Literature DB >> 25277096

"Is it going to hurt?": the impact of the diagnostic odyssey on children and their families.

Nikkola Carmichael1, Judith Tsipis, Gail Windmueller, Leslie Mandel, Elicia Estrella.   

Abstract

The pediatric diagnostic odyssey is a period of uncertainty and emotional turmoil for families, often characterized by multiple minor medical procedures (such as venipuncture) that children may find distressing. Interventions to reduce distress are rarely offered, despite evidence that this is crucial both for avoiding anticipatory anxiety before future procedures and for improving healthcare compliance in adulthood. We interviewed ten mothers of children with neuromuscular disorders, asking about their perceptions of their child's experiences with different medical procedures, the emotional impact of the diagnostic odyssey, implications of obtaining a diagnosis, and interactions with healthcare providers. We coded interviews in ATLAS.ti (version 7.0) based on a priori and emergent themes, and analyzed them based on the principles of interpretive description. We found that predicting and assessing children's reactions to procedures is challenging; parents reported non-invasive procedures such as x-rays were distressing for some children, and that providers did not detect subtle indicators of distress. Parents valued obtaining a diagnosis because it validated their concerns, enabled planning for the child's future healthcare needs, and allowed access to established support networks. This study suggests that healthcare providers can improve the experience of the diagnostic odyssey by validating family concerns and connecting them to support services that are available without a diagnosis.

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Mesh:

Year:  2014        PMID: 25277096     DOI: 10.1007/s10897-014-9773-9

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  31 in total

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10.  Parental perceived value of a diagnosis for intellectual disability (ID): a qualitative comparison of families with and without a diagnosis for their child's ID.

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  32 in total

1.  Factors Associated with Parental Adaptation to Children with an Undiagnosed Medical Condition.

Authors:  Tatiane Yanes; Linda Humphreys; Aideen McInerney-Leo; Barbara Biesecker
Journal:  J Genet Couns       Date:  2016-12-30       Impact factor: 2.537

2.  Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing?

Authors:  Allyn McConkie-Rosell; Stephen R Hooper; Loren D M Pena; Kelly Schoch; Rebecca C Spillmann; Yong-Hui Jiang; Heidi Cope; Christina Palmer; Vandana Shashi
Journal:  J Genet Couns       Date:  2018-01-02       Impact factor: 2.537

3.  'We Should View Him as an Individual': The Role of the Child's Future Autonomy in Shared Decision-Making About Unsolicited Findings in Pediatric Exome Sequencing.

Authors:  W Dondorp; I Bolt; A Tibben; G De Wert; M Van Summeren
Journal:  Health Care Anal       Date:  2021-01-02

4.  Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency.

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Journal:  J Clin Immunol       Date:  2017-05-24       Impact factor: 8.317

5.  Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era.

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Journal:  J Genet Couns       Date:  2019-01-24       Impact factor: 2.537

6.  A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network.

Authors:  Chloe M Reuter; Elise Brimble; Colette DeFilippo; Annika M Dries; Gregory M Enns; Euan A Ashley; Jonathan A Bernstein; Paul Graham Fisher; Matthew T Wheeler
Journal:  J Pediatr       Date:  2018-01-11       Impact factor: 4.406

Review 7.  Integrative omics for health and disease.

Authors:  Konrad J Karczewski; Michael P Snyder
Journal:  Nat Rev Genet       Date:  2018-02-26       Impact factor: 53.242

8.  Effective provider-patient communication of a rare disease diagnosis: A qualitative study of people diagnosed with schwannomatosis.

Authors:  Vanessa L Merker; Scott R Plotkin; Martin P Charns; Mark Meterko; Justin T Jordan; A Rani Elwy
Journal:  Patient Educ Couns       Date:  2020-09-28

9.  Diagnosing newborns with suspected mitochondrial disorders: an economic evaluation comparing early exome sequencing to current typical care.

Authors:  Samuel A Crawford; Cynthia L Gong; Leah Yieh; Linda M Randolph; Joel W Hay
Journal:  Genet Med       Date:  2021-05-26       Impact factor: 8.822

10.  Principles of Genomic Newborn Screening Programs: A Systematic Review.

Authors:  Lilian Downie; Jane Halliday; Sharon Lewis; David J Amor
Journal:  JAMA Netw Open       Date:  2021-07-01
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