Mettre la recherche en contexte : l'expérience de vie et les résultats des adultes appartenant au spectre de l'autisme recevant des services dans 29 États

Titre original en anglais : Putting the Research in Context: The Life Experience and Outcomes of Adults on the Autism Spectrum Receiving Services in 29 States

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Hiersteiner, D., Bradley, V. J., Ne'eman, A., Bershadsky, J., & Bonardi, A. (2017). Putting the Research in Context: The Life Experience and Outcomes of Adults on the Autism Spectrum Receiving Services in 29 States. Inclusion, 5(1), 45-59. https://doi.org/10.1352/2326-6988-5.1.45

Date de publication: 01/03/2017 Ajout dans AutiHub: 06/07/2026 Type: Article Langue de l’article: Anglais
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Auteurs

Auteur·ices des publications
5
Auteur·ices de la publication identifié·es comme autistes
1 / 5 (20,0 %)
  1. Dorothy Hiersteiner
  2. Valerie J. Bradley
  3. Ari Ne'eman *
  4. Julie Bershadsky
  5. Alexandra Bonardi

Résumé

Les réformes étatiques et fédérales dans le domaine du handicap ont entraîné l'élargissement des soutiens qui favorisent l'inclusion et l'intégration dans le courant dominant de la société américaine. Cependant, les adultes ayant reçu un diagnostic de trouble du spectre de l'autisme (TSA) ne semblent pas avoir bénéficié de ces changements dans la même mesure que ceux n'ayant pas reçu de diagnostic de TSA. Cet article utilise les données de la National Core Indicators Adult Consumer Survey pour examiner les caractéristiques démographiques et les résultats des adultes ayant reçu un diagnostic de TSA qui reçoivent des services des systèmes étatiques de déficiences intellectuelles et développementales (IDD). À partir des données, des approches en matière de politiques et de recherche sont proposées.

State and federal reforms in the disability field have resulted in the expansion of supports that foster inclusion and integration in the mainstream of American society. However, adults with an autism spectrum disorder (ASD) diagnosis do not appear to have benefited from these changes to the same extent as those without an ASD diagnosis. This article uses National Core Indicators Adult Consumer Survey data to examine the demographic characteristics and outcomes for adults with an ASD diagnosis who receive services from state intellectual and developmental disabilities (IDD) systems. Building on the data, policy and research approaches are suggested.

Bibliographie citée par cette référence

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Ces indicateurs décrivent la bibliographie citée importée pour cette publication. Les métriques de références citées utilisent le total des références citées comme dénominateur. Les métriques d’auteurices cité·es indiquent si elles utilisent toutes les occurrences d’auteurices cité·es ou seulement les occurrences rattachées à des auteurices déjà intégré·es à la base de données AutiHub. Ils utilisent les rattachements mis en cache entre les auteurices cité·es et les auteurices intégré·es à la base de données AutiHub. Dernier calcul : 16/08/2026 11:31.

Références citées
56
Nombre total de références citées intégrées pour cette publication.
Références citées avec un·e auteur·ice identifié·e comme autiste
1 / 56 (1,8 %)
Occurrences d’auteur·ices cité·es identifié·es comme autistes
1 / 110 (0,9 %)
Parmi les occurrences rattachées à des auteurices intégré·es à la base de données AutiHub : 1 / 13 (7,7 %). Auteurices cité·es distinct·es identifié·es comme autistes : 1 / 104 (1,0 %).
Occurrences citées rattachées à la base AutiHub
13 / 110 (11,8 %)
Auteurices cité·es distinct·es rattaché·es : 12 / 104 (11,5 %)
Occurrences rattachées, non identifiées comme autistes
12 / 13 (92,3 %)
Parmi les seules occurrences rattachées. Sur l’ensemble des occurrences d’auteurices cité·es : 12 / 110 (10,9 %). Auteurices cité·es distinct·es rattaché·es, non identifié·es comme autistes : 11 / 12 (91,7 %).
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