With advances in the treatment of childhood brain tumors, more children, some say up to 90 percent, survive and the numbers of caregivers have increased as have the demands placed upon them. Usually their caregivers are their mothers and other family members, especially for those survivors who do not gain independence in terms of their ability to live on their own, find work, make friends, and form partner relationships.
In the largest study of its kind, researchers led by the University of Pennsylvania School of Nursing have investigated the caregivers of 186 mothers to childhood brain tumor survivors aged 14-40 whose care needs last long into adulthood. They based their research on a model containing factors central to nursing practice, namely the caregiver, the survivor, and the family. They discovered that a complex interaction among components of the model, the health of the caregivers, the demands experienced by the caregiver, the caregiver’s perceptions about the health of the survivor, and the family’s support interact to explain how the caregiver assesses herself in her role. The study was recently published in Health Psychology.
“Based on the results of this study, either family functioning or caregiver’s perception about the survivor’s health can be targeted to improve competence for caregivers of adolescent and young adult brain tumor survivors,” said Janet A Deatrick, PhD, RN, FAAN, the Shearer Endowed Term Chair in Healthy Community Practices and Professor of Nursing. “Interventions targeted to survivor health could emphasize recovery expectations and reframe notions about the survivor’s functioning through family systems and cognitive-behavioral interventions.” The tumors and their treatment (i.e. surgery, chemotherapy, and cranial and/or spinal irradiation) can result in a range of late effects, including one of the most severe risk profiles for childhood cancer survivors (chronic morbidities and reduced health-related quality of life) and for their caregivers (ongoing care demands).