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Reacting to an Emerging Safety Threat: West Nile Virus in North America

机译:对新兴的安全威胁作出反应:北美的西尼罗河病毒

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West Nile virus (WNV) entered North America in 1999 and in 2002 was shown to be transfusion transmitted. With competent mosquito and bird vectors throughout the United States and Canada, WNV clinical disease continues at epidemic proportions. Due to these facts, blood donor screening was implemented prior to the 2003 mosquito season and occurs using a variety of strategies. A combination of minipool (MP) nucleic acid amplification testing (NAT) during the " non-season," coupled with the conversion tothe more sensitive individual donation (ID) NAT in epidemic locations during epidemic times, has been successful in detecting approximately 1500 infected blood donors. Assuming that each donation was infectious and manufactured into 1.45 blood components, testing has therefore prevented close to 2200 recipient infections and potential clinical disease. During this same time, transfusion transmission has occurred from seven MP NAT-nonreactive/ID NAT-reactive units (6 in 2003 and 1 in 2004), or a total of 30 transfusion transmitted cases since WNV has been identified in North America. Because WNV occurs in infected blood donors at low concentrations (i.e., lower viral loads than HIV or HCV with the highest viral load of 580,000 copies/ml observed in a blood donor), a trigger strategy that is used in most of the US consisting of two NAT-reactive donations detected by MP NAT and a frequency of 1:1000 or greater has been developed. Since the full implementation of the MP to ID NAT trigger strategy, therehave been no documented WNV transfusion transmissions. Because WNV is an acute infection that only occurs seasonally, other strategies have been proposed, such as seasonal testing, which has been implemented successfully in Canada (Quebec), coupled witha screening question used in the " non-season" of whether the donor has been in the US during the past 56 days; if so, WNV NAT is performed. WNV is an example of an emergent agent in which a rapid series of interventions has been successful in controlling transmission through blood transfusion.
机译:西尼罗河病毒(WNV)于1999年进入北美,并于2002年显示出输血。在美国和加拿大各地的蚊子和鸟类传染媒介,WNV临床疾病在流行性比例中持续存在。由于这些事实,在2003年蚊子季节之前实施了献血者筛查,并使用各种策略发生。 MiniPool(MP)核酸扩增检测(NAT)在“非季节”中的组合与疫情在流行病时的流行病地区的转​​化率更敏感的单独捐赠(ID)NAT,一直在检测约1500个感染献血者。假设每种捐赠都是传染性的,并制造成1.45血液成分,因此防止了检测接近2200个受体感染和潜在的临床疾病。在此同时,输血传输已经发生在七个MP NAT-NORERESCIVE / ID NAT-VATTIVE单元(2003年和2004年的1中),或者在北美已识别出WNV以来的总输血传输案例。因为WNV在低浓度下发生感染的血液供体(即,低于HIV或HCV的病毒载荷,具有580,000拷贝/ ml的最高病毒载荷,其大多数美国的触发策略包括在内已经开发出由MP NAT检测到的两个NAT反应捐赠和1:1000或更高的频率。由于MP的完整实现为ID NAT触发策略,因此没有记录的WNV输送传输。由于WNV是一种急性感染,只有季节性地发生季节性,所以已经提出了其他策略,例如季节性测试,这些策略在加拿大(魁北克省)成功实施,耦合在捐助者的“非季节”中使用的筛选问题。在过去的56天内在美国;如果是这样,则执行WNV NAT。 Wnv是一种突出剂的一个例子,其中一系列快速的干预措施在通过输血控制传播方面取得了成功。

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