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首页> 外文期刊>Journal of Education and Health Promotion >Modification of infant hypothyroidism and phenylketonuria screening program using electronic tools
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Modification of infant hypothyroidism and phenylketonuria screening program using electronic tools

机译:使用电子工具修改婴儿甲状腺功能减退症和苯丙酮尿症筛查程序

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Background: Congenital hypothyroidism and phenylketonuria (PKU) are the most common cause for preventable mental retardation in infants worldwide. Timely diagnosis and treatment of these disorders can have lasting effects on the mental development of newborns. However, there are several problems at different stages of screening programs that along with imposing heavy costs can reduce the precision of the screening, increasing the chance of undiagnosed cases which in turn can have damaging consequences for the society. Therefore, given these problems and the importance of information systems in facilitating the management and improving the quality of health care the aim of this study was to improve the screening process of hypothyroidism and PKU in infants with the help of electronic resources. Methods: The current study is a qualitative, action research designed to improve the quality of screening, services, performance, implementation effectiveness, and management of hypothyroidism and PKU screening program in Isfahan province. To this end, web-based software was designed. Programming was carried out using Delphi.net software and used SQL Server 2008 for database management. Findings: Given the weaknesses, problems, and limitations of hypothyroidism and PKU screening program, and the importance of these diseases in a national scale, this study resulted in design of hypothyroidism and PKU screening software for infants in Isfahan province. The inputs and outputs of the software were designed in three levels including Health Care Centers in charge of the screening program, provincial reference lab, and health and treatment network of Isfahan province. Immediate registration of sample data at the time and location of sampling, providing the provincial reference Laboratory and Health Centers of different eparchies with the ability to instantly observe, monitor, and follow-up on the samples at any moment, online verification of samples by reference lab, creating a daily schedule for reference lab, and receiving of the results from analysis equipment; and entering the results into the database without the need for user input are among the features of this software. Conclusion: The implementation of hypothyroidism screening software led to an increase in the quality and efficiency of the screening program; minimized the risk of human error in the process and solved many of the previous limitations of the screening program which were the main goals for implementation of this software. The implementation of this software also resulted in improvement in precision and quality of services provided for these two diseases and better accuracy and precision for data inputs by providing the possibility of entering the sample data at the place and time of sampling which then resulted in the possibility of management based on precise data and also helped develop a comprehensive database and improved the satisfaction of service recipients.
机译:背景:先天性甲状腺功能减退症和苯丙酮尿症(PKU)是全世界婴儿可预防的智力低下的最常见原因。及时诊断和治疗这些疾病会对新生儿的心理发育产生持久影响。但是,在筛查程序的不同阶段存在若干问题,这些问题加上巨额费用会降低筛查的准确性,增加未确诊病例的机会,进而对社会造成破坏性后果。因此,鉴于这些问题以及信息系统在促进管理和改善医疗保健质量方面的重要性,本研究的目的是借助电子资源改善婴儿甲状腺功能减退症和PKU的筛查过程。方法:本研究是一项定性,行动研究,旨在提高伊斯法罕省的筛查质量,服务质量,绩效,实施效果以及甲状腺功能减退症和PKU筛查计划的管理。为此,设计了基于Web的软件。使用Delphi.net软件进行编程,并将SQL Server 2008用于数据库管理。研究结果:鉴于甲状腺功能减退症和PKU筛查程序的弱点,问题和局限性,以及这些疾病在全国范围内的重要性,本研究导致了伊斯法罕省婴儿的甲状腺功能减退症和PKU筛查软件的设计。该软件的输入和输出被设计为三个级别,包括负责筛查程序的卫生保健中心,省级参考实验室以及伊斯法罕省的健康和治疗网络。在采样的时间和地点立即注册样品数据,使不同地区的省级参考实验室和卫生中心能够随时即时观察,监视和跟踪样品,并通过参考在线验证样品实验室,为参考实验室创建每日时间表,并从分析设备接收结果;该软件的功能包括将结果输入数据库,而无需用户输入。结论:甲状腺功能减退检查软件的实施导致检查程序质量和效率的提高;最大限度地减少了过程中的人为错误风险,并解决了筛选程序以前的许多局限性,这些限制是实现该软件的主要目标。通过提供在采样地点和时间输入样本数据的可能性,该软件的实施还提高了针对这两种疾病的服务的准确性和服务质量,并提高了数据输入的准确性和准确性,从而导致了基于精确数据的管理知识,还帮助开发了一个全面的数据库并提高了服务接受者的满意度。

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