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Risk prediction in medically treated chronic thromboembolic pulmonary hypertension

BACKGROUND: At present, there is no generally accepted comprehensive prognostic risk prediction model for medically treated chronic thromboembolic pulmonary hypertension (CTEPH) patients. METHODS: Consecutive medically treated CTEPH patients were enrolled in a national multicenter prospective regist...

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Detalles Bibliográficos
Autores principales: Quan, Ruilin, Yang, Yuanhua, Yang, Zhenwen, Tian, Hongyan, Li, Shengqing, Shen, Jieyan, Ji, Yingqun, Zhang, Gangcheng, Zhang, Caojin, Wang, Guangyi, Liu, Yuhao, Cheng, Zhaozhong, Yu, Zaixin, Song, Zhiyuan, Zheng, Zeqi, Cui, Wei, Chen, Yucheng, Liu, Shuang, Chen, Xiaoxi, Qian, Yuling, Xiong, Changming, Shan, Guangliang, He, Jianguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056726/
https://www.ncbi.nlm.nih.gov/pubmed/33879094
http://dx.doi.org/10.1186/s12890-021-01495-6
Descripción
Sumario:BACKGROUND: At present, there is no generally accepted comprehensive prognostic risk prediction model for medically treated chronic thromboembolic pulmonary hypertension (CTEPH) patients. METHODS: Consecutive medically treated CTEPH patients were enrolled in a national multicenter prospective registry study from August 2009 to July 2018. A multivariable Cox proportional hazards model was utilized to derive the prognostic model, and a simplified risk score was created thereafter. Model performance was evaluated in terms of discrimination and calibration, and compared to the Swedish/COMPERA risk stratification method. Internal and external validation were conducted to validate the model performance. RESULTS: A total of 432 patients were enrolled. During a median follow-up time of 38.73 months (IQR: 20.79, 66.10), 94 patients (21.8%) died. The 1-, 3-, and 5-year survival estimates were 95.5%, 83.7%, and 70.9%, respectively. The final model included the following variables: the Swedish/COMPERA risk stratum (low-, intermediate- or high-risk stratum), pulmonary vascular resistance (PVR, ≤ or > 1600 dyn·s/cm(5)), total bilirubin (TBIL, ≤ or > 38 µmol/L) and chronic kidney disease (CKD, no or yes). Compared with the Swedish/COMPERA risk stratification method alone, both the derived model [C-index: 0.715; net reclassification improvement (NRI): 0.300; integrated discriminatory index (IDI): 0.095] and the risk score (C-index: 0.713; NRI: 0.300; IDI: 0.093) showed improved discriminatory power. The performance was validated in a validation cohort of 84 patients (C-index = 0.707 for the model and 0.721 for the risk score). CONCLUSIONS: A novel risk stratification strategy can serve as a useful tool for determining prognosis and guide management for medically treated CTEPH patients. Trial registration: ClinicalTrials.gov (Identifier: NCT01417338). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-021-01495-6.