2001
DOI: 10.1055/s-2001-16682
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Wie nehmen Lebenspartner depressiver Patienten die Krankheit wahr und welche Informationen brauchen sie?

Abstract: Results are discussed in terms of the consequences of spouses' illness models for designing psychoeducational workshops for the families of depressive patients. The results document the great need for negotiated partnership between families and professionals. Furthermore, the need for educating the public about the disorder and its psychosocial costs for the patients' families is highlighted.

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Cited by 11 publications
(10 citation statements)
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“…Regarding emotional topics, excessive demands, helplessness, suicidality, feelings of guilt and shame as well as strains in the partnership are addressed most frequently. These contents are in accordance with findings about information needs [9,11] and burden of relatives [7,8]. From the PGIR-contact persons point of view, relatives’ most urgent need is dealing adequately with the patient.…”
Section: Discussionsupporting
confidence: 85%
See 1 more Smart Citation
“…Regarding emotional topics, excessive demands, helplessness, suicidality, feelings of guilt and shame as well as strains in the partnership are addressed most frequently. These contents are in accordance with findings about information needs [9,11] and burden of relatives [7,8]. From the PGIR-contact persons point of view, relatives’ most urgent need is dealing adequately with the patient.…”
Section: Discussionsupporting
confidence: 85%
“…Uncertainties about how to deal adequately with the patients and their illness-related behaviour [9] as well as negative emotions like guilt, anger or worries about the patients’ future are common [8]. A lack of illness-specific information and education, coupled with a high subjective need in this regard and a perceived lack of involvement in depression treatment, is also experienced as a burden [8,10,11]. Consequences are a diminished quality of life [12,13] and a significantly increased prevalence of depressive disorders in relatives themselves [14].…”
Section: Introductionmentioning
confidence: 99%
“…However, the demand for information often remains unmet (Angermeyer, Diaz Ruiz de Zarate & Matschinger, 2000; Gantt, Goldstein & Pinsky, 1989; Gümüş, 2008; Mueser et al, 1992; Wancata et al, 2006; Wei et al, 2010). Frequently, relatives do not know the correct diagnosis, do not get adequate information on the current medication or are not able to recognize the symptoms (Gantt, Goldstein & Pinsky, 1989; Gaskill & Cooney, 1991; Wittmund, Bischkopf & Angermeyer, 2001). They report a lack of involvement in the treatment process and often feel alone as they do not know other people being in the same situation (Gaskill & Cooney, 1991).…”
Section: Introductionmentioning
confidence: 99%
“…Die Gruppe der Fachvertreter psychiatrischer, psychotherapeutischer und psychologischer Abteilungen und Ambulanzen bilden die Autoren: Bickel [78], Frick [79], Häßler [80], Kilian [81], Kluge [82], Melchinger [83], Schützwohl [84], Soyka [85] und Wittmund [86].…”
Section: Introductionunclassified