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首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >Living With Classical Galactosemia: Health-Related Quality of Life Consequences
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Living With Classical Galactosemia: Health-Related Quality of Life Consequences

机译:患有典型的半乳糖血症:与健康相关的生活质量后果

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Objective. Classical galactosemia (McKusick 230400) is an autosomal recessive disorder of galactose metabolism caused by a deficiency of galactose-1-phosphate uridyltransferase (EC 2.7.712). Treatment, consisting of a severe restriction of dietary galactose, is life saving, but most patients develop abnormalities despite this diet. The aim of this study was to study the influence of galactosemia on the patients’ health-related quality of life (HRQoL), on educational levels, and on the specific galactosemia-related concerns of these families.Methods. Age-specific HRQoL questionnaires, a classical galactosemia-specific questionnaire designed by the authors, and a list of questions regarding educational attainment were handed out or sent to all 75 members of the Dutch Galactosemia Society and their families.Results. Sixty-three (84%) patients with classical galactosemia from 58 families returned the questionnaire. Concerning HRQoL, significant differences between patients aged 1 to 5 and healthy children were found on the domains of abdominal complaints and communication. Patients aged 8 to 15 years differed from their healthy peers on the domain of cognitive function. Mothers of patients aged 6 to 15 reported a significantly lower HRQoL on the domains of motor and cognitive function. Patients 16 years and older had significant lower scores on the domains of cognitive and social function. The percentage of patients who attend special schools is significantly higher than in the general population, and the educational attainment is significantly lower in patients with classical galactosemia.Conclusions. This is the first study to describe the HRQoL of patients with classical galactosemia using well-developed and validated instruments in different age groups. The results of the present study indicate that having galactosemia negatively influences the HRQoL. Early and regular evaluation and support of possible cognitive problems should be a major part of the protocol for the follow-up of patients with classical galactosemia.
机译:目的。经典的半乳糖血症(McKusick 230400)是一种由于半乳糖-1-磷酸尿嘧啶基转移酶(EC 2.7.712)缺乏引起的半乳糖代谢的常染色体隐性遗传疾病。严格限制饮食中的半乳糖饮食可以挽救生命,但是尽管如此,大多数患者仍会出现异常。这项研究的目的是研究半乳糖血症对患者健康相关生活质量(HRQoL),教育水平以及这些家庭与半乳糖血症相关的特殊关注的影响。由作者设计的针对年龄的HRQoL问卷,一份经典的针对半乳糖血症的问卷以及关于教育程度的问题清单已分发或发送给了荷兰半乳糖血症学会的所有75名成员及其家人。来自58个家庭的63名(84%)经典半乳糖血症患者返回了问卷。关于HRQoL,在腹部不适和交流方面,发现1至5岁患者与健康儿童之间存在显着差异。 8至15岁的患者在认知功能方面与健康同行不同。 6至15岁患者的母亲报告说,在运动和认知功能方面,HRQoL显着降低。 16岁及以上的患者在认知和社交功能方面得分明显较低。就读特殊学校的患者百分比显着高于普通人群,而经典半乳糖血症患者的受教育程度则明显较低。这是第一项使用成熟且经过验证的仪器在不同年龄组中描述经典半乳糖血症患者的HRQoL的研究。本研究的结果表明,半乳糖血症会对HRQoL产生负面影响。早期和定期评估以及对可能的认知问题的支持,应该是对经典半乳糖血症患者进行随访的方案的主要部分。

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