Loading…
Severe cough and hemoptysis induced reopening of patent foramen ovale leading to significant decrease in pulmonary artery pressure in a patient with idiopathic pulmonary arterial hypertension: A case report
Pulmonary arterial hypertension (PAH) is a perilous disease that precipitates right ventricular hypertrophy, induces right heart failure, and exerts deleterious ramifications on prognostic outcomes. The establishment of atrial communication can create a right-to-left shunt, thereby ameliorating hemo...
Saved in:
Published in: | Heliyon 2024-02, Vol.10 (3), p.e25386, Article e25386 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c449t-6f851ea6297e02a4febe6e4bd082ce04cc67a5483879a1755f9a6af893255f5e3 |
container_end_page | |
container_issue | 3 |
container_start_page | e25386 |
container_title | Heliyon |
container_volume | 10 |
creator | Wang, Li-Li Xu, Bing Yu, Xiao-Qing Zhang, Duan-Zhen |
description | Pulmonary arterial hypertension (PAH) is a perilous disease that precipitates right ventricular hypertrophy, induces right heart failure, and exerts deleterious ramifications on prognostic outcomes. The establishment of atrial communication can create a right-to-left shunt, thereby ameliorating hemodynamic parameters. Previous reports suggested that opening of a patent foramen ovale (PFO) was common in patients with severe PAH, but exhibited no discernible impact on long-term survival. We reported the case of a 39-year-old man with severe idiopathic PAH, who underwent reopening of the PFO due to severe cough and hemoptysis, followed by a marked amelioration in symptoms and a substantial decrease in pulmonary arterial pressure. The patient has survived for more than 12 years, persisting in World Health Organization functional class Ⅱ with mild PAH. |
doi_str_mv | 10.1016/j.heliyon.2024.e25386 |
format | article |
fullrecord | <record><control><sourceid>elsevier_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_4443446c8030453faade486c0615df87</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2405844024014178</els_id><doaj_id>oai_doaj_org_article_4443446c8030453faade486c0615df87</doaj_id><sourcerecordid>S2405844024014178</sourcerecordid><originalsourceid>FETCH-LOGICAL-c449t-6f851ea6297e02a4febe6e4bd082ce04cc67a5483879a1755f9a6af893255f5e3</originalsourceid><addsrcrecordid>eNqFklFu1DAQhiMEolXpEUC-wG7txHacJ1RVQCtV4gF4tmbt8carrB3Z2UV7Fc7SQ3ATroDTLaXlhSePZvx_Mx7_VfWW0SWjTF5slj0O_hDDsqY1X2ItGiVfVKc1p2KhOKcvn8Qn1XnOG0opE0p2bfO6OmlUU7ectafVzy-4x4TExN26JxAs6XEbx-mQfSY-2J1BSxLGEYMPaxIdGWHCMBEXE2wxkLiHAcmAYOf6FEn26-CdN1AuWTQJIWMhkXE3bGOAdCCQJizHmDDnXbovwoz1M_e7n3rirY8l0Xvzr8zDQPrDiCUO2cfw6-4HuSRm7pFwjGl6U71yMGQ8fzjPqm8fP3y9ul7cfv50c3V5uzCcd9NCOiUYgqy7FmkN3OEKJfKVpao2SLkxsgXBVaPaDlgrhOtAglNdU5dYYHNW3Ry5NsJGj8lvy4w6gtf3iZjWugzszYCac95wLo2iDeWicQAWuZKGSiasU21hvT-yxt1qi9aUPSQYnkGfV4Lv9TruNaOKt5KzQhBHgkkx54TuUcyoni2jN_rBMnq2jD5apujePe38qPpjkL-jYdnl3mPS2ZR_Kq7wCc1UHuv_0-I32ULeRw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Severe cough and hemoptysis induced reopening of patent foramen ovale leading to significant decrease in pulmonary artery pressure in a patient with idiopathic pulmonary arterial hypertension: A case report</title><source>Open Access: PubMed Central</source><source>ScienceDirect (Online service)</source><creator>Wang, Li-Li ; Xu, Bing ; Yu, Xiao-Qing ; Zhang, Duan-Zhen</creator><creatorcontrib>Wang, Li-Li ; Xu, Bing ; Yu, Xiao-Qing ; Zhang, Duan-Zhen</creatorcontrib><description>Pulmonary arterial hypertension (PAH) is a perilous disease that precipitates right ventricular hypertrophy, induces right heart failure, and exerts deleterious ramifications on prognostic outcomes. The establishment of atrial communication can create a right-to-left shunt, thereby ameliorating hemodynamic parameters. Previous reports suggested that opening of a patent foramen ovale (PFO) was common in patients with severe PAH, but exhibited no discernible impact on long-term survival. We reported the case of a 39-year-old man with severe idiopathic PAH, who underwent reopening of the PFO due to severe cough and hemoptysis, followed by a marked amelioration in symptoms and a substantial decrease in pulmonary arterial pressure. The patient has survived for more than 12 years, persisting in World Health Organization functional class Ⅱ with mild PAH.