Literature DB >> 21131618

Patients-in-waiting: Living between sickness and health in the genomics era.

Stefan Timmermans1, Mara Buchbinder.   

Abstract

What are the social consequences of the recent expansion of newborn screening in the United States? The adoption of new screening technologies has generated diagnostic uncertainty about the nature of screening targets, making it unclear not only whether a newborn will develop a disease but also what the condition actually is. Based on observations in a genetics clinic and in-depth interviews with parents and geneticists, we examine how parents and clinical staff work out the social significance of uncertain newborn screening results. We find that some newborns will experience a specific trajectory of prolonged liminality between a state of normal health and pathology. Based on a review of related literatures, we suggest "patients-in-waiting" as an umbrella concept for those under medical surveillance between health and disease.

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Year:  2010        PMID: 21131618     DOI: 10.1177/0022146510386794

Source DB:  PubMed          Journal:  J Health Soc Behav        ISSN: 0022-1465


  69 in total

1.  Qualitative Research on Expanded Prenatal and Newborn Screening: Robust but Marginalized.

Authors:  Rachel Grob
Journal:  Hastings Cent Rep       Date:  2019-05       Impact factor: 2.683

2.  Parsing the peanut panic: the social life of a contested food allergy epidemic.

Authors:  Miranda R Waggoner
Journal:  Soc Sci Med       Date:  2013-05-06       Impact factor: 4.634

3.  Parents' decisions to screen newborns for FMR1 gene expansions in a pilot research project.

Authors:  Debra Skinner; Summer Choudhury; John Sideris; Sonia Guarda; Allen Buansi; Myra Roche; Cynthia Powell; Donald B Bailey
Journal:  Pediatrics       Date:  2011-05-29       Impact factor: 7.124

Review 4.  Genetic screening.

Authors:  Wylie Burke; Beth Tarini; Nancy A Press; James P Evans
Journal:  Epidemiol Rev       Date:  2011-06-27       Impact factor: 6.222

5.  Genetic counselling for personalised medicine.

Authors:  Angus Clarke; Katie Thirlaway
Journal:  Hum Genet       Date:  2011-04-20       Impact factor: 4.132

6.  What's at stake? Genetic information from the perspective of people with epilepsy and their family members.

Authors:  Sara Shostak; Dana Zarhin; Ruth Ottman
Journal:  Soc Sci Med       Date:  2011-07-23       Impact factor: 4.634

7.  The Fracture of Relational Space in Depression: Predicaments in Primary Care Help Seeking.

Authors:  Elizabeth Bromley; David Kennedy; Jeanne Miranda; Cathy Donald Sherbourne; Kenneth B Wells
Journal:  Curr Anthropol       Date:  2016-08-15

8.  The fiduciary relationship model for managing clinical genomic "incidental" findings.

Authors:  Gabriel Lázaro-Muñoz
Journal:  J Law Med Ethics       Date:  2014       Impact factor: 1.718

Review 9.  Newborn Screening for Lysosomal Storage Disorders.

Authors:  Roy W A Peake; Olaf A Bodamer
Journal:  J Pediatr Genet       Date:  2016-12-02

10.  Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling.

Authors:  R Z Hayeems; R Babul-Hirji; N Hoang; R Weksberg; C Shuman
Journal:  J Genet Couns       Date:  2015-08-12       Impact factor: 2.537

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