Literature DB >> 25176315

Liminality as a conceptual frame for understanding the family caregiving rite of passage: an integrative review.

Susanne W Gibbons1, Alyson Ross, Margaret Bevans.   

Abstract

Family caregiving is a significant rite of passage experienced by family caregivers of individuals with protracted illness or injury. In an integrative review of 26 studies, we characterized family caregiving from the sociocultural perspective of liminality and explored associated psychosocial implications. Analysis of published evidence on this dynamic and formative transition produced a range of themes. While role ambiguity resolved for most, for others, uncertainty and suffering continued. The process of becoming a caregiver was transformative and can be viewed as a rebirth that is largely socially and culturally driven. The transition to family caregiving model produced by this review provides a holistic perspective on this phenomenon and draws attention to aspects of the experience previously underappreciated. Published 2014. This article is a U.S. Government work and is in the public domain in the USA. Published 2014. This article is a U.S. Government work and is in the public domain in the USA.

Entities:  

Keywords:  chronic illness; family caregiving; integrative review; liminality; qualitative; rite of passage

Mesh:

Year:  2014        PMID: 25176315      PMCID: PMC4180249          DOI: 10.1002/nur.21622

Source DB:  PubMed          Journal:  Res Nurs Health        ISSN: 0160-6891            Impact factor:   2.228


  51 in total

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Review 2.  Liminality as a framework for understanding the experience of cancer survivorship: a literature review.

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3.  The influence of orphan care and other household shocks on health status over time: a longitudinal study of children's caregivers in rural Malawi.

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4.  Carer experiences of life after stroke - a qualitative analysis.

Authors:  Cathy Bulley; Jane Shiels; Katie Wilkie; Lisa Salisbury
Journal:  Disabil Rehabil       Date:  2010       Impact factor: 3.033

5.  The concept of self in the context of crisis: a study of families of the severely brain-injured.

Authors:  C B Mwaria
Journal:  Soc Sci Med       Date:  1990       Impact factor: 4.634

6.  Quality of life in spite of an unpredictable future: the next of kin of patients with multiple sclerosis.

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Journal:  J Neurosci Nurs       Date:  2010-12       Impact factor: 1.230

7.  Uncertainty and alternate level of care: a narrative study of the older patient and family caregiver experience.

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8.  Transition as experienced by close relatives of people with traumatic brain injury.

Authors:  Åsa Engström; Siv Söderberg
Journal:  J Neurosci Nurs       Date:  2011-10       Impact factor: 1.230

9.  Ambiguity and uncertainty: the ongoing concerns of male partners of women treated for breast cancer.

Authors:  Alison Harrow; Mary Wells; Rosaline S Barbour; Stuart Cable
Journal:  Eur J Oncol Nurs       Date:  2008-06-10       Impact factor: 2.398

10.  Caring for heart transplant recipients: The lived experience of primary caregivers.

Authors:  Maria Lúcia Araújo Sadala; Noedir Groppo Stolf; Edimar A Bocchi; Maria Aparecida Viggiani Bicudo
Journal:  Heart Lung       Date:  2012-10-22       Impact factor: 2.210

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  10 in total

1.  Enhancing the cancer caregiving experience: Building resilience through role adjustment and mutuality.

Authors:  Susanne W Gibbons; Alyson Ross; Leslie Wehrlen; Stephen Klagholz; Margaret Bevans
Journal:  Eur J Oncol Nurs       Date:  2019-09-10       Impact factor: 2.398

2.  A National Profile Of End-Of-Life Caregiving In The United States.

Authors:  Katherine A Ornstein; Amy S Kelley; Evan Bollens-Lund; Jennifer L Wolff
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3.  Family Caregiving and Place of Death: Insights From Cross-national Analysis of the Harmonized End-of-Life Data.

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4.  Factors influencing loneliness in cancer caregivers: A longitudinal study.

Authors:  Alyson Ross; Avery Perez; Leslie Wehrlen; Lena J Lee; Li Yang; Robert Cox; Margaret Bevans; Alice Ding; Lori Wiener; Gwenyth R Wallen
Journal:  Psychooncology       Date:  2020-09-18       Impact factor: 3.955

5.  Cardiometabolic risk factors and health behaviors in family caregivers.

Authors:  Alyson Ross; Robert Shamburek; Leslie Wehrlen; Stephen D Klagholz; Li Yang; Elyssa Stoops; Sharon L Flynn; Alan T Remaley; Karel Pacak; Nonniekaye Shelburne; Margaret F Bevans
Journal:  PLoS One       Date:  2017-05-04       Impact factor: 3.240

6.  The Caregiving Experiences of Fathers and Mothers of Children With Rare Diseases in Italy: Challenges and Social Support Perceptions.

Authors:  Paola Cardinali; Laura Migliorini; Nadia Rania
Journal:  Front Psychol       Date:  2019-08-05

7.  [The first moments of the carer: The process of becoming a caregiver of a dependent elderly relative].

Authors:  Lourdes Moral-Fernández; Antonio Frías-Osuna; Sara Moreno-Cámara; Pedro A Palomino-Moral; Rafael Del-Pino-Casado
Journal:  Aten Primaria       Date:  2017-07-21       Impact factor: 1.137

8.  " … I felt completely stranded": liminality and recognition of personhood in the experiences of suicidal women admitted to psychiatric hospital.

Authors:  Julia Hagen; Birthe Loa Knizek; Heidi Hjelmeland
Journal:  Int J Qual Stud Health Well-being       Date:  2020-12

9.  The start of caring for an elderly dependent family member: a qualitative metasynthesis.

Authors:  Lourdes Moral-Fernández; Antonio Frías-Osuna; Sara Moreno-Cámara; Pedro A Palomino-Moral; Rafael Del-Pino-Casado
Journal:  BMC Geriatr       Date:  2018-09-25       Impact factor: 3.921

10.  Experiences of family caregivers of patients with COVID-19.

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  10 in total

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