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实施卑诗省先天性畸形监测系统(BCCASS)。

Implementation of the BC Congenital Anomalies Surveillance System (BCCASS).

机构信息

Office of the Provincial Health Officer, Ministry of Health, Victoria, British Columbia, Canada.

School of Health Information Science, University of Victoria, Victoria, BC, Canada.

出版信息

Can J Public Health. 2022 Jun;113(3):465-473. doi: 10.17269/s41997-021-00607-3. Epub 2022 Feb 11.

Abstract

SETTING

Congenital anomalies (CAs) can cause lifelong morbidity and accounted for 23.2% of infant deaths from 2003 to 2007. In British Columbia (BC), surveillance of CAs has been irregular since the early 2000s. To enhance CAs surveillance in BC, the Public Health Agency of Canada has provided funding for the implementation of the BC Congenital Anomalies Surveillance System (BCCASS).

INTERVENTION

BCCASS is a population-based surveillance system. The system leverages existing administrative data sources that capture information regarding vital events, disease status, drug prescription, and healthcare utilization. The system uses a series of algorithms to capture specific CAs diagnoses, some of which are further validated with the support of the Provincial Advisory Committee. This Advisory Committee is a multi-stakeholder coalition that includes the BC Office of the Provincial Health Officer, subject matter experts, data partners, users, and academia, and acts to provide support, expertise, and strategic guidance to BCCASS.

OUTCOMES

Through BCCASS, prevalence and historical trends for 35 CAs in BC are available. Information pertaining to maternal place of residence, risk, and protective factors can be used for association studies such as links to environmental hazards and cluster analysis.

IMPLICATIONS

BCCASS is a cost-effective and sustainable system that leverages existing data sources necessary to understand the overall burden of CAs across the BC population. This is fundamental to support data-driven decisions around policy development, program planning, and evaluation of preventive measures. Strong coalitions with stakeholders are instrumental to ensure successful implementation and expansion in the future.

摘要

背景

先天性异常(CA)可导致终生发病,2003 年至 2007 年占婴儿死亡人数的 23.2%。在不列颠哥伦比亚省(BC),自 21 世纪初以来,CA 的监测一直不规律。为了加强 BC 的 CA 监测,加拿大公共卫生局为实施不列颠哥伦比亚省先天性异常监测系统(BCCASS)提供了资金。

干预措施

BCCASS 是一个基于人群的监测系统。该系统利用现有的行政数据源,这些数据源可获取有关生命事件、疾病状况、药物处方和医疗保健利用的信息。该系统使用一系列算法来捕捉特定的 CA 诊断,其中一些诊断在省级咨询委员会的支持下进行了进一步验证。该咨询委员会是一个多利益相关者联盟,包括 BC 省卫生官员办公室、主题专家、数据合作伙伴、用户和学术界,为 BCCASS 提供支持、专业知识和战略指导。

结果

通过 BCCASS,可以获得 BC 35 种 CA 的患病率和历史趋势。与环境危害和聚类分析相关的母体居住地点、风险和保护因素的信息可用于关联研究。

意义

BCCASS 是一个具有成本效益和可持续性的系统,利用了了解整个 BC 人群中 CA 总体负担所需的现有数据源。这对于支持围绕政策制定、规划和评估预防措施的数据驱动决策至关重要。与利益相关者建立强大的联盟对于确保未来的成功实施和扩展至关重要。

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