Cardiovascular risk scores do not account for the effect of treatment: a review

S M Liew1, J Doust, P Glasziou

  • 1Department of Primary Care Medicine and Julius Center UM,University of Malaya, KualaLumpur, Malaysia. su.liew@phc.ox.ac.uk

Insights

This review found 21 cardiovascular risk scores, but most do not account for medications like statins or treatment changes. This limits their clinical use for predicting cardiovascular disease risk.

Area of Science:

  • Cardiology
  • Preventive Medicine
  • Biostatistics

Background:

  • Cardiovascular disease remains a leading cause of mortality globally.
  • Accurate assessment of cardiovascular risk is crucial for effective preventive strategies.
  • Numerous cardiovascular risk scores exist, but their clinical applicability and limitations require evaluation.

Purpose of the Study:

  • To compare the strengths and limitations of available cardiovascular risk scores.
  • To assess their utility in determining the absolute risk of cardiovascular disease for clinicians.

Main Methods:

  • A comprehensive review of cardiovascular risk scores was conducted.
  • Searched Medline (1966-2009) using keywords 'cardiovascular', 'risk prediction', and 'cohort studies'.
  • Included cohort studies of adults without prior cardiovascular disease, predicting 5-10 year absolute risk, usable by clinicians.

Main Results:

  • Identified 21 cardiovascular risk scores from 18 papers out of 3536 reviewed.
  • Cohort sizes varied significantly, from 4,372 to over 1.5 million participants.
  • Significant heterogeneity existed in definitions, risk predictors, and outcome measures. Most scores did not account for medication use (e.g., statins, antihypertensives) or treatment drop-ins.

Conclusions:

  • Current cardiovascular risk scores often fail to incorporate the impact of risk-factor-modifying drugs like statins.
  • The exclusion of treatment effects and variations in study design complicate clinical decision-making.
  • There is a need for risk scores derived from populations free from treatment bias to improve clinical utility.
Abstract

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