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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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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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><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 & 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 & 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 & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical cardiology (Mahwah, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Xiaoyi</au><au>Yuan, Ping</au><au>Chen, Jun</au><au>Wang, Shang</au><au>Zhao, Hui</au><au>Wei, Yaqin</au><au>Fu, Jiaqi</au><au>Chen, Fadong</au><au>Ruan, Hongyun</au><au>Zhang, Wei</au><au>Zhou, Yanli</au><au>Wang, Qiqi</au><au>Xu, Xiaoling</au><au>Feng, Kefu</au><au>Guo, Jianzhou</au><au>Gong, Sugang</au><au>Zhang, Ruifeng</au><au>Zhao, Qinhua</au><au>Wang, Lan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of different sequential triple oral combination therapies based selexipag on outcomes in pulmonary arterial hypertension</atitle><jtitle>Clinical cardiology (Mahwah, N.J.)</jtitle><addtitle>Clin Cardiol</addtitle><date>2024-02</date><risdate>2024</risdate><volume>47</volume><issue>2</issue><spage>e24245</spage><epage>n/a</epage><pages>e24245-n/a</pages><issn>0160-9289</issn><eissn>1932-8737</eissn><abstract>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.</abstract><cop>United States</cop><pub>John Wiley & 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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source | MEDLINE; Wiley Online Library Open Access; DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
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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