2018
DOI: 10.1080/02687038.2018.1486384
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Experiences of mood changes and depression after post-stroke aphasia

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Cited by 10 publications
(10 citation statements)
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“…The paucity of mental health identification and assessment methods validated on persons with CD could lead to under-identification of behavioral health disorders in this population. 32,33 Qualitative evidence from primary care indicates that persons with CDs interact with and convey messages to their physicians differently than those without CDs. [34][35][36] Persons with CDs rely heavily on caregivers for communication, need additional time to be understood, and are at risk of feeling misunderstood by their health care practitioners.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The paucity of mental health identification and assessment methods validated on persons with CD could lead to under-identification of behavioral health disorders in this population. 32,33 Qualitative evidence from primary care indicates that persons with CDs interact with and convey messages to their physicians differently than those without CDs. [34][35][36] Persons with CDs rely heavily on caregivers for communication, need additional time to be understood, and are at risk of feeling misunderstood by their health care practitioners.…”
Section: Discussionmentioning
confidence: 99%
“…Fortunately, approaches are emerging in the aphasia population, with several new behavioral health approaches under investigation. 32,44,[48][49][50] Another opportunity for addressing these needs is the addition of speech-language pathologists as part of the primary care and behavioral health team. 51 Such providers are specifically trained in addressing CDs and can work with both the patient and providers to improve communication and understanding of symptoms and treatment effects.…”
Section: Discussionmentioning
confidence: 99%
“…Increasing interest in psychosocial approaches has generated further knowledge of identity in aphasia. Approaches have focused on aspects such as: living successfully with aphasia (Brown et al 2012(Brown et al , 2013Grohn et al 2014); goal-setting (Worrall et al 2011); quality of life and wellbeing (Cruice et al 2003(Cruice et al , 2010Hilari 2011); participation (Dalemans et al 2010); the emotional impact of aphasia (Gainotti 1997;Herrmann 1997;Code et al 1999) including depression (Kauhanen et al 2000;Baker et al 2018) and anxiety (Morris et al 2017). A detailed account of 'Hope' following aphasia, despite making brief mention of spiritual beliefs, made no recourse to spiritual frameworks (Bright et al 2013).…”
Section: Introductionmentioning
confidence: 99%
“…Baker, C., Worrall, L., Rose, M., & Ryan, B (2018c). Experiences of mood changes and depression after post-stroke aphasia.…”
Section: Chapter 5 Statement Of Contributionmentioning
confidence: 99%
“…It is necessary for people with aphasia to contribute to the research and inform the translation of stepped psychological care to clinical practice. The aim of this chapter is to describe the perspective of people with aphasia regarding: a) their experience of mood changes, depression and current practice; and b) their preferences within a stepped psychological care approach.The content of this chapter is in preparation for publication, Baker, C., Worrall, L.,Rose, M., & Ryan, B (2018c). Experiences of mood changes and depression after post-stroke aphasia.…”
mentioning
confidence: 99%