A Validated Transthyretin Amyloid Cardiomyopathy Claims-Based Coding Algorithm: ValidATTR-US

Lack of a validated United States (US) claims-based method for identifying transthyretin amyloid cardiomyopathy (ATTR-CM) limits the reliability and comparability of real-world evidence. We developed and validated a US claims-based coding algorithm (ValidATTR-US) to identify patients with ATTR-CM. ValidATTR-US was developed by optimizing previously published algorithms using International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) codes and refining them using the STAnford Research Repository (STARR, claims/electronic health record-linked database; N = 61,908) to define the index cohort ( n = 694). The Stanford ATTR-CM Patient Registry ( N = 634) served as the validation cohort for cross-referencing the index cohort. Index cohort inclusion criteria were age ≥ 60 years at diagnosis and ≥ 2 ATTR-CM diagnosis codes (ICD-10-CM, E85.[0, 1, 2, 4, 82]) on separate days and ≥ 2 cardiac-related codes or ≥ 1 tafamidis claim. Exclusion criteria were multiple myeloma (C90), light chain amyloidosis (E85.81), hematopoietic stem cell transplantation (Z94.84), and organ-limited amyloidosis (E85.4) when co-occurring with cerebral amyloid angiopathy (I68.0), end-stage renal disease (N18.6), or skin disorders (L99). Performance metrics included accuracy ({true positives [TPs] + true negatives [TNs]}/total sample), specificity (TNs/{TNs + false positives [FPs]}), and sensitivity (TPs/{TPs + false negatives [FNs]}). Accuracy was 99.51% (95% confidence interval [CI] 99.45–99.56%), specificity 99.70% (99.65–99.74%), and sensitivity 80.76% (77.47–83.76%) for detecting patients with ATTR-CM (TP, n = 512; TN, n = 61,092; FP, n = 182; FN, n = 122). Individual ICD-10-CM codes were strongly predictive of ATTR-CM case status (area under the curve [AUC] 0.84) and genotype classification (AUC 0.88). ValidATTR-US is the first US claims-based ATTR-CM coding algorithm validated against a clinically confirmed ATTR-CM registry. Broader application may improve identification of patients with ATTR-CM in real-world datasets and help characterize prevalence and treatment patterns. Graphical abstract available for this article.

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Journal
Cardiology and Therapy
Published
2026-11-10
DOI
https://doi.org/10.1007/s40119-026-00484-2
Primary Topic
Amyloidosis: Diagnosis, Treatment, Outcomes
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article
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article

A Validated Transthyretin Amyloid Cardiomyopathy Claims-Based Coding Algorithm: ValidATTR-US

Gracia Fahed, Margarita Udall, Hiroki Kitakata, Kevin Michael Alexander et al.
Cardiology and Therapy
Amyloidosis: Diagnosis, Treatment, Outcomes
article

A Validated Transthyretin Amyloid Cardiomyopathy Claims-Based Coding Algorithm: ValidATTR-US

Gracia Fahed, Margarita Udall, Hiroki Kitakata, Kevin Michael Alexander, Nixuan Cai, Isaiah C. Jimenez
article en

Abstract

Lack of a validated United States (US) claims-based method for identifying transthyretin amyloid cardiomyopathy (ATTR-CM) limits the reliability and comparability of real-world evidence. We developed and validated a US claims-based coding algorithm (ValidATTR-US) to identify patients with ATTR-CM. ValidATTR-US was developed by optimizing previously published algorithms using International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) codes and refining them using the STAnford Research Repository (STARR, claims/electronic health record-linked database; N = 61,908) to define the index cohort ( n = 694). The Stanford ATTR-CM Patient Registry ( N = 634) served as the validation cohort for cross-referencing the index cohort. Index cohort inclusion criteria were age ≥ 60 years at diagnosis and ≥ 2 ATTR-CM diagnosis codes (ICD-10-CM, E85.[0, 1, 2, 4, 82]) on separate days and ≥ 2 cardiac-related codes or ≥ 1 tafamidis claim. Exclusion criteria were multiple myeloma (C90), light chain amyloidosis (E85.81), hematopoietic stem cell transplantation (Z94.84), and organ-limited amyloidosis (E85.4) when co-occurring with cerebral amyloid angiopathy (I68.0), end-stage renal disease (N18.6), or skin disorders (L99). Performance metrics included accuracy ({true positives [TPs] + true negatives [TNs]}/total sample), specificity (TNs/{TNs + false positives [FPs]}), and sensitivity (TPs/{TPs + false negatives [FNs]}). Accuracy was 99.51% (95% confidence interval [CI] 99.45–99.56%), specificity 99.70% (99.65–99.74%), and sensitivity 80.76% (77.47–83.76%) for detecting patients with ATTR-CM (TP, n = 512; TN, n = 61,092; FP, n = 182; FN, n = 122). Individual ICD-10-CM codes were strongly predictive of ATTR-CM case status (area under the curve [AUC] 0.84) and genotype classification (AUC 0.88). ValidATTR-US is the first US claims-based ATTR-CM coding algorithm validated against a clinically confirmed ATTR-CM registry. Broader application may improve identification of patients with ATTR-CM in real-world datasets and help characterize prevalence and treatment patterns. Graphical abstract available for this article.

Cardiology and Therapy
BridgeBio (United States) (US), Stanford Medicine (US), Stanford Cardiovascular Institute (US), Stanford University (US)
Amyloidosis: Diagnosis, Treatment, Outcomes
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