ASSOCIAÇÃO DA ATIVIDADE FÍSICA DE ADOLESCENTES, FAMILIARES E PARES: UMA REVISÃO SISTEMÁTICA

Objetivo: Analisar a associação entre a atividade física (AF) de pais, irmãos e pares à AF de adolescentes brasileiros por meio de uma revisão sistemática da literatura. Métodos: Realizou-se revisão sistemática em duas etapas, em junho de 2013 e fevereiro de 2014, nas bases de dados PubMed/MEDLINE, Web of Science, EBSCO e LILACS, utilizando-se quatro grupos de descritores, sendo estes “influência de pais e irmãos”, “atividade física”, “tipo de amostra” e “nacionalidade”, nos idiomas inglês e português, que atendesse aos seguintes critérios: (i) indivíduos saudáveis; (ii) adolescentes brasileiros; (iii) estudos abordando a AF; e (iv) estudos publicados entre janeiro de 2008 e fevereiro de 2014. Resultados: A busca nas bases de dados resultou em 2.094 títulos de artigos potencialmente relevantes, mas apenas 7 atenderam a todos os critérios de inclusão. Há uma associação positiva entre a AF de pais e filhos, porém, ao estratificar por sexo, esta é encontrada apenas no feminino, tanto para a inatividade quanto para estar fisicamente ativo. O apoio social possui grande influência na AF de crianças e adolescentes, no entanto, tal associação não foi encontrada em estudos longitudinais. Conclusão: Existe uma associação positiva entre a atividade física do pai e da mãe com suas filhas, tanto para a inatividade quanto para serem ativos, mas não foram encontradas associações entre os pais e os filhos, fato também observado para com irmãos inativos. O apoio social mostrou-se eficaz para aumentar o nível de atividade física de adolescentes.

CAREGIVING FOR A FAMILY MEMBER WITH HEAD AND NECK CANCER

Objective: To know the perception of informal caregivers regarding the care for a family member with head and neck cancer. Methods: Qualitative study conducted between March and May 2014 in the radiotherapy outpatient center of the Centro de Alta Complexidade em Oncologia – CACON (Oncology High Complexity Center) of the Hospital Universitário de Brasília – HUB (University Hospital of Brasília) using semi-structured interviews with nine caregivers about the experience of caring for family members. Data underwent Content Analysis and four units of meaning were identified: “Representation of cancer in the Family”, “The care as debt, individual reward or reconstruction of family ties”, “Repercussions of cancer on the caregiver’s personal life” and “Social support and network used by caregivers”. Results: Feelings of sadness and surprise at the moment of diagnosis were attributed to cancer, as well as the idea of punishment. The care was seen as personal satisfaction, accomplishment and opportunity for family rapprochement. Work overload and change in routine were altered functions. Religiosity, exchange of experience in the waiting room and institutional support appeared as coping strategies. Conclusion: The experience of caring for family members with head and neck cancer directly interferes in the lives of caregivers. Pointing out the institutional embracement as a strategy within the social network reinforces the importance of integrating the caregivers as a significant part of the health care plan developed by the health team.

NUTRITIONAL COUNSELING OFFERED TO CHILDREN AND ADOLESCENTS WITH DISABILITIES

Objective: To evaluate the nutritional counseling offered to children and adolescents with disabilities in the municipality of Santa Cruz, RN, Brazil. Methods: Observational, crosssectional, population-based study, developed from May to December 2013, with 102 children and adolescents attending a Children’s Rehabilitation Center. We conducted socioeconomic, demographic, health and lifestyle assessments, and evaluated the received nutritional assistance (whether they had received nutritional counseling from any health professional in relation to food and nutrition, how often it occurred and which professional conducted such counseling). Results: Only 37% (n=37) of parents had received some nutritional guidance. Regarding the frequency of counseling, only 11.8% (n=4) of the youngsters received it 7 or more times/year; 23.5% (n=8) received it 2 to 6 times/year; and most (64.7 %, n=22) received it 1 time/year or less. The length of the nutritional counseling was short: the majority (64.7%, n=22) received only one guidance session throughout the whole period attending the institution, and less than 15% (n=5) received counseling for more than six consecutive months. For the majority (73.5%, n=25), the amount of time receiving nutritional guidance has not reached half of the monitoring period. Nutritional counseling was carried out mainly by nutritionists (89.2%, n=33). Conclusion: There was a low frequency of nutritional counseling directed specifically to the disabilities presented by the participants. When such activity was conducted, it occurred irregularly during the participant´s follow-up, only during a short period of time, and lacking connection with the monitoring by the multidisciplinary team.