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Nutritional status of children and young adults with Ewing sarcoma or osteosarcoma at diagnosis and during multimodality therapy

机译:儿童和青少年尤文氏肉瘤或骨肉瘤在诊断和多式联运治疗期间的营养状况

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Objective: Objective of our study was to evaluate the nutritional status and growth of children and adolescents with common malignancies of the musculoskeletal system at diagnosis, and undergoing multimodality therapy. Methods: A retrospective analysis of data from 2001 to 2009 was conducted. Hospital charts were used as a source of clinical data. Primary endpoint of the analyses was to identify variations in anthropometric parameters at diagnosis and during the first 2 years of follow-up in children and adolescents with osteosarcoma or Ewing sarcoma. Factors contributing to disorders of growth in this population were sought. Results: A total of 139 children were registered, 62 with Ewing sarcoma and 77 with osteosarcoma. At diagnosis 72.7% of all patients were classified as adequately nourished (BMI 5th to <85th percentiles). During treatment all anthropometric parameters were markedly reduced (P<0.001) in both groups with extreme changes in body weight from -30% to +44%. This was pronounced in children affected by osteosarcoma (P<0.05). During follow-up, recovery of body weight was noted in both groups. Height Z-scores remained low (P<0.001) in comparison to the general population. After the observation period 43.4% of the children with osteosarcoma and 25.5% of the patients with Ewing sarcoma demonstrated an altered body mass. Conclusions: Pediatric patients with Ewing sarcoma or osteosarcoma are at an increased risk for developing malnutrition, in the form of either over- or underweight during multimodality therapy. Early recognition of abnormal body mass is required to prevent and to treat long-term comorbidities caused by malnutrition. Pediatr Blood Cancer 2012;59:621-626.
机译:目的:本研究的目的是评估诊断为肌肉骨骼系统常见恶性肿瘤并接受多模式治疗的儿童和青少年的营养状况和生长情况。方法:对2001年至2009年的数据进行回顾性分析。医院图表被用作临床数据的来源。分析的主要终点是确定患有骨肉瘤或尤因肉瘤的儿童和青少年在诊断时和随访的前2年中人体测量学参数的变化。寻找了导致该人群生长障碍的因素。结果:总共登记了139名儿童,其中62名患有尤因肉瘤,77名患有骨肉瘤。在诊断时,所有患者中有72.7%被归类为营养充足(BMI在第5至第85个百分位)。在治疗期间,两组的所有人体测量学参数均显着降低(P <0.001),体重从-30%急剧变化至+ 44%。这在受骨肉瘤影响的儿童中尤为明显(P <0.05)。在随访期间,两组均发现体重有所恢复。与一般人群相比,身高Z值仍然较低(P <0.001)。观察期后,有43.4%的骨肉瘤儿童和25.5%的尤因肉瘤患者表现出体重改变。结论:尤因肉瘤或骨肉瘤的小儿营养不良的风险增加,在多模式治疗期间体重过轻或过轻。需要早期发现体重异常,以预防和治疗营养不良引起的长期合并症。 Pediatr Blood Cancer 2012; 59:621-626。

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