Literature DB >> 31345846

Family caregivers of children and adolescents with rare diseases: a novel palliative care intervention.

Maureen E Lyon1, Jessica D Thompkins2, Karen Fratantoni3, Jamie L Fraser4, Sandra E Schellinger5, Linda Briggs5, Sarah Friebert6, Samar Aoun7,8, Yao Iris Cheng9, Jichuan Wang9,10.   

Abstract

OBJECTIVE: To develop and pilot test a palliative care intervention for family caregivers of children with rare diseases (FAmily-CEntered pediatric Advance Care Planning-Rare (FACE-Rare)).
METHODS: FACE-Rare development involved an iterative, family-guided process including review by a Patient and Family Advisory Council, semistructured family interviews and adaptation of two evidence-based person-centred approaches and pilot testing their integration. Eligible families were enrolled in FACE-Rare (the Carer Support Needs Assessment Tool (CSNAT) Approach Paediatric sessions 1 and 2; plus Respecting Choices Next Steps pACP intervention sessions 3 and 4). Satisfaction, quality of communication and caregiver appraisal were assessed.
RESULTS: Parents were mean age 40 years, and children 7 years. Children's diseases were rare enough that description would identify patients. All children were technology dependent. Telemedicine, used with four of seven families, was an effective engagement strategy and decreased subject burden. Families found FACE-Rare valuable following a strategy that first elicited palliative care needs and a support plan. Eight families were approached for pilot testing. Of the seven mothers who agreed to participate, six began session 1, and of those, 100% completed: all four FACE-Rare sessions, baseline and 2-week postintervention assessments, and a written pACP which described their preferences for medical decision-making to share with their providers. 100% reported FACE-Rare was helpful. The top three CSNAT concerns were: knowing what to expect in the future, having enough time for yourself and financial issues. Benchmarks were achieved and questionnaires were acceptable to parents and thus feasible to use in a larger trial.
CONCLUSIONS: FACE-Rare provides an innovative, structured approach for clinicians to deliver person-centred care. © Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  decision making; end-of-life; family caregiver; intervention; palliative care needs; pediatric advanced care planning; rare disease

Year:  2019        PMID: 31345846      PMCID: PMC8040699          DOI: 10.1136/bmjspcare-2019-001766

Source DB:  PubMed          Journal:  BMJ Support Palliat Care        ISSN: 2045-435X            Impact factor:   4.633


  35 in total

1.  Disparities in Inpatient Intensity of End-of-Life Care for Complex Chronic Conditions.

Authors:  Emily E Johnston; Jori Bogetz; Olga Saynina; Lisa J Chamberlain; Smita Bhatia; Lee Sanders
Journal:  Pediatrics       Date:  2019-04-10       Impact factor: 7.124

2.  Identifying and addressing the support needs of family caregivers of people with motor neurone disease using the Carer Support Needs Assessment Tool.

Authors:  Samar M Aoun; Kathleen Deas; Linda J Kristjanson; David W Kissane
Journal:  Palliat Support Care       Date:  2016-05-13

3.  The Spectrum of Caregiving in Palliative Care for Serious, Advanced, Rare Diseases: Key Issues and Research Directions.

Authors:  Lynn S Adams; Jeri L Miller; Patricia A Grady
Journal:  J Palliat Med       Date:  2016-06-01       Impact factor: 2.947

4.  The Impact of Supporting Family Caregivers Before Bereavement on Outcomes After Bereavement: Adequacy of End-of-Life Support and Achievement of Preferred Place of Death.

Authors:  Samar M Aoun; Gail Ewing; Gunn Grande; Chris Toye; Natasha Bear
Journal:  J Pain Symptom Manage       Date:  2017-10-10       Impact factor: 3.612

5.  Pediatric advance care planning.

Authors:  Bernard J Hammes; Judy Klevan; Michelle Kempf; Marc S Williams
Journal:  J Palliat Med       Date:  2005-08       Impact factor: 2.947

6.  Lived experiences of parents caring for a child with a life-limiting condition in Australia: A qualitative study.

Authors:  Anna Collins; Nicole Hennessy-Anderson; Sarah Hosking; Jenny Hynson; Cheryl Remedios; Kristina Thomas
Journal:  Palliat Med       Date:  2016-03-07       Impact factor: 4.762