</description><identifier>ISSN: 2405-8440</identifier><identifier>EISSN: 2405-8440</identifier><identifier>DOI: 10.1016/j.heliyon.2024.e25386</identifier><identifier>PMID: 38327417</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Case Report ; Hemoptysis ; Patent foramen ovale ; Pulmonary arterial hypertension</subject><ispartof>Heliyon, 2024-02, Vol.10 (3), p.e25386, Article e25386</ispartof><rights>2024 The Authors</rights><rights>2024 The Authors. Published by Elsevier Ltd.</rights><rights>2024 The Authors. Published by Elsevier Ltd. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c449t-6f851ea6297e02a4febe6e4bd082ce04cc67a5483879a1755f9a6af893255f5e3</cites><orcidid>0000-0002-3415-7343</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/PMC10847641/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2405844024014178$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3549,27924,27925,45780,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38327417$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Li-Li</creatorcontrib><creatorcontrib>Xu, Bing</creatorcontrib><creatorcontrib>Yu, Xiao-Qing</creatorcontrib><creatorcontrib>Zhang, Duan-Zhen</creatorcontrib><title>Severe cough and hemoptysis induced reopening of patent foramen ovale leading to significant decrease in pulmonary artery pressure in a patient with idiopathic pulmonary arterial hypertension: A case report</title><title>Heliyon</title><addtitle>Heliyon</addtitle><description>Pulmonary arterial hypertension (PAH) is a perilous disease that precipitates right ventricular hypertrophy, induces right heart failure, and exerts deleterious ramifications on prognostic outcomes. The establishment of atrial communication can create a right-to-left shunt, thereby ameliorating hemodynamic parameters. Previous reports suggested that opening of a patent foramen ovale (PFO) was common in patients with severe PAH, but exhibited no discernible impact on long-term survival. We reported the case of a 39-year-old man with severe idiopathic PAH, who underwent reopening of the PFO due to severe cough and hemoptysis, followed by a marked amelioration in symptoms and a substantial decrease in pulmonary arterial pressure. The patient has survived for more than 12 years, persisting in World Health Organization functional class Ⅱ with mild PAH.</description><subject>Case Report</subject><subject>Hemoptysis</subject><subject>Patent foramen ovale</subject><subject>Pulmonary arterial hypertension</subject><issn>2405-8440</issn><issn>2405-8440</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNqFklFu1DAQhiMEolXpEUC-wG7txHacJ1RVQCtV4gF4tmbt8carrB3Z2UV7Fc7SQ3ATroDTLaXlhSePZvx_Mx7_VfWW0SWjTF5slj0O_hDDsqY1X2ItGiVfVKc1p2KhOKcvn8Qn1XnOG0opE0p2bfO6OmlUU7ectafVzy-4x4TExN26JxAs6XEbx-mQfSY-2J1BSxLGEYMPaxIdGWHCMBEXE2wxkLiHAcmAYOf6FEn26-CdN1AuWTQJIWMhkXE3bGOAdCCQJizHmDDnXbovwoz1M_e7n3rirY8l0Xvzr8zDQPrDiCUO2cfw6-4HuSRm7pFwjGl6U71yMGQ8fzjPqm8fP3y9ul7cfv50c3V5uzCcd9NCOiUYgqy7FmkN3OEKJfKVpao2SLkxsgXBVaPaDlgrhOtAglNdU5dYYHNW3Ry5NsJGj8lvy4w6gtf3iZjWugzszYCac95wLo2iDeWicQAWuZKGSiasU21hvT-yxt1qi9aUPSQYnkGfV4Lv9TruNaOKt5KzQhBHgkkx54TuUcyoni2jN_rBMnq2jD5apujePe38qPpjkL-jYdnl3mPS2ZR_Kq7wCc1UHuv_0-I32ULeRw</recordid><startdate>20240215</startdate><enddate>20240215</enddate><creator>Wang, Li-Li</creator><creator>Xu, Bing</creator><creator>Yu, Xiao-Qing</creator><creator>Zhang, Duan-Zhen</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3415-7343</orcidid></search><sort><creationdate>20240215</creationdate><title>Severe cough and hemoptysis induced reopening