Impact of different sequential triple oral combination therapies based selexipag on outcomes in pulmonary arterial hypertension

Background While the GRIPHON study and others have confirmed the efficacy and safety of selexipag with single, dual, and initial triple combination therapy for patients with pulmonary arterial hypertension (PAH), multicenters studies concerning diverse triple oral combination therapies based on sele...

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Veröffentlicht in:Clinical cardiology (Mahwah, N.J.) N.J.), 2024-02, Vol.47 (2), p.e24245-n/a
Hauptverfasser: Hu, Xiaoyi, Yuan, Ping, Chen, Jun, Wang, Shang, Zhao, Hui, Wei, Yaqin, Fu, Jiaqi, Chen, Fadong, Ruan, Hongyun, Zhang, Wei, Zhou, Yanli, Wang, Qiqi, Xu, Xiaoling, Feng, Kefu, Guo, Jianzhou, Gong, Sugang, Zhang, Ruifeng, Zhao, Qinhua, Wang, Lan
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container_issue 2
container_start_page e24245
container_title Clinical cardiology (Mahwah, N.J.)
container_volume 47
creator Hu, Xiaoyi
Yuan, Ping
Chen, Jun
Wang, Shang
Zhao, Hui
Wei, Yaqin
Fu, Jiaqi
Chen, Fadong
Ruan, Hongyun
Zhang, Wei
Zhou, Yanli
Wang, Qiqi
Xu, Xiaoling
Feng, Kefu
Guo, Jianzhou
Gong, Sugang
Zhang, Ruifeng
Zhao, Qinhua
Wang, Lan
description Background While the GRIPHON study and others have confirmed the efficacy and safety of selexipag with single, dual, and initial triple combination therapy for patients with pulmonary arterial hypertension (PAH), multicenters studies concerning diverse triple oral combination therapies based on selexipag are limited. Hypothesis This study was conducted to evaluate the effects of various sequential triple oral combination therapies on PAH outcomes. Methods A retrospective study was carried out involving 192 patients from 10 centers, who were receiving sequential triple oral combination therapy consisting of an endothelin receptor antagonist (ERA), a phosphodiesterase 5 inhibitor (PDE5i)/riociguat and selexipag. Clinical parameters, event‐free survival, and all‐cause survival were assessed and analyzed at baseline and posttreatment. Results Among the 192 patients, 37 were treated with ERA + riociguat + selexipag, and 155 patients received ERA + PDE5i + selexipag. Both sequential triple oral combination therapies improved the World Health Organization functional class and raised the count of low‐risk parameters. As a result of the larger patients' population in the ERA + PDE5i + selexipag group, these individuals exhibited significant increases in 6‐minute walking distance (6MWD), pulmonary arterial systolic pressure, pulmonary arterial pressure, right ventricle, and eccentricity index, and significant decreases in N‐terminal probrain natriuretic peptide after 6 months of treatment. Nevertheless, both sequential triple oral combination therapy groups demonstrated similar shifts in these clinical parameters between baseline and 6 months. Baseline 6MWD and mean pulmonary arterial pressure were independent predictors of survival in patients undergoing ERA + PDE5i + selexipag therapy. Importantly, no significant differences were found in 6‐month event‐free survival and all‐cause survival between two groups. Conclusions Different oral sequential triple combination therapies based on selexipag could comparably improve outcomes in patients with PAH. Among the 192 pulmonary arterial hypertension patients, 37 were treated with endothelin receptor antagonist (ERA) + riociguat + selexipag, and 155 patients received ERA + phosphodiesterase 5 inhibitor + selexipag. Patients of various ages and genders were likely to be prescribed one of these six triple sequential oral combination therapies.
