Abstract:de produção em saúde, diante da implantação do Sistema Único de Saúde; C) construir um sistema de informação das práticas de enfermagem em saúde coletiva que permita a sua classificação, troca de experiências e interlocução nos níveis nacional e internacional.Subordinados a estes propósitos centrais, foram constituídos os objetivos específicos que se encontram descritos no Projeto.O marco teórico-metodológico adotado configurou as categorias analíticas -momento investigativo -e as categorias interpretativas -m… Show more
“…Suffering arising from the treatment and care demands often represent secondary gains to patients as the parental care system changes due to the parents' difficulties dealing with feelings of powerlessness to protect their child from painful and invasive procedures. As a consequence, limits are changed, responsibilities are reduced, and parents become more permissive (Santos & Gonçalves, 2008;Herman, Santos, & Miyazaki, 2007;Palmer et al, 2000;Woodgate, 2004;Young et al, 2002).…”
Section: Resultsmentioning
confidence: 99%
“…Mothers tend to report higher levels of anxiety than fathers, whether at the time the diagnosis is disclosed or in other stages of the disease, though these manifestations can be a result of how gender roles are constructed or the way parental caregivers split responsibilities; the primary caregiver role is usually attributed to mothers (Beck & Lopes, 2007a;Dahlquist, Czyzewski, & Jones, 1996;Santos & Gonçalves, 2008;Vrijmoet-Wiersma et al, 2008). Parents reporting high levels of anxiety at the diagnosis usually continue to experience significant manifestations even after the treatment ends (Vrijmoet-Wiersma et al).…”
A diagnosis of childhood cancer represents challenges for patients, family members, and health workers. The parents of a child or adolescent have to play an expanded role because they need to reconcile parental tasks and treatment demands. This study presents an integrative literature review concerning difficulties experienced by pediatric caregivers during onco-hematological treatment. The CAPES periodicals portal and the Scientific Library Online (SciELO) were searched for papers published between 1999 and 2009. Relevant themes are highlighted in Brazilian and international studies published in the field, such as psychological disorders experienced by caregivers, the professional and financial impact associated with treatment, changes in educative practices and family dynamics, and the influence of cultural practices on the experience of treatment. Suggestions for further research are presented to support efficient psychosocial interventions and minimize the psychosocial costs experienced by pediatric caregivers over the course of onco-hematological treatments.
“…Suffering arising from the treatment and care demands often represent secondary gains to patients as the parental care system changes due to the parents' difficulties dealing with feelings of powerlessness to protect their child from painful and invasive procedures. As a consequence, limits are changed, responsibilities are reduced, and parents become more permissive (Santos & Gonçalves, 2008;Herman, Santos, & Miyazaki, 2007;Palmer et al, 2000;Woodgate, 2004;Young et al, 2002).…”
Section: Resultsmentioning
confidence: 99%
“…Mothers tend to report higher levels of anxiety than fathers, whether at the time the diagnosis is disclosed or in other stages of the disease, though these manifestations can be a result of how gender roles are constructed or the way parental caregivers split responsibilities; the primary caregiver role is usually attributed to mothers (Beck & Lopes, 2007a;Dahlquist, Czyzewski, & Jones, 1996;Santos & Gonçalves, 2008;Vrijmoet-Wiersma et al, 2008). Parents reporting high levels of anxiety at the diagnosis usually continue to experience significant manifestations even after the treatment ends (Vrijmoet-Wiersma et al).…”
A diagnosis of childhood cancer represents challenges for patients, family members, and health workers. The parents of a child or adolescent have to play an expanded role because they need to reconcile parental tasks and treatment demands. This study presents an integrative literature review concerning difficulties experienced by pediatric caregivers during onco-hematological treatment. The CAPES periodicals portal and the Scientific Library Online (SciELO) were searched for papers published between 1999 and 2009. Relevant themes are highlighted in Brazilian and international studies published in the field, such as psychological disorders experienced by caregivers, the professional and financial impact associated with treatment, changes in educative practices and family dynamics, and the influence of cultural practices on the experience of treatment. Suggestions for further research are presented to support efficient psychosocial interventions and minimize the psychosocial costs experienced by pediatric caregivers over the course of onco-hematological treatments.
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