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首页> 外文期刊>Online Journal of Public Health Informatics >Validating Syndromic Data for Opioid Overdose Surveillance in Florida
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Validating Syndromic Data for Opioid Overdose Surveillance in Florida

机译:验证佛罗里达州阿片类药物过量监测的综合征数据

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Objective Assess the validity of Florida (FL) Enhanced State Opioid Overdose Surveillance (ESOOS) non-fatal syndromic case definitions. Introduction In 2017, FL Department of Health (DOH) became one of thirty-two states plus Washington, D.C funded by the Center for Disease Control and Prevention (CDC) under the ESOOS program. One of the objectives of this funding was to increase the timeliness of reporting on non-fatal opioid overdoses through syndromic surveillance utilizing either the emergency department (ED) or Emergency Medical Services (EMS) data systems. Syndromic case validation is an essential requirement under ESOOS for non-fatal opioid-involved overdose (OIOD). FL’s ESOOS program conducted OIOD validation and quality monitoring of EMS case definitions, using data from FL’s Emergency Medical Services Tracking and Reporting System (EMSTARS). We examined measurement validity with OIOD cases identified from FL’s statewide hospital billing database, FL Agency for Health Care Administration (AHCA). Methods From FL-EMSTARS, we extracted EMS data where the type of service requested was a 911 response, the patient was treated then transported by EMS to a hospital facility in Florida and was 11 years of age or older. Additionally, all incident-patient encounters excluded those who were dead at the scene. We included all responses with dispatch dates between January 1, 2016, and December 31, 2016. From FL-AHCA, we extracted ED and inpatient discharge information with admission dates and patient age covering the same ranges as our EMS encounters. We classified FL-EMSTARS cases based on combinations, like that of Rhode Island, 1 using providers primary impression (PPI), providers secondary impression (PSI) and response to the administration of naloxone. FL-AHCA cases were defined by the following T and F codes from the International Classification of Diseases 10: T40.0-T40.4, T40.60, T40.69, F11.12, F11.120, F11.121, F11.122, F11.129, F11.22, F11.220, F11.221, F11.222, F11.229, F11.92, F11.920, F11.921, F11.922, F11.929. For all “T” codes, the 6 th character was either a “1” or “4,” because ESOOS is focused on unintentional and undetermined drug overdoses, ergo we excluded ED visits that are related to intentional self-harm (i.e., “2”) or assault (i.e., “3”). Lastly, for all “T” codes, the 7 th character we included was the initial ED encounter (i.e., “A”) because the purpose of the system is to capture increases or decreases in acute overdoses. To improve our match rate, account for typographical errors, and account for the discriminatory power some values may contain, we employed probabilistic linkage using Link Plus software developed by the CDC Cancer Division. Blocking occurred among social security number (SSN), event date, patient age in years, and date of birth (DOB). Next, we matched both datasets on ten variables: event date, age, sex, DOB, ethnicity, facility code, hospital zip code, race, SSN, and patient’s residence zip code. Further pruning was performed to ensure all matches were within a 24-hour time interval. Data management and statistical analyses were performed using SAS? statistical software, version 9.4 (SAS Institute Inc., Cary, NC, USA). We assessed EMS measurement validity by sensitivity, specificity, and positive predictive value (PPV). Next, risk factors were