Risk Score for Predicting 2‐Year Mortality in Patients With Chagas Cardiomyopathy From Endemic Areas: SaMi‐Trop Cohort Study

Author:

Di Lorenzo Oliveira Claudia1,Nunes Maria Carmo P.2,Colosimo Enrico Antonio3,de Lima Emilly Malveira3,Cardoso Clareci S.1,Ferreira Ariela Mota4,de Oliveira Lea Campos5,Moreira Carlos Henrique Valente5,Bierrenbach Ana Luiza6,Haikal Desireé Sant′Ana4,Peixoto Sérgio Viana7,Lima‐Costa Maria Fernanda7,Sabino Ester Cerdeira8,Ribeiro Antonio Luiz P.2

Affiliation:

1. Federal University of São João del‐Rei Divinópolis Brazil

2. Hospital das Clínicas and Faculdade de Medicina Universidade Federal de Minas Gerais Belo Horizonte Brazil

3. Department of Statistics Instituto de Ciência Exatas Universidade Federal de Minas Gerais Belo Horizonte Brazil

4. Health Science Program Universidade Estadual de Montes Claros Montes Claros Brazil

5. Laboratório de Investigação Médica (LIM03) Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo São Paulo Brazil

6. Research and Education Institute – Hospital Sírio‐Libanês São Paulo Brazil

7. Instituto de Pesquisas René Rachou Fundação Oswaldo Cruz Belo Horizonte Brazil

8. Instituto de Medicina Tropical e Departamento de Moléstias Infecciosas e Parasitarias da Faculdade de Medicina da Universidade de São Paulo São Paulo Brazil

Abstract

Background Risk stratification of Chagas disease patients in the limited‐resource setting would be helpful in crafting management strategies. We developed a score to predict 2‐year mortality in patients with Chagas cardiomyopathy from remote endemic areas. Methods and Results This study enrolled 1551 patients with Chagas cardiomyopathy from Minas Gerais State, Brazil, from the SaMi‐Trop cohort (The São Paulo‐Minas Gerais Tropical Medicine Research Center). Clinical evaluation, ECG, and NT ‐proBNP (N‐terminal pro‐B‐type natriuretic peptide) were performed. A Cox proportional hazards model was used to develop a prediction model based on the key predictors. The end point was all‐cause mortality. The patients were classified into 3 risk categories at baseline (low, <2%; intermediate, ≥2% to 10%; high, ≥10%). External validation was performed by applying the score to an independent population with Chagas disease. After 2 years of follow‐up, 110 patients died, with an overall mortality rate of 3.505 deaths per 100 person‐years. Based on the nomogram, the independent predictors of mortality were assigned points: age (10 points per decade), New York Heart Association functional class higher than I (15 points), heart rate ≥80 beats/min (20 points), QRS duration ≥150 ms (15 points), and abnormal NT ‐pro BNP adjusted by age (55 points). The observed mortality rates in the low‐, intermediate‐, and high‐risk groups were 0%, 3.6%, and 32.7%, respectively, in the derivation cohort and 3.2%, 8.7%, and 19.1%, respectively, in the validation cohort. The discrimination of the score was good in the development cohort (C statistic: 0.82), and validation cohort (C statistic: 0.71). Conclusions In a large population of patients with Chagas cardiomyopathy, a combination of risk factors accurately predicted early mortality. This helpful simple score could be used in remote areas with limited technological resources.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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