Literature DB >> 22305806

'Doing the "right" thing': how parents experience and manage decision-making for children's 'normalising' surgeries.

Pauline Anne Nelson1, Ann-Louise Caress, Anne-Marie Glenny, Susan A Kirk.   

Abstract

Using cleft lip and palate as an exemplar, this article examines parents' decision-making for children in the context of elective treatments which aim to 'normalise' a child's function, appearance, communication or identity. Using purposive and theoretical sampling, 35 parents with children from infancy to young adulthood were recruited through a specialist cleft centre in England. Parents were interviewed in-depth between 2006 and 2008 about their beliefs and motivations in relation to treatment decision-making in this context. A grounded theory approach was used to analyse the data. Findings revealed a core category, 'doing the "right" thing', that encapsulated parents' main concern in relation to their children's treatment and highlighted several emotional, social and cultural considerations underpinning their decision-making stance. Parents fulfilled a perceived 'moral' obligation to be 'good' parents by pursuing the 'normalising' treatments, particularly surgeries, made available to their children. Such treatments were viewed as a way of facilitating their child's social inclusion and helping them reach their full potential. In order to enable their continued pursuit of treatments over the long-term, parents also constructed specialist practitioners as highly competent and particularly trustworthy. This article captures the complexities involved in parents' decision-making for children's elective 'normalising' treatments, where both functional and appearance-related concerns are involved. It suggests that social norms about parenting, physical appearance and healthcare practitioner power may significantly shape decision-making in this context, so that such choices may be viewed primarily as 'moral' rather than social. Services could support parents with such challenges, by gauging their needs for information about surgery and its likely outcomes and providing emotional/decisional support to consider all available options. Copyright Â
© 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22305806     DOI: 10.1016/j.socscimed.2011.11.024

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  13 in total

1.  Subjective need for psychological support (PsySupp) in parents of children and adolescents with disorders of sex development (dsd).

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Journal:  Eur J Pediatr       Date:  2015-04-14       Impact factor: 3.183

2.  Trust in Physicians, Anxiety and Depression, and Decision-Making Preferences among Parents of Children with Serious Illness.

Authors:  Vanessa N Madrigal; Douglas L Hill; Justine Shults; Chris Feudtner
Journal:  J Palliat Med       Date:  2021-09-13       Impact factor: 2.947

Review 3.  Parental experience and decision-making for epilepsy surgery: A systematic review of qualitative and quantitative studies.

Authors:  Debopam Samanta; Megan Leigh Hoyt; M Scott Perry
Journal:  Epilepsy Behav       Date:  2021-08-21       Impact factor: 3.337

4.  Psychosocial well-being of parents of children with oral clefts.

Authors:  N Nidey; L M Moreno Uribe; M M Marazita; G L Wehby
Journal:  Child Care Health Dev       Date:  2015-08-25       Impact factor: 2.508

5.  Parents' decision for helmet therapy in infants with skull deformation.

Authors:  Renske M van Wijk; Janine A van Til; Catharina G M Groothuis-Oudshoorn; Monique P L'Hoir; Magda M Boere-Boonekamp; Maarten J IJzerman
Journal:  Childs Nerv Syst       Date:  2014-03-19       Impact factor: 1.475

6.  Isolation, Uncertainty and Treatment Delays: Parents' Experiences of Having a Baby with Cleft Lip/Palate During the Covid-19 Pandemic.

Authors:  Bruna Costa; Danielle McWilliams; Sabrina Blighe; Nichola Hudson; Matthew Hotton; Marc C Swan; Nicola Marie Stock
Journal:  Cleft Palate Craniofac J       Date:  2021-11-29

7.  Society for Endocrinology UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development (Revised 2015).

Authors:  S Faisal Ahmed; John C Achermann; Wiebke Arlt; Adam Balen; Gerry Conway; Zoe Edwards; Sue Elford; Ieuan A Hughes; Louise Izatt; Nils Krone; Harriet Miles; Stuart O'Toole; Les Perry; Caroline Sanders; Margaret Simmonds; Andrew Watt; Debbie Willis
Journal:  Clin Endocrinol (Oxf)       Date:  2015-08-13       Impact factor: 3.478

8.  Experience of maintaining tooth brushing for children born with a cleft lip and/or palate.

Authors:  Yin-Ling Lin; Karen Davies; Peter Callery
Journal:  BMC Oral Health       Date:  2017-08-24       Impact factor: 2.757

9.  "I smile, but Without Showing My Teeth": The Lived Experience of Cleft, Lip, and Palate in Adults.

Authors:  Asgjerd Litleré Moi; Harald Gjengedal; Kari Lybak; Hallvard Vindenes
Journal:  Cleft Palate Craniofac J       Date:  2020-04-30

10.  Parental Perception of Children Affected by Amelogenesis Imperfecta (AI) and Dentinogenesis Imperfecta (DI): A Qualitative Study.

Authors:  Areej Alqadi; Anne C O'Connell
Journal:  Dent J (Basel)       Date:  2018-11-17
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