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商用沙门氏菌分组抗血清的可用性和有效性评估。

Assessment of availability and efficacy of commercial Salmonella grouping antisera.

作者信息

Evins G M, Linne L L, Colvin H M

出版信息

J Clin Microbiol. 1978 Oct;8(4):360-8. doi: 10.1128/jcm.8.4.360-368.1978.

Abstract

Salmonella somatic antisera for groups A to E were purchased from four commercial producers directly by the Center for Disease Control (CDC) and indirectly through two hospitals. CDC specifications and methods were used to evaluate antisera shipped directly to CDC. To assess the performance of the products under simulated user conditions, we used the commercial antisera purchased indirectly through the hospitals to group coded cultures. Of the 23 antisera ordered by CDC and the hospitals, the CDC received all 23, a large medical complex received 20, and a private hospital received 9. Similar results were obtained with producer and CDC test methods. Forty-five different lots of antisera were evaluated, of which 20% did not meet CDC specifications. The CDC specifications and latest revisions are discussed.

摘要

A至E组的沙门氏菌菌体抗血清由疾病控制中心(CDC)直接从四家商业生产商处购买,并通过两家医院间接购买。CDC的规格和方法用于评估直接运往CDC的抗血清。为了评估产品在模拟用户条件下的性能,我们使用通过医院间接购买的商业抗血清对编码培养物进行分组。在CDC和医院订购的23种抗血清中,CDC收到了全部23种,一家大型医疗综合机构收到了20种,一家私立医院收到了9种。生产商和CDC的测试方法得到了类似的结果。评估了45个不同批次的抗血清,其中20%不符合CDC的规格。讨论了CDC的规格和最新修订版。

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