseph Kreft; Brooke Swash
Journal:  BMC Palliat Care       Date:  2021-06-25       Impact factor: 3.234

Review 9.  Evaluating complex interventions in end of life care: the MORECare statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews.

Authors:  Irene J Higginson; Catherine J Evans; Gunn Grande; Nancy Preston; Myfanwy Morgan; Paul McCrone; Penney Lewis; Peter Fayers; Richard Harding; Matthew Hotopf; Scott A Murray; Hamid Benalia; Marjolein Gysels; Morag Farquhar; Chris Todd
Journal:  BMC Med       Date:  2013-04-24       Impact factor: 8.775

Review 10.  Alternative Consent Models in Pragmatic Palliative Care Clinical Trials.

Authors:  Joan G Carpenter; Connie Ulrich; Nancy Hodgson; Laura C Hanson; Mary Ersek
Journal:  J Pain Symptom Manage       Date:  2020-10-29       Impact factor: 5.576

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