Literature DB >> 32484432

Carer administration of as-needed subcutaneous medication for breakthrough symptoms in people dying at home: the CARiAD feasibility RCT.

Marlise Poolman1, Jessica Roberts1, Stella Wright1, Annie Hendry1, Nia Goulden2, Emily Af Holmes1, Anthony Byrne3, Paul Perkins4,5, Zoe Hoare2, Annmarie Nelson3, Julia Hiscock1, Dyfrig Hughes1, Julie O'Connor5, Betty Foster6, Liz Reymond7, Sue Healy8, Penney Lewis9, Bee Wee10, Rosalynde Johnstone11, Rossela Roberts12, Anne Parkinson5, Sian Roberts11, Clare Wilkinson1.   

Abstract

BACKGROUND: Most people who are dying want to be cared for at home, but only half of them achieve this. The likelihood of a home death often depends on the availability of able and willing lay carers. When people who are dying are unable to take oral medication, injectable medication is used. When top-up medication is required, a health-care professional travels to the dying person's home, which may delay symptom relief. The administration of subcutaneous medication by lay carers, although not widespread UK practice, has proven to be key in achieving better symptom control for those dying at home in other countries.
OBJECTIVES: To determine if carer administration of as-needed subcutaneous medication for common breakthrough symptoms in people dying at home is feasible and acceptable in the UK, and if it would be feasible to test this intervention in a future definitive randomised controlled trial.
DESIGN: We conducted a two-arm, parallel-group, individually randomised, open pilot trial of the intervention versus usual care, with a 1 : 1 allocation ratio, using convergent mixed methods.
SETTING: Home-based care without 24/7 paid care provision, in three UK sites. PARTICIPANTS: Participants were dyads of adult patients and carers: patients in the last weeks of their life who wished to die at home and lay carers who were willing to be trained to give subcutaneous medication. Strict risk assessment criteria needed to be met before approach, including known history of substance abuse or carer ability to be trained to competency. INTERVENTION: Intervention-group carers received training by local nurses using a manualised training package. MAIN OUTCOME MEASURES: Quantitative data were collected at baseline and 6-8 weeks post bereavement and via carer diaries. Interviews with carers and health-care professionals explored attitudes to, experiences of and preferences for giving subcutaneous medication and experience of trial processes. The main outcomes of interest were feasibility, acceptability, recruitment rates, attrition and selection of the most appropriate outcome measures.
RESULTS: In total, 40 out of 101 eligible dyads were recruited (39.6%), which met the feasibility criterion of recruiting > 30% of eligible dyads. The expected recruitment target (≈50 dyads) was not reached, as fewer than expected participants were identified. Although the overall retention rate was 55% (22/40), this was substantially unbalanced [30% (6/20) usual care and 80% (16/20) intervention]. The feasibility criterion of > 40% retention was, therefore, considered not met. A total of 12 carers (intervention, n = 10; usual care, n = 2) and 20 health-care professionals were interviewed. The intervention was considered acceptable, feasible and safe in the small study population. The context of the feasibility study was not ideal, as district nurses were seriously overstretched and unfamiliar with research methods. A disparity in readiness to consider the intervention was demonstrated between carers and health-care professionals. Findings showed that there were methodological and ethics issues pertaining to researching last days of life care.
CONCLUSION: The success of a future definitive trial is uncertain because of equivocal results in the progression criteria, particularly poor recruitment overall and a low retention rate in the usual-care group. Future work regarding the intervention should include understanding the context of UK areas where this has been adopted, ascertaining wider public views and exploring health-care professional views on burden and risk in the NHS context. There should be consideration of the need for national policy and of the most appropriate quantitative outcome measures to use. This will help to ascertain if there are unanswered questions to be studied in a trial. TRIAL REGISTRATION: Current Controlled Trials ISRCTN11211024. FUNDING: This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 24, No. 25. See the NIHR Journals Library website for further project information.

Entities:  

Keywords:  CARERS; COMMUNITY HEALTH CARE; INJECTIONS; PAIN, BREAKTHROUGH; PALLIATIVE CARE MEDICINE; SUBCUTANEOUS; SYMPTOM ASSESSMENT; TERMINAL CARE

Year:  2020        PMID: 32484432      PMCID: PMC7294396          DOI: 10.3310/hta24250

Source DB:  PubMed          Journal:  Health Technol Assess        ISSN: 1366-5278            Impact factor:   4.014


  54 in total

Review 1.  Qualitative research in health care. Analysing qualitative data.

Authors:  C Pope; S Ziebland; N Mays
Journal:  BMJ       Date:  2000-01-08

2.  The memorial symptom assessment scale: modified for use in understanding family caregivers' perceptions of cancer patients' symptom experiences.

Authors:  Michelle M Lobchuk
Journal:  J Pain Symptom Manage       Date:  2003-07       Impact factor: 3.612

Review 3.  Factors influencing death at home in terminally ill patients with cancer: systematic review.

Authors:  Barbara Gomes; Irene J Higginson
Journal:  BMJ       Date:  2006-02-08

4.  Lay caregivers' perspectives on injecting subcutaneous medications at home.

Authors:  Fiona Israel; Liz Reymond; Georgi Slade; Sharyn Menadue; Margaret A Charles
Journal:  Int J Palliat Nurs       Date:  2008-08

5.  Can symptom relief be provided in the home to palliative care cancer patients by the primary caregivers? An Indian study.

Authors:  Sheeba Chellappan; Punitha Ezhilarasu; Angela Gnanadurai; Reena George; Solomon Christopher
Journal:  Cancer Nurs       Date:  2014 Sep-Oct       Impact factor: 2.592

6.  Generalized method for adaptive randomization in clinical trials.

Authors:  D Russell; Z S J Hoare; Rh Whitaker; C J Whitaker; I T Russell
Journal:  Stat Med       Date:  2011-02-01       Impact factor: 2.373

7.  Using qualitative methods for attribute development for discrete choice experiments: issues and recommendations.

Authors:  Joanna Coast; Hareth Al-Janabi; Eileen J Sutton; Susan A Horrocks; A Jane Vosper; Dawn R Swancutt; Terry N Flynn
Journal:  Health Econ       Date:  2011-05-06       Impact factor: 3.046

8.  The Memorial Symptom Assessment Scale: an instrument for the evaluation of symptom prevalence, characteristics and distress.

Authors:  R K Portenoy; H T Thaler; A B Kornblith; J M Lepore; H Friedlander-Klar; E Kiyasu; K Sobel; N Coyle; N Kemeny; L Norton
Journal:  Eur J Cancer       Date:  1994       Impact factor: 9.162

9.  Comfort care kit: use of nonoral and nonparenteral rescue medications at home for terminally ill patients with swallowing difficulty.

Authors:  Richard Yap; R Akhileswaran; Chong Poh Heng; Angela Tan; David Hui
Journal:  J Palliat Med       Date:  2014-04-07       Impact factor: 2.947

10.  A process for Decision-making after Pilot and feasibility Trials (ADePT): development following a feasibility study of a complex intervention for pelvic organ prolapse.

Authors:  Carol Bugge; Brian Williams; Suzanne Hagen; Janet Logan; Cathryn Glazener; Stewart Pringle; Lesley Sinclair
Journal:  Trials       Date:  2013-10-25       Impact factor: 2.279

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