Skip to main content

Exploring comorbidities, triggers, and etiologies in heart failure. Insights from the SEPE registry subanalysis

Publication ,  Journal Article
Cristodulo, R; Espinoza, F; Vaca, C; Ureña, D; Rejas, IA; Rojas, J; Giorgi, J; Kaplinsky, E; Barbagelata, A
Published in: Rec Cardioclinics
January 1, 2025

Introduction and objectives Heart failure (HF) is a complex clinical syndrome characterized by a high burden of comorbidities and multiple underlying etiologies. This sub-analysis of the SEPE-Registry aimed to characterize the clinical profiles of hospitalized patients with HF and to analyze the incidence and association between etiologies, precipitating factors of decompensation and comorbidities. Methods A multicenter, cross-sectional study was conducted in Santa Cruz de la Sierra, Bolivia, including 418 patients hospitalized with a diagnosis of HF between January 2023 and April 2024. Results Hypertension was significantly associated with a higher prevalence of ischemic HF etiology (PR, 2.0; P = .001). Coronary artery disease was strongly associated with an ischemic etiology of HF (PR, 4.6; P < .001). Rheumatic HF etiology demonstrated a statistically significant inverse association with comorbidity. Chagas disease was the most prevalent HF etiology in the SEPE registry and was associated with a trend toward increased cardiovascular mortality, reaching borderline statistical significance (PR, 1.3; P = .052). Moreover, Chagasic HF showed a significant inverse association with hypertension (PR, 0.6; P = .001) but a higher prevalence of pacemakers (PR, 1.7; P = .001). The coexistence of Chagas disease and coronary artery disease within the same HF patient was statistically significant (χ 2: 15.0; P = .001) The overall cardiovascular mortality in HF patients on SEPE-HF Registry was founded as 5.5%. Conclusions HF exhibits significant clinical heterogeneity driven by the interplay between etiologies, comorbidities, and decompensating factors. The identification of distinct clinical profiles may support more personalized and effective treatment strategies.

Duke Scholars

Published In

Rec Cardioclinics

DOI

EISSN

2605-1575

ISSN

2605-1532

Publication Date

January 1, 2025
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Cristodulo, R., Espinoza, F., Vaca, C., Ureña, D., Rejas, I. A., Rojas, J., … Barbagelata, A. (2025). Exploring comorbidities, triggers, and etiologies in heart failure. Insights from the SEPE registry subanalysis. Rec Cardioclinics. https://doi.org/10.1016/j.rccl.2025.09.003
Cristodulo, R., F. Espinoza, C. Vaca, D. Ureña, I. A. Rejas, J. Rojas, J. Giorgi, E. Kaplinsky, and A. Barbagelata. “Exploring comorbidities, triggers, and etiologies in heart failure. Insights from the SEPE registry subanalysis.” Rec Cardioclinics, January 1, 2025. https://doi.org/10.1016/j.rccl.2025.09.003.
Cristodulo R, Espinoza F, Vaca C, Ureña D, Rejas IA, Rojas J, et al. Exploring comorbidities, triggers, and etiologies in heart failure. Insights from the SEPE registry subanalysis. Rec Cardioclinics. 2025 Jan 1;
Cristodulo, R., et al. “Exploring comorbidities, triggers, and etiologies in heart failure. Insights from the SEPE registry subanalysis.” Rec Cardioclinics, Jan. 2025. Scopus, doi:10.1016/j.rccl.2025.09.003.
Cristodulo R, Espinoza F, Vaca C, Ureña D, Rejas IA, Rojas J, Giorgi J, Kaplinsky E, Barbagelata A. Exploring comorbidities, triggers, and etiologies in heart failure. Insights from the SEPE registry subanalysis. Rec Cardioclinics. 2025 Jan 1;

Published In

Rec Cardioclinics

DOI

EISSN

2605-1575

ISSN

2605-1532

Publication Date

January 1, 2025