Development and Evaluation of a Prediction Model for Ascertaining Rheumatic Heart Disease Status in Administrative

D Bond-Smith1, R Seth1, N de Klerk1,2

  • 1School of Population and Global Health, The University of Western Australia, Perth, Australia.

Clinical Epidemiology
|August 6, 2020
PubMed

Insights

A new model accurately identifies rheumatic heart disease (RHD) in hospital data, significantly reducing misclassification errors from other heart conditions. This improves RHD surveillance and policy evaluation.

Area of Science:

  • Cardiology
  • Public Health
  • Health Informatics

Background:

  • Concerns exist regarding the accuracy of International Statistical Classification of Diseases (ICD) codes for rheumatic heart disease (RHD).
  • Misclassification of non-rheumatic valvular disease (non-rheumatic VHD) as RHD is a significant issue in administrative hospital data.
  • A validated, quantitative method for RHD case ascertainment in hospital records is lacking.

Purpose of the Study:

  • To develop and validate a predictive model for accurate RHD case ascertainment in administrative hospital data.
  • To address and reduce false-positive rates caused by misclassified non-rheumatic VHD and acute rheumatic fever (ARF).

Main Methods:

  • A dataset of validated Australian RHD cases was linked to inpatient hospital records (2000-2018).
  • A generalized linear mixed model was developed using demographic and clinical variables.
  • Internal and external validation was performed, calculating conditional optimal probability cutpoints.

Main Results:

  • The model reduced the false-positive rate for non-rheumatic VHD misclassified as RHD from 0.77 to 0.22.
  • It also reduced the false-positive rate for acute rheumatic fever (ARF) misclassified as RHD from 0.59 to 0.27.
  • The model demonstrated strong discriminant capacity (AUC: 0.93 internally, 0.88 externally) and can function with basic data.

Conclusions:

  • Misclassification of non-rheumatic VHD and ARF as RHD leads to substantial false-positive rates.
  • The proposed model effectively addresses these biases, offering a reliable solution for RHD case ascertainment.
  • This facilitates improved epidemiological disease monitoring and policy evaluation for RHD.
Abstract

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