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Developing and optimizing a computable phenotype for incident venous thromboembolism in a longitudinal cohort of patients with cancer.
Li, Ang; da Costa, Wilson L; Guffey, Danielle; Milner, Emily M; Allam, Anthony K; Kurian, Karen M; Novoa, Francisco J; Poche, Marguerite D; Bandyo, Raka; Granada, Carolina; Wallace, Courtney D; Zakai, Neil A; Amos, Christopher I.
Afiliação
  • Li A; Section of Hematology-Oncology Baylor College of Medicine Houston Texas USA.
  • da Costa WL; Section of Epidemiology and Population Science Baylor College of Medicine Houston Texas USA.
  • Guffey D; Institute for Clinical and Translational Research Baylor College of Medicine Houston Texas USA.
  • Milner EM; School of Medicine Baylor College of Medicine Houston Texas USA.
  • Allam AK; School of Medicine Baylor College of Medicine Houston Texas USA.
  • Kurian KM; School of Medicine Baylor College of Medicine Houston Texas USA.
  • Novoa FJ; School of Medicine Baylor College of Medicine Houston Texas USA.
  • Poche MD; School of Medicine Baylor College of Medicine Houston Texas USA.
  • Bandyo R; Bluetree Network Inc Madison Wisconsin USA.
  • Granada C; Harris Health System Houston Texas USA.
  • Wallace CD; Section of Hematology-Oncology Baylor College of Medicine Houston Texas USA.
  • Zakai NA; Harris Health System Houston Texas USA.
  • Amos CI; Departments of Medicine and Pathology and Laboratory Medicine Larner College of Medicine at the University of Vermont Burlington Vermont USA.
Res Pract Thromb Haemost ; 6(4): e12733, 2022 May.
Article em En | MEDLINE | ID: mdl-35647478
ABSTRACT

Background:

Research on venous thromboembolism (VTE) that relies only on the International Classification of Diseases (ICD) can misclassify outcomes. Our study aims to discover and validate an improved VTE computable phenotype for people with cancer.

Methods:

We used a cancer registry electronic health record (EHR)-linked longitudinal database. We derived three algorithms that were ICD/medication based, natural language processing (NLP) based, or all combined. We then randomly sampled 400 patients from patients with VTE codes (n = 1111) and 400 from those without VTE codes (n = 7396). Weighted sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were calculated on the entire sample using inverse probability weighting, followed by bootstrapped receiver operating curve analysis to calculate the concordance statistic (c statistic).

Results:

Among 800 patients sampled, 280 had a confirmed acute VTE during the first year after cancer diagnosis. The ICD/medication algorithm had a weighted PPV of 95% and a weighted sensitivity of 81%, with a c statistic of 0.90 (95% confidence interval [CI], 0.89-0.91). Adding Current Procedural Terminology codes for inferior vena cava filter removal or early death did not improve the performance. The NLP algorithm had a weighted PPV of 80% and a weighted sensitivity of 90%, with a c statistic of 0.93 (95% CI, 0.92-0.94). The combined algorithm had a weighted PPV of 98% at the higher cutoff and a weighted sensitivity of 96% at the lower cutoff, with a c statistic of 0.98 (95% CI, 0.97-0.98).

Conclusions:

Our ICD/medication-based algorithm can accurately identify VTE phenotype among patients with cancer with a high PPV of 95%. The combined algorithm should be considered in EHR databases that have access to such capabilities.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article