of patent foramen ovale leading to significant decrease in pulmonary artery pressure in a patient with idiopathic pulmonary arterial hypertension: A case report</title><author>Wang, Li-Li ; Xu, Bing ; Yu, Xiao-Qing ; Zhang, Duan-Zhen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c449t-6f851ea6297e02a4febe6e4bd082ce04cc67a5483879a1755f9a6af893255f5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Case Report</topic><topic>Hemoptysis</topic><topic>Patent foramen ovale</topic><topic>Pulmonary arterial hypertension</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Li-Li</creatorcontrib><creatorcontrib>Xu, Bing</creatorcontrib><creatorcontrib>Yu, Xiao-Qing</creatorcontrib><creatorcontrib>Zhang, Duan-Zhen</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Heliyon</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Li-Li</au><au>Xu, Bing</au><au>Yu, Xiao-Qing</au><au>Zhang, Duan-Zhen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Severe cough and hemoptysis induced reopening of patent foramen ovale leading to significant decrease in pulmonary artery pressure in a patient with idiopathic pulmonary arterial hypertension: A case report</atitle><jtitle>Heliyon</jtitle><addtitle>Heliyon</addtitle><date>2024-02-15</date><risdate>2024</risdate><volume>10</volume><issue>3</issue><spage>e25386</spage><pages>e25386-</pages><artnum>e25386</artnum><issn>2405-8440</issn><eissn>2405-8440</eissn><abstract>Pulmonary arterial hypertension (PAH) is a perilous disease that precipitates right ventricular hypertrophy, induces right heart failure, and exerts deleterious ramifications on prognostic outcomes. The establishment of atrial communication can create a right-to-left shunt, thereby ameliorating hemodynamic parameters. Previous reports suggested that opening of a patent foramen ovale (PFO) was common in patients with severe PAH, but exhibited no discernible impact on long-term survival. We reported the case of a 39-year-old man with severe idiopathic PAH, who underwent reopening of the PFO due to severe cough and hemoptysis, followed by a marked amelioration in symptoms and a substantial decrease in pulmonary arterial pressure. The patient has survived for more than 12 years, persisting in World Health Organization functional class Ⅱ with mild PAH.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>38327417</pmid><doi>10.1016/j.heliyon.2024.e25386</doi><orcidid>https://orcid.org/0000-0002-3415-7343</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2405-8440 |
ispartof | Heliyon, 2024-02, Vol.10 (3), p.e25386, Article e25386 |
issn | 2405-8440 2405-8440 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_4443446c8030453faade486c0615df87 |
source | Open Access: PubMed Central; ScienceDirect (Online service) |
subjects | Case Report Hemoptysis Patent foramen ovale Pulmonary arterial hypertension |
title | Severe cough and hemoptysis induced reopening of patent foramen ovale leading to significant decrease in pulmonary artery pressure in a patient with idiopathic pulmonary arterial hypertension: A case report |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T23%3A35%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Severe%20cough%20and%20hemoptysis%20induced%20reopening%20of%20patent%20foramen%20ovale%20leading%20to%20significant%20decrease%20in%20pulmonary%20artery%20pressure%20in%20a%20patient%20with%20idiopathic%20pulmonary%20arterial%20hypertension%EF%BC%9A%20A%20case%20report&rft.jtitle=Heliyon&rft.au=Wang,%20Li-Li&rft.date=2024-02-15&rft.volume=10&rft.issue=3&rft.spage=e25386&rft.pages=e25386-&rft.artnum=e25386&rft.issn=2405-8440&rft.eissn=2405-8440&rft_id=info:doi/10.1016/j.heliyon.2024.e25386&rft_dat=%3Celsevier_doaj_%3ES2405844024014178%3C/elsevier_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c449t-6f851ea6297e02a4febe6e4bd082ce04cc67a5483879a1755f9a6af893255f5e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/38327417&rfr_iscdi=true |