The American Journal of Medicine
Volume 122, Issue 6 , Pages 550-558, June 2009

Exceptional Mortality Prediction by Risk Scores from Common Laboratory Tests

  • Benjamin D. Horne, PhD, MPH

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
    • Genetic Epidemiology Division, Department of Biomedical Informatics, University of Utah, Salt Lake City
    • Corresponding Author InformationRequests for reprints should be addressed to Benjamin D. Horne, PhD, MPH, Cardiovascular Department, Intermountain Medical Center, 5121 S. Cottonwood St, Murray, UT 84157
  • ,
  • Heidi T. May, PhD, MSPH

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
  • ,
  • Joseph B. Muhlestein, MD

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
    • Cardiology Division, Department of Internal Medicine, University of Utah, Salt Lake City
  • ,
  • Brianna S. Ronnow, MS

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
  • ,
  • Donald L. Lappé, MD

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
    • Cardiology Division, Department of Internal Medicine, University of Utah, Salt Lake City
  • ,
  • Dale G. Renlund, MD

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
    • Cardiology Division, Department of Internal Medicine, University of Utah, Salt Lake City
  • ,
  • Abdallah G. Kfoury, MD

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
  • ,
  • John F. Carlquist, PhD

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
    • Cardiology Division, Department of Internal Medicine, University of Utah, Salt Lake City
  • ,
  • Patrick W. Fisher, DO, PhD

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
  • ,
  • Robert R. Pearson, PharmD

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
    • Current address: Clinical Development and Medical Affairs, GlaxoSmithKline, 5 Moore Drive, Research Triangle Park, NC 27709.
  • ,
  • Tami L. Bair, BS

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
  • ,
  • Jeffrey L. Anderson, MD

      Affiliations

    • Cardiovascular Department, Intermountain Medical Center, Murray, Utah
    • Cardiology Division, Department of Internal Medicine, University of Utah, Salt Lake City

Abstract 

Background

Some components of the complete blood count and basic metabolic profile are commonly used risk predictors. Many of their components are not commonly used, but they might contain independent risk information. This study tested the ability of a risk score combining all components to predict all-cause mortality.

Methods

Patients with baseline complete blood count and basic metabolic profile measurements were randomly assigned (60%/40%) to independent training (N = 71,921) and test (N = 47,458) populations. A third population (N = 16,372) from the Third National Health and Nutrition Examination Survey and a fourth population of patients who underwent coronary angiography (N = 2558) were used as additional validation groups. Risk scores were computed in the training population for 30-day, 1-year, and 5-year mortality using age- and sex-adjusted weights from multivariable modeling of all complete blood count and basic metabolic profile components.

Results

Area under the curve c-statistics were exceptional in the training population for death at 30 days (c = 0.90 for women, 0.87 for men), 1 year (c = 0.87, 0.83), and 5-years (c = 0.90, 0.85) and in the test population for death at 30 days (c = 0.88 for women, 0.85 for men), 1 year (c = 0.86, 0.82), and 5 years (c = 0.89, 0.83). In the test, the Third National Health and Nutrition Examination Survey, and the angiography populations, risk scores were highly associated with death (P <.001), and thresholds of risk significantly stratified all 3 populations.

Conclusion

In large patient and general populations, risk scores combining complete blood count and basic metabolic profile components were highly predictive of death. Easily computed in a clinical laboratory at negligible incremental cost, these risk scores aggregate baseline risk information from both the popular and the underused components of ubiquitous laboratory tests.

Keywords: Basic metabolic profile, Complete blood count, Risk assessment

 

 Funding: This study was funded by internal institutional funds.

 Conflict of Interest: BDH, HTM, BSR, and JLA are named as inventors on a patent protecting the risk scores; the authors have no other potential conflicts of interest to report.

 Authorship: All authors had access to the data and played a role in writing this manuscript.

 Trial Registration: Database registry of the Intermountain Heart Collaborative Study: NCT00406185 (ClinicalTrials.gov).

PII: S0002-9343(09)00103-X

doi:10.1016/j.amjmed.2008.10.043

The American Journal of Medicine
Volume 122, Issue 6 , Pages 550-558, June 2009