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Haemodynamic effects of riociguat in CTEPH and PAH: a 10-year observational study

BACKGROUND: Long-term treatment with riociguat has been shown to enhance exercise capacity in patients with pulmonary arterial hypertension (PAH) and inoperable or persistent/recurrent chronic thromboembolic pulmonary hypertension (CTEPH). This study sought to evaluate the long-term haemodynamic eff...

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Autores principales: Yang, Suqiao, Yang, Yuanhua, Zhang, Yixiao, Kuang, Tuguang, Gong, Juanni, Li, Jifeng, Li, Yidan, Wang, Jianfeng, Guo, Xiaojuan, Miao, Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419318/
https://www.ncbi.nlm.nih.gov/pubmed/34513985
http://dx.doi.org/10.1183/23120541.00082-2021
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author Yang, Suqiao
Yang, Yuanhua
Zhang, Yixiao
Kuang, Tuguang
Gong, Juanni
Li, Jifeng
Li, Yidan
Wang, Jianfeng
Guo, Xiaojuan
Miao, Ran
author_facet Yang, Suqiao
Yang, Yuanhua
Zhang, Yixiao
Kuang, Tuguang
Gong, Juanni
Li, Jifeng
Li, Yidan
Wang, Jianfeng
Guo, Xiaojuan
Miao, Ran
author_sort Yang, Suqiao
collection PubMed
description BACKGROUND: Long-term treatment with riociguat has been shown to enhance exercise capacity in patients with pulmonary arterial hypertension (PAH) and inoperable or persistent/recurrent chronic thromboembolic pulmonary hypertension (CTEPH). This study sought to evaluate the long-term haemodynamic effects of riociguat in patients with PAH and inoperable CTEPH. METHODS: During this single-centre long-term observational study, riociguat was administered at a three-times-daily dose of up to 2.5 mg. The primary outcome was pulmonary vascular resistance (PVR). The secondary outcomes included mean pulmonary arterial pressure (PAP), cardiac index, mortality, clinical worsening events, 6-min walk distance (6MWD) and World Health Organization functional class (WHO FC). RESULTS: 37 patients (CTEPH n=19; PAH n=18) were included. The median follow-up period was 96 months. The survival estimates for all the patients at 1/3/5/8 years were 0.97/0.86/0.72/0.61, without significant differences between patients with CTEPH and PAH. At the final data cut-off, PVR decreased (1232±462 dyn·s·cm(–5) versus 835±348 dyn·s·cm(–5), p<0.001), cardiac index increased (1.7±0.4 L·min(−1)·m(−2) versus 2.4±0.5 L·min(−1)·m(−2), p<0.001), 6MWD increased by 43.1±59.6 m, and WHO FC improved/stabilised/worsened in 40%/35%/25% of patients versus baseline. Improvement in PAP was not shown. Compared with patients in WHO FC I/II and III/IV at baseline, the 8-year clinical worsening-free survival estimates were 0.51 versus 0.19 (p=0.026). CONCLUSIONS: Riociguat improved PVR and cardiac index for up to 8 years, but not PAP. WHO FC may have certain predictive value for the long-term prognosis.
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spelling pubmed-84193182021-09-09 Haemodynamic effects of riociguat in CTEPH and PAH: a 10-year observational study Yang, Suqiao Yang, Yuanhua Zhang, Yixiao Kuang, Tuguang Gong, Juanni Li, Jifeng Li, Yidan Wang, Jianfeng Guo, Xiaojuan Miao, Ran ERJ Open Res Original Research Articles BACKGROUND: Long-term treatment with riociguat has been shown to enhance exercise capacity in patients with pulmonary arterial hypertension (PAH) and inoperable or persistent/recurrent chronic thromboembolic pulmonary hypertension (CTEPH). This study sought to evaluate the long-term haemodynamic effects of riociguat in patients with PAH and inoperable CTEPH. METHODS: During this single-centre long-term observational study, riociguat was administered at a three-times-daily dose of up to 2.5 mg. The primary outcome was pulmonary vascular resistance (PVR). The secondary outcomes included mean pulmonary arterial pressure (PAP), cardiac index, mortality, clinical worsening events, 6-min walk distance (6MWD) and World Health Organization functional class (WHO FC). RESULTS: 37 patients (CTEPH n=19; PAH n=18) were included. The median follow-up period was 96 months. The survival estimates for all the patients at 1/3/5/8 years were 0.97/0.86/0.72/0.61, without significant differences between patients with CTEPH and PAH. At the final data cut-off, PVR decreased (1232±462 dyn·s·cm(–5) versus 835±348 dyn·s·cm(–5), p<0.001), cardiac index increased (1.7±0.4 L·min(−1)·m(−2) versus 2.4±0.5 L·min(−1)·m(−2), p<0.001), 6MWD increased by 43.1±59.6 m, and WHO FC improved/stabilised/worsened in 40%/35%/25% of patients versus baseline. Improvement in PAP was not shown. Compared with patients in WHO FC I/II and III/IV at baseline, the 8-year clinical worsening-free survival estimates were 0.51 versus 0.19 (p=0.026). CONCLUSIONS: Riociguat improved PVR and cardiac index for up to 8 years, but not PAP. WHO FC may have certain predictive value for the long-term prognosis. European Respiratory Society 2021-09-06 /pmc/articles/PMC8419318/ /pubmed/34513985 http://dx.doi.org/10.1183/23120541.00082-2021 Text en Copyright ©The authors 2021 https://creativecommons.org/licenses/by-nc/4.0/This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions@ersnet.org (mailto:permissions@ersnet.org)
spellingShingle Original Research Articles
Yang, Suqiao
Yang, Yuanhua
Zhang, Yixiao
Kuang, Tuguang
Gong, Juanni
Li, Jifeng
Li, Yidan
Wang, Jianfeng
Guo, Xiaojuan
Miao, Ran
Haemodynamic effects of riociguat in CTEPH and PAH: a 10-year observational study
title Haemodynamic effects of riociguat in CTEPH and PAH: a 10-year observational study
title_full Haemodynamic effects of riociguat in CTEPH and PAH: a 10-year observational study
title_fullStr Haemodynamic effects of riociguat in CTEPH and PAH: a 10-year observational study
title_full_unstemmed Haemodynamic effects of riociguat in CTEPH and PAH: a 10-year observational study
title_short Haemodynamic effects of riociguat in CTEPH and PAH: a 10-year observational study
title_sort haemodynamic effects of riociguat in cteph and pah: a 10-year observational study
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419318/
https://www.ncbi.nlm.nih.gov/pubmed/34513985
http://dx.doi.org/10.1183/23120541.00082-2021
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