identified by stepwise multivariable logistic regression to improve the accuracy of the FL-ESOOS definition. Significant risk factors from the parsimonious multivariable model were used to simulate unique combinations to estimate the maximum sensitivity and PPV for OIOD. Results Prior to merging, FL-EMSTARS contained 1,308,825 unique incident-patient records, where FL-AHCA contained 8,862,566 unique incident-patient records. Of these, we conservatively linked 892,593 (68.2%) of the FL-EMSTARS dataset with FL-AHCA. Our probabilistic linkage represents an 18.2% linkage improvement over previous FL-DOH deterministic strategies (J Jiang, unpublished CSTE presentation, 2018). Among the matched pairs we estimated 8,526 OIOD, 0.96% prevalence, using the FL-AHCA case definition. Whereas the FL-ESOOS syndromic case definition estimated 6,188 OIOD, 0.69% prevalence. The FL-ESOOS OIOD syndromic case definition demonstrated 31.64% sensitivity, 99.61% specificity, and 43.60% PPV. Among false negatives, the response to administrated naloxone among OIOD was 39.37% “not known,” 37.95% “unchanged,” and 0.28% “worse.” We altered the FL-ESOOS EMSTARS case definition for OIOD to include those who were administered naloxone regardless of their response to the medication. We observed 12.37% sensitivity increase to 44.01%, 0.56% specificity decrease to 99.05%, and 12.78% PPV decrease to 30.82%. Are final multivariable model is as follows: lnOdds(Opioid Overdose)= 12.66 – 0.5459(Med Albuterol) – 0.9568(Med Aspirin) – 0.5765(Med Midazolam Hydrochloride) – 0.8690(Med Morphine Sulfate) + 1.4103 (Med Naloxone) – 0.7694(Med Nitroglycerine) + 0.3622(Med Ox
机译:目的评估佛罗里达州(FL)增强型阿片类药物过量监测(ESOOS)非致命综合征病例定义的有效性。简介2017年,佛罗里达州卫生部(DOH)成为美国疾病控制与预防中心(CDC)资助,由ESOOS计划资助的32个州以及华盛顿特区之一。这笔资金的目的之一是通过利用急诊科(ED)或急诊医疗服务(EMS)数据系统进行症状监测来提高非致命类鸦片药物过量报告的及时性。根据ESOOS,对于非致死性阿片类药物过量(OIOD),有症状的病例验证是一项基本要求。 FL的ESOOS计划使用了FL的紧急医疗服务跟踪和报告系统(EMSTARS)的数据,对EMS案例定义进行了OIOD验证和质量监控。我们检查了从佛罗里达州全州医院帐单数据库FL卫生保健管理局(AHCA)确定的OIOD病例的测量有效性。方法我们从FL-EMSTARS中提取了EMS数据,其中所请求的服务类型为911响应,对该患者进行了治疗,然后通过EMS将其运送到佛罗里达州的一家医院,年龄在11岁以上。此外,所有与病人接触的事件都排除了那些在现场死亡的人。我们包括了所有在2016年1月1日至2016年12月31日期间的回复。从FL-AHCA中,我们提取了ED和住院出院信息,其入院日期和患者年龄与EMS遇到的范围相同。我们根据组合对FL-EMSTARS病例进行了分类,例如使用供应商的主要印象(PPI),服务商的次要印象(PSI)和对纳洛酮的治疗反应,对罗得岛州的病例进行了分类。 FL-AHCA病例是根据国际疾病分类10中的以下T和F代码定义的:T40.0-T40.4,T40.60,T40.69,F11.12,F11.120,F11.121,F11 .122,F11.129,F11.22,F11.220,F11.221,F11.222,F11.229,F11.92,F11.920,F11.921,F11.922,F11.929。对于所有“ T”代码,第6个字符要么是“ 1”,要么是“ 4”,因为ESOOS着重于无意和不确定的药物过量,因此,我们排除了与故意自残有关的ED访问(即“ 2”)或攻击(即“ 3”)。最后,对于所有“ T”代码,我们包括的第7个字符是最初的ED遭遇(即“ A”),因为该系统的目的是捕获急性过量的增加或减少。为了提高匹配率,解决印刷错误,并考虑某些值可能包含的歧视能力,我们使用了由CDC Cancer Division开发的Link Plus软件进行概率链接。在社会安全号码(SSN),事件日期,以年为单位的患者年龄和出生日期(DOB)之间发生了阻止。接下来,我们将两个数据集匹配到十个变量:事件日期,年龄,性别,DOB,种族,机构代码,医院邮政编码,种族,SSN和患者的住所邮政编码。进行进一步修剪以确保所有匹配都在24小时的时间间隔内。数据管理和统计分析使用SAS?统计软件,版本9.4(SAS Institute Inc.,美国北卡罗来纳州卡里)。我们通过敏感性,特异性和阳性预测值(PPV)评估了EMS测量的有效性。接下来,通过逐步多变量logistic回归确定风险因素,以提高FL-ESOOS定义的准确性。来自简约多变量模型的重要风险因素用于模拟唯一组合,以估计OIOD的最大敏感性和PPV。结果合并之前,FL-EMSTARS包含1,308,825个独特的事件记录,其中FL-AHCA包含8,862,566个独特的事件记录。其中,我们将FL-EMSTARS数据集的892,593(68.2%)与FL-AHCA保守地关联起来。与以前的FL-DOH确定性策略相比,我们的概率关联表示关联改进了18.2%(J Jiang,未发表的CSTE演示文稿,2018年)。在配对中,使用FL-AHCA病例定义,我们估计了8,526个OIOD,患病率为0.96%。而FL-ESOOS综合征病例定义估计为6,188 OIOD,患病率为0.69%。 FL-ESOOS OIOD综合征病例定义显示出31.64%的敏感性,99.61%的特异性和43.60%的PPV。在假阴性中,在OIOD中,对纳洛酮给药的反应为“未知”为39.37%,“未改变”为37.95%,“更差”为0.28%。我们更改了OIOD的FL-ESOOS EMSTARS病例定义,以包括接受纳洛酮治疗的患者,无论其对药物的反应如何。我们观察到敏感性增加了12.37%,至44.01%,特异性降低了0.56%,至99.05%,PPV降低了12.78%,至30.82%。最终的多变量模型如下:lnOdds(阿片类药物过量)= 12.66 – 0.5459(Med Albuterol)– 0.9568(Med阿司匹林)– 0.5765(Med Midazolam盐酸盐)– 0.8690(Med吗啡硫酸盐)+ 1.4103(Med纳洛酮)– 0.7694(Med吗啡)硝酸甘油)+ 0.3622(Med Ox)

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