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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-61052

Jans, T; Ball, J; Preiss, M; Haberhausen, M; Warnke, A; Renner, T J (2011). Pervasive refusal syndrome. Three German cases provide further illustration. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie, 39(5):351-359.

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Abstract

Pervasive refusal syndrome (PRS) has been proposed as a new diagnostic entity among child and adolescent psychiatric disorders. It is characterized by a cluster of life-threatening symptoms including refusal of hood intake, decreased or complete lack of mobilization, and lack of communication as well as retreat from normal life activities. Active refusal to accept help as well as neglect of personal care have been core features of PRS in the limited number of cases reported in the last decade. There have, however; been cases with predominantly passive resistance, indicating the possibility that there may be a continuum from active refusal to passive resistance within PRS. Postulating this continuum allows for the integration of "depressive devitalization" -- a refusal syndrome mainly characterized by passive resistance -- into the concept of PRS. Here, three case vignettes of adolescent patients with PRS are presented. The patients' symptomatology can be allocated on this continuum of PRS. PRS and dissociative disorders are compared in greater detail and contrasted within this discussion of differential diagnoses at the poles of such a continuum. PRS is a useful diagnosis for cases involving symptoms of predominating refusal and retreat which cannot satisfactorily be classified by existing diagnostic categories, and which can mostly clearly be separated from dissociative disorder.

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3 citations in Web of Science®
2 citations in Scopus®
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Additional indexing

Item Type:Journal Article, refereed, further contribution
Communities & Collections:04 Faculty of Medicine > Center for Child and Adolescent Psychiatry
DDC:610 Medicine & health
Language:German
Date:2011
Deposited On:11 Mar 2012 07:49
Last Modified:05 Aug 2014 14:23
Publisher:Hans Huber
ISSN:1422-4917
Publisher DOI:10.1024/1422-4917/a000128
PubMed ID:21882157

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