2017
DOI: 10.1037/rep0000158
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The Kennedy Krieger Independence Scales-Sickle Cell Disease: Executive components of transition readiness.

Abstract: Results provide preliminary support for the KKIS-SCD as a reliable and valid tool for the assessment of executive components of self-care management skills for youth with SCD. Identifying specific weaknesses in executive function related to self-care management skills might assist in guiding intervention and individualizing transition planning in these at-risk youth. (PsycINFO Database Record

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Cited by 9 publications
(4 citation statements)
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“…Alternatively, it is possible that parents of medically complex children are more likely to overlook or underreport symptoms. Research with other medical populations (i.e., sickle cell disease, traumatic brain injury) has shown that parent ratings are often not as elevated as would be expected based on performance‐based measures 39–41 . Within the neuro‐oncology population, this may be due to a number of factors.…”
Section: Discussionmentioning
confidence: 97%
See 1 more Smart Citation
“…Alternatively, it is possible that parents of medically complex children are more likely to overlook or underreport symptoms. Research with other medical populations (i.e., sickle cell disease, traumatic brain injury) has shown that parent ratings are often not as elevated as would be expected based on performance‐based measures 39–41 . Within the neuro‐oncology population, this may be due to a number of factors.…”
Section: Discussionmentioning
confidence: 97%
“…Research with other medical populations (i.e., sickle cell disease, traumatic brain injury) has shown that parent ratings are often not as elevated as would be expected based on performance-based measures. [39][40][41] Within the neuro-oncology population, this may be due to a number of factors.…”
Section: Discussionmentioning
confidence: 99%
“…There are several manuscripts that target assessment and understanding of transition issues. Four manuscripts explore the topic of transition planning and the importance of managing key developmental transition points for individuals with congenital or acquired childhood disabilities (Jones, Jacobson, & Tarezi, 2017; Sung & Connor, 2017; Warschausky, Kaufman, Evitts, Schutt, & Hurvitz, 2017a, 2017b). Jones and colleagues utilize an existing measure for exploring adaptive behavior and transition readiness for individuals with spina bifida and explore the use of this measure in individuals with sickle cell disease.…”
Section: Pediatric Rehabilitation Psychology—research In Contextmentioning
confidence: 99%
“…Já no ambiente escolar, estão sujeitos a ausências constantes, constrangimentos devido a sintomas como incontinência urinária e icterícia, crises álgicas, incapacidade de participar de determinadas atividades esportivas, distúrbios sociais e emocionais (8)(9)(10)(11) . Na adolescência, diante das diversas mudanças psicológicas e somáticas, características do processo de crescimento, reagem melhor aos sintomas da DF, pois realizam atividades para melhorar sua saúde e bem-estar e costumam seguir as orientações médicas específicas (12,13) . É importante que os familiares busquem compreender a patologia e as corretas orientações de saúde, com vista a minimizar a dor e reduzir os riscos de internações hospitalares secundárias, pois a periodicidade de crises acontece constantemente ao decorrer da vida, com intensidade variável.…”
Section: Introductionunclassified