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导致儿童癌症幸存者接受治疗后随访护理的因素。

Factors that contribute to post-treatment follow-up care for survivors of childhood cancer.

机构信息

Division of Oncology, The Children's Hospital of Philadelphia, 3501 Civic Center Blvd., 10303 CTRB, Philadelphia, PA 19104, USA.

出版信息

J Cancer Surviv. 2012 Jun;6(2):155-62. doi: 10.1007/s11764-011-0206-6. Epub 2011 Dec 15.

Abstract

INTRODUCTION

As children complete cancer treatment and enter survivorship, follow-up care is critical to monitor for and treat relapses, secondary malignancies, and late effects of treatment. Relative contributions of cancer and treatment variables and sociodemographic factors in engagement with follow-up care are not fully understood. This study aimed to identify risk factors for inadequate follow-up care.

METHODS

The sample included a cohort of 173 children (birth-18 years) diagnosed with cancer in 2004 and treated at a children's hospital. Sociodemographics (gender, patient current age, ethnic minority status, distance from hospital, type of insurance), cancer and treatment variables (patient age at diagnosis, type of cancer, treatment modality, time off treatment, relapse, on clinical trial protocol), and follow-up care through 2009 were gathered via the hospital tumor registry and medical charts.

RESULTS

In simultaneous linear regression analysis (full model: F(12, 160) = 3.49, R2 = 0.21, p = 0.001), having a liquid tumor (p < 0.05), presence of relapse (p = 0.009), and shorter distance from hospital (p = 0.006) predicted total number of follow-up visits between completion of treatment and 5 years post-diagnosis. In simultaneous logistic regression analysis (full model: χ2 (12, N = 173) = 53.27, p < 0.001), being male (p = 0.077), having a brain tumor (p = 0.055), longer time off treatment (p = 0.004), and greater distance from hospital (p = 0.003) decreased the likelihood of completing a follow-up or survivorship visit between completion of treatment and 5 years post-diagnosis. In simultaneous linear regression analysis (full model: F(12, 160) = 4.52, R2 = 0.25, p = 0.001), non-White race (p = 0.001) and having public insurance (p = 0.002) predicted total number of no shows between completion of treatment and 5 years post-diagnosis.

DISCUSSION/CONCLUSIONS: These results extend knowledge of health disparities in pediatric cancer follow-up care suggesting that cancer and treatment-related variables (type of cancer, relapse, number of treatment modalities) and sociodemographic factors (distance from treatment center, non-White race, public insurance) are important predictors of engagement in follow-up care.

IMPLICATIONS FOR CANCER SURVIVORS

Survivors at risk for poor engagement may benefit from targeted interventions designed to increase likelihood of follow-up care.

摘要

简介

随着儿童完成癌症治疗并进入生存阶段,随访护理对于监测复发、继发性恶性肿瘤和治疗的晚期影响至关重要。癌症和治疗变量以及社会人口因素对随访护理的参与程度的相对贡献尚不完全清楚。本研究旨在确定随访护理不足的危险因素。

方法

该样本包括 2004 年在一家儿童医院接受治疗的 173 名(出生至 18 岁)癌症患儿队列。通过医院肿瘤登记处和病历收集社会人口统计学资料(性别、患者当前年龄、少数族裔地位、与医院的距离、保险类型)、癌症和治疗变量(患者诊断时的年龄、癌症类型、治疗方式、治疗中断时间、复发、临床试验方案)和 2009 年的随访护理情况。

结果

在同时进行的线性回归分析(全模型:F(12,160)=3.49,R2=0.21,p=0.001)中,液体肿瘤(p<0.05)、复发(p=0.009)和与医院距离较短(p=0.006)预测了治疗完成后至诊断后 5 年之间的随访次数。在同时进行的逻辑回归分析(全模型:χ2(12,N=173)=53.27,p<0.001)中,男性(p=0.077)、脑肿瘤(p=0.055)、治疗中断时间较长(p=0.004)和与医院距离较远(p=0.003)降低了治疗完成后至诊断后 5 年期间完成随访或生存随访的可能性。在同时进行的线性回归分析(全模型:F(12,160)=4.52,R2=0.25,p=0.001)中,非白人种族(p=0.001)和拥有公共保险(p=0.002)预测了治疗完成后至诊断后 5 年期间的总失约次数。

讨论/结论:这些结果扩展了儿科癌症随访护理中健康差异的知识,表明癌症和治疗相关变量(癌症类型、复发、治疗方式数量)和社会人口因素(治疗中心距离、非白人种族、公共保险)是参与随访护理的重要预测因素。

对癌症幸存者的影响

有不良参与风险的幸存者可能受益于旨在增加随访护理可能性的针对性干预措施。

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