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Evaluation of Syndromic Surveillance for Opioid Overdose Reporting in Illinois

机译:伊利诺伊州阿片类药物过量报告的综合监测评估

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Objective To evaluate capacity of the BioSense ESSENCE platform and pre-defined overdose queries to identify emergency department admissions related to opioid overdose, in compliance with 2018 mandatory overdose reporting laws in Illinois Introduction Accuracy in identifying drug-related emergency department admissions is critical to understanding local burden of disease and assessing effectiveness of drug abuse prevention and overdose-reduction initiatives. In 2018 the Illinois Department of Public Health (IDPH) began implementation of a mandatory opioid overdose reporting law, applicable to all hospital emergency departments (ED). The mandate requires reporting of patient demographics, causal substance and antagonist ED administration within 48 hours of presentation. This reporting is not name-based. IDPH currently utilizes a near real-time syndromic surveillance (SyS) reporting system for all hospital ED, capturing most of the mandated criteria. Leveraging this existing system facilitates adherence to the mandate while imposing minimal additional burden of reporting on local hospitals. The Division of Patient Safety and Quality at IDPH has thus chosen to evaluate the completeness of overdose reporting and compliance with the opioid overdose mandate that have resulted from use of the current syndromic surveillance system. Methods Multi-level internal and external validation methods are being employed to evaluate the accuracy of opioid overdose reporting through syndromic surveillance. An initial internal evaluation compared overdoses captured using hospital discharge data (HDD) and SyS data. This analysis compared daily overdose counts in the two datasets from 166 Illinois facilities, from admissions from April 1 through June 30 2017, inclusive. The opioid overdose query from HDD referenced ICD-10 poisoning codes; SyS utilized the preset Opioid Overdose Version 1 (v1.0) query in the ESSENCE Tool from the CDC’s National Syndromic Surveillance Program’s BioSense Platform. Daily and quarterly overdose counts by surveillance method were compared and visualized by facility. Three facilities were chosen for a secondary, case-level data comparison based on: magnitude of overdose discrepancies, overall overdose burden, and availability of linked data elements. Individual overdose visits were matched across SyS and HDD datasets based on: date of birth, sex and approximate date of admit. Cases identified in SyS but missing from (1) discharge diagnosis query and (2) discharge database overall were quantified. Cases identified by HDD that were (3) not identified in the SyS overdose query or (4) missing from the SyS database entirely were also counted. Results From April 1 to June 30 2017, among the 166 providers analyzed, the HDD query identified 2,998 opioid overdose-related visits; SyS identified 3,266 (268 cases or 8.9% difference) (Figure 1, r=0.724). A total of 25 (15%) of facilities had equivalent overdose visit counts between datasets: all were among those with low case burden (13 or fewer overdose visits per facility over the quarter). Among facilities with a higher number of overdose presentations, differences in quarterly case counts (SyS minus HDD) ranged