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首页> 外文期刊>Biosecurity and bioterrorism: Biodefense Strategy, Practice, and Science >Risk of occupationally acquired illnesses from biological threat agents in unvaccinated laboratory workers.
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Risk of occupationally acquired illnesses from biological threat agents in unvaccinated laboratory workers.

机译:未接种疫苗的实验室工作人员因生物威胁因子而患职业病的风险。

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摘要

Many vaccines for bioterrorism agents are investigational and therefore not available (outside of research protocol use) to all at-risk laboratory workers who have begun working with these agents as a result of increased interest in biodefense research. Illness surveillance data archived from the U.S. offensive biological warfare program (from 1943 to 1969) were reviewed to assess the impact of safety measures on disease prevention (including biosafety cabinets [BSCs]) before and after vaccine availability. Most laboratory-acquired infections from agents with higher infective doses (e.g., anthrax, glanders, and plague) were prevented with personal protective measures and safety training alone. Safety measures (including BSCs) without vaccination failed to sufficiently prevent illness from agents with lower infective doses in this high-risk research setting. Infections continued with tularemia (average 15/year), Venezuelan equine encephalitis (1.9/year), and Q fever (3.4/year) but decreased dramaticallyonce vaccinations became available (average of 1, 0.6, and 0 infections per year, respectively). While laboratory-acquired infections are not expected to occur frequently in the current lower-risk biodefense research setting because of further improvements in biosafety equipment and changes in biosafety policies, the data help to define the inherent risks of working with the specific agents of bioterrorism. The data support the idea that research with these agents should be restricted to laboratories with experience in handling highly hazardous agents and where appropriate safety training and precautions can be implemented.
机译:由于针对生物防御研究的兴趣增加,许多用于生物恐怖分子制剂的疫苗仍处于研究阶段,因此并非对所有有风险的实验室工作人员可用(在研究方案使用范围之外)。审查了从美国进攻性生物战计划(1943年至1969年)存档的疾病监测数据,以评估可获得疫苗之前和之后安全措施对疾病预防的影响(包括生物安全柜[BSC])。仅通过个人防护措施和安全培训就可以防止大多数实验室获得的感染剂量较高的病原体(例如炭疽,腺体和鼠疫)感染。在这种高风险的研究环境中,未进行疫苗接种的安全措施(包括BSC)未能充分预防感染剂量较低的药物引起的疾病。感染持续伴有妥拉血病(平均15 /年),委内瑞拉马脑炎(1.9 /年)和Q发热(3.4 /年),但一旦接种疫苗后感染率急剧下降(每年分别平均1、0.6和0次感染)。由于生物安全设备的进一步改进和生物安全政策的变化,在当前较低风险的生物防御研究环境中,预计实验室感染不会频繁发生,但这些数据有助于确定与特定的生物恐怖主义行为者合作的固有风险。数据支持这样的想法,即应将这些试剂的研究仅限于在处理高危试剂方面有经验的实验室,并在适当的地方进行安全培训和预防措施。

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