doi_str_mv 10.1002/clc.24245
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Hypothesis This study was conducted to evaluate the effects of various sequential triple oral combination therapies on PAH outcomes. Methods A retrospective study was carried out involving 192 patients from 10 centers, who were receiving sequential triple oral combination therapy consisting of an endothelin receptor antagonist (ERA), a phosphodiesterase 5 inhibitor (PDE5i)/riociguat and selexipag. Clinical parameters, event‐free survival, and all‐cause survival were assessed and analyzed at baseline and posttreatment. Results Among the 192 patients, 37 were treated with ERA + riociguat + selexipag, and 155 patients received ERA + PDE5i + selexipag. Both sequential triple oral combination therapies improved the World Health Organization functional class and raised the count of low‐risk parameters. As a result of the larger patients' population in the ERA + PDE5i + selexipag group, these individuals exhibited significant increases in 6‐minute walking distance (6MWD), pulmonary arterial systolic pressure, pulmonary arterial pressure, right ventricle, and eccentricity index, and significant decreases in N‐terminal probrain natriuretic peptide after 6 months of treatment. Nevertheless, both sequential triple oral combination therapy groups demonstrated similar shifts in these clinical parameters between baseline and 6 months. Baseline 6MWD and mean pulmonary arterial pressure were independent predictors of survival in patients undergoing ERA + PDE5i + selexipag therapy. Importantly, no significant differences were found in 6‐month event‐free survival and all‐cause survival between two groups. Conclusions Different oral sequential triple combination therapies based on selexipag could comparably improve outcomes in patients with PAH. Among the 192 pulmonary arterial hypertension patients, 37 were treated with endothelin receptor antagonist (ERA) + riociguat + selexipag, and 155 patients received ERA + phosphodiesterase 5 inhibitor + selexipag. Patients of various ages and genders were likely to be prescribed one of these six triple sequential oral combination therapies.</description><identifier>ISSN: 0160-9289</identifier><identifier>EISSN: 1932-8737</identifier><identifier>DOI: 10.1002/clc.24245</identifier><identifier>PMID: 38402556</identifier><language>eng</language><publisher>United States: John Wiley &amp; Sons, Inc</publisher><subject>Acetamides ; Blood pressure ; Body mass index ; Cardiovascular disease ; Clinical ; Congenital diseases ; Connective tissue diseases ; Ejection fraction ; Heart rate ; Hemodynamics ; Humans ; Medical prognosis ; Normal distribution ; oral sequential triple combination therapy ; Oxygen saturation ; Patients ; Peptides ; pulmonary arterial hypertension ; Pulmonary Arterial Hypertension - diagnosis ; Pulmonary Arterial Hypertension - drug therapy ; Pulmonary hypertension ; Pyrazines - adverse effects ; Retrospective Studies ; selexipag ; survival</subject><ispartof>Clinical cardiology (Mahwah, N.J.), 2024-02, Vol.47 (2), p.e24245-n/a</ispartof><rights>2024 The Authors. published by Wiley Periodicals, LLC.</rights><rights>2024 The Authors. Clinical Cardiology published by Wiley Periodicals, LLC.</rights><rights>2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4045-f72baffb14c5f678fceca4cebb1b5f7271d4a51dfeaa279a3f42f9a1cf5cceed3</cites><orcidid>0000-0002-8581-530X ; 0000-0003-1488-775X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10894617/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10894617/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1411,11541,27901,27902,45550,45551,46027,46451,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38402556$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Xiaoyi</creatorcontrib><creatorcontrib>Yuan, Ping</creatorcontrib><creatorcontrib>Chen, Jun</creatorcontrib><creatorcontrib>Wang, Shang</creatorcontrib><creatorcontrib>Zhao, Hui</creatorcontrib><creatorcontrib>Wei, Yaqin</creatorcontrib><creatorcontrib>Fu, Jiaqi</creatorcontrib><creatorcontrib>Chen, Fadong</creatorcontrib><creatorcontrib>Ruan, Hongyun</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Zhou, Yanli</creatorcontrib><creatorcontrib>Wang, Qiqi</creatorcontrib><creatorcontrib>Xu, Xiaoling</creatorcontrib><creatorcontrib>Feng, Kefu</creatorcontrib><creatorcontrib>Guo, Jianzhou</creatorcontrib><creatorcontrib>Gong, Sugang</creatorcontrib><creatorcontrib>Zhang, Ruifeng</creatorcontrib><creatorcontrib>Zhao, Qinhua</creatorcontrib><creatorcontrib>Wang, Lan</creatorcontrib><title>Impact of different sequential triple oral combination therapies based selexipag on outcomes in pulmonary arterial hypertension</title><title>Clinical cardiology (Mahwah, N.J.)