Evaluation of health-related quality of life and its domains in pediatric patients with cancer.

Mai Sabry Saleh, Asmaa Mahmoud Mohammed, Dina Bassiouni, Hend Helmy Mostafa, Zeinab Mohammed Monir
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Abstract

Background: Health-related quality of life has emerged as a significant component in pediatric oncology research during the last several decades. Measures of health-related quality of life provide a thorough assessment of the child's response to medical therapy, disease course, and adjustment outcomes in the context of pediatric oncology.

Methods: The aim of the present study was to assess the cancer-specific health-related quality of life in cancer pediatric patients and to evaluate the contribution of its domains and some of the anthropometric, sociodemographic, and treatment-related variables on the overall quality of life, by using the PedsQL™ 3.0 Cancer Module.

Results: The study included 110 cases. The mean value of the PedsQL™ 3.0 Cancer Module score was 49.3 ± 12.0. The lowest mean score of quality of life was for the "procedure anxiety" (8.7 ± 23.9), followed by the "worry" domains (16.6 ± 28.5). Higher "frequency of hospital visits" was associated with increased feeling of pain and treatment anxiety yet decrease in suffering from nausea and vice versa. The longer period of hospital admission for more than half of the recommended treatment period was associated with reduced pain suffering on the expense of increase in feeling of worry as well as communication problems. The perceived physical appearance was better among those patients who spent a treatment period for 3-6 months when compared to those who spent a treatment period less than 3 months or more than 6 months. There was a highly significant association between all the eight-cancer-specific quality-of-life domains except the pain domain- and the overall quality-of-life log scores. Nausea problem followed by worry and cognitive problems was the most effective domains on the overall quality-of-life score.

Conclusion: Cancer pediatric patients suffered low quality of life especially for anxiety procedure and worry domains with special consideration for the impact of nausea, worry, and cognitive problems on their perception of quality of life.

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儿童癌症患者健康相关生活质量及其领域的评估
背景:在过去的几十年里,与健康相关的生活质量已经成为儿科肿瘤学研究的一个重要组成部分。与健康相关的生活质量的测量提供了一个全面的评估儿童对药物治疗的反应,疾病过程,并在儿童肿瘤学的背景下调整结果。方法:本研究的目的是通过使用PedsQL™3.0癌症模块,评估癌症儿童患者的癌症特异性健康相关生活质量,并评估其域和一些人体测量学、社会人口学和治疗相关变量对整体生活质量的贡献。结果:纳入病例110例。PedsQL™3.0癌症模块评分的平均值为49.3±12.0。生活质量平均得分最低的是“程序焦虑”(8.7±23.9)分,其次是“担忧”(16.6±28.5)分。较高的“就诊频率”与疼痛感和治疗焦虑感增加有关,但恶心感减少,反之亦然。住院时间越长,超过推荐治疗时间的一半,就越能减轻疼痛,但代价是焦虑感和沟通问题增加。治疗期为3-6个月的患者与治疗期小于3个月或大于6个月的患者相比,其感知的身体外观更好。除疼痛外,所有八个癌症特异性生活质量领域与总体生活质量日志得分之间存在高度显著的关联。恶心问题紧随其后的是担忧和认知问题,这是总体生活质量得分中最有效的领域。结论:儿童癌症患者的生活质量较低,特别是在焦虑过程和担忧领域,特别要考虑恶心、担忧和认知问题对他们生活质量感知的影响。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
46
审稿时长
11 weeks
期刊介绍: As the official publication of the National Cancer Institute, Cairo University, the Journal of the Egyptian National Cancer Institute (JENCI) is an open access peer-reviewed journal that publishes on the latest innovations in oncology and thereby, providing academics and clinicians a leading research platform. JENCI welcomes submissions pertaining to all fields of basic, applied and clinical cancer research. Main topics of interest include: local and systemic anticancer therapy (with specific interest on applied cancer research from developing countries); experimental oncology; early cancer detection; randomized trials (including negatives ones); and key emerging fields of personalized medicine, such as molecular pathology, bioinformatics, and biotechnologies.
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