Improving an Administrative Case Definition for Longitudinal Surveillance of Sickle Cell Disease. (May 2019)
- Record Type:
- Journal Article
- Title:
- Improving an Administrative Case Definition for Longitudinal Surveillance of Sickle Cell Disease. (May 2019)
- Main Title:
- Improving an Administrative Case Definition for Longitudinal Surveillance of Sickle Cell Disease
- Authors:
- Snyder, Angela B.
Zhou, Mei
Theodore, Rodney
Quarmyne, Maa-Ohui
Eckman, James
Lane, Peter A. - Abstract:
- Objective: Several states are building infrastructure and data collection methods for longitudinal, population-based surveillance systems for selected hemoglobinopathies. The objective of our study was to improve an administrative case definition for sickle cell disease (SCD) to aid in longitudinal surveillance. Methods: We collected data from 3 administrative data sets (2004-2008) on 1998 patients aged 0-21 in Georgia who had ≥1 encounter in which an SCD International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) code was recorded, and we compared these data with data from a laboratory and medical record review. We assessed performance (sensitivity, specificity, positive predictive value [PPV], and negative predictive value [NPV]) of case definitions that differed by number and type of SCD-coded encounters; addition of SCD-associated treatments, procedures, and complications; and length of surveillance (1 vs 5 years). We identified correct diagnoses for patients who were incorrectly coded as having SCD. Results: The SCD case definition of ≥3 SCD-coded encounters in 5 years simplified and substantially improved the sensitivity (96.0% vs 85.8%) and NPV (68.2% vs 38.2%) of the original administrative case definition developed for 5-year, state-based surveillance (≥2 encounters in 5 years and ≥1 encounter for an SCD-related treatment, procedure, or complication), while maintaining a similar PPV (97.4% vs 97.4%) and specificity (76.5% vs 79.0%).Objective: Several states are building infrastructure and data collection methods for longitudinal, population-based surveillance systems for selected hemoglobinopathies. The objective of our study was to improve an administrative case definition for sickle cell disease (SCD) to aid in longitudinal surveillance. Methods: We collected data from 3 administrative data sets (2004-2008) on 1998 patients aged 0-21 in Georgia who had ≥1 encounter in which an SCD International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) code was recorded, and we compared these data with data from a laboratory and medical record review. We assessed performance (sensitivity, specificity, positive predictive value [PPV], and negative predictive value [NPV]) of case definitions that differed by number and type of SCD-coded encounters; addition of SCD-associated treatments, procedures, and complications; and length of surveillance (1 vs 5 years). We identified correct diagnoses for patients who were incorrectly coded as having SCD. Results: The SCD case definition of ≥3 SCD-coded encounters in 5 years simplified and substantially improved the sensitivity (96.0% vs 85.8%) and NPV (68.2% vs 38.2%) of the original administrative case definition developed for 5-year, state-based surveillance (≥2 encounters in 5 years and ≥1 encounter for an SCD-related treatment, procedure, or complication), while maintaining a similar PPV (97.4% vs 97.4%) and specificity (76.5% vs 79.0%). Conclusions: This study supports an administrative case definition that specifies ≥3 ICD-9-CM–coded encounters to identify SCD with a high degree of accuracy in pediatric patients. This case definition can be used to help establish longitudinal SCD surveillance systems. … (more)
- Is Part Of:
- Public health reports. Volume 134:Number 3(2019)
- Journal:
- Public health reports
- Issue:
- Volume 134:Number 3(2019)
- Issue Display:
- Volume 134, Issue 3 (2019)
- Year:
- 2019
- Volume:
- 134
- Issue:
- 3
- Issue Sort Value:
- 2019-0134-0003-0000
- Page Start:
- 274
- Page End:
- 281
- Publication Date:
- 2019-05
- Subjects:
- surveillance -- sickle cell disease -- administrative data
Public health -- United States -- Periodicals
614.0973 - Journal URLs:
- http://purl.access.gpo.gov/GPO/LPS23348 ↗
http://www.jstor.org/journals/00333549.html ↗
http://www.publichealthreports.org/archives/archives.cfm ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=347&action=archive ↗
https://uk.sagepub.com/en-gb/eur/public-health-reports/journal202574 ↗
http://www.sagepublications.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1177/0033354919839072 ↗
- Languages:
- English
- ISSNs:
- 0033-3549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6965.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10370.xml