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Predictors of risk-based medical follow-up: a report from the childhood cancer survivor study
Authors:Jeanne R. Steele  Melanie Wall  Nicholas Salkowski  Pauline Mitby  Toana Kawashima  Mark W. Yeazel  Melissa M. Hudson  Leslie L. Robison  Ann C. Mertens
Affiliation:1. Office of Statewide Health Improvement Initiatives, Minnesota Dept. of Health, St. Paul, MN, USA
2. Department of Biostatistics and Psychiatry, Columbia University, New York, NY, USA
3. Division of Biostatistics, University of Minnesota, Minneapolis, MN, USA
4. Children’s Hospitals and Clinics of Minnesota, Minneapolis, MN, USA
5. Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA, USA
6. Department of Family Medicine and Community Health, University of Minnesota, Minneapolis, MN, USA
7. Departments of Oncology and Epidemiology and Cancer Control, St. Jude Children’s Research Hospital, Memphis, TN, USA
8. Aflac Cancer Center, Children’s Healthcare of Atlanta, Department of Pediatrics, Emory University, 2015 Uppergate Dr, Atlanta, GA, 30322, USA
Abstract:

Purpose

The purpose of this study is to conduct an intervention study designed to assess the effectiveness of using a newsletter to increase medical follow-up in pediatric cancer survivors at risk of selected treatment complications.

Methods

Survivors participating in the Childhood Cancer Survivor Study who were at least 25 years of age and at risk of cardiovascular disease, breast cancer, or osteoporosis related to previous cancer treatment were randomly assigned to receive a newsletter featuring brief health risk information or a newsletter including an insert providing more comprehensive health risk information. A follow-up survey distributed 24 months after the newsletter intervention assessed predictors of medical follow-up.

Results

Overall, there were no differences found among the groups in terms of access to a treatment summary, medical follow-up, discussion of childhood cancer health risks, and medical screening for the targeted health behaviors. One exception, indicating borderline significance was that women at risk for osteoporosis who received the newsletter insert were more likely to have discussed their risk with a doctor than those who only received the brief information (10.1 % vs. 4.0 % p?=?0.05). Discussion of breast cancer (OR?=?2.15; 95 % CI?=?1.74-2.66), heart disease (OR?=?5.54; 95 % CI?=?4.67–6.57) and osteoporosis (OR?=?10.6; 95 % CI?=?8.34–13.47) risk with physician significantly predicted report of undergoing screening for targeted behavior in previous 2 years as did physician access to treatment summary.

Conclusions

More detailed content in a newsletter had minimal effect on recommended screening. However, survivor’s discussion of cancer-related risks with one’s doctor significantly influenced participation in health screening. These results highlight the integral role of communication in health behavior.

Implications for Cancer Survivors

This study is designed to assess communication strategies that increase medical follow-up in pediatric cancer survivors at risk of selected treatment complications. The results are of great importance not only to the pediatric oncology community but also the broad range of adult oncology medical specialties who are directly involved in the long-term medical care of this ever increasing population of cancer survivors.
Keywords:
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