Hypovitaminosis D in chronically ill children in Greece and its management

2013 ◽  
Author(s):  
Tsiamasfirou Damiani ◽  
Tsakiropoulos Charalambos ◽  
Vassilakis Alexandros ◽  
Paspati Ioanna
Keyword(s):  
Hypovitaminosis D ◽  
Chronically Ill ◽  
Chronically Ill Children

Neglect of Chronically Ill Children

1986 ◽  
Vol 140 (7) ◽  
pp. 655 ◽  
Author(s):  
Paula Kienberger Jaudes
Keyword(s):  
Chronically Ill ◽  
Chronically Ill Children

Children and schools: The special issues of chronically Ill children

1984 ◽  
Vol 61 (2) ◽  
pp. 10-15
Author(s):  
James M. Perrin ◽  
Henry T. Ireys ◽  
May W. Shayne ◽  
Linda Christie Oynihan
Keyword(s):  
Chronically Ill ◽  
Chronically Ill Children

Il vissuto di bambini e adolescenti con artrite idiopatica giovanile

2020 ◽  
Vol 39 (10) ◽  
pp. 638-641
Author(s):  
Lorenzoiara Mambelli ◽  
Agnese Menghi ◽  
Camilla Lama ◽  
Federico Marchetti
Keyword(s):  
Juvenile Idiopathic Arthritis ◽  
Chronically Ill ◽  
Behavioural Problems ◽  
Psychological Care ◽  
Voluntary Withdrawal ◽  
Increased Risk ◽  
Rheumatology Unit ◽  
Chronically Ill Children ◽  
Important Drug

Chronically ill children show an increased risk of developing a psychological-psychiatric disorder, with an important impact on their quality of life. The paper describes all the cases of Juvenile Idiopathic Arthritis (JIA) in the Paediatric Rheumatology Unit in Ravenna with documented psychological-behavioural problems. 23% of juvenile idiopathic arthritis patients have psychological-behavioural problems and 9% have requested cognitivebehavioural therapy, with good results. One of the most significant aspects is the treatment with methotrexate (MTX), which is an important drug in the management of JIA cases and, as it is known, is burdened with side effects such as malaise and vomiting, even before its intake. Half of the patients on MTX therapy show this "intolerance", which sometimes also leads to the voluntary withdrawal of the drug. Therefore, an anticipatory approach to these issues and an adequate and timely psychological care are increasingly necessary.

Mental Disorders in Chronically Ill Children: Parent-Child Discrepancy and Physician Identification

PEDIATRICS ◽  
1992 ◽  
Vol 90 (5) ◽  
pp. 692-696
Author(s):  
Emily Harris Canning ◽  
Suzanne B. Hanser ◽  
Kathryn A. Shade ◽  
W. Thomas Boyce
Keyword(s):  
Mental Disorders ◽  
Psychiatric Disorders ◽  
Mental Health Problems ◽  
Chronically Ill ◽  
Diagnostic Interview ◽  
Child Reports ◽  
Children And Parents ◽  
Child Psychiatric ◽  
Chronically Ill Children ◽  
Threshold Criteria

Mental disorders affect 18% to 20% of children and adolescents. The rate in children with chronic illness is probably higher. This study of chronically ill children addresses the discrepancy between parent and child reports of child psychiatric disorders and the extent to which pediatricians agree with reports by children and parents regarding such problems. Eighty-three subjects, aged 9 to 18 (mean = 12.6), were recruited; they had the following diagnoses: cystic fibrosis, diabetes, inflammatory bowel disease, and cancer. Subjects and one parent were interviewed separately, using the Diagnostic Interview Schedule for Children (DISC-2.1). The subject's physician completed a questionnaire asking about the presence of a range of mental disorders. Forty-one (49%) subjects reached threshold criteria for a psychiatric diagnosis, using both parent and child as informants. Psychiatric disorders were identified in only 22 subjects (54%) by the child and in 28 (68%) by parent alone. Thus, reliance on one informant resulted in failure to identify one third to one half of psychiatric disorders. Physicians' ratings agreed significantly with children's reports but not with parental reports, suggesting that physicians are sensitive to children's concerns but may underestimate the value and importance of parents' reports. Clinical and research evaluations of chronically ill children, as well as clinician identification of mental health problems, will be influenced by the choice of informant.

scholarly journals « Avoir un enfant différent dans un pays où on est différent ». Une étude des familles immigrées en Norvège

2017 ◽  
Author(s):  
Elena Albertini Früh ◽  
Zineb Rachedi ◽  
Hilde Lidén
Keyword(s):  
Labour Market ◽  
Present Article ◽  
Sickness Absence ◽  
Ethnic Differences ◽  
Research Council ◽  
Chronically Ill ◽  
Maladie Chronique ◽  
Labour Market Participation ◽  
Chronically Ill Children ◽  
Health And Sickness

Cadre de la recherche : En Norvège, vivre avec un enfant ayant des problèmes de santé est une réalité pour de nombreux parents et demande une adaptation de toute la famille ; cela peut être d’autant plus problématique pour des parents issus de l’immigration. Objectifs : Le présent article vise à comprendre comment les familles issues de différents types d’immigration gèrent le suivi de l’enfant ayant des besoins spécifiques. Méthodologie : Les données sont issues d’une recherche qualitative basée sur vingt-sept entretiens individuels semi-directifs et trois entretiens de groupe avec des parents immigrés ou issus de l’immigration. L’analyse inductive se fonde sur l’analyse de contenu des entretiens. Résultats : Vivre avec un enfant ayant des besoins spécifiques exige une redéfinition de l’investissement et des rôles de chacun des parents. On note, en effet, des stratégies conjugales et parentales qui prennent forme dans un rapport de genre marqué à la fois par des pratiques de changement et de reproduction. Pour les familles immigrées ayant un enfant aux besoins spécifiques, la question du travail aussi bien pour les hommes que pour les femmes est centrale tant elle montre la nécessité des bricolages, à la fois pour l’adaptation au mode de vie du pays d’accueil et pour sortir de « la famille soignante », où l’enfant est au centre des préoccupations. Conclusion : Les relations sociales (notamment par le travail ou par le maintien d’un réseau d’amis ou de la famille élargie) ainsi que le soutien apporté par les services médicosociaux restent des ressources précieuses pour faire face aux défis qu’entraînent le handicap ou la maladie chronique de l’enfant. Contributions: L’étude, réalisée en collaboration avec Lisbeth Gravdal Kvarme, est financée par The Research Council of Norway, dans le cadre du projet « Ethnic differences in labour market participation, health and sickness absence among parents caring for disabled or chronically ill children » ( n o 227022/H20).

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