Emma den Hartog, Marta Fiocco, Inge M van der Sluis, Patrick van der Torre, Wim J E Tissing, Emma J Verwaaijen
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引用次数: 0
Abstract
Purpose: Acute lymphoblastic leukaemia (ALL) and its treatment cause side effects in paediatric patients which increase the risk of walking inability, limiting functional independence and quality of life. However, the incidence of walking inability, the time until onset and potential risk factors are unknown.
Methods: We retrospectively retrieved data in ALL patients (≤ 18 years). Walking inability was defined as the incompetence to walk independently from diagnosis until the end of early treatment. A Kaplan-Meier analysis was conducted to estimate the time until walking inability. To assess the effect of risk factors, we estimated a Cox regression model and performed a landmark analysis.
Results: In total, 226 patients (age median, 5.5 years; interquartile range, 3.4-11.7) were included. Walking inability was experienced by 15.0% at diagnosis and 28.3% during induction/consolidation1. Age at diagnosis (hazard ratio (HR) 0.901; 95% confidence interval (CI) 0.847-0.959) was a risk factor during induction/consolidation1. The landmark analysis at end of induction identified age at diagnosis (HR 0.898; 95% CI 0.830-0.971), delta weight-to-height Z-score (HR 0.577; 95% CI 0.410-0.812) and duration of hospitalizations (HR 1.076; 95% CI 1.005-1.152) as risk factors during consolidation1.
Conclusion: Fifteen percent experienced walking inability at diagnosis and 28.3% temporarily stopped walking during early treatment. This is concerning because walking inability leads to isolation and loss of independence. Patients with younger age, decreasing weight and longer hospitalizations during the first month of treatment were at highest risk. Informing patients and parents about the occurrence of walking inability and studies on physiotherapy and nutritional interventions are indicated.
目的:急性淋巴细胞白血病(ALL)及其治疗在儿科患者中引起副作用,增加行走能力丧失的风险,限制功能独立性和生活质量。然而,行走障碍的发生率、发病时间和潜在的危险因素尚不清楚。方法:回顾性检索所有患者(≤18岁)的资料。行走障碍被定义为从诊断到早期治疗结束不能独立行走。通过Kaplan-Meier分析来估计到无法行走的时间。为了评估危险因素的影响,我们估计了Cox回归模型并进行了里程碑式分析。结果:共226例患者(中位年龄5.5岁;四分位数范围3.4-11.7)。15.0%的患者在诊断时出现行走障碍,28.3%的患者在诱导/巩固期间出现行走障碍1。诊断年龄(风险比(HR) 0.901;95%置信区间(CI) 0.847-0.959)是诱导/巩固期间的危险因素1。诱导结束时诊断年龄的标志性分析(HR 0.898;95% CI 0.830-0.971), δ体重-身高z分数(HR 0.577;95% CI 0.410-0.812)和住院时间(HR 1.076;95% CI 1.005-1.152)为盘整期间的风险因素1。结论:15%的患者在诊断时出现行走障碍,28.3%的患者在早期治疗时暂时停止行走。这是令人担忧的,因为无法行走会导致孤立和独立性的丧失。在治疗的第一个月,年龄较小、体重下降和住院时间较长的患者风险最高。向患者和家长告知行走障碍的发生,并进行物理治疗和营养干预的研究。
期刊介绍:
Supportive Care in Cancer provides members of the Multinational Association of Supportive Care in Cancer (MASCC) and all other interested individuals, groups and institutions with the most recent scientific and social information on all aspects of supportive care in cancer patients. It covers primarily medical, technical and surgical topics concerning supportive therapy and care which may supplement or substitute basic cancer treatment at all stages of the disease.
Nursing, rehabilitative, psychosocial and spiritual issues of support are also included.