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首页> 外文期刊>Haematologica >2nd Megma Conference on Thalassaemia & other Haemoglobinopathies Amman, Jordan, 11–12 November 2016
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2nd Megma Conference on Thalassaemia & other Haemoglobinopathies Amman, Jordan, 11–12 November 2016

机译:第二届地中海贫血症及其他血红蛋白病病虫害会议,2016年11月11日至12日,约旦安曼

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Haemoglobin disorders are a group of hereditary anaemias, which without opti- mum care, are lethal often in early childhood. In developing economies optimum care is often not provided and the result is premature death of patients, in their teens or early adulthood, who have lived the life of a chronic invalid. Such a situ- ation is an additional burden to the health economy, since all resources offered to the patients are lost before the patient can achieve any quality of life and be able to work as an independent member of society. Optimum care on the other hand has been shown to allow for a long and productive life with patients being able to integrate and contribute to society. While developing patient care services, a pro- gramme of prevention is also essential since increasing numbers of affected births will soon overwhelm the resources required for optimum care.
机译:血红蛋白异常是一类遗传性贫血,如果没有最佳护理,往往在儿童早期就致命。在发展中经济体中,通常不会提供最佳护理,其结果是使青少年或成年早期患者过早死亡,这些患者过着慢性病患者的生活。这样的局面给健康经济带来了额外的负担,因为提供给患者的所有资源在患者获得任何生活质量并能够作为独立的社会成员工作之前就已经流失了。另一方面,最佳护理已被证明可以延长患者的生产寿命,并使患者能够融入社会并为社会做出贡献。在开发患者护理服务时,预防计划也必不可少,因为越来越多的受影响的分娩会很快使最佳护理所需的资源不堪重负。

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