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1.
Child Care Health Dev ; 46(6): 682-691, 2020 11.
Article in English | MEDLINE | ID: mdl-32681520

ABSTRACT

INTRODUCTION: The input from practitioners in developmental assessment test revision is a crucial and leading component of the project. This paper highlights six key phases of the Griffiths III revision process and the value of having a guiding plan that includes test practitioner input. METHODS: The revision of the Griffiths III consisted of six separate phases that were supported by practitioner and user input and feedback. These six phases and practitioner views ensured that the necessary core constructs and new areas for item development were included in the revised version. These processes also underscored the construct development and task review, item design, piloting and standardization of the revised version, as well as its production, release and subsequent training methods. RESULTS: The six guiding phases provided a methodologically robust frame to the revision process. Practitioners valued an overall developmental measure with discrete data about and within the 'avenues of learning' allowing them to analyse a child's strengths and weaknesses. Communication with practitioners across the world demonstrated the wide disparity of culture and environments that the Griffiths Scales are deployed in. It is not possible to design a revised scale that is appropriate for all areas of use, so in this revision process, it was decided to design the scales as culturally fair as possible and support practitioners in other countries to translate and validate the scales for use. CONCLUSIONS: The revision of the Griffiths III found test users to be valuable sources of information on the basis of their experiences with the test and professional knowledge. Creating a continuous feedback mechanism within a phased process provided opportunities for the revision team to engage meaningfully with the data being obtained as well as test users to advance the scope and quality of the test. Revision teams are encouraged to consider the process and engagement methods explored in this study during their projects.


Subject(s)
Child Development/physiology , Developmental Disabilities/diagnosis , Psychological Tests , Attitude of Health Personnel , Child , Child, Preschool , Communication , Humans , Reproducibility of Results
2.
Dev Med Child Neurol ; 53(1): 34-9, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21126241

ABSTRACT

AIM: The aims of this study were to identify all people with Lesch-Nyhan disease (LND) born in the UK between 1988 and 2008, and to obtain a clinical profile including age at diagnosis, genetic background, family history, neurological signs, and medications. METHOD: Potential participants were contacted through the British Paediatric Neurology Surveillance Unit. Questionnaires were sent to each child's paediatric neurologist or primary consultant. Two purine laboratories provided metabolic information. RESULTS: Twenty-three live males with LND in the 0- to 20-year age band and eight live males over the age of 20 years were identified. Thirty-one live people with LND were identified in the UK in 2008, giving a prevalence of 1 in 2 million people. Over the 20 years of study, there was a mean incidence rate of 0.18 per 100 000 live births, range 0 to 0.5. INTERPRETATION: To our knowledge, this study is the first to provide details of the prevalence and incidence of LND in the UK. The data highlight that clinical profiles, at the time of diagnosis, and management of the disease are variable. There is the need for ongoing monitoring of allopurinol dosage and metabolic screening.


Subject(s)
Lesch-Nyhan Syndrome/epidemiology , Lesch-Nyhan Syndrome/physiopathology , Adolescent , Adult , Age Factors , Child , Child, Preschool , Community Health Planning , Health Surveys , Humans , Infant , Infant, Newborn , Lesch-Nyhan Syndrome/diagnosis , Lesch-Nyhan Syndrome/genetics , Longitudinal Studies , Male , Prevalence , Surveys and Questionnaires , United Kingdom/epidemiology , Young Adult
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