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Journal ArticleDOI

Profile of referrals for early childhood developmental delay to ambulatory subspecialty clinics.

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TLDR
A profile of referrals and the rationale thereof for a cohort of children with suspected developmental delay is presented that, although locale specific, has implications for service provision and training.
Abstract
The objective of this study was to determine the profile and pattern of referral to subspecialty clinics of young children with suspected developmental delay together with the factors prompting their referral. All children under 5 years of age referred to either developmental pediatrics or pediatric neurology clinics at a single tertiary hospital over an 18-month period were prospectively identified. Standardized demographic and referral information were collected at intake, final developmental delay subtype diagnosed was identified, and referring physicians were surveyed regarding factors prompting referral. A total of 224 children met study criteria. There was a marked male preponderance (166/224), especially among those with either cognitive or language delay. Two delay subtypes, global developmental delay and developmental language disorder, accounted for two thirds of the diagnoses made. For slightly more than one third of the children (75/224), the delay subtype diagnosed following specialty evaluation was different from that initially suspected by the referring physician. A mean delay of 15.5 months was observed for the cohort as a whole between initial parental concern and specialty assessment. For referring physicians, the major factor prompting referral was the severity of the observed delay. The most important aspects of the specialty evaluation according to referral sources were the identification of a possible etiology and confirmation of delay. A profile of referrals and the rationale thereof for a cohort of children with suspected developmental delay is presented that, although locale specific, has implications for service provision and training.

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Citations
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Journal ArticleDOI

Factors associated with age of diagnosis among children with autism spectrum disorders.

TL;DR: Improvements over time are suggested over time in decreasing the age at which children with ASD, especially higher functioning children, receive a diagnosis and a lack of resources in rural areas and for near-poor families and the importance of continuous pediatric care and specialty referrals are suggested.
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Race differences in the age at diagnosis among medicaid-eligible children with autism.

TL;DR: Important disparities exist in the early detection and treatment of autism and these disparities may be the result of differences in help-seeking, advocacy and support, and clinician behaviors.

Integration of Mental Health/Substance Abuse and Primary Care

TL;DR: There is a reasonably strong body of evidence to encourage integrated care, at least for depression, and there is no discernible effect of integration level, processes of care, or combination on patient outcomes for mental health services in primary care settings.
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Disparities in Diagnoses Received Prior to a Diagnosis of Autism Spectrum Disorder

TL;DR: Differences in diagnostic patterns by ethnicity suggest possible variations in parents’ descriptions of symptoms, clinician interpretations and expectations, or symptom presentation.
References
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Journal ArticleDOI

Diagnosis in Autism A Survey of Over 1200 Patients in the UK

TL;DR: The results of a survey of almost I300 parent members of autistic societies in the UK are described in this paper, which focused on parents' views of the diagnostic process and data were collected on the age at which diagnosis was made, the time taken to obtain a diagnosis and the professionals involved.
Book

Autistic spectrum disorders

Lorna Wing
TL;DR: Autism seems to be on the increase, this at least is the feeling of many professionals in the field of child development in Britain, who believe that in recent years they have been seeing more children with autistic spectrum disorders.
Journal ArticleDOI

Diagnostic yield of the neurologic assessment of the developmentally delayed child.

TL;DR: In this paper, the etiologic yield of the neurologic assessment of a consecutive cohort of developmentally delayed children was determined for a single university-based pediatric neurologist for evaluation of global developmental delay from July 1991 to December 1993.
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