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Psychosocial aspects of sickle cell disease (SCD) in childhood and adolescence: A review
Author(s) -
Midence Kenny,
Fuggle Peter,
Davies Sally C.
Publication year - 1993
Publication title -
british journal of clinical psychology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.479
H-Index - 92
eISSN - 2044-8260
pISSN - 0144-6657
DOI - 10.1111/j.2044-8260.1993.tb01057.x
Subject(s) - psychosocial , psychology , disease , coping (psychology) , personality , socioeconomic status , social support , interpersonal relationship , developmental psychology , interpersonal communication , clinical psychology , psychiatry , medicine , psychotherapist , population , social psychology , environmental health , pathology
This paper reviews the literature on the psychological and social aspects of Sickle Cell Disease (SCD) and discusses the clinical implications of its impact on children and their families. Sickle Cell Disease is a family of blood diseases including sickle cell anaemia (SS), SC disease (SC), and sickle B thalassaemia (SBThal). Research on the psychological and social aspects of SCD, particularly in the UK, has been limited and of varying methodological quality. The psychosocial adaptation of children and adolescents with SCD and their families has been associated with the personality and developmental stage of the child, family attitudes and behaviour, socioeconomic status, and social and environmental support. Concerns about the quality of interpersonal relationships within families have also led to investigations of family characteristics and social networks, and some research studies have pointed to different ways of coping associated with specific network and family structures.