Literature DB >> 12018738

Appropriate time frames for data collection in quality of life research among cancer patients at the end of life.

Siew Tzuh Tang1, Ruth McCorkle.   

Abstract

Longitudinal research has been recommended as the most appropriate research design to ensure the validity of quality of life assessments. However, high attrition and non-random missing data in quality of life studies for terminal cancer patients raise questions about generalizability of the study, and at worst they may jeopardize interpretation of the results. Appropriate time frames for eliciting information directly from terminal cancer patients can ensure the internal and external validity of quality of life research in end-of-life care, allow health care professionals to detect sensitively the effects of end-of-life care within the shortest intervention period, and make comparisons across studies possible. From a review of the literature, it is recommended that the appropriate time frame for interviewing terminal cancer patients about their quality of life be a weekly assessment schedule based on the following factors: (a) the median survival of terminal cancer patients enrolling in a hospice/palliative care program is approximately 30 days and there are substantial number of patients who die in each week; (b) at the final weeks of life, quality of life and symptoms of some terminal cancer patients change dramatically; and (c) the shortest intervention period that is likely to give a clinically significant effect of end-of-life care management is 1 week after the enrollment in end-of-life care.

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Year:  2002        PMID: 12018738     DOI: 10.1023/a:1015021531112

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  64 in total

1.  The use of the Rotterdam Symptom Checklist in palliative care.

Authors:  J R Hardy; P Edmonds; R Turner; E Rees; R A'Hern
Journal:  J Pain Symptom Manage       Date:  1999-08       Impact factor: 3.612

2.  Survival of Medicare patients after enrollment in hospice programs.

Authors:  N A Christakis; J J Escarce
Journal:  N Engl J Med       Date:  1996-07-18       Impact factor: 91.245

3.  Terminal cancer patients and timing of referral to palliative care: a multicenter prospective cohort study. Italian Cooperative Research Group on Palliative Medicine.

Authors:  M Costantini; F Toscani; M Gallucci; C Brunelli; G Miccinesi; M Tamburini; E Paci; P Di Giulio; C Peruselli; I Higginson; J Addington-Hall
Journal:  J Pain Symptom Manage       Date:  1999-10       Impact factor: 3.612

4.  The quality of life of patients with cancer receiving hospice care.

Authors:  S C McMillan
Journal:  Oncol Nurs Forum       Date:  1996-09       Impact factor: 2.172

5.  Historical and methodological perspectives on cancer outcomes research.

Authors:  J S Mandelblatt; J M Eisenberg
Journal:  Oncology (Williston Park)       Date:  1995-11       Impact factor: 2.990

6.  Hospice role in alleviating the emotional stress of terminal patients and their families.

Authors:  R L Kane; S J Klein; L Bernstein; R Rothenberg; J Wales
Journal:  Med Care       Date:  1985-03       Impact factor: 2.983

7.  Home palliative care for terminal cancer patients: a survey on the final week of life.

Authors:  C Peruselli; P Di Giulio; F Toscani; M Gallucci; C Brunelli; M Costantini; M Tamburini; E Paci; G Miccinesi; J M Addington-Hall; I J Higginson
Journal:  Palliat Med       Date:  1999-05       Impact factor: 4.762

8.  Assessing the effectiveness of a hospital palliative care team.

Authors:  J E Ellershaw; S J Peat; L C Boys
Journal:  Palliat Med       Date:  1995-04       Impact factor: 4.762

Review 9.  Quality of life assessment in palliative care.

Authors:  I G Finlay; R Dunlop
Journal:  Ann Oncol       Date:  1994-01       Impact factor: 32.976

10.  Are bereaved family members a valid proxy for a patient's assessment of dying?

Authors:  I Higginson; P Priest; M McCarthy
Journal:  Soc Sci Med       Date:  1994-02       Impact factor: 4.634

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  5 in total

1.  The feasibility, reliability and validity of the McGill Quality of Life Questionnaire-Cardiff Short Form (MQOL-CSF) in palliative care population.

Authors:  Pei Lin Lua; Sam Salek; Ilora Finlay; Chris Lloyd-Richards
Journal:  Qual Life Res       Date:  2005-09       Impact factor: 4.147

2.  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

3.  Evaluation of the palliative symptom burden score (PSBS) in a specialised palliative care unit of a university medical centre - a longitudinal study.

Authors:  Katharina Fetz; Hendrik Vogt; Thomas Ostermann; Andrea Schmitz; Christian Schulz-Quach
Journal:  BMC Palliat Care       Date:  2018-07-07       Impact factor: 3.234

4.  Proxy perspectives regarding end-of-life care for persons with cancer.

Authors:  Marie Bakitas; Tim A Ahles; Karen Skalla; Frances C Brokaw; Ira Byock; Brett Hanscom; Kathleen Doyle Lyons; Mark T Hegel
Journal:  Cancer       Date:  2008-04-15       Impact factor: 6.860

Review 5.  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

  5 in total

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