Samira Reschetti Marcon

Universidade Federal de Mato Grosso (UFMT), Vila Real do Senhor Bom Jesus de Cuiabá, Mato Grosso, Brazil

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Publications (9)2.04 Total impact

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    ABSTRACT: To evaluate the correlation between the presence of depressive symptoms and quality of life in users of psychoactive substances from Psychosocial Attention Centers in Mato Grosso.
    Revista da Escola de Enfermagem da U S P 08/2014; 48(4):663-9. · 0.39 Impact Factor
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    ABSTRACT: The aim of this study was to evaluate the quality of life and the presence of depressive symptoms among the caregivers and drug dependent people of the CAPSad. This is a cross-sectional study, with 109 users of four Psychosocial Care Centers for alcohol and other drugs of Mato Grosso and their caregivers, using the instruments: Medical Outcomes Studies 36 (SF-36), Beck Depression Inventory (BDI) and a sociodemographic variables questionnaire. The QoL of the caregivers in the domains functional capacity, physical aspect, pain and vitality were more affected when compared to the users. A strong correlation between QoL and depressive symptoms was found in both groups. The comparisons performed demonstrate a compromise in the quality of life of both, with the group of caregivers most affected, confirming the situation of drug dependence as an important factor in the perception of the caregiver regarding their quality of life.
    Revista Latino-Americana de Enfermagem 02/2012; 20(1):167-74. · 0.54 Impact Factor
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    ABSTRACT: OBJECTIVE: Compare clinical and sociodemographic profile of adolescents who stayed and did not stay in treatment at Centro de Atenção Psicossocial para Álcool e outras Drogas (CAPSad). METHOD: A transverse study based on medical records of 125 users who had been in treatment at CAPS ad Adolescer in Cuiabá/MT, from June 2009 to June 2011. RESULTS: The permanence in treatment was predominantly male among users who extensively used psychoactive substances, who were sent for this treatment by social and judicial sectors. They had a conflictual family relationship and also had a frequent participation of family in treatment. The biggest proportion of those who did not stay in treatment happened because of the lack of integration with other devices of the network. CONCLUSION: To know the characteristics of the adolescents and the interveners factors in the permanence reinforce the responsibility of CAPS in the effective articulation of the network, and moreover, reassure that family must be more and more close to treatment, as an fundamental part in the project of intervention.
    Jornal brasileiro de psiquiatria 12/2011; 61(4):227-234.
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    ABSTRACT: OBJETIVO: Avaliar a sobrecarga de cuidado e a qualidade de vida (QV) de cuidadores de crianças/adolescentes com câncer durante tratamento quimioterápico e relacioná-las entre si e aos dados sociodemográficos. MÉTODOS: Estudo transversal, com 160 cuidadores. Foram coletados dados sociodemográficos, sobrecarga de cuidado, conforme "Caregiver Burden Scale" e de QV pelo SF-36. RESULTADOS: 88,7% dos cuidadores eram mães, idade média 34,9 anos, escore geral de sobrecarga 2,09±0,04 e escores do SF-36 mais comprometidos: aspectos emocionais, vitalidade, saúde mental e aspectos físicos. O modelo de regressão respondeu 36,0% da sobrecarga. CONCLUSÃO: A QV dos cuidadores e sobrecarga de cuidados vivenciada mostram-se comprometidas em diversos domínios, e essas alterações podem afetar a qualidade da assistência prestada às crianças e adolescentes e propiciar desajustes na própria saúde.
    Acta Paulista de Enfermagem 12/2011; 25(4):567-573. · 0.14 Impact Factor
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    ABSTRACT: OBJECTIVE: To evaluate quality of life and presence of stress in caregivers of drug-addicted people. METHODS: This cross-sectional study was carried out at four Psychosocial Care Centers in Mato Grosso. Demographic and quality of life data were collected for 109 caregivers using the Medical Outcomes Study 36 – Item Short-form, depression symptoms (Beck Depression Inventory) and stress of caregivers (Caregiver Burden Scale). RESULTS: Of 109 caregivers, 55.9% were mothers with a mean age of 47.66 years; 23.8% had depressive symptoms. The SF36 scores most compromised were emotional aspects, vitality, pain and mental health. Mean stress among caregivers was 2.24. A significant correlation in quality of life, depression and stress of caregivers was seen. CONCLUSION: Findings confirmed that quality of life is compromised and stress is high among caregivers, highlighting the need for providing emotional support.
    Acta Paulista de Enfermagem 12/2011; 25(SPE2):7-12. · 0.14 Impact Factor
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    ABSTRACT: The focus of this study is mental health care in the Brazilian Family Health Program (FHP), with the complexity of such care as the main premise. The objectives were to analyze the actual conditions of mental health care in FHP services in Cuiabá, Mato Grosso State, describing the dynamics of such care and identifying situations and instruments used by different health professionals in dealing with problems of mental distress in the community. By means of a descriptive exploratory methodology, the discourses of eight health teams were studied, using content analysis. The study concluded that the demand for care for individuals with mental distress was not recorded on the patient charts, nor was it part of a proposal for individual or family interventions; some measures were taken according to a lay concept of 'mental illness' and treatment, while referral to the specialized mental health care network was frequently used, despite its precariousness, thus reflecting the need for continuing training in mental health.
    Cadernos de saúde pública / Ministério da Saúde, Fundação Oswaldo Cruz, Escola Nacional de Saúde Pública 09/2009; 25(9):2033-42. · 0.83 Impact Factor
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    Cadernos De Saude Publica - CAD SAUDE PUBLICA. 01/2009; 25(9).
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    ABSTRACT: RESUMO Objetivo: Avaliar a sobrecarga de cuidado e a qualidade de vida (QV) de cuidadores de crianças/adolescentes com câncer durante tratamento quimioterápico e relacioná-las entre si e aos dados sociodemográficos. Métodos: Estudo transversal, com 160 cuidadores. Foram coletados dados sociodemográficos, sobrecarga de cuidado, conforme "Caregiver Burden Scale" e de QV pelo SF-36. Resultados: 88,7% dos cuidadores eram mães, idade média 34,9 anos, escore geral de sobrecarga 2,09±0,04 e escores do SF-36 mais comprometidos: aspectos emocionais, vitalidade, saúde mental e aspectos físicos. O modelo de regressão respondeu 36,0% da sobrecarga. Conclusão: A QV dos cuidadores e sobrecarga de cuidados vivenciada mostram-se comprometidas em diversos domínios, e essas alterações podem afetar a qualidade da assistência prestada às crianças e adolescentes e propiciar desajustes na própria saúde. Descritores: Cuidadores; Qualidade de vida; Neoplasias/quimioterapia; Cuidado da criança; Adolescente ABSTRACT Objective: To evaluate the burden of care and quality of life (QOL) of caregivers of children/adolescents with cancer during chemotherapy treatment, and to relate them to each other and sociodemographic data. Methods: A transversal study, with 160 caregivers. We collected so-ciodemographic data, burden of care using the Caregiver Burden Scale and QOL using the SF-36. Results: 88.7% of caregivers were mothers, with the mean age of 34.9 years, overall burden score 2.09 ± 0.04 and the SF-36 scores most compromised were: emotional aspects, vitality, mental health and physical aspects. The regression model accounted for 36.0% of the burden. Conclusion: The QOL of caregivers and burden of care experienced showed compromise in various domains, and these alterations may affect the quality of care provided to children and adolescents, and lead to imbalances in their own health.