Abstract B121: Factors associated with HPV vaccination among childhood cancer survivors: Differences by Hispanic ethnicity and parental health literacy

Author(s):  
Yazmin San Miguel ◽  
Paula Aristizabal ◽  
Yesenia Avitia ◽  
Bianca P. Perdomo ◽  
Maria E. Martinez ◽  
...  
BMC Cancer ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Helena M. Linge ◽  
Cecilia Follin

Abstract Background The 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. Methods Survivors 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. Results The 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. Conclusions Reading 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.


Cancer ◽  
2021 ◽  
Author(s):  
Heather M. Brandt ◽  
Deanna Kepka ◽  
Anne C. Kirchhoff ◽  
Casey L. Daniel ◽  
Neel S. Bhatt

2020 ◽  
Author(s):  
Helena Linge ◽  
Cecilia Follin

Abstract Background: The 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. Methods Survivors 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. Results The 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. Conclusions Reading 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.


2019 ◽  
Vol 15 (7-8) ◽  
pp. 1767-1775 ◽  
Author(s):  
Anne C. Kirchhoff ◽  
Karely Mann ◽  
Echo L. Warner ◽  
Heydon K. Kaddas ◽  
Douglas Fair ◽  
...  

2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Lynda E Polgreen ◽  
Anna Petryk ◽  
Andrew C Dietz ◽  
Alan R Sinaiko ◽  
Wendy Leisenring ◽  
...  

2016 ◽  
Vol 58 (5) ◽  
pp. 331-337 ◽  
Author(s):  
Yasushi Ishida ◽  
Takashi Higaki ◽  
Mitsue Hayashi ◽  
Fumiko Inoue ◽  
Miwa Ozawa

2021 ◽  
Vol 73 ◽  
pp. 101950
Author(s):  
Claire Poulalhon ◽  
Stéphanie Goujon ◽  
Fabienne Marquant ◽  
Laure Faure ◽  
Sandra Guissou ◽  
...  

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