Literature DB >> 8584378

Parents' recollection of the initial communication of the diagnosis of cystic fibrosis.

I Jedlicka-Köhler1, M Götz, I Eichler.   

Abstract

BACKGROUND: The diagnosis of a chronic disease in children challenges parents' emotional coping abilities and cognitive capacities.
OBJECTIVE: To study parents' emotional and cognitive reactions to the diagnosis of cystic fibrosis (CF) in their children.
METHODS: Postal survey by means of a written questionnaire. PARTICIPANTS: Forty-six parents of 29 children with a median age of 2 months at diagnosis.
RESULTS: Most parents initially lacked knowledge of CF (76%) and were provided only oral information (96%). Parental estimates of how much of the information given they had understood and retained were 77% and 76%, respectively, with 15 parents (33%) having understood and remembered less than 50% of what the physicians had told them. The most frequent stressing feelings were fear (83%) and despair (56%). Fifty-four percent of parents had initial shocklike reactions. In this group, a significant decrease in the understanding and recall of information was noted compared with parents who had less-emotional responses.
CONCLUSIONS: Parents learning the diagnosis are, in effect, receiving a kind of lecture, which contains more information than they can possibly assimilate. Because of the incompatibility of emotional distress and optimum learning, impairment of early comprehension and retention of information about CF is unavoidable. Repeated interviews with both parents and the provision of written and audiovisual materials should be mandatory.

Entities:  

Mesh:

Year:  1996        PMID: 8584378

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  17 in total

1.  Parental information seeking following a positive newborn screening for cystic fibrosis.

Authors:  James Price Dillard; Lijiang Shen; Jeffrey D Robinson; Phillip M Farrell
Journal:  J Health Commun       Date:  2010-12

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Authors:  L Aite; A Zaccara; A Trucchi; A Nahom; B Iacobelli; P Bagolan
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3.  Psychosocial Distress and Knowledge Deficiencies in Parents of Children in Ireland Who Carry an Altered Cystic Fibrosis Gene.

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4.  Absorbing information about a child's incurable cancer.

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5.  A tailored approach to family-centered genetic counseling for cystic fibrosis newborn screening: the Wisconsin model.

Authors:  Audrey Tluczek; Christina Zaleski; Dania Stachiw-Hietpas; Peggy Modaff; Craig R Adamski; Megan R Nelson; Catherine A Reiser; Sumedha Ghate; Kevin D Josephson
Journal:  J Genet Couns       Date:  2010-10-09       Impact factor: 2.537

6.  Cause of Death of Infants and Children in the Intensive Care Unit: Parents' Recall vs Chart Review.

Authors:  Dorothy Brooten; JoAnne M Youngblut; Carmen Caicedo; Lynn Seagrave; G Patricia Cantwell; Balagangadhar Totapally
Journal:  Am J Crit Care       Date:  2016-05       Impact factor: 2.228

7.  Implications of resolving the diagnosis of PKU for parents and children.

Authors:  Bruce Lord; Judy Ungerer; Colin Wastell
Journal:  J Pediatr Psychol       Date:  2008-03-13

8.  Informing parents about positive newborn screen results: parents' recommendations.

Authors:  Natalie Salm; Elena Yetter; Audrey Tluczek
Journal:  J Child Health Care       Date:  2012-09-14       Impact factor: 1.979

9.  When the cystic fibrosis label does not fit: a modified uncertainty theory.

Authors:  Audrey Tluczek; Anne Chevalier McKechnie; Patrice A Lynam
Journal:  Qual Health Res       Date:  2010-02

10.  Day One Talk: parent preferences when learning that their child has cancer.

Authors:  Rachel M Kessel; Michael Roth; Karen Moody; Adam Levy
Journal:  Support Care Cancer       Date:  2013-06-13       Impact factor: 3.603

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