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Evaluation of the Implementation of CDC's Health Alert Related to the FDA LeadCare Recall From the State Health Department Perspective

机译:与国家卫生署视角下的FDA Leadcare Remall相关的CDC健康警报的实施

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On May 17, 2017, the Food and Drug Administration (FDA) issued a safety recall for the Magellan Diagnostics' LeadCare Testing Systems due to the potential for inaccurately low blood lead test results when used with venous blood samples. The Centers for Disease Control and Prevention (CDC) announced a health alert with retesting recommendations because those with a blood lead level of concern may have been missed and not connected to the appropriate follow-up services. A qualitative evaluation of 9 state childhood lead poisoning prevention programs' experiences is presented in this report. Interviewees reported using a variety of media and notification methods to inform key stakeholders about the recall and recommendations. Challenges experienced by programs in responding to retesting recommendations include incomplete and out-of-date lists of LeadCare users; missing or inaccurate information in their surveillance database; not having large laboratories and hospitals consider contacting persons for retesting to be within their purview; and having limited staff members to conduct emergency response activities. Two of the 9 states report subsequent challenges with their retesting rates. The retesting recommendations were generally viewed positively. The interviewees' comments provide insight into steps CDC might take to better serve state and local lead programs. Programs' experiences have led to a better understanding of the roles of their program when emergency events occur, their relationship with stakeholders as related to the blood lead testing and reporting process, and areas of improvement in surveillance databases. Public health agencies at all levels have important roles to play in preventing lead exposures and providing needed services when exposures occur. Programs may achieve long-term benefits by improving surveillance systems and having a better understanding of laboratory practices. CDC will continue to provide timely information and recommendations to state and local public health agencies to inform both routine and emergency response activities.
机译:2017年5月17日,由于与静脉血样使用时,食品和药物管理局(FDA)为Magellan Diagnostics的Leadcare测试系统发出了安全回忆,因为当与静脉血样时,由于不准确的血液铅测试结果。疾病控制和预防的中心(CDC)宣布了退休建议的健康警报,因为可能已经错过了血液领先的关注水平,并没有与适当的后续服务相关联。本报告中提出了对9州儿童铅中毒预防计划经验的定性评估。受访者报告使用各种媒体和通知方法通知关键利益相关者关于召回和建议。课程在回答重新测试建议时经历的挑战包括不完整和未婚的超出列表的超级领导者;在监视数据库中缺少或不准确的信息;没有大型实验室和医院考虑联系人以重新夺回他们的职权范围;并拥有有限的工作人员进行应急响应活动。 9个国家中的两个报告后续挑战率先。重新调整建议普遍认为是积极的。受访者的评论提供洞察力疾病疾病疾病疾病委员会的洞察力,可以采取更好的服务状态和当地主导计划。计划的经验导致在发生紧急事件发生时更好地了解他们的计划作用,与利益相关者与血铅测试和报告过程相关的关系,以及监督数据库的改进领域。各级公共卫生机构在防止铅风险和曝光时提供所需的服务具有重要作用。计划可以通过改善监视系统并更好地了解实验室实践来实现长期利益。 CDC将继续及时向州和地方公共卫生机构提供及时的信息和建议,以告知常规和应急响应活动。

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