Newborn Screening in a Pandemic-Lessons Learned.

IF 4 Q1 GENETICS & HEREDITY
Matej Mlinaric, James R Bonham, Viktor Kožich, Stefan Kölker, Ondrej Majek, Tadej Battelino, Ana Drole Torkar, Vanesa Koracin, Dasa Perko, Ziga Iztok Remec, Barbka Repic Lampret, Maurizio Scarpa, Peter C J I Schielen, Rolf H Zetterström, Urh Groselj
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Abstract

The COVID-19 pandemic affected many essential aspects of public health, including newborn screening programs (NBS). Centers reported missing cases of inherited metabolic disease as a consequence of decreased diagnostic process quality during the pandemic. A number of problems emerged at the start of the pandemic, but from the beginning, solutions began to be proposed and implemented. Contingency plans were arranged, and these are reviewed and described in this article. Staff shortage emerged as an important issue, and as a result, new work schedules had to be implemented. The importance of personal protective equipment and social distancing also helped avoid disruption. Staff became stressed, and this needed to be addressed. The timeframe for collecting bloodspot samples was adapted in some cases, requiring reference ranges to be modified. A shortage of essential supplies and protective equipment was evident, and laboratories described sharing resources in some situations. The courier system had to be adapted to make timely and safe transport possible. Telemedicine became an essential tool to enable communication with patients, parents, and medical staff. Despite these difficulties, with adaptations and modifications, some centers evaluated candidate conditions, continued developments, or began new NBS. The pandemic can be regarded as a stress test of the NBS under real-world conditions, highlighting critical aspects of this multidisciplinary system and the need for establishing local, national, and global strategies to improve its robustness and reliability in times of shortage and overloaded national healthcare systems.

Abstract Image

Abstract Image

大流行中的新生儿筛查——经验教训。
COVID-19大流行影响了公共卫生的许多重要方面,包括新生儿筛查计划。各中心报告了由于大流行期间诊断过程质量下降而丢失的遗传性代谢性疾病病例。在大流行开始时出现了一些问题,但从一开始,就开始提出和实施解决办法。制定了应急计划,本文对这些计划进行了审查和描述。工作人员短缺成为一个重要问题,因此必须执行新的工作时间表。个人防护装备和保持社交距离的重要性也有助于避免混乱。工作人员感到压力,这需要加以解决。在某些情况下,对采集血点样本的时间框架进行了调整,需要修改参考范围。基本用品和防护设备的短缺是显而易见的,实验室描述了在某些情况下共享资源的情况。快递系统必须进行调整,以使及时和安全的运输成为可能。远程医疗成为实现与患者、家长和医务人员沟通的重要工具。尽管存在这些困难,通过调整和修改,一些中心评估了候选人的条件,继续发展,或开始新的NBS。此次大流行可被视为国家统计局在现实条件下的压力测试,突出了这一多学科系统的关键方面,以及建立地方、国家和全球战略的必要性,以提高其在国家卫生保健系统短缺和超载时期的稳健性和可靠性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Neonatal Screening
International Journal of Neonatal Screening Medicine-Pediatrics, Perinatology and Child Health
CiteScore
6.70
自引率
20.00%
发文量
56
审稿时长
11 weeks
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