公开(公告)号：US08938409B2

公开(公告)日：2015-01-20

申请号：US14245333

申请日：2014-04-04

Applicant: Bio-Rad Laboratories, Inc.

Inventor： Curtis Alan Parvin ,  John C. Yundt-Pacheco

IPC: G06F11/00 ,  G06F15/18 ,  G01D3/00 ,  G06F11/24 ,  G06F15/78 ,  G06N99/00

CPC classification number: G06F11/24 ,  G06F15/781 ,  G06F19/00 ,  G06N99/005 ,  G16H10/40 ,  G16H40/20

Abstract: A method analyzes a quality control strategy. A quality control rule can define quality control events and specifying a control limit for determining whether a quality control event passes or fails. The quality control rule and a number of patient samples tested between quality control events can be received. A first expected number of correctible errors when a quality control event fails can be computed based on the quality control rule and the number of patient samples tested between quality control events. A second expected number of final errors that are not correctible when a quality control event fails can be computed based on the quality control rule and the number of patient samples tested between quality control events. An assessment of the quality control rule can include the first expected number of correctible errors and the second expected number of final errors as separate values.

Abstract translation: 一种方法分析质量控制策略。 质量控制规则可以定义质量控制事件并指定用于确定质量控制事件是否通过或失败的控制限制。 可以接收质量控制规则和在质量控制事件之间测试的多个患者样本。 可以基于质量控制规则和在质量控制事件之间测试的患者样本的数量来计算质量控制事件失败时的第一预期数量的可纠正错误。 可以基于质量控制规则和在质量控制事件之间测试的患者样本的数量来计算质量控制事件失败时不可校正的最终错误的第二预期数量。 质量控制规则的评估可以包括第一预期数量的可纠正错误和第二预期数量的最终错误作为单独的值。

公开(公告)号：US20140223234A1

公开(公告)日：2014-08-07

申请号：US14245333

申请日：2014-04-04

Applicant: Bio-Rad Laboratories, Inc.

Inventor： Curtis Alan Parvin ,  John C. Yundt-Pacheco

IPC: G06F11/24

CPC classification number: G06F11/24 ,  G06F15/781 ,  G06F19/00 ,  G06N99/005 ,  G16H10/40 ,  G16H40/20

Abstract: A method analyzes a quality control strategy. A quality control rule can define quality control events and specifying a control limit for determining whether a quality control event passes or fails. The quality control rule and a number of patient samples tested between quality control events can be received. A first expected number of correctible errors when a quality control event fails can be computed based on the quality control rule and the number of patient samples tested between quality control events. A second expected number of final errors that are not correctible when a quality control event fails can be computed based on the quality control rule and the number of patient samples tested between quality control events. An assessment of the quality control rule can include the first expected number of correctible errors and the second expected number of final errors as separate values.

Abstract translation: 一种方法分析质量控制策略。 质量控制规则可以定义质量控制事件并指定用于确定质量控制事件是否通过或失败的控制限制。 可以接收质量控制规则和在质量控制事件之间测试的多个患者样本。 可以基于质量控制规则和在质量控制事件之间测试的患者样本的数量来计算质量控制事件失败时的第一预期数量的可纠正错误。 可以基于质量控制规则和在质量控制事件之间测试的患者样本的数量来计算质量控制事件失败时不可校正的最终错误的第二预期数量。 质量控制规则的评估可以包括第一预期数量的可纠正错误和第二预期数量的最终错误作为单独的值。