ABSTRACT
Objective:
To understand the perception and knowledge of caregivers of children with microcephaly on oral health care.
Methods:
This is a qualitative study with a research-action method, in which semi-structured interviews - diagnostic and evaluative - and oral health workshop were adopted as techniques for data collection and intervention.The study was conducted in a group aimed at caregivers of children with microcephaly, offered in the public health network of the capital Maceió, Alagoas. Nine women caring for children with microcephaly participated in the study. The participants statements were transcribed and, through the thematic analysis, the data was categorized and discussed.
Results:
The main caregivers of children with microcephaly were mothers and grandmothers. Of these, 45% had incomplete secondary education. Most reported self-care with their impaired oral health, were unaware of the risk of transmission of dental caries-related bacteria, did not offer exclusive breastfeeding until 6 months of age, and offered artificial milk to the children with sugared and farinaceous milk.
Conclusion:
For caregivers of children with microcephaly, oral health care is a less valuable topic when compared to other demands, both at home and other physical treatments. Responsibility for care is aimed at the maternal figures, which makes it difficult for them to take care of their own oral health. Educational action on oral health minimized doubts and fragilities for the self-care and care of children related to oral health.
Indexing terms
Disabled person; Microcephaly; Oral health