Skip to main content

Chief Complaint

Description

The National Syndromic Surveillance Program (NSSP) is a community focused collaboration among federal, state, and local public health agencies and partners for timely exchange of syndromic data. These data, captured in nearly real time, are intended to improve the nation's situational awareness and responsiveness to hazardous events and disease outbreaks. During CDC’s previous implementation of a syndromic surveillance system (BioSense 2), there was a reported lack of transparency and sharing of information on the data processing applied to data feeds, encumbering the identification and resolution of data quality issues. The BioSense Governance Group Data Quality Workgroup paved the way to rethink surveillance data flow and quality. Their work and collaboration with state and local partners led to NSSP redesigning the program’s data flow. The new data flow provided a ripe opportunity for NSSP analysts to study the data landscape (e.g., capturing of HL7 messages and core data elements), assess end-to-end data flow, and make adjustments to ensure all data being reported were processed, stored, and made accessible to the user community. In addition, NSSP extensively documented the new data flow, providing the transparency the community needed to better understand the disposition of facility data. Even with a new and improved data flow, data quality issues that were issues in the past, but went unreported, remained issues in the new data. However, these issues were now identified. The newly designed data flow provided opportunities to report and act on issues found in the data unlike previous versions. Therefore, an important component of the NSSP data flow was the implementation of regularly scheduled standard data quality checks, and release of standard data quality reports summarizing data quality findings.

Objective:

Review the impact of applying regular data quality checks to assess completeness of core data elements that support syndromic surveillance.

Submitted by elamb on
Description

In January 2017, the NSSP transitioned their BioSense analytical tools to Electronic Surveillance System for Early Notification of Community-Based Epidemics (ESSENCE). The chief complaint field in BioSense 2.0 was a concatenation of the record's chief complaint, admission reason, triage notes, and diagnostic impression. Following the transition to ESSENCE, the chief complaint field was comprised of the first chief complaint entered or the first admission reason, if the chief complaint was blank. Furthermore, the ESSENCE chief complaint field was electronically parsed (i.e., the original chief complaint text was altered to translate abbreviations and remove punctuation). This abstract highlights key findings from Maricopa County Department of Public Health's evaluation of the new chief complaint field, its impact on heat-related illness syndromic surveillance, and implications for ongoing surveillance efforts.

Objective:

To evaluate the effect and implications of changing the chief complaint field during the National Syndromic Surveillance Program (NSSP) transition from BioSense 2.0 analytical tools to BioSense Platform ESSENCE.

Submitted by elamb on
Description

EDCC data provides an opportunity for capturing the early mental health impact of disaster events at the community level, and to track their impact over time. However, while rapid mental health assessment can facilitate a better understanding of the acute post-disaster period and aid early identification of persons at long-term risk,1 determining how wide a net to effectively capture the critical range of mental health sub-categories has not yet been clearly defined. This project creates a comprehensive set of mental health sub-category keywords, and applies them to evaluate short- and long-term trends in postHurricane Sandy mental health outcomes in New York State.

Objective

To define mental health keywords using daily hospital emergency department chief complaint (EDCC) data during and after Hurricane Sandy 2) To track short- and long-term trends in mental health EDCCs. 3) To compare mental health EDCCs in affected counties to the rest of the New York State population.

Submitted by uysz on
Description

The number of US adults who use the internet to access health information has increased from about 95 million in 2005 to 220 million in 2014. The public health impact of this trend is unknown; in theory, patients may be able to better help the doctor arrive at the correct diagnosis, but self-diagnosed patients may also inappropriately self-treat or delay going to the doctor. The current study examines trends in self-diagnoses in NYC EDs, identifies the demographic characteristics of self-diagnosed patients, and compares hospital admission rates of self-diagnosed patients with those who do not self-diagnose.

Objective

To monitor self-reported diagnosis from New York City (NYC) emergency department (ED) chief complaints (CC).

Submitted by teresa.hamby@d… on