Pediatric patients and their quality of life
Annals of General Psychiatry
Poster presentation Pediatric patients and their quality of life Alexandra Michopoulou*, Angeliki Nikolaou, Vasiliki Goula, Athina Iliadou, Kalliopi Voikli, Dimitrios Giannios, Georgios Stefanou and Stavroula- Maria Papatheodorou
Address: Penteli's Children Hospital
Greece
Corresponding author
References 1. Eiser C, Morse R: A review of measures of quality of life for children with chronic illness. Archives of disease in childhood 2001, 84:205-211. 2. Ravens-Sieberer U, Bullinger M: Assessing health-related quality of life in chronically ill children with the German KINDL: first psychometric and content analytical results. Quality of life 1998, 7:399-407. 3. Eiser C: Children's quality of life measures. Archives of disease in childhood 1997, 37:359-354.
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from International Society on Brain and Behaviour: 2nd International Congress on Brain and Behaviour
Thessaloniki, Greece. 1720 November 2005
Background
This study aims to compare quality of life between healthy
and ill children (distinction between chronic and
nonchronic illness). Five domains of quality of life were
evaluated: somatic, psychological, social, family and school
life. Hypothesis was that healthy children had better
quality of life than the other two groups of ill children and
especially hospitalized and chronically ill children.
Materials and methods
The sample consisted of 201 children, aged 6 to 14 years
old. 53,5% were boys and 46,5% were girls. The children
were categorized into three target groups: a) control group
(95 children), b) outpatient group (74 children) and c)
inpatient group (32 children). 54 children of the total
sample had a chronic disease. Actually, the ill children
consulted the following departments: 6,7% Dermatology,
37,5% Psychology and Development departments, 7,7%
Endokrinology, 12,5% Allergiology, 25% Pediatric and
10,6% Surgery department. Children were given a
questionnaire of quality of life constructed by our Department,
based on Kid-KINDL questionnaire for children,
translated and standardized by Vidalis A and Vidali LE.
Results
Hypothesis was confirmed that the control group had a
better quality of life than the ill children (outpatient and
inpatient group). Especially, the somatic and school life
domains were affected more negatively for the
hospitalized children. The chronicity of the disease is an
important factor for the aggravation of the children's difficulties
and especially of their school life. It also affects their
selfconcept. The sex of the child was proved to be an
important factor. Girls were generally more affected, especially
(statistically significant results) on the somatic and
psycho-emotional domain. The age group, to which the
children belonged, was also important for their school life
(school difficulties, concentration, school performance).
Adolescents were found to present lower self-esteem than
the children, so that their contact with friends was less
frequent.
Discussion
Hospitalization is experienced as a traumatic period of the
children's life, so that their main wish is to be healthy and
capable of physical activities. The long duration of the
illness makes them believe that they are different and
inferior than the other children. As a result, feelings of fear
and aggressiveness appear, so that the contact with other
children becomes difficult. As a consequence of this lack
of contact, children choose friends and relationships as
the most important factors for a better quality of life.
(...truncated)