7.  Advance Care Planning and HIV Symptoms in Adolescence.

Authors:  Maureen E Lyon; Patricia A Garvie; Lawrence J D'Angelo; Ronald H Dallas; Linda Briggs; Patricia M Flynn; Ana Garcia; Yao I Cheng; Jichuan Wang
Journal:  Pediatrics       Date:  2018-10-19       Impact factor: 7.124

8.  Impaired Health-Related Quality of Life in Children and Families Affected by Methylmalonic Acidemia.

Authors:  Kimberly Splinter; Anna-Kaisa Niemi; Rachel Cox; Julia Platt; Monisha Shah; Gregory M Enns; Mureo Kasahara; Jonathan A Bernstein
Journal:  J Genet Couns       Date:  2015-12-14       Impact factor: 2.537

9.  Increased burden on caregivers of having a child with haemophilia complicated by inhibitors.

Authors:  Karin Lindvall; Sylvia von Mackensen; Sölve Elmståhl; Kate Khair; Ann Marie Stain; Rolf Ljung; Erik Berntorp
Journal:  Pediatr Blood Cancer       Date:  2013-11-26       Impact factor: 3.167

10.  Improving the analysis of composite endpoints in rare disease trials.

Authors:  Martina McMenamin; Anna Berglind; James M S Wason
Journal:  Orphanet J Rare Dis       Date:  2018-05-22       Impact factor: 4.123

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  7 in total

Review 1.  Age-Appropriate Advance Care Planning in Children Diagnosed with a Life-Limiting Condition: A Systematic Review.

Authors:  Julie Brunetta; Jurrianne Fahner; Monique Legemaat; Esther van den Bergh; Koen Krommenhoek; Kyra Prinsze; Marijke Kars; Erna Michiels
Journal:  Children (Basel)       Date:  2022-06-03

2.  The profile and support needs of parents in paediatric palliative care: comparing cancer and non-cancer groups.

Authors:  Samar M Aoun; Fenella J Gill; Marianne B Phillips; Suzanne Momber; Lisa Cuddeford; Renee Deleuil; Roswitha Stegmann; Denise Howting; Maureen E Lyon
Journal:  Palliat Care Soc Pract       Date:  2020-09-25

3.  Documentation of Psychosocial Distress and Its Antecedents in Children with Rare or Life-Limiting Chronic Conditions.

Authors:  Sarah R McCarthy; Elizabeth H Golembiewski; Derek L Gravholt; Jennifer E Clark; Jeannie Clark; Caree Fischer; Hannah Mulholland; Kristina Babcock; Victor M Montori; Amie Jones
Journal:  Children (Basel)       Date:  2022-05-05

4.  Conceptualising paediatric advance care planning: a qualitative phenomenological study of paediatricians caring for children with life-limiting conditions in Australia.

Authors:  Sidharth Vemuri; Jenny Hynson; Katrina Williams; Lynn Gillam
Journal:  BMJ Open       Date:  2022-05-16       Impact factor: 3.006

5.  Towards a Comprehensive Strategy for the Management of Rare Diseases in Slovenia: Outlining an IT-Enabled Ecosystemic Approach.

Authors:  Dalibor Stanimirovic; Eva Murko; Tadej Battelino; Urh Groselj; Mojca Zerjav Tansek
Journal:  Int J Environ Res Public Health       Date:  2021-11-25       Impact factor: 3.390

6.  "It Is a Whole Different Life from the Life I Used to Live": Assessing Parents' Support Needs in Paediatric Palliative Care.

Authors:  Samar M Aoun; Roswitha Stegmann; Renee Deleuil; Suzanne Momber; Lisa Cuddeford; Marianne B Phillips; Maureen E Lyon; Fenella J Gill
Journal:  Children (Basel)       Date:  2022-03-01

7.  Family-Centered Advance Care Planning: What Matters Most for Parents of Children with Rare Diseases.

Authors:  Karen Fratantoni; Jessica Livingston; Sandra E Schellinger; Samar M Aoun; Maureen E Lyon
Journal:  Children (Basel)       Date:  2022-03-21
  7 in total

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