from –56 to 120. Discrepant counts were found in 85% of centers (Figure 2). HDD captured a larger number of overdoses in 93 facilities (56%). SyS captured a larger number of overdoses in 48 facilities (29%). The ten facilities with highest syndromic caseload accounted for 33% of overall case burden (1069); the ten with the highest discharge counts accounted for 29% (897 cases). However, the top ten facilities by surveillance type were notably different: the 2nd and 3rd highest using syndromic surveillance ranked 30th and 41st using discharge surveillance over the same period. The center with 5th highest caseload by discharge criteria ranked 38th using syndromic surveillance. In secondary case-level analyses: across datasets from three facilities, both HDD and SyS captured 43.5% of overdoses, while 56% were only in SyS data and 0.5% were only in HDD. Discrepancies in the all-visit (“denominator”) datasets were found, requiring follow-up with facilities directly. Conclusions Next steps in these evaluations include further characterization of cases missed differentially by syndromic and discharge surveillance. An external validation phase will engage facility staff to query the Electronic Medical Record directly. Hospital personnel will review and confirm opioid overdose events captured by SyS and hospital facilities will investigate and resolve discrepancies in data quality. These analyses have the potential to inform more accurate definitions for opioid-related overdose seen in emergency departments. Such improved surveillance can aid allocation of medication (naloxone and naltrexone), promotion of intervention (i.e. methadone-assisted treatment programs), and drug abuse prevention. Engagement of facility staff in public health surveillance has resulted i
机译:目的根据伊利诺伊州2018年强制性过量报告法律,评估BioSense ESSENCE平台的能力和预定义的过量查询以识别与阿片类药物过量有关的急诊室入院简介识别与药物有关的急诊室入院的准确性对于了解当地情况至关重要疾病负担和评估预防滥用药物和减少药物滥用举措的有效性。 2018年,伊利诺伊州公共卫生部(IDPH)开始实施适用于所有医院急诊科(ED)的强制性阿片类药物过量报告法。该任务要求在报告后的48小时内报告患者的人口统计资料,病因物质和拮抗剂ED的使用情况。此报告不是基于名称的。 IDPH当前为所有医院急诊使用近实时的综合症状监测(SyS)报告系统,捕获了大多数强制性标准。利用此现有系统有助于遵守任务规定,同时将对本地医院的报告负担最小化。因此,IDPH的患者安全与质量司选择评估过量使用药物的报告的完整性以及对由于使用当前症状监测系统而产生的阿片类药物过量使用的要求。方法采用多层次的内部和外部验证方法,通过症状监测评估阿片类药物过量报告的准确性。初步的内部评估比较了使用医院出院数据(HDD)和SyS数据捕获的过量。该分析比较了166个伊利诺伊州设施的两个数据集中的每日过量用药计数,这些数据来自2017年4月1日至6月30日(含)的入院人数。来自硬盘的阿片类药物过量查询参考了ICD-10中毒代码; SyS利用了CDC国家综合监控计划BioSense平台在ESSENCE工具中预设的阿片类药物过量版本1(v1.0)查询。通过监控方法比较每日和每季度的过量用药计数,并通过设施进行可视化。基于以下三个条件,选择了三种设施用于进行二级病例数据比较:过量用药差异的大小,过量用药的总体负担以及链接数据元素的可用性。在SyS和HDD数据集上根据以下因素对个体过量用药进行了匹配:出生日期,性别和大概入院日期。对在SyS中确定但从(1)出院诊断查询和(2)出院数据库整体中丢失的病例进行了量化。由HDD识别的病例(3)在SyS用药过量查询中未发现或(4)在SyS数据库中完全缺失的病例也被计数。结果2017年4月1日至6月30日,在分析的166家医疗服务提供者中,HDD查询确定了2,998例与阿片类药物过量相关的就诊; SyS识别出3266(268例,差异8.9%)(图1,r = 0.724)。总共25个(15%)的设施在数据集之间具有相同的过量就诊次数:所有病例负担较低(在该季度中每个设施的过量就诊13次或更少)。在过量用药次数较多的医疗机构中,每季度病例数(SyS减去HDD)的差异在–56至120之间。在85%的中心中发现了不正确的计数(图2)。 HDD在93个设施中捕获了更多的过量药物(56%)。 SyS在48个机构中捕获了更多的药物过量(29%)。十个综合症病例最多的十个机构占总病例负担的33%(1069);出院率最高的十个占了29%(897例)。但是,按监视类型排在前十位的设施明显不同:使用综合监视的第二和第三高的设施,在同期使用排泄监视的位置分别排在第30和第41。根据出院标准,病例量排在第五位的中心在综合监测中排名第38位。在二级病例级分析中:在来自三个机构的数据集中,HDD和SyS都捕获了过量的43.5%,而56%仅在SyS数据中,而0.5%仅在HDD中。发现所有访问(“分母”)数据集中的差异,需要直接跟进设施。结论这些评估的下一步包括对症候群和出院监测差异性遗漏的病例进行进一步鉴定。外部验证阶段将邀请设施工作人员直接查询电子病历。医院工作人员将审查并确认由SyS捕获的阿片类药物过量事件,医院机构将调查并解决数据质量差异。这些分析有可能为急诊科中发现的与阿片类药物相关的过量用药提供更准确的定义。这种改进的监测可以帮助分配药物(纳洛酮和纳曲酮),促进干预(即美沙酮辅助治疗方案)和预防药物滥用。设施工作人员参与公共卫生监督的结果是

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