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Establishment and verification of a nomogram that predicts the risk for coronary slow flow.
Yu, Jiang; Ran, Yangshan; Yi, Dan; Yang, Chengyu; Zhou, Xiang; Wang, Sibin; Li, Hao; Yu, Wensi; Sun, Zhijun; Zhang, Zhengbo; Yan, Muyang.
Afiliación
  • Yu J; Department of Hyperbaric Oxygen, The First Medical Centre of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
  • Ran Y; Graduate School, Chinese People's Liberation Army Medical School, Beijing, China.
  • Yi D; Department of Internal Medicine, Xuanhan Chinese Medicine Hospital, Dazhou, Sichuan, China.
  • Yang C; Graduate School, Chinese People's Liberation Army Medical School, Beijing, China.
  • Zhou X; West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, China.
  • Wang S; Department of Hyperbaric Oxygen, The First Medical Centre of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
  • Li H; Graduate School, Chinese People's Liberation Army Medical School, Beijing, China.
  • Yu W; Department of Hyperbaric Oxygen, The First Medical Centre of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
  • Sun Z; Graduate School, Chinese People's Liberation Army Medical School, Beijing, China.
  • Zhang Z; Department of General Medicine, Zhige Township Hospital, Meishan, Sichuan, China.
  • Yan M; Graduate School, Guangxi University of Chinese Medicine, Nanning, Guangxi, China.
Front Endocrinol (Lausanne) ; 15: 1337284, 2024.
Article en En | MEDLINE | ID: mdl-38501108
ABSTRACT

Background:

Coronary slow flow (CSF) has gained significance as a chronic coronary artery disease, but few studies have integrated both biological and anatomical factors for CSF assessment. This study aimed to develop and validate a simple-to-use nomogram for predicting CSF risk by combining biological and anatomical factors.

Methods:

In this retrospective case-control study, 1042 patients (614 CSF cases and 428 controls) were randomly assigned to the development and validation cohorts at a 73 ratio. Potential predictive factors were identified using least absolute shrinkage and selection operator regression and subsequently utilized in multivariate logistic regression to construct the nomogram. Validation of the nomogram was assessed by discrimination and calibration.

Results:

N-terminal pro brain natriuretic peptide, high density lipoprotein cholesterol, hemoglobin, left anterior descending artery diameter, left circumflex artery diameter, and right coronary artery diameter were independent predictors of CSF. The model displayed high discrimination in the development and validation cohorts (C-index 0.771, 95% CI 0.737-0.805 and 0.805, 95% CI 0.757-0.853, respectively). The calibration curves for both cohorts showed close alignment between predicted and actual risk estimates, demonstrating improved model calibration. Decision curve analysis suggested high clinical utility for the predictive nomogram.

Conclusion:

The constructed nomogram accurately and individually predicts the risk of CSF for patients with suspected CSF and may be considered for use in clinical care.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenómenos Fisiológicos Cardiovasculares / Nomogramas Límite: Humans Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenómenos Fisiológicos Cardiovasculares / Nomogramas Límite: Humans Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza