Developing and validating a diabetes database in a large health system

https://doi.org/10.1016/j.diabres.2006.07.007Get rights and content

Abstract

Background

One component of clinical information systems is a registry of patients. Registries allow providers to identify gaps in care at the population level. Registries also allow for rapid cycle continuous quality improvement, targeted practice change and improved outcomes. Most registries are built based on membership with an insurer or other selection criteria. Little, if any data exist on registries representing demographically heterogeneous populations.

Methods

Administrative and clinical data for the period 1/1/2000–12/30/03 were examined. In total, 46,082,941 lab reports, 233,292,544 medical records, and 9,351,415 medical record abstracts, representing approximately 2 million unique patients were searched. The diabetes source population was identified by presence of any one of the following criteria: ICD-9 code 250 (diabetes) for inpatient, emergency room or outpatient visits; any hemoglobin A1c result; blood glucose >200 mg/dl; or diabetes medication. A diagnosis of diabetes was verified by trained chart reviewers on a sample of patients. Single indicators and combinations were examined to determine optimal identification of these cases.

Results

In two separate validation studies, using two or more indicators or outpatient diagnosis maximized positive predictive value (PPV) (96 and 97%) and sensitivity (99 and 100%) and identified 55,807 individuals. When all patients with a single indicator of outpatient diagnosis (which had the highest single PPV of 94 and 95%) were included together with those having ≥2 indicators, the final sample size was 65,725.

Conclusion

Two or more indicators or an out-patient-diagnosis identifies a sizeable and unselective diabetes database which can be used to track processes and outcomes.

Introduction

There are currently 18 million people in the U.S. with diabetes. This number is expected to rise to 30.3 million people by the year 2030 [1]. Diabetes thus represents a major health burden, especially as an increase in the prevalence of diabetes complications is also anticipated, given the current level of suboptimal diabetes care in this country [2]. Diabetes therefore poses a major challenge to healthcare systems.

The Chronic Care Model [3] outlines the components of a health care delivery system that promotes quality disease management and provides a potential useful framework with which to respond to this challenge. The use of clinical information systems is a key element of this model [2], [4], [5], [6]. Information systems that contain data on the level of care, including both processes and outcomes, offer a valuable tool for health systems. These information systems allow for continuous quality improvement, practice change, and improved outcomes. However traditional systems used to track quality of care, such as chart audit or patient and provider self-report, lack internal validity, are expensive, and inefficient.

A number of diabetes registries are currently available in the United States (Table 1). They have examined key issues, including quality of care [7], sociodemographic differences in health care delivery [7], [8], [9], outcomes [10], [11], risk stratification [12], and costs [13], [14]. In general, these databases are derived from homogenous populations, defined by a health plan, insurer or membership in another group, limiting the translation of methodologies to other populations. Further, specific criteria employed to identify people with diabetes vary within these registries, making comparisons between populations and registries difficult. It would thus be helpful to develop a registry that reflects a more general population that receives diabetes care in a variety of provider settings, and includes a broad spectrum of patient demographics and insurers. It would also facilitate further study to develop a standardized method of identifying patients with diabetes, in such settings, in order to optimize estimation of cases, and comparison of findings.

With these considerations in mind, our objectives were to: (1) develop a diabetes registry using administrative and clinical data in a major health care system serving a large heterogeneous population; (2) develop a set of criteria that most reproducibly and accurately identifies people with diabetes.

Section snippets

The setting

The University of Pittsburgh Medical Center (UPMC) is a large health care system and academic medical center in western Pennsylvania. UPMC is one of the largest non-profit integrated health care systems in the United States comprised of 19 tertiary care, specialty and community hospitals, physician practices, imaging and surgery facilities, post-acute rehabilitation and in-home services, long-term care facilities, pharmacy services, a managed care health plan, and a Community Health Division.

Validation study

Results of the validation studies are displayed in Table 2. In the first validation the six screening criteria were applied to patients from three local outpatient clinics (endocrine, internal medicine, and family practice). A total of 254 charts were reviewed. In this test-population, with at least one potential indicator of diabetes, 54.6% of patients were confirmed to have diabetes. When indicators were combined, as the number of indicators increased, the PPV and specificity increased, while

Discussion

As part of our efforts to improve diabetes care in our healthcare system we developed a diabetes registry as a key first step. This project involved the unique opportunity to use currently existing administrative and clinical data representing a heterogeneous diabetic population. This registry is applicable to a broad range of ages, races, and insurers, reflective of the general diabetes population of western Pennsylvania. To the best of our knowledge, this diabetes registry is the first

References (20)

  • K.M. Newton et al.

    The use of automated data to identify complications and comorbidities of diabetes: a validation study

    J. Clin. Epidmiol.

    (1999)
  • S. Wild et al.

    Global prevalence of diabetes. estimates for the year 2000 and projections for 2030

    Diabetes Care

    (2004)
  • J.B. Saaddine et al.

    A diabetes report card for the United States: quality of care in the 1990s

    Ann. Intern. Med.

    (2002)
  • E.G. Wagner

    Meeting the needs of chronically ill people

    BMJ

    (2001)
  • Institute for Health Care Improvement, vol. 2005, Institute for Health Care Improvement,...
  • E.H. Wagner et al.

    Improving outcomes in chronic illness

    Managed Care Quarterly

    (1996)
  • E.H. Wagner et al.

    Organizing care for patients with chronic illness

    The Mill Bank Quarterly

    (1996)
  • D.R. Arday et al.

    Variation in diabetes care among states. Do patient characteristics matter?

    Diabetes Care

    (2002)
  • A.M. McBean et al.

    Racial variation in the control of diabetes among elderly medicare managed care beneficiaries

    Diabetes Care

    (2003)
  • T.L. Gary et al.

    Racial comparisons of health care and glycemic control for African American and white diabetic adults in an urban managed care organization

    Dis. Manag.

    (2004)
There are more references available in the full text version of this article.

Cited by (62)

  • The local geographic distribution of diabetic complications in New York City: Associated population characteristics and differences by type of complication

    2016, Diabetes Research and Clinical Practice
    Citation Excerpt :

    We used unique identifiers within SPARCS to identify ED visits by the same individual throughout the study period. As previously published [4], we identified any individual who had ever received a primary or secondary ICD-9 diagnosis code with the prefix 250 during any ED visit including ED admissions [14]. We used the ED patient population as our prior study demonstrated that the demographics of unique ED users is similar to Census estimates after accounting for repeat ED users.

  • Association between blood alcohol concentration and mortality in critical illness

    2015, Journal of Critical Care
    Citation Excerpt :

    Diabetes mellitus is defined by ICD-9-CM code 250. xx in the 2-years before hospital discharge [67,68]. Early ICU admission is defined as ICU admission within 48 hours of hospital admission.

View all citing articles on Scopus
View full text