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1.
J Soc Work End Life Palliat Care ; 15(2-3): 99-110, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31230584

RESUMO

Children receiving palliative care services are held within the context of a family and often within multiple-generational arms. The purpose of this case series paper is to recognize grandparents' roles in their family system from a personal, cultural, and anthropological perspective; to explore emotions and experiences as applies to grandparents of children receiving palliative care; and to provide tangible insight into caring well for families across the generational arc.


Assuntos
Cuidadores/psicologia , Avós/psicologia , Cuidados Paliativos/organização & administração , Pediatria/organização & administração , Criança , Características Culturais , Emoções , Características da Família , Humanos , Cuidados Paliativos/psicologia , Apoio Social , Meios de Transporte
2.
Cardiol Young ; 29(9): 1143-1148, 2019 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-31391137

RESUMO

BACKGROUND: Understanding perceptions of family caregivers' roles and responsibilities regarding their child with complex cardiac needs has potential to help care teams better support parents. Paternal experience has been under-explored in pediatric cardiac cohorts. METHODS: Ten fathers of children undergoing cardiac surgery completed quantitative surveys on their knowledge needs and preferred format of communication. In face-to-face recorded interviews, they responded to open-ended questions about the definition of being a good father to a child with a complex cardiac condition, perceived paternal responsibilities, personal growth as a parent to a child with a complex heart condition, support needs, and recommendations to medical staff for paternal inclusion. Semantic content analysis was utilised. The study reports strictly followed COnsolidated criteria for REporting Qualitative research guidelines. RESULTS: The fathers reported high preference for knowledge about the child's heart condition, communication about the treatment plan, and desire for inclusion in the care of their child. Paternal role was defined thematically as: providing a supportive presence, being there, offering bonded insight, serving as strong provider, and acting as an informed advocate. The fathers revealed that their responsibilities sometimes conflicted as they strove to serve as an emotional and economic stabiliser for their family, while also wanting to be foundationally present for their child perioperatively. CONCLUSION: This study provides insight into paternal experience and strategies for paternal inclusion. This summary of the self-defined experience of the fathers of pediatric cardiac patients offers constructive and specific advice for medical teams.


Assuntos
Adaptação Psicológica , Procedimentos Cirúrgicos Cardíacos/psicologia , Emoções/fisiologia , Pai/psicologia , Cardiopatias Congênitas/cirurgia , Comportamento Paterno/psicologia , Apoio Social , Adulto , Criança , Pré-Escolar , Feminino , Seguimentos , Cardiopatias Congênitas/psicologia , Humanos , Lactente , Masculino , Estudos Retrospectivos , Estresse Psicológico/psicologia
4.
J Palliat Med ; 24(8): 1161-1166, 2021 08.
Artigo em Inglês | MEDLINE | ID: mdl-33404324

RESUMO

Background: Hospital-based support for bereaved parents is regarded as best practice. Little is known about parental perceptions or programmatic potential of online grief support. Objectives: To learn from bereaved parent participants' experiences with an online support group to include perceptions of technology acceptance and group communication dynamics. Design: Descriptive study reporting on an eight-week online bereavement support group offered during summer 2020. Subjects and Setting: Inclusive of six bereaved parent participants in the Midwestern United States. Measurements: Post-intervention survey consisting of 49-items with the Technology Acceptance Model and Other Communicated Perspective-Taking Ability instruments embedded. Results: Five bereaved mothers and one father (mean age 32 years) residing an average 126 miles from hospital participated in an online support group in a timeframe seven months to one year from the death of their child. Intensity of grief emotion (5/6 parents) and physical distance (4/6 parents) were notable barriers to in-person visits to the hospital, where bereavement support was to be offered. Parents uniformly reported feeling benefit from the program and satisfaction with the program. Respondents self-reported gaining improved communication (4/6 parents), coping (3/6 parents), peer support (3/6 parents), education (3/6 parents), and emotional expression (3/6 parents). Mean scores on the technology acceptance and communication experiences scales were 4.7/5. The virtual format was an acceptable modality with perceived supportive interpersonal communication dynamics. Conclusion: Pediatric palliative care teams may consider the offering of online bereavement support groups. Further research is warranted on the impact and outcomes of online bereavement support groups for bereaved parents.


Assuntos
Luto , Adulto , Criança , Feminino , Pesar , Humanos , Mães , Pais , Grupos de Autoajuda
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