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Verfasst von:Bühren, Katharina [VerfasserIn]   i
 Kaess, Michael [VerfasserIn]   i
Titel:First sociodemographic, pretreatment and clinical data from a German web-based registry for child and adolescent anorexia nervosa
Verf.angabe:Katharina Bühren, Beate Herpertz-Dahlmann, Astrid Dempfle, Katja Becker, Karin M. Egberts, Stefan Ehrlich, Christian Fleischhaker, Alexander von Gontard, Freia Hahn, Charlotte Jaite, Michael Kaess, Tanja Legenbauer, Tobias J. Renner, Ellen Schrötter, Ulrike Schulze, Judith Sinzig, Gisela Antony, Johannes Hebebrand, and Manuel Föcker
E-Jahr:2017
Jahr:August 21, 2017
Umfang:8 S.
Fussnoten:Onlineveröffentlichung: August 21, 2017 ; Gesehen am 06.09.2018
Titel Quelle:Enthalten in: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie
Ort Quelle:Bern : Huber, 1999
Jahr Quelle:2017
Band/Heft Quelle:45(2017), 5, Seite 393-400
ISSN Quelle:1664-2880
Abstract:Objective: The first web-based registry for childhood and adolescent anorexia nervosa (AN) in Germany was established to systematically collect demographic and clinical data. These data as well as information on how young individuals with AN can find access to healthcare services are presented. Method: Patients´ data from child and adolescent psychiatry departments of 12 university hospitals and two major nonuniversity hospitals in Germany were collected between January 2015 and December 2016. All patients met the ICD-10 diagnostic criteria for (atypical) AN. Sociodemographic data, type and amount of healthcare utilization before admission, and clinical data at admission and discharge were compiled. Results: 258 patients with a mean age of 14.7 years and a mean BMI at admission of 15.3 kg/m2 were included. The parents and patients had a higher educational level than the general German population. More than 80 % of the patients reported having utilized healthcare before hospitalization. The mean duration of outpatient treatment before hospitalization was 7 months. Conclusions: There seem to be major barriers to specialist treatment for young patients with AN in Germany, which should be analyzed in future studies.
DOI:doi:10.1024/1422-4917/a000544
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: http://dx.doi.org/10.1024/1422-4917/a000544
 Volltext: https://econtent.hogrefe.com/doi/10.1024/1422-4917/a000544
 DOI: https://doi.org/10.1024/1422-4917/a000544
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1580737692
Verknüpfungen:→ Zeitschrift

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