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1.
J Autism Dev Disord ; 48(5): 1780-1791, 2018 05.
Article in English | MEDLINE | ID: mdl-29247310

ABSTRACT

Simple and low-cost observational-tools to detect symptoms of Autism Spectrum Disorder (ASD) are still necessary. The OERA is a new assessment tool to screen children eliciting observable behaviors with no substantial knowledge on ASD required. The sample was 99 children aged 3-10: 76 with ASD and 23 without ASD (11/23 had intellectual disability). The 13 remained items exhibited high interrater agreement and high reliability loaded onto a single latent trait. Such model showed excellent fit indices evaluated via confirmatory factor analysis and no item showed differential function in terms of age/sex/IQ. A cutoff of five points or higher resulted in the highest sensitivity (92.75) and specificity (90.91) percentages. OERA is a brief, stable, low-cost standardized observational-screening to identify ASD children.


Subject(s)
Autism Spectrum Disorder/diagnosis , Autism Spectrum Disorder/economics , Behavior Observation Techniques/economics , Behavior Observation Techniques/standards , Mass Screening/economics , Mass Screening/standards , Autism Spectrum Disorder/psychology , Child , Child, Preschool , Cost-Benefit Analysis , Factor Analysis, Statistical , Female , Humans , Intellectual Disability/diagnosis , Intellectual Disability/economics , Intellectual Disability/psychology , Male , Reproducibility of Results
2.
Med Care ; 55(1): 57-63, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27547947

ABSTRACT

BACKGROUND: Several states have passed Medicaid Home and Community-based Services (HCBS) waivers that expand eligibility criteria and available services for children with autism spectrum disorder (ASD). Previous research has shown considerable variation in these waivers, but little is known about the extent to which they address the health care needs of children with ASD. OBJECTIVE: To determine the effects of Medicaid HCBS waivers, and their characteristics, on unmet health care needs among children with ASD. METHODS: We used data from the 2003, 2007, and 2011 waves of the National Survey of Children's Health with detailed information on the Medicaid HCBS waiver programs of 35 states. Quasi-difference-in-difference-in-differences models were used to determine the effects of waivers and their characteristics on parent report of unmet health care needs of children with ASD compared with children without ASD. RESULTS: Greater waiver cost limits per child, estimated costs of services, and enrollment limits were associated with significant decreases in the adjusted rate of unmet health care needs, with considerable variation by household income level. CONCLUSIONS: These findings suggest that Medicaid HCBS waivers significantly decrease the unmet need for health care among children with ASD, most substantially among those who would not otherwise qualify for Medicaid. The findings regarding the effects of specific aspects of these waivers can inform the development of insurance policies in other states to address the needs of children with ASD.


Subject(s)
Autism Spectrum Disorder/economics , Community Health Services/economics , Health Services Needs and Demand/statistics & numerical data , Home Care Services/economics , Medicaid/statistics & numerical data , Adolescent , Child , Child, Preschool , Community Health Services/statistics & numerical data , Female , Health Services Accessibility/economics , Health Services Accessibility/statistics & numerical data , Health Services Needs and Demand/economics , Home Care Services/statistics & numerical data , Humans , Insurance Coverage/economics , Insurance Coverage/statistics & numerical data , Male , Medicaid/legislation & jurisprudence , United States
3.
J Dev Behav Pediatr ; 37(9): 687-693, 2016.
Article in English | MEDLINE | ID: mdl-27801720

ABSTRACT

OBJECTIVE: To identify challenges primary care providers (PCPs) experience providing a Medical Home for children with autism spectrum disorders (ASDs) and to describe the role developmental behavioral pediatricians (DBPs) play in the Medical Home Neighborhood. METHODS: The authors used purposeful sampling to recruit 25 PCPs from around Colorado to participate in 4 focus groups. Member checking was performed at the end of each group. Sampling continued until themes repeated and saturation was achieved. Focus groups were transcribed verbatim, and transcripts were analyzed using content analysis; an outside reviewer audited the data. RESULTS: Qualitative analysis yielded 30 codes that fell into 7 themes: provider education, shared model of care, initial diagnostic evaluation by the DBP, communication, office factors, cost and coverage, and access. PCPs identified knowledge gaps that led to decreased comfort and desired ongoing education and a centralized resource for providers. They envisioned a shared care model with ongoing specialist collaboration and improved communication within the care team. A specific role desired of the DBP was to provide the initial diagnostic evaluation and treatment plan with specific resources. Office factors, high cost and variable coverage, and poor access to services were barriers to providing a Medical Home for children with ASD. CONCLUSION: Working to remove barriers to shared care as well as providing continued educational opportunities will help improve access to a Medical Home Neighborhood for children with ASD. Advocacy is needed to help remove barriers related to cost, coverage, and access to services.


Subject(s)
Autism Spectrum Disorder/diagnosis , Autism Spectrum Disorder/therapy , Patient-Centered Care/standards , Pediatricians/standards , Primary Health Care/standards , Autism Spectrum Disorder/economics , Child , Humans , Qualitative Research
4.
Salud Publica Mex ; 58(6): 694-707, 2016.
Article in English | MEDLINE | ID: mdl-28225946

ABSTRACT

OBJECTIVE:: This study aims to generate evidence on intellectual development disorders (IDD) in Mexico. MATERIALS AND METHODS:: IDD disease burden will be estimated with a probabilistic model, using population-based surveys. Direct and indirect costs of catastrophic expenses of families with a member with an IDD will be evaluated. Genomic characterization of IDD will include: sequencing participant exomes and performing bioinformatics analyses to identify de novo or inherited variants through trio analysis; identifying genetic variants associated with IDD, and validating randomly selected variants by polymerase chain reaction (PCR) and sequencing or real-time quantitative PCR (qPCR). Delphi surveys will be done on best practices for IDD diagnosis and management. An external evaluation will employ qualitative case studies of two social and labor inclusion programs for people with IDD. CONCLUSIONS:: The results will constitute scientific evidence for the design, promotion and evaluation of public policies, which are currently absent on IDD.


Subject(s)
Intellectual Disability , Attention Deficit and Disruptive Behavior Disorders/diagnosis , Attention Deficit and Disruptive Behavior Disorders/economics , Attention Deficit and Disruptive Behavior Disorders/genetics , Attention Deficit and Disruptive Behavior Disorders/therapy , Autism Spectrum Disorder/diagnosis , Autism Spectrum Disorder/economics , Autism Spectrum Disorder/genetics , Autism Spectrum Disorder/therapy , Catastrophic Illness/economics , Cost of Illness , Costs and Cost Analysis , Genetic Variation , Genomics , Humans , Intellectual Disability/diagnosis , Intellectual Disability/economics , Intellectual Disability/genetics , Intellectual Disability/therapy , Mexico , Pediatric Obesity/diagnosis , Pediatric Obesity/economics , Pediatric Obesity/genetics , Pediatric Obesity/therapy , Surveys and Questionnaires
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