Abstract

BackgroundThe survival rate after childhood cancer has improved to 80%. The majority of childhood cancer survivors (CCS) will experience late complications which require follow up care, including access to their individual cancer treatment summary. The need to understand CCS needs and preferences in terms of ways to receive information e.g. digitally, becomes important. This study aims to through a mixed methods approach a) examine how CCS’ health awareness was impacted by viewing their personalized digital treatment summary and follow-up recommendations, b) explore E health literacy, and c) determine self-reported survivorship experiences and health care usage.MethodsSurvivors with a recent visit to the Late effects clinic were eligible for the study (n = 70). A representative sample of primary diagnoses were invited (n = 28). 16 CCS were enrolled. Recent medical visits, e health literacy and impressions of the digital treatment summary were assessed by a survey in conjunction with viewing their digital treatment summary on a computer screen. Their experience of reading and understanding their digital treatment summary in the context of their health related survivorship experiences were assessed in focus groups. The transcribed data was analyzed with conventional qualitative content analysis.ResultsThe self-reported medical problems largely reflected that, only 6,3% reported no cancer-related reasons for seeking medical attention. Of the medical specialists, the primary care physician was the most frequently visited specialist (68.8%). High E health literacy was not associated with treatment features but with educational level (p = 0.003, CI: 3.9–14.6) and sex (p = 0.022, CI: − 13.6- -1.3). All survivors graded the digital treatment summary above average in terms of being valuable, agreeable and comprehensive. The focus group interviews identified three themes: 1) The significance of information, 2) The impact of awareness; and 3) Empowerment.ConclusionsReading the treatment summaries furthered the survivors understanding of their health situation and consequently aided empowerment. A digital treatment summary, provided by knowledgeable health care professionals, may increase the self-managed care and adherence to follow-up recommendations. Further insights into e health literacy in larger samples of CCS may determine to what extent health-related information can be communicated via digital resources to this at risk population.

Highlights

  • IntroductionThe majority of childhood cancer survivors (CCS) will experience late complications which require follow up care, including access to their individual cancer treatment summary

  • Further insights into e health literacy in larger samples of cancer survivor (CCS) may determine to what extent health-related information can be communicated via digital resources to this at risk population

  • This study aims to 1) examine the impact of viewing and understanding a personalized digital treatment summary and follow-up recommendations on CCSs’ health awareness, 2) explore E health literacy among the survivors and 3) determine self-reported survivorship experiences and health care visits

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Summary

Introduction

The majority of childhood cancer survivors (CCS) will experience late complications which require follow up care, including access to their individual cancer treatment summary. Reports indicate that 70–90% of CCS will experience one or several late complications due to cancer treatment, resulting in excess morbidity and mortality compared to gender matched controls [3, 4]. These complications require regular follow-up care to preserve health, improve quality of life and increase empowerment [5]. In addition to the follow-up care at the hospital and a long-term relationship with qualified healthcare professionals, the survivors need education about their diagnosis, treatment history and follow-up plans, including access to their individual cancer treatment summary

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