Literature DB >> 17533941

Children's behaviour following diagnosis of acute lymphoblastic leukaemia: a qualitative longitudinal study.

Emily Anne Earle1, Christine Eiser.   

Abstract

Survival rates for children with cancer have improved significantly, but lengthy and painful treatments compromise the quality of life of children and their families. The aim of this article is to describe children's behaviour and coping over the 2- or 3-year-course of treatment. We interviewed 32 mothers of children newly diagnosed with Acute Lymphoblastic Leukaemia (ALL) shortly following diagnosis, 1 and 2 years later. Thematic analysis was used to extract themes related to adjustment and behaviour. The results were organized separately for children in three age groups: 0-4 years, 5-9 years and 10-14 years. Mothers described children in the 0-4-year age group as adjusting well, and attributed this to their limited understanding and ability to integrate treatments into normal life. Children in the 5-9-year group were adjusting less well, experiencing social problems and worries about appearance. Older children (10-14 years) adjusted least well. Many withdrew socially and were concerned about the need to look and feel normal. These findings will be useful for parents and clinicians in identifying typical behaviours of children coping with ALL. They also have implications for the development of child-centred age-specific measures of quality of life in children treated for ALL.

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Mesh:

Year:  2007        PMID: 17533941     DOI: 10.1177/1359104507075935

Source DB:  PubMed          Journal:  Clin Child Psychol Psychiatry        ISSN: 1359-1045            Impact factor:   2.544


  7 in total

1.  Psychological morbidity in children undergoing chemotherapy for acute lymphoblastic leukemia.

Authors:  Vineeta Gupta; Aparna Singh; Tej Bali Singh; Shashikala Upadhyay
Journal:  Indian J Pediatr       Date:  2013-08-29       Impact factor: 1.967

2.  Healthcare and psychosocial experiences of individuals with craniofacial microsomia: Patient and caregivers perspectives.

Authors:  Daniela V Luquetti; Michelle R Brajcich; Nicola M Stock; Carrie L Heike; Alexis L Johns
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2018-02-07       Impact factor: 1.675

3.  Parental perceptions of health-related quality of life in children with leukemia in the second week after the diagnosis: a quantitative model.

Authors:  Marta Tremolada; Sabrina Bonichini; Gianmarco Altoè; Marta Pillon; Modesto Carli; Thomas S Weisner
Journal:  Support Care Cancer       Date:  2010-03-13       Impact factor: 3.603

4.  Coping with cancer: a Web-based educational program for early and middle adolescents.

Authors:  Susan O'Conner-Von
Journal:  J Pediatr Oncol Nurs       Date:  2009-05-15       Impact factor: 1.636

5.  The personal experience of parenting a child with juvenile Huntington's disease: perceptions across Europe.

Authors:  Virginia Eatough; Helen Santini; Christine Eiser; Marie-Louise Goller; Wioletta Krysa; 'Annunziata' de Nicola; Matteo Paduanello; Martina Petrollini; Maria Rakowicz; Ferdinando Squitieri; Aad Tibben; Katie Lee Weille; Bernhard Landwehrmeyer; Oliver Quarrell; Jonathan A Smith
Journal:  Eur J Hum Genet       Date:  2013-02-27       Impact factor: 4.246

6.  Quality of Life and Pain Experienced by Children and Adolescents With Cancer at Home Following Discharge From the Hospital.

Authors:  Joana Duran; Lilian Bravo; Vanessa Torres; Alexandra Craig; Jasmine Heidari; Kathleen Adlard; Rita Secola; Renee Granados; Eufemia Jacob
Journal:  J Pediatr Hematol Oncol       Date:  2020-01       Impact factor: 1.170

7.  The psychosocial experience of adolescents with haematological malignancies in Jordan: an interpretive phenomenological analysis study.

Authors:  Omar Al Omari; Dianne Wynaden
Journal:  ScientificWorldJournal       Date:  2014-01-05
  7 in total

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