阿尔巴尼亚β-地中海贫血患者步态评价

G. Pano
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引用次数: 0

摘要

地中海贫血是世界上最普遍的遗传性疾病之一。血红蛋白合成因地中海贫血而减少。地中海贫血患者表现出一系列骨骼问题,包括脊柱畸形、骨质减少和骨质疏松以及生长衰竭。本研究的主要目的是评估阿尔巴尼亚β-地中海贫血患者的步态和平衡。在这项研究中,来自阿尔巴尼亚三个不同流行病学城市的18名年龄在17至29岁之间的参与者(5名男性和13名女性)参加了研究。使用“T&T mediilogic medizintechnik gmbh”wi-fi鞋垫进行步态分析。“一般步态参数”,“有效脚长,左[%]”参数平均结果[67.59%],与相对规范平均值[69.7%]相比,显示出约2%的差异。此外,“有效脚长,左[%]”均值结果[65.49%]与相对规范均值[69.7%]相比,显示出约3.5%的差异。“一般步态参数”,数据比较显示,“is”和“nom”测量的“Rel双步长”、“双步持续时间”、“有效脚长右”和“步态右宽度”的变量差异有统计学意义(p<0.005)。其余变量的结果没有统计学上的显著差异。该研究的目的是评估阿尔巴尼亚地中海贫血患者的步态参数。根据“一般步态参数”的结果,数据显示平均步态线的百分比存在差异,这与鞋垫长度的有效分布有关,显示了步态不安全的特定指示。根据研究结果,步态问题是地中海贫血患者的一个重要健康问题,这很可能是由疾病相关的副作用引起的,如输血后高钙水平、肌肉量不足引起的不活动,以及所有其他与健康相关的疾病。建议将步态分析检查纳入定期健康检查。未来的研究应涉及更大的ß-地中海贫血患者,考虑到这类患者的独特状态,以更好地评估与一般静态和动态姿势问题相关的步态问题。临床医生的健康专家和康复专家在规划B-Thal康复项目时,应将步态分析检查作为常规健康检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Gait in Albanian β-thalassemia Patients
Abstract One of the most prevalent genetic diseases in the world is beta thalassemia. Hemoglobin synthesis is decreased by the blood condition beta thalassemia. Patients with thalassemia exhibit a range of bone problems, including as spinal deformities, osteopenia and osteoporosis, as well as growth failure. This study’s main goal was to evaluate gait and balance in Albanian β-thalassemia patients. In this study, 18 participants aged 17 to 29 years old (5 males and 13 females) from three distinct epidemiological cities in Albania took part. Gait analysis was performed using “T&T medilogic medizintechnik gmbh” wi-fi insoles. “General Gait Parameters”, results of the “Effective Foot Length, left [%]” parameter mean results [67.59%], reveals approx a 2% difference compared with the relative normative mean [69.7%]. Also, “Effective Foot Length, left [%]” mean results [65.49%], reveals approximately a 3.5% difference compared with the relative normative mean [69.7%]. “General Gait Parameters”, data comparisons revealed statistically significant differences between “is” and “nom.” measurements for the following variables: “Rel Double Step Length”, “Double Step Duration”, “Effective Foot Length Right” and “Width Of Gait Right” (p<0.005). Results for the rest of the variables shwed a not statistically significant difference. The aim of the study was to assess the gait parameter in Albanian individuals with thalassemia. Based on the result of the “General Gait Parameters”, data reveal a difference in the % of the average gait line which is related to effective distribution in the insole length showing a specific indication of insecure gait. According to the findings, gait issues are a significant health issue for beta thalassemia patients which are most likely caused by disease-related side-effects such high calcium levels after blood transfusions, inactivity caused by insufficient muscle mass, and all other health-related disease conditions. It is advised that the gait analysis exam to be included in their regular health check-ups. Future studies should be conducted involving larger ß-thalassemia patients take into account the unique state of this category to better evaluate the gait problems related with general static and dynamic posture problems. Clinicians’ health specialists and rehabilitation experts when planning B-Thal rehabilitation programs sholud use gait analysis exam as a regular health check-up.
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