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新生儿疾病筛查管理中常见问题与对策

机译:新生儿疾病筛查管理中常见问题与对策

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Abstract:Objective To discuss the common problems and countermeasures in the management of neonatal disease screening. Methods  The clinical data of neonatal metabolic disease screening in hospital between January 2015 and December 2015 were selected and analyzed retrospectively. Results  TSH, Phe, G6PD and 17-OHP related diseases were four of major hereditary metabolic disease in neonatal metabolic screening. The number of participants with suspicious positive response was 30 cases in the first quarter, 135 cases in the second quarter, 158 cases in the third quarter and 116 cases in the fourth quarter. The actual number of recalled patients was 28 cases, 135 cases, 150 cases, 113 cases, respectively. The number of those failed to recall for reexamination was 2 cases, 0 case, 8 cases, 3 cases. The main problems were as follows, insufficient of propaganda of health education, imperfect screening network, poor quality of blood film, inadequate training of technology, poor quality of service. Conclusion  A lot of problems still exist in the management of neonatal screening. It is required to strengthen staff training and health education, regulate the work procedures for health administrative departments at all levels of attention, so as to improve the quality of newborn screening.
机译:摘要:目的探讨新生儿疾病筛查管理中的常见问题及对策。方法回顾性分析2015年1月至2015年12月住院新生儿代谢疾病筛查的临床资料。结果TSH,Phe,G6PD和17-OHP相关疾病是新生儿代谢筛查中的四种主要遗传性代谢疾病。第一季度可疑阳性反应的参与者数量为30例,第二季度为135例,第三季度为158例,第四季度为116例。实际召回患者分别为28例,135例,150例,113例。未召回复查的人数为2例,0例,8例,3例。主要问题如下:健康教育宣传不足,筛查网络不完善,血膜质量差,技术培训不足,服务质量差。结论新生儿筛查的管理仍然存在许多问题。要加强人员培训和健康教育,规范各级卫生行政部门的工作程序,提高新生儿筛查质量。

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