</title><addtitle>Clin Cardiol</addtitle><description>Background While the GRIPHON study and others have confirmed the efficacy and safety of selexipag with single, dual, and initial triple combination therapy for patients with pulmonary arterial hypertension (PAH), multicenters studies concerning diverse triple oral combination therapies based on selexipag are limited. Hypothesis This study was conducted to evaluate the effects of various sequential triple oral combination therapies on PAH outcomes. Methods A retrospective study was carried out involving 192 patients from 10 centers, who were receiving sequential triple oral combination therapy consisting of an endothelin receptor antagonist (ERA), a phosphodiesterase 5 inhibitor (PDE5i)/riociguat and selexipag. Clinical parameters, event‐free survival, and all‐cause survival were assessed and analyzed at baseline and posttreatment. Results Among the 192 patients, 37 were treated with ERA + riociguat + selexipag, and 155 patients received ERA + PDE5i + selexipag. Both sequential triple oral combination therapies improved the World Health Organization functional class and raised the count of low‐risk parameters. As a result of the larger patients' population in the ERA + PDE5i + selexipag group, these individuals exhibited significant increases in 6‐minute walking distance (6MWD), pulmonary arterial systolic pressure, pulmonary arterial pressure, right ventricle, and eccentricity index, and significant decreases in N‐terminal probrain natriuretic peptide after 6 months of treatment. Nevertheless, both sequential triple oral combination therapy groups demonstrated similar shifts in these clinical parameters between baseline and 6 months. Baseline 6MWD and mean pulmonary arterial pressure were independent predictors of survival in patients undergoing ERA + PDE5i + selexipag therapy. Importantly, no significant differences were found in 6‐month event‐free survival and all‐cause survival between two groups. Conclusions Different oral sequential triple combination therapies based on selexipag could comparably improve outcomes in patients with PAH. Among the 192 pulmonary arterial hypertension patients, 37 were treated with endothelin receptor antagonist (ERA) + riociguat + selexipag, and 155 patients received ERA + phosphodiesterase 5 inhibitor + selexipag. Patients of various ages and genders were likely to be prescribed one of these six triple sequential oral combination therapies.</description><subject>Acetamides</subject><subject>Blood pressure</subject><subject>Body mass index</subject><subject>Cardiovascular disease</subject><subject>Clinical</subject><subject>Congenital diseases</subject><subject>Connective tissue diseases</subject><subject>Ejection fraction</subject><subject>Heart rate</subject><subject>Hemodynamics</subject><subject>Humans</subject><subject>Medical prognosis</subject><subject>Normal distribution</subject><subject>oral sequential triple combination therapy</subject><subject>Oxygen saturation</subject><subject>Patients</subject><subject>Peptides</subject><subject>pulmonary arterial hypertension</subject><subject>Pulmonary Arterial Hypertension - diagnosis</subject><subject>Pulmonary Arterial Hypertension - drug therapy</subject><subject>Pulmonary hypertension</subject><subject>Pyrazines - adverse effects</subject><subject>Retrospective Studies</subject><subject>selexipag</subject><subject>survival</subject><issn>0160-9289</issn><issn>1932-8737</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kU9v1DAQxS0EokvhwBdAlrjAIa3t2HFyQmjFn0orcYGz5TjjrisnDnZS2BNfnVm2VIDEaUZ6v3mamUfIc84uOGPi0kV3IaSQ6gHZ8K4WVatr_ZBsGG9Y1Ym2OyNPSrlBlLWifkzO6lYyoVSzIT-uxtm6hSZPh-A9ZJgWWuDrijXYSJcc5gg0ZexdGvsw2SWkiS57yHYOUGhvCww4EuF7mO01RTGtC7KohYnOaxzTZPOB2rxAPnruDzNgPxU0ekoeeRsLPLur5-TL-3eftx-r3acPV9u3u8pJJlXlteit9z2XTvlGt96Bs9JB3_Neoaj5IK3igwdrhe5s7aXwneXOK-cAhvqcvDn5zms_wuDwPDzJzDmMuJtJNpi_lSnszXW6NZy1nWy4RodXdw454XvKYsZQHMRoJ0hrMQIfz7judIPoy3_Qm7TmCe87UlxxrTVH6vWJcjmVksHfb8OZOeZqMFfzK1dkX_y5_j35O0gELk_AtxDh8H8ns91tT5Y_AWw7sl4</recordid><startdate>202402</startdate><enddate>202402</enddate><creator>Hu, Xiaoyi</creator><creator>Yuan, Ping</creator><creator>Chen, Jun</creator><creator>Wang, Shang</creator><creator>Zhao, Hui</creator><creator>Wei, Yaqin</creator><creator>Fu, Jiaqi</creator><creator>Chen, Fadong</creator><creator>Ruan, Hongyun</creator><creator>Zhang, Wei</creator><creator>Zhou, Yanli</creator><creator>Wang, Qiqi</creator><creator>Xu, Xiaoling</creator><creator>Feng, Kefu</creator><creator>Guo, Jianzhou</creator><creator>Gong, Sugang</creator><creator>Zhang, Ruifeng</creator><creator>Zhao, Qinhua</creator><creator>Wang, Lan</creator><general>John Wiley &amp; Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8581-530X</orcidid><orcidid>https://orcid.org/0000-0003-1488-775X</orcidid></search><sort><creationdate>202402</creationdate><title>Impact of different sequential triple oral combination therapies based selexipag on outcomes in pulmonary arterial hypertension</title><author>Hu, Xiaoyi ; Yuan, Ping ; Chen, Jun ; Wang, Shang ; Zhao, Hui ; Wei, Yaqin ; Fu, Jiaqi ; Chen, Fadong ; Ruan, Hongyun ; Zhang, Wei ; Zhou, Yanli ; Wang, Qiqi ; Xu, Xiaoling ; Feng, Kefu ; Guo, Jianzhou ; Gong, Sugang ; Zhang, Ruifeng ; Zhao, Qinhua ; Wang, Lan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4045-f72baffb14c5f678fceca4cebb1b5f7271d4a51dfeaa279a3f42f9a1cf5cceed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acetamides</topic><topic>Blood pressure</topic><topic>Body mass index</topic><topic>Cardiovascular disease</topic><topic>Clinical</topic><topic>Congenital diseases</topic><topic>Connective tissue diseases</topic><topic>Ejection fraction</topic><topic>Heart rate</topic><topic>Hemodynamics</topic><topic>Humans</topic><topic>Medical prognosis</topic><topic>Normal distribution</topic><topic>oral sequential triple combination therapy</topic><topic>Oxygen saturation</topic><topic>Patients</topic><topic>Peptides</topic><topic>pulmonary arterial hypertension</topic><topic>Pulmonary Arterial Hypertension - diagnosis</topic><topic>Pulmonary Arterial Hypertension - drug therapy</topic><topic>Pulmonary hypertension</topic><topic>Pyrazines - adverse effects</topic><topic>Retrospective Studies</topic><topic>selexipag</topic><topic>survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Xiaoyi</creatorcontrib><creatorcontrib>Yuan, Ping</creatorcontrib><creatorcontrib>Chen, Jun</creatorcontrib><creatorcontrib>Wang, Shang</creatorcontrib><creatorcontrib>Zhao, Hui</creatorcontrib><creatorcontrib>Wei, Yaqin</creatorcontrib><creatorcontrib>Fu, Jiaqi</creatorcontrib><creatorcontrib>Chen, Fadong</creatorcontrib><creatorcontrib>Ruan, Hongyun</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Zhou, Yanli</creatorcontrib><creatorcontrib>Wang, Qiqi</creatorcontrib><creatorcontrib>Xu, Xiaoling</creatorcontrib><creatorcontrib>Feng, Kefu</creatorcontrib><creatorcontrib>Guo, Jianzhou</creatorcontrib><creatorcontrib>Gong, Sugang</creatorcontrib><creatorcontrib>Zhang, Ruifeng</creatorcontrib><creatorcontrib>Zhao, Qinhua</creatorcontrib><creatorcontrib>Wang, Lan</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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Hypothesis This study was conducted to evaluate the effects of various sequential triple oral combination therapies on PAH outcomes. Methods A retrospective study was carried out involving 192 patients from 10 centers, who were receiving sequential triple oral combination therapy consisting of an endothelin receptor antagonist (ERA), a phosphodiesterase 5 inhibitor (PDE5i)/riociguat and selexipag. Clinical parameters, event‐free survival, and all‐cause survival were assessed and analyzed at baseline and posttreatment. Results Among the 192 patients, 37 were treated with ERA + riociguat + selexipag, and 155 patients received ERA + PDE5i + selexipag. Both sequential triple oral combination therapies improved the World Health Organization functional class and raised the count of low‐risk parameters. As a result of the larger patients' population in the ERA + PDE5i + selexipag group, these individuals exhibited significant increases in 6‐minute walking distance (6MWD), pulmonary arterial systolic pressure, pulmonary arterial pressure, right ventricle, and eccentricity index, and significant decreases in N‐terminal probrain natriuretic peptide after 6 months of treatment. Nevertheless, both sequential triple oral combination therapy groups demonstrated similar shifts in these clinical parameters between baseline and 6 months. Baseline 6MWD and mean pulmonary arterial pressure were independent predictors of survival in patients undergoing ERA + PDE5i + selexipag therapy. Importantly, no significant differences were found in 6‐month event‐free survival and all‐cause survival between two groups. Conclusions Different oral sequential triple combination therapies based on selexipag could comparably improve outcomes in patients with PAH. Among the 192 pulmonary arterial hypertension patients, 37 were treated with endothelin receptor antagonist (ERA) + riociguat + selexipag, and 155 patients received ERA + phosphodiesterase 5 inhibitor + selexipag. Patients of various ages and genders were likely to be prescribed one of these six triple sequential oral combination therapies.</abstract><cop>United States</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>38402556</pmid><doi>10.1002/clc.24245</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-8581-530X</orcidid><orcidid>https://orcid.org/0000-0003-1488-775X</orcidid><oa>free_for_read</oa></addata></record>
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subjects Acetamides
Blood pressure
Body mass index
Cardiovascular disease
Clinical
Congenital diseases
Connective tissue diseases
Ejection fraction
Heart rate
Hemodynamics
Humans
Medical prognosis
Normal distribution
oral sequential triple combination therapy
Oxygen saturation
Patients
Peptides
pulmonary arterial hypertension
Pulmonary Arterial Hypertension - diagnosis
Pulmonary Arterial Hypertension - drug therapy
Pulmonary hypertension
Pyrazines - adverse effects
Retrospective Studies
selexipag
survival
title Impact of different sequential triple oral combination therapies based selexipag on outcomes in pulmonary arterial hypertension
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