Literature DB >> 22261754

A qualitative secondary evaluation of statewide follow-up interviews for abnormal newborn screening results for cystic fibrosis and sickle cell hemoglobinopathy.

Alison La Pean1, Jenelle L Collins, Stephanie A Christopher, Kerry L Eskra, Sara J Roedl, Audrey Tluczek, Michael H Farrell.   

Abstract

PURPOSE: The purpose of this qualitative analysis was to assess parental acceptability of large-scale, telephone follow-up regarding their infants' newborn screening (NBS) results, indicating carrier status for sickle cell hemoglobinopathy (SCH) and cystic fibrosis (CF).
METHODS: Analysis of 195 interview transcripts focused on parents' responses to two open-ended questions: "What was your reaction to being called by me?" and "What do you think of the state NBS program having follow-up people calling parents like you?" Responses were coded using conventional content analysis procedures, and nonparametric tests were performed to analyze quantitative data.
RESULTS: Most parents reported favorable opinions about the follow-up. Favorable opinions were associated with several emotional reactions to receiving follow-up (P <0.001) and three reasons why parents found the interview beneficial (P < 0.05): it provided information, clarified NBS results, and answered questions. Seventeen parents of SCH carriers reportedly had not been told their infant's NBS results and received them for the first time during the follow-up interview.
CONCLUSION: Parents of CF and SCH carrier infants had favorable opinions and identified specific benefits to receiving follow-up contact. This analysis demonstrates an information deficit among carrier parents and illustrates the importance of NBS follow-up and need for comprehensive communication and counseling.

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Year:  2012        PMID: 22261754      PMCID: PMC3246552          DOI: 10.1038/gim.0b013e31822dd7b8

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  24 in total

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Journal:  Am J Med       Date:  2009-04-24       Impact factor: 4.965

2.  Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop report.

Authors:  Anne Marie Comeau; Frank J Accurso; Terry B White; Preston W Campbell; Gary Hoffman; Richard B Parad; Benjamin S Wilfond; Margaret Rosenfeld; Marci K Sontag; John Massie; Philip M Farrell; Brian P O'Sullivan
Journal:  Pediatrics       Date:  2007-02       Impact factor: 7.124

Review 3.  An overview of international literature from cystic fibrosis registries 2. Neonatal screening and nutrition/growth.

Authors:  Donatello Salvatore; Roberto Buzzetti; Ermanno Baldo; Maria Pia Forneris; Vincenzina Lucidi; Daniela Manunza; Italo Marinelli; Barbara Messore; Anna Silvia Neri; Valeria Raia; Maria Lucia Furnari; Gianni Mastella
Journal:  J Cyst Fibros       Date:  2009-12-02       Impact factor: 5.482

4.  Newborn screening for Duchenne muscular dystrophy: a psychosocial study.

Authors:  E P Parsons; A J Clarke; K Hood; E Lycett; D M Bradley
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2002-03       Impact factor: 5.747

5.  Factors that influence parents' experiences with results disclosure after newborn screening identifies genetic carrier status for cystic fibrosis or sickle cell hemoglobinopathy.

Authors:  Jenelle L Collins; Alison La Pean; Faith O'Tool; Kerry L Eskra; Sara J Roedl; Audrey Tluczek; Michael H Farrell
Journal:  Patient Educ Couns       Date:  2012-01-11

6.  Qualitative content analysis: a guide to paths not taken.

Authors:  D L Morgan
Journal:  Qual Health Res       Date:  1993-02

7.  Psychosocial risk associated with newborn screening for cystic fibrosis: parents' experience while awaiting the sweat-test appointment.

Authors:  Audrey Tluczek; Rebecca L Koscik; Philip M Farrell; Michael J Rock
Journal:  Pediatrics       Date:  2005-06       Impact factor: 7.124

8.  Comparison of the clinical manifestations of cystic fibrosis in black and white patients.

Authors:  A Hamosh; S C FitzSimmons; M Macek; M R Knowles; B J Rosenstein; G R Cutting
Journal:  J Pediatr       Date:  1998-02       Impact factor: 4.406

9.  Long-term evaluation of genetic counseling following false-positive newborn screen for cystic fibrosis.

Authors:  Laura Cavanagh; Cecilia J Compton; Audrey Tluczek; Roger L Brown; Philip M Farrell
Journal:  J Genet Couns       Date:  2010-02-04       Impact factor: 2.537

10.  Evaluation of a state-wide neonatal screening programme.

Authors:  E F Robertson; G N Hill; A C Pollard
Journal:  Med J Aust       Date:  1979-05-05       Impact factor: 7.738

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  6 in total

1.  Adherence to Quality of Care Indicators and Location of Sickle Cell Care Within Indiana.

Authors:  Emily Riehm Meier; Isaac A Janson; Kisha Hampton; Ellen Bloom; Natalie Duncan; Chris Roberson; Angeli Rampersad
Journal:  J Community Health       Date:  2020-02

2.  Effort required to contact primary care providers after newborn screening identifies sickle cell trait.

Authors:  Stephanie A Christopher; Jenelle L Collins; Michael H Farrell
Journal:  J Natl Med Assoc       Date:  2012 Nov-Dec       Impact factor: 1.798

3.  Improving the quality of physician communication with rapid-throughput analysis and report cards.

Authors:  Michael H Farrell; Stephanie A Christopher; Alison La Pean Kirschner; Sara J Roedl; Faith O O'Tool; Nadia Y Ahmad; Philip M Farrell
Journal:  Patient Educ Couns       Date:  2014-08-28

4.  Frequency of high-quality communication behaviors used by primary care providers of heterozygous infants after newborn screening.

Authors:  Michael H Farrell; Stephanie A Christopher
Journal:  Patient Educ Couns       Date:  2012-11-26

5.  Benefit of Report Card Feedback After Point-of-Care Assessment of Communication Quality Indicators.

Authors:  Michael H Farrell; Clair R Sprenger; Shelbie L Sullivan; Bree A Trisler; Jessica J F Kram; Erin K Ruppel
Journal:  J Patient Cent Res Rev       Date:  2017-01-31

6.  Type 2 Diabetes Education and Support in a Virtual Environment: A Secondary Analysis of Synchronously Exchanged Social Interaction and Support.

Authors:  Allison A Lewinski; Ruth A Anderson; Allison A Vorderstrasse; Edwin B Fisher; Wei Pan; Constance M Johnson
Journal:  J Med Internet Res       Date:  2018-02-21       Impact factor: 5.428

  6 in total

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