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タイトル: | Comparison of Psychological Quality of Life Between Long-term Survivors of Childhood Cancer and Their Families |
著者: | Shinohara, Yuki Morino, Tappei Shimoura, Kanako Niu, Qian Mukaiyama, Kohei Chen, Changyu Matsumura, Natsuki Shimizu, Hiroki Tabata, Ami Hanai, Akiko Nagai-Tanima, Momoko Ogawa, Masahiro Kato, Toshihiro Tanimukai, Hitoshi Matsuoka, Mari Adachi, Souichi Takita, Junko Tsuboyama, Tadao Aoyama, Tomoki |
著者名の別形: | 篠原, 有紀 森野, 達平 下浦, 佳南子 牛, 茜 向山, 耕平 松村, 奈都季 清水, 博己 田畑, 阿美 華井, 明子 谷間, 桃子 小川, 真寛 加藤, 寿宏 谷向, 仁 松岡, 真里 足立, 壯一 滝田, 順子 坪山, 直生 青山, 朋樹 |
キーワード: | survivors of childhood cancer follow-up care psychosocial support system squality of life family caregivers |
発行日: | 14-Jun-2023 |
出版者: | Mary Ann Liebert Inc |
誌名: | Journal of Adolescent and Young Adult Oncology |
巻: | 12 |
号: | 3 |
開始ページ: | 297 |
終了ページ: | 302 |
抄録: | [Purpose:] Although treatment outcomes for childhood cancer have improved in recent years, some patients continue to experience physical symptoms and psychological stress several years after the end of treatment. This study aimed to examine the correlation between the quality-of-life (QOL) scores of childhood cancer survivors (CCSs) aged 18–39 and (1) their families and (2) the time since the end of treatment. [Methods:] Measuring the QOL of CCSs attending the long-term follow-up (LTFU) and those of their families. The Short-Form Health Survey (SF-36) was used for CCSs and the Caregiver Quality of Life Index-Cancer (CQOLC) for their families. Spearman's rank correlation analyses were used to examine the relationship between the CCSs' and their families' QOL and the time since the end of treatment. [Results:] Twenty-nine CCSs (mean age, 24.2 years; mean the time since the end of treatment, 13.9 years), each paired with one family member, were included. Time since the end of treatment was positively correlated with the CCSs' QOL on the physical component score (ρ = 0.42, p = 0.03) and negatively correlated with mental health (MH) (ρ = −0.50, p = 0.01), a subscale of the mental component score (MCS). Furthermore, the CCSs' QOL on the MCS was positively correlated with their families' QOL scores (ρ = 0.58, p < 0.01). [Conclusion:] Psychological stress may persist in CCSs long after treatment, even when physical symptoms improve. Therefore, it is necessary to establish a comprehensive support system for the LTFU of CCSs, including MH care and QOL monitoring for patients and their families. |
著作権等: | This is the accepted version of the following article: [Yuki Shinohara, Tappei Morino, Kanako Shimoura, Qian Niu, Kohei Mukaiyama, Changyu Chen, Natsuki Matsumura, Hiroki Shimizu, Ami Tabata, Akiko Hanai, Momoko Nagai-Tanima, Masahiro Ogawa, Toshihiro Kato, Hitoshi Tanimukai, Mari Matsuoka, Souichi Adachi, Junko Takita, Tadao Tsuboyama, and Tomoki Aoyama. Comparison of Psychological Quality of Life Between Long-Term Survivors of Childhood Cancer and Their Families. Journal of Adolescent and Young Adult Oncology 2023 12:3, 297-302.], which has now been formally published in final form at Journal of Adolescent and Young Adult Oncology at https://doi.org/10.1089/jayao.2021.0217. This original submission version of the article may be used for non-commercial purposes in accordance with the Mary Ann Liebert, Inc., publishers’ self-archiving terms and conditions. This is not the published version. Please cite only the published version. この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。 |
URI: | http://hdl.handle.net/2433/283348 |
DOI(出版社版): | 10.1089/jayao.2021.0217 |
PubMed ID: | 35969380 |
出現コレクション: | 学術雑誌掲載論文等 |
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