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家长对儿科癌症治疗后未来受限风险的理解。

Parent understanding of the risk of future limitations secondary to pediatric cancer treatment.

机构信息

Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.

Division of Population Sciences, Dana-Farber Cancer Institute, Boston, Massachusetts.

出版信息

Pediatr Blood Cancer. 2018 Jul;65(7):e27020. doi: 10.1002/pbc.27020. Epub 2018 Mar 30.

Abstract

BACKGROUND

Parents and physicians may have different understandings of a child's risk of future limitations due to cancer or cancer treatment. We evaluated alignment between parent- and physician-estimated risk of late effects.

METHODS

We surveyed 352 parents of children with cancer within 12 weeks of diagnosis, and the children's oncologists, at Dana-Farber/Boston Children's Cancer and Blood Disorders Center and Children's Hospital of Philadelphia. We assessed parent and physician estimations of the child's risk of future limitations in physical abilities, intelligence, or quality of life (QOL) due to cancer treatment. Physician-estimated risk of limitations ≥50% was considered high risk.

RESULTS

Physicians considered 22% of children at high risk of physical impairments, 9% at high risk for impaired intelligence, and 6% at high risk for impaired QOL. Among high-risk children, 38% of parents recognized this risk in physical abilities, 21% in intelligence, and 5% in QOL. In multivariable analysis, parental understanding of risk, defined as concordant parent and physician estimates, was greater among parents of children at lower risk of future limitations (odds ratio 2.59; 95% confidence interval 1.35-4.96). Regardless of risk, 92% of parents considered it very/extremely important to receive information about potential health implications of cancer treatment.

CONCLUSIONS

Although most parents want information about life after cancer, most parents of children at high risk of future impairment do not recognize this risk. Strategies to improve communication about late effects throughout pediatric cancer treatment should prioritize meeting information needs and improving parent understanding of the risk of impairment.

摘要

背景

父母和医生可能对孩子因癌症或癌症治疗而未来出现身体受限的风险有不同的理解。我们评估了父母和医生对晚期影响风险的估计是否一致。

方法

我们在诊断后 12 周内在丹娜-法伯/波士顿儿童癌症和血液疾病中心和费城儿童医院调查了 352 名癌症患儿的父母,以及他们的肿瘤医生。我们评估了父母和医生对孩子因癌症治疗而未来在身体能力、智力或生活质量(QOL)方面出现受限的风险估计。医生估计的限制风险≥50%被认为是高风险。

结果

医生认为 22%的孩子有身体损伤的高风险,9%的孩子有智力受损的高风险,6%的孩子有 QOL 受损的高风险。在高风险儿童中,38%的父母认识到身体能力方面的风险,21%的父母认识到智力方面的风险,5%的父母认识到 QOL 方面的风险。在多变量分析中,父母对风险的理解,定义为父母和医生的估计一致,在未来有较低限制风险的孩子的父母中更高(优势比 2.59;95%置信区间 1.35-4.96)。无论风险如何,92%的父母认为了解癌症治疗潜在健康影响的信息非常/极其重要。

结论

尽管大多数父母都希望了解癌症治疗后的生活,但大多数未来有身体损伤高风险的孩子的父母并没有认识到这种风险。在整个儿科癌症治疗过程中改善关于晚期影响的沟通的策略应优先满足信息需求,并提高父母对损伤风险的理解。

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