Literature DB >> 16924639

Posttraumatic stress disorder in children affected by sickle-cell disease and their parents.

Michel Hofmann1, Mariane de Montalembert, Bérengère Beauquier-Maccotta, Philippe de Villartay, Bernard Golse.   

Abstract

Children affected with sickle-cell disease experience painful crises that may be life threatening, or felt as if they were. We evaluated by semistructured interviews and questionnaires the presence of posttraumatic stress disorder in 11 children affected by sickle-cell disease and having suffered at least one hospitalization for a painful crisis, and in their parents (10 mothers, 1 father). Three children (27%) and four parents (40%) were diagnosed with the disorder. It was not correlated to the disease severity but, in parents, to a feeling of powerlessness over the child's illness (P = 0.04). (c) 2006 Wiley-Liss, Inc.

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Year:  2007        PMID: 16924639     DOI: 10.1002/ajh.20722

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  8 in total

1.  The Cellie Coping Kit for Sickle Cell Disease: Initial acceptability and feasibility.

Authors:  Meghan L Marsac; Olivia G Klingbeil; Aimee K Hildenbrand; Melissa A Alderfer; Nancy Kassam-Adams; Kim Smith-Whitley; Lamia P Barakat
Journal:  Clin Pract Pediatr Psychol       Date:  2014-12-01

2.  Sickle cell disease: primum non nocere (first do no harm).

Authors:  Mariane de Montalembert; Irene Roberts
Journal:  Haematologica       Date:  2010-01       Impact factor: 9.941

3.  A pilot study comparing traumatic stress symptoms by child and parent report across pediatric chronic illness groups.

Authors:  Lisa M Ingerski; Kimberly Shaw; Wendy N Gray; David M Janicke
Journal:  J Dev Behav Pediatr       Date:  2010 Nov-Dec       Impact factor: 2.225

4.  Sickle cell disease: a comprehensive program of care from birth.

Authors:  Mariane de Montalembert; Léon Tshilolo; Slimane Allali
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

5.  Understanding the social networks of parents of children with sickle cell disease.

Authors:  Lisa M Vaughn; Daniel McLinden; Farrah Jacquez; Lori Crosby; Shalonda Slater; Monica Mitchell
Journal:  J Health Care Poor Underserved       Date:  2011-08

6.  Coping and coping assistance among children with sickle cell disease and their parents.

Authors:  Aimee K Hildenbrand; Lamia P Barakat; Melissa A Alderfer; Meghan L Marsac
Journal:  J Pediatr Hematol Oncol       Date:  2015-01       Impact factor: 1.289

7.  Bright IDEAS problem-solving skills training for caregivers of children with sickle cell disease: A two-site pilot feasibility trial.

Authors:  Melissa Young; Megan Voll; Robert B Noll; Diane L Fairclough; Cate Flanagan-Priore
Journal:  Pediatr Blood Cancer       Date:  2020-12-23       Impact factor: 3.167

8.  Quality of life among caregivers of sickle cell disease patients: a cross sectional study.

Authors:  Badr M Madani; Rajaa Al Raddadi; Soad Al Jaouni; Mohab Omer; Marie-Isabelle Al Awa
Journal:  Health Qual Life Outcomes       Date:  2018-09-10       Impact factor: 3.186

  8 in total

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