The Effect of Adding Comorbidities to Current Centers for Disease Control and Prevention Central-Line-Associated

Sarah S Jackson1, Surbhi Leekha1, Laurence S Magder1

  • 11Department of Epidemiology and Public Health,University of Maryland School of Medicine,Baltimore,Maryland.

Insights

Improving central-line-associated bloodstream infection (CLABSI) risk adjustment is crucial for fair hospital comparisons. Incorporating patient comorbidities significantly enhances the accuracy of CLABSI rate predictions.

Area of Science:

  • Healthcare Quality Improvement
  • Infectious Disease Epidemiology
  • Health Services Research

Background:

  • Accurate risk adjustment is essential for comparing hospital-acquired infection rates, specifically central-line-associated bloodstream infections (CLABSI).
  • Current Centers for Disease Control and Prevention (CDC) methodologies for CLABSI risk adjustment have limitations, primarily focusing on intensive care unit (ICU) type, hospital size, and medical school affiliation.

Purpose of the Study:

  • To evaluate the effectiveness of incorporating patient demographics and comorbidities, extracted from electronic hospital discharge codes, into risk adjustment models for CLABSI rates.
  • To compare the discriminatory power of a new risk-adjustment model against the existing CDC methodology.

Main Methods:

  • A cohort study analyzed data from 85,849 ICU patients across 22 hospitals between January 2012 and December 2013.
  • CLABSIs were identified by infection preventionists, and patient data, including International Classification of Diseases, Ninth Edition, Clinical Modification (ICD-9-CM) codes, were collected.
  • Two models were compared: one adjusting for ICU type alone, and another incorporating ICU type plus patient case-mix (demographics and comorbidities). Model performance was assessed using C statistics and changes in hospital rankings based on standardized infection ratios (SIRs).

Main Results:

  • The inclusion of patient comorbidities (coagulopathy, paralysis, renal failure, malnutrition, and age) significantly improved the risk-adjustment model's predictive ability (C statistic increased from 0.55 to 0.64).
  • Hospital rankings based on SIRs changed for 45% of hospitals when comorbidity data was added, indicating a substantial impact on comparative performance.
  • The overall CLABSI rate in the study cohort was 0.2% (162 cases).

Conclusions:

  • Risk-adjustment models for CLABSI that utilize electronically available comorbidity data demonstrate superior discrimination compared to the current CDC model.
  • The findings strongly suggest that the CDC should consider integrating comorbidity-based risk adjustment to achieve more accurate and equitable comparisons of CLABSI rates across healthcare facilities.

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